Programme at a Glance
Programme a Glance Programme atat a Glance
Thursday Thursday 19 19 September September
S1
WG1
WG2
WG3
WG4
Gold [14]
Brown 1 [15]
Brown 3 [16]
Amber 3 [17]
Space 1+2 [18] Space 3 [19]
Safety and Bone and Appropriateness Growth Plate of GH (BGP) Treatment in Europe (SAGhE)
Obesity (O)
Global Paediatric Endocrinology and Diabetes (GPED)
Paediatric and Adolescent Gynaecology (PAG): Hyperinsulinaemic Androgen Excess (PCOS) in Adolescents
WG5
WG6
Turner Syndrome (TS): Controversies on the Care of TS
Disorders of Sex Development (DSD): Information and Communication in the Context of DSD
Space 4 [20]
LUNCH
POSTER AND EXHIBITION
07:30 07:45 08:00 08:15 08:30 08:45 09:00 09:15 09:30 09:45 10:00 10:15 10:30 10:45 11:00 11:15 11:30 11:45 12:00 12:15 12:30 12:45 13:00 13:10 13:30 13:40 14:00 14:10 14:15 14:45 15:00 15:15 15:30 15:45 16:00 16:15 16:30 16:45 17:00 17:15 17:30 17:45 18:00 18:15 18:30 18:45 19:00 19:15 19:30 19:45 20:00
Opening Ceremony Gold [21] PL1 Stem Cell-derived Islet Cells for Transplantation – PES Gold [21] PL2 Prevention of Type 1 Diabetes in Children – ESPE Gold [21] COFFEE BREAK. Visit to the Posters and Exhibition Area Guided Poster Tours 14:20–15:20 – P1-d1, P2-d1 [80]
S2
S3
CPE1
S4
Gold [22]
Brown 1 [22]
Brown 3 [23]
Space 1+2 [23]
Gender Identity and Behaviour
Rare Forms of Diabetes: the Euro-WABB Project
Diagnosis and Treatment of Early Puberty
Congenital Hypothyroidism Revisited
S5
Hypoglycaemia in Children with Diabetes – ISPAD/ESPE Space 3 [24]
SAT1
SAT2
SAT3
Gold [26]
Brown 3 [26]
Space 4 [27]
Optimising Therapy in Children with Growth Disorders from Diagnosis to Adult Height: Case Study Debate Sponsored by Novo Nordisk
Taking GH Therapy to New Frontiers Sponsored by Merck Serono
S6
Rare Diseases – Epigenetic Mechanisms Space 4 [25]
Is It Hypophosphatasia or Osteogenesis Imperfecta? Clarifying the Diagnostic Approach to Challenging Patient Cases Sponsored by Alexion
Welcome Reception in the Exhibition Hall
[242]
CPE = Controversies in Paediatric Endocrinology FC = Free Communication Session MTE = Meet the Expert NP = New Perspectives PL = Plenary Lecture
S = Symposium S = Meeting Theme Symposium SAT = Joint Meeting Satellite Symposium WG = Joint Meeting Working Group YB = Yearbook of Paediatric Endocrinology
Rooms and Halls in italics [Page in Final Programme]
9th Joint Meeting of Paediatric Endocrinology 2013
1
Friday 20 20 September September Friday 07:30 07:45 08:00 08:15 08:30 08:45 09:00 09:15 09:30 09:45 10:00 10:15 10:30 10:45 11:00 11:15 11:30 11:45 12:00 12:15 12:30 12:45 13:00 13:15 13:30 13:45 14:00 14:15 14:30 14:45 15:00 15:15 15:30 15:45 16:00 16:15 16:30 16:45 17:00 17:15 17:30 17:45 18:00 18:15 18:30 18:45 19:00 19:15 19:30
NP1
Imaging in Paediatric Endocrinology Gold [30]
YB1
Yearbook of Paediatric Endocrinology Gold [35]
MTE1:1
Molecular Diagnosis and Management of Hereditary Gynaecomastia Brown 1 [30]
MTE4:1
Beta-Cell Dysfunction of the Newborn Brown 1 [35]
MTE2:1
FC1
FC3
Space 1+2 [33]
Space 3 [34]
FC4
MTE5:1
MTE6:1
FC5
FC6
Brown 3 [36]
Amber 3 [37]
Amber 4 [37]
Space 1+2 [38]
Space 3 [39]
Controversies in the Management of Hyperthyroidism in Children and Adolescents
Puberty
Pituitary Adenoma and Incidentaloma Amber 4 [32]
FC2
Brown 3 [31]
Endocrine Issues in Boys and Adolescents with Klinefelter Syndrome
Bone and Growth Plate
Programming and Epigenetics
Growth
Glucose Metabolism
PL3 Programming Effects of Early Life Adversity – APPES Gold [40]
PL4
Joint Meeting Award Session 1
Gold [40]
PL5 Novel Therapy for the Metabolic Complications of Obesity – JSPE Gold [41]
LUNCH. Visit to the Posters and Exhibition Area Guided Poster Tours 13:00–14:00 – P1-d2, P2-d2 [81]
S7
CPE2
S8
S9
S10
Gold [41]
Brown 3 [42]
Space 1+2 [43]
Space 3 [44]
Space 4 [44]
Vitamin D in Health and Disease
Idiopathic Short Stature: To Treat or Not To Treat?
The Adipose Organ: All Fat Is Not Created Equal
The Testis in 3D Endocrine Tumours (Development, Descent, in Childhood Dysfunction)
COFFEE BREAK. Visit to the Posters and Exhibition Area Business Meeting SLEP
Business Meeting ESPE
Brown 1 [45]
Space 3 [45]
SAT4
SAT5
SAT6
Gold [45]
Space 1+2 [45]
Space 4 [45]
What’s New in Adrenal Disorders Sponsored by Sandoz
Practical Application of Personalised Medicine in Paediatric and Adolescent Endocrinology Sponsored by Pfizer Specialty Care
CPE = Controversies in Paediatric Endocrinology FC = Free Communication Session MTE = Meet the Expert NP = New Perspectives PL = Plenary Lecture Rooms and Halls in italics [Page in Final Programme]
2
MTE3:1
Type 1 Diabetes in Preschool Children Amber 3 [32]
Gonads and Gynaecology
COFFEE BREAK. Visit to the Posters and Exhibition Area
POSTER AND EXHIBITION
Programme at a Glance
Programme at a Glance
Programme at a Glance
9th Joint Meeting of Paediatric Endocrinology 2013
SHOX-ing News about Growth: Updates on Genetics, Clinical Characteristics and Treatment of Children with SHOX Deficiency Sponsored by Eli Lilly and Company
S = Symposium S = Meeting Theme Symposium SAT = Joint Meeting Satellite Symposium WG = Joint Meeting Working Group YB = Yearbook of Paediatric Endocrinology
Programme at a Glance
Programme a Glance Programme atat a Glance
Saturday Saturday 21 21 September September MTE1:2
Molecular Diagnosis and Management of Hereditary Gynaecomastia
Brown 1 [48]
FC7
GH and IGF in Health and Disease Brown 3 [48]
MTE3:2
Pituitary Adenoma and Incidentaloma Amber 3 [49]
MTE4:2
Beta-Cell Dysfunction of the Newborn Amber 4 [49]
FC8
FC9
Space 1+2 [50]
Space 3 [51]
Disorders of Sex Differentiation
Adrenal Steroidogenesis
MTE2:2
Type 1 Diabetes in Preschool Children Space 4 [52]
PL6 Long-term Follow-up of Patients with Disorders of Sex Development – SLEP “Cesar Bergadá Lecture“ Gold [52]
PL7
Joint Meeting Award Session 2 Gold [52]
PL8 The Nature of Nutrition: an Integrative Framework from Animal Adaptation to Human Obesity – APEG Gold [52]
COFFEE BREAK. Visit to the Posters and Exhibition Area POSTER AND EXHIBITION
07:30 07:45 08:00 08:15 08:30 08:45 09:00 09:15 09:30 09:45 10:00 10:15 10:30 10:45 11:00 11:15 11:30 11:45 12:00 12:15 12:30 12:45 13:00 13:15 13:30 13:45 14:00 14:15 14:30 14:45 15:00 15:15 15:30 15:45 16:00 16:15 16:30 16:45 17:00 17:15 17:30 17:45 18:00 18:15 18:30 18:45 19:00 19:15 19:30 19:45 20:00 20:15
MTE7:1
FC10
MTE8:1
Brown 1 [52]
Brown 3 [53]
Amber 3 [54]
Management of Hyponatraemia
Pituitary and Neu- The Child with roendocrinology Very Small Penis
MTE9:1
Clinical Prediction Tools: the Example of Growth Monitoring Amber 4 [54]
NP2
Genome Sequencing Promise in Paediatric Endocrinology Space 1+2 [54]
FC11
FC12
Space 3 [55]
Space 4 [56]
Congenital Hyperinsulinism
Mineral Metabolism
LUNCH. Visit to the Posters and Exhibition Area Guided Poster Tours 12:45–13:45 – P1-d3, P2-d3 [81]
S11
S12
Gold [57]
Brown 3 [57]
Environmental and Genetic Disorders of Puberty
Glucocorticoid Effects in Bone and Cartilage Tissues
S19
Symposium for Nurses and Allied Healthcare Professionals Amber 3 [58]
CPE3
Detection and Treatment of Congenital Subclinical Hypothyroidism Space 1+2 [58]
S13
Why Doesn’t Everyone Become Obese: Energy Intake and Expenditure Space 3 [59]
S14
Autoimmunity in Paediatric Endocrinology Space 4 [60]
COFFEE BREAK. Visit to the Posters and Exhibition Area
MTE10:1
Diagnosis and Treatment of Adrenal Insufficiency Brown 1 [60]
SAT7
FC13
Endocrine Oncology Brown 3 [61]
MTE11:1
Clinical Management of Hypocalcaemia Amber 3 [62]
The First 1000 Days – Early Nutrition and Long-term Consequences Sponsored by Nestlé Nutrition Brown 3 [65]
MTE12:1
Molecular Genetic Investigation of the Child with Short Stature Amber 4 [62]
YB2
Yearbook of Paediatric Endocrinology Space 1+2 [62]
FC14
Perinatal and Neonatal Endocrinology Space 3 [63]
FC15
Adipose Tissue Space 4 [64]
SAT9
SAT8
Overcoming the Hypoglycaemia Barrier for Optimal Metabolic Control: the Role of New Technologies Sponsored by Medtronic Space 1+2 [65]
Growth Hormone and IGF-1: Ready to Wear or Bespoke Treatment for the Short Child? Sponsored by Ipsen Space 4 [65]
Children’s Charity Concert and Joint Meeting Evening at MiCo
[242]
CPE = Controversies in Paediatric Endocrinology FC = Free Communication Session MTE = Meet the Expert NP = New Perspectives PL = Plenary Lecture
S = Symposium S = Meeting Theme Symposium SAT = Joint Meeting Satellite Symposium WG = Joint Meeting Working Group YB = Yearbook of Paediatric Endocrinology
Rooms and Halls in italics [Page in Final Programme]
9th Joint Meeting of Paediatric Endocrinology 2013
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Programme at a Glance
Programme a Glance Programme atat a Glance
Sunday Sunday 22 22 September September 07:30 07:45 08:00 08:15 08:30 08:45 09:00 09:15 09:30 09:45 10:00 10:15 10:30 10:45 11:00 11:15 11:30 11:45 12:00 12:15 12:30 12:45 13:00 13:15
FC16
Novel Growthpromoting Treatment Gold [68]
YB3
Yearbook of Paediatric Endocrinology Gold [71]
MTE5:2
Controversies in the Management of Hyperthyroidism in Children and Adolescents Brown 1 [68]
MTE9:2
Clinical Prediction Tools: the Example of Growth Monitoring Brown 1 [71]
FC17
MTE7:2
MTE8:2
FC18
Brown 3 [69]
Amber 3 [69]
Amber 4 [70]
Space 1+2 [70]
Endocrine Issues in Boys and Adolescents with Klinefelter Syndrome Space 4 [71]
FC19
MTE11:2
MTE12:2
FC20
MTE10:2
Obesity
Management of Hyponatraemia
Thyroid
Clinical Management of Hypocalcaemia Amber 3 [73]
Brown 3 [71]
Molecular Genetic Investigation of the Child with Short Stature Amber 4 [73]
MTE6:2
Adrenal Disorders
Late Breaking Abstracts Space 1+2 [74]
Diagnosis and Treatment of Adrenal Insufficiency Space 4 [74]
S15
CPE4
S16
S17
S18
Gold [75]
Brown 1 [76]
Brown 3 [76]
Space 1+2 [77]
Space 4 [77]
Emerging Etiologies of Hypopituitarism
Fertility Preservation in Pre-Pubertal Children
Hyperandrogenism/ PCOS during Adolescence
Noonan Syndrome and Other RAS-opathies
Biochemical and Molecular Bases of Diabetic Complications – SIRP/ISPR
PL9 New Insights into the Genetic Regulation of Growth – Dedicated to Rita Levi Montalcini Gold [78]
PL10 Endocrine Disruptors and Their Effects on Reproductive Health – ASPAE Gold [78]
PL11 President’s Poster Awards Gold [78] Closing Ceremony Gold [78]
CPE = Controversies in Paediatric Endocrinology FC = Free Communication Session MTE = Meet the Expert NP = New Perspectives PL = Plenary Lectures Rooms and Halls in italics [Page in Final Programme]
4
The Child with Very Small Penis
9th Joint Meeting of Paediatric Endocrinology 2013
S = Symposium S = Meeting Theme Symposium SAT = Joint Meeting Satellite Symposium WG = Joint Meeting Working Group YB = Yearbook of Paediatric Endocrinology
Programme at a Glance
Welcome from the President Dear Friends, Colleagues and Paediatric Endocrinologists from around the globe! Welcome to Milan. It is my sincere pleasure, and privilege, to welcome you to the 9th Joint Meeting of Paediatric Endocrinology on behalf of the Joint Programme Organising Committee (JPOC). This prestigious occasion marks the reunion of the European Society for Paediatric Endocrinology (ESPE) with the Pediatric Endocrine Society (PES), Australasian Paediatric Endocrine Group (APEG), Asia Pacific Paediatric Endocrine Society (APPES), African Society for Paediatric and Adolescent Endocrinology (ASPAE), Japanese Society for Pediatric Endocrinology (JSPE), and the Sociedad Latino-Americana de Endocrinologia Pediátrica (SLEP). “Predictive Medicine to Improve the Care of Children” is the fitting theme for this occasion, paying homage to the innovation we have observed in the field of Paediatric Endocrinology in recent years. Scientific research, technological advances and the consequent development of our understanding now, more than ever, impacts directly on patient care. The exciting implications of this theme will be explored through plenary lectures, symposia and meet the expert sessions. This emphasis on a global sharing of knowledge will be complimented by the privileging of free communications and poster sessions in a truly international forum of the latest scientific and clinical research. The city’s architecture and gastronomy reflect Milan’s position as the historic crossroads between Italy and Europe, further underlining its appropriateness as a setting for this meeting. The social programme foregrounds this dynamic aspect of the city, whilst not forgetting its Italian heritage. On Saturday, I look forward to seeing you all at the Joint Meeting evening where you will have the opportunity to verify for yourselves the culinary pride for which Italians are famed! Before the Joint Meeting evening, a classical concert will be given by the prestigious children’s orchestra of the ‘Civica Scuola di Musica’ of Milan. I have chosen this event to help the ‘Civica Scuola di Musica’ in its mission to enable underprivileged children to study classical music – everybody is invited to attend the concert and your support is greatly appreciated. All members of the Italian Society for Paediatric Endocrinology and Diabetes (ISPED/ SIEDP) join me in wishing you the most enjoyable stay. We are counting on your participation to render this a fruitful meeting and we extend to you all warmest welcome to Milan and welcome to Italy!
Franco Chiarelli ESPE President 2013
9th Joint Meeting of Paediatric Endocrinology 2013
5
Programme at a Glance
Committees President Joint Meeting 2013
Professor Franco Chiarelli Joint Programme Organising Committee (JPOC) ESPE
Franco Chiarelli, Chieti, Italy (Chairman) Jean-Claude Carel, Paris, France Olle Söder, Stockholm, Sweden Chris Kelnar, Edinburgh, United Kingdom Lars Sävendahl, Stockholm, Sweden PES
David Allen, Madison, United States Cheri Deal, Montreal, Canada Peter Lee, Hershey, United States Philip Zeitler, Denver, United States Alan Rogol, Charlottesville, United States APEG
Paul Hofman, Auckland, New Zealand APPES
Aman Pulungan, Jakarta, Indonesia Reiko Horikawa, Tokyo, Japan ASPAE
Abiola Oduwole, Lagos, Nigeria JSPE
Tsutomu Ogata, Hamamatsu, Japan Tomonobu Hasegawa, Tokyo, Japan SLEP
Fernando Cassorla, Santiago, Chile Ivo Arnhold, São Paulo, Brazil Honorary Committee
Giuseppe Chiumello, Milan Sergio Bernasconi, Parma Gianni Bona, Novara Mauro Bozzola, Pavia Brunetto Boscherini, Rome Luciano Cavallo, Bari Alessandro Cicognani, Bologna Filippo De Luca, Messina Renata Lorini, Genoa Giuseppe Saggese, Pisa Francesca Severi, Pavia
6
9th Joint Meeting of Paediatric Endocrinology 2013
Local Organising Committee
Franco Chiarelli, Chieti Marco Cappa, Rome Stefano Cianfarani, Rome Lucia Ghizzoni, Turin Sandro Loche, Cagliari Mohamad Maghnie, Genoa Angelika Mohn, Chieti (Summer School Coordinator) Franco Meschi, Milan Giorgio Radetti, Bolzano Gianni Russo, Milan Giovanna Weber, Milan ESPE Council
Lars Sävendahl, Sweden – Secretary General Franco Chiarelli, Italy – President 2013 Hilary Hoey, Ireland – President-elect 2014 Anita Hokken-Koelega, The Netherlands – Treasurer Gary Butler, United Kingdom – Chairman of Clinical Practice Committee Jan Lebl, Czech Republic – Chairman of Education and Training Committee Jean-Claude Carel, France – Chairman of Programme Organising Committee Mehul Dattani, United Kingdom – Chairman–elect of Programme Organising Committee Peter Clayton, United Kingdom – Chairman of Corporate Liaison Board George Chrousos – Member responsible for communication The President would like to thank Loredana Marcovecchio and Cosimo Giannini for their assistance in the organisation of the free communication and poster sessions.
Programme at a Glance
Societies The 9th Joint Meeting of Paediatric Endocrinology is organised by the following societies:
ESPE – European Society for Paediatric Endocrinology – www.eurospe.org
PES – Pediatric Endocrine Society – www.lwpes.org
APEG – Australasian Paediatric Endocrine Group – www.apeg.org.au
APPES – Asia Pacific Paediatric Endocrine Society – www.appes.org
ASPAE - African Society for Pediatric and Adolescent Endocrinology – www.aspae.co.za
JSPE – Japanese Society for Paediatric Endocrinology – http://jspe.umin.jp
SLEP – Sociedad Latino-Americana de Endocrinología Pediátrica – www.slep.com.br
9th Joint Meeting of Paediatric Endocrinology 2013
7
Programme at a Glance
Meeting Information Meeting Secretariat
Meeting website
Congrex Sweden AB Attn: Joint Meeting 2013 P.O. Box 5619 SE-114 86 Stockholm Sweden Telephone: +46 8 459 66 00
www.jointmeeting2013.org
Exhibition Organiser
Congrex Sweden AB Attn: Joint Meeting 2013 P.O. Box 5619 SE-114 86 Stockholm Sweden Telephone: +44 7830 221032 European Society for Paediatric Endocrinology
Society Secretariat BioScientifica Euro House 22 Apex Court Woodlands Bristol BS32 4JT United Kingdom Telephone: +44 1454 642246 Fax: +44 1454 642222 Email:
[email protected] www.eurospe.org Email Addresses Scientific Programme and Speakers’ Contact
[email protected] Registration
[email protected] Hotel
[email protected] Exhibition
[email protected] General Issues and Practical Matters
[email protected]
8
9th Joint Meeting of Paediatric Endocrinology 2013
Meeting Opening Hours Registration Desk and Meeting Secretariat
Wednesday Thursday Friday Saturday Sunday
18 September 19 September 20 September 21 September 22 September
14:00–18:00 07:30–19:00 07:00–18:00 07:00–18:00 07:00–12:30
Speakers’ Support Centre
Wednesday Thursday Friday Saturday Sunday
18 September 19 September 20 September 21 September 22 September
14:00–18:00 07:30–19:00 07:00–18:00 07:00–18:00 07:00–12:30
Commercial Exhibition and Poster Exhibition
Thursday Friday Saturday
19 September 20 September 21 September
09:45–20:00 08:30–17:00 08:30–17:00
Programme at a Glance
Acknowledgements The 9th Joint Meeting of Paediatric Endocrinology express their gratitude to the following companies who, through their generosity, have helped to make this meeting possible: Platinum Sponsors
Sponsored Items
Ferring Pharmaceuticals Novo Nordisk A/S Genzyme – a Sanofi company IBSA
Bookmark Abstracts on USB Lunch Boxes Email Centre
Other Sponsors
Alexion Medtronic Nestlé Nutrition The following companies have contributed to the Joint Meeting in Milan as a contribution to the Italian Society for Paediatric Endocrinology and Diabetes (ISPED): Eli Lilly Italy Ferring Italy Ipsen Italy
Medtronic Italy Merck Serono Italy Novo Nordisk Italy
Pfizer Italy Sanofi-aventis Italy
In addition to supporting the 9th Joint Meeting 2013, the following companies have committed themselves to support the following ESPE awards and events: Eli Lilly and Company – ESPE Sabbatical Leave Programme Ferring Pharmaceuticals – ESPE Summer and Winter School Programmes; Symposium for Healthcare Professionals S. Karger AG – Medical and Scientific Publishers – ESPE Hormone Research in Paediatrics Prize Merck Serono SA – ESPE Clinical Fellowship Programme, ESPE Website Novo Nordisk A/S – Henning Andersen Prizes for best clinical and basic abstracts, ESPE Research Fellowship Programme ESPE – ESPE Andrea Prader Prize, ESPE Research Award and Lecture, ESPE Outstanding Clinician Award, ESPE Young Investigator Awards, ESPE International Award, ESPE Yearbook of Paediatric Endocrinology, ESPE Visiting Scholarship, ESPE Travel Grants, ESPE Science School, ESPE Maghreb School Sandoz International GmBh – ESPE e-learning programme, ESPE Research Unit
9th Joint Meeting of Paediatric Endocrinology 2013
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How to read the scientific Programme
12:45 – 13:10 session title:
Room: Gold Opening Ceremony
How to read the Scientific Programme chairs:
franco chiarelli, chieti, italy marco cappa, rome, italy
Welcome to Milan Franco Chiarelli, Chieti, Italy Quality of care of children with endocrine disorders and diabetes in Italy
Cappa, Rome,Room Italy Start/end of theMarco session
Abstract number
Session type and code
Thursday 19 September
Programme at a Glance
scientific Programme | Thursday 19 September 2013
Session title
13:10 – 13:40
Room: Gold
session type: session title:
PL1 Stem Cell-derived Islet Cells for Transplantation – PES
chair:
Dorothy Becker, Pittsburgh, Usa
Plenary session
PL1-1 Camillo Ricordi, Miami, USA
Speaker 13:40 – 14:10
Room: Gold
session type: session title:
PL2 Prevention of Type 1 Diabetes in Children – ESPE
chair:
to be announced
Plenary session
Session Codes and Abstract Numbers
The Scientific Programme is coded to facilitate finding the sessions in the Programme at a Glance PL2-2 Knip, Helsinki, Finland and in the DailyMichael Programme. The first characters indicate the type of session. Session codes for each session type: 14:20 – 15:20
Room: Exhibition Hall
session type:
Poster sessions
CPE = Controversies in Paediatric Endocrinology FC = Free Communication Session guided Poster tours – P1-d1, P2-d1, P3-d1 MTE = Meet the Expert For further details see page xx. NP = New Perspectives PL = Plenary Lecture
S = Symposium S = Meeting Theme Symposium SAT = Joint Meeting Satellite Symposium WG = Joint Meeting Working Group YB = Yearbook of Paediatric Endocrinology
Rooms and Halls in italics [Page in Final Programme]
The abstract number consists of the session code and a unique running number which starts with one for the first Plenary abstract (PL1-1) through to the last poster with running number 1528. The abstract number for the posters indicates in addition the area and day of presentation. The first number indicates the assigned poster area: P1 = closest to the commercial exhibition P2 = end part of the Exhibition Hall P3 = under the balcony Posters in P1 are those which scored highest in the anonymous peer evaluation. Second part of the posters’ abstract number indicate the day of presentation and when the author is present by their poster; that is, d1 for Thursday 19 September; d2 for Friday 20 September; and d3 for Saturday 21 September. The third part is the unique running number.
9th Joint meeting of Paediatric endocrinology 2013
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9th Joint Meeting of Paediatric Endocrinology 2013
21
Plenary Lecture (PL)
A Plenary Lecture is a stand-alone session on a topic every ESPE member should know more about. The lecturers are all outstanding researchers selected to provide a state of the art review of a wider field of Paediatric Endocrinology. The aim of the Plenary Lecture is to inspire the meeting participants by addressing some particular areas of Paediatric Endocrinology, raise interest in the field, and challenge conventional ways of thinking. A Plenary Lecture is 30 minutes in length. Symposium and Meeting Theme Symposium (S)
A Symposium is 90 minutes in length and consists of three presentations of 25 minutes each. Each presentation is followed by 5 minutes for discussion. One symposium a day is a Meeting Theme Symposium, based on the theme “Predictive Medicine to Improve the Care of Children”. A Symposium normally starts with a lecture on basic mechanisms, followed by one or two more clinically orientated lectures. New Perspectives (NP)
The New Perspectives sessions include two lectures of approximately 25 minutes followed by 5 minutes for discussion. The aim of these sessions is to provide a thorough update on new methodologies and techniques which have had a major impact in the field of Paediatric Endocrinology. Controversies in Paediatric Endocrinology (CPE)
The Controversies sessions consist of two experts discussing a controversial topic in the field of Paediatric Endocrinology. The sessions will have a debate format; each speaker will take questions and answers and challenge each other’s knowledge. The speakers will have 15 minutes each to present their views, and thereafter there will be 25 minutes for discussion and 5 minutes for the chairpersons’ summary. Meet the Expert (MTE)
The Meet the Expert sessions are small interactive sessions, devoted to a clinical problem and how to manage it in the clinical setting. All Meet the Expert speakers are requested to prepare handouts and discuss 1–2 cases during the session. The handout is distributed to all participants in the meeting bag and available on the Meeting website after the Meeting. The speakers are also requested to provide a mini-review/personal practice update for consideration for publication in the Clinical Practice section of Hormone Research in Paediatrics, and to add to the clinical practice pages of the ESPE website. Joint Meeting Working Group (WG)
The ESPE Working Groups aim to study and debate in detail a disease or a group of diseases, a treatment, a biologic process, a diagnostic method, or a new technology. This could foster exchange of ideas and share experiences, and potentially plan multicentre trials. This year the ESPE WG are open to all delegates coming from all over the world, in order to share further knowledge, generate lively debate and expand the possibility of studies and trials. Yearbook of Paediatric Endocrinology (YB)
The Yearbook of Paediatric Endocrinology sessions consist of presentations of the most relevant papers published over the last 12 months. During each of the three YB sessions, experts in specific fields of Paediatric Endocrinology will summarise the year’s breakthrough developments, achieved through basic and clinical research. Abstract-based Sessions
The abstract submission process is an excellent opportunity for all delegates to share their research, findings, knowledge and experience with medical professionals in the Paediatric Endocrinology community.
9th Joint Meeting of Paediatric Endocrinology 2013
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Programme at a Glance
How to read the scientific Programme
Programme at a Glance
How to read the scientific Programme
The abstracts are presented in the following formats: Free Communications (FC)
The Free Communication sessions contain oral presentations where the authors are allowed eight minutes for presentation and two minutes for discussion. Posters (P1, P2, P3)
The posters are on display on the first three days of the meeting with a dedicated poster presentation during each of these three days. The presenting author is requested to stand by their poster throughout the given presentation time. The posters in areas P1 and P2 are included in Guided Poster Tours. The Guided Tours give the authors a chance to interactively discuss the posters with the chairs and audience. There will be two minutes for presentation and two minutes for discussion. Electronic Posters (P1, P2, P3)
The posters on display in the Poster Exhibition during the meeting are also available online to view as electronic posters. This is to increase the visibility of the poster authors as well as to facilitate contacts between authors and delegates. It is possible to email the presenting author and request a copy of the poster yourself. The programme displays the posters in a uniform format and posters can be searched for by number, title, author or free text search. Joint Meeting Satellite Symposium (SAT)
Satellite Symposia will take place after the main programme each day. These symposia have been prepared by companies who have selected the scientific content, which is then approved by the Joint Programme Organising Committee. This year several Satellite Symposia have been proposed on various fields of Paediatric Endocrinology.
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Thursday 19 September 2013
Programme at a Glance
Thursday 19 September Daily programme
WG1
WG2
WG3
WG4
Gold [14]
Brown 1 [15]
Brown 3 [16]
Amber 3 [17]
Space 1+2 [18] Space 3 [19]
Obesity (O)
Global Paediatric Endocrinology and Diabetes (GPED)
Paediatric and Adolescent Gynaecology (PAG): Hyperinsulinaemic Androgen Excess (PCOS) in Adolescents
WG5
(PasteWG6 PAAG)
S1
Safety and Bone and Appropriateness Growth Plate of GH (BGP) Treatment in Europe (SAGhE)
Thursday 19 September
Thursday 19 September Turner Syndrome (TS): Controversies on the Care of TS
Disorders of Sex Development (DSD): Information and Communication in the Context of DSD
Space 4 [20]
LUNCH
POSTER AND EXHIBITION
07:30 07:45 08:00 08:15 08:30 08:45 09:00 09:15 09:30 09:45 10:00 10:15 10:30 10:45 11:00 11:15 11:30 11:45 12:00 12:15 12:30 12:45 13:00 13:10 13:30 13:40 14:00 14:10 14:15 14:45 15:00 15:15 15:30 15:45 16:00 16:15 16:30 16:45 17:00 17:15 17:30 17:45 18:00 18:15 18:30 18:45 19:00 19:15 19:30 19:45 20:00
Opening Ceremony Gold [21] PL1 Stem Cell-derived Islet Cells for Transplantation – PES Gold [21] PL2 Prevention of Type 1 Diabetes in Children – ESPE Gold [21] COFFEE BREAK. Visit to the Posters and Exhibition Area Guided Poster Tours 14:20–15:20 – P1-d1, P2-d1 [80]
S2
S3
CPE1
S4
Gold [22]
Brown 1 [22]
Brown 3 [23]
Space 1+2 [23]
Gender Identity and Behaviour
Rare Forms of Diabetes: the Euro-WABB Project
Diagnosis and Treatment of Early Puberty
Congenital Hypothyroidism Revisited
S5
Hypoglycaemia in Children with Diabetes – ISPAD/ESPE Space 3 [24]
SAT1
SAT2
SAT3
Gold [26]
Brown 3 [26]
Space 4 [27]
Optimising Therapy in Children with Growth Disorders from Diagnosis to Adult Height: Case Study Debate Sponsored by Novo Nordisk
Taking GH Therapy to New Frontiers Sponsored by Merck Serono
S6
Rare Diseases – Epigenetic Mechanisms Space 4 [25]
Is It Hypophosphatasia or Osteogenesis Imperfecta? Clarifying the Diagnostic Approach to Challenging Patient Cases Sponsored by Alexion
Welcome Reception in the Exhibition Hall
[242]
CPE = Controversies in Paediatric Endocrinology FC = Free Communication Session MTE = Meet the Expert NP = New Perspectives PL = Plenary Lecture
S = Symposium S = Meeting Theme Symposium SAT = Joint Meeting Satellite Symposium WG = Joint Meeting Working Group YB = Yearbook of Paediatric Endocrinology
Rooms and Halls in italics [Page in Final Programme]
9th Joint Meeting of Paediatric Endocrinology 2013
13
Thursday 19 September
scientific Programme | Thursday 19 September 2013
09:00 – 12:00
Room: Gold
Session type:
Symposium S1
Session title:
Safety and Appropriateness of GH Treatment in Europe (SAGhE)
Chairs:
Marc Maes, Brussels, Belgium Roland Pfaeffle, Leipzig, Germany Peter Clayton, Manchester, UK Anita Hokken-Koelega, Rotterdam, Netherlands
SESSION AIM: The aim of this symposium is to provide an update on the results of the SAGhE study.
Preliminary data on long-term efficacy, quality of life, mortality and morbidity from a European cohort of about 25,000 patients treated with recombinant human GH during childhood will be presented and discussed. S1-11
SAGhE: project presentation. Investigation plan and objectives Stefano Cianfarani, Rome, Italy State of the art, rationale, investigation plan and objectives of SAGhE project will be presented. S1-12
SAGhE efficacy results Jean-Claude Carel, Paris, France Preliminary results on the long-term efficacy of GH treatment in a European cohort of short children treated with recombinant human GH will be presented. S1-13
SAGhE quality of life results Joël Coste, Paris, France Preliminary data on the quality of life of young adults treated with recombinant human GH during childhood and tested with SF-36 questionnaire will be presented. S1-14
SAGhE: Preliminary report of all-cause mortality analyses Lars Sävendahl, Stockholm, Sweden Preliminary data on all-cause and cause specific mortality in subjects treated with recombinant human GH during childhood will be presented. Coffee break 10:20 – 10:40 S1-15
SAGhE: Preliminary report of cancer incidence and cancer mortality analyses Anthony Swerdlow, London, UK Preliminary data on morbidity associated with GH treatment will be presented. S1-16
Critical appraisal of SAGhE results Leslie L. Robison, Memphis, USA Mortality and morbidity SAGhE data will be critically appraised by an external expert in the field.
14
9th Joint Meeting of Paediatric Endocrinology 2013
09:00 – 12:00
Room: Brown 1
Session type:
Joint Meeting Working Group WG1
Session title:
Bone and Growth Plate (BGP)
Chairs:
Wolfgang Högler, Birmingham, UK Masanori Minagawa, Chiba, Japan Klaus Mohnike, Magdeburg, Germany Serap Turan, Istanbul, Turkey
Thursday 19 September
scientific Programme | Thursday 19 September 2013
WG1-80
Genetic changes affecting growth plate cartilage Ola Nilsson, Stockholm, Sweden WG1-81
Role of obesity in the growth process and timing of puberty Shlomit Shalitin, Petah Tikva, Israel WG1-82
Vitamin D in infancy: how much is needed Outi Mäkitie, Helsinki, Finland Coffee break 10:15 – 10:45 WG1-83
What is new in LRP5? Matthew Warman, Boston, USA WG1-84
The effect of leukaemia therapy on linear growth and the development of bone strength Leanne Ward, Ottawa, Canada WG1-85
Phenotypes and genotypes: from TGF-β to SHOX Valerie Cormier-Daire, Paris, France
9th Joint Meeting of Paediatric Endocrinology 2013
15
Thursday 19 September
scientific Programme | Thursday 19 September 2013
09:00 – 12:00
Room: Brown 3
Session type:
Joint Meeting Working Group WG2
Session title:
Obesity (O)
Chairs:
Bessie Spiliotis, Patras, Greece Matthew Sabin, Melbourne, Australia Claudio Maffeis, Verona, Italy Ram Weiss, Jerusalem, Israel
WG2-86
Bone morphogenetic proteins in the regulation of thermogenesis in brown adipose tissue Andrew Whittle, Cambridge, UK WG2-87
Mitochondrial dysfunction in white adipose tissue and obesity Martin Wabitsch, Ulm, Germany Coffee break 10:15 – 10:45 WG2-88
Regulation of obesity associated chronic inflammation and insulin resistance via apoptosis inhibitor of macrophage Toru Miyazaki, Tokyo, Japan WG2-89
Declining β-cell function in children relative to insulin sensitivity with escalating OGTT 2-h glucose concentrations Hala Tfayli, Beirut, Lebanon Obesity Study Group Meeting
16
9th Joint Meeting of Paediatric Endocrinology 2013
09:00 – 12:00
Room: Amber 3
Session type:
Joint Meeting Working Group WG3
Session title:
Global Paediatric Endocrinology and Diabetes (GPED)
Chairs:
Vijayalakshmi Bhatia, Lucknow, India Hugo Fideleff, Buenos Aires, Argentina Kerstin Albertsson-Wikland, Gothenburg, Sweden Stuart Brink, Boston, USA
Thursday 19 September
scientific Programme | Thursday 19 September 2013
WG3-90
World issues in paediatric endocrinology Ze’ev Hochberg, Haifa, Israel WG3-91
Global Paediatric Endocrinology and Diabetes (GPED): a joint effort by world paediatric endocrinologists Jean-Pierre Chanoine, Vancouver, Canada WG3-92
Paediatric endocrinology management in low resources societies Margaret Zacharin, Melbourne, Australia WG3-93
The changing face of diabetes in Africa Abiola Oduwole, Lagos, Nigeria Coffee break 10:15 – 10:45 Free Communications (related to GPED) WG3-94
At last, an adult height prediction model for black children David D. Martin1, Hans Henrik Thodberg2, John Pettifor3 1 Tübingen, Germany, 2Holte, Denmark, 3Johannesburg, South Africa WG3-95
Reduction in incidence of type 1 diabetes mellitus complications in adolescents in Uzbekistan Nasiba U. Alimova, Gulnara N. Rakhimova Tashkent, Uzbekistan WG3-96
Congenital hypothyroidism: world birth population undergoing newborn screening and economic impact George Ford, Stephen LaFranchi Portland, USA WG3-97
Newborn screening for congenital hypothyroidism in an underprivileged region of India Kriti Joshi, Vignesh Gopalakrishnan, Vijaylakshmi Bhatia, Preeti Dabadghao, Shubha Rao Phadke, Vineeta Das, Meenal Agarwal Lucknow, India WG3-98
Dyshormonogenesis seems to be more frequent in a group of Cameroonian patients with congenital hypothyroidism Suzanne Annette Ngo Um, Louis De Djob, Félicitée Dongmo, Paul Koki Yaounde, Cameroon
9th Joint Meeting of Paediatric Endocrinology 2013
17
Thursday 19 September
scientific Programme | Thursday 19 September 2013
09:00 – 12:00
Room: Space 1+2
Session type:
Joint Meeting Working Group WG4
Session title:
Paediatric and Adolescent Gynaecology (PAG): Hyperinsulinaemic Androgen Excess (PCOS) in Adolescents
Chairs: Reiko Horikawa, Tokyo, Japan Charles Sultan, Montpellier, France Warren Lee, Singapore, Singapore Jean-Pierre Bourguignon, Liège, Belgium WG4-99
Early development and prevention of PCOS Francis de Zegher, Leuven, Belgium WG4-100
Genetics of PCOS Ken Ong, Cambridge, UK WG4-101
Hyperinsulinaemic androgen excess in patients with type 1 diabetes Ethel Codner, Santiago, Chile Coffee break 10:15 – 10:45 WG4-102
PCOS in girls: what the world can learn from India Preeti Dabadghao, Lucknow, India WG4-103
Treatment of PCOS in obese girls: weight loss, oral contraceptives and/or insulin sensitisation Hala Tfayli, Beirut, Lebanon WG4-104
Treatment of PCOS in non-obese adolescents Lourdes Ibáñez, Barcelona, Spain WG4-105
Contraceptive options for adolescents with PCOS Catherine Gordon, Boston, USA
18
9th Joint Meeting of Paediatric Endocrinology 2013
09:00 – 12:00
Room: Space 3
Session type:
Joint Meeting Working Group WG5
Session title:
Turner Syndrome (TS): Controversies on the Care of TS
Chairs:
Laura Mazzanti, Bologna, Italy Catherine Dacou-Voutetakis, Athens, Greece Berit Kriström, Umeå, Sweden Aneta Gawlik, Katowice, Poland
Thursday 19 September
scientific Programme | Thursday 19 September 2013
WG5-106
Ovarian failure in TS Paolo Beck-Peccoz, Milan, Italy WG5-107
Puberty induction in TS: early, late or super early? Judith Ross, Philadelphia, USA WG5-108
TS patient as a candidate for IVF Outi Hovatta, Stockholm, Sweden Coffee break 10:15 – 10:45 WG5-109
Cardiac evaluation in TS using new imaging techniques: is MRI the first-line study also in paediatric population with TS? Carolyn Bondy, USA WG5-110
Transition of females with TS from paediatrics to adulthood: the paediatric endocrinologist Alan Rogol, Charlottesville, USA WG5-111
Transition of females with TS from paediatrics to adulthood: the adult endocrinologist Claus H. Gravholt, Aarhus C, Denmark
9th Joint Meeting of Paediatric Endocrinology 2013
19
Thursday 19 September
scientific Programme | Thursday 19 September 2013
09:00 – 12:00
Room: Space 4
Session type:
Joint Meeting Working Group WG6
Session title:
Disorders of Sex Development (DSD): Information and Communication in the Context of DSD
Chairs:
Anna Nordenström, Stockholm, Sweden Shinobu Ida, Osaka, Japan Paul-Martin Holterhus, Kiel, Germany Carlos Alberto Longui, São Paulo, Brazil
WG6-112
Biochemical information necessary to reach a diagnosis Christa Flück, Bern, Switzerland WG6-113
Chances, pitfalls, risks and how genetic information should be relayed to the clinician Ken McElreavey, Paris, France WG6-114
Communication around the DSD patient in the clinical setting S. Faisal Ahmed, Glasgow, UK WG6-115
Decision impossible - what does the parent want/need to hear? Julia Marie Kriegler, Berlin, Germany Coffee break 10:15 – 10:45 WG6-116
Communication with children and adolescents about their DSD condition Tom Mazur, Buffalo, USA WG6-117
The I-DSD registry update Jillian Bryce, Glasgow, UK WG6-118
dsd-LIFE: Clinical European study on the outcome of and experiences with hormonal therapies, surgery, psychological support and psychological intervention in DSD Birgit Köhler, Berlin, Germany WG6-119
DSDnet: building a network for studies of differences of sex development Olaf Hiort, Lübeck, Germany
20
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Thursday 19 September 2013
12:45 – 13:10 Session title: Chairs:
Room: Gold Opening Ceremony Franco Chiarelli, Chieti, Italy Marco Cappa, Rome, Italy
Thursday 19 September
Welcome to Milan Franco Chiarelli, Chieti, Italy Quality of care of children with endocrine disorders and diabetes in Italy Marco Cappa, Rome, Italy
13:10 – 13:40
Room: Gold
Session type:
Plenary Session PL1 Stem Cell-derived Islet Cells for Transplantation – PES
Session title:
Chair: Dorothy Becker, Pittsburgh, USA PL1-1 Camillo Ricordi, Miami, USA
13:40 – 14:10
Room: Gold
Session type: Session title:
Plenary Session PL2 Prevention of Type 1 Diabetes in Children – ESPE
Chair: Giuseppe Chiumello, Milan, Italy PL2-2 Michael Knip, Helsinki, Finland
14:20 – 15:20
Room: Exhibition Hall
Session type:
Poster Sessions
Guided Poster Tours – P1-d1, P2-d1
For further details see page 80.
9th Joint Meeting of Paediatric Endocrinology 2013
21
Thursday 19 September
scientific Programme | Thursday 19 September 2013
15:30 – 17:00
Room: Gold
Session type:
Symposium S2
Session title:
Gender Identity and Behaviour
Chairs:
Xiaoping Luo, Wuhan, China S. Faisal Ahmed, Glasgow, UK
SESSION AIM: Gender identity is a crucial component of sex assignment in DSD. This symposium will
give an update on the epidemiology, neuroanatomy and endocrinology of gender identity disorders. S2-17
Gender identity disorders in childhood Peggy Cohen-Kettenis, Amsterdam, Netherlands This speaker will give an update on the epidemiology and clinical presentation of gender identity disorders in children. S2-18
Brain imaging in gender identity disorders Ivanka Savic, Stockholm, Sweden This presentation will demonstrate neuroimaging patterns in gender identity disorders in humans. S2-19
Sex steroids and behaviour Melissa Hines, Cambridge, UK This presentation will give an update on the impact of sex steroids on gender typic behaviour.
15:30 – 17:00 Session type: Session title: Chairs:
Room: Brown 1 Symposium S3 Rare Forms of Diabetes: the Euro-WABB Project Vallo Tillmann, Tartu, Estonia Mark Harris, Brisbane, Australia
SESSION AIM: Rare forms of diabetes are often difficult to diagnose. This presentation focuses on three monogenic diabetes syndromes, the recent advances in diagnosis research through an international registry, and lessons from the underlying molecular mechanisms for commoner forms of diabetes.
S3-20
Rare diabetes syndromes, and the development of a Europe-wide registry Timothy Barrett, Birmingham, UK Monogenic forms of diabetes are difficult to study due their rarity. This presentation describes the establishment of a European registry for monogenic diabetes and the outcomes in terms of management guidelines, genetic testing and natural history of the diseases. S3-21
Diagnostic markers and treatment for Wolfram syndrome, a prototype for human endoplasmic reticulum disease Fumihiko Urano, St. Louis, USA Wolfram syndrome is a form of neurodegeneration and diabetes, due to endoplasmic reticulum stress. This will be explored as a model for stress in common forms of diabetes. S3-22 Endocrine abnormalities in the ciliopathies with examples of Bardet-Biedl syndrome and Alström syndrome
Vincent Marion, Strasbourg, France Ciliopathies are a group of diseases sharing pathology in the non-motile cilia. This presentation will explore ciliopathies as a model for obesity and insulin resistance.
22
9th Joint Meeting of Paediatric Endocrinology 2013
15:30 – 17:00
Room: Brown 3
Session type:
Controversies in Paediatric Endocrinology CPE1
Session title:
Diagnosis and Treatment of Early Puberty
Chairs:
Fatimah Harun, Kuala Lumpur, Malaysia Gary Butler, London, UK
SESSION AIM: This is a controversial area for many clinicians with important implications for the patient and her family; this session will present an evidence-based discussion of the potential costs and benefits of analog therapy in girls with early puberty.
CPE1-72
Pros of treatment of early (but not precocious) puberty in girls Lucia Ghizzoni, Turin, Italy This lecture will present the pro treatment point of view, by stressing the favorable effects of GnRH therapy for girls with this condition. Special attention will be directed towards the potential social and emotional benefits of analog therapy for girls with early puberty. CPE1-73
Cons of treatment of early (but not precocious) puberty in girls Mark Palmert, Toronto, Canada This lecture gives the against therapy point of view, by reviewing the secular trend towards early pubertal development in most parts of the world, and the potential negative metabolic effects of analog therapy in these girls.
15:30 – 17:00 Session type: Session title:
Room: Space 1+2 Symposium S4 Congenital Hypothyroidism Revisited
Chairs: Gianni Bona, Novara, Italy Tomonobu Hasegawa, Tokyo, Japan SESSION AIM: Congenital hypothyroidism is the most frequent congenital endocrine disorder. This symposium will deal with some fundamental and important issues, which have not been elucidated regarding CH.
S4-23
Genetics of thyroid development: facts and mysteries Roberto Di Lauro, Naples, Italy The speaker will review and summarise the most recent understanding of nature of the signals that lead to the biochemical and morphogenetic events responsible for thyroid development, such as intrinsic factors, extrinsic factors, and gene interactions. S4-24
Unveiling the genetic landscape of congenital hypothyroidism Satoshi Narumi, Tokyo, Japan Recently, genetic defects in the pathogenesis of congenital hypothyroidism have been unveiled. The speaker will review and summarise the genetic defects, primarily focusing on “nonclassic TSH resistance”. S4-25
Congenital hypothyroidism: the screening programs and epidemiology Johnny Deladoey, Montreal, Canada The incidence of congenital hypothyroidism was reported to have doubled over two decades. Is this true or due to the change in the newborn screening cutoff? It remains controversial that such increased cases benefit from early detection and treatment.
9th Joint Meeting of Paediatric Endocrinology 2013
23
Thursday 19 September
scientific Programme | Thursday 19 September 2013
Thursday 19 September
scientific Programme | Thursday 19 September 2013
15:30 – 17:00
Room: Space 3
Session type:
Symposium S5
Session title:
Hypoglycaemia in Children with Diabetes – ISPAD/ESPE
Chairs:
Maria Craig, Sydney, Australia Morey Haymond, Houston, USA
SESSION AIM: Hypoglycaemia still remains the major limitation to further improvement of glycaemic control in diabetic children, particularly in the first years of life. This symposium will highlight the effect of hypoglycaemia on the brain and how to prevent it.
S5-26
Hypoglycaemia: physiological responses in children and adolescents with type 1 diabetes Geremia B. Bolli, Perugia, Italy This presentation will review the principles of the defense against hypoglycaemia which integrates the autonomic nervous system, hormones, their receptors and enzymes to allow adequate glucose for the brain and other tissues. S5-27
The impact of hypoglycaemia on the brain of children with diabetes Neil H. White, St. Louis, USA This lecture will review how hypoglycaemia in infants, children and adolescents can affect cognition, memory and learning. Hypoglycaemia in children can also impact long-term spatial memory. S5-28
Hypoglycaemia in children and adolescents with diabetes: Who is at risk? How to prevent? Reinhard Holl, Ulm, Germany This presentation will point out how the diabetes team may use insulin, nutrition and physical exercise to prevent hypoglycaemia in children with diabetes. The role of new technologies will also be discussed.
24
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Thursday 19 September 2013
15:30 – 17:00
Room: Space 4
Session type:
Meeting Theme Symposium S6
Session title:
Rare Diseases – Epigenetic Mechanisms
Chairs:
Horacio Domené, Buenos Aires, Argentina Mitchell Geffner, Los Angeles, USA
Thursday 19 September
SESSION AIM: Genome imprinting plays a critical role in the body and placental growth and development. This symposium focuses on rare but important imprinting diseases in the field of paediatric endocrinology.
S6-29
Prader-Willi Syndrome Dan Driscoll, Gainesville, USA Prader-Willi syndrome (PWS) is the first disorder identified as an imprinting disease. Recent studies have clarified the imprinting centre and the critical role of SnoRNA in the development of PWS. S6-30
Silver-Russell Syndrome: from epigenetic/phenotype correlations to clinical care Irene Netchine, Paris, France Silver-Russell syndrome is caused by maternal chromosome 7 disomy (5–10%) and by epimutation of the H19-DMR (30–60%). Phenotype-(epi)genotype correlations reveal characteristic features of each entity. S6-31
Clarification of (epi)genetic mechanisms leading to upd(14)pat and upd(14)mat phenotypes Masayo Kagami, Tokyo, Japan This lecture focuses on the identification of the body and placental imprinting centres and their relevance to the development of clinical features in paternal and maternal chromosome 14 disomies.
9th Joint Meeting of Paediatric Endocrinology 2013
25
scientific Programme | Thursday 19 September 2013
17:15 – 18:45
Room: Gold
Session type:
Joint Meeting Satellite Symposium SAT1
Session title:
Optimising Therapy in Children with Growth Disorders from Diagnosis to Adult Height: Case Study Debate
Thursday 19 September
Sponsored by Novo Nordisk Chairs: David Dunger, Cambridge, UK Susumu Yokoya, Tokyo, Japan The impact of early GH treatment on outcomes for the patient: case of a SGA child Jesús Argente, Madrid, Spain The importance of using an appropriate dose of GH: case of girls with Turner syndrome Theo Sas, Rotterdam, Netherlands Can patients with GHD benefit from IGF-based dosing? Case-based discussion of efficacy, safety, and cost-effectiveness Pinchas Cohen, Los Angeles, USA Managing the transition of patients with GHD: a case illustrating metabolic effects and stopping/ continuing treatment Mohamad Maghnie, Genoa, Italy
17:15 – 18:45
Room: Brown 3
Session type:
Joint Meeting Satellite Symposium SAT2
Session title:
Taking GH Therapy to New Frontiers Sponsored by Merck Serono
Chairs:
Marco Cappa, Rome, Italy Carlo Acerini, Cambridge, UK
Grant for Growth Innovation Andrew Galazka, Coinsins, Switzerland Genetic modulation of IGF-1 generation in children with growth hormone deficiency or Turner syndrome treated with GH Pierre Chatelain, Lyon, France Health care at a distance in a global context Kristina Groth, Stockholm, Sweden The link between adherence and clinical outcome: ECOS study Peter Davies, Brisbane, Australia
26
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Thursday 19 September 2013
17:15 – 18:45
Room: Space 4
Session type:
Joint Meeting Satellite Symposium SAT3
Session title:
Is It Hypophosphatasia or Osteogenesis Imperfecta? Clarifying the Diagnostic Approach to Challenging Patient Cases Sponsored by Alexion Jeremy Allgrove, London, UK Dov Tiosano, Haifa, Israel
Thursday 19 September
Chairs:
Case 1: Rare metabolic bone disorders: common presentation and clinical challenges Jeremy Allgrove, London, UK Case 2: Osteogenesis imperfecta Nick Shaw, Birmingham, UK Case 3: Hypophosphatasia Michael P. Whyte, St. Louis, USA Case 4: The diagnostic challenge Jay Shapiro, Baltimore, USA
18:45 – 20:00 Welcome Reception in the Exhibition Hall For further details see page 242.
9th Joint Meeting of Paediatric Endocrinology 2013
27
Thursday 19 September
scientific Programme | Thursday 19 September 2013
28
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Friday 20 September 2013
Daily programme
Programme at a Glance
Friday 20 SeptemberFriday 20 September NP1
Imaging in Paediatric Endocrinology Gold [30]
YB1
Yearbook of Paediatric Endocrinology Gold [35]
MTE1:1
Molecular Diagnosis and Management of Hereditary Gynaecomastia Brown 1 [30]
MTE4:1
Beta-Cell Dysfunction of the Newborn Brown 1 [35]
MTE2:1
FC1
MTE3:1
(PasteFC3 PAAG)
Brown 3 [31]
FC4
MTE5:1
MTE6:1
FC5
FC6
Brown 3 [36]
Amber 3 [37]
Amber 4 [37]
Space 1+2 [38]
Space 3 [39]
Controversies in the Management of Hyperthyroidism in Children and Adolescents
Puberty
Pituitary Adenoma and Incidentaloma Amber 4 [32]
FC2
Type 1 Diabetes in Preschool Children Amber 3 [32]
Gonads and Gynaecology
Endocrine Issues in Boys and Adolescents with Klinefelter Syndrome
Bone and Growth Plate
Growth
Space 1+2 [33]
Space 3 [34]
Programming and Epigenetics
Glucose Metabolism
Friday 20 September
COFFEE BREAK. Visit to the Posters and Exhibition Area
PL3 Programming Effects of Early Life Adversity – APPES Gold [40]
PL4
Joint Meeting Award Session 1
POSTER AND EXHIBITION
07:30 07:45 08:00 08:15 08:30 08:45 09:00 09:15 09:30 09:45 10:00 10:15 10:30 10:45 11:00 11:15 11:30 11:45 12:00 12:15 12:30 12:45 13:00 13:15 13:30 13:45 14:00 14:15 14:30 14:45 15:00 15:15 15:30 15:45 16:00 16:15 16:30 16:45 17:00 17:15 17:30 17:45 18:00 18:15 18:30 18:45 19:00 19:15 19:30
Gold [40]
PL5 Novel Therapy for the Metabolic Complications of Obesity – JSPE Gold [41]
LUNCH. Visit to the Posters and Exhibition Area Guided Poster Tours 13:00–14:00 – P1-d2, P2-d2 [81]
S7
CPE2
S8
S9
S10
Gold [41]
Brown 3 [42]
Space 1+2 [43]
Space 3 [44]
Space 4 [44]
Vitamin D in Health and Disease
Idiopathic Short Stature: To Treat or Not To Treat?
The Adipose Organ: All Fat Is Not Created Equal
The Testis in 3D Endocrine Tumours (Development, Descent, in Childhood Dysfunction)
COFFEE BREAK. Visit to the Posters and Exhibition Area Business Meeting SLEP
Business Meeting ESPE
Brown 1 [45]
Space 3 [45]
SAT4
SAT5
SAT6
Gold [45]
Space 1+2 [45]
Space 4 [45]
What’s New in Adrenal Disorders Sponsored by Sandoz
Practical Application of Personalised Medicine in Paediatric and Adolescent Endocrinology Sponsored by Pfizer Specialty Care
CPE = Controversies in Paediatric Endocrinology FC = Free Communication Session MTE = Meet the Expert NP = New Perspectives PL = Plenary Lecture
SHOX-ing News about Growth: Updates on Genetics, Clinical Characteristics and Treatment of Children with SHOX Deficiency Sponsored by Eli Lilly and Company
S = Symposium S = Meeting Theme Symposium SAT = Joint Meeting Satellite Symposium WG = Joint Meeting Working Group YB = Yearbook of Paediatric Endocrinology
Rooms and Halls in italics [Page in Final Programme]
9th Joint Meeting of Paediatric Endocrinology 2013
29
scientific Programme | Friday 20 September 2013
07:30 – 08:30
Room: Gold
Session type: New Perspectives NP1 Session title:
Imaging in Paediatric Endocrinology
Chairs: George Werther, Melbourne, Australia David Allen, Madison, USA SESSION AIM: This is a symposium which will review the recent advances in neuroimaging in pituitary disorders and functional imaging of the pancreas in children.
NP1-68
Advances in neuroimaging of pituitary disorders Giovanni Morana, Genoa, Italy The use of neuroimaging for assessing disorders of pituitary development will be discussed. In addition, advances in neuroimaging of pituitary tumours will be highlighted.
Friday 20 September
NP1-69
Functional imaging of the pancreas in children Francoise Montravers, Paris, France The presentation will review the role of functional imaging of the pancreas in the diagnosis of hyperinsulinism of infancy. Clinical advice on the use of [18F]fluoro-L-DOPA PET will be given.
07:30 – 08:30
Room: Brown 1
Session type:
Meet the Expert MTE1:1
Session title:
Molecular Diagnosis and Management of Hereditary Gynaecomastia
Maki Fukami, Tokyo, Japan SESSION AIM: Hereditary gynaecomastia is caused by overexpression of CYP19A1 encoding aromatase. This session is aimed to introduce underlying genomic rearrangements and successful treatment of gynaecomastia.
30
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Friday 20 September 2013
07:30 – 08:30
Room: Brown 3
Session type:
Free Communication FC1
Session title:
Gonads and Gynaecology
Chairs: Raimo Voutilanen, Kuopio, Finland Toshihiro Tajima, Sapporo, Japan FC1-120
Lack of expression of Gamete Specific Function 1 gene in cryptorchid boys at high risk of infertility Faruk Hadziselimovic, Nils Hadziselimovic Liestal, Switzerland FC1-121
FC1-122
Sexuality, fertility and gonadotropic axis evaluation in 191 men born with classic 21-hydroxylase deficiency: first results of a French multicentre survey Laure Esterle1, Véronique Tardy2, Peggy Renoult-Pierre3, Sophie Christin-Maitre4, Véronique Kerlan5, Jerôme Bertherat4, Jean-Marc Kuhn6, Philippe Caron7, Maryse Cartigny8, Delphine Drui9, Olivier Chabre10, Didier Dewailly8, Philippe Touraine4, Jacques Young1, Claire Bouvattier1, Y-BLOC21 Network 1 Le Kremlin Bicêtre, France, 2Lyon, France, 3Tours, France, 4Paris, France, 5Brest, France, 6Rouen, France, 7 Toulouse, France, 8Lille, France, 9Nantes, France, 10Grenoble, France FC1-123
Assisted reproductive therapies and Prader-Willi syndrome: a preliminary Italian survey Graziano Grugni1, Antonino Crino’2, Maurizio Delvecchio3, Stefania Di Candia4, Giorgio Radetti5, Letizia Ragusa6, Nadia Beltrami5, Marco Cappa2, Andrea Corrias7, Donatella Greco6, Michele Sacco3, Alessandro Sartorio1, Giuseppe Chiumello4, Luigi Gargantini8, on behalf of the Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology 1 Verbania, Italy, 2Rome, Italy, 3S. Giovanni Rotondo, Italy, 4Milan, Italy, 5Bolzano, Italy, 6Troina, Italy, 7 Turin, Italy, 8Treviglio, Italy FC1-124
Preliminary results of the fertility preservation in a group of Klinefelter adolescents Ingrid Plotton, Aurelie Brosse, Yves Morel, Herve Lejeune, Group Fertipreserve Bron, France FC1-125
Genome-wide methylation analysis in Klinefelter syndrome Anne Skakkebæk1, Michal Switnicki1, Anders Bojesen2, Jens Michael Hertz3, John R. Østergaard1, Anders D. Pedersen1, Mikkel Wallentin1, Karina D. Sørensen1, Claus H. Gravholt1 1 Aarhus, Denmark, 2Vejle, Denmark, 3Odense, Denmark
9th Joint Meeting of Paediatric Endocrinology 2013
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Friday 20 September
Cryptorchidism and testicular abnormalities related to a novel correlation of gene variants of insulin-like 3 hormone in boys Rosa Mourelatou, Alexia Karvela, Xenophon Sinopidis, Efstathia Tsekoura, George Georgiou, Bessie E. Spiliotis Patras, Greece
scientific Programme | Friday 20 September 2013
07:30 – 08:30
Room: Amber 3
Session type:
Meet the Expert MTE2:1
Session title:
Type 1 Diabetes in Preschool Children
Ragnar Hanas, Uddevalla, Sweden SESSION AIM: This Meet the Expert session will focus on peculiar management of children with diabetes during the first months and years of life. In preschool children diabetes is difficult to manage for the instability of glycaemia and particularly for the risk of brain damage consequent to hypoglycaemia. Insulin treatment, glucose monitoring and indications for the use of continuous subcutaneous insulin infusion will also be discussed.
Friday 20 September
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
07:30 – 08:30
Room: Amber 4
Session type:
Meet the Expert MTE3:1 Pituitary Adenoma and Incidentaloma
Session title:
Annamaria Colao, Naples, Italy SESSION AIM: Most pituitary MRI abnormalities are microincidentalomas and non-functional, but endocrinopathies or visual field defects may be present. The differential diagnosis of pituitary adenoma and incidentaloma will be reviewed.
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Friday 20 September 2013
07:30 – 08:30
Room: Space 1+2
Session type:
Free Communication FC2
Session title:
Bone and Growth Plate
Chairs:
Agnès Linglart, Kremlin-Bicêtre, France Keiichi Ozono, Osaka, Japan
FC2-126
IGF-1 signalling is essential for differentiation of mesenchymal stem cells for peak bone mass Janet L. Crane1, Luo Zhao2, Joseph S. Frye3, Lingling Xian1, Tao Qiu1, Xu Cao1 1 Baltimore, USA, 2Beijing, China, 3Columbia, USA FC2-127
Evidence that estrogen hastens epiphyseal fusion and cessation of longitudinal bone growth by irreversibly depleting the number of resting zone progenitor cells Ola Nilsson, Martina Weise, Jeffrey Baron Bethesda, USA FC2-128
Friday 20 September
Patients with mutations in PHEX or FGF23 share FGF23 excess but present distinct bone and mineral metabolism features Claire Théret1, Laure Esterle2, Pierre-François Souchon3, Emma Allain-Launay4, Gwenaelle Roussey4, Georges Deschenes5, Catherine Chaussain5, Anya Rothenbuhler2, Dominique Prié5, Caroline Silve5, Peter Kamenicky5, Agnès Linglart2 1 Lons-le-Saunier, France, 2Kremlin-Bicêtre, France, 3Reims, France, 4Nantes, France, 5Paris, France FC2-129
Neuroradiologic and neurophysiologic study of the cranio-cervical junction in children affected by achondroplasia Mila Ann Kalapurackal, Valentina Donghi, Stefania Acerno, Cristina Baldoli, Stefania Medaglini, Giovanna Weber Milan, Italy FC2-130
High spontaneous osteoclastogenesis in paediatric osteogenesis imperfecta patients receiving and not receiving intravenous neridronate Maria Felicia Faienza, Albina Tummolo, Laura Piacente, Rita Fischetto, Maria Ciccarelli, Annamaria Ventura, Francesco Papadia, Maria Grano, Luciano Cavallo, Giacomina Brunetti Bari, Italy FC2-131
Adult Prader-Willi patients have smaller and weaker bones Silvia Longhi1, Graziano Grugni2, Davide Gatti3, Emiliano Spinozzi2, Giorgio Radetti1 1 Bolzano, Italy, 2Verbania, Italy, 3Verona, Italy
9th Joint Meeting of Paediatric Endocrinology 2013
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scientific Programme | Friday 20 September 2013
07:30 – 08:30
Room: Space 3
Session type:
Free Communication FC3
Session title:
Growth
Chairs:
Mauro Bozzola, Pavia, Italy Helen Storr, London, UK
FC3-132
An activating mutation of the natriuretic peptide receptor 2 causes extremely tall stature Sabine Elisabeth Hannema1, Hermine A. van Duyvenvoorde1, Thomas Premsler2, Ruey-Bing Yang3, Thomas D. Mueller2, Birgit Gaßner2, Heike Oberwinkler2, Ferdinand Roelfsema1, Gijs W.E. Santen1, Timothy Prickett4, Sarina G. Kant1, Annemieke J.M.H. Verkerk5, André G. Uitterlinden5, Eric Espiner4, Claudia A.L. Ruivenkamp1, Wilma Oostdijk1, Alberto M. Pereira1, Monique Losekoot1, Michaela Kuhn2, Jan M. Wit1 1 Leiden, Netherlands, 2Würzburg, Germany, 3Taipei, Taiwan, 4Christchurch, New Zealand, 5Rotterdam, Netherlands
Friday 20 September
FC3-133
Excess mortality in children born short Kerstin Albertsson-Wikland1, Lars Sävendahl2, Anton Mårtensson1, Aimon Niklasson1, Ann Hellström1, Nils-Gunnar Pehrson1, Anders Odén1 1 Gothenburg, Sweden, 2Stockholm, Sweden FC3-134
Heterozygous mutations in natriuretic peptide receptor-B gene as a cause of idiopathic short stature Gabriela A. Vasques1, Naoko Amano2, Ana Jung1, Mariana F.A. Funari1, Elisangela P.S. Quedas1, Ivo J.P. Arnhold1, Tomonobu Hasegawa2, Alexander A.L. Jorge1 1 Sao Paulo, Brazil, 2Tokyo, Japan FC3-135
The physiological role of circulating and breast milk adiponectin and leptin in infancy growth Philippa Prentice1, Ken Ong1, Marieke Schoemaker2, Eric van Tol2, Carlo Acerini1, Ieuan Hughes1, David Dunger1 1 Cambridge, UK, 2Nijmegen, Netherlands FC3-136
Trajectory analysis – a method to show growth patterns proceeding to obesity in children Nina Vuorela, Tiina Hakanen, Ulla Harjunmaa, Ludmila Lipiäinen, Marja-Terttu Saha, Matti Salo, Tapio Nummi Tampere, Finland FC3-137
Bone age assessment by a novel quantitative ultrasound based device, SonicBone, is comparable to the conventional Greulich and Pyle method Marianna Rachmiel1,2, Larisa Naugolny1, Kineret Mazor-Aronovitch2, Amnon Levin2, Nira Koren-Morag2, Tzvi Bistritzer1,2 1 Zerifin, Israel, 2Tel Aviv, Israel
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Friday 20 September 2013
08:45 – 09:45
Room: Gold
Session type:
Yearbook of Paediatric Endocrinology YB1
Session title:
Yearbook of Paediatric Endocrinology
Chairs:
Vũ Chí Dũng, Hanoi, Vietnam Hector Jasper, Buenos Aires, Argentina
Type 2 diabetes, metabolic syndrome, lipids Orit Pinhas-Hamiel, Ramat-Gan, Israel Obesity and weight regulation Martin Wabitsch, Ulm, Germany Growth and growth factors Stefano Cianfarani, Rome, Italy
08:45 – 09:45
Room: Brown 1
Session type:
Meet the Expert MTE4:1
Session title:
Beta-Cell Dysfunction of the Newborn
Friday 20 September
Growth plate, bone, calcium Outi Mäkitie, Helsinki, Finland
Khalid Hussain, London, UK SESSION AIM: Identification of molecular defects in glucose regulation of insulin secretion in the pancreas has expanded the options for diagnosis and treatment of neonatal diabetes and hyperinsulinism.
9th Joint Meeting of Paediatric Endocrinology 2013
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scientific Programme | Friday 20 September 2013
08:45 – 09:45
Room: Brown 3
Session type:
Free Communication FC4
Session title:
Puberty
Chairs:
Maria Carolina Salerno, Naples, Italy Jorma Toppari, Turku, Finland
FC4-138
Loss-of-function mutations in a gene cause central precocious puberty Ana Paula Abreu1,2, Andrew Dauber3, Delanie Bulcão Macedo2, Sekoni D. Noel1, Vinicius Nahime Brito2, John C. Gill1, Priscilla Cukier2, Iain R. Thompson1, Victor M. Navarro1, Priscila C. Gagliardi4, Tânia M. Rodrigues5, Cristiane Kochi6, Carlos A. Longui6, Dominique Beckers7, Francis de Zegher7, Luciana R. Montenegro2, Berenice B. Mendonca2, Rona S. Carroll1, Joel N. Hirschhorn3, Ana Claudia Latronico2, Ursula B. Kaiser1 1 Boston, USA, 2Sao Paulo, Brazil, 3Boston, USA, 4Jacksonville, USA, 5Belo Horizonte, Brazil, 6Sao Paulo, Brazil, 7Leuven, Belgium
Friday 20 September
FC4-139
The diagnostic value of first-voided urinary LH compared with GnRH-stimulated gonadotropins in differentiating slowly-progressive from rapidly progressive-precocious puberty in girls Amnon Zung, Ella Burundukov, Mira Ulman, Tamar Glaser, Moshe Rosenberg, Malka Chen, Zvi Zadik Rehovot, Israel FC4-140
Treated and untreated women with idiopathic precocious puberty in the 3rd and 4th decades: longterm follow-up and reproductive outcome Yael Lebenthal1, Joseph Meyerovitch1,2, Liat de Vries1,2, Moshe Phillip1,2, Liora Lazar1,2 1 Petah Tikva, Israel, 2Tel Aviv, Israel FC4-141
Novel genes underlying pubertal delay Sasha R.R. Howard, Helen Storr, Michael Barnes, Claudia Cabrera, Louise A. Metherell, Leo Dunkel London, UK FC4-142
Novel rare variants in POLR3A and POLR3B genes identified in 4H syndrome patients with and without isolated hypogonadotropic hypogonadism Luciana R. Montenegro, Marcela R. Freitas, Ericka B. Trabarch, Fernando Kok, Ana Claudia Latronico, Leticia G. Silveira Sao Paulo, Brazil FC4-143
Study of gender identity disorder in children and adolescents Sophie N. Khadr1, Polly Carmichael1, Victoria Holt1, Edna Roche2, Russell Viner1 1 London, UK, 2Dublin, Ireland
36
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Friday 20 September 2013
08:45 – 09:45
Room: Amber 3
Session type:
Meet the Expert MTE5:1
Session title:
Controversies in the Management of Hyperthyroidism in Children and Adolescents
Donald Zimmerman, Chicago, USA SESSION AIM: This session will review the options for medical, radioactive iodine and surgical therapy for hyperthyroidism. One should take into account the age of the patient, degree of disease and wishes of the patient.
08:45 – 09:45
Room: Amber 4
Session type:
Meet the Expert MTE6:1
Session title:
Endocrine Issues in Boys and Adolescents with Klinefelter Syndrome
Friday 20 September
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
Claus Højbjerg Gravholt, Aarhus, Denmark SESSION AIM: Klinefelter syndrome is much more than androgen deficiency. I will review the developmental and behavioral issues that might lead to earlier diagnosis and possible therapies given that only approximately 1:10 boys with this condition are diagnosed during childhood and adolescence.
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
9th Joint Meeting of Paediatric Endocrinology 2013
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scientific Programme | Friday 20 September 2013
08:45 – 09:45
Room: Space 1+2
Session type:
Free Communication FC5
Session title:
Programming and Epigenetics
Chairs:
Junfen Fu, Hangzhou, China Elizabeth Crowne, Bristol, UK
FC5-144
Paternal trans-generational effects of weaning age on maturational tempo-related gene expression in the newborn rat liver Philippa Melamed, Lilach Pnueli, Yonatan Crispel, Michael Shmoish, Ze’ev Hochberg Haifa, Israel
Friday 20 September
FC5-145
From bench to bedside: miR-155 and miR-370 are related with genotype and glucose tolerance state in cystic fibrosis Luisa Montanini1, Mariolina Gullì2, Arianna Smerieri1, Giovanna Pisi1, Sergio Bernasconi1, Nelson Marmiroli2, Maria E. Street1 Parma, Italy FC5-146
Chromatin profiling of germ cell cancer cell lines reveals differences in active enhancer states between seminomas and non-seminomas: a genvironmental connection? Yvonne G. van der Zwan1, Amanda Notini2, Fernando Rossello2, Suzan de Boer2, Leendert H.J. Looijenga1, Stefan White2 1 Rotterdam, Netherlands, 2Clayton, Australia FC5-147
CDKN1C mutation in the PCNA domain is a new mechanism for Silver-Russell syndrome Frederic Brioude1, Isabelle Oliver-Petit2, Annick Blaise1, Sylvie Rossignol1, Marilyne Le Jule1, Nathalie Thibaud1, Francoise Praz1, Anne-Marie Faussat1, Maithe Tauber2, Yves Le Bouc1, Irene Netchine1 1 Paris, France, 2Toulouse, France FC5-148
Higher blood pressure in 5- to 7-year-old children born preterm as compared to children born at term is not related to cortisol excretion rate Eva Landmann1, Verena Huke1, Stefan A. Wudy1, Michaela F. Hartmann1, Markus Brugger2, Konstantin Strauch2, Silvia Rudloff1 1 Giessen, Germany, 2Munich, Germany FC5-149
Clustering of cardio-metabolic risk factors during childhood and adolescence in subjects born small and large for gestational age Valentina Chiavaroli, Tommaso de Giorgis, M. Loredana Marcovecchio, Stefania De Marco, Cosimo Giannini, Francesco Chiarelli, Angelika Mohn Chieti, Italy
38
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Friday 20 September 2013
08:45 – 09:45
Room: Space 3
Session type:
Free Communication FC6
Session title:
Glucose Metabolism
Chairs:
Fergus Cameron, Melbourne, Australia Susana Campos, Manila, Philippines
FC6-150
IGFBP-2 enhances insulin signalling and glucose uptake in human skeletal myotubes Steven W. Yau, Vincenzo C. Russo, Iain J. Clarke, George A. Werther, Matthew A. Sabin Melbourne, Australia FC6-151
GLP1 levels and HMW adiponectin in children born small for gestational age with catch-up vs children born small for gestational age without catch-up; a possible explanation for their differences in carbohydrate metabolism and food intake Mario Angulo1, Marisol Badiel1, Enrique Jaramillo1, Contreras Catalina1, Diaz Marta2 1 Cali, Colombia, 2Barcelona, Spain
Friday 20 September
FC6-152
Higher relative risk for multiple sclerosis in a paediatric diabetes population: analysis from DPV database Susanne Bechtold1, Astrid Blaschek1, Klemens Raile2, Axel Dost3, Clemens Freiberg4, Meik Askenas5, Elke Fröhlich-Reiterer6, Esther Molz7, Reinhard W. Holl7 1 Munich, Germany, 2Berlin, Germany, 3Jena, Germany, 4Göttingen, Germany, 5Bielefeld, Germany, 6 Graz, Austria, 7Ulm, Germany FC6-153
Linear association between household income and metabolic control in children with insulindependent diabetes mellitus in spite of free access to health care Johnny Deladoey, Mélanie Henderson, Louis Geoffroy Montreal, Canada FC6-154
Early onset diabetes and hypoglycaemic seizures are associated with deteriorating IQ: evidence from a cohort with type 1 diabetes mellitus followed-up for 12 years from diagnosis Ashleigh Lin1, Elisabeth A. Northam2, George A. Werther2, Fergus J. Cameron2 1 Birmingham, UK, 2Melbourne, Australia FC6-155
Neonatal diabetes mellitus in a prospective cohort of 174 patients: frequent association with developmental defects and neuropsychological dysfunction Kanetee Busiah1, Séverine Drunat1, Laurence Vaivre-Douret1, Amélie Bonnefond2, Albane Simon3, Isabelle Flechtner1, Bénédicte Gérard1, Nathalie Pouvreau1, Caroline Elie1, Revital Nimri4, Liat De Vries4, Nadia Tubiana Rufi1, Chantal Metz5, Anne-Marie Bertrand6, Sylvie Nivot-Adamiak7, Marc de Kerdanet7, Chantal Stuckens2, Farida Jennane8, Véronique Sulmont9, Claire Le Tallec10, Nicole Ser10, Christelle Désirée1, Sabrina Pereira1, Aurélie Dechaume2, Moshe Phillip4, Raphael Scharfmann1, Paul Czernichow1, Philippe Froguel2,11, Martine Vaxillaire2, Michel Polak1, Hélène Cavé1, French NDM Study Group 1 Paris, France, 2Lille, France, 3Le Chesnay, France, 4Petah Tikva, Israel, 5Brest, France, 6Besançon, France, 7 Rennes, France, 8Casablanca, Morocco, 9Reims, France, 10Toulouse, France, 11London, UK
9th Joint Meeting of Paediatric Endocrinology 2013
39
scientific Programme | Friday 20 September 2013
10:15 – 10:45
Room: Gold
Session type:
Plenary Session PL3
Session title:
Programming Effects of Early Life Adversity – APPES
Chair:
Aman Pulungan, Jakarta, Indonesia
Friday 20 September
PL3-3 Wayne Cutfield, Auckland, New Zealand
10:45 – 12:15
Room: Gold
Session type:
Plenary Session PL4
Session title:
Joint Meeting Award Session 1
Chairs:
Jan Lebl, Prague, Czech Republic Anita Hokken-Koelega, Rotterdam, The Netherlands
ESPE Summer and Winter Schools – sponsored by Ferring Pharmaceuticals ESPE Science and Maghreb Schools – sponsored by Pfizer Endocrine Care ESPE Clinical Fellowships – sponsored by Merck Serono SA ESPE Research Fellowships – sponsored by ESPE and Novo Nordisk ESPE Sabbatical Leave Programme – sponsored by Eli Lilly and Company ESPE Research Unit Awards – sponsored by ESPE and Sandoz International GmbH IFCAH-ESPE Awards – supported by the International Fund for Research on Congenital Adrenal Hyperplasia ESPE Hormone Research in Paediatrics Prizes – sponsored by S. Karger AG – Medical and Scientific Publishers APPES Award – sponsored by APPES Henning Andersen Prizes – sponsored by Novo Nordisk A/S Presentation of best basic and clinical science abstracts. PL4-4 Basic
Rabconnectin-3α is a synaptic protein that controls pubertal onset and reproduction Juliane Leger1, Lukas Huijbregts1, Brooke Tata1, Sandrine Jacquier1, Emmanuelle Genin2, Sofia Leka1, Alexandra Durr1, Jeannette Nardelli1, Jean-Claude Carel1, Nicolas de Roux1 1 Paris, France, 2Brest, France PL4-5 Clinical
New molecular mechanism for severe familial isolated growth hormone deficiency type I due to mutations in the RNPC3 gene encoding the minor spliceosome 65KDa protein Jesus Argente1, Ivon Cusco2, Bhupendra Verma3, Gabriel A. Martos-Moreno1, Armand Gutierrez2, Raquel Flores2, Ali Oghabian3, Julie A. Chowen1, Mikko J. Frilander3, Luis A. Perez-Jurado2 1 Madrid, Spain, 2Barcelona, Spain, 3Helsinki, Finland ESPE Research Award and Lecture – sponsored by Pfizer Endocrine Care ESPE International Award – sponsored by Pfizer Endocrine Care
40
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Friday 20 September 2013
12:15 – 12:45
Room: Gold
Session type:
Plenary Session PL5
Session title:
Novel Therapy for the Metabolic Complications of Obesity – JSPE
Chair:
Tsutomo Ogata, Tokyo, Japan
PL5-6 Toru Miyazaki, Tokyo, Japan
13:00 – 14:00
Room: Exhibition Hall
Session type:
Poster Sessions
Guided Poster Tours – P1-d2, P2-d2
14:15 – 15:45
Room: Gold
Session type:
Symposium S7
Session title:
Vitamin D in Health and Disease
Friday 20 September
For further details see page 81.
Chairs: Giuseppe Saggese, Pisa, Italy Rasa Verkauskiene, Kaunas, Lithuania SESSION AIM: The aim of this session is to provide an update on vitamin D deficiency and its role in health and disease
S7-32
Clinical risk factors and impact of vitamin D deficiency in children Giovanna Weber, Milan, Italy Maternal vitamin D status is the determinant of neonate’s vitamin D reserve. Maternal deficiency can result in various consequences in newborn, including congenital rickets, affects the skeletal growth, tooth enamel formation, and calcium homeostasis. S7-33
Rickets, past, present and future Nick Shaw, Birmingham, UK In the past, rickets has been considered being defeated. But recently, there are evidences of increasing prevalence worldwide. Without any significant action regarding vitamin D status, rickets will become a huge health threat in the future. S7-34
Extra-skeletal effects of vitamin D Rebecca Mason, Sydney, Australia Vitamin D not only affects bone health, but is also considered as having a major role in preventing infection, cancer, autoimmune diseases, and diabetes mellitus. However, this will need further research.
9th Joint Meeting of Paediatric Endocrinology 2013
41
scientific Programme | Friday 20 September 2013
14:15 – 15:45
Room: Brown 3
Session type:
Controversies in Paediatric Endocrinology CPE2
Session title:
Idiopathic Short Stature: To Treat or Not To Treat?
Chairs:
Sandro Loche, Cagliari, Italy Toshiaki Tanaka, Tokyo, Japan
SESSION AIM: This session will debate whether and/or when hGH therapy for children with idiopathic short stature is justified by its rationale, benefits, potential risks, and costs.
CPE2-74
GH for ISS: A decade of safety and efficacy post-FDA approval Pinchas Cohen, Los Angeles, USA hGH treatment is justified for idiopathic short stature.
Friday 20 September
CPE2-75
Idiopathic short stature: still an enigma for therapy and response Martin O. Savage, London, UK hGH treatment is not justified for idiopathic short stature.
42
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Friday 20 September 2013
14:15 – 15:45
Room: Space 1+2
Session type:
Meeting Theme Symposium S8
Session title:
The Adipose Organ: All Fat Is Not Created Equal
Chairs:
Wieland Kiess, Leipzig, Germany Tohru Yorifuji, Osaka, Japan
SESSION AIM: This session will improve the understanding of the biology of adiposity by exploring how fat location, sex, race, and other factors affect function and dysfunction of this new endocrine organ.
S8-35
Development of the adipose organ Peter Arner, Stockholm, Sweden This lecture will discuss the development of the fat cell – its differentiation, structure, and function in energy homeostasis. S8-36
Friday 20 September
Adipose tissue as endocrine organ Philipp Scherer, Dallas, USA This lecture will discuss adipose tissue as endocrine organ, and how caloric excess contributes to its dysregulation and the metabolic syndrome. S8-37
Sex and racial influences on adipose organ function and dysfunction Sonia Caprio, New Haven, USA This lecture will discuss recently recognised genetic effects on adipose organ function which lead to sex and racial differences in morbidities associated with obesity.
9th Joint Meeting of Paediatric Endocrinology 2013
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scientific Programme | Friday 20 September 2013
14:15 – 15:45
Room: Space 3
Session type:
Symposium S9
Session title:
The Testis in 3D (Development, Descent, Dysfunction)
Chairs:
Alfonso Vargas, New Orleans, USA Peter Lee, Hershey, USA
SESSION AIM: This symposium gives a translational update on testicular development and markers of testicular function in childhood.
S9-38
Update on testis development Richard Sharpe, Edinburgh, UK The speaker will give a translational update on testis development.
Friday 20 September
S9-39
Next generation sequencing reveals new genetic factors involved in human testicular development Ken McElreavey, Paris, France This talk will present an extended list of genes involved in testicular development and implicated in disorders of sexual development. S9-40
Anti-Müllerian hormone as a marker of paediatric male hypogonadism Rodolfo Rey, Buenos Aires, Argentina This presentation will give an overview of what markers to use to evaluate testis function in a clinical setting.
14:15 – 15:45
Room: Space 4
Session type:
Symposium S10
Session title:
Endocrine Tumours in Childhood
Chairs:
Chris Kelnar, Edinburgh, UK Cheri Deal, Montreal, Canada
SESSION AIM: This session will provide an update on basic mechanisms underlying tumour susceptibility in childhood and their practical consequences in terms of screening and management.
S10-41
SDH mutations and susceptibility to paraganglioma Anne-Paule Gimenez-Roqueplo, Paris, France Multiple molecular mechanisms underlie the pathogenesis of paragangliomas. Their identification allows specific follow-up and familial screening. S10-42
Genetic origin of pituitary adenomas Marta Korbonits, London, UK AIP (aryl hydrocarbon–interacting protein gene) mutations underlie familial pituitary, in particular GH-producing, adenomas. The clinical presentation and implications for managements will be discussed. S10-43
Familial forms of thyroid cancer Steven Waguespack, Houston, USA Familial forms of thyroid cancers concern not only medullary cell cancer, as part of MEN type 2, but also differentiated thyroid cell cancers. This has important implications for the management and for familial counseling.
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Friday 20 September 2013
16:15 – 17:45
Room: Brown 1
Session type:
Business Meetings
Session title:
Business Meeting – SLEP
For members only
16:15 – 17:45
Room: Space 3
Session type:
Business Meetings
Session title:
Business Meeting – ESPE
18:00 – 19:30
Room: Gold
Session type:
Joint Meeting Satellite Symposium SAT4
Session title:
What’s New in Adrenal Disorders
Friday 20 September
For members only
Sponsored by Sandoz Chairs:
Lucia Ghizzoni, Turin, Italy Jérôme Bertherat, Paris, France
The conundrum of premature adrenarche – clues from the steroid metabolome Wiebke Arlt, Birmingham, UK Adrenalectomy for paediatric Cushing’s syndrome Martin O. Savage, London, UK Congenital adrenal hyperplasia: an update Christa Flück, Bern, Switzerland
18:00 – 19:30
Room: Space 1+2
Session type:
Joint Meeting Satellite Symposium SAT5 Practical Application of Personalised Medicine in Paediatric and Adolescent Endocrinology
Session title:
Sponsored by Pfizer Specialty Care Chairs: Ron Rosenfeld, Portland, USA Jovanna Dahlgren, Gothenburg, Sweden How can personalised medicine aid the management of patients during transition? Ajay Thankamony, Cambridge, UK Patient-centred care during transition John Gregory, Cardiff, UK Practical illustrations of growth prediction Wayne Cutfield, Auckland, New Zealand Health economic considerations in the management of growth disorders in children Joris Kleintjens, Brussels, Belgium
9th Joint Meeting of Paediatric Endocrinology 2013
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scientific Programme | Friday 20 September 2013
18:00 – 19:30
Room: Space 4
Session type:
Joint Meeting Satellite Symposium SAT6
Session title:
SHOX-ing News about Growth: Updates on Genetics, Clinical Characteristics and Treatment of Children with SHOX Deficiency Sponsored by Eli Lilly and Company
Chairs:
Stenvert L.S. Drop, Rotterdam, Netherlands Alexander A.L. Jorge, Sao Paulo, Brazil
Basic research: new insights into role and regulation of SHOX in linear bone growth Karen Heath, Madrid, Spain An update: who should be tested for SHOX deficiency and how? Gerhard Binder, Tübingen, Germany
Friday 20 September
Long-term outcomes of somatropin treatment of short stature associated with SHOX deficiency Charmian A. Quigley, Indianapolis, USA
46
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
Programme at a Glance
Daily programme
Saturday 21 September Saturday 21 September MTE1:2
Molecular Diagnosis and Management of Hereditary Gynaecomastia
Brown 1 [48]
FC7
GH and IGF in Health and Disease Brown 3 [48]
MTE3:2
Pituitary Adenoma and Incidentaloma Amber 3 [49]
MTE4:2
Beta-Cell Dysfunction of the Newborn Amber 4 [49]
FC8
FC9
Space 1+2 [50]
Space 3 [51]
Disorders of Sex Differentiation
Adrenal Steroidogenesis
MTE2:2
Type 1 Diabetes in Preschool Children Space 4 [52]
PL6 Long-term Follow-up of Patients with Disorders of Sex Development – SLEP “Cesar Bergadá Lecture“ Gold [52]
PL7
Joint Meeting Award Session 2 Gold [52]
PL8 The Nature of Nutrition: an Integrative Framework from Animal Adaptation to Human Obesity – APEG Gold [52]
COFFEE BREAK. Visit to the Posters and Exhibition Area
MTE7:1
FC10
MTE8:1
Brown 1 [52]
Brown 3 [53]
Amber 3 [54]
Management of Hyponatraemia
Pituitary and Neu- The Child with roendocrinology Very Small Penis
MTE9:1
Clinical Prediction Tools: the Example of Growth Monitoring Amber 4 [54]
NP2
Genome Sequencing Promise in Paediatric Endocrinology Space 1+2 [54]
FC11
FC12
Space 3 [55]
Space 4 [56]
Congenital Hyperinsulinism
Mineral Metabolism
LUNCH. Visit to the Posters and Exhibition Area Guided Poster Tours 12:45–13:45 – P1-d3, P2-d3 [81]
S11
S12
Gold [57]
Brown 3 [57]
Environmental and Genetic Disorders of Puberty
Glucocorticoid Effects in Bone and Cartilage Tissues
S19
Symposium for Nurses and Allied Healthcare Professionals Amber 3 [58]
CPE3
Detection and Treatment of Congenital Subclinical Hypothyroidism Space 1+2 [58]
S13
Why Doesn’t Everyone Become Obese: Energy Intake and Expenditure Space 3 [59]
Saturday 21 September
POSTER AND EXHIBITION
07:30 07:45 08:00 08:15 08:30 08:45 09:00 09:15 09:30 09:45 10:00 10:15 10:30 10:45 11:00 11:15 11:30 11:45 12:00 12:15 12:30 12:45 13:00 13:15 13:30 13:45 14:00 14:15 14:30 14:45 15:00 15:15 15:30 15:45 16:00 16:15 16:30 16:45 17:00 17:15 17:30 17:45 18:00 18:15 18:30 18:45 19:00 19:15 19:30 19:45 20:00 20:15
S14
Autoimmunity in Paediatric Endocrinology Space 4 [60]
COFFEE BREAK. Visit to the Posters and Exhibition Area
MTE10:1
Diagnosis and Treatment of Adrenal Insufficiency Brown 1 [60]
SAT7
FC13
Endocrine Oncology Brown 3 [61]
MTE11:1
Clinical Management of Hypocalcaemia Amber 3 [62]
The First 1000 Days – Early Nutrition and Long-term Consequences Sponsored by Nestlé Nutrition Brown 3 [65]
MTE12:1
Molecular Genetic Investigation of the Child with Short Stature Amber 4 [62]
YB2
Yearbook of Paediatric Endocrinology Space 1+2 [62]
FC14
Perinatal and Neonatal Endocrinology Space 3 [63]
FC15
Adipose Tissue Space 4 [64]
SAT9
SAT8
Overcoming the Hypoglycaemia Barrier for Optimal Metabolic Control: the Role of New Technologies Sponsored by Medtronic Space 1+2 [65]
Growth Hormone and IGF-1: Ready to Wear or Bespoke Treatment for the Short Child? Sponsored by Ipsen Space 4 [65]
Children’s Charity Concert and Joint Meeting Evening at MiCo
[242]
CPE = Controversies in Paediatric Endocrinology FC = Free Communication Session MTE = Meet the Expert NP = New Perspectives PL = Plenary Lecture
S = Symposium S = Meeting Theme Symposium SAT = Joint Meeting Satellite Symposium WG = Joint Meeting Working Group YB = Yearbook of Paediatric Endocrinology
Rooms and Halls in italics [Page in Final Programme]
9th Joint Meeting of Paediatric Endocrinology 2013
47
scientific Programme | Saturday 21 September 2013
07:30 – 08:30
Room: Brown 1
Session type:
Meet the Expert MTE1:2
Session title:
Molecular Diagnosis and Management of Hereditary Gynaecomastia
Maki Fukami, Tokyo, Japan SESSION AIM: Hereditary gynaecomastia is caused by overexpression of CYP19A1 encoding aromatase. This session is aimed to introduce underlying genomic rearrangements and successful treatment of gynaecomastia.
07:30 – 08:30
Room: Brown 3
Session type:
Free Communication FC7
Session title:
GH and IGF in Health and Disease
Chairs:
Akira Shimatsu, Kyoto, Japan Jan-Maarten Wit, Leiden, Netherlands
FC7-156
GH signalling independent of IGF-1 induces increased linear bone growth in SOCS2 knockout mice Ross Dobie1, Vicky MacRae1, Chloe Pass1, Seema Jasim1, Faisal Ahmed2, Colin Farquharson1 1 Edinburgh, UK, 2Glasgow, UK
Saturday 21 September
FC7-157
Multiple perturbations to the insulin-like growth factor 1 pathway and adult energy homeostasis following disruption of mouse chromosome 12 imprinting Marika Charalambous1,2, Simao T. Da Rocha2,3, Arturo Hernandez4, Anne C. Ferguson-Smith2 1 London, UK, 2Cambridge, UK, 3Paris, France, 4Maine, USA FC7-158
Changes in serum insulin, insulin-like growth factor-I and growth in GH deficient children treated with GH are associated with distinct gene expression networks Adam Stevens1, Chiara De Leonibus1, Benoit Destenaves2, Pierre Chatelain3, Peter Clayton1, the PREDICT Investigator Group 1 Manchester, UK, 2Geneva, Switzerland, 3Lyon, France FC7-159
Body composition changes in adolescents with childhood-onset GH deficiency during the transition phase in relation to the GH retest peak: sex matters Gerhard Binder, Bettina Becker, Jana-Leonie Bauer, Roland Schweizer Tuebingen, Germany FC7-160
Genetic characterisation of short children with potential defects of GH action by single gene sequencing Julia Kowalczyk, Evelien F. Gevers, Martin O. Savage, Leo Dunkel, Louise A. Metherell, Helen L. Storr London, UK FC7-161
Increased IGF-1R affinity of insulin glargine, but not its metabolites, is caused by a faster association rate and, less, by a slower dissociation rate Peter Bang1, Christine Skwirut-Carlsson2 1 Linköping, Sweden, 2Stockholm, Sweden
48
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
07:30 – 08:30
Room: Amber 3
Session type:
Meet the Expert MTE3:2
Session title:
Pituitary Adenoma and Incidentaloma
Annamaria Colao, Naples, Italy SESSION AIM: Most pituitary MRI abnormalities are microincidentalomas and non-functional, but endocrinopathies or visual field defects may be present. The differential diagnosis of pituitary adenoma and incidentaloma will be reviewed.
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
07:30 – 08:30
Room: Amber 4
Session type:
Meet the Expert MTE4:2 Beta-Cell Dysfunction of the Newborn
Session title:
Khalid Hussain, London, UK SESSION AIM: Identification of molecular defects in glucose regulation of insulin secretion in the pancreas has expanded the options for diagnosis and treatment of neonatal diabetes and hyperinsulinism.
Saturday 21 September
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
9th Joint Meeting of Paediatric Endocrinology 2013
49
scientific Programme | Saturday 21 September 2013
07:30 – 08:30
Room: Space 1+2
Session type:
Free Communication FC8
Session title:
Disorders of Sex Differentiation
Chairs:
Kenichi Kashimada, Tokyo, Japan Marco Rivarola, Buenos Aires, Argentina
FC8-162
Endocrine disruption in the human fetal testis. The effects of exposure to acetominophen (paracetamol) on testosterone production and steroidogenesis Rod T. Mitchell, Richard M. Sharpe, Zoe Johnston, Chris J.H. Kelnar, Hamish Wallace, Richard A. Anderson, Sander van den Driesche Edinburgh, UK FC8-163
Gonadal localization and tumor risk markers in disorder of sexual development patients during prepuberty Esperanza Berensztein, Costanzo Mariana, Gabriela Guercio, Roxana Marino, Pablo Ramirez, Natalia Perez Garrido, Mercedes Maceiras, Marcela Bailez, Marco A. Rivarola, Alicia Belgorosky Buenos Aires, Argentina FC8-164
A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties Evangelia Charmandari1, Meilin Zhang2, Letícia Gontijo Silveira3, George P. Chrousos1, Amalia Sertedaki1, Ana Claudia Latronico3, Deborah L. Segaloff2 1 Athens, Greece, 2Iowa City, USA, 3São Paulo, Brazil
Saturday 21 September
FC8-165
APOD bioassay confirms CAIS in a 46,XY newborn with female external genitalia in the absence of a coding AR-gene mutation Nadine C.D. Hornig1, Martine Cools2, Carine De Beaufort3, Alexandra E. Kulle1, Maik Welzel1, Ralf Werner4, Olaf Hiort4, Ole Ammerpohl1, Paul-Martin Holterhus1 1 Kiel, Germany, 2Ghent, Belgium, 3Luxembourg, Luxembourg, 4Lübeck, Germany FC8-166
Temporal changes in sex assignment based on data gathered from the I-DSD Registry Zofia Kolesinska1, S. Faisal Ahmed2, Jillian Bryce2, Mona Alkhawari3, Wiebke Arlt4, Antonio Balsamo5, Silvano Bertelloni6, Pierre Chatelain7, Martine Cools8, Feyza Darendeliler9, An Desloovere8, Sten Drop10, Mona Ellaith11, Tulay Guran12, Olaf Hiort13, Paul-Martin Holterhus14, Ieuan Hughes15, Katherine Lachlan16, Lidka Lisa17, Inas Mazen18, Harriet Miles15, Anna Nordenstrom19, Martina Rodie2, Olle Soder19, Rieko Tadokoro-Cuccaro15, Naomi Weintrob20, Yvonne van der Zwan10, Marek Niedziela1 1 Poznan, Poland, 2Glasgow, UK, 3Kuwait City, Kuwait, 4Birmingham, UK, 5Bologna, Italy, 6Pisa, Italy, 7 Lyon, France, 8Ghent, Belgium, 9İstanbul, Turkey, 10Rotterdam, Netherlands, 11Khartoum, Sudan, 12 Istanbul, Turkey, 13Lübeck, Germany, 14Kiel, Germany, 15Cambridge, UK, 16Southampton, UK, 17Prague, Czech Republic, 18Cairo, Egypt, 19Stockholm, Sweden, 20Tel Aviv, Israel FC8-167
Phalloplasty: a valuable treatment for men with disorders of sex development and micropenis? Nina Callens, Griet De Cuypere, Eline Van Hoecke, Guy T’Sjoen, Stan Monstrey, Piet Hoebeke, Martine Cools Ghent, Belgium
50
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
07:30 – 08:30
Room: Space 3
Session type:
Free Communication FC9
Session title:
Adrenal Steroidogenesis
Chairs: Olaf Hiort, Lubeck, Germany Wiebke Arlt, Birmingham, UK FC9-168
Identification and developmental changes in the expression of the enzymes from the “backdoor pathway” in prepubertal and pubertal human adrenal tissues Maria Sonia Baquedano, Sabrina Madjinca, Marco A. Rivarola, Alicia Belgorosky Buenos Aires, Argentina FC9-169
New insights into the in vivo regulation of steroidogenesis: P450 side-chain cleavage enzyme and ferredoxin specifically regulate interrenal steroid synthesis in zebrafish Silvia Parajes, Aliesha Griffin, Angela E. Taylor, Cedric Shackleton, Ferenc Müller, Nils Krone Birmingham, UK FC9-170
Compensated mild androgen deficiency in boys with steroid sulfatase deficiency: evidence from steroid metabolomics Jan Idkowiak1, Angela E. Taylor1, Donna M. O’Neil1, Sandra Subtil1, Raymon Vijzelaar2, Renuka P. Dias1, Rakesh Amin3, Timothy G. Barrett1, Jeremy Kirk1, Cedric H. Shackleton1, Celia Moss1, Wiebke Arlt1 1 Birmingham, UK, 2Amsterdam, Netherlands, 3London, UK Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites Yuhei Koyama1, Keiko Homma1, Maki Fukami1, Masayuki Miwa1, Kazushige Ikeda1, Tsutomu Ogata1,2, Mitsuru Murata1, Tomonobu Hasegawa1 1 Tokyo, Japan, 2Shizuoka, Japan FC9-172
The effect of a novel compound heterozygous PAPSS2 mutation in two brothers with spondyloepimetaphyseal dysplasia on DHEA sulfation and androgen synthesis and metabolism Wilma Oostdijk1, Jan Idkowiak2, Jonathan W. Mueller2, Angela E. Taylor2, Beverley A. Hughes2, Martine C. de Vries1, Sarina G. Kant1, Annemieke J.M.H. Verkerk3, Andre G. Uitterlinden3, Jan M. Wit1, Monique Losekoot1, Wiebke Arlt2 1 Leiden, Netherlands, 2Birmingham, UK, 3Rotterdam, Netherlands FC9-173
Androgen receptor CAG repeat length in relation to phenotype of females with non-classical 21-hydroxylase deficiency Itay Ayalon1, Shay Ben-Shachar2,3, Yardena Tenenbaum-Rakover4,5, Nehama Zukerman-Levin6, Anita Schachter-Davidov7, Shoshana Israel8, Ilana Koren9, Dalit Modan10, Ori Eyal3,7, Naomi Weintrob3,7 1 Tel Aviv, Israel, 2Tel Aviv, Israel, 3Tel Aviv, Israel, 4Afula, Israel, 5Haifa, Israel, 6Haifa, Israel, 7Tel Aviv, Israel, 8Jerusalem, Israel, 9Haifa, Israel, 10Tel-Hashomer, Israel
9th Joint Meeting of Paediatric Endocrinology 2013
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Saturday 21 September
FC9-171
scientific Programme | Saturday 21 September 2013
07:30 – 08:30
Room: Space 4
Session type:
Meet the Expert MTE2:2
Session title:
Type 1 Diabetes in Preschool Children
Ragnar Hanas, Uddevalla, Sweden SESSION AIM: This Meet the Expert session will focus on peculiar management of children with diabetes during the first months and years of life. In preschool children diabetes is difficult to manage for the instability of glycaemia and particularly for the risk of brain damage consequent to hypoglycaemia. Insulin treatment, glucose monitoring and indications for the use of continuous subcutaneous insulin infusion will also be discussed.
08:45 – 09:15
Room: Gold
Session type:
Plenary Session PL6
Session title:
Long-term Follow-up of Patients with Disorders of Sex Development – SLEP “Cesar Bergadá Lecture”
Chair:
Fernando Cassorla, Santiago, Chile
Saturday 21 September
PL6-7 Berenice Mendonca, São Paulo, Brazil
09:15 – 10:30
Room: Gold
Session type:
Plenary Session PL7
Session title:
Joint Meeting Award Session 2
Chairs:
Laura Audi, Barcelona, Spain Lars Sävendahl, Stockholm, Sweden
ESPE Young Investigator Award 1+2 – sponsored by Pfizer Endocrine Care APEG Young Investigator Presentation – sponsored by APEG SLEP Young Investigator Lecture – sponsored by by SLEP ESPE Outstanding Clinician Award – sponsored by Pfizer Endocrine Care ESPE Andrea Prader Prize – sponsored by Pfizer Endocrine Care
10:30 – 11:00
Room: Gold
Session type:
Plenary Session PL8
Session title:
The Nature of Nutrition: an Integrative Framework from Animal Adaptation to Human Obesity – APEG
Chair:
Paul Hoffman, Auckland, New Zealand
PL8-8 Stephen Simpson, Sydney, Australia
11:30 – 12:30
Room: Brown 1
Session type:
Meet the Expert MTE7:1
Session title:
Management of Hyponatraemia
Mohamad Maghnie, Genoa, Italy SESSION AIM: Hyponatraemia is defined as a serum sodium concentration of less than 136 mmol/L. Its appropriate management may be challenging and reliant on the accurate identification of the underlying cause.
52
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
11:30 – 12:30
Room: Brown 3
Session type:
Free Communication FC10
Session title:
Pituitary and Neuroendocrinology
Chairs:
Susan Rose, Cincinnati, USA Primus Mullis, Bern, Switzerland
FC10-174
Novel syndrome of microcephaly, endocrine, visual and renal abnormalities caused by ARNT2 mutation Emma A. Webb1, Angham Almutair2, Dan Kelberman1, Chiara Bacchelli1, Estelle Chanudet1, Francesco Lescai1, Cynthia Andoniadou1, Derek Burke1, Mark Mccabe1, Tessa Kasia1, Robert Kleta1, Fowzan Alkuraya2, Juan Pedro Martinez-Barbera1, Jane C. Sowden1, Mehul T. Dattani1 1 London, UK, 2Riyadh, Saudi Arabia FC10-175
The repressor activity of the Wnt/β-Catenin effector Tcf3/TCF7L1 is required for normal hypothalamic-pituitary development Carles Gaston-Massuet1, Mark McCabe1, Wu Chun-I.2, Neda Mousavy1, Sergei Y. Sokol3, Mehul T. Dattani1, Juan Pedro Martinez-Barbera1 1 London, UK, 2Chicago, USA, 3New York, USA FC10-176
Five novel mutations of IGSF1 in six Japanese patients with X-linked congenital central hypothyroidism Syuntarou Morikawa1, Beata Bak2, Jessica Lam2, Tomoyuki Hotsubo1, Toru Yorifuji3, Akie Nakamura1, Katura Ishizu1, Daniel J. Bernard2, Toshihiro Tajima1 1 Sapporo, Japan, 2Montreal, Canada, 3Osaka, Japan The IGSF1 deficiency syndrome: clinical and biochemical characteristics of male and female patients Sjoerd Joustra1, Nadia Schoenmakers2, Wilma Oostdijk1, Nienke R. Biermasz1, Marco Bonomi3, Giorgio Radetti4, Luca Persani3, Irene Campi3, Alberto M. Pereira1, Aimée Varewijck5, Joop A.M.J.L. Janssen5, Krishna Chatterjee2, Mehul T. Dattani6, A. S. Paul van Trotsenburg7, Jan Maarten Wit1 1 Leiden, Netherlands, 2Cambridge, UK, 3Milan, Italy, 4Bolzano, Italy, 5Rotterdam, Netherlands, 6London, UK, 7Amsterdam, Netherlands FC10-178
Linkage analysis of autosomal dominant hypopituitarism and maternal gingival fibromatosis in a large Finnish pedigree Johanna Tommiska1, Rainer Fagerholm1, Johanna Känsäkoski1, Päivi Lahermo1, Mari Kaunisto1, Riikka Keski-Filppula2, Kari Kaunisto2, Franziska Phan-Hug3, Nelly Pitteloud3, Riitta Veijola2, Taneli Raivio1 1 Helsinki, Finland, 2Oulu, Finland, 3Lausanne, Switzerland FC10-179
Ancestral origin of two most prevalent mutations in the PROP1 gene causing combined pituitary hormone deficiency in selected European populations Petra Dusatkova1, Roland Pfäffle2, Barbora Obermannova1, Rasa Verkauskiene3, Natallia Akulevich4, Jana Malikova1, Zuzana Pribilincova5, Agnes Sallai6, Gordana Stipancic7, Ciril Krzisnik8, Werner Blum2, John Parks9, Ondrej Cinek1, Jan Lebl1 1 Prague, Czech Republic, 2Leipzig, Germany, 3Kaunas, Lithuania, 4Minsk, Belarus, 5Bratislava, Slovakia, 6 Budapest, Hungary, 7Zagreb, Croatia, 8Ljubljana, Slovenia, 9Atlanta, USA
9th Joint Meeting of Paediatric Endocrinology 2013
53
Saturday 21 September
FC10-177
scientific Programme | Saturday 21 September 2013
11:30 – 12:30
Room: Amber 3
Session type:
Meet the Expert MTE8:1
Session title:
The Child with Very Small Penis
Tomohiro Ishii, Tokyo, Japan SESSION AIM: Very small penis (“micropenis”) is a penis of very small size with a normal morphology. Paediatric endocrinologists face a lot of difficult clinical questions on very small penis. This Meet the Expert will mainly focus on initial evaluation and management.
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
11:30 – 12:30
Room: Amber 4
Session type:
Meet the Expert MTE9:1 Clinical Prediction Tools: the Example of Growth Monitoring
Session title:
Martin Chalumeau, Paris, France SESSION AIM: Clinical decision is a complex process that should be aided by evaluated clinical decision rules. Their use in paediatric endocrinology for the selection of short children for GH testing and for MRI examination in precocious puberty will be discussed.
Saturday 21 September
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
11:30 – 12:30
Room: Space 1+2
Session type: New Perspectives NP2 Session title:
Genome Sequencing Promise in Paediatric Endocrinology
Chairs: Osamu Arisaka, Shimotsuga, Japan Durval Damiani, Sao Paulo, Brazil SESSION AIM: New technologies, such as next generation or massively parallel DNA sequencing, have great potential in genetics research. The large quantities of data produced require advances in informatics and new clinical skills.
NP2-70
The impact of next generation sequencing on paediatric endocrine research Louise A. Metherell, London, UK An update on emerging genetic technology and its power to uncover molecular roots of clinical disorders. NP2-71
Application of genome-wide association studies to childhood diseases Struan Grant, Philadelphia, USA Genome-wide association studies in key paediatric populations have provided insight into the genetics of childhood diseases and are changing our understanding of pathophysiology and treatment.
54
9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
11:30 – 12:30
Room: Space 3
Session type:
Free Communication FC11
Session title:
Congenital Hyperinsulinism
Chairs:
Franco Meschi, Milan, Italy Timo Otonkoski, Helsinki, Finland
FC11-180
Gene expression profiling reveals possible role of growth factors in beta-cell hyperplasia in congenital hyperinsulinism Senthil Senniappan, Peter Hindmarsh, Khalid Hussain London, UK FC11-181
Network analysis can be used to predict signalling pathways associated with the pathobiology of congenital hyperinsulinism Adam Stevens, Karen E. Cosgrove, Mars S. Skae, Raja Padidela, Peter E. Clayton, Indi Banerjee, Mark J. Dunne Manchester, UK FC11-182
Islet somatostatin receptor expression is altered in children with congenital hyperinsulinism Yanqin Shi, Adam Stevens, Mars S. Skae, Bindu Avatapalle, Lindsey Rigby, Raja Padidela, Karen E. Cosgrove, Peter E. Clayton, Indi Banerjee, Mark J. Dunne Manchester, UK Understanding the molecular basis of congenital hyperinsulinism due to autosomal dominant ABCC8 and KCNJ11 mutations Azizun Nessa1, Alison Thomas1, Qadeer H. Aziz1, Steve Harmer1, Amanda Heslegrave1, Chela James1, Ved B. Arya1, Sofia Rahman1, Maha Sherif1, Sarah E. Flanagan2, Ritika R. Kapoor1, Sian S. Ellard2, Andrew Tinker1, Khalid Hussain1 1 London, UK, 2Exeter, UK FC11-184
A pilot trial of supplemental omega-3-polyunsaturated fatty acids may reduce risk of hypoglycaemia in children with congenital hyperinsulinism Bindu Avatapalle, Mars Skae, Indraneel Banerjee, Andy Vail, Lindsey Rigby, Louise Caine, Raja Padidela, Leena Patel, Sarah Ehtisham, Karen E. Cosgrove, Mark J. Dunne, Peter E. Clayton Manchester, UK FC11-185
Successful treatment of five patients with severe hyperinsulinaemic hypoglycaemia with a novel therapy using mTOR inhibitor Senthil Senniappan1, Pratik Shah1, Ved Arya1, Sarah Flanagan2, Sian Ellard2, Dyanne Rampling1, Michael Ashworth1, Khalid Hussain1 1 London, UK, 2Exeter, UK
9th Joint Meeting of Paediatric Endocrinology 2013
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Saturday 21 September
FC11-183
scientific Programme | Saturday 21 September 2013
11:30 – 12:30
Room: Space 4
Session type:
Free Communication FC12
Session title:
Mineral Metabolism
Chairs:
Feyza Darendeliler, Istanbul, Turkey Toshimi Michigami, Osaka, Japan
FC12-186 Functional rescue of inactivating and activating mutant CASRs by allosteric modulators
Akie Nakamura, Syuntarou Morikawa, Katsura Ishizu, Toshihiro Tajima Sapporo, Japan FC12-187
Anticalciuric effect of recombinant PTH in patients with activating mutations of the calciumsensing receptor causing autosomal dominant hypocalcaemia-hypercalciuria Anya Rothenbuhler1, Jeremy Allgrove2, Regis Coutant3, Klaus Kapelari4, Lucie Bessenay5, Myriam Isnard6, Wolfgang Hogler7, Pierre Bougneres1, Agnès Linglart1, ESPE Working Group on Bone and Growth Plate 1 Le Kremlin-Bicêtre, France, 2London, UK, 3Angèrs, France, 4Innsbruck, Austria, 5Clermont Ferrand, France, 6Riom, France, 7Birmingham, UK FC12-188
Effects of the anti-rank ligand denusomab on adolescents with beta thalassaemia major-induced osteoporosis Ashraf Soliman1, Mohamed Yassin1, Ahmed Elawwa1, Aml Sabt1, Vincenzo De Sanctis2 1 Doha, Qatar, 2Ferrara, Italy
Saturday 21 September
FC12-189
The effect of nutritional rickets on bone mineral density Tom D. Thacher1, Philip R. Fischer1, John M. Pettifor2 1 Rochester, USA, 2Johannesburg, South Africa FC12-190
Patterns of renal distal tubule PTH sensitivity in subtypes of pseudohypoparathyroidism Emmanuelle Motte, Virginie Grybek, Caroline Silve, Agnès Linglart Le Kremlin-Bicêtre, France FC12-191
Comprehensive genetic analyses of primary hypoparathyroidism using next-generation sequencing Toshikatsu Mitsui1, Satoshi Narumi1, Mikako Inokuchi1, Keisuke Nagasaki2, Hironori Shibata1, Tomohiro Ishii1, Yasumasa Iwasaki3, Tomonobu Hasegawa1 1 Tokyo, Japan, 2Niigata, Japan, 3Kochi, Japan
12:45 – 13:45
Room: Exhibition Hall
Session type:
Poster Sessions
Guided Poster Tours – P1-d3, P2-d3
For further details see page 81.
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
14:00 – 15:30
Room: Gold
Session type:
Symposium S11
Session title:
Environmental and Genetic Disorders of Puberty
Chairs:
Yves Morel, Lyon, France Carine de Beaufort, Luxembourg, Luxembourg
SESSION AIM: Environmental factors and many new genes have been associated with early or late onset of puberty. These novel findings shed new insights into the mechanisms that control the reproductive axis.
S11-44
Trends in puberty timing and environmental modifiers Anders Juul, Copenhagen, Denmark The earlier onset of puberty cannot be explained by genetic factors. Environmental factors, such as obesity and endocrine disruptors have been suspected. S11-45
Multigenetic control of the onset of puberty Ken Ong, Cambridge, UK Genome-wide association studies revealed a genetic basis for the timing of puberty as well as a link to body weight regulation. S11-46
14:00 – 15:30
Room: Brown 3
Session type:
Symposium S12
Session title:
Glucocorticoid Effects in Bone and Cartilage Tissues
Chairs:
Alicia Belgorosky, Buenos Aires, Argentina Nalini Shah, Mumbai, India
Saturday 21 September
Genetic causes of central precocious puberty Ana Claudia Latronico, Sao Paulo, Brazil The first genetic causes of central precocious puberty have been recently described. In parallel, several genes have been implicated in the etiology of normosmic hypogonadotropic hypogonadism.
SESSION AIM: This is a symposium which will review the biochemical and molecular mechanisms of glucocorticoid actions in bone and cartilage tissues, facilitating our understanding of how glucocorticoids negatively influence bone growth and bone health in children and adolescents.
S12-47
Mechanisms of glucocorticoid action in bone and cartilage tissues Farasat Zaman, Stockholm, Sweden The presentation will review biochemical and molecular mechanisms of glucocorticoid actions in bone and cartilage tissues. Possible targets for the prevention of glucocorticoid-induced side effects will also be highlighted. S12-48
Clinical management of growth impairment in chronic disease S. Faisal Ahmed, Glasgow, UK The talk will review the clinical problem of glucocorticoid-induced bone growth impairment in growing individuals. In addition, possible ways to reduce the negative impact of glucocorticoids on bone growth will be reviewed. S12-49
Manifestations, prevention and treatment of osteoporosis in children with glucocorticoid-treated diseases Leanne Ward, Ottawa, Canada The lecture will highlight the effects of glucocorticoids on bone healths in children and adolescents. Different strategies to prevent the negative effects of glucocorticoids on bone tissue will be discussed.
9th Joint Meeting of Paediatric Endocrinology 2013
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scientific Programme | Saturday 21 September 2013
14:00 – 15:30
Room: Amber 3
Session type:
Symposium S19
Session title:
Symposium for Nurses and Allied Healthcare Professionals
Chairs:
Jenny Walker, Leeds, UK Eileen Pyra, Calgary, Canada
Clinical management of diabetes insipidus Mohamad Maghnie, Genoa, Italy The challenging management of childhood craniopharyngioma Guftar Shaik, Glasgow, UK The long and short of it! Nicky Nicoll, Bristol, UK Rebecca Myers, Bristol, UK Endocrine nursing: a Canadian perspective Melissa Anne Benoit, Toronto, Canada Eileen Pyra, Calgary, Canada Children’s endocrine nursing in Europe
Saturday 21 September
This session is supported by Ferring with an unrestricted educational grant.
14:00 – 15:30
Room: Space 1+2
Session type:
Controversies in Paediatric Endocrinology CPE3
Session title:
Detection and Treatment of Congenital Subclinical Hypothyroidism
Chairs: Giorgio Radetti, Bolzano, Italy Carlos Alberto Longui, São Paulo, Brazil SESSION AIM: This session debates whether the importance of detection and treatment of subclinical congenital hypothyroidism merits inclusion as an objective of all newborn screening programs.
CPE3-76
The benefits of screening for mild forms of congenital hypothyroidism Juliane Léger, Paris, France All newborn screening programs should be designed to detect and provide early treatment for subclinical congenital hypothyroidism. CPE3-77
Screening for subclinical hypothyroidism: the burden of global over treatment Heiko Krude, Berlin, Germany Detection and treatment of subclinical hypothyroidism should not be a mandatory objective of newborn screening programs.
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
14:00 – 15:30
Room: Space 3
Session type:
Meeting Theme Symposium S13 Why Doesn’t Everyone Become Obese: Energy Intake and Expenditure
Session title: Chairs:
Philip Zeitler, Aurora, USA George Chrousos, Athens, Greece
SESSION AIM: Regulation of body weight and adiposity requires orchestration of energy intake and expenditure, accomplished by dynamic interactions among body fat, nutrient availability, and hypothalamic signalling.
S13-50
Neuroendocrine regulation of energy expenditure Stephen O’Rahilly, Cambridge, UK Gut hormones, nutrients and the hypothalamus regulate activity and energy expenditure. S13-51
Metabolic effects on neuroregulation of homeostasis in the brain Tamas L. Horvath, New Haven, USA Disordered metabolism leads to plasticity and permanent change to hypothalamic regulatory pathways. S13-52
Saturday 21 September
Lifestyle interventions for weight loss: principles and pitfalls Judy Regensteiner, Denver, USA This talk will review lessons from the Diabetes Prevention Program and other behavioural modification studies and discuss their translation to adolescents at risk for and with type 2 diabetes.
9th Joint Meeting of Paediatric Endocrinology 2013
59
scientific Programme | Saturday 21 September 2013
14:00 – 15:30
Room: Space 4
Session type:
Symposium S14
Session title:
Autoimmunity in Paediatric Endocrinology
Chairs:
Jean-Claude Carel, Paris, France Tadej Battelino, Ljubljana, Slovenia
SESSION AIM: To provide an update on the mechanisms concurring to endocrine autoimmunity and their increasing prevalence in children.
S14-53
Mechanisms of endocrine autoimmunity in children Roberto Mallone, Paris, France The identification of the Aire gene function has allowed a leap in the understanding of endocrine autoimmmunity. An update on how these discoveries will impact on management of this and other forms of autoimmunity will be provided. S14-54
The clinical spectrum of APS-1 and beyond Olle Kämpe, Uppsala, Sweden APS1 or APECED is the prismatic model for endocrine autoimmunity. However, even in this apparently homogeneous disease, things are not so simple and variable clinical presentations can occur. S14-55
Saturday 21 September
Environmental and epigenetic factors in type 1 diabetes autoimmunity – where are we? Jill Norris, Aurora, USA Environmental or epigenetics factors obviously play an important role in the occurrence of endocrine autoimmunity. However, the identification of these potentially modifiable factors has so far been elusive.
16:00 – 17:00
Room: Brown 1
Session type:
Meet the Expert MTE10:1
Session title:
Diagnosis and Treatment of Adrenal Insufficiency
Nils Krone, Birmingham, UK SESSION AIM: In this session typical and atypical presentations, etiologies of primary and secondary causes, medical replacement therapy involving glucocorticoids and mineralocorticoids, aspects of patient education and potential associated diagnoses will be discussed.
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
16:00 – 17:00
Room: Brown 3
Session type:
Free Communication FC13
Session title:
Endocrine Oncology
Chairs:
Suttipong Wacharasindhu, Bangkok, Thailand Stephen Shalet, Manchester, UK
FC13-192
Differential expression profile of miRNAs in paediatric non-neoplastic adrenal tissue, metastatic and non-metastatic paediatric adrenocortical tumors Paola F. Fedatto1, David S. Marco Antonio1, Rodrigo A. Panepucci1, Amélia G. Araújo1, Carlos E. Martinelli Jr1, Sonir R.R. Antonini1, Margaret Castro1, Silvio Tucci Jr.1, Luciano Neder1, Ana L. Seidinger2, Maria J. Mastellaro2, José A. Yunes2, Silvia R. Brandalise2, Luiz G. Tone1, Carlos A. Scrideli1 1 Ribeirão Preto, Brazil, 2Campinas, Brazil FC13-193
Correlations between gene expression of IGF1R and IGF2 and WNT/B-catenin pathways in paediatric adrenocortical tumors Régia C.P. Lira1, Letícia F. Leal1, Paola F. Fedatto1, Carlos E. Martinelli Jr.1, Margaret Castro1, Silvio Tucci Jr.1, Luciano Neder1, Leandra Z. Ramalho1, Ana L. Seidinger2, Izilda Cardinalli2, Maria J. Mastellaro2, José A. Yunes2, Silvia R. Brandalise2, Luiz G. Tone1, Sonir R.R. Antonini1, Carlos A. Scrideli1 1 Ribeirão Preto, Brazil, 2Campinas, Brazil Factors influencing prognosis of stage I and II adrenocortical tumor in children and adolescents: experience of 101 cases Rosana Marques Pereira, Heyde Francine Pinto, Mara Albonei Dudeque Pianovski, Luciane Costa Neto, Marina Bressiani, Julienne Angela Ramirez de Carvalho, Suzana Nesi França, Romolo Sandrini, Luiz De Lacerda Curitiba, Brazil FC13-195
The use of 123I in diagnostic radioactive iodine uptake scans in children with differentiated thyroid carcinoma and metastatic disease: a case series at a single academic centre Melissa J. Bauters, Donald Zimmerman, Richard Shore, Jami L. Josefson Chicago, USA FC13-196
Disease- and treatment-related factors implicated in late neuroendocrine morbidity after paediatric optic pathway gliomas: a preliminary multivariate analysis of 128 patients over 30 years Hoong-Wei Gan, Helen A. Spoudeas London, UK FC13-197
Local deficiency of insulin-like growth factor-I receptor modulates the initial steps of experimental pheochromocytoma development Ayelen Martin, María Celia Fernández, Cecilia Mathó, Marcela Cristina Venara, Patricia A. Pennisi Buenos Aires, Argentina
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Saturday 21 September
FC13-194
scientific Programme | Saturday 21 September 2013
16:00 – 17:00
Room: Amber 3
Session type:
Meet the Expert MTE11:1
Session title:
Clinical Management of Hypocalcaemia
Outi Mäkitie, Helsinki, Finland SESSION AIM: This Meet the Expert Session will cover the pathogenesis and clinical management of hypocalcaemia of infancy and childhood.
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
16:00 – 17:00
Room: Amber 4
Session type:
Meet the Expert MTE12:1
Session title:
Molecular Genetic Investigation of the Child with Short Stature
Alexander A.L. Jorge, Sao Paulo, Brazil SESSION AIM: This session explores novel molecular findings in short, but healthy children, and to what degree in clinical practice such variations explaining differences in stature should be searched for.
Saturday 21 September
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
16:00 – 17:00
Room: Space 1+2
Session type:
Yearbook of Paediatric Endocrinology YB2
Session title:
Yearbook of Paediatric Endocrinology
Chairs:
Patricia A. Crock, Newcastle, Australia Yung Seng Lee, Singapore, Singapore
Pituitary Mehul Dattani, London, UK Reproductive endocrinology Olle Söder, Stockholm, Sweden Thyroid Michel Polak, Paris, France Adrenals Evangelia Charmandari, Athens, Greece Science & Medicine Ze’ev Hochberg, Haifa, Israel
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
16:00 – 17:00
Room: Space 3
Session type:
Free Communication FC14
Session title:
Perinatal and Neonatal Endocrinology
Chairs:
Verónica Mericq, Santiago, Chile Jesús Argente, Madrid, Spain
FC14-198
Placental expression of SPRY2: relation to maternal metabolism and placental growth Judit Bassols1, Jose Moreno-Navarrete1, Gemma Carreras-Badosa1, Marta Díaz2, Anna Prats-Puig1, Ferran Díaz-Roldán1, Francis de Zegher3, Lourdes Ibáñez2, Jose Manuel Fernandez-Real1, Abel López-Bermejo1 1 Girona, Spain, 2Barcelona, Spain, 3Leuven, Belgium FC14-199
Placental expression of ATG7, an autophagy gene, associates to weight partitioning among the mother, the placenta and the fetus Gemma Carreras-Badosa1, Anna Prats-Puig1, Ferran Díaz-Roldán1, Monserrat Vázquez-Ruíz2, Montserrat Bruel2, Francis de Zegher3, Lourdes Ibáñez4, Abel Lopez-Bermejo1, Judit Bassols1 1 Girona, Spain, 2Figueres, Spain, 3Leuven, Spain, 4Barcelona, Spain FC14-200
Prematurity should not prevent genetic testing for neonatal diabetes Rachel E.J. Besser1,2, Sarah E. Flanagan1, Deborah J. Mackay2, I.K. Temple2, Maggie H. Shepherd1, Beverley M. Shields1, Sian Ellard1, Andrew T. Hattersley1 1 Exeter, UK, 2Southampton, UK Hormone levels in extreme prematurity: establishment of gestational appropriate reference intervals for FSH, LH and prolactin Ronda F. Greaves1,2, Janne Pitkin2, Chung Shun Ho3, James Baglin1, Rodney W. Hunt2, Margaret R. Zacharin2 1 Bundoora, Australia, 2Parkville, Australia, 3Shatin, Hong Kong FC14-202
Involvement of gonadal control in gonadotropin secretion in infancy Tanja Kuiri-Hänninen1, Ulla Sankilampi1, Leo Dunkel2 1 Kuopio, Finland, 2London, UK FC14-203
Transient postnatal gonadal activation regulates linear growth in infants Panu Kiviranta1, Tanja Kuiri-Hänninen1, Antti Saari1, Marja-Leena Hannila1, Leo Dunkel2, Ulla Sankilampi1 1 Kuopio, Finland, 2London, UK
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Saturday 21 September
FC14-201
scientific Programme | Saturday 21 September 2013
16:00 – 17:00
Room: Space 4
Session type:
Free Communication FC15
Session title:
Adipose Tissue
Chairs:
Ciril Kržišnik, Ljubljana, Slovenia Charlotte Boney, Providence, USA
FC15-204
Peroxiredoxin 3 regulates adipogenic differentiation and glucose uptake in human adipocytes Azahara I. Ruperez1,2, Eveliina Enlund1, Concepcion Aguilera2, Martin Wabitsch1, Pamela Fischer-Posovszky1 1 Ulm, Germany, 2Granada, Spain FC15-205
Resveratrol inhibits inflammation-induced fibrosis in human adipocytes Ivana Zagotta, Daniel Tews, Hansjörg Habisch, Shaoxia Zhou, Klaus-Michael Debatin, Martin Wabitsch, Pamela Fischer-Posovszky Ulm, Germany FC15-206
Adipose tissue selective TSH receptor knockout alters the gene expression in brown but not in white adipose tissue Aziz Elgadi, Claude Marcus Stockholm, Sweden
Saturday 21 September
FC15-207
Exposure to increased androgens during early development modifies circulating adipokine levels and adipokine expression in visceral adipose tissue in adult female rats Purificación Ros-Pérez1, Pilar Argente-Arizón2, Esther Fuente-Martín2, Miguel Ángel Sánchez-Garrido2,3, David Castro-González2, Manuel Tena-Sempere2,3, Vicente Barrios2, Jesús Argente2, Julie A. Chowen2 1 Majadahonda, Spain, 2Madrid, Spain, 3Córdoba, Spain FC15-208
The expression of the adipocyte “insulin sensitivity” cellular markers, protein kinase B and glucose transporter 4, in relation to adipocyte aquaglyceroporin 7 in childhood obesity Eleni Oikonomou, Alexia Karvela, Eirini Matsigou, George Georgiou, Bessie E. Spiliotis Patras, Greece FC15-209
Anti-inflammatory SFRP5 and pro-inflammatory WNT5A are abundantly released by adipose tissue and closely related in prepubertal children Anna Prats-Puig1, Pilar Soriano Rodríguez2, Gemma Carreras-Badosa1, Elena Riera-Pérez2, Montserrat Ros-Miquel1, Antoni Gomila-Borja1, Francis de Zegher3, Lourdes Ibáñez4, Judit Bassols1, Abel López-Bermejo1 1 Girona, Spain, 2Figueres, Spain, 3Leuven, Belgium, 4Barcelona, Spain
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Saturday 21 September 2013
17:15 – 18:45
Room: Brown 3
Session type:
Joint Meeting Satellite Symposium SAT7
Session title:
The First 1000 Days – Early Nutrition and Long-term Consequences Sponsored by Nestlé Nutrition
Chairs:
Muhammad Yazid Jalaludin, Kuala Lumpur, Malaysia Ece Bober, Izmir, Turkey
The first 1000 days – early nutrition and long-term consequences Mike Possner, Frankfurt/Main, Germany Maternal nutrition in pregnancy: role in fetal development Irene Cetin, Milan, Italy Macronutrient intakes in the 6 to 24 month period and later non-communicable disorders Carlo Agostoni, Milan, Italy
17:15 – 18:45
Room: Space 1+2
Session type:
Joint Meeting Satellite Symposium SAT8 Overcoming the Hypoglycaemia Barrier for Optimal Metabolic Control: the Role of New Technologies
Session title:
Sponsored by Medtronic Chairs:
Carine de Beaufort, Luxembourg, Luxembourg Henk Veeze, Rotterdam, the Netherlands
Saturday 21 September
Hypoglycaemia in paediatric diabetes and other endocrine disorders Orit Pinhas-Hamiel, Ramat-Gan, Israel Sensor augmented pump therapy for hypoglycaemia risk reduction Tadej Battelino, Ljubljana, Slovenia Looking at the future of artificial pancreas: the DREAM project Moshe Phillip, Petah Tikva, Israel
17:15 – 18:15
Room: Space 4
Session type:
Joint Meeting Satellite Symposium SAT9
Session title:
Growth Hormone and IGF-1: Ready to Wear or Bespoke Treatment for the Short Child? Sponsored by Ipsen
Chairs:
Michel Polak, Paris, France Joachim Wölfle, Bonn, Germany
Increlex: an update on an essential medicine Peter Bang, Stockholm, Sweden The continuum model: GH therapy in the context of the continuum model Martin O. Savage, London, UK Q&A Joachim Wölfle, Bonn, Germany
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scientific Programme | Saturday 21 September 2013
19:00 – 23:59 Children’s Charity Concert and Joint Meeting Evening at MiCo
Saturday 21 September
For further details see page 242.
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Sunday 22 September 2013
Programme at a Glance
Daily programme
Sunday 22 September
Sunday 22 September
FC16
Novel Growthpromoting Treatment Gold [68]
YB3
Yearbook of Paediatric Endocrinology Gold [71]
MTE5:2
Controversies in the Management of Hyperthyroidism in Children and Adolescents Brown 1 [68]
MTE9:2
Clinical Prediction Tools: the Example of Growth Monitoring Brown 1 [71]
(PasteMTE6:2 PAAG)
FC17
MTE7:2
MTE8:2
FC18
Brown 3 [69]
Amber 3 [69]
Amber 4 [70]
Space 1+2 [70]
Endocrine Issues in Boys and Adolescents with Klinefelter Syndrome Space 4 [71]
FC19
MTE11:2
MTE12:2
FC20
MTE10:2
Obesity
Management of Hyponatraemia
Thyroid
Clinical Management of Hypocalcaemia Amber 3 [73]
Brown 3 [71]
The Child with Very Small Penis
Molecular Genetic Investigation of the Child with Short Stature Amber 4 [73]
Adrenal Disorders
Late Breaking Abstracts Space 1+2 [74]
Diagnosis and Treatment of Adrenal Insufficiency Space 4 [74]
S15
CPE4
S16
S17
S18
Gold [75]
Brown 1 [76]
Brown 3 [76]
Space 1+2 [77]
Space 4 [77]
Emerging Etiologies of Hypopituitarism
Fertility Preservation in Pre-Pubertal Children
Hyperandrogenism/ PCOS during Adolescence
Noonan Syndrome and Other RAS-opathies
Biochemical and Molecular Bases of Diabetic Complications – SIRP/ISPR
PL9 New Insights into the Genetic Regulation of Growth – Dedicated to Rita Levi Montalcini Gold [78]
PL10 Endocrine Disruptors and Their Effects on Reproductive Health – ASPAE Gold [78]
PL11 President’s Poster Awards Gold [78] Closing Ceremony Gold [78]
Sunday 22 September
07:30 07:45 08:00 08:15 08:30 08:45 09:00 09:15 09:30 09:45 10:00 10:15 10:30 10:45 11:00 11:15 11:30 11:45 12:00 12:15 12:30 12:45 13:00 13:15
CPE = Controversies in Paediatric Endocrinology FC = Free Communication Session MTE = Meet the Expert NP = New Perspectives PL = Plenary Lectures
S = Symposium S = Meeting Theme Symposium SAT = Joint Meeting Satellite Symposium WG = Joint Meeting Working Group YB = Yearbook of Paediatric Endocrinology
Rooms and Halls in italics [Page in Final Programme]
9th Joint Meeting of Paediatric Endocrinology 2013
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scientific Programme | Sunday 22 September 2013
07:30 – 08:30
Room: Gold
Session type:
Free Communication FC16
Session title:
Novel Growth-promoting Treatment
Chairs:
Peter Bang, Linkoping, Sweden Luciano Cavallo, Bari, Italy
FC16-210
Sodium butyrate helps to rescue the aberrant splicing in the autosomal dominant form of isolated growth hormone deficiency type II Maria Consolata Miletta, Vibor Petkovic, Andrée Eblé, Christa E. Flück, Primus E. Mullis Bern, Switzerland FC16-211
Effect of genetic background and latitude of study site on growth response to recombinant human growth hormone in patients with GH deficiency: a post-hoc analysis of PREDICT Chiara De Leonibus1, Pierre Chatelain2, Benoit Destenaves3, Peter Clayton1, Adam Stevens1, the PREDICT Investigator Group 1 Manchester, UK, 2Lyon, France, 3Geneva, Switzerland FC16-212
Pubertal height gain and adult height in growth hormone treated short children born small for gestational age Judith Renes, Petra Breukhoven, Maria De Ridder, Anita Hokken-Koelega Rotterdam, Netherlands FC16-213
Intranasal administration of human growth hormone (CP024) results in a linear dose response relationship with Cmax and AUC increasing with dose Faron Jordan1, Stephen Shalet2, Gareth King1 1 Nottingham, UK, 2Manchester, UK FC16-214
A phase 1b/2a study of a new long-acting growth hormone (VRS-317) in pre-pubertal children with growth hormone deficiency George M. Bright1, Teresa Quattrin2, Gad B. Kletter3, Wayne V. Moore4, John S. Fuqua5, Paul M. Desrosiers6, Eric Humphriss1, Jeffrey L. Cleland1 1 Redwood City, USA, 2Buffalo, USA, 3Seattle, USA, 4Kansas City, USA, 5Indianapolis, USA, 6Orlando, USA
Sunday 22 September
FC16-215
Analytical and bioanalytical characterization of MOD-4023, a long-acting growth hormone Oren Hershkovitz1, Laura Moschcovich1, Rachel Guy1, Yana Felikman1, Ahuva Bar Ilan1, Ron Rosenfeld2, Vivian Hwa2, Gili Hart1, Eyal Fima1 1 Nes Ziona, Israel, 2Portland, USA
07:30 – 08:30
Room: Brown 1
Session type:
Meet the Expert MTE5:2
Session title:
Controversies in the Management of Hyperthyroidism in Children and Adolescents
Donald Zimmerman, Chicago, USA SESSION AIM: This session will review the options for medical, radioactive iodine and surgical therapy for hyperthyroidism. One should take into account the age of the patient, degree of disease and wishes of the patient.
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Sunday 22 September 2013
07:30 – 08:30
Room: Brown 3
Session type:
Free Communication FC17
Session title:
Obesity
Chairs:
Elizabeth Davis, Perth, Australia Antje Körner, Leipzig, Germany
FC17-216
Study of circulating microRNAs in prepubertal obesity Anna Prats-Puig1, Francisco J. Ortega1, Josep M. Mercader2, Gemma Carreras-Badosa1, Ferran Díaz-Roldán1, Judit Bassols1, Abel López-Bermejo1, José M. Fernández-Real1 1 Girona, Spain, 2Barcelona, Spain FC17-217
POMC DNA hypermethylation variant in obese children and obese adults Peter Kuehnen1, Marcus Brandt1, Daniela Handke1, Anke Hinney2, Johannes Hebebrand2, Antje Fischer-Rosinsky1, Joachim Spranger1, Annette Grüters1, Heiko Krude1 1 Berlin, Germany, 2Essen, Germany FC17-218
Identification of copy number variants associated with severe early-onset obesity Clara Serra-Juhé1, Gabriel Á. Martos-Moreno2, Francisca Díaz2, Raquel Flores1, Armand Gutiérrez1, Benjamín Rodríguez Santiago1, Luis A. Pérez-Jurado1, Jesús Argente2 1 Barcelona, Spain, 2Madrid, Spain FC17-219
Mutation in an intronic CpG island causes deregulation of MEST in a family with severe early-onset obesity Clara Serra-Juhé1, Gabriel Á. Martos-Moreno2, Raquel Flores1, José M. Fernández-Real3, Jesús Argente2, Luis A. Pérez-Jurado1 1 Barcelona, Spain, 2Madrid, Spain, 3Girona, Spain FC17-220
Aberrant hepatic microRNA expression in non-alcoholic fatty liver disease Yueying Feng1, Chenbo Ji2, Xiaoqin Xu1, Chunmei Shi2, Xirong Guo2, Junfen Fu1 1 Hangzhou, China, 2Nanjing, China Hypothalamic suppressor of cytokine signalling 3 decreases drastically during development in both normal and overweight rats David Castro-González, Pilar Argente-Arizón, Esther Fuente-Martín, Francisca Díaz, Vicente Barrios, Julie A. Chowen, Jesús Argente Madrid, Spain
07:30 – 08:30
Room: Amber 3
Session type:
Meet the Expert MTE7:2 Management of Hyponatraemia
Session title:
Mohamad Maghnie, Genoa, Italy SESSION AIM: Hyponatraemia is defined as a serum sodium concentration of less than 136 mmol/L. Its appropriate management may be challenging and reliant on the accurate identification of the underlying cause.
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
9th Joint Meeting of Paediatric Endocrinology 2013
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Sunday 22 September
FC17-221
scientific Programme | Sunday 22 September 2013
07:30 – 08:30
Room: Amber 4
Session type:
Meet the Expert MTE8:2
Session title:
The Child with Very Small Penis
Tomohiro Ishii, Tokyo, Japan SESSION AIM: Very small penis (“micropenis”) is a penis of very small size with a normal morphology. Paediatric endocrinologists face a lot of difficult clinical questions on very small penis. This Meet the Expert will mainly focus on initial evaluation and management.
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
07:30 – 08:30
Room: Space 1+2
Session type:
Free Communication FC18
Session title:
Adrenal Disorders
Chairs: Naomi Weintrob, Ramat Aviv, Israel Gianni Russo, Milan, Italy FC18-222
A mutation in thioredoxin reductase 2 is associated with familial glucocorticoid deficiency Rathi Prasad1, Claire R. Hughes1, Li F. Chan1, Julia Kowalczyk1, Catherine J. Peters1, Nisha Nathwani2, Adrian J.L. Clark1, Helen L. Storr1, Louise A. Metherell1 1 London, UK, 2Luton, UK FC18-223
A novel point mutation in the ligand-binding domain of the human glucocorticoid receptor gene causing primary generalised glucocorticoid resistance Nicolas C. Nicolaides1, Eliza Geer2, Amalia Sertedaki1, George P. Chrousos1, Evangelia Charmandari1 1 Athens, Greece, 2New York, USA FC18-224
Digenic inheritance of mutations in antioxidant pathway genes in a patient with familial glucocorticoid deficiency? Julia Kowalczyk, Eirini Meimaridou, Rathi Prasad, Leo Guasti, Adrian J.L. Clark, Louise A. Metherell London, UK
Sunday 22 September
FC18-225
Utility of whole-exome sequencing in the diagnosis of adrenal insufficiency Li F. Chan, Tatiana V. Novoselova, Daniel C. Campbell, Claire R. Hughes, Adrian J.L. Clark, Louise A. Metherell London, UK FC18-226
A 13-year-old girl with aldosterone-producing adenoma having a somatic mutation of KCNJ5 Noboru Uchida1, Naoko Amano1, Tomohiro Ishii1, Yui Yamaoka2, Ayumi Uematsu2, Makoto Suzuki2, Jun Watanabe2, Ryuji Fukuzawa1, Tomonobu Hasegawa1 1 Tokyo, Japan, 2Shizuoka, Japan FC18-227
Are female paediatricians more stress resistant than their male colleagues? A study on the endocrine impact of 24h-shifts in physicians based on urinary steroid metabolomics Claudia Boettcher, Michaela F. Hartmann, Klaus-Peter Zimmer, Stefan A. Wudy Giessen, Germany
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Sunday 22 September 2013
07:30 – 08:30
Room: Space 4
Session type:
Meet the Expert MTE6:2
Session title:
Endocrine Issues in Boys and Adolescents with Klinefelter Syndrome
Claus Højbjerg Gravholt, Aarhus, Denmark SESSION AIM: Klinefelter syndrome is much more than androgen deficiency. I will review the developmental and behavioral issues that might lead to earlier diagnosis and possible therapies given that only approximately 1:10 boys with this condition are diagnosed in childhood and adolescence.
08:45 – 09:45
Room: Gold
Session type:
Yearbook of Paediatric Endocrinology YB3
Session title:
Yearbook of Paediatric Endocrinology
Chairs:
Sei-Won Yang, Seoul, Korea Paul Saenger, New York, USA
Neuroendocrinology Nicolas De Roux, Paris, France Oncology and chronic disease Helmuth G. Dörr, Erlangen, Germany Type 1 diabetes M. Loredana Marcovecchio, Chieti, Italy Evidence based paediatric endocrinology Christopher J. Kelnar, Edinburgh, UK
08:45 – 09:45
Room: Brown 1
Session type:
Meet the Expert MTE9:2
Session title:
Clinical Prediction Tools: the Example of Growth Monitoring
Martin Chalumeau, Paris, France SESSION AIM: Clinical decision is a complex process that should be aided by evaluated clinical decision rules. Their use in paediatric endocrinology for the selection of short children for GH testing and for MRI examination in precocious puberty will be discussed.
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Sunday 22 September
Editor’s choice Ken K. Ong, Cambridge, UK
scientific Programme | Sunday 22 September 2013
08:45 – 09:45
Room: Brown 3
Session type:
Free Communication FC19
Session title:
Thyroid
Chairs:
Malgorzata Wasniewska, Messina, Italy Guy van Vliet, Montreal, Canada
FC19-228
Novel mutations in the carboxy-terminal region of DEHAL1 and iodotyrosine dehalogenase deficiency Ainhoa Iglesias1, María Güemes2, Laura García3, Jean Louis Wemeau4, Monique Vincens5, Aubene Lèger5, Ernest Brunet1, José Ángel Cocho3, José Carlos Moreno1 1 Madrid, Spain, 2Toledo, Spain, 3Santiago de Compostela, Spain, 4Lille, France, 5Paris, France FC19-229
Monoallelic mutations in TSHR and DUOX2 do not act as single Mendelian factors but as risk factors for congenital hypothyroidism: pathway burden hypothesis Kiyomi Abe1, Satoshi Narumi1, Naoko Amano1, Tomohiro Ishii1, Koji Muroya2, Yumi Asakura2, Masanori Adachi2, Goro Sasaki3, Keisuke Nagasaki4, Takayuki Abe1 1 Tokyo, Japan, 2Yokohama, Japan, 3Ichikawa, Japan, 4Niigata, Japan FC19-230
Dual-specificity tyrosine (Y)-phosphorylation regulated kinase 1A overexpression is linked to congenital hypothyroidism in Down syndrome Dulanjalee Kariyawasam1, Latif Rachdi1, Mercè Martin-Pena2, Aurore Carré3, Marine Houlier1, Corinne Dupuy3, Nathalie Janel1, Jean-Maurice Delabar1, Raphaël Scharfmann1, Michel Polak1 1 Paris, France, 2Barcelona, Spain, 3Villejuif, France FC19-231
Permanent congenital hypothyroidism due to a novel heterozygous mutation in the promoter region of the PAX8 gene in a girl with Down syndrome Pia Hermanns1, Jeremy Jones2, Scott Shepherd2, Mohamed Mansor3, John Schulga3, Malcolm Donaldson2, Joachim Pohlenz1 1 Mainz, Germany, 2Glasgow, UK, 3Larbert, UK FC19-232
Sunday 22 September
Dynamics of TSH secretion under TRH stimulation and genetics of central congenital hypothyroidism Marta García, María Antonia Molina, Julio Guerrero, Inés María Toscano, Lucía Sentchordi, Cristina Álvarez Escolá, Purificación Ros, Isabel González, José Carlos Moreno Madrid, Spain FC19-233
Factors associated with hearing impairment in young adult patients with congenital hypothyroidism treated since the neonatal period: a national population-based study Lydia Lichtenberger, Sophie Dos Santos, Yasmine Hassani, Emmanuel Ecosse, Thierry Van Den Abbeele, Juliane Léger Paris, France
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9th Joint Meeting of Paediatric Endocrinology 2013
scientific Programme | Sunday 22 September 2013
08:45 – 09:45
Room: Amber 3
Session type:
Meet the Expert MTE11:2
Session title:
Clinical Management of Hypocalcaemia
Outi Mäkitie, Helsinki, Finland SESSION AIM: This Meet the Expert session will cover the pathogenesis and clinical management of hypocalcaemia of infancy and childhood.
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
08:45 – 09:45
Room: Amber 4
Session type:
Meet the Expert MTE12:2
Session title:
Molecular Genetic Investigation of the Child with Short Stature
Alexander A.L. Jorge, Sao Paulo, Brazil SESSION AIM: This session explores novel molecular findings in short, but healthy children, and to what degree in clinical practice such variations explaining differences in stature should be searched for.
Sunday 22 September
This session is interactive and located in a smaller room. Seats are limited and will therefore be allocated on a “first-come-first-served” basis.
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scientific Programme | Sunday 22 September 2013
08:45 – 09:45
Room: Space 1+2
Session type:
Free Communication FC20
Session title:
Late Breaking Abstracts
Chairs:
Atilla Buyukgebiz, Istanbul, Turkey Tim Jones, Perth, Australia
FC20-1483
Whole exome sequencing identifies FAM111A as a new cause of autosomal recessive Kenny-Caffey syndrome Dong Li1, Hakon Hakonarson1, Matthew A. Deardorff1, Michael A. Levine1 1 Philadelphia, USA FC20-1484
Loss of function of the melanocortin 2 receptor accessory protein 2 is associated with mammalian obesity Masato Asai1,2, Shwetha Ramachandrappa3, Maria Joachim1, Yuan Shen1, Rong Zhang1, Nikhil Nuthalapati1, Visali Ramanathan1, David E. Strochlic1, Peter Ferket4, Kirsten Linhart1, Caroline Ho1, Tatiana V. Novoselova5, Sumedha Garg3, Martin Ridderstråle6, Claude Marcus7, Joel N. Hirschhorn1,8, Julia M. Keogh3, Stephen O’Rahilly3, Li F. Chan3, Adrian J. Clark5, I. Sadaf Farooqi3, Joseph A. Majzoub1 1 Boston, USA, 2Nagoya, Japan, 3Cambridge, UK, 4Raleigh, USA, 5London, UK, 6Malmö, Sweden, 7 Stockholm, Sweden, 8Boston/Cambridge, USA FC20-1485
Absence of renal resistance to PTH in PDE4D-mutated acrodysostosis patients: regulation of cAMP/PKA pathway by PDE4 may be tissue and agonist-specific – example of renal PTH signaling pathway Emmanuelle Motte1, Catherine Le Stunff1, Agnès Linglart1, Caroline Silve1 1 Le Kremlin-Bicêtre, France FC20-1486
Sonic Hedgehog pathway involvement in adrenal cortex development and tumorigenesis Debora C. Gomes1, Leticia F. Leal1, Livia M. Mermejo1, Carlos A. Scrideli1, Carlos E. Martinelli Jr.1, Maria Candida V. Fragoso2, Ana Claudia X. Latronico2, Luis G. Tone1, Silvio Tucci1, Jose A. Yunes3, Maria Jose Mastellaro3, Silvia Brandalise3, Ayrton C. Moreira1, Fernando Ramalho1, Leandra Z. Ramalho1, Margaret Castro1, Sonir R. Antonini1 1 Ribeirao Preto, Brazil, 2Sao Paulo, Brazil, 3Campinas, Brazil
Sunday 22 September
FC20-1487
Whole exome sequencing and functional studies identify a germline gain-of-function mutation in GNA11 as a novel cause of autosomal dominant hypoparathyroidism Li Dong1, Hakon Hakonarson1, Daniel Metzger2, Evan Opas1, Florin Tuluc1, Michael A. Levine1 1 Philadelphia, USA, 2Vancouver, Canada FC20-1488
Asfotase alfa improves skeletal mineralisation and respiratory function in infants and young children with hypophosphatasia: results from up to 12 months’ treatment Cheryl R. Greenberg1, Jerry Vockley2, Paul Harmatz3, Marc Vallée4, Camille L. Bedrosian5, Johannes G. Liese6 1 Winnipeg, Canada, 2Pittsburgh, USA, 3Oakland, USA, 4Cambridge, USA, 5Cheshire, USA, 6Wuerzburg, Germany
08:45 – 09:45
Room: Space 4
Session type:
Meet the Expert MTE10:2
Session title:
Diagnosis and Treatment of Adrenal Insufficiency
Nils Krone, Birmingham, UK SESSION AIM: In this session typical and atypical presentations, etiologies of primary and secondary causes, medical replacement therapy involving glucocorticoids and mineralocorticoids, aspects of patient education and potential associated diagnoses will be discussed.
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scientific Programme | Sunday 22 September 2013
10:00 – 11:30
Room: Gold
Session type:
Meeting Theme Symposium S15
Session title:
Emerging Etiologies of Hypopituitarism
Chairs:
Ivo Arnhold, São Paulo, Brazil Christopher Cowell, Sydney, Australia
SESSION AIM: This symposium summarises new genes and new mechanisms involved in hypopituitarism, emphasises the relevance of oligogenic mutations and autoimmunity in the development of hypopituitarism.
S15-56
Novel genes involved in hypopituitarism Mehul Dattani, London, UK Recent advance in molecular technologies has served to identify novel genes involved in the development of hypopituitarism. This lecture will focus on updated topics on this matter. S15-57
Oligogenic bases of hypopituitarism Nelly Pitteloud, Lausanne, Switzerland The relevance of oligogenicity has become evident in hypopituitarism. This will provide a useful clue to clarify the underlying factors for clinical variability in this entity. S15-58
Sunday 22 September
Novel mechanism leading to hypopituitarism Yutaka Takahashi, Kobe, Japan Identification of genetic abnormalities remains infrequent in hypopituitarism. Recently, an autoimmune disorder has been identified in hypopituitarsim, providing a novel diseasecausing factor.
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scientific Programme | Sunday 22 September 2013
10:00 – 11:30
Room: Brown 1
Session type:
Controversies in Paediatric Endocrinology CPE4
Session title:
Fertility Preservation in Pre-Pubertal Children
Chairs: Olle Söder, Stockholm, Sweden Hiroyuki Ishiguro, Kanagawa, Japan SESSION AIM: This session will deal with the prospects and potential risks of the rapidly developing technologies to preserve future fertility of children with cancer subjected to gonadotoxic treatment regimens and other conditions.
CPE4-78
Fertility preservation in 47,XXY: from childhood to adulthood Herman Tournaye, Brussels, Belgium This talk will give an overview of the methodology and discuss the selection of patients to be offered gonadal rescue programs. CPE4-79
Fertility after childhood cancer treatment – indications for fertility preservation Kirsi Jahnukainen, Helsinki, Finland This lecturer will discuss the best timing of gonadal tissue sampling and the gender differences.
10:00 – 11:30
Room: Brown 3
Session type:
Symposium S16
Session title:
Hyperandrogenism/PCOS during Adolescence
Chairs:
Henriette Delemarre-van de Waal, Leiden, Netherlands Pierre Bougneres, Paris, France
SESSION AIM: This session will discuss the role of childhood obesity in the early onset of hyperandrogenism, the specific diagnostic criteria for PCOS during adolescence and the therapeutical options for adolescents with PCOS.
Sunday 22 September
S16-59
Obesity and hyperandrogenism Thomas Reinehr, Datteln, Germany This session will discuss the potential mechanisms underlying the relationship between hyperandrogenism and obesity during adolescence, and the management of this condition. S16-60
A critical assessment of the criteria to diagnose PCOS during adolescence Ethel Codner, Santiago, Chile At least three different sets of diagnostic criteria have been postulated to diagnose PCOS in adult women. This session will discuss the most reliable ultrasonographic and hormonal criteria to make the diagnosis of PCOS in adolescent girls. S16-61
Transition of care in PCOS Selma Witchel, Pittsburgh, USA Transition care for the adolescent girl with PCOS has several relevant aspects which must be addressed by the paediatric endocrinologist, since changes in management during this period may be very confusing to the patient with this condition.
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scientific Programme | Sunday 22 September 2013
10:00 – 11:30
Room: Space 1+2
Session type:
Symposium S17
Session title:
Noonan Syndrome and Other RAS-opathies
Chairs:
Pik To Cheung, Hong Kong, China Martin Ritzén, Stockholm, Sweden
SESSION AIM: The RAS-MAPk intracellular signalling pathway links metabolism, cell differentiation, and cell proliferation. A growing spectrum of abnormalities in this pathway have been identified as the causes of genetic syndromes and cancer.
S17-62
The Ras pathway – a critical signalling pathway in health and disease Marco Tartaglia, Rome, Italy A review of the Ras signalling pathway and principles of function and dysfunction. S17-63
Spectrum of mutations in Noonan and other RAS-opathies and their correlation with phenotype Han-Wook Yoo, Seoul, Republic of Korea Noonan syndrome is the paradigmatic RAS-opathy with everyday relevance to the paediatric endocrinologist. S17-64
Noonan’ syndrome: clinical features and management Amy E. Roberts, Boston, USA An understanding of the role of RAS mutations and the spectrum of phenotypes in Noonan syndrome has implications for the approach to diagnosis and treatment.
10:00 – 11:30
Room: Space 4
Session type:
Symposium S18
Session title:
Biochemical and Molecular Bases of Diabetic Complications – SIRP/ISPR
SESSION AIM: This is a symposium which will review the biochemical and molecular mechanisms determining diabetic angiopathy, paving the way for better understanding its pathophysiology and, consequently, improving treatment and prevention of diabetes vascular complications.
The symposium is held in collaboration with the Italian Society for Paediatric Research (SIRP/ISPR). S18-65
Biochemical mechanisms of diabetic angiopathy Ida Giardino, Foggia, Italy This lecture will review the main biochemical mechanisms with special reference to alterations of mitochondrial function. Damaged mitochondria generate an excess of superoxide, which may mediate tissue injury in diabetes. S18-66
Molecular machinery of diabetic vascular disease Hans P. Hammes, Heidelberg, Germany This presentation will review the mechanisms by which chronic hyperglycaemia causes vascular desease focusing in particular on the molecular changes that induce intraretinal vasoregression and the subsequent angiogenesis. S18-67
Clinical outcomes of diabetic angiopathy in children and adolescents Kim C. Donaghue, Sydney, Australia This lecture will show the clinical consequences of diabetic angiopathy. Early detection and prevention of diabetic vascular disease in children will also be pointed out.
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Sunday 22 September
Chairs: Renata Lorini, Genoa, Italy Lynne Levitsky, Boston, USA
scientific Programme | Sunday 22 September 2013
11:45 – 12:15
Room: Gold
Session type:
Plenary Session PL9
Session title:
New Insights into the Genetic Regulation of Growth Dedicated to Rita Levi Montalcini
Chair:
Hilary Hoey, Dublin, Ireland
PL9-9 Jeffrey Baron, Bethesda, USA
12:15 – 12:45
Room: Gold
Session type:
Plenary Session PL10
Session title:
Endocrine Disruptors and Their Effects on Reproductive Health – ASPAE
Chair:
Abiola Oduwole, Lagos, Nigeria
PL10-10 Niels Erik Skakkebaek, Copenhagen, Denmark
12:45 – 13:00
Room: Gold
Session type:
Plenary Session PL11
Session title:
President’s Poster Awards – Sponsored by ESPE
Chairs:
Franco Chiarelli, Chieti, Italy David Allen, Madison, USA Hilary Hoey, Dublin, Ireland Lars Sävendahl, Stockholm, Sweden
Sunday 22 September
Joint Meeting President Poster Awards
The Joint Meeting President Poster Awards are voted by members of the Joint Programme Organising Committee after the last poster session and are given to five presenting authors (among 50 nominees). The winners will be announced by the President at the Joint Meeting President Poster Awards Session prior to the Closing Ceremony. The voting criteria will be based on the scientific content and style of poster presentation. The Awards consist of an official Joint Meeting Award Diploma, a Presidential gift and a place in the official listing on the society website among Joint Meeting Award Winners in the following year.
13:00 – 13:15 Session type:
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Room: Gold Closing Ceremony
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions
Poster Sessions The Poster Exhibition is located within the Exhibition Hall. The posters are on display the first three days of the meeting. By looking at the poster number you can find the area and the day of presentation for the poster.
Area
Day
Unique number
P1-d1-234 The first number indicates the assigned poster area where the poster is displayed: P1 = closest to the commercial exhibition; P2 = end part of the Exhibition Hall; and P3 = under the balcony. Posters in P1 are those which scored highest in the anonymous peer evaluation. The second number indicates the day of presentation (e.g. d1 for Thursday 19 September; d2 for Friday 20 September; and d3 for Saturday 21 September). Guided Poster Tours
The posters in areas P1 and P2 are included in Guided Poster Tours. The Guided Tours give the authors a chance to interactively discuss the posters with the chairpersons and the audience. Display of Posters
Posters should be put up for display on Thursday 19 September between 09:45 and 13:30 Posters must be removed by Saturday 21 September 17:00*.
Poster Sessions
*Please note that the posters need to be removed due to the exhibition closing on the end of Saturday 21 September.
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Poster sessions
Thursday 19 September (d1), 14:20 – 15:20 P1
Abstract no.
Page
Adrenals and HPA Axis 1.........................................................................234 – 246.................................83 Autoimmune Endocrine Diseases 1........................................................272 – 281.................................87 Bone, Growth Plate and Mineral Metabolism 1....................................282 – 293.................................88 Fat Metabolism, Obesity 1........................................................................307 – 318.................................91 Fat Metabolism, Obesity 4........................................................................343 – 354.................................95 GH and IGF Physiology and Treatment 1..............................................380 – 391.................................99 Glucose Metabolism 1..............................................................................416 – 425...............................104 Glucose Metabolism 4..............................................................................446 – 455...............................107 Growth 1.....................................................................................................466 – 477...............................110 Perinatal and Neonatal Endocrinology 1...............................................491 – 502...............................113 Pituitary and Neuroendocrinology 1......................................................503 – 512...............................114 Programming/Epigenetics 1....................................................................522 – 528...............................116 Puberty and Gonads 1..............................................................................529 – 540...............................117 Sex Differentiation 1.................................................................................565 – 576...............................121 Thyroid 1....................................................................................................589 – 598...............................124 P2
Abstract no.
Page
Adrenals and HPA Axis 4.........................................................................619 – 630...............................128 Adrenals and HPA Axis 7.........................................................................655 – 666...............................132 Autoimmune Endocrine Diseases 2........................................................667 – 674...............................133 Bone, Growth Plate and Mineral Metabolism 3....................................683 – 694...............................135 Bone, Growth Plate and Mineral Metabolism 6....................................719 – 731...............................139 Endocrine Oncology 1..............................................................................732 – 740...............................140 Fat Metabolism, Obesity 7........................................................................741 – 752...............................141 Fat Metabolism, Obesity 10......................................................................777 – 788...............................145 GH and IGF Physiology and Treatment 4..............................................813 – 824...............................149 Glucose Metabolism 6..............................................................................849 – 859...............................153 Glucose Metabolism 9..............................................................................882 – 892...............................157 Glucose Metabolism 12............................................................................915 – 925...............................161 Growth 3.....................................................................................................950 – 961...............................164 Growth 6.....................................................................................................986 – 997...............................168 Perinatal and Neonatal Endocrinology 2...............................................998 – 1009.............................170 Pituitary and Neuroendocrinology 3......................................................1010 – 1021...........................171 Programming/Epigenetics 2....................................................................1034 – 1039...........................174 Puberty and Gonads 4..............................................................................1040 – 1051...........................174 Puberty and Gonads 7..............................................................................1076 – 1087...........................178 Sex Differentiation 3.................................................................................1099 – 1110...........................181 Thyroid 4....................................................................................................1135 – 1146...........................184 Thyroid 7....................................................................................................1171 – 1182...........................188
Poster Sessions
P3
Abstract no.
Page
Adrenals and HPA Axis 8.........................................................................1195 – 1205...........................191 Autoimmune Endocrine Diseases 4........................................................1216 – 1223...........................193 Bone, Growth Plate and Mineral Metabolism 7....................................1224 – 1235...........................194 Endocrine Oncology 2..............................................................................1249 – 1257...........................196 Fat Metabolism, Obesity 13......................................................................1258 – 1270...........................197 GH and IGF Physiology and Treatment 7..............................................1285 – 1295...........................199 Glucose Metabolism 15............................................................................1320 – 1332...........................203 Growth 7.....................................................................................................1359 – 1370...........................207 Perinatal and Neonatal Endocrinology 3...............................................1396 – 1403...........................211 Pituitary and Neuroendocrinology 5......................................................1404 – 1412...........................212 Puberty and Gonads 9..............................................................................1422 – 1432...........................214 Sex Differentiation 6.................................................................................1452 – 1460...........................217 Thyroid 9....................................................................................................1461 – 1471...........................218
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poster sessions
Friday 20 September (d2), 13:00 – 14:00 P1
Abstract no.
Page
Adrenals and HPA Axis 2.........................................................................247 – 259.................................84 Bone, Growth Plate and Mineral Metabolism 2....................................294 – 306.................................90 Fat Metabolism, Obesity 2........................................................................319 – 330.................................93 Fat Metabolism, Obesity 5........................................................................355 – 366.................................97 GH and IGF Physiology and Treatment 2..............................................392 – 403...............................101 Glucose Metabolism 2..............................................................................426 – 435...............................105 Glucose Metabolism 5..............................................................................456 – 465...............................109 Growth 2.....................................................................................................478 – 490...............................111 Pituitary and Neuroendocrinology 2......................................................513 – 521...............................115 Puberty and Gonads 2..............................................................................541 – 552...............................119 Sex Differentiation 2.................................................................................577 – 588...............................123 Thyroid 2....................................................................................................599 – 608...............................125 P2
Abstract no.
Page
Adrenals and HPA Axis 5.........................................................................631 – 642...............................129 Autoimmune Endocrine Diseases 3........................................................675 – 682...............................134 Bone, Growth Plate and Mineral Metabolism 4....................................695 – 706...............................136 Fat Metabolism, Obesity 8........................................................................753 – 764...............................143 Fat Metabolism, Obesity 11......................................................................789 – 800...............................147 GH and IGF Physiology and Treatment 5..............................................825 – 836...............................151 Glucose Metabolism 7..............................................................................860 – 870...............................155 Glucose Metabolism 10............................................................................893 – 903...............................158 Glucose Metabolism 13............................................................................926 – 937...............................162 Growth 4.....................................................................................................962 – 973...............................166 Pituitary and Neuroendocrinology 4......................................................1022 – 1033...........................172 Puberty and Gonads 5..............................................................................1052 – 1063...........................176 Puberty and Gonads 8..............................................................................1088 – 1098...........................180 Sex Differentiation 4.................................................................................1111 – 1122...........................182 Thyroid 5....................................................................................................1147 – 1158...........................186 Thyroid 8....................................................................................................1183 – 1194...........................189 P3
Abstract no.
Page
Adrenals and HPA Axis 9.........................................................................1206 – 1215...........................192 Bone, Growth Plate and Mineral Metabolism 8....................................1236 – 1248...........................195 Fat Metabolism, Obesity 14......................................................................1271 – 1284...........................198 GH and IGF Physiology and Treatment 8..............................................1296 – 1307...........................201 Glucose Metabolism 16............................................................................1333 – 1345...........................204 Growth 8.....................................................................................................1371 – 1382...........................208 Pituitary and Neuroendocrinology 6......................................................1413 – 1421...........................213 Puberty and Gonads 10............................................................................1433 – 1443...........................215 Thyroid 10..................................................................................................1472 – 1482...........................219
Saturday 21 September (d3), 12:45 – 13:45 Abstract no.
Page
Adrenals and HPA Axis 3.........................................................................260 – 271.................................86 Fat Metabolism, Obesity 3........................................................................331 – 342.................................94 Fat Metabolism, Obesity 6........................................................................367 – 379.................................98 GH and IGF Physiology and Treatment 3..............................................404 – 415...............................102 Glucose Metabolism 3..............................................................................436 – 445...............................106 Puberty and Gonads 3..............................................................................553 – 564...............................120 Thyroid 3....................................................................................................609 – 618...............................126
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Poster Sessions
P1
Poster sessions
P2
Abstract no.
Page
Adrenals and HPA Axis 6.........................................................................643 – 654...............................130 Bone, Growth Plate and Mineral Metabolism 5....................................707 – 718...............................137 Fat Metabolism, Obesity 9........................................................................765 – 776...............................144 Fat Metabolism, Obesity 12......................................................................801 – 812...............................148 GH and IGF Physiology and Treatment 6..............................................837 – 848...............................152 Glucose Metabolism 8..............................................................................871 – 881...............................156 Glucose Metabolism 11............................................................................904 – 914...............................159 Glucose Metabolism 14............................................................................938 – 949...............................163 Growth 5 ....................................................................................................974 – 985...............................167 Puberty and Gonads 6..............................................................................1064 – 1075...........................177 Sex Differentiation 5.................................................................................1123 – 1134...........................183 Thyroid 6....................................................................................................1159 – 1170...........................187 P3
Abstract no.
Page
GH and IGF Physiology and Treatment 9..............................................1308 – 1319...........................202 Glucose Metabolism 17............................................................................1346 – 1358...........................206 Growth 9 ....................................................................................................1383 – 1395...........................209 Puberty and Gonads 11............................................................................1444 – 1451...........................216
Late breaking posters Saturday 21 September (d3), 12:45 – 13:45 P1
Abstract no.
Page
Poster Sessions
LB1 – Adrenals, Bone, Endocrine Oncology.........................................1489 – 1495...........................220 LB2 – Fat Metabolism, Obesity...............................................................1496 – 1505...........................221 LB3 – Glucose Metabolism......................................................................1506 – 1518...........................222 LB4 – Pituitary, Growth, Thyroid...........................................................1519 – 1528...........................223
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poster sessions | P1
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1 Adrenals and HPA Axis 1
Session title: Chairs:
Antonio Balsamo, Bologna, Italy Rebecca Perry, Calgary, Canada
P1-d1-234
Clinical features and mutation spectrum of the StAR gene of patients with congenital lipoid adrenal hyperplasia Yoo-Mi Kim, Ja Hye Kim, Jae-Min Kim, Ju-Hyun Kim, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo Seoul, Republic of Korea P1-d1-235
Plasma matrix metalloproteinases activity in children with hypertension due to 11ß-hsd2 deficiency activity Alejandro Martinez-Aguayo, Carmen Campino, Hernan Garcia, Marlene Aglony, Carolina Avalos, Lilian Bolte, Rodrigo Bancalari, Cristian A. Carvajal, Lorena Garcia, Sergio Lavanderos, Carlos E. Fardella Santiago de Chile, Chile P1-d1-236
Adrenarche has no major association with dietary factors or physical activity Aino Mäntyselkä, Jarmo Jääskeläinen, Virpi Lindi, Timo Lakka Kuopio, Finland P1-d1-237
Glucocorticoid replacement therapy in children with hypoadrenalism during physiological stress Keiko Aso, Mari Sato, Tsutomu Saji, Yukihiro Hasegawa Tokyo, Japan P1-d1-238
Bilateral adrenalectomy in 7 women and 1 girl with salt-wasting congenital adrenal hyperplasia of difficult management Miquel Gussinyer Canadell, Anai Nuñez, Marino Asensio Llorente, Diego Yeste Fernández, Antonio Carrascosa Lezcano Barcelona, Spain P1-d1-239
Circadian rhythm of salivary cortisol in children and adolescents using an ultrasensitive electrochemiluminescence immunoassay María G. Ballerini, Andrea Amaro, Patricia Otero, Ignacio Bergadá, María G. Ropelato Buenos Aires, Argentina P1-d1-240
Poster Sessions P1
Biochemical diagnosis of classic 3β-hydroxysteroid dehydrogenase deficiency in term newborns using urine metabolites of Δ5 steroids Keiko Homma, Yuhei Koyama, Kei Takasawa, Tomohiro Ishii, Masayuki Miwa, Kazushige Ikeda, Nobuko Shimizu, Ayako Shibata, Masatoshi Wakui, Mitsuru Murata, Tomonobu Hasegawa Tokyo, Japan P1-d1-241
The novel mutation in the nicotinamide nucleotide transhydrogenase gene with a classical case of familial glucocorticoid deficiency Fatih Gurbuz1, Eda Mengen1, Leman Damla Kotan1, Ali Kemal Topaloglu1, Louise A. Metherell2, Bilgin Yuksel1 1 Adana, Turkey, 2London, UK P1-d1-242
Cushing syndrome due to POMC secretion from a malignant yolk sac tumor in a two year old child Evelien F. Gevers1, Pratik Shah1, Suzanne Meredith2, John Torpiano3, Catherine J. Peters1, Neil Sebire1, Anne White2, Olga Slater1, Mehul T. Dattani1 1 London, UK, 2Manchester, UK, 3Msida, Malta
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Poster sessions | P1
P1-d1-243
Comprehensive genetic analyses of primary adrenal failure of unknown etiologies: expanding phenotypic spectrum of NNT mutations Naoko Amano1, Mie Hayashi1, Satoshi Narumi1, Kazuhide Imai2, Hiroki Matsuura3, Hiroshi Mochizuki4, Koji Muroya5, Rika Kizu5, Izumi Tamada6, Yuko Taniguchi7, Atsuko Sasaki8, Shiro Yamada9, Keiko Homma1, Tomohiro Ishii1, Tomonobu Hasegawa1 1 Tokyo, Japan, 2Oita, Japan, 3Nagano, Japan, 4Saitama, Japan, 5Kanagawa, Japan, 6Kagoshima, Japan, 7 Tochigi, Japan, 8Fukuoka, Japan, 9Gunma, Japan P1-d1-244
Utility of early morning cortisol and cortisone for the identification of patients with adrenal insufficiency during inhaled corticosteroid therapy for asthma Joanne C. Blair1, Mohammed Didi1, Das Urmi1, Poonam Dharmaraj1, Paul Newland1, Catherine Collingwood1, Gill Lancaster2, Andrew Titman2, Matthew T. Peak1, Jonathan Couriel1 1 Liverpool, UK, 2Lancaster, UK P1-d1-245
Definition of a practical sampling interval in 24h serum cortisol profiling to optimise treatment in children with 21-hydroxylase deficiency Karen M. Logan1, Leonor Boto1, Pietro Lazzeroni2, Nathan R. Hill3, Peters Catherine1, David R. Matthews1, Evangelia Charmandari4, Felix G. Riepe5, Mehul T. Dattani1, Peter C. Hindmarsh1 1 London, UK, 2Parma, Italy, 3Oxford, UK, 4Athens, Greece, 5Kiel, Germany P1-d1-246
Atypical presentation of apparent mineralocorticoid excess Ranita Kuryan, Tina Cheng, Dennis E. Carey New Hyde Park, USA
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2 Adrenals and HPA Axis 2
Session title: Chairs:
Christa Flück, Bern, Switzerland María Gabriela Ballerini, Buenos Aires, Argentina
P1-d2-247
Diagnostic mysteries solved by exome sequencing Caroline Hasselmann, Mark E. Samuels, Jacek Majewski, Cheri L. Deal, Céline Huot, Guy Van Vliet, Johnny Deladoey Montréal, Canada P1-d2-248
Decreased 11β-hydroxysteroid dehydrogenase type 2 activity in neonates with 21-hydroxylase deficiency Clemens Kamrath, Michaela F. Hartmann, Stefan A. Wudy Giessen, Germany
Poster Sessions P1
P1-d2-249
Clinical follow-up in girls with non-classical congenital adrenal hyperplasia: can oral contraceptives replace steroid treatment? Liat de Vries1,2, Michal Horovitz1, Yael Lebenthal1,2, Moshe Phillip1,2 1 Petah Tikva, Israel, 2Tel Aviv, Israel P1-d2-250
Evaluation of the hypothalamic-pituitary-adrenal axis and polysomnography in Prader-Willi children Wesley Buysse1, Veronique Beauloye2, Jean De Schepper2, Sara Van Aken1, Kathleen De Waele1, Margarita Craen1, Inge Gies2, Inge Francois3, Dominique Beckers4, An Desloovere1, G. Francois2, Karlien Dhondt1, Martine Cools1 1 Ghent, Belgium, 2Brussels, Belgium, 3Leuven, Belgium, 4Louvain-la-Neuve, Belgium
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poster sessions | P1
P1-d2-251
Application of liquid chromatography-tandem mass spectrometry for diagnosis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency in a 5-year-old boy Karine Khatchadourian, Graham Sinclair, Daniel L. Metzger Vancouver, Canada P1-d2-252
Adrenal insufficiency in children and risk of hypoglycaemia: usefulness of continuous glucose monitoring Paola Cambiaso, Riccardo Schiaffini, Novella Rapini, Stefania Pedicelli, Romana Marini, Gianluigi Spadoni, Marco Cappa Rome, Italy P1-d2-253
Three novel CYP21A2 mutations in patients with nonclassical 21-hydroxylase deficiency Débora Paula Michelatto, Fernanda Caroline Soardi, Fernanda Borchers Coeli, Denise Pedrosa, Sofia Helena Valente Lemos-Marini, Maria Tereza Matias Baptista, Gil Guerra-Júnior, Maricilda Palandi de Mello Campinas, Brazil P1-d2-254
N323K mutation of HSD3B2 gene in two siblings: sexual ambiguity limited to male gender Alessandro Salvatoni1, Adolfo Trettene1, Anita De Paoli2, Carlo Corbetta3, Yves Morel4 1 Varese, Italy, 2Gallarate, Italy, 3Milan, Italy, 4Lyon-Bron, France P1-d2-255
Different clinical presentation of X-linked congenital adrenal hypoplasia in four patients with new mutations in the NR0B1 gene Arianna Boiani1, Carla Bizzarri1, Romana Marini1, Paola Cambiaso1, Graziamaria Ubertini1, Stefano Cianfarani1,2, Marco Cappa1 1 Rome, Italy, 2Stockholm, Sweden P1-d2-256
11β-hydroxylase deficiency: functional characterisation of three novel CYP11B1 mutations Seher Polat1, Alexandra Kulle2, Züleyha Karaca1, Ilker Akkurt3, Selim Kurtoglu1, Fahrettin Kelestimur1, Joachim Grötzinger2, Paul-Martin Holterhus2, Felix G. Riepe2 1 Kayseri, Turkey, 2Kiel, Germany, 3Hamburg, Germany P1-d2-257
Hypercortisolism results in a differential delay in bone maturation of the bones of the wrist and hand Antony R. Lafferty1, Valeska Philippi2, Eric Richmond3, George P. Chrousos2,4, Alan D. Rogol5, Ze’ev Hochberg6 1 Canberra, Australia, 2Bethesda, USA, 3San José, Costa Rica, 4Athens, Greece, 5Charlottesville, USA, 6 Haifa, Israel P1-d2-258
Poster Sessions P1
Corticotropin tests for assessment of the hypothalamus-pituitary-adrenal axis in patients with Prader-Willi syndrome Graziano Grugni1, Andrea Corrias2, Antonino Crinò3, Luciano Beccaria4, Stefania Di Candia5, Lorenzo Iughetti6, Alessandro Mussa2, Letizia Ragusa7, Alessandro Salvatoni8, Alessandro Sartorio1, Giuseppe Chiumello5, Luigi Gargantini9, on behalf of the Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetes 1 Verbania, Italy, 2Turin, Italy, 3Rome, Italy, 4Lecco, Italy, 5Milan, Italy, 6Modena, Italy, 7Troina, Italy, 8 Varese, Italy, 9Treviglio, Italy P1-d2-259
Molecular genetic analysis of CYP21A2 gene and genotype-phenotype correlations in Croatian patients with classical form of 21-hydroxylase deficiency Katja K. Dumic1, Katarina Stingl1, Zorana Grubic1, Vesna Kušec1, Tony Yuen2, Robert Wilson2, Ingeborg Barisic1, Veselin Skrabic3, Miroslav Dumic1, Maria I. New2 1 Zagreb, Croatia, 2New York, USA, 3Split, Croatia
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Poster sessions | P1
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d3 Adrenals and HPA Axis 3
Session title: Chairs:
Ignacio Bergadá, Buenos Aires, Argentina Marc Nicolino, Lyon, France
P1-d3-260
Mutations of the KCNJ5 gene in patients with hypertension and increased aldosterone response to ACTH Amalia Sertedaki, Athina Markou, Geoarge Piaditis, George P. Chrousos, Evangelia Charmandari Athens, Greece P1-d3-261
Low body mass index at birth is associated with early adiposity rebound in 21-hydroxylase deficiency patients Shigeru Takishima1,2, Yohei Matsubara1, Makoto Ono1, Keisuke Nakajima1, Kentaro Miyai1, Kei Takasawa1, Shuki Mizutani1, Kenichi Kashimada1 1 Tokyo, Japan, 2Saitama, Japan P1-d3-262
Mutation analysis of CYP21A2 and correlation between genotype – phenotype in Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency Vũ Chí Dũng1, Khanh Van Tran1, Phuong Thi Le1, Ha Thi Nguyen1, Maki Fukami2, Liem Thanh Nguyen1, Van Thanh Ta1 1 Hanoi, Vietnam, 2Tokyo, Japan P1-d3-263
A novel SF1 mutation in a boy with late onset adrenal insufficiency, normal external genitalia and hypergonadotrophic hypogonadism Antonis Voutetakis1, Pascal Philibert2, Themistoklis Karpathios1, Amalia Sertedaki1, George P. Chrousos1, Charles Sultan2, Catherine Dacou-Voutetakis1 1 Athens, Greece, 2Montpellier, France P1-d3-264
Implementation of a LC-MSMS method for routine determination of 17-hydroxypregnenolone and dehydroepiandrosterone-sulfate and its application in endocrine diagnoses Alexandra E. Kulle1, Maik Welzel1, Nadine C. Hornig1, Thomas Reinehr2, Felix G. Riepe1, Paul-Martin Holterhus1 1 Kiel, Germany, 2Datteln, Germany P1-d3-265
A novel StAR splice site mutation in a 46,XX patient with lipoid congenital adrenal hyperplasia Núria Camats1, Amit V. Pandey1, Mónica Fernández-Cancio2, Juan Manuel Fernández3, Sameer Udhane1, Primus E. Mullis1, Antonio Carrascosa2, Laura Audí2, Christa E. Flück1 1 Bern, Switzerland, 2Barcelona, Spain, 3Granada, Spain
Poster Sessions P1
P1-d3-266
Molecular mechanisms of action of the natural human glucocorticoid receptor mutant hGRαT556I causing primary generalised glucocorticoid resistance Nicolas Nicolaides, Amalia Sertedaki, George P. Chrousos, Evangelia Charmandari Athens, Greece P1-d3-267
Pitfalls in the diagnosis of 11β-hydroxylase deficiency – new insights from four patients carrying novel CYP11B1 mutations Silvia Parajes1, Roxana Marino2, Ian T. Rose1, Angela E. Taylor1, Natalia Perez Garrido2, Mercedes Maceiras2, Pablo Ramirez2, Diana Warman2, Marco A. Rivarola2, Wiebke Arlt1, Alicia Belgorosky2, Nils Krone1 1 Birmingham, UK, 2Buenos Aires, Argentina
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poster sessions | P1
P1-d3-268
Newborn screening for congenital adrenal hyperplasia in Tokyo, Japan: lessons learned from 23 years’ experience Atsumi Tsuji, Konishi Kaoru, Satomi Hasegawa, Akira Anazawa, Teruo Kitagawa, Shuki Mizutani, Kenichi Kashimada Tokyo, Japan P1-d3-269
A novel mutation of the human glucocorticoid receptor gene causing mild primary generalised glucocorticoid resistance Amalia Sertedaki, Nicolas C. Nikolaides, George P. Chrousos, Evangelia Charmandari Athens, Greece P1-d3-270
Clinical, laboratory and genetic evaluation in 46,XX patient with P450c17 deficiency Luciane Carneiro de Carvalho1, Regina Martin Matsunaga1, Elaine Maria Frade Costa1, Sorahia Domenice1, Rosana Barbosa Silva1, Aline Zamboni Machado1, Margaret de Castro2, Livia Mermejo2, Fernanda Borchers Coeli-Lacchini2, Rosana Quezado3, Virginia Ribeiro Teixeira3, Fabrícia Torres Gonçalves4, Alexandre José Faria Carrilho5, Kenny Yelena Del Toro Camargo6, Gabriela Paula Finkielstain7, Ignacio Bergadá7, Giselle Fernandes Taboada8, Berenice Bilharinho Mendonça1 1 São Paulo, Brazil, 2Ribeirão Preto, Brazil, 3Fortaleza, Brazil, 4Uberlândia, Brazil, 5Londrina, Brazil, 6 Barranquilla, Colombia, 7Buenos Aires, Argentina, 8Rio de Janeiro, Brazil P1-d3-271
Evaluation of cognitive function and behavioural performances in girls with non-classical congenital adrenal hyperplasia Maria Pecoraro, Malgorzata Wasniewska, Tommaso Aversa, Silvestro Mirabelli, Giuseppina Zirilli, Giuseppina Salzano, Filippo De Luca Messina, Italy
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1 Autoimmune Endocrine Diseases 1
Session title: Chairs:
Zvi Laron, Petah Tikva, Israel Keisuke Nagasaki, Niigata, Japan
P1-d1-272
Defective transitional B cell compartment in APECED patients: correlation with the development of clinical symptoms of the disease Antonella Meloni1, Alessandra Magnani2, Maria Furcas1, Marco Gattorno2, Alberto Martini2, Elisabetta Traggiai3 1 Cagliari, Italy, 2Genoa, Italy, 3Basel, Switzerland Investigation of osteopontin levels and genomic variation of osteopontin and its receptors in type 1 diabetes mellitus Zohereh Karamizadeh, Forough Saki, Eskandar Kamali Sarvestani Shiraz, Islamic Republic of Iran P1-d1-274
Prevalence of early allergic sensitization in children with HLA-conferred susceptibility to type 1 diabetes Aleksandr Peet1, Anu-Maaria Hämäläinen2, Pille Kool1, Jorma Ilonen3,4, Vallo Tillmann1, Mikael Knip2,5 1 Tartu, Estonia, 2Helsinki, Finland, 3Turku, Finland, 4Kuopio, Finland, 5Tampere, Finland P1-d1-275
Endocrine autoimmunity in Turner syndrome: retrospective analysis of 67 patients and review of the literature Armando Grossi, Marco Cappa, Alessandra Fierabracci Rome, Italy
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Poster Sessions P1
P1-d1-273
Poster sessions | P1
P1-d1-276
Time lying down and energy expenditure are important determinants of vascular health in children with type 1 diabetes Jemma J. Anderson1, Oana Maftei1, Jenny Couper1, Bronwyn D’Arcy1, Adine Mayenburg1, Roger Gent1, Kate Dowling1, Tim Olds2, Alexia Pena1 1 North Adelaide, Australia, 2Adelaide, Australia P1-d1-277
21-hydroxylase and interferon omega autoantibodies in Turner syndrome Line Cleemann1, Bergithe Oftedal2, Christian Trolle3, Kirsten Holm1, Eystein S. Husebye2, Claus H. Gravholt3 1 Hillerød, Denmark, 2Bergen, Norway, 3Aarhus, Denmark P1-d1-278
The prevalence of ZnT8 autoantibodies in Czech children at onset of type 1 diabetes mellitus and dynamic changes of serum ZnT8 autoantibody concentrations over time Lenka Petruzelkova1, Rossi Ananieva-Jordanova2, Jana Vcelakova1, Katerina Stechova1, Jan Lebl1, Petr Dušátkova1, Zdenek Sumnik1, Rebecca Coles2, Mike Powell2, Jadwiga Furmaniak2, Bernard Rees Smith2, Stanislava Kolouskova1 1 Prague, Czech Republic, 2Cardiff, UK P1-d1-279
Cerebellar ataxia in a patient with autoimmune polyglandular syndrome type 1 Leila Sozaeva, Elizaveta Orlova, Svetlana Mikhailova, Natalya Pechatnicova, Alexey Maschan Moscow, Russian Federation P1-d1-280
Vitamin D status and the effects of vitamin D treatment in children with vitiligo Gülay Karagüzel, Nil Palancı Sakarya, Sevgi Bahadır, Selçuk Yaman, Aysenur Ökten Trabzon, Turkey P1-d1-281
Cytokines and high sensitive CRP before and after meal-induced hyperglycaemia in children with type 1 diabetes Niels H. Birkebaek1, Jesper S. Sørensen1, Bjarne K. Møller1, Kurt Kristensen1, Kristin Skogstrand2, David M. Hougaard2 1 Aarhus, Denmark, 2Copenhagen, Denmark
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1 Bone, Growth Plate and Mineral Metabolism 1
Session title: Chairs:
Eckhard Schoenau, Koeln, Germany Natascia Di Iorgi, Genoa, Italy
Poster Sessions P1
P1-d1-282
Brittle bones caused by mutations in WNT1 – new gene, new therapeutic approach? Heike Hoyer-Kuhn1, Oliver Semler1, Katharina Keupp1, Joan Marini2, Bernhard Zabel3, Christian Netzer1, Bernd Wollnik1, Eckhard Schoenau1 1 Cologne, Germany, 2Bethesda, USA, 3Freiburg, Germany P1-d1-283
Compound heterozygous mutations of SLC34A3 can cause idiopathic hypercalciuria without rickets: novel mutations detected in a sporadic case of a girl with idiopathic haematuria Yuki Abe1, Keisuke Nagasaki1,2, Maki Fukami2 1 Niigata, Japan, 2Tokyo, Japan P1-d1-284
A family with autosomal dominant hypocalcaemia with sensorineural hearing impairment and low urine excretion of calcium Hironori Shibata1, Naoaki Hori2, Makoto Yoshida2, Toshikata Mitui1, Satoshi Narumi1, Tomonobu Hasegawa1 1 Tokyo, Japan, 2Tochigi, Japan
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
P1-d1-285
Hyperparathyroidism and low sclerostin are the main causes of smaller and weaker bones in obese children Silvia Longhi1, Roberto Franceschi2, Davide Gatti3, Giorgio Radetti1 1 Bolzano, Italy, 2Trento, Italy, 3Verona, Italy P1-d1-286
A transient reduction in bone quality in nutrition-induced short-term catch-up growth Rakefet Pando1, Anna Idelevich2, Biana Shtaif1, Majdi Masarwi1, Efrat Monsonego-Ornan2, Ron Shahar2, Moshe Phillip3, Galia Gat-Yablonski3 1 Tel Aviv, Israel, 2Rehovot, Israel, 3Petah Tikva, Israel P1-d1-287
Inverse relationship between vitamin D status and insulin resistance and the risk of impaired fasting glucose in Korean children and adolescents Young Ah Lee, Choong Ho Shin, Sei Won Yang Seoul, Republic of Korea P1-d1-288
Effect of β-Estradiol on C-type natriuretic peptide induced endochondral ossification in ATDC5 cells Hua-Mei Ma, Zhe Su, Yan-Hong Li Guangzhou, China P1-d1-289
Hereditary 1,25-dihydroxyvitamin D-resistant rickets with homozygous VDR mutation – an extremely rare case of maternal uniparental disomy of chromosome 12 detected by genome-wide SNP array Mayuko Tamura1, Tsuyoshi Isojima1, Hideki Yoshida2, Minae Kawashima1, Keiko Yamamoto3, Taichi Kitaoka3, Noriyuki Namba3, Keiichi Ozono3, Katsushi Tokunaga1, Sachiko Kitanaka1 1 Tokyo, Japan, 2Kyoto, Japan, 3Osaka, Japan P1-d1-290
Mouse polycomb regulates infantile long bone growth and development Yuko Katoh-Fukui, Maki Fukami Tokyo, Japan P1-d1-291
Nutritional rickets: vitamin D, calcium or the genetic make up? Laura Audi1, Heba Elsedfy2, Monica Fernandez-Cancio1, Mohamed El Kholy2 1 Barcelona, Spain, 2Cairo, Egypt P1-d1-292
Children and adolescents with cystic fibrosis have normal volumetric BMD and geometry at the radius, but low muscle area at the forearm Ondrej Soucek, Jan Lebl, Veronika Skalicka, Dana Zemkova, Miloslav Rocek, Zdenek Sumnik Prague, Czech Republic P1-d1-293
9th Joint Meeting of Paediatric Endocrinology 2013
Poster Sessions P1
Ex vivo model reveals an important role for PDGFR-β in development of fetal mouse metacarpal growth plate Henna Joki1, Mirja Nurmio1, Anna-Marja Säämänen1, Kirsi Jahnukainen2,3, Jorma Toppari1, Tiina Laitala-Leinonen1 1 Turku, Finland, 2Stockholm, Sweden, 3Helsinki, Finland
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Poster sessions | P1
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2 Bone, Growth Plate and Mineral Metabolism 2
Session title: Chairs:
Hiroyuki Tanaka, Okayama, Japan Ashraf Soliman, Doha, Qatar
P1-d2-294
Bone disease in children with geroderma osteodysplasticum: a 25-year experience from a single tertiary centre Jaya Sujatha Gopal-Kothandapani, Raja Padidela, Jill Clayton-Smith, Kate E. Chandler, Judith E. Adams, Anthony J. Freemont, M. Zulf Mughal Manchester, UK P1-d2-295
Hereditary 1,25-dihydroxyvitamin D-resistant rickets inherited as a dominant trait caused by a novel vitamin D receptor mutation with dominant negative effect Tsuyoshi Isojima1, Kazuko Yoshimura2, Michiyasu Ishizawa1, Shinichi Hirose2, Makoto Makishima1, Sachiko Kitanaka1 1 Tokyo, Japan, 2Fukuoka, Japan P1-d2-296
FGF23 is modulated by calcium in children under peritoneal dialysis Francisco Cano, María Luisa Ceballos, Marta Azocar, Angelica Rojo, María José Ibacache, Angela Delucchi, Luisa Quiroz, Carlos Irarrazabal, Iris Delgado, Francisca Ugarte Santiago, Chile P1-d2-297
Altered bone geometry, strength and quality in children born SGA at term and in children born AGA and SGA prematurely Silvia Longhi1, Laura Carloni1, Federico Mercolini1, Roberto Franceschi2, Giorgio Radetti1 1 Bolzano, Italy, 2Trento, Italy P1-d2-298
Cardiovascular involvement in children with osteogenesis imperfecta Hamdollah Karamifar, Homa Ilkhanipoor, Gholamhossein Ajami, Zohreh Karamizadeh, Gholamhossein Amirhakimi, Alimohammmad Shakiba Shiraz, Islamic Republic of Iran P1-d2-299
The evaluation of vitamin D supplementation dose during pregnancy in a high-risk population Gul Yesiltepe Mutlu1, Elif Ozsu1, Sibel Kalaca2, Aysegul Yuksel1, Filiz Mine Cizmecioglu1, Sukru Hatun1 1 Kocaeli, Turkey, 2Istanbul, Turkey P1-d2-300
Fibroblast growth factor-23 and matrix extracellular phosphoglycoprotein levels in healthy children and pregnant and lactating women, and their roles in phosphate metabolism Serap Turan, Ahu Ozsen, Andrzej Furman, Abdullah Bereket Istanbul, Turkey
Poster Sessions P1
P1-d2-301
Microcephaly, multiple dysmorfisms and diabetes mellitus: multiple genetic involvement Andrea Accogli1, Dicky J. Halley2, M. Grazia Mancini2, Martina Wilke2, Renata Lorini1, Giuseppe d’Annunzio1 1 Genoa, Italy, 2Rotterdam, Netherlands P1-d2-302
The role of growth hormone in enchondroplasia and chondral osteogenesis: evaluation by hand x-ray Lea Even1, Björn Andersson2, Berit Kristöm3, Ze’ev Hochberg4, Kerstin Albertsson-Wikland2 1 Naharia, Israel, 2Gothenburg, Sweden, 3Umeå, Sweden, 4Haifa, Israel
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
P1-d2-303
Bone microarchitecture and vertebral bone marrow adiposity in young women with childhoodonset type 1 diabetes mellitus Naiemh Abdalrahaman, Christie McComb, John E. Foster, Russel Drummond, Derak Gordon, Robert Lindsay, Gerard McKay, Collin Perry, Guftar M. Shaikh, Faisal S. Ahmed Glasgow, UK P1-d2-304
25-Hydroxyvitamin D, osteocalcin, under-carboxylated osteocalcin and N-terminal propeptide of type 1 procollagen in prepubertal and pubertal survivors of childhood cancer compared with healthy controls Kristen A. Neville, Jan L. Walker, Richard J. Cohn, Chris Cowell, Chris P. White Sydney, Australia P1-d2-305
Autosomal recessive hypophosphatemic rickets type 2 and hypertension due to novel compound heterozygous mutations within the ENPP1 gene Klaus Kapelari1, Bettina Lorenz-Depiereux2, Tim Strom2, Elisabeth Steichen-Gersdorf1 1 Innsbruck, Austria, 2Muenchen, Germany P1-d2-306
Hip structural analysis in adolescent boys with anorexia nervosa and controls Madhusmita Misra1, Debra K. Katzman2, Hannah Clarke1, Karen K. Miller1, Anne Klibanski1 1 Boston, USA, 2Toronto, Canada
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1 Fat Metabolism, Obesity 1
Session title: Chairs:
Jennifer Couper, Adelaide, Australia Antonino Crinò, Rome, Italy
P1-d1-307
Use of a sex- and ethnicity-specific childhood continuous metabolic syndrome risk score to detect risk of glucose intolerance Mark D. DeBoer1, Matthew J. Gurka2 1 Charlottesville, USA, 2Morgantown, USA P1-d1-308
Exposure to androgens during early development predisposes females to hypothalamic gliosis and metabolic syndrome Pilar Argente-Arizón1, Esther Fuente-Martín1, Purificación Ros-Pérez1, Francisca Díaz1, Miguel Ángel Sánchez-Garrido1,2, David Castro-González1, Manuel Tena-Sempere1,2, Vicente Barrios1, Jesús Argente1, Julie A. Chowen1 1 Madrid, Spain, 2Córdoba, Spain P1-d1-309
Poster Sessions P1
A new human adipocyte model derived from a PTEN-deficient lipoma Franziska Käßner1, Antje Garten1, Gordian Schmid1, Astrid Tannert1, Franziska Wilhelm1, Jenny Leipert1, Martin Wabitsch2, Wieland Kiess1, Antje Körner1 1 Leipzig, Germany, 2Ulm, Germany P1-d1-310
Renin-angiotensin-aldosterone axis and cortisoluria in obese children and adolescents with or without arterial hypertension measured by 24-hour ambulatory blood pressure monitoring Esperanza Moreno-Villamil, Diego Yeste Fernández, Antonio Carrascosa Lezcano, Luis Lara Moctezuma, Laura Audi Parera, Carolina Forero Torres, María Clemente León, Marian Albisu Aparicio Barcelona, Spain
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Poster sessions | P1
P1-d1-311
Up-regulation of hippocampal somatostatin receptors may attenuate acute leptin action after its central infusion Vicente Barrios1, Arancha Perianes-Cachero2, Emma Burgos-Ramos1, Lilian Puebla-Jiménez2, Jesús Argente1, Julie A. Chowen1, Eduardo Arilla-Ferreiro2 1 Madrid, Spain, 2Alcalá de Henares, Spain P1-d1-312
GPR120 R270H polymorphism is a risk factor for liver injury in obese children Anna Grandone, Mariasole Conte, Francesco Capuano, Enrica Emanuela Cascone, Francesco Di Mauro, Manuela Rinaldi, Grazia Cirillo, Emanuele Miraglia Del Giudice, Laura Perrone Napoli, Italy P1-d1-313
Role of oncostatin M, a novel gp130 cytokine secreted in adipose tissue, in the development of obesity and type 2 diabetes David Sanchez-Infantes1,2, Gemma Aragones1, Marta Diaz1, Lourdes Ibañez1, Eric Ravussin2, Jacqueline M. Stephens2 1 Esplugues de Llobregat, Spain, 2Baton Rouge, USA P1-d1-314
Novel variants of aquaglyceroporin 7 gene promoter in relation to serum glycerol and susceptibility to low birth weight and type 2 diabetes in prepubertal children and adolescents Alexia Karvela1, Eleni Oikonomou1, Aliki Pappa1, Andrea Paola Roja-Gil2, George Georgiou1, Bessie E. Spiliotis1 1 Patras, Greece, 2Sparta, Greece P1-d1-315
Diet supplementation with betaine during lactation prevents the development of glucose intolerance in a mouse model of childhood obesity Marta Ramon-Krauel1, Thais Pentinat Pelegrin1, Judith Cebrià Romeo1, Ruben Diaz Naderi1, Carles Lerín2, Josep Jiménez-Chillarón1 1 Esplugues de Llobregat, Spain, 2Barcelona, Spain P1-d1-316
Higher serum levels of the Wnt-signalling antagonist DKK1 in obese compared to Prader-Willi syndrome Giacomina Brunetti1, Maurizio Delvecchio2, Graziano Grugni3, Annamaria Ventura1, Maria Ciccarelli1, Claudia Carbone1, Silvia Colucci1, Maria Grano1, Luciano Cavallo1, Maria Felicia Faienza1 1 Bari, Italy, 2San Giovanni Rotondo, Italy, 3Verbania, Italy P1-d1-317
Fitness and fatness have a biomarker in children: chemokine C-C ligand 2 M. Constantine Samaan, Joyce Obeid, Thanh Nguyen, Brian Timmons Hamilton, Canada P1-d1-318
Poster Sessions P1
Short-term intervention improves endothelial progenitor cell count and reduces cardiovascular markers in obese children and adolescents Isabel Viola Wagner1, Kathrin Dittrich1, Julia Gesing1, Julia Bielitz1, Friebe Daniela1, Firoz Ahmadi2, Wieland Kiess1, Antje Körner1 1 Leipzig, Germany, 2Bad-Frankenhausen, Germany
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2
Session title: Fat Metabolism, Obesity 2 Chairs: Raul Calzada, Mexico City, Mexico Cosimo Giannini, Chieti, Italy P1-d2-319
Bariatric surgery in adolescents and young adults Belinda S. Lennerz1, Christian Knoll2, Hans Lippert2, Thomas Manger3, Rudolf Weiner4, Stephanie Wolff2, Christine Stroh3, Martin Wabitsch1 1 Ulm, Germany, 2Magdeburg, Germany, 3Gera, Germany, 4Sachsenhausen, Germany P1-d2-320
Leptin substitution results in increased insulin and changes in gut hormone secretion, but unchanged BDNF in an adolescent with leptin deficiency Christian L. Roth1, Julia von Schnurbein2, Clinton Elfers1, Anja Moss2, Martin Wabitsch2 1 Seattle, USA, 2Ulm, Germany P1-d2-321
Neutrophil-to-lymphocyte ratio: ontogeny of a cardiovascular-risk marker Judit Bassols1, Ferran Díaz-Roldán1, Anna Prats-Puig1, Montserrat Gispert-Saüch1, Inés Osiniri2, Gemma Carreras-Badosa1, Lluís Mayol1, Francis de Zegher3, Lourdes Ibánez4, Abel López-Bermejo1 1 Girona, Spain, 2Figueres, Spain, 3Leuven, Belgium, 4Barcelona, Spain P1-d2-322
Cardiovascular risk factors and carotid intima media thickness in prepubertal children Fernanda M. Gazolla, Isabel R. Madeira, Paulo F. Collett-Solberg, Cecilia N.M. Carvalho, Alexandra V. Monteiro, Nadia Cristina P. Rodrigues, Ana Paula N. Bordallo, Clarice M. Borschiver, Marcos Antonio Borges, Maria Alice N. Bordallo, Bruna M. Muniz, Suellen M. Pinheiro Rio de Janeiro, Brazil P1-d2-323
Association between two genetic variants in APOA1 and CET and loss of adiposity after intervention in obese/overweight adolescents: Evasyon study Cristina Azcona1, Adriana Moleres1, Fermín Milagro1, Ascensión Marcos2, Eduardo González-Zorzano1, Cristina Campoy3, Jesús María Garagorri4, José Alfredo Martínez1, Amelia Marti1, Evasyon Study 1 Pamplona, Spain, 2Madrid, Spain, 3Granada, Spain, 4Zaragoza, Spain P1-d2-324
Adipocyte oxidative stress produces glutathionylated lipid aldehydes, novel activators of macrophage inflammation Brigitte I. Frohnert, Eric K. Long, Wendy Hahn, David A. Bernlohr Minneapolis, USA P1-d2-325
Increased metalloproteinase-9 activities in children with metabolic syndrome Hernan Garcia, Alejandro Martinez-Aguayo, Carmen Campino, Carolina Loureiro, Marlene Aglony, Rodrigo Bancalari, Lilian Bolte, Carolina Avalos, Cristian A. Carvajal, Lorena Garcia, Sergio Lavanderos Santiago de Chile, Chile
Poster Sessions P1
P1-d2-326
Severe early-onset obesity caused by compound heterozygosity for two novel leptin receptor mutations Sabine Elisabeth Hannema1, Abraham Felius1, Jan M. Wit1, Monique M. ten Dam1, Annemieke J.M.H. Verkerk2, André G. Uitterlinden2, Sarina G. Kant1, Wilma Oostdijk1, Monique Losekoot1, Henriette A. Delemarre-van de Waal1 1 Leiden, Netherlands, 2Rotterdam, Netherlands P1-d2-327
Is increased insulin sensitivity in Prader-Willi syndrome due to hyperghrelinaemia? Elena Bogova, Natalya Volevodz, Valentina Peterkova Moscow, Russian Federation
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Poster sessions | P1
P1-d2-328
Endocrine counter-regulation after weight-loss in obese children and adolescents: a controlled trial Susanna Wiegand, Annika Bickenbach, Almut Dannemann, Anne-Madeleine Bau, Andrea Ernert, Knut Mai, Joachim Spranger, Heiko Krude Berlin, Germany P1-d2-329
The smallest paternally transmitted SNORD 116 deletion in a young female displays a typical Prader-Willi Syndrome phenotype Sanaa Eddiry1, Eric Bieth1, Françoise Lorenzini1, Veronique Gaston1, Alexandre Buffet1, Françoise Auriol1, Catherine Molinas1, Benoit Arveiler2, Jean Pierre Salles1, Maithe Tauber1 1 Toulouse, France, 2Bordeaux, France P1-d2-330
Abstract has been withdrawn
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d3 Fat Metabolism, Obesity 3
Session title: Chairs:
Angelika Mohn, Chieti, Italy Sangeeta Yadav, New Delhi, India
P1-d3-331
Deep breathing acutely improves arterial dysfunction in obese children: evidence of functional impairment Valeria Calcaterra, Daniela Larizza, Matteo Vandoni, Irene Bonomelli, Roberto Raschetti, Marisa Arpesella, Bernardi Luciano Pavia, Italy P1-d3-332
Consumption of sugar-sweetened beverages is associated with prospective weight gain in preschoolers Mark D. DeBoer, Rebecca J. Scharf Charlottesville, USA P1-d3-333
Central leptin infusion increases insulin sensitivity and glycogen levels in the rat liver Vicente Barrios1, Emma Burgos-Ramos1, Amaia Rodríguez2, Sandra Canelles1, Javier Gómez-Ambrosi2, Gema Frühbeck2, Jesús Argente1 1 Madrid, Spain, 2Pamplona, Spain P1-d3-334
Poster Sessions P1
Clinical and genetic characteristics of the paediatric heterozygous familial hypercholesterolaemia population in Slovenia: a preliminary report Urh Groselj, Gasper Klancar, Natasa Bratina, Nevenka Bratanic, Katarina Trebusak Podkrajsek, Tadej Battelino Ljubljana, Slovenia P1-d3-335
Perinephric adipose tissue thickness in relation to blood pressure, plasma apelin and C-reactive protein levels in obese adolescents Ayse Nurcan Cebeci, Ayla Guven, Lutfi Ihsan Kuru Istanbul, Turkey P1-d3-336
Direct TBI effects contribute to increased cardiovascular risk in adult survivors of childhood acute lymphoblastic leukaemia treated with bone marrow transplantation and total body irradiation Christina Wei, Manigandan Thyagiarajan, Linda P. Hunt, Rachel M. Cox, Karin J. Bradley, Ruth Elson, Michael C.G. Stevens, Elizabeth C. Crowne Bristol, UK
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poster sessions | P1
P1-d3-337
The role of gut microbiota in obesity aetiology. Cause or effect? Muhammad Jaffar Khan1,2, Mohamad Guftar Shaikh1, Christopher Quince1, Christine Anne Edwards1, Konstantinos Gerasimidis1 1 Glasgow, UK, 2Peshawar, Pakistan P1-d3-338
Immune cell dysregulation – contributing to the risk of the development of metabolic disease and malignancies Eirin Carolan1, Andrew Hogan1, Michelle Corrigan1, Jean O’Connell2, Niamh Foley1, Luke O’Neill1, Declan Cody1, Donal O’Shea1,2, Obesity Immunology Group 1 Dublin, Ireland, 2Loughlinstown, Ireland P1-d3-339
Abdominal fat in newborns: relation to circulating long-chain poly-unsaturated fatty acids Nuria Sanz1, Cristina Sierra1, Marta Diaz1,2, Aroa Fernandez1, Abel López-Bermejo3, Francis de Zegher4, Lourdes Ibáñez1,2 1 Barcelona, Spain, 2Madrid, Spain, 3Girona, Spain, 4Leuven, Belgium P1-d3-340
BDNF and FTO gene variants modified the response to short-term weight management in overweight and obese adolescents Lenka Dusatkova, Hana Zamrazilova, Barbora Sedlackova, Josef Vcelak, Petr Hlavaty, Bela Bendlova, Marie Kunesova, Vojtech Hainer Prague, Czech Republic P1-d3-341
Timing and body mass index at adiposity rebound are associated with metabolic risk in 7-year old children Laura González1, Jeannette Linares1, Maria Luisa Garmendia1, Juliana Kain1, Ricardo Uauy1,2, Camila Corvalan1 1 Santiago, Chile, 2London, UK P1-d3-342
Miglitol increases energy expenditure by up-regulating uncoupling protein 1 in brown adipose tissue of diet-induced obesity mice Satoru Sugimoto, Hisakazu Nakajima, Kensuke Matsuo, Kitaro Kosaka, Hajime Hosoi Kyoto, Japan
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1
Session title: Chairs:
Fat Metabolism, Obesity 4 Luigi Gargantini, Treviglio, Italy Shigetaka Sugihara, Tokyo, Japan
An association between markers of endothelial dysfunction and early signs of renal damage in obese children and adolescents Cosimo Giannini, M. Loredana Marcovecchio, Simone Franchini, Valentina Chiavaroli, Tommaso de Giorgis, Francesco Chiarelli, Angelika Mohn Chieti, Italy P1-d1-344
Abstract has been withdrawn P1-d1-345
Impact of MTHFR genotype on HDL cholesterol in obese adolescents Esko J. Wiltshire1,2, Alexia S. Pena2, Tulika Sundernathan2, Jennifer J. Couper2 1 Wellington, New Zealand, 2Adelaide, Australia
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Poster Sessions P1
P1-d1-343
Poster sessions | P1
P1-d1-346
If I say: “a small bottle of soft drink a day means 24 kg of sugar a year” do you understand? A new communication strategy for adolescent health promotion Adriana Franzese, Lorena Morabito, Mary Lista, Enza Mozzillo, Eugenio Zito, Clelia Natale, Eleanna De Nitto, Giuseppe Mazzarella, Paola Iaccarino Idelson Naples, Italy P1-d1-347
Lack of growth hormone action modifies the serum lipid profile and metabolic parameters in response to a high fat diet Eva Baquedano1, Laura M. Frago1, Ana Ruiz-López1, Elahu S. Gosney2, James Herpy2, Julie A. Chowen1, John J. Kopchick2, Jesús Argente1 1 Madrid, Spain, 2Athens, USA P1-d1-348
Paediatric obesity and vitamin D deficiency: a proteomic approach identifies multimeric adiponectin as a key link between these conditions Gillian E. Walker, Flavia Prodam, Roberta Ricotti, Marta Roccio, Stefania Moia, Simonetta Bellone, Gianni Bona Novara, Italy P1-d1-349
Mutations in the leptin receptor gene in patients with early onset extreme obesity – a case series Belinda S. Lennerz1, Franziska Degenhardt2, Ulrich Paetow3, Gudrun Weinhandel4, Hansjosef Böhles3, Pamela Fischer-Posovszky1, Elke Fröhlich-Reiterer4, Georgia Lahr1, Klaus-Michael Debatin1, Martin Wabitsch1 1 Ulm, Germany, 2Bonn, Germany, 3Frankfurt, Germany, 4Graz, Austria P1-d1-350
Efficacy, safety and tolerability of statin therapy in adolescents with familial hypercholesterolaemia Lorenzo Iughetti, Simona Madeo, Zaira Pietrangiolillo, Barbara Predieri, Patrizia Bruzzi Modena, Italy P1-d1-351
Metformin prevents weight gain in youth on second generation antipsychotics David J. Klein, Jane Khoury, Keith Marsolo, Lawrence Dolan, Lindsey Hornung, Rajesh Ganta, Michael Sorter Cincinnati, USA P1-d1-352
The utility of natriuretic peptides as novel cardiovascular biomarkers in girls with Turner syndrome: comparison of findings to obese children and adolescents Ahmet Uçar, Fahrettin Oz, Firdevs Baş, Hüseyin Oflaz, Melike Tuğrul Kabasakal, Nurçin Saka, Rüveyde Bundak, Şükran Poyrazoğlu, Feyza Darendeliler Istanbul, Turkey P1-d1-353
Adipocyte selective TSH receptor knockout mice increased susceptibility to obesity Aziz Elgadi, Yingting Cao, Claude Marcus Stockholm, Sweden
Poster Sessions P1
P1-d1-354
Adiposity and inflammatory markers associated with non-alcoholic fatty liver disease Rosaura Leis1, Antía M. González1, Concepción Aguilera2, Josune Olza2, Mercedes Gil-Campos3, Nazareth Martinón1, Vanesa Crujeiras1, Gloria Bueno4, Rocio Vázquez1, Lidia Castro1, Rafael Tojo1 1 Santiago de Compostela, Spain, 2Granada, Spain, 3Córdoba, Spain, 4Zaragoza, Spain
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2
Session title: Fat Metabolism, Obesity 5 Chairs: Graziano Grugni, Verbania, Italy Edgar Van Mil, Den Bosch, Netherlands P1-d2-355
Abdominal fat distribution correlates to aromatase activity in pre-school girls Ann-Katrine Karlsson1, Joel Kullberg2, Per-Arne Svensson1, Kerstin Allvin1, Jovanna Dahlgren1 1 Gothenburg, Sweden, 2Uppsala, Sweden P1-d2-356
Liver dysfunction and its association with pro- and anti-inflammatory adipokines in healthy prepubertal children with abdominal obesity Sonya Galcheva1, Violeta Iotova1, Dilyana Baleva1, Yoto Yotov1, Davide Martorana2, Maria E. Street2 1 Varna, Bulgaria, 2Parma, Italy P1-d2-357
Pre-pregnant BMI is a predictor of the offspring’s adult risk for overweight and obesity Fredrik Ahlsson, Barbro Diderholm, Maria Lundgren Uppsala, Sweden P1-d2-358
A novel heterozygous splice-site mutation in two siblings with Bardet-Biedl syndrome Liana Gabriel, Moris Angulo, Monika Zak, Paul Saenger Mineola, USA P1-d2-359
Manganese superoxide dismutase Ala16Val gene polymorphism in obese children with metabolic syndrome Ilker T. Ozgen, Emel Torun, Arzu Ergen, Hande Karagedik, Yasar Cesur, Mehmet S. Aksu, Faruk Oktem, Umit Zeybek Istanbul, Turkey P1-d2-360
Influence of metformin on weight reduction and metabolic comorbidities in obese children and adolescents Andrea Bartucci, Gabriel Á. Martos-Moreno, Vicente Barrios, María Teresa Muñoz-Calvo, Jesús Pozo, Jesús Argente Madrid, Spain P1-d2-361
Toward early protection against endocrine-metabolic complications of later obesity: breastfed, large-for-gestational-age infants from non-diabetic mothers are more sensitive to insulin and gain more lean mass and less fat mass across infancy Giorgia Sebastiani1, Miriam Perez1, Marta Díaz1, Abel Lopez- Bermejo2, Francis De Zegher3, Lourdes Ibañez1 1 Barcelona, Spain, 2Girona, Spain, 3Leuven, Belgium P1-d2-362
Poster Sessions P1
Dyslipidaemia in survivors of childhood acute lymphoblastic leukaemia post bone marrow transplantation and total body irradiation is associated with abnormal differential fat deposition and adipocytokine levels Christina Wei, Manigandan Thyagiarajan, Linda P. Hunt, Rachel M. Cox, Karin J. Bradley, Ruth Elson, Michael C.G. Stevens, Elizabeth C. Crowne Bristol, UK P1-d2-363
Quantitative MRI - not ALT- allows for early diagnosis of hepatic steatosis Jennifer L. Rehm1, Peter Wolfgram1, Ellen Connor1, Vanessa Curtis2, Scott Reeder1, David B. Allen1 1 Madison, USA, 2Iowa City, USA
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Poster sessions | P1
P1-d2-364
Association of cardiac changes with serum adiponectin and resistin levels in obese children Ayşehan Akıncı, Cemşit Karakurt, Sibel Gürbüz, Özlem Elkıran Malatya, Turkey P1-d2-365
Low omentin-1 levels are related with clinical and metabolic parameters in obese children Gonul Catli, Ahmet Anik, Ayhan Abaci, Tuncay Kume, Ece Bober Izmir, Turkey P1-d2-366
An age-dependent association between a single nucleotide polymorphism in the MC4R gene and adiposity indexes in a population of Caucasian school-children M. Loredana Marcovecchio, Ebe D’Adamo, Rita Capanna, Sandra Mammarella, Cosimo Giannini, Francesco Chiarelli, Alessandro Cama, Angelika Mohn Chieti, Italy
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d3
Session title: Chairs:
Fat Metabolism, Obesity 6 Kenji Ihara, Fukuoka, Japan Maria Street, Parma, Italy
P1-d3-367
Liver transplantation as a successful therapy in a patient with homozygous familial hypercholesterolaemia – long-term follow up Nina Bratanič, Urh Grošelj, Gašper Klančar, Valentin Sojar, Nataša Bratina, Tadej Battelino Ljubljana, Slovenia P1-d3-368
PI3K/mTOR signalling and IGFBP2 production in human adipocyte models Franziska K. Wilhelm1, Franziska Kässner1, Gordian Schmid1, Jürgen Kratzsch1, Antje Körner1, Martin Wabitsch2, Wieland Kiess1, Antje Garten1 1 Leipzig, Germany, 2Ulm, Germany P1-d3-369
Serum uric acid levels and albuminuria-to-creatininuria ratio in obese children are associated with obesity comorbidities Flavia Prodam, Simonetta Bellone, Agostina Marolda, Matteo Castagno, Alice Monzani, Roberta Ricotti, Enza Giglione, Giulia Genoni, Elena Altieri, Gianni Bona Novara, Italy P1-d3-370
Poster Sessions P1
Early identification of impaired renal function in obese children with non-alcoholic fatty liver disease Hu Lin, Jun Fen Fu, Xue Feng Chen, Ke Huang, Wei Wu, Li Liang Hangzhou, China P1-d3-371
Predictive factors for insulin resistance in children Anzhalika Solntsava, Liudmila Viazava, Elena Aksionava, Alexandr Sukalo, Nina Danilenko Minsk, Belarus P1-d3-372
Early menarche and cardiovascular risk in Chilean adolescents of low- to mid- socioeconomic level Raquel Burrows1, Paulina Correa-Burrows2, Marcela Reyes1, Estela Blanco3, Cecilia Albala1, Sheila Gahagan3 1 Santiago de Chile, Chile, 2Madrid, Spain, 3San Diego, USA
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
P1-d3-373
Melatonin secretion in obese prepubertal patients and its correlation with metabolic syndrome and other cardiovascular risk factors Hugo L. Fideleff, Gabriel Fideleff, Hugo R. Boquete, Gabriela Ruibal, Martha Suárez, María De Luján Calcagno, Claudio González, Miriam Azaretzky Buenos Aires, Argentina P1-d3-374
Influence of prepubertal adiposity, insulin resistance and asymmetric dimethylarginine on blood pressure during puberty in obese subjects Tommaso de Giorgis, Cosimo Giannini, M. Loredana Marcovecchio, Valentina Chiavaroli, Stefania De Marco, Francesco Chiarelli, Angelika Mohn Chieti, Italy P1-d3-375
Effect of pre-pregnancy BMI and gestational weight gain on the timing of adiposity rebound Jeannette Linares, Camila Corvalan, Juliana Kain, Maria Luisa Garmendia, Laura González, Verónica Mericq Santiago, Chile P1-d3-376
Growth restraint before birth, weight catch-up in infancy, and central adiposity in childhood: a placebo-controlled pilot study of early metformin intervention Marta Díaz1,2, Lourdes Ibañez1,2, Abel López-Bermejo3, David Sanchez-Infantes1, Judit Bassols3, Francis de Zegher4 1 Esplugues, Spain, 2Madrid, Spain, 3Girona, Spain, 4Leuven, Belgium P1-d3-377
C242T polymorphims in p22phox in normotensive and hypertensive children and its relation with vascular inflammatory markers Francisca Riera, Alejandro Martinez-Aguayo, Alejandra Tapia, Cristian Carvajal, Carmen Campino, Hernan García, Carlos Fardella Santiago, Chile P1-d3-378
Non-obese girls exhibit different metabolic effects of ectopic fat based on race and ethnicity Peter Wolfgram, Jennifer Rehm, Ellen L. Connor, Jens C. Eickhoff, Scott B. Reeder, David B. Allen Madison, USA P1-d3-379
A proteomic approach to evaluate the role of cocoa consumption in the inflammatory pathway Marta Roccio, Flavia Prodam, Gillian Elisabeth Walker, Stefania Moia, Simonetta Bellone, Marco Arlorio, Gianni Bona Novara, Italy
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1 GH and IGF Physiology and Treatment 1 Stefan Riedl, Vienna, Austria Titania Pasqualini, Buenos Aires, Argentina
Poster Sessions P1
Session title: Chairs:
P1-d1-380
Autosomal dominant isolated growth hormone deficiency resulting from a recurrent GH1 gene mutation (p.Arg183His) in three unrelated families Alicia Martínez1, Paula A. Scaglia1, María Gabriela Ropelato1, Juan J. Heinrich1, Miguel Blanco2, Héctor G. Jasper1, Horacio M. Domené1 1 Buenos Aires, Argentina, 2Pilar, Argentina P1-d1-381
Effect of growth hormone for induced seizures Shigeru Nagaki, Kumiko Miwa, Makiko Osawa Tokyo, Japan
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster sessions | P1
P1-d1-382
Intracellular response to growth hormone in fibroblast cultures from normal adolescent boys Germán Iñiguez, Pedro Gallardo, Paula Ocaranza, Ximena Gaete, Fernando Cassorla Santiago, Chile P1-d1-383
50 years of the insulin tolerance test. Are we using the optimal sampling times? Nikolaos Daskas, Janet Stone, Wolf Woltersdorf, Elizabeth Crowne Bristol, UK P1-d1-384
A novel (p.Leu213Phe) and 2 recurrent (p.E35GfsX17 and p.Asn276Ser) IGFALS gene mutations in two children presenting IGF-I and IGFBP-3 deficiencies Angela Spinola-Castro1, Paula A. Scaglia2, Adriana Siviero-Miachon1, Juliana Saito Tartuci1, Héctor G. Jasper2, Horacio M. Domené2 1 Sao Paulo, Brazil, 2Buenos Aires, Argentina P1-d1-385
IGF-I in children with non-alcoholic fatty liver disease Valentina Pampanini1, Elena Inzaghi1, Rossana Fiori1, Arianna Boiani1, Paola Alessio1, Valerio Nobili1, Stefano Cianfarani1,2 1 Rome, Italy, 2Stockholm, Sweden P1-d1-386
Coexistence of growth hormone and glucocorticoid resistance in cases of Laron syndrome can be the reason of poor response to IGF-1 therapy Bryan Ghanny1, Aristotle Panayiotopoulos1, Yevgenly Apostolov2, Steven Ghanny3, Natia Pantsulaia4, Christina Tatsi1, Amrit Bhangoo5, Joseph Michl1, Svetlana Ten1 1 Brooklyn, USA, 2Little Rock, USA, 3Hackensack, USA, 4Mt Vernon, USA, 5Long Beach, USA P1-d1-387
Identification of two novel heterozygous molecular defects in the IGF-1R gene in familial short stature with intrauterine growth retardation and normal cognitive development Bich Lam1, Nathalie Thibaud1, Salah Azzi1, Cecile Brachet2, Laurence Berard1, Claudine Heinrichs2, Thuy-Ai Vu-Hong1, Frederic Brioude1, Yves Le Bouc1, Irene Netchine1 1 Paris, France, 2Brussels, Belgium P1-d1-388
Optimisation of growth hormone treatment in children born small-for-gestational-age: addition of metformin raises adiponectin levels and reduces the gain of visceral fat Paula Casano- Sancho1,2, Marta Diaz1,2, Abel López-Bermejo3, Francis de Zegher4, Lourdes Ibáñez1,2 1 Esplugues, Spain, 2Madrid, Spain, 3Girona, Spain, 4Leuven, Belgium P1-d1-389
Three years growth response to growth hormone treatment in very young children born small for gestational age: data from KIGS Margaret Boguszewski1, Anders Lindberg2, Hartmut Wollmann3, KIGS 1 Curitiba, Brazil, 2Sollentuna, Sweden, 3Surrey, UK
Poster Sessions P1
P1-d1-390
Four years of safety and efficacy of a once-weekly formulation of rhGH (LB03002) in children with GHD Vaman Khadilkar1, Rajesh Khadgawat2, Heba Elsedfy3, Meena Desai4, Shriraam Mahadevan5, Mala Dharmalingam6, Dieter Martin7, E. Christine Siepl7, Yoon Ju Bae8, Hyi-Jeong Ji8, Paul Saenger9 1 Pune, India, 2New Delhi, India, 3Cairo, Egypt, 4Mumbai, India, 5Chennai, India, 6Bangalore, India, 7 Baar, Switzerland, 8Seoul, Republic of Korea, 9New York, USA P1-d1-391
Pre-clinical characterisation of MOD-4023, a long acting growth hormone supporting phase II in GHD paediatric population Gili Hart, Oren Herskovits, Ahuva Bar-Iilan, Leanne Amitzi, Eyal Fima Nes Ziona, Israel
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2 GH and IGF Physiology and Treatment 2
Session title: Chairs:
Maité Tauber, Toulouse, France Junko Ito, Tokyo, Japan
P1-d2-392
Improvements in cognitive function following GH treatment: is there a catch-up effect? John E. Chaplin1, Berit Kriström2, Björn Jonsson3, Torsten Tuvemo3, Kerstin Albertson Wikland1 1 Gothenburg, Sweden, 2Umeå, Sweden, 3Uppsala, Sweden P1-d2-393
Aromatase inhibitor treatment in peri-pubertal males with growth disorders augments height while maintaining bone age/chronological age ratio Judith L. Ross1,2, Peter A. Lee3, Robert Z. Gut4, John A. Germak4 1 Philadelphia, USA, 2Wilmington, USA, 3Hershey, USA, 4Princeton, USA P1-d2-394
Recombinant human insulin-like growth factor 1 therapy in Duchenne muscular dystrophy Meilan M. Rutter, James Collins, Brenda L. Wong, Paul Horn, Michael D. Taylor, Shengyong Hu, Samantha Blum, Paula Morehart, Hemant Sawnani, Philippe Backeljauw Cincinnati, USA P1-d2-395
Efficacy of rhGH/rhIGF-1 co-administration therapy in children with short stature, low IGF-1 and GH sufficiency: results from a phase II, randomized, open-label, active-controlled trial Philippe Backeljauw1, Bradley S. Miller2, Pascale Dutailly3, Aude Sicsic3, Elizabeth Lawson4, Daniel E. Hale5, Barry J. Reiner6, Mark A. Sperling7 1 Cincinnati, USA, 2Minneapolis, USA, 3Les Ulis, France, 4Brisbane, USA, 5San Antonio, USA, 6Baltimore, USA, 7Pittsburgh, USA P1-d2-396
Factors influencing the final adult height of girls with Turner syndrome treated with recombinant human growth hormone and stanazolol Hui Xiong, Hong-Shan Chen, Min-Lian Du, Yan-Hong Li, Zhe Su, Hua-Mei Ma, Qiu-Li Chen Guangzhou, China P1-d2-397
Is there a dose-dependent effect of long-term growth hormone treatment on insulin sensitivity and β-cell function in pubertal short children born small for gestational age? Manouk van der Steen, Annemieke J. Lem, Judith S. Renes, Anita C.S. Hokken-Koelega Rotterdam, Netherlands P1-d2-398
P1-d2-399
The effect of prolonged GH treatment on upper airways and sleep-disordered breathing of 50 non-severely obese children with Prader-Willi syndrome Jenny Berini1, Stefania Di Candia2, Valeria Spica Russotto1, Lorenzo Iughetti3, Luigi Gargantini4, Alba Pilotta5, Graziano Grugni6, Giovanni Padoan1, Mariangela Cisternino7, Giuliana Trifirò8, Paolo Castelnuovo1, Giuseppe Chiumello2, Alessandro Salvatoni1, ISPED Study Group on Genetic Obesity 1 Varese, Italy, 2Milan, Italy, 3Modena, Italy, 4Treviglio, Italy, 5Brescia, Italy, 6Verbania, Italy, 7Pavia, Italy, 8 Rho, Italy
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster Sessions P1
Effects of varying growth hormone dose regimens on glucose metabolism in children born small for gestational age Ajay Thankamony1, Rikke B. Jensen2, Jeremy Kirk3, Sten Ivarsson4, Olle Söder5, Edna Roche6, Hilary Hoey6, David B. Dunger1 1 Cambridge, UK, 2Copenhagen, Denmark, 3Birmingham, UK, 4Malmo, Sweden, 5Stockholm, Sweden, 6 Dublin, Ireland
Poster sessions | P1
P1-d2-400
Population PK model of insulin-like growth factor after single and repeated administration of recombinant human IGF-1 in subjects with IGF deficiency Josep-Maria Cendrós Carreras1, Marion Dehez2, Angel Menargues2, Sandra Blethen3 1 Barcelona, Spain, 2Les Ulis, France, 3Basking Ridge, USA P1-d2-401
Pubertal height gain and adult height in pre- and pubertal short SGA patients treated with GH Muriel Thomas1, Inge François2, Kathleen De Waele3, Véronique Beauloye1, Annick France4, Cécile Brachet1, Marie-Christine Lebrethon5, Inge Gies1, Geneviève Thiry-Counson5, Dominique Beckers6, Guy Massa7, Franciska Verlinde1, Jean De Schepper1 1 Brussels, Belgium, 2Leuven, Belgium, 3Gent, Belgium, 4Antwerpen, Belgium, 5Liège, Belgium, 6Yvoir, Belgium, 7Hasselt, Belgium P1-d2-402
Most subjects with non-severe GH deficiency do not require GH treatment until final height Stefano Zucchini, Mirella Scipione, Anna Lisa Martini, Giulio Maltoni, Federico Baronio, Laura Mazzanti Bologna, Italy P1-d2-403
The association between growth hormone response and baseline body composition of children with growth hormone deficiency Ihsan Esen, Fatma Demirel, Derya Tepe, Ozlem Kara, Nevra Koc Ankara, Turkey
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d3 GH and IGF Physiology and Treatment 3
Session title: Chairs:
Jürgen Brämswig, Münster, Germany Masanori Ohta, Yamanashi, Japan
P1-d3-404
A preliminary report: from the database on growth hormone treatment in Japanese, NordiPAD GH effect on lipid metabolism Toshihiro Tajima1, Masanori Adachi2, Keiichi Ozono3, Toshiaki Tanaka4, Tomonobu Hasegawa4, Reiko Horikawa4, Susumu Yokoya4 1 Sapporo, Japan, 2Yokohama, Japan, 3Osaka, Japan, 4Tokyo, Japan P1-d3-405
Relationship between either total anti-IGF-1 antibodies or specific anti-IGF-1 IgE titres and the occurrence of apparent hypersensitivity reactions in a paediatric population treated with rhIGF-1 (Increlex®) Julie Legrand1, Bruno Fiorentino2, Pascale Dutailly1 1 Les Ulis, France, 2Boulogne Billancourt, France
Poster Sessions P1
P1-d3-406
Effects of the two-year treatment with recombinant IGF-1 of children with primary IGF-1 deficiency in Poland: a multicentre study Elzbieta Petriczko1, Anita Horodnicka-Jozwa1, Beata Wikiera2, Anna Noczynska2, Maria Korpal- Szczyrska3, Dorota Birkholz-Walerzak3, Ewa Malecka-Tendera4, Barbara Kalina-Faska4, Ewa Barg2, Iwona Ben-Skowronek5, Leszek Szewczyk5, Maciej Hilczer6, Katarzyna Ziora4, Artur Bossowski7, Beata Pyrzak8, Andrzej Kedzia9, Mieczyslaw Szalecki8, Joanna Smyczynska6, Maria Kalina4, Edyta Pietrewicz7, Tomasz Jackowski1, Agnieszka Kilian1, Mieczyslaw Walczak1 1 Szczecin, Poland, 2Wroclaw, Poland, 3Gdansk, Poland, 4Katowice, Poland, 5Lublin, Poland, 6Lodz, Poland, 7Bialystok, Poland, 8Warsaw, Poland, 9Poznan, Poland
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
P1-d3-407
Ten years after the United States Food and Drug Administration approval of GH treatment for idiopathic short stature: who is being treated and what is the response to treatment? Charmian A. Quigley1, Christopher J. Child2, Alan G. Zimmermann1, Judith L. Ross3, Ron G. Rosenfeld4, Werner F. Blum5 1 Indianapolis, USA, 2Windlesham, UK, 3Philadelphia, USA, 4Palo Alto, USA, 5Bad Homburg, Germany P1-d3-408
Sleep-related breathing disorders in patients with Prader-Willi syndrome depending on period of growth hormone treatment Agnieszka Lecka-Ambroziak1, Mieczyslaw Szalecki1,2 1 Warsaw, Poland, 2Kielce, Poland P1-d3-409
Impact of age at the onset of growth hormone treatment on weight status at the end of treatment in children with idiopathic growth hormone deficiency Thomas Reinehr1, Anders Lindberg2, Ferah Aydin2, Matthias Heinze3, Maria Koltowska-Häggström2, KIGS 1 Datteln, Germany, 2Sollentuna, Sweden, 3Berlin, Germany P1-d3-410
Predictors of growth hormone responsiveness during transition from childhood to adult GH treatment Ajay Thankamony1, Donatella Capalbo1, Helen L. Simpson1, Hartmut A. Wollmann2, Peter Jonsson3, Maria Koltowska-Haggstrom3, David B. Dunger1 1 Cambridge, UK, 2Tadworth, UK, 3Sollentuna, Sweden P1-d3-411
Eight years of growth hormone treatment in children with Prader-Willi syndrome: maintaining the positive effects Nienke Bakker, Renske Kuppens, Elbrich Siemensma, Roderick Tummers de Lind van Wijngaarden, Dederieke Festen, Maria De Ridder, Anita Hokken-Koelega Rotterdam, Netherlands P1-d3-412
Secondary IGF-I deficiency as a prognostic factor of growth hormone therapy effectiveness in children with isolated, non-acquired growth hormone deficiency Joanna Smyczynska, Renata Stawerska, Andrzej Lewinski, Maciej Hilczer Lodz, Poland P1-d3-413
Evaluation of serum IGF-I, IGFBP-3 and IGF-I/IGFBP-3 molar ratio in children with growth hormone deficiency, Turner syndrome and small for gestational age on rhGH treatment María G. Ballerini, Débora Braslavsky, Ana Keselman, Alicia Martinez, María E. Rodriguez, Horacio M. Domené, Paula Scaglia, Analía V. Freire, Héctor G. Jasper, Ignacio Bergadá, María G. Ropelato Buenos Aires, Argentina P1-d3-414
Poster Sessions P1
Poor growth response and responsiveness to growth hormone therapy in children with growth failure Saartje Straetemans1,2, Jean De Schepper2,3, Raoul Rooman2,4, Belgian Study Group for Paediatric Endocrinology 1 Maastricht, Netherlands, 2Brussels, Belgium, 3Ghent, Belgium, 4Antwerp, Belgium P1-d3-415
Quality of life after growth hormone treatment in young adults with isolated GH deficiency Annalisa Deodati1, Roberto Sorge1, Claudio Giacomozzi1, Riccardo Torre1, Flavia Pricci1, Cristina Fazzini1, Pietro Panei1, Patrizia Matarazzo2, Laura Perrone3, Marco Cappa1, Antonella Puglianiello1, Daniela Germani1, Stefano Cianfarani1,4 1 Rome, Italy, 2Turin, Italy, 3Naples, Italy, 4Stockholm, Sweden
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster sessions | P1
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1
Session title: Chairs:
Glucose Metabolism 1 Luis Castaño, Vizcaya, Spain Chunxiu Gong, Beijing, China
P1-d1-416
Long-term changes of visual evoked potentials in children and adolescents with type 1 diabetes mellitus Jae Hong Yu1, Heon-Seok Han2 1 Daejeon, Republic of Korea, 2Cheongju, Republic of Korea P1-d1-417
Gut microbiota in children with type 1 diabetes differs from healthy children: a case-control study Isabel Leiva Gea1, Ana Leiva Gea2, Mª Isabel Queipo Ortuño1, Juan Pedro López Siguero1, Antonio Urda1, Federico Soriguer1 1 Málaga, Spain, 2Jaén, Spain P1-d1-418
Development of a prediction model for a ‘best-fit’ basal insulin infusion pattern in children and adolescents with diabetes mellitus type 1 on insulin pumps Paul-Martin Holterhus1, Jessica Bokelmann1, Felix Riepe1, Bettina Heidtmann2, Verena Wagner3, Birgit Rami-Merhar4, Thomas Kapellen5, Klemens Raile6, Wulf Quester7, Reinhard W. Holl8, German/Austrian DPV-initiative and the German Pediatric CSII Working Group 1 Kiel, Germany, 2Hamburg, Germany, 3Lübeck, Germany, 4Vienna, Austria, 5Leipzig, Germany, 6Berlin, Germany, 7Bad Oeynhausen, Germany, 8Ulm, Germany P1-d1-419
Diminished serum estrogenic activity in girls with type 1 diabetes Daniela Martínez, Andrea Castro, Cecilia Lardone, Germán Iñiguez, Patricia López, Paulina Merino, Fernando Cassorla, Ethel Codner Santiago, Chile P1-d1-420
Retinal thinning in young patients with type 1 diabetes mellitus: is it the first sign of diabetic retinopathy? Anna Saporiti, Gianluca Musolino, Matteo Marazza, Roberta Cardani, Muna Al Oum, Adolfo Trettene, Simone Donati, Claudio Azzolini, Alessandro Salvatoni Varese, Italy P1-d1-421
Performance of meglitinide analogues in 117 adolescent patients with HNF1A-MODY (MODY3): experience from the prospective German/Austrian DPV database Klemens Raile1, Katja Konrad2, Angelika Thon3, Jürgen Grulich-Henn4, Thomas Meissner5, Joachim Woelfle6, Edith Schober7, Reinhard Holl8, DPV Initiative and the German BMBF Competence Network Diabetes Mellitus. 1 Berlin, Germany, 2Essen, Germany, 3Hannover, Germany, 4Heidelberg, Germany, 5Düsseldorf, Germany, 6 Bonn, Germany, 7Vienna, Austria, 8Ulm, Germany
Poster Sessions P1
P1-d1-422
The Euro-WABB Registry: analysis of obesity and diabetes prevalence in the first 115 patients affected by Wolfram, Alstrom or Bardet-Biedl syndrome recruited to the registry (www.euro-wabb.org) Tim Barrett1, Ségolène Aymé2, Miguel Lopez de Heredia3, Pietro Maffei4, Susan Mccafferty5, Wojciech Mlynarski6, Virginia Nunes3, Véronique Paquis7, Kay Parkinson8, Richard Sinnott5, Vallo Tillmann9, Amy C. Farmer1 1 Birmingham, UK, 2Paris, France, 3Barcelona, Spain, 4Padua, Italy, 5Glasgow, UK, 6Poland, Poland, 7Nice, France, 8Torbay, UK, 9Tartu, Estonia P1-d1-423
The gene for a novel syndrome of diazoxide-responsive hyperinsulinaemic hypoglycaemia and polycystic kidney disease maps to chromosome 16 Oscar Rubio-Cabezas1, Elena García-Martínez2, Montserrat Antón-Gamero2 1 Madrid, Spain, 2Córdoba, Spain
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poster sessions | P1
P1-d1-424
Are environmental and genetic factors at type 1 diabetes diagnosis associated with the development of microvascular complications? Myra S. Y. Poon1, Maria E. Craig1,2,3, Albert K. F. Chan1, Janine M. Cusumano1, Kim C. Donaghue1,2 1 Westmead, Australia, 2Sydney, Australia, 3Randwick, Australia P1-d1-425
Oleate protects INS1 cells from palmitate-induced apoptosis by down-regulating ER stress and GSK3β through stearoyl-CoA desaturase 1 Shan Huang, Wei Wu, Yan Liang, Qin Ning, Xiao-Ping Luo Wuhan, China
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2
Session title: Chairs:
Glucose Metabolism 2 Tatsuhiko Urakami, Tokyo, Japan Thomas Kapellen, Leipzig, Germany
P1-d2-426
F-DOPA PET MRI as a new imaging modality for the precise localisation of focal congenital hyperinsulinism Senthil Senniappan, Pratik Shah, Marguerite du Preez, Raymond Endozo, Celia O’Meara, Caroline Townsend, Clare Gilbert, Kate Morgan, Louise Hinchey, Agostino Pierro, Lorenzo Biassoni, Oystein Olsen, Jamshed Bomanji, Khalid Hussain London, UK 18
P1-d2-427
Subclinical diabetic cardiomyopathy in children Viktoriya Furdela Ternopil, Ukraine P1-d2-428
Measuring the effect of diabetic ketoacidosis on brain compliance using a non-invasive device Matthew Stenerson1, Peter Neild2, Nicole Schleifer1, Kristin Schleifer1, Joseph Malo2, Darrell Wilson1, Tandy Aye1 1 Stanford, USA, 2Mountain View, USA P1-d2-429
Diazoxide-responsive hyperinsulinaemic hypoglycaemia caused by a de novo novel HNF4A mutation Barbora Obermannova, Petra Dusatkova, Stepanka Pruhova, Zdenek Sumnik, Jan Lebl Prague, Czech Republic Utilizing bedside ultrasound measurements of optic nerve sheath diameter to assess increased intracranial pressure in children with diabetic ketoacidosis Miladys M. Palau-Collazo, Eda Cengiz, Vince Faustino, Stuart Weinzimer, Cicero Silva, Lei Chen, William Tamborlane New Haven, USA P1-d2-431
Efficacy and safety of closed-loop insulin delivery during reduction or omission of meal boluses in adolescents with type 1 diabetes Daniela Elleri1, Janet Allen1, Giulio Maltoni1, Marianna Nodale1, Kavita Kumareswaran1, Lalantha Leelarathna1, Hood Thabit1, Karen Caldwell1, Malgorzata E. Wilinska1, Peter Calhoun2, Craig Kollman2, David B. Dunger1, Roman Hovorka1 1 Cambridge, UK, 2Tampa, USA
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Poster Sessions P1
P1-d2-430
Poster sessions | P1
P1-d2-432
A mutation in the ABCC8 gene (c.1773delC) causing congenital hyperinsulinaemia evolving into postprandial hyperglycaemia Tohru Yorifuji1, Yuki Hosokawa1, Rie Kawakita1, Rika Fujimaru1, Akiko Saito-Hakoda2, Ikuma Fujiwara2 1 Osaka, Japan, 2Sendai, Japan P1-d2-433
Pancreatic enzyme supplementation slows gastric emptying and improves post prandial glycaemia in adolescents with cystic fibrosis Shiree Perano, Jennifer Couper, Christopher Rayner, James Martin, Stamatiki Kritas, Kate Dowling, Michael Horowitz Adelaide, Australia P1-d2-434
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism Maria Carla Proverbio1, Eleonora Mangano2, Alessandra Gessi1, Roberta Bordoni2, Roberta Spinelli2, Rosanna Asselta1, Paola Sogno Valin1, Stefania Di Candia2, Ilaria Zamproni2, Cecilia Diceglie2, Stefano Mora2, Manuela Caruso-Nicoletti3, Cristina Battaglia1,2, Giuseppe Chiumello1, Gianluca De Bellis2, Alessandro Salvatoni4 1 MIlan, Italy, 2Segrate, Italy, 3Catania, Italy, 4Varese, Italy P1-d2-435
Molecular analysis of congenital hyperinsulinism: genotype/phenotype correlations Luis Salamanca Fresno, Isabel González-Casado, Guillermo Barreno-Sardiña, Julio Guerrero-Fernández, Juan Tovar-Larrucea, Ana Gómez-Núñez, Angel Campos-Barros Madrid, Spain
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d3 Glucose Metabolism 3
Session title: Chairs:
Stephen O’Riordan, Cork, Ireland Declan Cody, Dublin, Ireland
P1-d3-436
Long-term follow-up of individuals diagnosed with type 1 diabetes mellitus during childhood Mary White, Michele A. O’Connell, Peter Colman, Fergus J. Cameron Melbourne, Australia P1-d3-437
A mathematical model to predict HbA1c levels from mean blood glucose in young type 1 diabetic patients Houda El Arabi, Dominique Willems, Christian Mélot, Harry Dorchy Bruxelles, Belgium
Poster Sessions P1
P1-d3-438
Obesity and diabetes in youth: distinguishing characteristics at diagnosis and follow-up between islet cell antibody positive vs. negative patients Michelle Y. Rivera-Vega, Amanda Flint, Ingrid Libman, Silva Arslanian Pittsburgh, USA P1-d3-439
The role of glucagon-like peptide-1, glucose-dependent inhibitory peptide and peptide YY in congenital hyperinsulinism Sofia A. Rahman, Efthimia Karra, Pratik Shah, Ved B. Arya, Senthil Senniappan, Azizun Nessa, Maha Sherif, Khalid Hussain London, UK
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poster sessions | P1
P1-d3-440
A randomised controlled trial of a psychological intervention to improve metabolic control in children with type 1 diabetes Elisabeth A. Northam, Elizabeth M. Westrupp, Michael Combie, Shannon Scratch, Fergus J. Cameron Melbourne, Australia P1-d3-441
The efficacy of using the internet-based CareLink® therapy management system for diabetes in patients with type 1 diabetes Shlomit Shalitin1,2, Tal Sakal Ben Ari1, Michal Yackobovitch Gavan1,2, Moshe Phillip1,2 1 Petah Tikva, Israel, 2Tel Aviv, Israel P1-d3-442
Cognitive and neuroanatomical differences in young children with type 1 diabetes and association with dysglycaemia: the diabetes research in children network (DirecNet) experience Nelly Mauras1, Neil H. White2, Eva Tsalikian3, Stuart Weinzimer4, Tandy Aye5, Allison Cato1, Peiyao Cheng6, Craig Kollman6, Roy W. Beck6, Katrina J. Ruedy6, Tamara Hershey2, Paul Mazaika5, Naama Barnea-Goraly5, Matthew Marzelli5, Larry Fox1, William Tamborlane4, Ana Maria Arbelaez2, Allan Reiss5, Diabetes Research in Children Network (DirecNet) 1 Jacksonville, USA, 2St. Louis, USA, 3Iowa City, USA, 4New Haven, USA, 5Stanford, USA, 6Tampa, USA P1-d3-443
Higher albumin creatinine ratio is associated with cardiac autonomic dysfunction in adolescents with type 1 diabetes Yoon Hi Cho1, Maria E. Craig1, Elizabeth A. Davis2, Andrew M. Cotterill3, Jennifer J. Couper4, Fergus J. Cameron5, Paul Z. Benitez-Aguirre1, R. Neil Dalton6, David B. Dunger7, Timothy W. Jones2, Kim C. Donaghue1, Adolescent Type 1 Diabetes Cardio-Renal Intervention Trial (AdDIT) 1 Sydney, Australia, 2Perth, Australia, 3Brisbane, Australia, 4Adelaide, Australia, 5Melbourne, Australia, 6 London, UK, 7Cambridge, UK P1-d3-444
First child with glucagonoma: multiple endocrine neoplasia type 1 presenting with hyperinsulinaemic hypoglycaemia and simultaneous glucagonoma and insulinoma, identified by [68Ga]DOTATATE PET/CT and [111]In-Exendin-3 SPECT, respectively Henrik Thybo Christesen1, Henrik Petersen1, Lars Rasmussen1, Lennart Friis-Hansen2, Cees Noordam3, Claus Hovendal1, Sven Pörksen4, Martin Gotthardt3 1 Odense C, Denmark, 2Copenhagen, Denmark, 3Nijmegen, Netherlands, 4Roskilde, Denmark P1-d3-445
Adverse inflammatory profile during luteal phase in adolescents with type 1 diabetes Paulina M. Merino, Patricia Lopez, Daniela Martinez, Claudia Godoy, German Iñiguez, Andrea Castro, Fernando Cassorla, Francisco Perez-Bravo, Ethel Codner Santiago, Chile
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1 Glucose Metabolism 4 Claude Marcus, Stockholm, Sweden Fortunato Lombardo, Messina, Italy
Poster Sessions P1
Session title: Chairs:
P1-d1-446
Pesticides immunotoxicity in diabetic Egyptian children during first presentation Rania H. Abdel Rahman, Doaa A. El-Morsi, Sherin M. Abd El-Aziz, Ashraf A. Elsharkawy Mansoura, Egypt P1-d1-447
The relationship between metabolic dyslipidaemia and insulin sensitivity versus hyperglycaemia in obese adolescents Sheela N. Magge1, Raymond C. Boston2, Justine Shults1, Nicolas Stettler3, Lorraine E.L. Katz1, Daniel J. Rader1 1 Philadelphia, USA, 2Kennett Square, USA, 3Washington, USA
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Poster sessions | P1
P1-d1-448
Impact of protein and fat rich meals on glucose levels. A study in adolescent patients with type 1 diabetes Roland Schweizer, Susan Herrlich, Martina Lösch-Binder, Regina Braun, Fabian Behret, Angelika Schneider, Andreas Neu Tübingen, Germany P1-d1-449
Improvement of diabetes self-management skills in children and adolescents with type 1 diabetes mellitus Manmohan Kamboj, David Repaske, Sean Gleeson, Kathryn Stephens, Lindsey Rauch, Jeff Lewis, Setenay Kara, Richard Brilli Columbus, USA P1-d1-450
In children with type 1 diabetes mellitus, anti-tissue transglutaminase antibody levels may spontaneously normalise despite a gluten normal intake Maria Carmela Oliva, Albina Tummolo, Federica Ortolani, Francesca Carella, Maristella Masciopinto, Marcella Vendemiale, Sabino Pesce, Ruggiero Francavilla, Stefania Paola Castellaneta, Francesco Papadia, Elvira Piccinno Bari, Italy P1-d1-451
Both homoarginine and asymmetric dimethylarginine are decreased in children and adolescents with type 1 diabetes, and are unaffected by statin treatment Karl Otfried Schwab1, Andreas Krebs1, Juergen Doerfer1, Jan Woehrl1, Bernhard Stier2, Kai Lichte3, Karl Winkler1, Juergen Grulich-Henn4, Martin Holder5, Arno Schmidt-Trucksaess6 1 Freiburg, Germany, 2Butzbach, Germany, 3Villingen-Schwenningen, Germany, 4Heidelberg, Germany, 5 Stuttgart, Germany, 6Basel, Switzerland P1-d1-452
Is insulin resistance more frequent in children born small for gestational age? Ramona Stroescu, Teofana Bizerea, Otilia Marginean, Monica Marazan, Ioana Micle Timisoara, Romania P1-d1-453
Profile and outcome of diabetic ketoacidosis treated in a tertiary care referral centre in a developing country Janani Sundaram, Saranya Subburayalu, Hemchand Krishna Prasad, Anitha Pannagasayanan, Thangavelu Sangaralingam Chennai, India P1-d1-454
A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes: a case report Gonul Catli1, Ayhan Abaci1, Sarah E. Flanagan2, Elisa De Franco2, Sian Ellard2, Andrew Hattersley2, Handan Guleryuz1, Ece Bober1 1 Izmir, Turkey, 2Exeter, UK
Poster Sessions P1
P1-d1-455
Medication induced diabetes during induction treatment for ALL, an early marker for future metabolic risk? Yonatan Yeshayahu1,2, Dror Koltin3, Jill Hamilton3, Stacey Urbach3 1 Ramat-Gan, Israel, 2Tel Aviv, Israel, 3Toronto, Canada
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poster sessions | P1
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2 Glucose Metabolism 5
Session title: Chairs:
Adriana Franzese, Naples, Italy Pauliina Utriainen, Kuopio, Finland
P1-d2-456
A study on correlation between blood glucose fluctuations and activation of oxidative stress in type 1 diabetes children during the acute metabolic disturbance period Chunxiu Gong, Di Wu, Xi Meng, Qiulan Yang Beijing, China P1-d2-457
Plasma insulin levels during an OGTT are positively correlated with height in obese pre-pubertal children and adolescents: implications for OGTT interpretation Primož Kotnik, Martina Žakelj, Zinka Velagić, Nataša Bratina, Tadej Battelino Ljubljana, Slovenia P1-d2-458
Vitamin D deficiency and insulin resistance in Korean girls So Hyun Park1, Won Kyung Cho2, Kyung Soon Cho3, Min Ho Jung2, Byung Kyu Suh2 1 Suwon-si, Republic of Korea, 2Seoul, Republic of Korea, 3Bucheon-si, Republic of Korea P1-d2-459
Abstract has been withdrawn P1-d2-460
Mutations of monogenic forms of diabetes, especially INS gene mutation, in Japanese children with type 1B diabetes Ichiro Yokota1, Maki Moritani1, Shigetaka Sugihara2, Shin Amemiya3, the Japanese Study Group of Insulin Therapy for Children and Adolescent Diabetes (JSGIT) 1 Zentsuji, Japan, 2Tokyo, Japan, 3Saitama, Japan P1-d2-461
Physical activity, fitness and screen time in childhood: how these lifestyle habits predict insulin sensitivity 2 years later Mélanie Henderson, Andrea Benedetti, Katherine Gray-Donald, QUALITY Cohort Research Group Montreal, Canada P1-d2-462
Use of metformin in paediatric patients with diabetes mellitus type 1: an analysis based on a German/Austrian paediatric registry for the German/Austrian DPV Initiative and the German BMBF competence networks diabetes and obesity Katja Konrad1, Nicolin Datz2, Ilse Engelsberger3, Jürgen Grulich-Henn4, Thomas Hoertenhuber5, Burkhild Knauth6, Thomas Meissner7, Susanne Wiegand8, Joachim Wöllfle9, Berthold P. Hauffa1, Reinhard W. Holl10 1 Essen, Germany, 2Hannover, Germany, 3München, Germany, 4Heidelberg, Germany, 5Vienna, Austria, 6 Berchtesgarden, Germany, 7Düsseldorf, Germany, 8Berlin, Germany, 9Bonn, Germany, 10Ulm, Germany P1-d2-463
Poster Sessions P1
Diagnostic and management in 33 focal forms of congenital hyperinsulinism – limits of the 18 F-DOPA PET/CT Peter Kuehnen1, Khalid Hussain2, Wolfgang Mohnike1, Karin Rothe1, Oliver Blankenstein1 1 Berlin, Germany, 2London, UK P1-d2-464
Higher insulin detemir doses are required for similar glycaemic control: comparison of insulin detemir and insulin glargine in children with type 1 diabetes Saygın Abalı, Serap Turan, Zeynep Atay, Tülay Güran, Belma Haliloğlu, Abdullah Bereket Istanbul, Turkey
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster sessions | P1
P1-d2-465
Use of glucagon-like peptide 1 receptor agonists in Prader-Willi syndrome: report of six cases Danilo Fintini1, Claudia Brufani1, Sarah Bocchini1, Graziano Grugni2, Arianna Boiani1, Marco Cappa1, Antonino Crinò1 1 Rome, Italy, 2Piancavallo, Italy
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1
Session title: Chairs:
Growth 1 Peter Hindmarsh, London, UK Philippe Backeljauw, Cincinnati, USA
P1-d1-466
FGF21 causes GH resistance in human chondrocytes through activation of SOCS2 and inhibition of IGF-1 expression Leonardo Guasti, Patrizia Ferretti, Leo Dunkel London, UK P1-d1-467
Duplication of the NSD 1 (Sotos) gene causes the reverse phenotype of short stature and IUGR Georgina M.G. Williams, Elizabeth C. Crowne, Ruth Newbury-Ecob Bristol, UK P1-d1-468
Designing informative growth charts for specialist use. A novel evidence-based approach using two methods to evaluate pubertal progress Gary E. Butler1, Tim J. Cole1, Stef van Buuren2, Benjamin Holter1, Nishat Rahman1, John Short3, Charlotte M. Wright4, Royal College of Paediatrics and Child Health Growth Chart Expert Working Group 1 London, UK, 2Leiden, Netherlands, 3South Shields, UK, 4Glasgow, UK P1-d1-469
Evaluation of submicroscopic chromosomal deletions and duplications in dysmorphic patients born small for gestational age Ana P.M. Canton, Tatiane Rodrigues, Ivo J.P. Arnhold, Berenice B. Mendonca, Carla Rosenberg, Alexander A.L. Jorge São Paulo, Brazil P1-d1-470
Recombinant growth hormone increases intact FGF23 level Justine Bacchetta, Laurence Chardon, Ingrid Plotton, Bruno Ranchin, Pascaline Arsac, Behrouz Kassai, Pierre Cochat, Marc Nicolino Lyon, France
Poster Sessions P1
P1-d1-471
Impaired growth hormone signalling pathway in fibroblasts of children with chronic renal failure under peritoneal dialysis therapy. Preliminary data Francisca Ugarte, Teresa Salazar, Cristian Suazo, Carlos Irarrazabal, Marta Azocar, María Luisa Ceballos, Francisco Cano Santiago, Chile P1-d1-472
Individuals heterozygous for the c.424_427del STAT5B mutation have mild growth and immunological phenotypes Renata C. Scalco1, Carlos A. Tonelli2, Patricia N. Pugliese-Pires1, Julio C. Cechinel2, Ivo J.P. Arnhold1, Alexander A.L. Jorge1 1 Sao Paulo, Brazil, 2Criciuma, Brazil
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
P1-d1-473
Short stature and severe insulin resistance associated with double heterozygous mutations of IGF1R and INSR genes: a physiologic role of IGF1R-INSR hybrids in longitudinal growth? Carlo Colombo1, Laura Proietti Pannunzi1, Valeria Grasso1, Cristina Rofani1, Ornella Massa1, Maria Grazia Deiana1, Claudia Motta1, Domenico Accili2, Vincenzo Toscano1, Fabrizio Barbetti1 1 Rome, Italy, 2New York, USA P1-d1-474
Are recent references for length/height influenced by the presence of overweigth or obese children? Pétur Júlíusson1, Mathieu Roelants2, Bente Brannsether1, Hege Kristiansen3, Robert Bjerknes1 1 Bergen, Norway, 2Brussels, Belgium, 3Førde, Norway P1-d1-475
Factors affecting growth velocity after discontinuation of gonadotropin-releasing hormone agonist treatment in girls with central precocious or early puberty Yun Jung Choi, Shin Hee Kim, Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Seung Hoon Hahn, Min Ho Jung, Byung Kyu Suh, Byung Churl Lee Seoul, Republic of Korea P1-d1-476
The easypodTM connect observational study: adherence to recombinant human growth hormone therapy in younger and older children Peter Davies1, Jeremy Kirk2, Jan Lebl3, Andrea Luczay4, John VanderMeulen5, Sandro Loche6, Svante Norgren7, Ludmila Kostalova8, Ho-Seong Kim9, Marc Nicolino10, Evangelia Charmandari11, George Stoyanov12 1 Herston, Brisbane, Australia, 2Birmingham, UK, 3Prague, Czech Republic, 4Budapest, Hungary, 5 Hamilton, Canada, 6Cagliari, Italy, 7Stockholm, Sweden, 8Bratislava, Slovakia, 9Seoul, Republic of Korea, 10 Lyon, France, 11Athens, Greece, 12Mississauga, Canada P1-d1-477
Cardiofaciocutaneous syndrome, a Noonan syndrome related disorder: clinical and molecular findings Atilano Carcavilla1,2, Sixto García-Miñáur2, Antonio Pérez-Aytés3, Vendrell Teresa4, Pinto Isabel5, Encarna Guillén-Navarro6, Sánchez-Pozo Jaime2, Lilian Galbis2, Luis Santomé2, Juan P. López-Siguero7, Begoña Ezquieta2 1 Toledo, Spain, 2Madrid, Spain, 3Valencia, Spain, 4Barcelona, Spain, 5Leganés, Spain, 6Murcia, Spain, 7 Málaga, Spain
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2
Session title: Chairs:
Growth 2 Han Heon Seok, Seoul, Republic of Korea Haruo Mizuno, Nagoya, Japan
Whole exome sequencing is an effective tool for discovering the genetic causes of familial endocrine disorders Monique Losekoot1, Gijs W.E. Santen1, Hermine A. van Duyvenvoorde1, Michiel J.R. van der Wielen1, Annemieke J.M.H. Verkerk2, Andre G. Uitterlinden2, Sabine E. Hannema1, Jan-Maarten Wit1, Sarina G. Kant1, Wilma Oostdijk1 1 Leiden, Netherlands, 2Rotterdam, Netherlands P1-d2-479
QEPS – a new mathematical model describing individual human growth Andreas F.M. Nierop1, Aimon Niklasson1, Anton Holmgren1, Lars Gelander1, Stefan Aronsson2, Kerstin Albertsson-Wikland1 1 Gothenburg, Sweden, 2Halmstad, Sweden P1-d2-480
Reference values for IGF-I, IGFBP-3 and ALS in the diagnostic work-up for short stature Diana-Alexandra Ertl, Andreas Gleiss, Susanne Sagmeister, Gabriele Haeusler Vienna, Austria
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Poster Sessions P1
P1-d2-478
Poster sessions | P1
P1-d2-481
Does muscle training increase growth velocity in children with cerebral palsy? Oliver Semler, Christina Stark, Heike Hoyer-Kuhn, Ibrahim Duran, Eckhard Schoenau Cologne, Germany P1-d2-482
The sitting height/height ratio for age is a simple and useful tool to select children with idiopathic short stature for SHOX studies Alexsandra C. Malaquias1, Eveline G.P. Fontenele2, Everlayny F. Costalonga3, Renata C. Scalco1, Mariana F.A. Funari1, Mirian Y. Nishi1, Ivo J.P. Arnhold1, Berenice B. Mendonca1, Alexander A.L. Jorge1 1 Sao Paulo, Brazil, 2Fortaleza, Brazil, 3Vila Velha, Brazil P1-d2-483
Current growth and metabolic syndrome components in Korean adolescents according to birth weight at gestational age: results from the Korea National Health and Nutrition Examination Surveys (KNHANES) 2010 – 2011 In Ah Jung, Shin Hee Kim, Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byung-Kyu Suh Seoul, Republic of Korea P1-d2-484
Percutaneous epiphysiodesis is an efficient and safe method to reduce adult height in extremely tall adolescent boys and girls Emelie Benyi1, Dionisios Chrysis2, Ola Nilsson1,3, Henrik Wehtje1, Lars Sävendahl1 1 Stockholm, Sweden, 2Rion, Greece, 3Bethesda, USA P1-d2-485
Short stature and GH deficiency caused by zinc deficiency in a 6-month-old breast-fed infant due to a dominant negative heterozygous G87R mutation in the Zinc Transporter ZnT-2 (SLC30A2) in the mother Andreas Bieri, Vibor Petkovic, Maria C. Miletta, Christa E. Flück, Primus E. Mullis Bern, Switzerland P1-d2-486
Extending WHO weight-for-age reference curves to older children: a CPEG initiative Sarah E. Lawrence1, Jean Pierre Chanoine2, Elizabeth A. Cummings3, Daniel L. Metzger2, Mark R. Palmert4, Celia Rodd5, Atul K. Sharma5, Canadian Pediatric Endocrine Group (CPEG) 1 Ottawa, Canada, 2Vancouver, Canada, 3Halifax, Canada, 4Toronto, Canada, 5Montreal, Canada P1-d2-487
Severity of the disease negatively influences growth in children suffering from homozygous SS sickle-cell disease: results of a single centre study Fatiha Guemazi, Malika Benkerrou, Mohamed Damir, Zineddine Houari, Corinne Alberti, Jean-Claude Carel, Dominique Simon Paris, France P1-d2-488
Study on the role of amino-terminal propeptide of C-type natriuretic peptide in children with short stature Woo Yeong Chung, Seung Hwan Oh, Tae Min Eom Busan, Republic of Korea
Poster Sessions P1
P1-d2-489
Endocrine and genetic assessment of a girl with Weaver syndrome Yoko Miyoshi1, Noriyuki Namba1, Kohji Miura1, Naomichi Matsumoto2, Keiichi Ozono1 1 Osaka, Japan, 2Yokohama, Japan P1-d2-490
Accuracy of different GH provocative tests for the diagnosis of GH deficiency in children Chiara Guzzetti1, Anastasia Ibba1, Sabrina Pilia1, Nadia Beltrami2, Natascia Di Iorgi3, Alessandra Rollo4, Giorgio Radetti2, Stefano Zucchini4, Mohamad Maghnie3, Marco Cappa5, Sandro Loche1 1 Cagliari, Italy, 2Bolzano, Italy, 3Genoa, Italy, 4Bologna, Italy, 5Rome, Italy
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poster sessions | P1
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1
Session title: Perinatal and Neonatal Endocrinology 1 Chairs: Giuliana Trifirò, Rho, Italy Melinda Atienza, Manila, Philippines P1-d1-491
Alterations in protein expression in small for gestational age infants born at term Maria D. Ruiz-González, María D. Cañete-Vázquez, José L. Gómez-Chaparro, Juan L. Lopez-Barea, Ramón Cañete Córdoba, Spain P1-d1-492
Higher expression of Klotho/FGF system in placentas from small for gestational age newborns: relation with birth growth and length Germán Iñiguez, Andy Torres, Juan José Castro, Verónica Mericq, María Cecilia Johnson, Fernando Cassorla Santiago, Chile P1-d1-493
Following the Canadian Pediatric Society and the American Academy of Pediatrics guidelines for the management of neonatal hypoglycaemia will miss some neonates with transient perinatal stress hyperinsulinism Paul Thornton, Lisa Tran Fort Worth, USA P1-d1-494
Hypophosphataemia in small for gestational age extremely low birth weight infants receiving parenteral nutrition in the first week after birth Go Ichikawa, Junko Ichikawa, Yoshiyuki Watabe, Akihisa Nitta, Hiroshi Suzumura, Toshimi Sairenchi, Takashi Muto, Osamu Arisaka Tochigi, Japan P1-d1-495
Differences in IR/IRS-1/AKT/mTOR protein contents and their response to IGF-I in human term and preterm placentas Germán Iñiguez, Juan José Castro, Ernesto Torres, Verónica Peña, Verónica Mericq, María Cecilia Johnson, Fernando Cassorla Santiago, Chile P1-d1-496
Identifying the growth-restricted neonate Popi Sifianou, Helen Karga Athens, Greece P1-d1-497
Poster Sessions P1
Adiponectin and serum leptin levels of large for gestational age newborns with a weight gain more than 1.0 Kg during the first month of life Viktoria L. Butyhina, Angelika Solntsava Minsk, Belarus P1-d1-498
Relation of gestational age to ratios of serum insulin-like growth factor-II to serum insulin-like growth factor binding protein-3 in the not-life-threatened newborn: relevance of the proportion between estimated birth brain weight and birth body weight beyond the presence of caesarean section and of a small birth body weight for gestational age Cesare Terzi1, Werner F. Blum2, Sergio Zani1, Marco Riani1, Gabriele Tridenti3, Andrea Cerioli1, Lidia Garavelli3, Sergio Bernasconi1, Raffaele Virdis1, Giacomo Banchini3 1 Parma, Italy, 2Giessen, Germany, 3Reggio Emilia, Italy
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster sessions | P1
P1-d1-499
Higher PINP in small for gestational-age preterm infants is associated with increased growth during the first six months post-term Monique van de Lagemaat1, Eline van der Veer2, Mirjam M. van Weissenbruch1, Harrie N. Lafeber1, Joost Rotteveel1 1 Amsterdam, Netherlands, 2Groningen, Netherlands P1-d1-500
Body mass index and ponderal index references for newborn at 28-42 weeks gestation Nihal Hatipoglu, Selim Kurtoglu, Mumtaz Mustafa Mazicioglu, Mustafa Ali Akin, Sonay Gokoglu, Coban Dilek, Osman Bastug Kayseri, Turkey P1-d1-501
Concurrent argininosuccinic aciduria in a patient with Russell-Silver syndrome caused by maternal uniparental isodisomy of chromosome 7 Dau-Ming Niu1, Fu-Sung Lo2, Hao-Chuan Liu1, Sheng-Fong Chiang1, Chia-Feng Yang1, Yu-Hsiu Huang1, Yung-Hsiu Lu1, Cheng-Fang Li1, Ming-Yu Lo1 1 Taipei, Taiwan 2Taoyuan, Taiwan P1-d1-502
Catch-up growth by itself following fetal growth restriction is an adaptive compensation and does not induce metabolic changes until three years of age Ivana Milovanovic, Falucar Njuieyon, Samia Deghmoun, Didier Chevenne, Claire Lévy-Marchal, Jacques Beltrand Paris, France
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1
Session title: Chairs:
Pituitary and Neuroendocrinology 1 José Ignacio Labarta Aizpún, Zaragoza, Spain Malgorzata Wasniewska, Messina, Italy
P1-d1-503
Genotypic classification of Wolfram syndrome patients: insights into the natural history of the disease and correlation with phenotype Miguel López de Heredia1, Ramón Clèries1,2, Virginia Nunes1,2 1 L’Hospitalet de Llobregat, Spain, 2Barcelona, Spain P1-d1-504
Novel mutations in PAX6 cause congenital hypopituitarism with or without ocular malformation Masaki Takagi1, Keisuke Nagasaki2, Tomohiro Ishii1, Naoko Amano1, Yumi Asakura3, Koji Muroya3, Yukihiro Hasegawa1, Masanori Adachi3, Tomonobu Hasegawa1 1 Tokyo, Japan, 2Niigata, Japan, 3Kanagawa, Japan
Poster Sessions P1
P1-d1-505
Prevalence of microadenomas in children with isolated growth hormone deficiency and central precocious puberty Stefania Pedicelli1, Gian Luigi Spadoni1, Paola Alessio1, Giuseppe Scirè1, Diego De Angelis1, Marco Cappa1, Stefano Cianfarani1,2 1 Rome, Italy, 2Stockholm, Sweden P1-d1-506
Copy number variants in Brazilian patients with congenital hypopituitarism Fernanda A. Correa, Marcela M. Franca, Ana P.M. Canton, Aline P. Otto, Everlayne F. Costalonga, Vinicius N. Brito, Luciani R. Carvalho, Silvia Costa, Ivo J.P. Arnhold, Alexander A.L. Jorge, Carla Rosenberg, Berenice B. Mendonca Sao Paulo, Brazil
114
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
P1-d1-507
Contribution of OTX2 mutations in the aetiology of congenital hypopituitarism in a selected cohort of patients: novel changes and functional consequences Kyriaki S. Alatzoglou1, Mark J. Mccabe1, Louise C. Gregory1, Emanuela Spadoni1, Juan-Pedro Martinez-Barbera1, Mohamad Maghnie2, Mehul T. Dattani1 1 London, UK, 2Genoa, Italy P1-d1-508
Diencepephalic syndrome before diagnosis of childhood craniopharyngioma: results of multinational studies on 485 long-term survivors after childhood craniopharyngioma Hermann Lothar Müller1, Anthe S. Sterkenburg2, Ursel Gebahrdt1, Anika Hoffmann1, Kraniopharyngeom 2007 1 Oldenburg, Germany, 2Groningen, Netherlands P1-d1-509
Lowered FT4 concentrations after starting growth hormone treatment: unmasking of mild congenital central hypothyroidism? Laura van Iersel1, Hanneke M. van Santen1, Gladys R.J. Zandwijken2, Petra Oomen3, Anita C.S. Hokken-Koelega2, A.S. Paul van Trotsenburg1 1 Amsterdam, Netherlands, 2Rotterdam, Netherlands, 3Bilthoven, Netherlands P1-d1-510
Long-term health outcomes of adults with McCune Albright syndrome Sze Choong Wong, Margaret Zacharin Melbourne, Australia P1-d1-511
Contribution of GLI2 mutations to pituitary deficits and delineation of the associated phenotypic spectrum Marie Legendre1, Florence Dastot1, Nathalie Collot1, Chantal Lacombe1, Alexandra Afenjar1, Louise Brueton2, Sylvie Cabrol1, Enzo Cohen1, Stéphanie Friszer1, Jean Furioli3, Anne-Marie Guerrot4, Juliane Legér1, Catherine Naud-Saudreau5, Sylvie Nivot6, Chirag Patel2, Michel Polak1, Sophie Rose1, Marie-Laure Sobrier1, Aude Soleyan1, Amnon Zung7, Serge Amselem1 1 Paris, France, 2Birmingham, UK, 3Mantes-La-Jolie, France, 4Rouen, France, 5Lorient, France, 6Rennes, France, 7Rehovot, Israel P1-d1-512
Treatment of growth hormone excess in two children with neurofibromatosis type 1 with the longacting somatostatin analogue lanreotide Theda Wessel, Erwin Lankes, Heiko Krude, Dirk Schnabel Berlin, Germany
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2
Session title: Chairs:
Pituitary and Neuroendocrinology 2 Joseph Majzoub, Boston, USA Suh Byung-Kyu, Seoul, Republic of Korea
Poster Sessions P1
P1-d2-513
Thyroid hormone transporter expression in the murine anterior pituitary lobe Makoto Fujiwara1, Noriyuki Namba1, Masanobu Kawai2, Keiko Yamamoto1, Kohji Miura1, Taichi Kitaoka1, Takuo Kubota1, Keiichi Ozono1 1 Suita, Japan, 2Izumi, Japan P1-d2-514
Abstract has been withdrawn
9th Joint Meeting of Paediatric Endocrinology 2013
115
Poster sessions | P1
P1-d2-515
Anterior hypopituitarism in adult childhood cancer survivors: a report from the St. Jude Lifetime cohort Wassim Chemaitilly1, Zhenghong Li1, Kirsten K. Ness1, Karen L. Clark1, Daniel M. Green1, Nicole Barnes1, Gregory T. Armstrong1, Matthew J. Krasin1, Deo Kumar Srivastava1, Ching-Hon Pui1, Thomas E. Merchant1, Larry E. Kun1, Amar Gajjar1, Melissa M. Hudson1, Leslie L. Robison1, Charles A. Sklar2 1 Memphis, USA, 2New York, USA P1-d2-516
Unusual presentation of craniopharyngioma with acute haemorrhage and syndrome of inappropriate antidiuretic hormone secretion Chibuzor N. Ihe, Jennifer Kalitsi, Charles R. Buchanan London, UK P1-d2-517
Managing rare, resistant, macro- and giant prolactinomas causing raised intracranial pressure in children: lessons learnt at a single centre Chloe Bulwer, Hoong-Wei Gan, Eve Stern, Micheal Powell, Owase Jeelani, Marta Korbonits, Helen Spoudeas London, UK P1-d2-518
A single sample triptorelin stimulation test in diagnosing the onset of hypothalamic-pituitarygonadal axis in girls Zhuangjian Xu, Yaping Ma, Qing Wang, Junying Lu, Jinling Zhao WuXi, China P1-d2-519
Management of central diabetes insipidus with oral desmopressin lyophilisate in infants Hüseyin Anil Korkmaz, Korcan Demir, Fatma Kaya Kiliç, Demet Terek, Sertaç Arslanoglu, Ceyhun Dizdarer, Behzat Ozkan Izmir, Turkey P1-d2-520
Pulsatility of the hypothalamus-pituitary-adrenal axis in depressed male survivors of childhood traumatic brain injury Nik Daskas, Peta Sharples, Wolf Woltersdorf, Elizabeth Crowne, KHINES (Kids Head Injury NeuroEndocrine Study) Bristol, UK P1-d2-521
Poster Sessions P1
Trans-sphenoidal approach for the treatment of childhood craniopharyngiomas can reduce the risk of hypothalamic obesity Junko Ito, Naomi Mito, Shozo Yamada, Susumu Yokoya Tokyo, Japan
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1 Programming/Epigenetics 1
Session title: Chairs:
Fredrik Ahlsson, Uppsala, Sweden Paolo Ghirri, Pisa, Italy
P1-d1-522
Altered protein arginine methylation in offspring of diabetic mice Corinna Grasemann1, Berthold P. Hauffa1, Ralf Herrmann1, Cordula Kiewert1, Wei-Shih Liu1, Michael M. Schündeln1, Mark R. Palmert2, Hartmut Grasemann2 1 Essen, Germany, 2Toronto, Canada
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
P1-d1-523
Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome Tomoko Fuke1, Seiji Mizuno2, Toshiro Nagai3, Tomonobu Hasegawa1, Reiko Horikawa1, Yoko Miyoshi4, Koji Muroya5, Tatsuro Kondoh6, Chikahiko Numakura7, Seiji Sato3, Shinichiro Sano1,8, Keiko Matsubara1, Masayo Kagami1, Kazuki Yamazawa1, Tsutomu Ogata1,8 1 Tokyo, Japan, 2Aichi, Japan, 3Saitama, Japan, 4Suita, Japan, 5Kanagawa, Japan, 6Isahaya, Japan, 7Yamagata, Japan, 8Hamamatsu, Japan P1-d1-524
Reduced insulin sensitivity in children born to mothers with severe hyperemesis gravidarum Ahila Ayyavoo, Paul L. Hofman, Jose Derraik, Sarah Mathai, Peter Stone, Frank Bloomfield, Barbara Cormack, Wayne S. Cutfield Auckland, New Zealand P1-d1-525
Early markers of the metabolic syndrome in children born post-term Ahila Ayyavoo, Paul L. Hofman, Jose G.. Derraik, Sarah Mathai, Wayne S. Cutfield Auckland, New Zealand P1-d1-526
Methylation of the PGC-1alpha promoter is associated with the mitochondrial content and insulin resistance in liver of IUGR rats with catch-up growth Xuemei Xie, Lihong Liao, Meihui Zhang, Xiaoping Luo Wuhan, China P1-d1-527
Methylation defects of GNAS cluster in two patients with PHP-Ia Shinichiro Sano1, Akira Endoh2, Tomoko Fuke1, Keiko Matsubara1, Masayo Kagami1, Maki Fukami1, Tsutomu Ogata3 1 Setagayaku, Japan, 2Iwata, Japan, 3Hamamatsu, Japan P1-d1-528
Intrafamilial correlations of metabolic risk factors: results from the Ulm Birth Cohort Study Stephanie Brandt1, Anja Moß1, Wolfgang Koenig1, Melanie Weck2, Chad Logan1, Herrmann Brenner2, Dietrich Rothenbacher1, Martin Wabitsch1 1 Ulm, Germany, 2Heidelberg, Germany
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1 Puberty and Gonads 1
Session title: Chairs:
Manuela Caruso-Nicoletti, Catania, Italy Gerhard Binder, Tübingen, Germany
P1-d1-529
P1-d1-530
Effects of metformin and oral contraceptive on serum anti-Mullerian hormone levels in adolescent patients with polycystic ovary syndrome Fatma Dursun, Ayla Güven, Metin Yıldız Istanbul, Turkey P1-d1-531
Excess of ovarian nerve growth factor causes a polycystic ovary-like syndrome in mice, which closely resembles both reproductive and metabolic aspects of the human syndrome Jenny Wilson1, Michael A. Cowley1, Sergio R. Ojeda2, Pablo J. Enriori1, Maria C. Garcia-Rudaz1 1 Clayton, Australia, 2Beaverton, USA
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster Sessions P1
Treatment of 11 newborns with congenital hypogonadotropic hypogonadism with continuous subcutaneous infusion of recombinant FSH and LH Ariane Cuny, Pierre Bougneres, Claire Bouvattier Le Kremlin-Bicêtre, France
Poster sessions | P1
P1-d1-532
Replacement therapy with recombinant human FSH in Japanese males with congenital hypogonadotropic hypogonadism Tatsuya Miyoshi, Yukihiro Hasegawa, Noriko Nishina Tokyo, Japan P1-d1-533
Evaluation of puberty and gonadal function in women with congenital disorders of glycosylation syndrome Maud Bidet, Marion Keller, Hélene Crosnier, Pascale Delonlay, Michel Polak Paris, France P1-d1-534
Impact of gonadotrophin analogues therapy on body mass index of children with central precocious puberty Hemchand Krishna Prasad, Angela Casey, Jeremy Kirk Birmingham, UK P1-d1-535
Oral contraception versus insulin sensitisation for 18 months in non-obese adolescents with androgen excess: post-treatment differences in C-reactive protein, intima-media thickness, visceral adiposity, insulin sensitivity and menstrual regularity Lourdes Ibáñez1,2, Marta Díaz1,2, Giorgia Sebastiani1,2, Maria Victoria Marcos2,3, Abel López-Bermejo4, Francis de Zegher5 1 Esplugues, Barcelona, Spain, 2Madrid, Spain, 3Terrassa, Spain, 4Girona, Spain, 5Leuven, Belgium P1-d1-536
Human testicular peritubular cells: a source of Leydig cells? Luise Landreh1, Katrin Spinnler2, Olle Söder1, Konstantin Svechnikov1, Artur Mayerhofer2 1 Stockholm, Sweden, 2Munich, Germany P1-d1-537
Regulation and roles of anti-Müllerian hormone in the maturating rat testis Masanori Ohta, Hideaki Yagasaki, Kisho Kobayashi, Kanji Sugita, Kenji Ohyama Yamanashi, Japan P1-d1-538
Turner-Down syndrome mosaicism with spontaneous pregnancy and birth of a normal female Graciela del Rey, Viviana Pipman Buenos Aires, Argentina P1-d1-539
Benefit of testosterone in paediatric genital trauma Mary White, Margaret Zacharin Melbourne, Australia P1-d1-540
Poster Sessions P1
Efficacy of the hyperinsulinaemia treatment with metformin on androgen plasma levels and early adolescence PCOS features in obese prepubertal females Laura Guazzarotti, Silvia Mauri, Mariangela Petruzzi, Federica Occhipinti, Maddalena Macedoni, Alessandra Bosetti, Tarcisio Vago, Gian Vincenzo Zuccotti Milan, Italy
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2 Puberty and Gonads 2
Session title: Chairs:
Assunta Albanese, London, UK Patricia Vuguin, New York, USA
P1-d2-541
The effect of CYP21A2 heterozygous mutations on the values of DHEAS and other androgens in women with PCOS Nikolaos Settas1, Maria Dracopoulou-Vabouli1, Antonia Dastamani1, Ilias Katsikis2, George Chrousos1, Dimitrios Panidis2, Catherine Dacou-Voutetakis1 1 Athens, Greece, 2Thessaloniki, Greece P1-d2-542
Abstract has been withdrawn P1-d2-543
Evaluation of diagnostic criteria of polycystic ovary syndrome during adolescence Claudio Villarroel, Patricia López, Paulina M. Merino, Germán Iñiguez, Ethel Codner Santiago, Chile P1-d2-544
Gonadal impairment in children with acute lymphoblastic leukaemia treated by bone marrow transplantation: prevalence and risk factors Huda Abdulfatah Elhaj Burrani1, Mohamed Guftar Shaikh2, Anna Maria Ewin2, Brenda Gibson2, Malcolm Donaldson2 1 Tripoli, Libyan Arab Jamahiriya, 2Glasgow, UK P1-d2-545
Anti-Müllerian hormone deficiency in female children and adolescents with congenital multiple pituitary hormone deficiency Beate Deubzer, Karin Weber, Barbara Lawrenz, Gerhard Binder Tübingen, Germany P1-d2-546
Hormonal intervention in the management of adolescents with gender identity disorders Henriette Delemarre-van de Waal, Sabine E. Hannema, Sebastian E.E. Schagen Leiden, Netherlands P1-d2-547
Absence of functional TAC3 and TACR3 mutations in a cohort of patients affected by familial central precocious puberty Mariangela Cisternino1, Paolo Duminuco2, Giulia Rossetti1, Ilaria Brambilla1, Alexandra Madè1, Lorenzo Andrea Bassi1, Laura Losa1, Luca Persani2, Marco Bonomi2 1 Pavia, Italy, 2Milan, Italy New puberty growth model for estimation of individual pubertal growth parameters and their precision Anton Holmgren1, Andreas F.M. Nierop2, Aimon Niklasson1, Lars Gelander1, Stefan Aronsson3, Kerstin Albertsson-Wikland1 1 Gothenburg, Sweden, 2Leiderdorp, Netherlands, 3Halmstad, Sweden P1-d2-549
Idiopathic central precocious puberty, adult lung function and asthma Rossella Gaudino, Virginia Murri, Michele Piazza, Grazia Morandi, Paolo Cavarzere, Evelina Maines, Franco Antoniazzi, Attilio Boner Verona, Italy
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster Sessions P1
P1-d2-548
Poster sessions | P1
P1-d2-550
Serum inhibin, but not AMH or INSL3 levels, are helpful in discriminating between prepubertal boys with constitutional delay of growth and puberty and hypogonadotropic hypogonadism Julia Rohayem, Sabine Kliesch, Zitzmann Michael Münster, Germany P1-d2-551
Differentiation of olfactory placodal cells and their derivatives from human pluripotent stem cells Carina Lund1, Parinya Noisa1,2, Karolina Lundin1, Timo Tuuri1, Taneli Raivio1 1 Helsinki, Finland, 2Nakhon Ratchasima, Thailand P1-d2-552
Urinary bisphenol A levels in Turkish girls with idiopathic central precocious puberty Erdem Durmaz1, Ali Ascı2, Pinar Erkekoglu2, Sema Akcurin3, Belma Kocer Giray2, İffet Bircan3 1 Mersin, Turkey, 2Ankara, Turkey, 3Antalya, Turkey
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d3 Puberty and Gonads 3
Session title: Chairs:
Bradley Miller, Minneapolis, USA Sabine Heger, Hannover, Germany
P1-d3-553
Association analyses of CYP19A1 gene polymorphisms with central precocious puberty in girls Jung Sub Lim1, Hae Sang Lee2, Jin Soon Hwang2 1 Seoul, Republic of Korea, 2Suwon, Republic of Korea P1-d3-554
Thirty-six months treatment experience of two leuprolide acetate 3 month depot formulations for children with central precocious puberty Peter Lee1, Karen Klein2, Nelly Mauras3, Lois Larsen4, Wangang Xie4, Tali Lev-Vaisler4, H. Peter Bacher4 1 Hershey, USA, 2San Diego, USA, 3Jacksonville, USA, 4North Chicago, USA P1-d3-555
Seasonality of menarche in normal weight and obese school children Susanna Wiegand1, Peter Kuehnen1, Andrea Ernert1, Anne-Madeleine Bau1, Celine Vetter2, Till Roenneberg2, Heiko Krude1 1 Berlin, Germany, 2Munich, Germany P1-d3-556
Serum vascular endothelial growth factor-A levels in normal children and adolescents and precocious puberty girls Hyo-Kyoung Nam, Joon Woo Baek, Young Jun Rhie, Kee-Hyoung Lee Seoul, Republic of Korea
Poster Sessions P1
P1-d3-557
Once-yearly histrelin subcutaneous implants provide continuous suppression of the hypothalamicpituitary-gonadal axis for up to 6 years in children with central precocious puberty Gad B. Kletter1, Lawrence A. Silverman2, E. Kirk Neely3, Erica A. Eugster4, Surya Chitra5, Gay Owens5 1 Seattle, USA, 2Morristown, USA, 3Stanford, USA, 4Indianapolis, USA, 5Malvern, USA P1-d3-558
New puberty growth model for estimation of age for peak height velocity compared with a manual method Anton Holmgren1, Andreas F.M. Nierop2, Aimon Niklasson1, Lars Gelander1, Stefan Aronsson3, Kerstin Albertsson-Wikland1 1 Gothenburg, Sweden, 2Leiderdorp, Netherlands, 3Halmstad, Sweden
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
P1-d3-559
Different patterns of pubertal growth in girls with different pathways through puberty (pubarche pathway vs thelarche pathway) Yanhong Li, Minlian Du, Huamei Ma, Hongshan Chen, Zhe Su, Yufen Gu Guangzhou, China P1-d3-560
Leptin during treatment of precocious puberty with GnRH-analogue or a combination of GnRHanalogue and growth hormone Lemm Proos, Torsten Tuvemo, Björn Jonsson, Jan Gustafsson Uppsala, Sweden P1-d3-561
Idiopathic central precocious puberty and maternal attachment security Rossella Gaudino1, Virginia Murri1, Nicole Adami1, Grazia Morandi1, Evelina Maines1, Paolo Cavarzere1, Elena Monti2, Franco Antoniazzi1 1 Verona, Italy, 2Legnago, Italy P1-d3-562
Usefulness of basal serum LH in the diagnosis of central precocious puberty Carmen Riu, Elisa Vaiani, Silvia M. Gil, Juan M. Lazzati, Mercedes Maceiras, Marco A. Rivarola, Alicia Belgorosky Buenos Aires, Argentina P1-d3-563
Usefulness of a basal LH level to diagnose central precocious puberty in girls Analía V. Freire, Andrea J. Arcari, María G. Ballerini, María E. Escobar, Ignacio Bergadá, Mirta G. Gryngarten, María G. Ropelato Buenos Aires, Argentina P1-d3-564
Biological reference intervals for serum estradiol and testosterone in children Carina Ankarberg-Lindgren1, Birgitte T. Mahler2, Ensio Norjavaara1 1 Gothenburg, Sweden, 2Aarhus, Denmark P1-d3-564b
Fertility screening in men with acquired undescended testes: a long-term follow-up study Jocelyn Van Brakel, Gert R. Dohle, Frans W.J. Hazebroek, Sabine M.P.F. De Muinck Keizer- Schrama Rotterdam, Netherlands
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1 Sex Differentiation 1
Session title: Chairs:
Annemieke Boot, Groningen, Netherlands Silvano Bertelloni, Pisa, Italy
Cardiovascular monitoring with echo and MRI during spontaneous and assisted pregnancy in Turner syndrome Laura Mazzanti, Federica Tamburrino, Emanuela Scarano, Luigi Lovato, Annamaria Perri, Benedetta Vestrucci, Daniela Prandstraller Bologna, Italy P1-d1-566
Blood cell chimerism in dizygotic twins following in vitro fertilisation Gabriel Á. Martos-Moreno1, Clara Campos1, Raquel Flores2, Rafael Yturriaga1, Luis A. Pérez-Jurado2, Jesús Argente1 1 Madrid, Spain, 2Barcelona, Spain
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Poster Sessions P1
P1-d1-565
Poster sessions | P1
P1-d1-567
Pseudoautosomal region abnormalities in patients with Y-chromosome terminal AZFb+c deletions Andrea Castro, Fernando Rodríguez, Daniela Martínez, Patricia López, Cecilia Lardone, Martha Flórez, Felipe Argandoña, Mauricio Ebensperger, Raúl Valdevenito, Andrés Estrugo, Fernando Cassorla Santiago, Chile P1-d1-568
Low expression of X-linked inhibitor of apoptosis in Turner syndrome patients with bicuspid aortic valves: possible role of apoptosis Ganesh Jevalikar1,2, Margaret Zacharin1, Steven Yau1, Vincenzo Russo1, Matthew Sabin1 1 Melbourne, Australia, 2Gurgaon, India P1-d1-569
The prevalence of neoplasm in Turner syndrome Daniela Larizza, Valeria Calcaterra, Rossana Toglia, Anna Chiara Malvezzi, Chiara Gertosio, Alice Brambilla, Gloria Cantamessa, Irene Bonomelli Pavia, Italy P1-d1-570
Gonadoblastoma and dysgerminoma in girls with Turner syndrome and Y chromosome material: a single centre experience Ursula M. Waldthausen1, Désirée P.A. Dunstheimer1, Tobias Schuster1, Bruno Märkl1, Michael Frühwald1, Peter H. Heidemann2 1 Augsburg, Germany, 2Ulm, Germany P1-d1-571
Y-chromosome mosaicism in Turner syndrome: body proportions and final height reached with GH-therapy Federica Tamburrino, Emanuela Scarano, Annamaria Perri, Benedetta Vestrucci, Mirella Scipione, Angela Rizzello, Laura Mazzanti Bologna, Italy P1-d1-572
Characteristic testicular histology is useful for the identification of NR5A1 gene mutations in prepuberty 46,XY patients Noriko Nishina1, Ryuji Fukuzawa1, Chikahiko Numakura2, Ayuko Suwanai1, Tomonobu Hasegawa1, Yukihiro Hasegawa1 1 Tokyo, Japan, 2Yamagata, Japan P1-d1-573
Lims1: a new androgen receptor coregulator expressed during male genital development Helga Grötsch, Marlene Kunert, Dagmar Struve, Olaf Hiort, Ralf Werner Lübeck, Germany P1-d1-574
Satisfaction with hormone replacement therapy and vaginal function in orchiectomised women with complete androgen insensitivity syndrome Erica A. Eugster1, Julia R. Heiman2, Kristina L. Bryk3, Charmian A. Quigley1 1 Indianapolis, USA, 2Bloomington, USA, 3University Park, USA
Poster Sessions P1
P1-d1-575
Duplication of the SOX3 gene in a SRY negative 46,XX male hypoplasia of the right kidney and hypospadias Zoran S. Gucev1, Felix Riepe2, Marina Krstevska-Konstantinova1, Aleksandra Janchevska1, Ali G. Gharavi3, Simone Sanna-Cherchi3, Velibor Tasic1 1 Skopje, The Former Yugoslav Republic of Macedonia, 2Kiel, Germany, 3New York, USA P1-d1-576
Abstract has been withdrawn
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2
Session title: Sex Differentiation 2 Chairs: Nella Greggio, Padua, Italy Agota Muzsnai, Budapest, Hungary P1-d2-577
Molecular analysis of 5-alpha-reductase type 2 gene in patients with 46,XY DSD Flávia Leme Calais1, Reginaldo José Petroli1, Fernanda Soardi1, Adriana Aparecida Siviero-Miachon2, Angela Maria Spinola de Castro2, Isabella L. Monlleó1, Sarah Baccarini Cunha3, Andréa Trevas Maciel-Guerra1, Gil Guerra-Júnior1, Maricilda Palandi de Mello1 1 Campinas, Brazil, 2São Paulo, Brazil, 3Belo Horizonte, Brazil P1-d2-578
Molecular analyses using next-generation technologies for 141 patients with disorders of sex development Maki Igarashi1, Vũ Chí Dũng2, Erina Suzuki1, Shinobu Ida3, Kentaro Mizuno4, Yoshiyuki Kojima4,5, Kouji Muroya6, Satoshi Takakuwa7, Yuji Oto1, Kei Takazawa1, Yoshikazu Stuji8, Yukihiro Hasegawa1, Reiko Horikawa1, Tsutomu Ogata1,9, Maki Fukami1 1 Tokyo, Japan, 2Hanoi, Vietnam, 3Osaka, Japan, 4Nagoya, Japan, 5Fukushima, Japan, 6Kanagawa, Japan, 7 Okinawa, Japan, 8Nagaya, Japan, 9Hamamatsu, Japan P1-d2-579
Effect of exposure to bisphenol A on hippocampal cell proliferation: a sexual dimorphism Sofie Pieter Janssen, Elise Naveau, Jean-Pierre Bourguignon, Anne-Simone Parent Liège, Belgium P1-d2-580
Pubertal course of 45,X/46,XY MGD patients raised as girls Laetitia Martinerie1, Yves Morel2, Claire-Lise Gay3, Catherine Pienkowski4, Marc de Kerdanet5, Sylvie Cabrol1, Claudine Lecointre6, Regis Coutant7, Sabine Baron8, Michel Colle9, Raja Brauner1, Elisabeth Thibaud1, Juliane Legér1, Claire Nihoul-Fekete1, Claire Bouvattier1 1 Paris, France, 2Bron, France, 3Lyon, France, 4Toulouse, France, 5Rennes, France, 6Rouen, France, 7 Angers, France, 8Nantes, France, 9Bordeaux, France P1-d2-581
Characterisation of a novel CYP19A1 (aromatase) R192H mutation with severe virilisation of the 46,XX newborn but without virilization of the mother during pregnancy Nadia Bouchoucha1, Dinane Samara-Boustani2, Amit V. Pandey1, Helene Bony-Trifunovic3, Yves Aigrain2, Michel Polak2, Christa E. Flueck1 1 Bern, Switzerland, 2Paris, France, 3Amiens, France P1-d2-582
Molecular studies in four patients with SRY-positive 46,XX disorders of sex development: implications for the development of normal and abnormal male external genitalia Shinichi Nakashima1, Eiko Nagata1, Rie Yamaguchi1, Akira Ohishi1, Shinichiro Sano2, Eiichiro Satake1, Fumio Takada3, Maki Fukami2, Tsutomu Ogata1 1 Hamamatsu, Japan, 2Tokyo, Japan, 3Sagamihara, Japan P1-d2-583
Poster Sessions P1
Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia Marina Fanelli, Rosana B. Silva, Sorahia Domenice, Berenice B. Mendonca, Elaine M.F. Costa São Paulo, Brazil P1-d2-584
Achieving clarity in the molecular pathogenesis of 46,XY DSD Rieko Tadokoro-Cuccaro, Ranna Khairi, Harriet Miles, Trevor Bunch, Nigel Mongan, Ieuan Hughes Cambridge, UK P1-d2-585
Sexual dimorphism of in vivo rodent brain chemistry using magnetic resonance spectroscopy Martina Rodie, Michelle Welsh, William Holmes, Martin McMillan, Mhairi Macrae, Faisal Ahmed Glasgow, UK
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Poster sessions | P1
P1-d2-586
Progestogen exposure in the male programming window reduces birth weight and affects sex development of offspring Kathryn J. Cox, S. Faisal Ahmed, Michelle Welsh Glasgow, UK P1-d2-587
Decreased expression of four memory genes in non-syndromic cryptorchid males Faruk Hadziselimovic, Nils Hadziselimovic Liestal, Switzerland P1-d2-588
A novel heterozygous mutation in steroidogenic factor 1 in a 46,XY patient with ambiguous genitalia but without adrenal insufficiency Nicola Improda1, Carla Ungaro1, Donatella Capalbo1, Martina Rezzuto1, Fulvia Baldinotti2, Paolo Simi2, Mariacarolina Salerno1 1 Naples, Italy, 2Pisa, Italy
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d1
Session title: Chairs:
Thyroid 1 Peter Laurberg, Aalborg, Denmark Alessandra Cassio, Bologna, Italy
P1-d1-589
Clinical usefulness of sonoelastography in differential diagnosis of thyroid nodules in children and in young adults Urszula Zaleska-Dorobisz, Teresa Żak, Mateusz Łasecki, Cyprian Olchowy, Aleksander Pawluś Wrocław, Poland P1-d1-590
The improvement of mental development by early L-thyroxine therapy of secondary hypothyroidism in preterm-born children with low body weight Iwona Ben-Skowronek, Magdalena Wisniowiecka Lublin, Poland P1-d1-591
Maternal hypothyroxinaemia in pregnancy and impact on the mental development of their children Gema Grau1, Anibal Aguayo1, Amaia Vela1, M. Angeles Aniel-Quiroga1, Mercedes Espada2, Gorka Miranda1, Yeray Duque1, Pedro Martul1, Luis Castaño1, Itxaso Rica1 1 Barakaldo, Spain, 2Derio, Spain P1-d1-592
Poster Sessions P1
Clinical and biochemical risk factors in children with untreated long-term idiopathic subclinical hypothyroidism Manuela Cerbone1, Malgorazata Wasniewska2, Sara Alfano1, Iolanda Di Donato1, Raffaella Di Mase1, Filippo De Luca2, Mariacarolina Salerno1 1 Naples, Italy, 2Messina, Italy P1-d1-593
Two novel mutations in the TITF1/NKX2.1 gene in two Japanese families with Brain-Thyroid-Lung syndrome Hiroyuki Shinohara1, Masaki Takagi1, Kimiko Ito2, Eri Suzuki1, Tatsuya Miyoshi1, Terutaka Tajima3, Yukihiro Hasegawa1 1 Tokyo, Japan, 2Gifu, Japan, 3Saitama, Japan
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poster sessions | P1
P1-d1-594
Thyroid disorders in children and adolescents with Prader-Willi syndrome: data from 299 Italian patients Lorenzo Iughetti1, Giulia Vivi1, Antonio Balsamo2, Giuseppe Chiumello3, Andrea Corrias4, Antonino Crinò5, Maurizio Delvecchio6, Luigi Gargantini7, Nella A. Greggio8, Graziano Grugni9, Uros Hladnik10, Alba Pilotta11, Letizia Ragusa12, Alessandro Salvatoni13, Malgorzata Wasniewska14, Barbara Predieri1 1 Modena, Italy, 2Bologna, Italy, 3Milan, Italy, 4Turin, Italy, 5Rome, Italy, 6San Giovanni Rotondo, Italy, 7 Treviglio, Italy, 8Padova, Italy, 9Verbania, Italy, 10Vicenza, Italy, 11Brescia, Italy, 12Troina, Italy, 13Varese, Italy, 14Messina, Italy P1-d1-595
Twin study emphasises the importance of foetal environment as a determinant of individual T4 setpoint Nitash Zwaveling-Soonawala, Toos C. van Beijsterveldt, Dorret I. Boomsma, A.S. Paul van Trotsenburg Amsterdam, Netherlands P1-d1-596
Relationship between Th17 cells and antithyroid antibodies in patients with autoimmune thyroid disease Artur Bossowski, Marcin Moniuszko, Milena Dąbrowska, Malgorzata Rusak, Marta Jeznach, Anna Bodzenta-Łukaszyk, Beata Sawicka, Anna Bossowska Bialystok, Poland P1-d1-597
Abstract has been withdrawn P1-d1-598
Clinical re-evaluation of congenital hypothyroidism in preterm infants with eutopic thyroid Maria Cristina Vigone, Silvana Caiulo, Marianna Di Frenna, Stefano Ghirardello, Carlo Corbetta, Fabio Mosca, Giovanna Weber Milan, Italy
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d2
Session title: Chairs:
Thyroid 2 Kazumichi Onigata, Shimane, Japan Jose Moreno, Madrid, Spain
P1-d2-599
Expression of preproghrelin gene and ghrelin receptor family in thyroid tissues from paediatric patients with immune and non-immune thyroid diseases Artur Bossowski1, Barbara Czarnocka2, Jerzy Harasymczuk3, Krzysztof Bardadin2, Anna Łyczkowska2, Anna Bossowska1 1 Bialystok, Poland, 2Warsaw, Poland, 3Poznań, Poland P1-d2-600
Poster Sessions P1
Predictors of malignancy in paediatric thyroid nodules Alessandro Mussa, Arianna Santanera, Nicola Palestini, Maurilio De Andrea, Andrea Corrias Turin, Italy P1-d2-601
Thyroid disease in children with PTEN Hamartoma tumor syndrome: when should we start to screen? Michaela Hamm, Janina Kionke, Bettina Gohlke, Felix Schreiner, Joachim Woelfle Bonn, Germany P1-d2-602
Evaluating the cognitive functions in subclinical hypothyroidism by P300 event related potential Ozlem Sangun1, Serpil Demirci1, Nihal Dundar2, Ozgur Pirgon1, Tugba Koca1, Melike Dogan1, Bumin Dundar2 1 Isparta, Turkey, 2Izmir, Turkey
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Poster sessions | P1
P1-d2-603
Cognitive outcome in congenital hypothyroidism and initial L-thyroxin dose: a meta- analysis Paulina Aleksander1, Maria Craig2, Heiko Krude1, Oliver Blankenstein1 1 Berlin, Germany, 2Sydney, Australia P1-d2-604
Should we treat euthyroid children with autoimmune Hashimoto thyroiditis with levothyroxine? Results of a multicentre, randomised, controlled clinical trial Helmuth Dörr1, Markus Bettendorf2, Gerhard Binder3, Beate Karges4, Carolin Kneppo2, Heinrich Schmidt5, Egbert Voss6, Martin G. Wabitsch7, Jörg Dötsch8 1 Erlangen, Germany, 2Heidelberg, Germany, 3Tübingen, Germany, 4Stollberg, Germany, 5Munich, Germany, 6Nürnberg, Germany, 7Ulm, Germany, 8Köln, Germany P1-d2-605
High prevalence of single gene mutations in severe congenital hypothyroidism Hiroyuki Adachi, Ikuko Takahashi, Hirokazu Arai, Tsutomu Takahashi Akita, Japan P1-d2-606
High blood TSH values in newborns hospitalised in NICU Antonella Olivieri1, Stefano Ghirardello2, Carlo Corbetta2, Giovanna Weber2, Maria Cristina Vigone2, Daniela Rotondi1, Flavia Chiarotti1, Fabio Mosca2 1 Rome, Italy, 2Milan, Italy P1-d2-607
When is it justifiable to await venous thyroid function tests before starting thyroxine treatment in infants referred with capillary TSH elevation? Tzveta Pokrovska, Jeremy Jones, Guftar Shaikh, Malcolm Donaldson Glasgow, UK P1-d2-608
Abstract has been withdrawn
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type:
Poster Session P1-d3
Session title: Chairs:
Thyroid 3 Michel Polak, Paris, France Graziano Cesaretti, Pisa, Italy
P1-d3-609
Subclinical hypothyroidism in in vitro fertilisation babies Hasan Onal, Oya Ercan, Atilla Ersen, Erdal Adal, Zerrin Onal Istanbul, Turkey
Poster Sessions P1
P1-d3-610
High prevalence of positive anti-thyroid antibodies, low serum thyroid hormones and high serum TSH associated with a low vitamin D status in a paediatric cohort Veronica Zaidman, Mercedes Maceiras, Juan M. Lazzati, Gabriela D’Isa, Chilelli Carla, Cristina Tau, Gisela Viterbo, Marco A. Rivarola, Alicia Belgorosky, Eduardo A. Chaler Buenos Aires, Argentina P1-d3-611
Functional characterisation of a novel iodide transport defect causing Na+/I- symporter mutation Juan Pablo Nicola1, Paul Saenger2, David F. Rodriguez-Buritica3, Radhika Muzumdar4, Nancy Carrasco1 1 New Haven, USA, 2Mineola, USA, 3Birmingham, USA, 4Bronx, USA P1-d3-612
Capacity building and training of personnel for congenital hypothyroidism screening in Nigeria Iroro Yarhere1,2, Oliver Bankenstein2, Paulina Aleksander2 1 Rivers, Nigeria, 2Berlin, Germany
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poster sessions | P1
P1-d3-613
The effect of thyroxine treatment during the first two years of life in children with Down syndrome on development and growth at the age of 10.7 years Jan Pieter Marchal1, Femke Klouwer1, Emma Witteveen1, Nadine A. Ikelaar1, Kim Verhorstert1, Bregje A. Houtzager2, Martha A. Grootenhuis1, A. S. Paul van Trotsenburg1 1 Amsterdam, Netherlands, 2Deventer, Netherlands P1-d3-614
Mutations in the TTF1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders Pia Hermanns1, Małgorzata Kumorowicz-Czoch2, Joachim Pohlenz1 1 Mainz, Germany, 2Cracow, Poland P1-d3-615
Ectopic intrathyroid thymus in childhood: a sonographic finding leading to misdiagnosis Marina Vakaki, Elpis Vlachopapadopoulou, Feneli Karachaliou, Kleanthi Kalogerakou, Christina Gali, Irene Kaloumenou, Stefanos Michalacos Athens, Greece P1-d3-616
Subclinical hypothyroidism in childhood: presentation modes and evolution over time Aneta Gawlik1, Berenika Norek1, Kamila Such1, Aleksandra Dejner1, Tomasz Gawlik2, Ewa Malecka-Tendera1 1 Katowice, Poland, 2Gliwice, Poland P1-d3-617
Natural regulatory T cells: CD4 FoxP3 and CD8+CD122+ T in children with autoimmune thyroiditis Anna M. Kucharska, Anna Stelmaszczyk-Emmel, Katarzyna Popko, Beata Pyrzak Warszawa, Poland P1-d3-618
Poster Sessions P1
Molecular basis and oligogenic causes of permanent and transient congenital hypothyroidism with enlarged- or normal-sized eutopic thyroid glands Yoo-Mi Kim, Ja Hye Kim, Hye Young Jin, Sun-Hee Heo, Ju-Hyun Kim, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo Seoul, Republic of Korea
9th Joint Meeting of Paediatric Endocrinology 2013
127
Poster sessions | P2
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Adrenals and HPA Axis 4
Session title: Chairs:
Jarmo Jääskelainen, Kuopio, Finland Iroro Yarhere, Port Harcourt, Nigeria
P2-d1-619
Molecular and phenotypical characterisation of ten families with 11ß-hydroxylase deficiency Soara Menabò1, Lilia Baldazzi1, Felix Riepe2, Gabriella Cherchi3, Gianni Russo4, Alessandra Franzoni5, Alessandra Gambineri1, Flaminia Fanelli1, Anna Lisa Martini1, Diego Rinaldini1, Antonio Balsamo1 1 Bologna, Italy, 2Kiel, Germany, 3Cagliari, Italy, 4Milan, Italy, 5Udine, Italy P2-d1-620
Premature adrenarche and glucocorticoid sensitivity Aristotle Panayiotopoulos1, Bryan Ghanny1, Steven Ghanny2, Yevgenly Apostolov3, Amrit Bhangoo4, Joseph Michl1, Svetlana Ten1 1 Brooklyn, USA, 2Hackensack, USA, 3Little Rock, USA, 4Long Beach, USA P2-d1-621
Optimisation of hydrocortisone treatment in children with hypopituitarism using 24-hour serum cortisol profiling Evelien F. Gevers1, Sarra Ahmed1, Karen Logan1, Pietro Lazzeroni1,2, Peter C. Hindmarsh1, Mehul T. Dattani1 1 London, UK, 2Parma, Italy P2-d1-622
Paediatric reference intervals for FSH, LH, estradiol, testosterone, DHEA-S and cortisol by electrochemiluminescence Cintia Tarifa, Liliana Silvano, Cecilia Aguirre, Gabriela Sobrero, Maria Lescurat, Ivan Collet, Mariana Ochetti, Silvia Martin, Mirta Miras, Liliana Muñoz Córdoba, Argentina P2-d1-623
Highly elevated basal cortisol levels and their association with disease severity in critically ill paediatric patients Yael Levy-Shraga1,2, Vered Molina-Hazan1, Marina Rubinshtein1,2, Rina Hemi1, Hana Kanety1, Gidi Paret1,2, Orit Pinhas-Hamiel1,2 1 Ramat Gan, Israel, 2Tel Aviv, Israel P2-d1-624
Two novel mutations in CYP21A2 gene causing classic and non-classic congenital adrenal hyperplasia Ming Chen1, Jiayan Liu1, Nils Krone2, Richard J. Auchus1 1 Ann Arbor, USA, 2Birmingham, UK P2-d1-625
Poster Sessions P2
Blood pressure, fludrocortisone dose and plasma renin activity in infants with classical adrenal hyperplasia due to 21-hydroxylase deficiency Walter Bonfig, Hans Peter Schwarz München, Germany P2-d1-626
Assessment of adrenal function in patients with Prader-Willi syndrome Keiko Matsubara1,2, Masahisa Shiraishi2, Nobuyuki Murakami2, Takayoshi Tsuchiya2, Yuji Oto2, Masayo Kagami1, Maki Fukami1, Tsutomu Ogata3, Toshiro Nagai2 1 Tokyo, Japan, 2Saitama, Japan, 3Shizuoka, Japan P2-d1-627
Normal ranges of basal and glucagon-stimulated free cortisol in children: a pilot study Anita Schachter Davidov, Ori Eyal, Asaf Oren, Naftali Stern, Rona Limor, Naomi Weintrob Tel Aviv, Israel
128
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-628
A large heterozygous deletion in the CYP21A2 gene in a girl with premature adrenarche and precocious puberty: divergence between genotype and phenotype and the diagnostic role of multiplex ligation-dependent probe amplification technology Nicoletta Cresta, Anna Grandone, Alberto M. Corona, Francesco Di Mauro, Enrica E. Cascone, Emanuele Miraglia Del Giudice, Laura Perrone Naples, Italy P2-d1-629
Adrenocortical tumors in childhood Claudia Hernandez, Gabriela Rampi, Romina de la Puente, Verónica Figueroa, Valeria Santidrian, Diego Amaral, Oscar H. Brunetto Buenos Aires, Argentina P2-d1-630
Age and gender affect cortisol levels to simplified low dose short synacthen test in children with asthma Dinesh Giri1, Mohammed Didi1, Peter Laing1, Zoe Yung1, Gill Lancaster2, Andrew Titman2, Paul Newland1, Catherine Collingwood1, Matthew T. Peak1, Jonathan Couriel1, Joanne C. Blair1 1 Liverpool, UK, 2Lancaster, UK
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Adrenals and HPA Axis 5
Session title: Chairs:
Evangelia Charmandari, Athens, Greece Thomas Völkl, Erlangen, Germany
P2-d2-631
Cushing syndrome in children and adolescents: a retrospective review at presentation, diagnosis, management and outcome Maria Güemes, Philip Murray, Caroline Brain, Catherine Peters, Helen Spoudeas, Peter Hindmarsh, Mehul Dattani London, UK P2-d2-632
Double mutated allele [IVS2+5G>A; p.V281L] in non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency patients. Implications in genetic counseling Roxana Marino, Pablo Ramirez, Natalia Pasqualini, Natalia Perez Garrido, Carlos Rocco, Maria E. Escobar, Marco Aurelio Rivarola, Alicia Belgorosky Buenos Aires, Argentina The variability of mutations in patients with 21-hydroxylase deficiency in some ethnic populations resident in the Russian Federation Sofya Blokh1, Maria Kareva1, Olga Ivanova1, Oleg Malievsky2, Galina Chistousova3, Irina Kostrova4, Olga Kunaeva5 1 Moscow, Russian Federation, 2Ufa, Russian Federation, 3Perm, Russian Federation, 4Mahachkala, Russian Federation, 5Igevsk, Russian Federation P2-d2-634
Functional analysis of novel mutations inactivating the HSD3B2 gene Elizabeth S. Baranowski1, Pilar Bahillo-Curieses2, Sarah Ehtisham3, Phillip Murray4, John Achermann4, Mehul Dattani4, Claire Hughes4, Angela Taylor1, Silvia Parajes1, Nils Krone1 1 Birmingham, UK, 2Valladolid, Spain, 3Manchester, UK, 4London, UK P2-d2-635
Adrenal steroid determinations by ultra performance liquid chromatography tandem mass spectrometry in healthy newborn babies Guillermo F. Alonso, Mariana Mendez, María I. Gimenez, Titania Pasqualini Buenos Aires, Argentina
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster Sessions P2
P2-d2-633
Poster sessions | P2
P2-d2-636
Girls with precocious pubarche: SHBG levels at age 8 are followed by lower SHBG and higher C-reactive protein levels at age 22 Ana M. Velásquez Rodríguez1, Marta Díaz1,2, Judit Bassols3, Abel López-Bermejo3, Francis de Zegher4, Lourdes Ibáñez1,2 1 Esplugues, Spain, 2Madrid, Spain, 3Girona, Spain, 4Leuven, Belgium P2-d2-637
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency derived from novel compound heterozygous mutations (IVS2-13 A/C>G and p.E431K) Yuki Kawashima1, Yoshiki Okayama1, Masanobu Fujimoto1, Naoki Miyahara1, Rei Nishimura1, Keiichi Hanaki1, Takeshi Usui2, Susumu Kanzaki1 1 Yonago, Japan, 2Kyoto, Japan P2-d2-638
Is maximal isometric grip force a potential long-term parameter to monitor metabolic control in children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency? Thomas M.K. Völkl, Sonja Kern, Helmuth-G. Dörr Erlangen, Germany P2-d2-639
Utility of urinary steroid profiling to distinguish causes of urinary salt loss in infancy: evidence for adaptive response of steroid biosynthetic pathways and of characteristic presence of urinary cholesterol in secondary pseudohypoaldosteronism Vimmi Abbot1, Lea Ghataore1, Pandina Kwong2, D. Jaco Pieterse1, Gill Rumsby1, Charles R. Buchanan1, Norman F. Taylor1 1 London, UK, 2Goodmayes, UK P2-d2-640
Assessment of central adrenal insufficiency in children and adolescents with Prader-Willi syndrome Anna Wedrychowicz, Katarzyna Dolezal-Oltarzewska, Anna Kalicka-Kasperczyk, Katarzyna Tyrawa, Malgorzata Wojcik, Jerzy Starzyk Cracow, Poland P2-d2-641
Prevalence of late-onset congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhoea Cigdem Binay, Enver Simsek, Oguz Cilingir, Zafer Yuksel, Ozden Kutlay Eskisehir, Turkey P2-d2-642
Poster Sessions P2
Prevalence and characterisation of testicular adrenal rest tumors in Chinese children and adolescent males with congenital adrenal hyperplasia Zhe Su, Hua-Mei Ma, Yan-Hong Li, Min-Lian Du Guangzhou, China
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3 Adrenals and HPA Axis 6
Session title: Chairs:
Anatoly Tiulpakov, Moscow, Russian Federation Helmuth Dörr, Erlangen, Germany
P2-d3-643
Prevalence and long-term follow-up outcomes of testicular adrenal rest tumors in children and adolescent males with congenital adrenal hyperplasia Zehra Aycan, Veysel Nijat Baş, Semra Çetinkaya, Sebahat Yilmaz Agladioglu, Tuğrul Tiryaki Ankara, Turkey
130
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d3-644
The 17α-hydroxyprogesterone neonatal screening in Bulgaria 2010-2012 Iva H. Stoeva, Antoaneta I. Kostova, Radoslava E. Grozdanova, Ani V. Aroyo, Shina M. Pashova Sofia, Bulgaria P2-d3-645
Cushing disease in paediatric population: diagnostic and therapeutic difficulties Elzbieta Moszczynska1, Karolina Kot1, Agnieszka Lecka-Ambroziak1, Mieczyslaw Szalecki1,2 1 Warsaw, Poland, 2Kielce, Poland P2-d3-646
Reduced uterus body length in girls with congenital adrenal hyperplasia Irina Kopylova, Irina Yarovaya, Tatyana Glybyna, Maria Kareva Moscow, Russian Federation P2-d3-647
Final height in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with glucocorticoids: factors influencing the outcome Moira Gianninoto, Teresa Genoni, Alessandra di Lascio, Silvia L.C. Meroni, Ilaria Colombo, Gianni Russo Milan, Italy P2-d3-648
Management of Cushings disease in children and adolescents after first line treatment failure: report of a single centre experience Federico Baronio, Angelica Marsigli, Matteo Zoli, Angela Rizzello, Benedetta Vestrucci, Emanuela Zazzetta, Andrea Pession, Antonio Balsamo Bologna, Italy P2-d3-649
Non-classical CAH: molecular evaluation of 287 subjects from Northern and Southern Italy with comparison between genetic and hormonal results Antonio Balsamo1, Soara Menabò1, Malgorzata Wasniewska2, Silvestro Mirabelli2, Annalisa Nicoletti1, Angelica Marsigli1, Diego Rinaldini1, Filippo De Luca2, Laura Mazzanti1, Lilia Baldazzi1 1 Bologna, Italy, 2Messina, Italy P2-d3-650
Puberty is critical for the development of bone mineral density impairment and increasing fat mass in patients with congenital adrenal hyperplasia Marco Pitea1, Stefano Mora2, Alessandra Di Lascio2, Silvia Meroni2, Moira Gianninoto2, Teresa Genoni2, Gianni Russo2 1 Lecco, Italy, 2Milan, Italy P2-d3-651
Congenital generalised hypertrichosis terminalis with gingival hyperplasia Zdravka Todorova, Elissaveta Stefanova, Krasimira Kazakova, Emil Simeonov, Desislava Jordanova, Mihaela Dimitrova Sofia, Bulgaria P2-d3-652
Poster Sessions P2
Pelvic ultrasound findings in prepubertal girls with precocious adrenarche born appropriate for gestational age with evidence of metabolic correlates of PCOS Ahmet Uçar, Nurçin Saka, Firdevs Baş, Şükran Poyrazoğlu, Serdar Bozlak, Özge Umur, Rüveyde Bundak, Feyza Darendeliler Istanbul, Turkey P2-d3-653
Late-onset congenital adrenal hyperplasia: new treatment strategy with sub-physiological dose dexamethasone preserves endogenous cortisol stress-response Danielle C.M. van der Kaay, Erica L.T. van den Akker Rotterdam, Netherlands
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster sessions | P2
P2-d3-654
Clinical characteristics and genetic analysis of patients with autoimmune polyendocrinopathycandidiasis-ectodermal dystrophy syndrome – single centre experience during 44 years (1968-2012) Katarina Mitrovic1, Katarina T. Podkrajšek2, Tatjana Milenkovic1, Sladjana Todorovic1, Rade Vukovic1, Dragan Zdravkovic1 1 Belgrade, Serbia, 2Ljubljana, Slovenia
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1
Session title: Chairs:
Adrenals and HPA Axis 7 Tokuo Mukai, Asahikawa, Japan Michaela Hartmann, Giessen, Germany
P2-d1-655
Carrier status for 21-hydroxylase deficiency can be a factor in the variable phenotype of hyperandrogenism Nicos Skordis1, Christos Shammas1, Alexia A.P. Phedonos1, Andreas Kyriakou1, Meropi Toumba2, Vassos Neocleous1, Leonidas Phylactou1 1 Nicosia, Cyprus, 2Paphos, Cyprus P2-d1-656
Reproducibility and utility of an overnight 0.25 mg dexamethasone suppression test as a marker for corticosteroid sensitivity in children with asthma Ruben Willemsen, Leonie van Leeuwen, Sandra Voorend-van den Bergen, Yolanda de Rijke, Marielle Pijnenburg, Erica van den Akker Rotterdam, Netherlands P2-d1-657
Cheilognathopalatoschisis and cognitive disturbances after prenatal dexamethasone treatment in a girl with congenital adrenal hyperplasia Annelieke van der Linde, Viviane van de Crommert, Janielle van Alfen-van der Velden, Hedi Claahsen-van der Grinten Nijmegen, Netherlands P2-d1-658
Testicular adrenal rest tumors in children with congenital adrenal hyperplasia Igor Chugunov, Maria Kareva, Elizaveta Orlova, Sergey Bogolubov Moscow, Russian Federation P2-d1-659
Neonatal massive bilateral adrenal haemorrhage associated with subclinical hypoadrenalism spontaneously recovering Sarah Bocchini, Danilo Fintini, Aurora Rossodivita, Mauro Colajacomo, Enzo Pacciani, Marco Cappa, Antonino Crinò Rome, Italy
Poster Sessions P2
P2-d1-660
Clinical and biochemical characteristics of classic 21-hydroxylase deficiency patients with central precocious puberty Karn Wejaphikul1, Taninee Sahakitrungruang2 1 Chiang Mai, Thailand, 2Bangkok, Thailand P2-d1-661
Variable manifestation of pseudohypoaldosteronism type 1b in consanguineous brothers Usha Niranjan1, Pooja Sachdev1, Tafadzwa Makaya2, Paul Dimitri1 1 Sheffield, UK, 2Oxford, UK P2-d1-662
Genotype-phenotype correlations in Turkish children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency Enver Simsek, Oguz Cilingir, Cigdem Binay, Zafer Yuksel, Ozden Kutlay, Birgul Kirel, Sevilhan Artan Eskisehir, Turkey
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-663
Successful treatment of childhood recurrent Cushing disease after trans-sphenoidal surgery with different treatment modalities: long-term follow-up Ayla Güven1, Ayse Nurcan Cebeci2, Feyyaz Baltacıoğlu1, Selçuk Peker1, Kenan Coşkun1 1 Istanbul, Turkey, 2Kocaeli, Turkey P2-d1-664
Atypical clinical presentation of ACTH dependent Cushing syndrome in a patient treated with retinoic acid Malgorzata Wojcik, Katarzyna Tyrawa, Agata Zygmunt-Górska, Anna Kalicka-Kasperczyk, Jerzy B. Starzyk Krakow, Poland P2-d1-665
A challenging early diagnosis in a case of prepubertal Cushing disease Julia Hoppmann1, Isabel Wagner1, Stefan Wudy2, Michael Buchfelder3, Wieland Kiess1, Roland Pfaeffle1 1 Leipzig, Germany, 2Giessen, Germany, 3Erlangen, Germany P2-d1-666
Tall stature in two sisters with a homozygous mutation in the CYP17A1 gene Niels Birkebaek, Ida Vogel, Birgitta Trolle Aarhus, Denmark
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Autoimmune Endocrine Diseases 2
Session title: Chairs:
Mona Al-Khawari, Kuwait City, Kuwait Maria Francesca Messina, Messina, Italy
P2-d1-667
Total body bone mineral density, total body bone mineral content and body composition in children with type 1 diabetes Mieczyslaw Szalecki1,2, Elzbieta Wierzbicka1, Anna Swiercz1, Pawel Pludowska1, Maciej Jaworski1 1 Warsaw, Poland, 2Kielce, Poland P2-d1-668
Cardiovascular risk evaluation in a type 1 diabetes paediatric population and comparison with a control cohort Paolo Brambilla1, Marco Giussani2, Simonetta Genovesi2, Laura Antolini2, Silvana Mastriani2, Michela Nava2, Riccardo Bonfanti1, Andrea Rigamonti1, Giulio Frontino1, Roseila Battaglino1, Valeria Favalli1, Clara Bonura1, Giusy Ferro1, Franco Meschi1, Giuseppe Chiumello1 1 Milan, Italy, 2Monza, Italy P2-d1-669
Polyglandular autoimmune syndromes type III in children with type 1 diabetes mellitus Iwona Ben-Skowronek, Aneta Michalczyk, Robert Piekarski, Beata Wysocka-Łukasik, Bozena Banecka Lublin, Poland
Poster Sessions P2
P2-d1-670
The incentive trial: do financial rewards improve glycaemic control in teenagers with poorly controlled type 1 diabetes? Carley Frerichs1, Thomas Douglas2, Randell Tabitha1 1 Nottingham, UK, 2Lincoln, UK P2-d1-671
High prevalence of negative islet autoantibody status in children with type 1 diabetes in a region of inner city London Reena Perchard1, Jemma Say1, Jeremy Allgrove1, Kausik Banerjee2, Rakesh Amin1 1 London, UK, 2Romford, UK
9th Joint Meeting of Paediatric Endocrinology 2013
133
Poster sessions | P2
P2-d1-672
Proinflamatory cytokines (IL-1β and TNF-α) in childhood autoimmune thyroid diseases Hanna Mikos, Marcin Mikos, Marek Niedziela Poznan, Poland P2-d1-673
Autoimmune hypoparathyroidism as the only clinical manifestation of autoimmune polyglandular syndrome type 1: a case report Divya Khurana1, Aristotle Panayiotopoulos1, Andrey Mamkin1, Svetlana Ten1, Eystein S. Husebye2 1 Brooklyn, USA, 2Bergen, Norway P2-d1-674
Fulminant type 1 diabetes mellitus and chronic mucocutaneous candidiasis with STAT1-mutation: a case report Misako Okuno1, Remi Kuwabara1, Masako Habu1, Ayako Yoshida1, Junichi Suzuki1, Tomohiro Morio1, Masao Kobayashi2, Tatsuhiko Urakami1 1 Tokyo, Japan, 2Hiroshima, Japan
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Autoimmune Endocrine Diseases 3
Session title: Chairs:
Franco Cerutti, Turin, Italy Abdulaziz Al Twaim, Jeddah, Saudi Arabia
P2-d2-675
Role of C-peptide in the pathogenesis of microvascular complications of type 1 diabetes with paediatric age onset Valeria Favalli, Andrea Rigamonti, Giulio Frontino, Roseila Battaglino, Clara Bonura, Franco Meschi, Giuseppe Chiumello, Riccardo Bonfanti, Gianpaolo Zerbini Milan, Italy P2-d2-676
Incidence and trends of childhood (years 0-14) type 1 diabetes in Lombardy from 2002 to 2007 Clara Bonura, Andrea Rigamonti, Giulio Frontino, Roseila Battaglino, Valeria Favalli, Giusy Ferro, Franco Meschi, Giuseppe Chiumello, Riccardo Bonfanti Milan, Italy P2-d2-677
Peer review: a tool to improve paediatric diabetes services Chizo Juliana Agwu1, John Scanlon2, Kathryn MCcrea3, Parakkal Raffeeq4, Melanie Kershaw5, Sarah Broomhead1, Jane Eminson1, West Midlands Paediatric Diabetes Network 1 West Bromwich, UK, 2Worcester, UK, 3Shrewsbury, UK, 4Stoke on Trent, UK, 5Birmingham, UK P2-d2-678
Poster Sessions P2
22q11.2 microdeletion syndrome: analysis of 7 children diagnosed in a tertiary hospital Marta DeToro-Codes, Gabriela Martínez-Moya, Jesús De La Cruz Moreno, Victoria Esteban-Marfil, Juan Francisco Expósito-Montes Jaén, Spain P2-d2-679
Dietary intake of Australian children with type 1 diabetes exceeds recommendations for energy intake, total sugar and saturated fat Bronwen D’Arcy1, Jemma Anderson1, Oana Maftei1, Jennifer Couper1, Adine Mayenburg1, Timothy Olds2, Alexia Pena1 1 North Adelaide, Australia, 2Adelaide, Australia P2-d2-680
Characterisation of polyglandular autoimmune syndrome in endocrinology paediatric consult: cases reports Audrey Matallana, Francisco Montero, Liliana Mejia de Beldjenna Cali, Colombia
134
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d2-681
Vitamin D status in new onset type 1 diabetes Ana Almeida, Ana Fitas, Catarina Limbert, Lurdes Lopes Lisbon, Portugal P2-d2-682
Genetic markers of autoimmune endocrinopathy in Krasnodar region Elena Kondratyeva1, Irina Chernyak1, Asiet Tlif1, Nataliya Tarasenko2 1 Krasnodar, Russian Federation, 2Tomsk, Russian Federation
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Bone, Growth Plate and Mineral Metabolism 3
Session title: Chairs:
Ikuma Fujiwara, Sendai, Japan Gabriele Haeusler, Vienna, Austria
P2-d1-683
Cross-sectional and longitudinal comparison of bone mass and quality determinants in young adults with juvenile systemic lupus erythematosus and juvenile idiopathic arthritis Franco Ricci, Stefano Stagi, Loredana Cavalli, Marco Matucci-Cerinic, Maria-Luisa Brandi, Maurizio de Martino, Salvatore Seminara, Fernanda Falcini Florence, Italy P2-d1-684
A new mechanism of reduced efficacy of vitamin D therapy in hypoparathyroidism Nicoletta Cresta, Anna Grandone, Francesco Capuano, Enrica E. Cascone, Mariasole Conte, Francesco Di Mauro, Maria Carmen Affinita, Carmine Ficociello, Laura Perrone Naples, Italy P2-d1-685
Response to vitamin D therapy in obese vs. non-obese children and adolescents Fatemeh Saffari, Parisa Shahroodi, Sonia Oveisi, Neda Esmailzadehha Qazvin, Islamic Republic of Iran P2-d1-686
Comparison of bone mineral density in adolescent girls with hypogonadotropic hypogonadism and hypergonadotropic hypogonadism Huseyin Demirbilek, Mehmet Nuri Ozbek, Riza Taner Baran Diyarbakır, Turkey P2-d1-687
Marked phenotypic variability and different response to bisphosphonate treatment in osteogenesis imperfecta type V caused by c.-14C>T mutation in IFITM5 gene Nina Bratanic1, Bojana Dzodan2, Katarina Trebusak Podkrajsek1, Sara Bertok1, Janja Marc1, Tadej Battelino1 1 Ljubljana, Slovenia, 2Maribor, Slovenia 25-hydroxyvitamin D and bone formation markers (osteocalcin, under-carboxylated osteocalcin and N-terminal propeptide of type 1 procollagen) in adult survivors of childhood cancer Kristen A. Neville, Jan L. Walker, Richard J. Cohn, Chris P. White Sydney, Australia P2-d1-689
Vitamin D-dependent rickets, type 1A causes disproportioned short stature and increased risk of caesarean section Signe Sparre Beck-Nielsen1,2, Klaus Brusgaard2,3, Kim Brixen2, Jeppe Gram1 1 Esbjerg, Denmark, 2Odense C, Denmark, 3Odense, Denmark
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster Sessions P2
P2-d1-688
Poster sessions | P2
P2-d1-690
The incidence and aetiology of childhood hypercalcaemia Jane D. McNeilly, Rachel Boal, M. Guftar Shaikh, S. Faisal Ahmed Glasgow, UK P2-d1-691
Bone health evolution over time in childhood solid cancer survivors Laura G. González Briceño1, Alexandra Goischke1, Jean-Claude Souberbielle1, Marie Piketty1, Ghania Daoud1, Marie-Pierre Lorrain1, Jacques Grill2, Laurence Brugières2, Christelle Dufour2, Dominique Valteau-Couanet2, Veronique Minard2, François Doz1, Isabelle Aerts1, Jean Michon1, Hélène Pacquement1, Daniel Orbach1, Christian Sainte-Rose1, Michel Zerah1, Stéphanie Puget1, Caroline Elie1, Michel Polak1 1 Paris, France, 2Villejuif, France P2-d1-692
Bone mass in children with Marfan syndrome: a longitudinal study Giuliana Trifirò1, Susan Marelli2, Stefano Mora2, Alessandro Pini2 1 Rho, Italy, 2Milan, Italy P2-d1-693
Assessment of bone markers and osteoporosis in thalassemia major Tanju Celik, Ozlem Sangun, Sule Unal, Ali Balci, Sedat Motor Hatay, Turkey P2-d1-694
Acrodysostosis with hormone resistance: case report Federico Baronio, Claudio Graziano, Elisa Ballarini, Daniela Turchetti, Emanuela Scarano, Laura Mazzanti Bologna, Italy
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Bone, Growth Plate and Mineral Metabolism 4
Session title: Chairs:
Francesco Massart, Pisa, Italy Luciano Beccaria, Lecco, Italy
P2-d2-695
Bone mineral density in adolescents with hypogonadism Marta Giaccardi, Serena Noli, Barbara Roviglione, Flavia Napoli, Erika Calandra, Teresa Battaglia, Maria Luisa Garrè, Mohamad Maghnie, Natascia Di Iorgi Genoa, Italy P2-d2-696
Poster Sessions P2
Evaluation of nephrocalcinosis and nephrolithiasis in eleven children with X-linked hypophosphataemic rickets confirmed with mutations in PHEX gene Guido De Paula Colares Neto, Pedro H. Silveira Corrêa, Regina M. Martin Sāo Paulo, Brazil P2-d2-697
High prevalence of overweight and obesity in paediatric patients with severe osteogenesis imperfecta: further injury to bone tissue Lilian Argentino Pinchiari, Luciana Felipe Ferrer, Hamilton Cabral Menezes- Filho, Joyce De Brito Pupo, Caroline De Gouveia Buff Passone, Renata Nobile, Hilton Kuperman, Thais Della Manna, Vaê Dichtchekenian, Nuvarte Setian, Durval Damiani São Paulo, Brazil P2-d2-698
BMD measured by quantitative ultrasound and biochemical parameters in SGA newborn infants Mustafa Kendirci, Ferhat Vatankulu, Tamer Güneş, Leyla Behice Akin, Alper Özcan Kayseri, Turkey
136
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d2-699
Vitamin D supplementation in pregnancy and its effect on cord blood 25-hydroxycholecalciferol and anthropometry of the newborn Vijayalakshmi Bhatia1, Kishore Katam1, Anjoo Agarwal2, Vinita Das2, Venkataraman Ramesh3 Lucknow, India P2-d2-700
Bone markers and indirect measures of body composition and metabolic markers in early childhood Josefine Roswall1, Stefan Bergman2, Gerd Almqvist-Tangen1, Bernt Alm1, Jovanna Dahlgren1 1 Gothenburg, Sweden, 2Halmstad, Sweden P2-d2-701
Comparison of calcitonin and pamidronate treatments in children with osteogenesis imperfecta Fatih Gurbuz, Neslihan Onenli Mungan, Eda Mengen, Ozden Ozgur, Ali Kemal Topaloglu, Bilgin Yuksel Adana, Turkey P2-d2-702
Longitudinal study of the effect of Fok-I gene polymorphism of vitamin D receptor on bone mineral density in young patients with β-thalassaemia major Meropi Dimitriadou, Athanasios Christoforidis, Panagiota Triantafyllou, Eirini Kazantzidou, Liana Fidani, Aikaterini Teli, Efthimia Vlachaki, Marina Economou, Miranda Athanassiou-Metaxa, George Katzos Thessaloniki, Greece P2-d2-703
Acrodysostosis and pseudohypoparathyroidism: different diseases with similar clinical symptoms Sara Berrade1, Mirentxu Oyarzabal1, Maria Chueca1, Maite Ruiz1, Amaia Sagastibeltza1, Guiomar Perez de Nanclares2 1 Pamplona, Spain, 2Vitoria-Gasteiz, Spain P2-d2-704
Successful and uncomplicated treatment of generalised arterial calcification of infancy with weekly oral risedronate – a four-year follow-up Maja Marinkovic, Hiba Al-Zubedi, Paul Grossfeld, Kenneth Lee Jones San Diego, USA P2-d2-705
Case report: juvenile Paget´s disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation Forough Saki1, Zohereh Karamizadeh1, Michael Whyte2 1 Shiraz, Islamic Republic of Iran, 2St. Louis, USA P2-d2-706
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3 Bone, Growth Plate and Mineral Metabolism 5
Session title: Chairs:
Poster Sessions P2
Decreased vitamin D levels in children with familial Mediterranean fever Ahmet Anik, Gonul Catli, Balahan Makay, Ayhan Abaci, Tuncay Kume, Erbil Unsal, Ece Bober Izmir, Turkey
Francesco De Luca, Philadelphia, USA Takehisa Yamamoto, Osaka, Japan
P2-d3-707
Does medication use during pregnancy in patients with rheumatoid arthritis, influence bone density of children aged 5-8 years? Florentien D.O. de Steenwinkel, Anita C.S. Hokken-Koelega, Johanna M.W. Hazes, Radboud J.E.M. Dolhain Rotterdam, Netherlands
9th Joint Meeting of Paediatric Endocrinology 2013
137
Poster sessions | P2
P2-d3-708
GH-induced short-term changes of serum bone markers in children with idiopathic short stature Inge Gies1, Martine Cools2, Kathleen De Waele2, Marc Maes1, Véronique Beauloye1, Cécile Brachet1, Erika Boros1, Olivia Chivu3, Marieke den Brinker4, Annick France4, Raoul Rooman4, Jean De Schepper1,2,4 1 Brussels, Belgium, 2Gent, Belgium, 3Liege, Belgium, 4Antwerpen, Belgium P2-d3-709
Does disease treatment influence bone mineral density in children and adolescents with inflammatory bowel disease? Francesca Mangiantini1, Stefano Stagi2, Monica Lo Russo2, Ivana Pela2, Maurizio de Martino2, Salvatore Seminara2, Paolo Lionetti2 1 Pistoia, Italy, 2Florence, Italy P2-d3-710
Increased serum interferon-γ concentration is positively associated with increased total body bone mineral content and density in 10- to 11-year-old overweight boys Liina Utsal, Vallo Tillmann, Mihkel Zilmer, Jarek Mäestu, Priit Purge, Meeli Saar, Evelin Lätt, Katre Maasalu, Toivo Jürimäe, Jaak Jürimäe Tartu, Estonia P2-d3-711
Management of a new case of neonatal hypocalciuric hypercalcaemia related to mutation of the calcium-sensing receptor gene with bone abnormalities Thomas Edouard1, Céline Mouly1, Emmanuelle Mimoun1, Isabelle Gennero1, Corine Magdelaine2, Jean-Pierre Salles1 1 Toulouse, France, 2Limoges, France P2-d3-712
A novel cytoplasmatic mutation of the calcium-sensing receptor in a newborn resulting in familial hypocalciuric hypercalcaemia Felix Reschke, Judith Lohse, Angela Huebner Dresden, Germany P2-d3-713
Kearns-Sayre syndrome presenting with hypoparathyroidism in a child Sarar Mohamed, Muddathir H.A. Hamad, Khalid K. Abu-Amero, Thomas M. Bosley, Hisham Alkhaldi, Mustafa A.M. Salih Riyadh, Saudi Arabia P2-d3-714
The effect of vitamin D on childhood migraine attacks Atilla Cayir1, Mehmet Ibrahim Turan1, Huseyin Tan1, Behzat Ozkan2 1 Erzurum, Turkey, 2Istanbul, Turkey P2-d3-715
Short stature, osteoporosis and fractures are not always due to osteogenesis imperfecta: two cases diagnosed with lysinuric protein intolerance Saygın Abalı, Zeynep Atay, Belma Haliloğlu, Tülay Güran, Abdullah Bereket, Serap Turan Istanbul, Turkey
Poster Sessions P2
P2-d3-716
A novel de novo activating mutation of calcium-sensing receptor in a patient with hypocalcaemia and long QT syndrome Mariangela Cisternino1, Lorenzo Andrea Bassi1, Giulia Rossetti1, Patrizia Bulzomì1, Alessia C. Codazzi1, Silvia Magrassi1, Laura Losa1, Giovanni Pieri1, Katia Maruka2, Stefano Mora2 1 Pavia, Italy, 2Milan, Italy P2-d3-717
Different phenotypes associated with inactivating mutations of the GNAS gene María José Alcázar Villar, María José Rivero Martín, Araceli Serrano Barral, Constanza Navarro Moreno, María Sanz Fernández Fuenlabrada, Spain
138
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d3-718
Bone health determinants in spinal muscular atrophy Natascia Di Iorgi, Giorgia Brigati, Irene Olivieri, Marta Giaccardi, Serena Noli, Barbara Roviglione, Claudio Bruno, Mohamad Maghnie Genoa, Italy
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Bone, Growth Plate and Mineral Metabolism 6
Session title: Chairs:
Merih Berberoglu, Ankara, Turkey Leandro Soriano-Guillen, Madrid, Spain
P2-d1-719
Is anaemia and neutropaenia always associated with primary disease in hereditary bone marrow syndrome? Myelofibrosis associated with vitamin D deficiency Bayram Ozhan, Mehmet Akin Denizli, Turkey P2-d1-720
Risk of over the counter vitamin D supplements: a case of unintentional chronic vitamin D intoxication of an infant Jose M. Jimenez-Vega1, Heidi Kamrath2, Laura Gandrud2, Jesse Hennum2 1 Cincinnati, USA, 2Minneapolis, USA P2-d1-721
Vitamin D levels in children diagnosed with acute otitis media Atilla Cayir1, Mehmet I. Turan1, Ozalkan Ozkan1, Behzat Ozkan2 1 Erzurum, Turkey, 2Istanbul, Turkey P2-d1-722
Assessment of the effects of levothyroxine treatment on bone turnover parameters in children with subclinical hypothyroidism Mesut Parlak1, Sema Akçurin2, Sebahat Ozdem2, Adil Boz2 1 Kahramanmaras, Turkey, 2Antalya, Turkey P2-d1-723
Calcium disorders in childhood malignancies in the University of Port Harcourt Teaching Hospital, Nigeria: when should bone mineral density studies start? Iroro Yarhere, Gracia Eke, Nwadiuto Akani Port Harcourt, Nigeria P2-d1-724
Hypocalcaemia and seizures in a 5-week-old girl due to autosomal dominant hypocalcaemia: a case study and review of the literature Signe B. Thim1, Niels H. Birkebæk2, Peter H. Nissen3, Christian Høst2 1 Randers, Denmark, 2Aarhus N, Denmark, 3Aarhus, Denmark P2-d1-725
Poster Sessions P2
Improvement of growth and bone mineral density in two cases of osteogenesis imperfecta with recombinant human growth hormone therapy and pamidronate Takahiro Mochizuki, Keinosuke Fujita, Yuko Tanaka, Nahoko Inada, Chiyoko Fukuda, Toshinori Nishigaki Osaka, Japan P2-d1-726
Association of serum 25-hydroxyvitamin D concentration and metabolic syndrome in Korean children and adolescents Seung Yang, Il Tae Hwang Seoul, Republic of Korea
9th Joint Meeting of Paediatric Endocrinology 2013
139
Poster sessions | P2
P2-d1-727
Effects of steroid treatment on bone mineral density in children with nephrotic syndrome and congenital adrenal hyperplasia: comparison between drug and replacement therapy Maria Felicia Faienza1, Gabriella Aceto1, Lucia Soldano1, Olinda D’Addato1, Giovanni Messina1, Giacomina Brunetti1, Maurizio Delvecchio2, Luciano Cavallo1 1 Bari, Italy, 2San Giovanni Rotondo, Italy P2-d1-728
Short-term intravenous calcium infusion followed by high dose oral calcium therapy in hereditary vitamin D resistant rickets Noman Ahmad Jeddah, Saudi Arabia P2-d1-729
Ceasing vitamin D replacement in infants with premature closure of frontal fontanelle: true or false? Tolga Unuvar1, Turkan Uygur2, Erdal Adal2 1 Aydin, Turkey, 2Istanbul, Turkey P2-d1-730
Vitamin D levels in adolescent inpatients with eating disorders Dalit Modan-Moses1,2, Orit Pinhas-Hamiel1,2, Yael Levy-Shraga1,2, Beigitte Kochavi1, Adi Hanoch-Levi1, Daniel Stein1,2 1 Ramat-Gan, Israel, 2Tel Aviv, Israel P2-d1-731
Clinical course and aetiology of primary hypoparathyroidism in childhood Ja Hye Kim, Yoo-Mi Kim, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo Seoul, Republic of Korea
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Endocrine Oncology 1
Session title: Chairs:
Martine Cools, Ghent, Belgium Maryam Razzaghy-Azar, Tehran, Islamic Republic of Iran
P2-d1-732
Chemosensitisation of leukaemia cells through an inhibition of Nampt Theresa Gorski, Stefanie Petzold-Quinque, Sandy Laue, Susanne Schuster, Melanie Penke, Wieland Kiess, Antje Garten Leipzig, Germany P2-d1-733
Poster Sessions P2
A girl with androgen secreting adrenal oncocytoma Galina Yordanova1, Violeta Iotova1, Krasimir Ivanov1, Nikola Kolev1, Anton Tonev1, Kalin Kalchev1, J. Wolter Oosterhuis2 1 Varna, Bulgaria, 2Rotterdam, Netherlands P2-d1-734
Risk of metabolic syndrome in adolescents treated for liquid and solid non-central tumors Vera Morsellino, Federica Ceroni, Marta Giaccardi, Serena Noli, Barbara Roviglione, Silvia Caruso, Maura Faraci, Riccardo Haupt, Natascia Di Iorgi, Mohamad Maghnie Genoa, Italy P2-d1-735
Spectacular shrinkage of a giant, invasive and resistant paediatric prolactinoma under temozolomide Fetta Amel Yaker, Said Azzoug, Faiza Belhimer, Farida Chentli Algiers, Algeria
140
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-736
Follow-up of endocrine functions in children treated for malignant haemopathies: careful attention must be payed to the body weight even in cases of chemotherapy only Aurélie Armougon, Pascale Schneider, Jean Pierre Vannier, Mireille Castanet Rouen, France P2-d1-737
Multicentre study on final height and body mass index in adult survivors of childhood acute lymphoblastic leukaemia treated on AIEOP 87-2000 protocols excluding cranial radiotherapy Patrizia Bruzzi1, Barbara Predieri1, Simona Madeo1, Aurora Rossodivita2, Alberto Marsciani3, Maria Elisabeth Street4, Andrea Corrias5, Lorenzo Iughetti1 1 Modena, Italy, 2Rome, Italy, 3Rimini, Italy, 4Parma, Italy, 5Turin, Italy P2-d1-738
Water and electrolyte disorders in a large cohort of 159 paediatric patients with suprasellar tumours – at a distance from surgery Laura G. González Briceño1, Jacques Grill2, François Doz1, Imane Benabbad1, Laurence Brugières2, Christelle Dufour2, Dominique Valteau-Couanet2, Franck Bourdeaut1, Isabelle Aerts1, Jean Michon1, Hélène Pacquement1, Daniel Orbach1, Christian Sainte-Rose1, Michel Zerah1, Stéphanie Puget1, Caroline Elie1, Michel Polak1 1 Paris, France, 2Villejuif, France P2-d1-739
An audit of endocrine late effects in survivors of childhood brain tumours Emmeline C. Heffernan, Anthony Mc Carthy, Robert Johnston, Noina Abid Belfast, UK P2-d1-740
Tumor origin and growth pattern at diagnosis and surgical hypothalamic damage predict obesity in paediatric craniopharyngioma Young Ah Lee, Choong Ho Shin, Sei Won Yang Seoul, Republic of Korea
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Fat Metabolism, Obesity 7
Session title: Chairs:
Jan Gustafsson, Uppsala, Sweden Barbara Predieri, Modena, Italy
P2-d1-741
Effect of weight loss on markers of inflammation and endothelial function in obese children and adolescents Maria L. Iezzi1, Patrizia Bruzzi2, Alessia Salvatore1, Marina Saccomandi1, Barbara Predieri2, Lorenzo Iughetti2 1 L’ Aquila, Italy, 2Modena, Italy The relationship between hepcidin concentrations in serum with iron homeostasis in obese children Didem Helvacioglu, Serap Turan, Tulay Guran, Zeynep Atay, Belma Haliloglu, Saygin Abali, Cengiz Canpolat, Abdullah Bereket Istanbul, Turkey P2-d1-743
Improvement in anxiety-depression manifestations, eating behaviour and growth velocity by exercise in obese children with moderate short stature Andrea Aguirre, Wilson Acosta, Alvaro P. Aguirre Sucre, Bolivia
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster Sessions P2
P2-d1-742
Poster sessions | P2
P2-d1-744
Early puberty in obese girls: effect of weight reduction on menarche timing Shokery Awadalla Bogota, Colombia P2-d1-745
Changes in metabolic syndrome and fibrinolysis as a function of BMI, insulin resistance and leptin levels following lifestyle intervention in obese prepubertal children M. Valle1, R. Martos1, M.D. Cañete2, R.M. Morales1, F. Gascón1, F. Bermudo1, E.L. van Donkelaar1, R. Cañete3 1 Pozoblanco, Spain, 2Córdoba, Spain P2-d1-746
Timing of puberty and physical growth in obese children: a longitudinal study in boys and girls M. Loredana Marcovecchio, Chiara De Leonibus, Valentina Chiavaroli, Tommaso De Giorgis, Cosimo Giannini, Francesco Chiarelli, Angelika Mohn Chieti, Italy P2-d1-747
Circadian rhythm of NAMPT, metabolic parameters and hormone levels and the impact of obesity and physical exercise Isabel Viola Wagner, Kathrin Dittrich, Dennis Löffler, Julia Gesing, Daniela Friebe, Wieland Kiess, Antje Körner Leipzig, Germany P2-d1-748
Relation between consumption of sugar-sweetened drinks and childhood obesity: a prospective, observational analysis Elham Zare Tehran, Islamic Republic of Iran P2-d1-749
Impairment of inflammatory markers in children and adolescents with familial hypercholesterolaemia Barbara Predieri, Giovanni Malmusi, Laura Lucaccioni, Viviana Dora Patianna, Patrizia Bruzzi, Lorenzo Iughetti Modena, Italy P2-d1-750
More new clinic manifestations in adolescents and youths with metabolic syndrome and benefits of insulinosensitizers and antidepressants Rodrigo Ribera, Mónica Pereyra, Alvaro P. Aguirre Sucre, Bolivia P2-d1-751
Salt intake and insulin resistance in obese children and adolescents Gianpaolo De Filippo1, Viviana D. Patianna2, Domenico Rendina3, Catherine Piquard1, Pierre Bougnères1 1 Le Kremlin-Bicêtre, France, 2Modena, Italy, 3Naples, Italy
Poster Sessions P2
P2-d1-752
Orlistat prescribing in Scottish children and adolescents and the potential of treatment discontinuation as a signal for adverse drug reactions Pei-Chen Sun1, Bradley Kirby1, Corri Black1, Peter J. Helms1, Marion Bennie2, James S. McLay1 1 Aberdeen, UK, 2Edinburgh, UK
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poster sessions | P2
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Fat Metabolism, Obesity 8
Session title: Chairs:
Emanuele Miraglia Del Giudice, Naples, Italy Ewa Malecka-Tendera, Katowice, Poland
P2-d2-753
Short-term intervention improves cardiorespiratory fitness, glucose metabolism and lipid profile in obese children and adolescents Julia Gesing1, Kathrin Dittrich1, Isabel V. Wagner1, Julia Bielitz1, Daniela Friebe1, Firooz Ahmadi2, Wieland Kiess1, Antje Körner1 1 Leipzig, Germany, 2Bad Frankenhausen, Germany P2-d2-754
Associations between weight variation, thyroid function and other metabolic variables in obese children Maria Inês Santos1, Catarina Limbert1, Filipa Carlota Marques1, Frederico Rosário2, Daniela Amaral1, Rosa Pina1, Laura Oliveira1, Lurdes Lopes1 1 Lisbon, Portugal, 2Tondela, Portugal P2-d2-755
Melatonin in obese pubertal patients: correlation with metabolic syndrome and other cardiovascular risk factors Hugo R. Boquete, Gabriel Fideleff, Hugo L. Fideleff, Miriam Azaretzky, Gabriela Ruibal, María De Luján Calcagno, Claudio González, Martha Suárez Buenos Aires, Argentina P2-d2-756
Evaluation of waist-to-height ratio as an indicator of cardio-metabolic risk in 6-10-year-old children Valesca Mansur Kuba1, Cláudio Leone2, Durval Damiani2 1 Campos dos Goytacazes, Brazil, 2São Paulo, Brazil P2-d2-757
Cardio-metabolic risk profile in Chilean adolescents of mid-low socioeconomic level: association with sex and obesity Raquel Burrows1, Paulina Correa-Burrows2, Marcela Reyes1, Estela Blanco3, Sheila Gahagan3, Cecilia Albala1 1 Santiago de Chile, Chile, 2Madrid, Spain, 3San Diego, USA P2-d2-758
Abstract has been withdrawn P2-d2-759
Trends in lipid profile components and lifestyle factors in Korean adolescents; the KNHANES study 1998-2010 Young-Hwan Song1, Shin-Hye Kim1, Sangshin Park2, Mi-Jung Park1 1 Seoul, Republic of Korea, 2Texas, USA Metabolic syndrome criteria predicting non-alcoholic fatty liver disease: comparison of two methods Mehmet Emre Atabek, Beray Selver Eklioglu, Nesibe Akyurek Konya, Turkey P2-d2-761
Polycystic ovary syndrome treatment during adolescence: improvement of clinical and metabolic parameters with metformin versus oestroprogestins and antiandrogens Graziamaria Ubertini, Ilaria Menghi, Armando Grossi, Chiara Carducci, Danila Benevento, Rossana Fiori, Marco Cappa Rome, Italy
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster Sessions P2
P2-d2-760
Poster sessions | P2
P2-d2-762
Impaired theory of mind and symptoms of autism spectrum disorder in children with Prader-Willi syndrome Renske Kuppens1, Sin Ting Lo1, Philippe Collin2, Elbrich Siemensma1, Anita Hokken-Koelega1 1 Rotterdam, Netherlands, 2Sittard, Netherlands P2-d2-763
Evaluation of early markers of risk for metabolic syndrome and vascular function in children with intrauterine growth restriction Zulema M. Chaila, Maria De Los Angeles Peral de Bruno, Claudio M. Joo Turoni, Rossana Chahla, Olga Graiff, Alejandro Negrete, Adriana Elias, Maria E. Bruno, Maria C. Bazan Tucuman, Argentina P2-d2-764
Association of pre-pregnancy weight with weight status and classical cardiovascular factors at 4 years Isolina Riaño-Galán1, Cristina Rodriguez-Dehli1, Ana Fernandez-Somoano2, Ana Souto2, Rafael Venta Obaya1, Adonina Tardon2 1 Aviles, Spain, 2Oviedo, Spain
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3
Session title: Chairs:
Fat Metabolism, Obesity 9 Michele De Simone, L’Aquila, Italy Mirjana Kocova, Skopje, The Former Yugoslav Republic of Macedonia
P2-d3-765
Serum apelin12 levels in obese youngsters with altered glucose homeostasis-insulin resistance Eleni P. Kotanidou, Smaragda Efraimidou, Efimia Papadopoulou-Alataki, Styliani Fidani, Assimina Galli-Tsinopoulou Thessaloniki, Greece P2-d3-766
The relationship between carotid-intima thickness and fibrin monomers in obese children Esra Yazarlı, Bülent Alioğlu, Betül Şimşek, Ozlem Engiz, Uğur Koşar, Yıldız Dallar Bilge Ankara, Turkey P2-d3-767
16p11.2 deletion accounting for early-onset morbid obesity and intellectual disability in two sisters Mary White, Margaret Zacharin, Mathew A. Sabin Melbourne, Australia
Poster Sessions P2
P2-d3-768
Maternal BMI predicts therapy outcome in obese children independent of the presence of metabolic syndrome: results of a national evaluation study of multiprofessional group programs Lallemand Dagmar1, Esther Kirchhoff2, Margarete Bolten3, Andrea Zumbrunn4, Xavier Martin5, Robert Sempach2, Nathalie Farpour-Lambert5 1 St. Gallen, Switzerland, 2Aarau, Switzerland, 3Basel, Switzerland, 4Olten, Switzerland, 5Geneva, Switzerland P2-d3-769
Weight status and risk behaviours in urban Bulgarian preschool children (2009-2013) Mina Pl. Lateva1, Sonya Galcheva1, Wouter De Witte2, Violeta Iotova1 1 Varna, Bulgaria, 2Ghent, Belgium P2-d3-770
Evaluation of serum chemerin levels in childhood obesity Anıl Er, Orhun M. Çamurdan, Aysun Bideci, Hamdi Cihan Emeksiz, Çelik Nurullah, Esra Döğer, Özge Yüce, Peyami Cinaz Ankara, Turkey
144
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d3-771
A case of rapid-onset obesity with hypothalamic dysfunction, hypoventilation, autonomic dysregulation: ROHHAD syndrome Ahmet Uçar, Firdevs Baş, Özge Umur, Yasin Yılmaz, Şükran Poyrazoğlu, Rüveyde Bundak, Nurçin Saka, Feyza Darendeliler Istanbul, Turkey P2-d3-772
Association between trace element urinary profile and body mass index in a representative adolescent population Primož Kotnik, Simona Murko, Mitja Vahčič, Jernej Kovač, Mirjana Zupančič, Darja Mazej, Ciril Kržišnik, Tadej Battelino, Milena Horvat Ljubljana, Slovenia P2-d3-773
Overweight/obesity and serum total cholesterol trends in Slovenian 5-year old children, 2001-2009 Katarina Sedej, Primož Kotnik, Magdalena Avbelj Stefanija, Urh Grošelj, Andreja Širca Čampa, Lara Lusa, Tadej Battelino, Nataša Bratina Ljubljana, Slovenia P2-d3-774
Preventing childhood obesity by reducing consumption of carbonated drinks: cluster randomised controlled trial Mojtaba Homayon Tehran, Islamic Republic of Iran P2-d3-775
Waist-to-height ratio as screening tool for metabolic risk factors in children and adolescents Emilio García-García1, Rafael Galera2, Patricia Oliva2, Icíar García-Escobar2, Jerónimo Momblan2, José L. Gómez-Llorente2, Angeles Vázquez2, Antonio Bonillo2 1 Sevilla, Spain, 2Almería, Spain P2-d3-776
Myeloperoxidase G-463A polymorphism in obese children with metabolic syndrome Ilker T. Ozgen, Emel Torun, Arzu Ergen, Yasar Cesur, Faruk Oktem, Mehmet S. Aksu, Umit Zeybek, Hande Karagedik Istanbul, Turkey
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Fat Metabolism, Obesity 10
Session title: Chairs:
Ivana Rabbone, Turin, Italy Susanna Wiegand, Berlin, Germany
The serum ferritin level is higher in Korean male adolescents with abdominal obesity: results from the Korea National Health and Nutrition Examination Surveys 2010 In Ah Jung, Shin Hee Kim, Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byung Kyu Suh Seoul, Republic of Korea P2-d1-778
No difference in serum adiponectin, resistin, TNFR1 and TNFR2 in obese adolescents with or without insulin resistance Fengyang Huang1, Blanca Estela del Río Navarro1, José Alfredo Pérez Ontiveros1, Saúl Torres Alcántara1, Efraín Navarro Olivos2, Mireya Figueroa Barrón1, Leticia Hernandez Cadena2 1 Mexico City, Mexico, 2Cuernavaca, Mexico
9th Joint Meeting of Paediatric Endocrinology 2013
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Poster Sessions P2
P2-d1-777
Poster sessions | P2
P2-d1-779
The distinction of metabolically ‘healthy’ from metabolically ‘unhealthy’ obese children and adolescents Guy Massa1, Liene Bervoets1,2 1 Hasselt, Belgium, 2Diepenbeek, Belgium P2-d1-780
Family history, perinatal factors and feeding behaviour during the first year of life in obese children with metabolic syndrome and those with healthy metabolic phenotype Nayely Garibay, Mayra Bustos, Flor Alvarez, Fernando Ramírez, América Miranda, Armando Espinosa, Xochitl Prado, Yolotzin Flores, Raúl López, López-Alvarenga Juan, Gloria Queipo Mexico City, Mexico P2-d1-781
Sitosterolaemia in a 2-year-old girl with dermal and haematological expression Javier Nuñez Rodriguez, Maria J. Garcia Barcina, Begoña Lejona Martinez de Lecea, Concepcion Fernandez Ramos, Elena Sanchez Gonzalez Bilbao, Spain P2-d1-782
ACE inhibitors have positive effects on insulin resistance and lipid profile in children with metabolic syndrome Korkut Ulucan1, Teoman Akcay1, Eda Celebi Bitkin2, Mehmet Boyraz3, Necati Taskin1, Hande Kızılocak1, Arzu Akcay1 1 Istanbul, Turkey, 2Van, Turkey, 3Ankara, Turkey P2-d1-783
Experiences implementing obesity services for children and adolescents consensus guidelines in a secondary care setting for children with obesity Kristina Marshall, Jane McIvor, Vijith Reddy Puthi Peterborough, UK P2-d1-784
To study the HDL-cholesterol metabolism in the offspring of patients with type 2 diabetes mellitus Sumayya Wani1, Iram Shabir1, Ishrat Hussain2, Madan L. Khurana1 1 New Delhi, India, 2Srinagar, India P2-d1-785
Clinical and analytical characteristics of children with severe hypercholesterolaemia. Genetic and ultrasound carotid intima-media thickness studies Maria C. Luzuriaga Tomás, María L. Bertholt, Lidia Urbón López de Linares Santander, Spain P2-d1-786
Vitamin D supplementation in an urban paediatric weight management program Melissa Putman1, Rebecca Persky2, Catherine Gordon1,3, Erinn Rhodes1 1 Boston, USA, 2Hartford, USA, 3Providence, USA P2-d1-787
Poster Sessions P2
Association between non-alcoholic fatty liver disease and mean platelet volume in obese children and adolescents Nihal Hatipoglu1, Selim Kurtoglu1, Deniz Okdemir1, Oznur Ozturk2, Leyla Akin1 1 Kayseri, Turkey, 2Washington DC, USA P2-d1-788
Vitamin D levels in obese compared to normal weight children Shokery Awadalla Bogota, Colombia
146
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Fat Metabolism, Obesity 11
Session title: Chairs:
Kuben Pillay, Durban, South Africa Lorenzo Iughetti, Modena, Italy
P2-d2-789
Body image of normal, overweight and obese adolescent girls Hashmat Moayeri, Katayoon Bidad Tehran, Islamic Republic of Iran P2-d2-790
Relationship of FABP4 and adiponectin levels in adolescents with obesity Olga Vasyukova, Pavel Okorokov, Valentina Peterkova Moscow, Russian Federation P2-d2-791
The role of leptin and ghrelin in obesity development after adenoidectomy or adenotonsillectomy Zeynep Selen Karalok, Mehmet Akdag, Murat Turhan, Gulbahar Uzun, Sebahat Ozdem, Oktay Dinc, Iffet Bircan Antalya, Turkey P2-d2-792
Six-month outcomes of family-based multidisciplinary treatment of childhood obesity Tali Sinai, Limor Tal-Pony Rehovot, Israel P2-d2-793
The role of hereditary risk factors in children and adolescents with overweight and obesity Vira Yakovenko1, Tatiana Kobez1, Igor Lebid2, Galina Solovyova2 1 Simferopol, Ukraine, 2Kiev, Ukraine P2-d2-794
C-reactive protein and food consumption: interrelationship with features and frequency of metabolic syndrome in obese and non obese children and adolescents Vanessa Vieira Lopes Borba, Rosalia Gouveia Filizola, Roberto Sampaio De Lucena, Roberto Teixeira De Lima Joao Pessoa, Brazil P2-d2-795
Determinants and correlates of vitamin D deficiency in obese adolescents Inge Gies1, Inge Roggen1, Jesse Vanbesien1, Maria Van Helvoirt2, Patrick Debode2, Bettina Würth2, Hilde Franckx2, Ann De Guchtenaere2, Ellen Anckaert1, Jean De Schepper1 1 Jette, Belgium, 2De Haan, Belgium P2-d2-796
P2-d2-797
Unique treatment and rapid resolution of extreme hyperlipidaemia in a 7-year-old female with new onset diabetes, treated with L-carnitine and continuous insulin infusion Yelena S. Nicholson, Paul Bryer, Marisa VanSchuyver Dayton, USA P2-d2-798
Are body mass index and family history of cardiovascular disease predictors of abnormal lipid profiles in children and adolescents? Zacharoula Karabouta1, Dimitrios Papandreou1, Areti Hitoglou-Makedou2, Israel Rousso1, Fani Athanassiadou-Piperopoulou1 1 Thessaloniki, Greece, 2Thessaloníki, Greece
9th Joint Meeting of Paediatric Endocrinology 2013
147
Poster Sessions P2
The relationship between serum 25-hydroxyvitamin D and inflammatory cytokines in obese children Ling Feng, Fan Yang Chengdu, China
Poster sessions | P2
P2-d2-799
Long-term efficacy (12 months) after a treatment program for treating obesity Ainhoa Sarasua Miranda, Ignacio Diez Lopez, Isabel Lorente Blazquez, Victor Rodríguez Rivera, M.P. Portillo Baquedano, M.T. Macarulla Arenaza Vitoria, Spain P2-d2-800
Serum adipokines profile and metabolic syndrome in obese children and adolescents Iuliana Gherlan, Suzana Vladoiu, Florin Alexiu, Mihaela Giurcaneanu, Andreea-Cristiana Brehar, Camelia Procopiuc, Cristina-Patricia Dumitrescu, Andra Caragheorgheopol Bucharest, Romania
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3
Session title: Chairs:
Fat Metabolism, Obesity 12 Claire Levy-Marchal, Paris, France Valentino Cherubini, Ancona, Italy
P2-d3-801
Clinical, behavioural and family characteristics as predictors to response to therapeutic lifestyle change among overweight and obese children Tali Sinai, Limor Tal-Pony Rehovot, Israel P2-d3-802
The number of smoked cigarettes per day influences adverse blood pressure and lipid levels in adolescents with obesity Jurgita Gailite, Iveta Dzivite-Krisane, Una Lauga-Tunina, Inara Kirillova, Ieva Strele, Dace Gardovska Riga, Latvia P2-d3-803
Hypothalamic obesity in children: a life-threatening disease Belma Haliloglu, Serap Turan, Zeynep Atay, Tulay Guran, Saygın Abalı, Abdullah Bereket Istanbul, Turkey P2-d3-804
Altered blood pressure circadian rhythm in obese children and adolescents: an initial cardiovascular risk marker? Esperanza Moreno Villamil, Diego Yeste Fenandez, Antonio Carrascosa Lezcano, Luis L. Moctezuma, Carolina Forero Torres, Maria C. Leon, Marian Albisu Aparicio, Laura Audi Parera Barcelona, Spain P2-d3-805
Metabolic syndrome in children cardiometabolic disorders and social background Tetyana Chaychenko, Ganna Senatorova Kharkiv, Ukraine
Poster Sessions P2
P2-d3-806
Food addiction in obese children Alev Keser, Ayşegül Yüksel, Asuman Bayhan, Gül Yeşiltepe Mutlu, Elif Özsu, Filiz Mine Çizmecioğlu, Şükrü Hatun Kocaeli, Turkey P2-d3-807
Advanced bone age and hyperinsulinaemia in overweight and obese children Orit Pinhas-Hamiel1,2, Doreen Benary1, Kineret Mazor-Aronovich1,2, Michal Ben-Ami1,2, Yael Levy-Shraga1,2, Valentina Boyko1, Liat Lerner-Geva1,2, Dalit Modan-Moses1,2 1 Ramat-Gan, Israel, 2Tel Aviv, Israel
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d3-808
The associations of osteocalcin level and metabolic profile on different ethnic groups in South-West Romania Otilia Marginean, Ioan Simidrea, Camelia Daescu, Andreea Militaru, Oana Belei, Giorgiana Brad, Andreea Dobrescu Timisoara, Romania P2-d3-809
Adverse influence of the number of smoked cigarettes per day on blood pressure and lipid level in adolescents with obesity Jurgita Gailite, Ieva Strele, Una Lauga-Tunina, Inara Kirillova, Dace Gardovska, Iveta Dzivite-Krisane Riga, Latvia P2-d3-810
An attempt to evaluate the efficacy of psychodynamic group therapy for obese children and their families in a hospital setting Nicoletta Bisacchi, Anna Lisa Martini, Diego Rinaldini, Elisa Serra, Franco D’Alberton, Laura Mazzanti, Antonio Balsamo Bologna, Italy P2-d3-811
Vasodilatory potential in obese children: an investigation of F-RHI using Endo-PAT Noriyuki Takubo1, Misako Yokoyama1, Mari Ito1, Kazuhiro Mibu1, Daisuke Kamekawa1, Kazuteru Kitsuda1, Noriko Suyama1, Yumiko Takubo1, Shigeyuki Outsu1, Mayumi Kazahari1, Yukifumi Yokota1, Chii Kato2, Masahiro Ishii1 1 Sagamihara, Japan, 2Hino, Japan P2-d3-812
The prevalence of childhood obesity and central obesity in a rural Greek island and their association with gender, puberty and nationality Maria Sourani1, Kostas Kakleas2, Charalambos Tsentidis2, Ilias Haramaras2, Maria Dimoula1, Eleni Kotsani1, Marianna Armaou1, Triantafyllia Sdogou2, Christina Karayianni2, Elisabeta Baltaretsou1, Kyriaki Karavanaki2 1 Cyclades, Greece, 2Athens, Greece
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 GH and IGF Physiology and Treatment 4
Session title: Chairs:
Fabio Buzi, Mantova, Italy Claudio Giacomozzi, Glasgow, UK
P2-d1-813
P2-d1-814
Effects of GH treatment on oxygen-transporting properties of erythrocytes and blood antioxidant system in girls with Turner syndrome Svetlana Kovalenko, Alexander Yusipovich, Maria Vorontsova, Maria Pankratova, Tatiana Shiryaeva, Elena Nagaeva, Adil Baizhumanov, Evgenia Parshina, Valentina Peterkova, Georgy Maksimov Moscow, Russian Federation P2-d1-815
A novel nonsense mutation at carboxyl terminal region of IGF-1R (p.Q1220X) causes reduction of the IGF-1R protein, and results in SGA short stature Masanobu Fujimoto1, Yuki Kawashima1, Naoki Hamajima2, Rei Nishimura1, Keiichi Hanaki1, Susumu Kanzaki1 1 Yonago, Japan, 2Nagoya, Japan
9th Joint Meeting of Paediatric Endocrinology 2013
149
Poster Sessions P2
Oxygen-transporting properties of erythrocytes and the blood antioxidant system in children with growth hormone deficiency and girls with Turner syndrome Maria Vorontsova, Maria Pankratova, Svetlana Kovalenko, Alexander Yusipovich, Tatiana Shiryaeva, Olga Chikulaeva, Adil Baizhumanov, Evgenia Parshina, Georgy Maksimov, Valentina Peterkova Moscow, Russian Federation
Poster sessions | P2
P2-d1-816
A precocious GH peak at GHRH plus arginine test in GH sufficient short children is predictive of a lower growth velocity Simonetta Bellone, Flavia Prodam, Matteo Castagno, Giulia Genoni, Cristina Fiorito, Sandra Esposito, Antonella Petri, Gianluca Aimaretti, Gianni Bona Novara, Italy P2-d1-817
Evaluation of asymmetric dimethylarginine levels in children with growth hormone deficiency Asan Onder, Zehra Aycan, Cemile Koca, Merve Ergin, Semra Cetinkaya, Sebahat Yilmaz Agladıoglu, Havva Nur Peltek Kendirci, Veysel Nijat Bas Ankara, Turkey P2-d1-818
Birth seasonality in Japanese patients with growth hormone deficiency Tadayuki Ayabe1,2, Maki Fukami2, Kenji Takehara2, Naoko Kakee2, Akira Matsui2, Susumu Yokoya2 1 Koshigaya, Japan, 2Tokyo, Japan P2-d1-819
Effect of long-term growth hormone therapy on adult height in children born small for gestational age Dominique Simon1, Graziella Pinto1, Marc De Kerdanet2, Michel Polak1, Nicole Mairon3, Juergen Zieschang4, Paul Czernichow1 1 Paris, France, 2Rennes, France, 3Geneva, Switzerland, 4Darmstadt, Germany P2-d1-820
Growth hormone improves short stature in children with Diamond-Blackfan anaemia Jonathan C. Howell1, Sarita Joshi2, Lindsey Hornung1, Jane Khoury1, Richard Harris1, Susan R. Rose1 1 Cincinnati, USA, 2Columbus, USA P2-d1-821
Growth hormone devices changeovers: causes and effects Jeremy Kirk, Julia Prior, Angela Casey Birmingham, UK P2-d1-822
Is there any evidence that GH increases the risk to develop leukaemia in children treated for malignant tumors? Patrick Wilton1, Björn Jonsson2 1 Stockholm, Sweden, 2Uppsala, Sweden P2-d1-823
Quality of life in adolescents and young adults with childhood-onset growth hormone deficiency Joanna Oswiecimska1, Dagmara Plywacz1, Magdalena Pys-Spychala2, Agnieszka Szymlak1, Agata Mikolajczak3, Katarzyna Ziora1 1 Zabrze, Poland, 2Strzelce Opolskie, Poland, 3Gliwice, Poland P2-d1-824
Poster Sessions P2
Changes of male prevalence in the treatment observed during the GH era within KIGS Michael B. Ranke1, Anders Lindberg2, Hartmut Wollmann3, Cecilia Camacho-Hubner4 1 Tuebingen, Germany, 2Sollentuna, Sweden, 3Tadworth, UK, 4New York, USA
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 GH and IGF Physiology and Treatment 5
Session title: Chairs:
Ives Le Bouc, Paris, France Stephen Duck, Evanston, USA
P2-d2-825
Safety and effectiveness of Increlex® therapy in children enrolled in the Increlex Growth Forum Database in Europe: 3 years interim results Joachim Woelfle1, Peter Bang2, Michel Polak3, Pascal Maisonobe4, Pascale Dutailly5, on behalf of the EU IGFD Registry Study Group 1 Bonn, Germany, 2Linköping, Sweden, 3Paris, France, 4Boulogne Billancourt, France, 5Les Ulis, France P2-d2-826
Low vitamin D levels affect height velocity in growth hormone deficient children treated with growth hormone Maria Xatzipsalti, Andriani Vazeou, Ioanna Polychroni, Lampros Fotis, Sotiris Konstantakopoulos, Alexsandra Papadopoulou, Lela N. Stamogiannou Athens, Greece P2-d2-827
Management of childhood-onset growth hormone deficiency in young adulthood Mahjouba Ahmid1, Ethel McNeil1, Victoria Fisher1, Jennifer Roach2, Louise Bath2, Nicola Zammitt2, Malcolm Donaldson1, Colin G. Perry1, Syed Faisal Ahmed1, Mohamad Guftar Shaikh1 1 Glasgow, UK, 2Edinburgh, UK P2-d2-828
A population pharmacokinetic and pharmacodynamic model following a phase II study of MOD4023 in growth hormone deficient adults supporting the assessment of pharmacokinetic and pharmacodynamic in growth hormone deficient children Gili Hart1, Serge Guzy2, Leanne Amitzi1, Oren Herskovitz1, Eyal Fima1 1 Nes Ziona, Israel, 2Albany CA, USA P2-d2-829
Two-year safety and efficacy data from PAtients TReated with Omnitrope® (PATRO) children − a multi-centre, non-interventional study in infants/children/adolescents requiring growth hormone treatment Roland Pfaeffle1, Shankar Kanumakala2, Charlotte Hoeybye3, Berit Kristroem4, Ellen Schuck5, Markus Zabransky5, Tadej Battelino6, Michel Colle7 1 Leipzig, Germany, 2Brighton, UK, 3Stockholm, Sweden, 4Umea, Sweden, 5Holzkirchen, Germany, 6 Ljubljana, Slovenia, 7Bordeaux, France P2-d2-830
One month change in insulin-like growth factor binding protein 3 consistently associates with changes in growth markers from year one to five of recombinant human growth hormone treatment in short children with GH Deficiency but not with Turner syndrome Pierre Chatelain1, Adam Stevens2, Benoit Destenaves3, Peter Clayton2, the PREDICT Investigator Group 1 Lyon, France, 2Manchester, UK, 3Geneva, Switzerland P2-d2-831
Poster Sessions P2
Baseline characteristics of GH-treated patients enrolled in the prospective genetics and neuroendocrinology of short stature international study (GeNeSIS): trends over time Christopher J. Child1, Charmian A. Quigley2, Alan G. Zimmermann2, Jan Lebl3, Judith L. Ross4, Tomonobu Hasegawa5, Werner F. Blum6 1 Windlesham, UK, 2Indianapolis, USA, 3Prague, Czech Republic, 4Philadelphia, USA, 5Tokyo, Japan, 6 Bad Homburg, Germany P2-d2-832
Final height after long-term growth hormone treatment of short children with GH-deficiency, born small for gestational age and Turner syndrome Elena Nagaeva, Tatiana Shiryaeva, Valentina Peterkova, Olga Chikulaeva, Olga Bezlepkina Moscow, Russian Federation
9th Joint Meeting of Paediatric Endocrinology 2013
151
Poster sessions | P2
P2-d2-833
The effect of gonadotropin-releasing hormone analog combined with anabolic steroid hormone and/or growth hormone on adult height in boys who enter puberty with short stature Toshiaki Tanaka1, Masamichi Ogawa2, Eiichi Kinoshita3, Yukiko Nakano4, Osamu Nose4, Study Group of Out-patient Clinics on Short Stature 1 Tokyo, Japan, 2Nagoya, Japan, 3Nagasaki, Japan, 4Osaka, Japan P2-d2-834
Adult height of girls with Turner syndrome treated from before six years of age with a fixed per kilo GH dose Malgorzata Wasniewska1, Tommaso Aversa1, Laura Mazzanti2, Maria Pia Guarneri3, Patrizia Matarazzo4, Filippo De Luca1, Fortunato Lombardo1, Maria Francesca Messina1, Mariella Valenzise1 1 Messina, Italy, 2Bologna, Italy, 3Milan, Italy, 4Turin, Italy P2-d2-835
Normalised pubertal growth and adult height in children with multiple pituitary hormone deficiency, results from a randomised clinical trial Elena Lundberg1, Berit Kriström1, Björn Jonsson2, Kerstin Albertsson-Wikland2 1 Umeå, Sweden, 2Gothenburg, Sweden P2-d2-836
Vitamin D and growth hormone treatment Björn Andersson1, Diana Swolin-Eide1, Berit Kriström2, Kerstin Albertsson-Wikland1 1 Gothenburg, Sweden, 2Umeå, Sweden
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3 GH and IGF Physiology and Treatment 6
Session title: Chairs:
Päivi Tapanainen, Oulu, Finland Alessandro Salvatoni, Varese, Italy
P2-d3-837
Effects of treatment with recombinant growth hormone in children with transient partial growth hormone deficiency Barbara Krukowska-Andrzejczyk, Maria A. Kalina, Barbara Kalina-Faska, Ewa Malecka-Tendera Katowice, Poland P2-d3-838
Comparison of IGF-1 secretion in children with short stature with respect to growth hormone secretion after falling asleep and in stimulating tests Maciej Hilczer, Joanna Smyczynska, Renata Stawerska, Andrzej Lewinski Lodz, Poland
Poster Sessions P2
P2-d3-839
Contrasting factors that impact the response to growth hormone therapy in children with idiopathic growth hormone deficiency and idiopathic short stature Jo Blair1, Judith Ross2, Lars Sävendahl3, Pétur Júlíusson4, John Germak5, Birgitte T. Pedersen6, Peter Lee7 1 Liverpool, UK, 2Philadelphia, USA, 3Stockholm, Sweden, 4Bergen, Norway, 5Princeton, USA, 6Søborg, Denmark, 7Hershey, USA P2-d3-840
A 4-year, open-label, multi-centre, randomised, 2-arm study of Genotropin® growth hormone in patients with idiopathic short stature: analysis of 4-year data comparing efficacy, glucose homeostasis, and IGF-I between an individualised, target-driven regimen and standard dosing Debra R. Counts1, Mitchell Geffner2, Ronald Newfield3, Lawrence Silverman4, Lynne Levitsky5, Natasa Rajicic6, Deborah Bowlby7, Judith Hey-Hadavi6, Michael Wajnrajch6, ISS Study Group 1 Baltimore, USA, 2Los Angeles, USA, 3San Diego, USA, 4Morristown, USA, 5Boston, USA, 6New York, USA, 7Charleston, USA
152
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d3-841
Audit of patients who have ceased treatment in a national growth hormone program Ian Hughes1, Catherine Choong2, Mark Harris1, Andrew Cotterill1 1 South Brisbane, Australia, 2Subiaco, Australia P2-d3-842
Paternally inherited deletion of 6q24.3 with Silver-Russell like syndrome phenotype and GH deficiency Elisabetta Lapi1, Stefano Stagi1, Perla Scalini1, Andrea Riccio2, Maurizio de Martino1, Leopoldo Zelante2, Massimo Carella2, Salvatore Seminara1 1 Florence, Italy, 2Caserta, Italy P2-d3-843
Growth response (year 1 delta height SDS) and percentage of poor responders in GH-treated patients are functions of the position of the diagnosis in the continuum of short stature disorders Martin O. Savage1, Aude Sicsic2, Bruno Fiorentino2, Robin Kingswell2 1 London, UK, 2Boulogne Billancourt, France P2-d3-844
Increased growth rate response to rhGH treatment in a patient with a novel homozygous IGFALS mutation Marta Ramon-Krauel1, Ana María Velásquez-Rodríguez1, Ana María Prado-Carro1, Ana Gómez-Núñez2, Angel Campos-Barros2 1 Barcelona, Spain, 2Madrid, Spain P2-d3-845
Bone structure change in childhood-onset GH deficient adolescents after cessation of GH treatment is mild and does not indicate the severity of GHD Roland Schweizer, Bettina Becker, Jana L. Bauer, Gerhard Binder Tübingen, Germany P2-d3-846
SOX3 duplication and growth hormone deficiency: a case with long-term follow-up Stefano Stagi, Elisabetta Lapi, Sabrina Giglio, Marilena Pantaleo, Cristina Manoni, Maurizio de Martino, Salvatore Seminara Florence, Italy P2-d3-847
Long-term auxological and endocrinological evaluation of patients with 9p trisomy: a focus on growth hormone-insulin-like growth factor-I axis Elisabetta Lapi, Stefano Stagi, Silvia Guarducci, Sabrina Giglio, Marilena Pantaleo, Giulia Anzilotti, Maurizio de Martino, Salvatore Seminara Florence, Italy P2-d3-848
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1
Session title: Chairs:
Glucose Metabolism 6
Poster Sessions P2
The influence of growth hormone therapy on carbohydrate and lipid metabolism in children with growth hormone deficiency Corina Paul, Mirela Mogoi, Puiu Iulian Velea Timisoara, Romania
Feihong Luo, Shanghai, China Dario Iafusco, Naples, Italy
P2-d1-849
GCK gene mutations are a common cause of childhood-onset maturity-onset diabetes of the young in a Turkish cohort Belma Haliloglu1, Gerald Hysenaj2, Zeynep Atay1, Tulay Guran1, Saygın Abalı1, Serap Turan1, Sian Elllard2, Abdullah Bereket1 1 Istanbul, Turkey, 2Exeter, UK
9th Joint Meeting of Paediatric Endocrinology 2013
153
Poster sessions | P2
P2-d1-850
Long-term endocrine and exocrine outcome of medically unresponsive diffuse congenital hyperinsulinism managed with near-total pancreatectomy: 18-years experience Ved Bhushan Arya1, Syeda Alam1, Senthil Senniappan1, Azizun Nessa1, Sophia Rahman1, Maha Sherif1, Sarah E. Flanagan2, Sian Ellard2, Khalid Hussain1 1 London, UK, 2Exeter, UK P2-d1-851
Glucose response curve shape and diabetes risk in a cystic fibrosis population María Martín-Frías, Patricia Enes, Adelaida Lamas, Rosa Yelmo, M. Angeles Alvarez, Raquel Barrio Madrid, Spain P2-d1-852
A novel ABCC8 misssense mutation in two siblings with variable expression of neonatal hyperinsulinism Violeta Iotova1, Sonya Galcheva1, Kevin Colclough2, Irina Halvadzhiyan1, Chaika Petrova3, Khalid Hussein4, Sian Ellard2 1 Varna, Bulgaria, 2Exeter, UK, 3Pleven, Bulgaria, 4London, UK P2-d1-853
Glycaemic control and concomitant autoimmune diseases in paediatric type 1 diabetes patients Patricia Enes, María Martín-Frías, María Álvarez, Rosa Yelmo, Milagros Alonso, Raquel Barrio Madrid, Spain P2-d1-854
Catch-up growth pattern as early predictor of deranged insulin sensitivity in term SGA children at 12-18 months Deepika Rustogi, Sangeeta Yadav, Siddharth Ramji, T. K. Mishra New Delhi, India P2-d1-855
Impact of glycaemic control on LDL cholesterol in type 1 diabetes from childhood to young adulthood Michelle Katz, Carly E. Dougher, Lisa K. Volkening, Lori M. Laffel Boston, USA P2-d1-856
The relationship between glucose variability and oxidative stress in children with type 1 diabetes Xi Meng, Chunxiu Gong Beijing, China P2-d1-857
Next-generation sequencing to identify a novel INS gene mutation in a family with maturity onset diabetes of the young Stephanie R. Johnson1,2, Ivan N. McGown1, Louise Conwell3, Mark Harris1, Emma L. Duncan2,3 1 South Brisbane, Australia, 2Woolloongabba, Australia, 3Herston, Australia P2-d1-858
BMI changes after diagnosis of type 1 diabetes mellitus in children and adolescents Liat de Vries1,2, Maayan Kuperberg Bar-Niv1,2, Yael Lebenthal1,2, Shlomit Shalitin1,2, Liora Lazar1,2, Ariel Tenenbaum1, Moshe Phillip1,2 1 Petah Tikva, Israel, 2Tel Aviv, Israel
Poster Sessions P2
P2-d1-859
18F-DOPA PET and enhanced CT imaging for congenital hyperinsulinism: our experience of using oral sedation Pratik Shah, Senthil Senniappan, Marguerite du Preez, Raymond Endozo, Caroline Townsend, Clare Gilbert, Kate Morgan, Louise Hinchey, Agostino Pierro, Lorenzo Biassoni, Oystein Olsen, Jamshed Bomanji, Khalid Hussain London, UK
154
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Glucose Metabolism 7
Session title: Chairs:
Marco Janner, Bern, Switzerland Riccardo Bonfanti, Milan, Italy
P2-d2-860
Clinical and genetic characteristics of Turkish patients with congenital hyperinsulinism Ayla Guven1, Ayse Nurcan Cebeci2, Sarah Flanagan3, Sian Ellard3 1 Istanbul, Turkey, 2Izmit, Turkey, 3Exeter, UK P2-d2-861
Interdisciplinary challenges in focal congenital hyperinsulinism Emine Varol1, Klaus Mohnike2, Carsten Müller1, Hagen Bahlmann1, Carmen Schröder1, Wolfgang Mohnike3, Martin Zenker2, Ilse Wieland2, Silke Vogelgesang1, Winfried Barthlen1 1 Greifswald, Germany, 2Magdeburg, Germany, 3Berlin, Germany P2-d2-862
Transient neonatal diabetes mellitus in a Turkish patient with three novel homozygous variants in the ZFP57gene Teoman Akcay1, Mehmet Boyraz2, Korkut Ulucan1, Hande Kızılok1, Sarah E. Flanagan3, Deborah J.G. Mackay4 1 Istanbul, Turkey, 2Ankara, Turkey, 3Exeter, UK, 4Salisbury, UK P2-d2-863
Schizophrenia in adolescents and young adults with type 1 diabetes: prevalence and clinical characteristics – analysis from the prospective nationwide German and Austrian diabetes survey (DPV) Angela Galler1, Esther Molz2, Michael Meusers3, Bela Bartus4, Andrea Näke5, Holger Haberland1, Edith Schober6, Reinhard W. Holl2 1 Berlin, Germany, 2Ulm, Germany, 3Herdecke, Germany, 4Stuttgart, Germany, 5Dresden, Germany, 6 Wien, Austria P2-d2-864
Serum osteoprotegerin, s-rankl and carotid intima-media thickness in the diagnosis of endothelial dysfunction in children and adolescents with type 1 diabetes mellitus Irene Lambrinoudaki, Emmanouil Tsouvalas, Marina Vakaki, Georgios Kaparos, Kimon Stamatelopoulos, Areti Augoulea, Andreas Alexandrou, Maria Kreatsa, Kyriaki Karavanaki Athens, Greece P2-d2-865
Ambulatory blood pressure and subclinical cardiovascular disease in children and adolescents with type 1 diabetes Mehmet Emre Atabek, Nesibe Akyürek, Beray Selver Eklioğlu, Hayrullah Alp Konya, Turkey Frequency of fetal and neonatal complications in children of diabetic mothers assisted at a tertiary University Centre Beatriz Pires Ferreira, Taciana C.M. Feilbelmann, Adriana P. Silva, Evelyne G. Schmaltz Chaves, Priscila Melo Franciscon, Marina Melo Paschoini, Maria F. Borges Uberaba, Brazil P2-d2-867
A case report of congenital hyperinsulinism due to a focal lesion resulting from a frameshift mutation in KCNJ11 Chelsey Grimbly, Robert Couch, Bryan Dicken, Andrea Haqq, Elizabeth Rosolowsky, Mary Jetha Edmonton, Canada P2-d2-868
Increased frequency of vitamin D deficiency/insufficiency among children and adolescents with type 1 diabetes Maria Xatzipsalti, Sotiris Konstantakopoulos, Konstantina Papadopoulou, Eirini Eleutheriou, Symeon Tournis, Maria Dracopoulou, Andriani Vazeou Athens, Greece
9th Joint Meeting of Paediatric Endocrinology 2013
155
Poster Sessions P2
P2-d2-866
Poster sessions | P2
P2-d2-869
Dynamics of glucose response curve during an oral glucose tolerance test and risk of type 2 diabetes in an obese paediatric population Patricia Enes, María Martín-Frías, Yoko Oyakawa, Daniel Alonso, Milagros Alonso, Raquel Barrio Madrid, Spain P2-d2-870
Prevalence of Wolfram syndrome is not necessarily so infrequent as generally expected Giuseppina Salzano, Fortunato Lombardo, Gilberto Candela, Fernanda Chiera, Federica Porcaro, Maria Ausilia Catena, Filippo De Luca Messina, Italy
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3
Session title: Glucose Metabolism 8 Chairs: Diane Wherrett, Toronto, Canada M. Loredana Marcovecchio, Chieti, Italy P2-d3-871
Relationship between Gilbert syndrome and rate of nephropathy in patients with type 1 diabetes Sigal Singer1, Nurit Pilpel1, Orit Pinhas-Hamiel1,2 1 Ra’anana, Israel, 2Tel-Aviv, Israel P2-d3-872
Insulin pump treatment in neonates and infants below 1 year. Recommendations for initial choice of bolus and basal rate based on the experiences from the German working group for paediatric pump treatment Thomas M. Kapellen1, Bettina Heidtmann2, Eggert Lilienthal3, Birgit Rami4, Charlotte Engler-Schmidt5, Reinhard W. Holl6 1 Leipzig, Germany, 2Hamburg, Germany, 3Bochum, Germany, 4Vienna, Austria, 5Worms, Germany, 6 Ulm, Germany P2-d3-873
Effective management of hypoglycaemia during a children’s diabetes camp Lindsay McTavish, Esko J. Wiltshire Wellington, New Zealand P2-d3-874
Italian translation, cultural adaptation and validation of the PedsQL™ 3.0 Diabetes Module questionnaire in children with type 1 diabetes and their parents Sara Gialetti1, Ornella Della Casa Alberighi1, Sara Bolloli1, Chiara Carducci2, Ivana Rabbone3, Donatella Lo Presti4, Sonia Toni5, Eugenio Zito6, Renata Lorini1, Giuseppe d’Annunzio1 1 Genoa, Italy, 2Rome, Italy, 3Turin, Italy, 4Catania, Italy, 5Florence, Italy, 6Naples, Italy
Poster Sessions P2
P2-d3-875
Increased incidence of type 1 diabetes mellitus during the pandemic H1N1 influenza in 2009 in eastern Santiago Carolina Valdes, Maria Isabel Hernandez, Nancy Unanue, Roberto Garcia, Magdalena Castro, Leticia Vasquez, Carolina Sepúlveda, Verónica Mericq Santiago, Chile P2-d3-876
Improving diabetes management in adolescents via continuous glucose monitoring technology Pei Kwee Lim, Rashida Vasanwala, Yuen Ching Hui, Soo Ting Lim, Ngee Lek, Fabian Yap Singapore, Singapore P2-d3-877
Congenital hyperinsulinism due to homozygous ABCC8 in a 47 XYY child Sameh Tawfik1, Sarah Flanagan2, Jayne Houghton2, Tina Libretto2, Sian Ellard2, Khalid Hussain3, Malcolm Donaldson4 1 Cairo, Egypt, 2Exeter, UK, 3London, UK, 4Glasgow, UK
156
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d3-878
Indeterminate glucose tolerance in youth with cystic fibrosis: transient decline in body mass index z-score Arti Shah, Matthew Fenchel, Rhonda Szczesniak, Laurie Kahill, Deborah Elder Cincinnati, USA P2-d3-879
Genotype, phenotype and outcome of Vietnamese patients with congenital hyperinsulinism: a report of 41 cases Vũ Chí Dũng1, Liem Thanh Nguyen1, Thao Phuong Bui1, Ngoc Thi Bich Can1, Khanh Ngoc Nguyen1, Duong Anh Dang1, Hoan Thi Nguyen1, Dat Phu Nguyen1, Sarah Flanagan2, Jayne Houghton2, Sian Ellard2 1 Hanoi, Vietnam, 2Exeter, UK P2-d3-880
Low levels of plasma free fatty acids and monounsaturated fatty acids are associated with insulin resistance in obese children Paulina Bustos, Karen Toledo, Katia Sáez, Mario Aranda, Sylvia Asenjo Concepcion, Chile P2-d3-881
Two cases of congenital central hypoventilation syndrome with a PHOX2B gene mutation complicated by hyperinsulinaemic hypoglycaemia Ryojun Takeda1,2, Masahiro Goto1, Junko Igaki1, Masaki Takagi1, Nao Tachibana1, Hiroshi Yoshihashi1, Chikahiko Numakura3, Kiyoshi Hayasaka3, Yukihiro Hasegawa1 1 Fuchu City, Japan, 2Fussa City, Japan, 3Yamagata City, Japan
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1
Session title: Chairs:
Glucose Metabolism 9 Päivi Miettinen, Helsinki, Finland Zdenek Sumnik, Prague, Czech Republic
P2-d1-882
Effect of 2012 earthquake on glycaemic control in children and adolescents with type 1 diabetes: the experience of Modena, Italy Patrizia Bruzzi, Eleonora Balestri, Simona Madeo, Barbara Predieri, Lorenzo Iughetti Modena, Italy P2-d1-883
Neurocognitive and neuroimaging profile in children with hyperinsulinaemic hypoglycaemia and ketotic hypoglycaemia Anitha Kumaran, Jemima Bullock, Holly Clisby, Lisa Walker, Jessica Jackson, Polly Carmichael, W.K. Chong, Fareneh Vargha-Khadem, David Gadian, Chris Clark, Ritika R. Kapoor, Khalid Hussain London, UK Hypoglycaemia: an unrecognised problem in cystic fibrosis patients unmasked by continuous glucose monitoring Belma Haliloglu, Yasemin Gokdemir, Zeynep Atay, Saygın Abalı, Tulay Guran, Fazilet Karakoc, Refika Ersu, Bulent Karadag, Serap Turan, Abdullah Bereket Istanbul, Turkey P2-d1-885
Analysis of clinical characteristics and potassium channel gene mutations in 25 cases of congenital hyperinsulinism in a Chinese population Chang Su, Chunxiu Gong Beijing, China
9th Joint Meeting of Paediatric Endocrinology 2013
157
Poster Sessions P2
P2-d1-884
Poster sessions | P2
P2-d1-886
Use of insulin pump tools and metabolic control in children and adolescents with type 1 diabetes María Martín-Frias, Patricia Enes, M. Angeles Alvarez, Rosa Yelmo, Milagros Alonso, Raquel Barrio Madrid, Spain P2-d1-887
Clinical outcome and molecular defects of congenital hyperinsulinism Ja Hye Kim, Yoo-Mi Kim, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo Seoul, Republic of Korea P2-d1-888
Evaluation of anxiety and glicaemic control of teenagers with type 1 diabetes mellitus Erdal Adal, Koray Yalcın, Atilla Ersen, Zerrin Onal, Hasan Onal Istanbul, Turkey P2-d1-889
Residual beta-cell function and growth velocity in children with type 1 diabetes Carla Bizzarri1, Arianna Boiani1, Marzia Bongiovanni1, Concetta Fusco1, Danila Benevento1, Ippolita Patrizia Patera1, Stefano Cianfarani1,2, Marco Cappa1 1 Rome, Italy, 2Stockholm, Sweden P2-d1-890
The efficacy and safety of long-acting somatostatin analog depot in young patients with persistent hyperinsulinaemic hypoglycaemia of infancy Chie Takahashi, Satsuki Nishigaki, Yusuke Mizuno, Kengo Miyashita, Yasuhiro Naiki, Reiko Horikawa Tokyo, Japan P2-d1-891
The role of pump therapy in pregnant women with type 1 diabetes and its impact on development of fetopathy Julia Samoylova, Oksana Oleynik, Mariia Novoselova Tomsk, Russian Federation P2-d1-892
Psychological characteristics of children and adolescents with type 1 diabetes mellitus Young Jun Rhie1, Joon Woo Baek2, Hyo-Kyoung Nam2, Kee-Hyoung Lee2 1 Ansan-si, Republic of Korea, 2Seoul, Republic of Korea
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Glucose Metabolism 10
Session title: Chairs:
Jadranka Popovic, Pittsburgh, USA Fabrizio Barbetti, Rome, Italy
Poster Sessions P2
P2-d2-893
Molecular genetics in children with neonatal diabetes at Vietnam National Hospital of Pediatrics Ngoc Thi Bich Can1, Vũ Chí Dũng1, Thao Phuong Bui1, Khanh Ngoc Nguyen1, Dat Phu Nguyen1, Hoan Thi Nguyen1, Maria Craig2, Sian Ellard3 1 Hanoi, Vietnam, 2Sydney, Australia, 3Exeter, UK P2-d2-894
Insulin resistance in Chilean adolescents: the role of family history of type 2 diabetes Paulina Correa-Burrows1, Raquel Burrows2, Marcela Reyes2, Estela Blanco3, Cecilia Albala2, Sheila Gahagan3 1 Madrid, Spain, 2Santiago de Chile, Chile, 3San Diego, USA P2-d2-895
Two cases of diabetic ketoacidosis in HNF1A-MODY linked to severe dehydration: is it time to change the diagnostic criteria for MODY? Stepanka Pruhova1, Petra Dusatkova1, David Neumann2, Erik Hollay1, Ondrej Cinek1, Jan Lebl1, Zdenek Sumnik1 1 Prague, Czech Republic, 2Hradec Kralove, Czech Republic
158
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d2-896
Poor evidence of enterovirus infection in newly diagnosed diabetic children in the area of Bologna (Italy) Giulio Maltoni, Liliana Gabrielli, Tiziana Lazzarotto, Francesca Bellini, Mirella Scipione, Alessandra Rollo, Claudia Balsamo, Stefano Zucchini Bologna, Italy P2-d2-897
Incidence rates of childhood type 1 diabetes mellitus in Liguria region, Italy, from 2006 to 2011 Giuseppe d’Annunzio, Sara Bolloli, Angela Pistorio, Nicola Minuto, Renata Lorini Genoa, Italy P2-d2-898
Quality of life in a group of Chilean adolescents with type 1 diabetes mellitus Carolina Mendoza, Maria Isabel Hodgson, Lissete Slaibe, Hanna Rumié Santiago, Chile P2-d2-899
Identification of a novel WFS1 gene mutation in an Italian family with Wolfram syndrome Federica Ortolani1, Elvira Piccinno1, Marcella Vendemiale1, Maria Pia Natale1, Albina Tummolo1, Maristella Masciopinto1, Concetta Aloi2, Alessandro De Luca3, Rita Fischetto1, Francesco Papadia1 1 Bari, Italy, 2Genoa, Italy, 3Rome, Italy P2-d2-900
iPro glucose sensor improves glycaemic control in children and adolescents with type 1 diabetes Sotiris Konstantakopoulos, Maria Xatzipsalti, Konstantina Papadopoulou, Dimitris Delis, Andriani Vazeou Athens, Greece P2-d2-901
Endothelial dependent vasodilatation across glucose tolerance categories in obese adolescents Preneet C. Brar1, Payal R. Patel2, Stuart D. Katz1 1 New York, USA, 2Los Angeles, USA P2-d2-902
Renal function in children and adolescents with type 1 diabetes mellitus Vivian Gallardo, Francisca Ugarte, Carolina Garfias, Jorge Saba, Gabriel Cavada, Anahi Yizmeyian, Soledad Villanueva, Antonio Barrera, Carolina Sepúlveda Santiago, Chile P2-d2-903
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3 Glucose Metabolism 11
Session title: Chairs:
Poster Sessions P2
The effect of sulfonylurea therapy in neonatal diabetes mellitus patients with highly heterogeneous genetic background Feihong Luo, Miaoying Zhang, Shuixian Shen, Ruoqian Cheng, Li Xi, Zhuhui Zhao, Wei Lu, Rong Ye Shanghai, China
Annalisa Blasetti, Chieti, Italy Violeta Iotova, Varna, Bulgaria
P2-d3-904
Transient neonatal diabetes in Spanish patients: natural evolution during the two first decades of life Itxaso Rica, Anibal Aguayo, Rosa Martinez, Inés Urrutia, Maria Ortiz, Luis Castaño, Grupo Español de Diabetes Neonatal Barakaldo, Spain
9th Joint Meeting of Paediatric Endocrinology 2013
159
Poster sessions | P2
P2-d3-905
Vitamin D level as a predictive factor of certain parameters in patients with type 1 diabetes Shamita Trivedi1, Ramon Durazo2, Carla Minutti2 1 Dallas, USA, 2Maywood, USA P2-d3-906
Case report: use of long-acting octreotide in a child with congenital hyperinsulinism on diazoxide Pratik Shah, Clare Gilbert, Kate Morgan, Louise Hinchey, Hannah Levy, Khalid Hussain London, UK P2-d3-907
KCNJ11 gene mutation analysis in 27 patients with infancy and early childhood diabetes mellitus Yanmei Sang1, Huiqin Wei2, Wenli Yang1, Jie Yan1, Zidi Xu1, Yujun Wu1, Cheng Zhu1, Guichen Ni1 1 Beijing, China, 2Urumqi, China P2-d3-908
Glycaemic profile during remission in a patient with 6q24 transient neonatal diabetes Yasuhiro Sato, Eishin Ogawa, Yoichi Izumi, Kahoko Motoyama, Hiroko Kodama, Akira Kikuchi Tokyo, Japan P2-d3-909
Characterisation of cases of congenital hyperinsulinism in a tertiary paediatric endocrinology clinic: high yield from genetic testing and prevalence of dominantly inherited ABCC8 mutations Caoimhe Howard1, Ioana D. Maris1, Caroline Joyce1, Sian Ellard2, Sarah Flanagan2, Nuala Murphy3, Andrew Green3, Stephen M.P. O’Riordan1, Susan M. O’Connell1 1 Cork, Ireland, 2Exeter, UK, 3Dublin, Ireland P2-d3-910
Hyperinsulinaemic hypoglycaemia and brain injury in term babies with no risk factors: how long is too long? Clare Gilbert, Kate Morgan, Louise Hinchey, Pratik Shah, Anitha Kumaran, Khalid Hussain London, UK P2-d3-911
Variations in cumulative incidence of the association between coeliac disease and type 1 diabetes in northern Italy Giulio Maltoni1, Roberto Franceschi2, Giovanna Ignaccolo3, Barbara Piccini4, Anna Lisa Martini1, Alessandra Rollo1, Vittoria Cauvin2, Ivana Rabbone3, Lorenzo Lenzi4, Stefano Zucchini1 1 Bologna, Italy, 2Trento, Italy, 3Turin, Italy, 4Florence, Italy P2-d3-912
The incidence trend of type 1 diabetes mellitus in children in Beijing based on hospitalisation data during 1995-2010 Xi Meng, Chunxiu Gong Beijing, China P2-d3-913
New technologies for promoting hypoglycaemia self-management in type 1 diabetic children Elvira Piccinno, Federica Ortolani, Marcella Vendemiale, Albina Tummolo, Elda Frezza, Cataldo Torelli, Pierpaolo Di Bitonto, Veronica Rossano, Stefano Rossello, Ivan Salinaro, Teresa Roselli Bari, Italy
Poster Sessions P2
P2-d3-914
Focal congenital hyperinsulinism due to a novel mutation of ABCC8 gene Natasa Rojnic Putarek1, Nevena Krnic1, Katja Kubat Dumic1, Christine Bellanné-Chantelot2, Cecile Saint-Martin2, Winfried Barthlen3, Ingeborg Barisic1 1 Zagreb, Croatia, 2Paris, France, 3Greifswald, Germany
160
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1
Session title: Glucose Metabolism 12 Chairs: Geoffrey Ambler, Sydney, Australia Hernan Garcia, Santiago de Chile, Chile P2-d1-915
Screening results for microvascular complications according to recent consensus in adolescents with type 1 diabetes Fatma Demirel, Derya Tepe, Ozlem Kara, Ihsan Esen Ankara, Turkey P2-d1-916
The effect of education on glycaemic parameters in children with diabetes type 1 mellitus Diana Stimjanin-Koldzo, Salem Alajbegovic, Ena Stimjanin Zenica, Bosnia and Herzegovina P2-d1-917
No evidence for heart dysfunction and blood pressure disorders in pubertal children after 5-10 years of type 1 diabetes duration: results of a pilot study Malgorzata Wojcik, Andrzej Rudziński, Malgorzata Stelmach, Marta Ciechanowska, Joanna Nazim, Krystyna Sztefko, Jerzy B. Starzyk Krakow, Poland P2-d1-918
Novel case of insulin resistant diabetes secondary to newly described autoinflammatory disorder: CANDLE syndrome Rashida Farhad Vasanwala Singapore, Singapore P2-d1-919
Does type 1 diabetes influence lung function? Results of a pneumo-allergological follow-up study Giuseppe d’Annunzio, Maria Angela Tosca, Michela Silvestri, Andrea Accogli, Giulia Romanisio, Angela Pistorio, Giovanni A. Rossi, Renata Lorini Genoa, Italy P2-d1-920
Non-alcoholic fatty liver disease: a novel risk factor for the development of type 2 diabetes in childhood? Carolina Loureiro, Carmen Campino, Alejandro Martínez-Aguayo, Marlene Aglony, Carolina Avalos, Lilian Bolte, Rodrigo Bancalari, Cristian Carvajal, Carlos Fardella, Hernán García Santiago, Chile P2-d1-921
Hypoglycaemia rate during diabetic ketoacidosis, managed with the two-bag system Heba Ismail, Katherine Cochrane, Carolyn Paris, Ildiko H. Koves Seattle, USA P2-d1-922
Poster Sessions P2
Epidemiology of childhood type 1 diabetes in Extremadura (1996-2011) Noemi A. Fuentes-Bolaños1, Francisco J. Arroyo Díez1, Ana Rodríguez González2, Manuela Núñez Estévez1, Jesus González de Buitrago Amigo3, Enrique Galán Gómez1 1 Badajoz, Spain, 2Valladolid, Spain, 3Cáceres, Spain P2-d1-923
The role of diabetic ketoacidosis in the evolution of type 1 diabetes in children Ileana Puiu, Elena Carmen Niculescu, Veronica Elena Maria, Alexandra Oltea Puiu Craiova, Romania P2-d1-924
Novel fructose-1,6-biphosphatase gene mutation in two siblings Erdal Eren1, Tuba Edgunlu2, Ilhan Yetkin1 1 Sanliurfa, Turkey, 2Mugla, Turkey
9th Joint Meeting of Paediatric Endocrinology 2013
161
Poster sessions | P2
P2-d1-925
Improving paediatric diabetic ketoacidosis: lessons from a multidisciplinary quality improvement initiative in the computerized era of medicine Ildiko H. Koves, Jean C. Popalisky, Kate Drummond, Michael G. Leu, Elaine Beardsley, Kristi Klee, Carolyn Paris, Suzanne Spencer, Troy L. McGuire, Joel S. Tieder, Jerry J. Zimmerman, Diabetic Ketoacidosis Guideline Development Workgroup Seattle, USA
Session date:
Friday 20 September (d2), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Glucose Metabolism 13
Session title: Chairs:
Andrea Scaramuzza, Milan, Italy Asma Deeb, Abu Dhabi, United Arab Emirates
P2-d2-926
Permanent neonatal diabetes mellitus caused by a novel mutation in KCNJ11 gene Hakan Doneray1, Jayne Houghton2, Kadir Serafettin Tekgunduz1, Ferat Balkir1, Ibrahim Caner1 1 Erzurum, Turkey, 2Exeter, UK P2-d2-927
A survey of monogenic diabetes forms in Switzerland Philippe Klee, Mirjam Dirlewanger, Jean-Louis Blouin, Valérie M. Schwitzgebel Geneva, Switzerland P2-d2-928
Management of Rabson-Mendenhall syndrome Ilker T. Ozgen, Yasar Cesur, Demet Demirkol, Hakan Gedik, Mehmet S. Aksu Istanbul, Turkey P2-d2-929
A novel type heterozygous mutation in the glucose-6-phosphatase gene in a patient with glycogen storage disease Ia Jie Zhu, Yan Xing, Guoping He, Xuenong Xing, An Ren, Shandong Ye Hefei, China P2-d2-930
Achievement of internationally established metabolic goals in Spanish paediatric patients with type 1 diabetes Milagros Alonso, Patricia Enes, María Martín-Frías, Luz Golmayo, Rosa Yelmo, María Álvarez, Raquel Barrio Madrid, Spain P2-d2-931
Poster Sessions P2
A screening test for the cause of hypoglycaemia is a valuable tool for identification of the underlying diagnosis Julie Green, Dinesh Giri, Swathi Upadrasta, Joanne Blair, Poonam Dharmaraj, Urmi Das, Renuka Ramakrishnan, Mohammed Didi Liverpool, UK P2-d2-932
Identification of a novel mutation in an Egyptian infant with microcephaly, epilepsy, and permanent neonatal diabetes syndrome Nancy Samir Elbarbary1, Sarah E. Flanagan2, Sian Ellard2 1 Cairo, Egypt, 2Exeter, UK P2-d2-933
Frequency of glutamic acid dehydrogenase antibodies among paediatric Filipino with type 1 diabetes mellitus Marichu Pacanan Mabulac Manila, Philippines
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9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d2-934
A new case of exercise-induced hyperinsulinism caused by MCT1-expressing insulinoma Alena Welters1, Jan Marquard1, Dirk Klee1, Winfried Barthlen1, Timo Otonkoski2, Eckhard Lammert1, Ertan Mayatepek1, Thomas Meissner1 1 Düsseldorf, Germany, 2Helsinki, Finland P2-d2-935
Development and implementation of clinical practice guidelines in diabetic ketoacidosis: NICE is also nice in the Middle East Sarar Mohamed, Nasir Al-Juryyan, Amir Babiker, Hessah Al-Otibi, Rana Hasanato, Hala Omer, Mohamed Elfaki Osman, Abdelrahman Al-Nemri Riyadh, Saudi Arabia P2-d2-936
Assessing service satisfaction levels of adolescents with diabetes in out-patient clinic setting: a patient response outcome measure Amith Nuti1,2, Rebekah Pryce1,2 1 Morriston, UK, 2Newport, UK P2-d2-937
Efficacy analysis of MDI or CSII in type 1 diabetes mellitus children of different duration Li Y. Wei, Chun X. Gong, Di Wu, Xi Meng, Bing Y. Cao Beijing, China
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3
Session title: Glucose Metabolism 14 Chairs: Riitta Veijola, Oulu, Finland Stefano Tumini, Chieti, Italy P2-d3-938
Ketoacidosis related to alcohol consumption but not to type 1 diabetes in an adolescent with type 1 diabetes Oya Ercan, Hasan Onal, Serdar Celebi, İlhan Ocak, Metin Karabocuoglu Istanbul, Turkey P2-d3-939
Neonatal diabetes mellitus in Vietnam: clinical features and outcome Ngoc Thi Bich Can1, Vũ Chí Dũng1, Thao Phuong Bui1, Khanh Ngoc Nguyen1, Dat Phu Nguyen1, Hoan Thi Nguyen1, Sian Ellard2, Maria Craig3 1 Hanoi, Vietnam, 2Exeter, UK, 3Sydney, Australia P2-d3-940
Poster Sessions P2
Inflammatory cytokines and the adipokines visfatin, apelin, adiponectin are not upregulated in children with type 1 diabetes without complications Mirjam Dirlewanger, Ivaine Droz, Pascale Roux-Lombard, Nathalie Farpour-Lambert, Valérie Schwitzgebel Geneva, Switzerland P2-d3-941
Ovarian dysgerminoma associated with diabetes mellitus Yvonne Yijuan Lim, Kah-Yin Loke, Cindy Weili Ho, Yung-Seng Lee Singapore, Singapore P2-d3-942
Effective treatment with metformin of a teenager with MODY3 and oligomenorrhoea: case presentation Anna Wedrychowicz, Marta Ciechanowska, Malgorzata Stelmach, Jerzy Starzyk Cracow, Poland
9th Joint Meeting of Paediatric Endocrinology 2013
163
Poster sessions | P2
P2-d3-943
Successful transition from insulin pump therapy to glyburide treatment in a 5-month-old male infant with a KJN11 mutation Kathryn Jackson1, Jadranka Popovic2, Figen Ugrasbul1 1 Kansas City, USA, 2Pittsburgh, USA P2-d3-944
Octreotide-induced long QT syndrome in a child with congenital hyperinsulinaemia Peyami Cinaz1, Çelik Nurullah1, Hamdi Cihan Emeksiz1, Khalid Hussain2, Orhun Mahmut Çamurdan1, Aysun Bideci1, Esra Döğer1, Özge Yüce1, Zafer Türkyılmaz1, Deniz Oğuz1 1 Ankara, Turkey, 2London, UK P2-d3-945
A novel mutation for thiamine responsive megaloblastic anaemia and diabetes Ramlah H. Alsaif1,2 1 Dammam, Saudi Arabia, 2Riyadh, Saudi Arabia P2-d3-946
Hyperglycaemia and kidney disease: which MODY can be suspected? Concetta Aloi, Sara Bolloli, Alessandro Salina, Marta Marchi, Renata Lorini, Giuseppe d’Annunzio Genoa, Italy P2-d3-947
Changing profile of GAD and IA2 positivity in children with type 1 diabetes in India Sudip Chatterjee, Debmalya Sanyal Kolkata, India P2-d3-948
Evaluation of depression and glicaemic control of teenagers with type 1 diabetes Erdal Adal, Umit A Sarıtas, Huriye Ersen, Hasan Onal Istanbul, Turkey P2-d3-949
Neonatal hypoglycaemia due to glucose 6 phosphatase deficiency Lenira Cristina Stella1, Marina Dallal1, Cecília Oliveira Barbosa Buck2, Fadlo Fraige Filho1, Alexander A.L. Jorge1 1 São Paulo, Brazil, 2Campinas, Brazil
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1
Session title: Growth 3 Chairs: Daniela Larizza, Pavia, Italy Susumu Kanzaki, Tottori, Japan
Poster Sessions P2
P2-d1-950
The determinants of short stature in HIV infected children Dipesalema Joel, Seeletso Nchingane, Vincent Mabikwa, Jerry Makhanda, Michael A. Tolle, Gabriel Anabwani Gaborone, Botswana P2-d1-951
Idiopathic short stature: final results of the growth evolution and analysis of the GH1, GHR and IGF1 genes in a control study with therapeutic intervention Lidia Castro-Feijoo, Celsa Quinteiro, Lourdes Loidi, Jesús Barreiro, Paloma Cabanas, Claudia Heredia, Rosaura Leis, Manuel Pombo Santiago de Compostela, Spain
164
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-952
Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiency in a cohort of Brazilian patients Andria C.V. Lido, Marcela M. França, Aline P. Otto, Luciani R. Carvalho, Berenice B. Mendonca, Ivo J.P. Arnhold, Alexander A.L. Jorge Sao Paulo, Brazil P2-d1-953
Breast milk analytes and infancy growth Philippa Prentice1, Ken Ong1, Marieke Schoemaker2, Eric van Tol2, Jacques Vervoort3, Carlo Acerini1, Ieuan Hughes1, David Dunger1 1 Cambridge, UK, 2Nijmegen, Netherlands, 3Wageningen, Netherlands P2-d1-954
Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 gene is associated with children height in a Brazilian cohort Eveline Gadelha Pereira Fontenele1, Catarina B. d’Alva1, Daniel P. Pinheiro1, Ericka B. Trarbarch2, Berenice B. Mendonca2, Maria Elisabete A. Moraes1, Alexander A.L. Jorge2 1 Fortaleza, Brazil, 2São Paulo, Brazil P2-d1-955
Identification of FGFR3 and SHOX mutations in patients with hypochondroplasia and Léri-Weill dyschondrosteosis: clinical overlap or clinical misdiagnosis? Sara Benito-Sanz1, Beatriz Paumard-Hernández1, Miriam Gayo-Escribano1, Fernando Santos-Simarro1, Pilar Bahillo-Curieses2, Jaime Sánchez del Pozo1, Isabel González-Casado1, Karen E. Heath1 1 Madrid, Spain, 2Valladolid, Spain P2-d1-956
Incidence of SHOX deficiency in a cohort of Italian children with idiopathic short stature Roberta Minari1, Alessandra Vottero1, Sara Azzolini2, Daniele Barbaro3, Carlo Burrai4, Giuliana M. Cardinale5, Daniela Cioffi6, Maria S. Coccioli7, Mara Ferrari8, Federica Gallarotti9, Francesco Gallo10, Raffaele Montinaro11, Giovanna Municchi12, Angela Panariello13, Maria Parpagnoli14, Laura Perrone15, Giorgio Radetti16, Antonio F. Radicioni17, Aurora Rossodivita17, Maria C. Salerno15, Luca Tafi18, Albina Tummolo19, Malgorzata Wasniewska20, Lorenzo Iughetti21, Sergio Bernasconi1 1 Parma, Italy, 2Padua, Italy, 3Livorno, Italy, 4Sassari, Italy, 5Casarano, Italy, 6Naples, Italy, 7Francavilla Fontana, Italy, 8Massa-Carrara, Italy, 9Cuneo, Italy, 10Brindisi, Italy, 11Galatina, Italy, 12Siena, Italy, 13 Pesaro, Italy, 14Florence, Italy, 15Naples, Italy, 16Bolzano, Italy, 17Rome, Italy, 18Arezzo, Italy, 19Bari, Italy, 20 Messina, Italy, 21Modena, Italy P2-d1-957
Final adult height and body proportions in young adults with childhood onset and adult onset Crohn disease Avril Mason, Jelena Lljuhhina, Daniel R. Gaya, Faisal S. Ahmed, Konstantinos Gerasimidis Glasgow, UK P2-d1-958
Electronic auto-injection device prevents growth hormone wastage in comparison to non-electronic injection devices Maria Trendafilow1, Isabel Baur1, Rene Ramseger2, Klaus K.P. Hartmann1 1 Frankfurt, Germany, 2Darmstadt, Germany Growth pattern in Kabuki syndrome Dina A. Schott1, Nicole Aj Cramers1, Willem J. Gerver1, Christine Fauth2, Koenraad Devriendt3, Constance T. Schrander-Stumpel1 1 Maastricht, Netherlands, 2Innsbruck, Austria, 3Leuven, Belgium P2-d1-960
Heterozygous expression of a new acide-labile subunit mutation: anthropometric and biochemical characterisation and response to growth hormone therapy Anna Grandone, Emanuele Miraglia del Giudice, Grazia Cirillo, Mariasole Conte, Francesco Capuano, Ciro Abbondanza, Laura Perrone Naples, Italy
9th Joint Meeting of Paediatric Endocrinology 2013
165
Poster Sessions P2
P2-d1-959
Poster sessions | P2
P2-d1-961
Adherence to the treatment with ZOMAJETTM, a needle-free device transjecting growth hormone: results of French observational survey Jacques Weill1, Philippe Niez2 1 Lille, France, 2Gentilly, France
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2
Session title: Chairs:
Growth 4 Julie Chowen, Madrid, Spain Giovanni Farello, L’Aquila, Italy
P2-d2-962
Clinical features of a series of patients with Rubinstein-Taybi syndrome from Brazil Cristiane Kopacek, Janaina Borges Polli, Rafael Fabiano Machado Rosa, Vinicius Freitas de Mattos, Patrícia Trevisan, Alessandra Pawelec da Silva, Mônica Léon Bacil, Samira Hasan Musa, Carla Graziadio, Paulo Ricardo Gazzola Zen Porto Alegre, Brazil P2-d2-963
Microcephalic osteodysplastic primordial dwarfism type II with severe insulin resistance Sukriye Pinar Isguven, Nursel Elcioglu, Metin Yildiz Istanbul, Turkey P2-d2-964
Comparison of serial bone age determination by BoneXpert image analysis and manual assessment using Greulich and Pyle method in children with congenital adrenal hyperplasia Bradley S. Miller1, Maria T. Gonzalez1, Tara L. Holm1, Khalid M. Khan2, Kyriakie Sarafoglou1 1 Minneapolis, USA, 2Washington, USA P2-d2-965
Growth retardation and autoimmune hypothyroidism with skeletal dysplasia based on mutation in ACP5 gene (Spondylenchondrodysplasia) Sebastian Kummer1, Carsten Doeing1, Markus Vogel1, Joerg Schaper1, Ekkehart Lausch2, Prasad Thomas Oommen1, Ertan Mayatepek1, Thomas Meissner1 1 Duesseldorf, Germany, 2Freiburg, Germany P2-d2-966
Short stature by SHOX gene deletion due to a chromosomal traslocation Marta DeToro-Codes, Gabriela Martínez-Moya, Jesús De La Cruz Moreno, Victoria Esteban-Marfil, Juan Francisco Expósito-Montes Jaén, Spain P2-d2-967
Poster Sessions P2
Familial isolated growth hormone deficiency due to P89L mutation Mirjana Kocova1, Elena Kochova1, Jurgen Klammt2, Elena Sukarova-Angelovska1, Heike Stobbe2, Roland Pfaeffle2 1 Skopje, The Former Yugoslav Republic of Macedonia, 2Leipzig, Germany P2-d2-968
Study on the defect of SHOX gene and its conserved noncoding elements and the relationships with phenotypes and X-ray in idiopathic short stature Min Zhu, Shujuan Guo, Yueshuang Cun, Fang Xie, Feng Xiong Chongqing, China P2-d2-969
Identification of an intragenic SHOX duplication and FGFR3 mutation (p.K650T) in a family with multiple members affected by disproportionate short stature Sara Benito-Sanz, Beatriz Paumard-Hernández, Miriam Gayo-Escribano, Fernando Santos-Simarro, Karen E. Heath Madrid, Spain
166
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d2-970
The heart and aorta MRI usefulness in the diagnostics of girls with Turner syndrome Monika Obara-Moszynska, Magdalena Lanocha, Anna Kociemba, Barbara Rabska-Pietrzak, Magdalena Janus, Andrzej Siniawski, Bartlomiej Mrozinski, Pawel Prycki, Marek Niedziela, Malgorzata Pyda Poznan, Poland P2-d2-971
Hyperbolic function shows close correlation between GH secretion rate and GH sensitivity Ralph Decker1, Berit Kriström2, Jovanna Dahlgren1, Björn Andersson1, Kerstin Albertsson-Wikland1 1 Gothenburg, Sweden, 2Umeå, Sweden P2-d2-972
Plasma midkine concentrations in healthy children and children with short stature Youn Hee Jee1, Kun Song Lee2, David B. Sacks1, Alan Remaley1, Young Pyo Chang2, Ellen W. Leschek1, Jack Yanovski1, Jeffrey Baron1 1 Bethesda, USA, 2Cheonan, Republic of Korea P2-d2-973
Adult height in individuals with Silver-Russell syndrome treated with growth hormone from childhood – correlations to pubertal growth Jovanna Dahlgren, Clara Velander, Christini Ladaki Gothenburg, Sweden
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3
Session title: Growth 5 Chairs: Gian Luigi Spadoni, Rome, Italy Yael Lebenthal, Petah Tikva, Israel P2-d3-974
Comparative analyses of prevalence of thinness, overweight and obesity of semi–urban Nigerian school children using three international references Bolanle Fetuga1, Tinuade Ogunlesi1, Björn Jonsson2, Kerstin Albertsson-Wikland3 1 Saguma, Nigeria, 2Uppsala, Sweden, 3Gothenburg, Sweden P2-d3-975
Pituitary gland size is a useful marker in diagnosing growth hormone deficiency in short children Asma Deeb Abu Dhabi, United Arab Emirates P2-d3-976
Growth and pubertal timing in patients with phenylketonuria Milva Orquidea Bal, Ilaria Bettocchi, Emanuela Zazzetta, Antonella Cantasano, Martina Zanotti, Andrea Pession, Laura Mazzanti, Alessandra Cassio Bologna, Italy P2-d3-977
Poster Sessions P2
Endocrine complications in patients with β-thalassaemia major Zhe Meng, Liyang Liang, Lina Zhang, Lele Hou, Xiangyang Luo, Dongfang Li, Zhanwen He, Jianpei Fang Guangzhou, China P2-d3-978
IGF-1 levels in term SGA children with catch up at 12-18 months Sangeeta Yadav, Deepika Rustogi, Siddharth Ramji, T.K. Mishra New Delhi, India P2-d3-979
Congenital hypopituitarism: clinical, biochemical and neuroradiological correlation Laura Cecilia Castro, Constanza Pelliza, Silvia Martín, Liliana Muñoz, Adriana Boyanovsky, Mirta Miras Córdoba, Argentina
9th Joint Meeting of Paediatric Endocrinology 2013
167
Poster sessions | P2
P2-d3-980
Phenotypic and genotypic variability in SHOX gene haploinsufficiency Francesca Simi, Maria F. Tutera, Giuseppe Saggese Pisa, Italy P2-d3-981
Comparative analyses of prevalence of short and tall stature of semi-urban Nigerian school children using three international references Bolanle Fetuga1, Tinuade Ogunlesi1, Björn Jonsson2, Kerstin Albertsson-Wikland3 1 Saguma, Nigeria, 2Uppsala, Sweden, 3Gothenburg, Sweden P2-d3-982
Clinical, biochemical and neuroimaging findings as predictors of growth hormone deficiency in children Florencia Clément, Débora Braslavsky, Ana C. Keselman, Alicia Martinez, María G. Ropelato, María G. Ballerini, Romina P. Grinspon, Ignacio Bergadá, Rodolfo A. Rey, Gabriela P. Finkielstain Buenos Aires, Argentina P2-d3-983
Longitudinal studies of growth and pubertal progress in adolescents with inflammatory bowel disease Avril Mason1, Jonathan Bishop2, Paraic McGrogan1, Martin McMillan1, Jane McNeilly1, Richard K. Russell1, Faisal S. Ahmed1 1 Glasgow, UK, 2Auckland, New Zealand P2-d3-984
Measurement of birth length and parental height for SGA babies and follow-up of short children at 2 years Colette M. Sardar1, Sheena Kinmond2, Jamila Siddique2, Andrew Cooper2, Sheena Mcgowan1, Wendy Paterson1, Sharon Donnelly2, Emma Jane Gault1, Malcolm Donaldson1 1 Glasgow, UK, 2Ayrshire, UK P2-d3-985
The effect of alteration in breast milk leptin concentration during a suckling period on neonatal weight gain Hakan Doneray, Elif Oruc, Mehmet Ali Gul, Zerrin Orbak Erzurum, Turkey
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1
Session title: Chairs:
Growth 6 PSN Menon, New Delhi, India Julia Boiko, Minsk, Belarus
P2-d1-986
Poster Sessions P2
Concentration of selected metals in blood, plasma and urine of short stature and healthy children Maria Klatka, Anna Błażewicz, Iwona Beń-Skowronek, Małgorzata Partyka Lublin, Poland P2-d1-987
Genetic diagnosis of a patient with manifestations of both Prader-Willi syndrome and Angelman syndrome Kenichi Miyako1, Atsuko Kawano1, Yuichi Mushimoto1, Koji Muroya2, Yukiko Kuroda2, Kenji Kurosawa2 1 Fukuoka, Japan, 2Yokohama, Japan P2-d1-988
Preterm twins with discordant birth weight: auxological, hormonal and metabolic follow-up during the first two years of life Marta Baricco, Sheila Beux, Maria F. Fissore, Francesca Giuliani, Luisa de Sanctis Turin, Italy
168
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-989
Sitting height/standing height ratio from birth to adulthood: normal reference values Antonio de Arriba, María Mercedes Domínguez, José Ignacio Labarta, Carmen Rueda, Esteban Mayayo, Ángel Ferrández-Longás Zaragoza, Spain P2-d1-990
Natural history of congenital growth hormone deficiency Eva Deillon1, Sophie Stoppa1, Michael Hauschild1, Gérald-Edouard Theintz1, Jean-Michel Dubuis2, René Tabin3, Nelly Pitteloud1, Franziska Phan-Hug1 1 Lausanne, Switzerland, 2Genève, Switzerland, 3Sion, Switzerland P2-d1-991
Comparison of the WHO child growth standards and references and the Sempé and Pedron growth references in a population of 1023 Algerian children referred for short stature Asmahane Ladjouze1, Yasmine Ouarezki1, Adel Djermane2, Leila Kedji1, Abdennour Laraba1 1 Algiers, Algeria, 2Gouraya, Algeria P2-d1-992
Linear growth of Indonesian children: growth declines and their association with parental height Leni Sri Rahayu1, I. Made Alit Gunawan2, Madarina Julia2 1 Jakarta, Indonesia, 2Yogyakarta, Indonesia P2-d1-993
Early postnatal growth retardation as a first sign of progeria Barbora Obermannova, Petra Dusatkova, Jana Kaprova, Daniela Zemkova, Stanislava Kolouskova, Zdenek Sumnik, Jan Lebl Prague, Czech Republic P2-d1-994
Long-term efficacy and safety of recombinant human growth hormone in children with chronic kidney disease: a single-centre experience Athanasios Christoforidis, Panagiota Triantafyllou, Nikoleta Printza, John Dotis, Fotios Papachristou Thessaloniki, Greece P2-d1-995
Short stature, complex cardiac defects and developmental delay associated with a de novo microduplication of chromosome 15q13.2q13 Michael Hauschild, Danielle Martinet, Franziska Phan-Hug, Sophie Stoppa, Daniele Cassatella, Andrew Dwyer, Nelly Pitteloud, Marie-Claude Addor Lausanne, Switzerland P2-d1-996
Familial 17q23.3 deletion and Xp 22.31 duplication detected using array-CGH in a girl with Silver Russell phenotype Laura Losa1, Lorenzo A. Bassi1, Manuela Seminara1, Giovanni Pieri1, Giulia Rossetti1, Palma Finelli2, Silvia Russo2, Lidia Larizza2, Mariangela Cisternino1 1 Pavia, Italy, 2Milan, Italy P2-d1-997
Poster Sessions P2
Early detection of coeliac disease in children by using height and weight in screening Antti Saari1, Samuli Harju1, Outi Mäkitie2, Marja-Terttu Saha3, Leo Dunkel4, Ulla Sankilampi1 1 Kuopio, Finland, 2Helsinki, Finland, 3Tampere, Finland, 4London, UK
9th Joint Meeting of Paediatric Endocrinology 2013
169
Poster sessions | P2
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Perinatal and Neonatal Endocrinology 2
Session title: Chairs:
Laura Guzzarotti, Milan, Italy Yukihiro Hasegawa, Tokyo, Japan
P2-d1-998
Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15 Ikuko Takahashi1, Hiroyuki Adachi1, Hidenobu Soejima2, Michiya Masue3, Tsutomu Takahashi1 1 Akita, Japan, 2Saga, Japan, 3Gifu, Japan P2-d1-999
Cardiovascular fitness in prepubertal children born small for gestational age Giulia Cafiero, Danilo Fintini, Caludia Brufani, Emanuele Fabrizi, Marco Cappa, Attilio Turchetta, Melania Manco, Stefano Cianfarani Rome, Italy P2-d1-1000
Immediate severe hyperglycaemia enables the differential diagnosis between transient idiopathic hyperglycaemia and neonatal diabetes mellitus in premature newborns Julie Auger, Kanetee Busiah, Nathalie Pouvreau, Sonia Dahan, Christelle Désirée, Hélène Cavé, Delphine Mitanchez, Michel Polak Paris, France P2-d1-1001
Neonatal Wolfram syndrome: novel de-novo dominant mutation presenting as an unusual clinical phenotype Abdulsalam Abu-Libdeh1, Ranit Jaron1, Tom Walsh2, Mary-Claire King2, Efrat Levy-Lahad1, David Zangen1 1 Jerusalem, Israel, 2Seattle, USA P2-d1-1002
Intra-uterine growth restriction associates with more severe hyperinsulinaemic hypoglycaemia in children born small for gestation age Jaya Sujatha Gopal-Kothandapani, Rajesh Chidanandaswamy, Raja Padidela, Lindsey Rigby, Louise Caine, Sarah Ehtisham, Mars Skae, Leena Patel, Indraneel Banerjee, Peter E. Clayton Manchester, UK P2-d1-1003
The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea Rimm Huh1, Sung Yoon Cho1, Chang-Seok Ki1, Young Bae Sohn2, Se Hyun Maeng1, You Jin Jung1, Su Jin Kim3, Dong-Kyu Jin1 1 Seoul, Republic of Korea, 2Suwon, Republic of Korea, 3Goyang, Republic of Korea
Poster Sessions P2
P2-d1-1004
The safety and patterns of use of octreotide in the treatment of congenital hyperinsulinism Ann W. McMahon1, Pamela Weinel1, Gerold Wharton1, B. Abrams1, Cecilia P. Damilano2, Diva De Leon2, Phuong Lieu3, Lilly Yen3, Carol Taketomo3, Beena Sood4, B. Jackson5, William Rodriguez1, Dianne Murphy1, Paul S. Thornton6, Ann W. McMahon1 1 Silver Spring, USA, 2Philadelphia, USA, 3Los Angeles, USA, 4Detroit, USA, 5Washington, USA, 6 Fort Worth, USA P2-d1-1005
“Crocodile” thyropathy in newborns: a novel cause of neonatal goiter with hypothyrosis Oleg Malievsky Ufa, Russian Federation P2-d1-1006
Neonatal waist circumference reference curves and its relationship with body mass index and ponderal index Selim Kurtoglu, Mustafa Ali Akin, Nihal Hatipoglu, Mumtaz Mustafa Mazicioglu, Leyla Akin, Deniz Okdemir Kayseri, Turkey
170
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-1007
The clinical and chromosome 11p15 imprinting defects study in Silver Russell syndrome Chunxiu Gong, Di Wu, Mingqiang Zhu Beijing, China P2-d1-1008
A report of neonatal screening for phenylketonuria in the past 20 years in Chengdu Xinran Cheng, Fang Tang, Li Yan, Yan Wei, Na Shu Chengdu, China P2-d1-1009
Miliaria rubra revealing systemic pseudohypoaldosteronism type 1 Laure Warin1, Jessica Jaillet1, Prisca Dealberti2, Maria-Christina Zennaro3, Michel David2, Philippe Rebaud1 1 Villefranche sur Saône Cedex, France, 2Lyon, France, 3Paris, France
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1
Session title: Pituitary and Neuroendocrinology 3 Chairs: Giovanni Federico, Pisa, Italy Stefano Zucchini, Bologna, Italy P2-d1-1010
A novel homozygous LHX4 mutation associated with severe panhypopituitarism leading to neonatal death Louise C. Gregory1, Khadija N. Humayun2, Mark J. McCabe1, James Greening3, Simon J. Rhodes4, Miles J. Levy3, Mehul T. Dattani1 1 London, UK, 2Karachi, Pakistan, 3Leicester, UK, 4Indianapolis, USA P2-d1-1011
Development of multiple pituitary hormone deficiencies in paediatric patients originally diagnosed with isolated GH deficiency of organic aetiology Christopher J. Child1, Cheri L. Deal2, Alan G. Zimmermann3, Charmian A. Quigley3, Elena P. Shavrikova4, Gordon B. Cutler Jr.5, Stenvert L.S. Drop6, Ron G. Rosenfeld7, Werner F. Blum8 1 Windlesham, UK, 2Montreal, Canada, 3Indianapolis, USA, 4St. Petersburg, Russian Federation, 5 Deltaville, USA, 6Rotterdam, Netherlands, 7Portland, USA, 8Bad Homburg, Germany P2-d1-1012
Impact of athletic activity vs. hypogonadism on regional body composition, haemodynamic and haematological parameters, and liver function tests Kathryn E. Ackerman, Lisa Pierce, Gabriela Guereca, Meghan Slattery, Madhusmita Misra Boston, USA P2-d1-1013
P2-d1-1014
Septo-optic dysplasia: clinical, endocrinological and neuroradiological phenotype Barbara Roviglione, Marta Giaccardi, Serena Noli, Maria Savina Severino, Anna E.M. Allegri, Roberto Gastaldi, Angela Pistorio, Natascia Di Iorgi, Andrea Rossi, Mohamad Maghnie Genoa, Italy P2-d1-1015
Long-term weight development and psychosocial status in childhood craniopharyngioma patients Hermann Lothar Müller1, Anthe S. Sterkenburg2, Ursel Gebahrdt1, Anika Hoffmann1, Kraniopharyngeom 2007 1 Oldenburg, Germany, 2Groningen, Netherlands
9th Joint Meeting of Paediatric Endocrinology 2013
171
Poster Sessions P2
Significance of PSIS diagnosis in the management for GHD patients Hongshan Chen, Minlian Du, Bonin Luo GuangZhou, China
Poster sessions | P2
P2-d1-1016
Serum prolactin concentration in children with coeliac disease and role of gluten free diet: a longitudinal study Maurizio Delvecchio1, Sonia Peruzzi2, Ruggiero Francavilla2, Vincenzo Rutigliano2, Antonella Lonero2, Luciano Cavallo2, Maria Felicia Faienza2 1 San Giovanni Rotondo, Italy, 2Bari, Italy P2-d1-1017
Thiazide diuretic treatment of neonatal central diabetes insipidus Amanda Scott, Andrew Cotterill, Mark Harris, Gary Leong, Stephanie Johnson Brisbane, Australia P2-d1-1018
Male prolactinomas in the paediatric population Katia Daffeur, Lina Akkache, Hadjer Zellagui, Fetta Amel Yaker, Farida Chentli Algiers, Algeria P2-d1-1019
Anterior pituitary gland aplasia: neuroradiological, phenotypical and hormonal evaluation Chiara Maria Damia, Maria Piera Ferrarello, Gabriella Pozzobon, Giuseppe Cannalire, Andrea Voto, Gisella Garbetta, Sara Osimani, Giovanna Weber Milan, Italy P2-d1-1020
Evaluation of pituitary function after infectious meningitis in childhood Claudia Giavoli, Claudia Tagliabue, Eriselda Profka, Laura Senatore, Silvia Bergamaschi, Paolo Beck-Peccoz, Susanna Esposito Milan, Italy P2-d1-1021
Craniopharyngioma: clinical, metabolic and auxological evolution Alessandra Musio, Gabriella Pozzobon, Maria Piera Ferrarello, Chiara Maria Damia, Andrea Voto, Giuseppe Cannalire, Gisella Garbetta, Sara Osimani, Giovanna Weber, Giuseppe Chiumello Milan, Italy
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Pituitary and Neuroendocrinology 4
Session title: Chairs:
Antonis Voutetakis, Athens, Greece Mohamed El Kholy, Cairo, Egypt
P2-d2-1022
Evaluation of hypothalamic-pituitary function in children following acute bacterial meningitis Eda Karadag Oncel, Meltem Didem Cakir, Ates Kara, Nazli Gonc, Ali Bulent Cengiz, Alev Ozon, Ergin Ciftci, Ayfer Alikasifoglu, Mehmet Ceyhan, Nurgun Kandemir Ankara, Turkey
Poster Sessions P2
P2-d2-1023
Screening for POU1F1 mutations among Bulgarian patients with congenital hyposomatotropism Ani V. Aroyo, Iva H. Stoeva, Daniela D. Dacheva, Atanaska M. Mitkova, Rada R. Kaneva, Shina I. Pashova, Vanio I. Mitev Sofia, Bulgaria P2-d2-1024
Endocrine problems in children with neurofibromatosis type 1 Meltem Tayfun, Hacı Ahmet Demir, Suna Emir, Fatma Demirel, Ozlem Kara, Derya Tepe Ankara, Turkey
172
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d2-1025
Endocrinopathies in beta-thalassaemia major: evidences from ten years of follow-up and evaluation of combined iron chelation therapy Valeria Chirico, Luciana Rigoli, Basilia Piraino, Mariangela La Rosa, Carmelo Salpietro, Teresa Arrigo Messina, Italy P2-d2-1026
Response of medical treatment in female paediatric and adolescents prolactinomas Lina Azzoug Akkache, Katia Daffeur, Hadjer Zellagui, Fetta Amel Yaker, Farida Chentli Algiers, Algeria P2-d2-1027
Thyrotropinoma in an 11-year-old boy with type 1 autoimmune polyglandular syndrome Nadezhda Mazerkina, Sergey Gorelyshev, Yury Trunin, Andrey Golanov, Elisabet Orlova, Maxim Karmanov Moscow, Russian Federation P2-d2-1028
GH- and prolactin-producing pituitary adenoma with low somatostatin receptor 2 expression in a 16-year-old girl 15 years after heart transplantation Angela Huebner, Gabriele Hahn, Sascha Ifflaender, Norbert Lorenz, Bettina Tittel, Thomas Pinzer, Kathrin Geiger, Lorenz Hofbauer Dresden, Germany P2-d2-1029
Etiologies of central diabetes insipidus in children Mourad Kesraoui, Said Azzoug, Fetta A. Yaker, Farida Chentli Algiers, Algeria P2-d2-1030
Wolfram syndrome in twelve patients from a mountainous area where consanguineous unions are not unusual: phenotypical expression Giuseppina Salzano, Fortunato Lombardo, Gilberto Candela, Federica Porcaro, Vincenzo Ramistella, Giuseppina Zirilli, Filippo De Luca Messina, Italy P2-d2-1031
Pitfalls in the diagnosis of GHD in children with hypothalamic and pituitary abnormalities Romana Marini, Paola Cambiaso, Carla Bizzarri, Marco Cappa Rome, Italy P2-d2-1032
Congenital hypopituitarism and early onset of ACTH deficiency in a boy with 301-302delAG/150delA mutation of PROP1 Iva H. Stoeva1, Ani V. Aroyo1, Silvia I. Andonova1, Radoslava E. Grozdanova1, Shina I. Pashova1, Daniela M. Avdjieva1, Reni I. Koleva2, Alexei S. Savov1 1 Sofia, Bulgaria, 2Stara Zagora, Bulgaria P2-d2-1033
Poster Sessions P2
An adolescent girl with McCune Albright syndrome combined with pituitary gigantism treatment with lanreotide and cabergoline Jeannette Linares, Patricio Romero, Francisca Grob, Hernán García, Ximena Gaete Santiago, Chile
9th Joint Meeting of Paediatric Endocrinology 2013
173
Poster sessions | P2
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Programming/Epigenetics 2
Session title: Chairs:
Barbro Diderholm, Uppsala, Sweden Luisa de Sanctis, Turin, Italy
P2-d1-1034
Birth weight is associated with insulin resistance, dyslipidaemia, and hypertension in children, adolescents and young adults with type 1 diabetes mellitus Christian Denzer1, Marion Flechtner-Mors1, Joachim Wölfle2, Joachim Rosenbauer3, Holger Haberland4, Edith Schober5, Martin Wabitsch1, Reinhard W. Holl1, DPV Initiative and the BMBF-Competence Network for Diabetes Mellitus 1 Ulm, Germany, 2Bonn, Germany, 3Duesseldorf, Germany, 4Berlin, Germany, 5Vienna, Austria P2-d1-1035
Serum biochemical markers related to insulin sensitivity in children born from pre-eclamptic pregnancies Satu Seppä1, Sirpa Tenhola1, Eero Rahiala1, Raimo Voutilainen2 1 Kotka, Finland, 2Kuopio, Finland P2-d1-1036
Clinical characterisation and molecular classification of fifteen Korean patients with pseudohypoparathyroidism type Ia, Ib, Ic and pseudopseudohypoparathyroidism Sung Yoon Cho1, Chang-Seok Ki2, Young Ahn Yoon2, Dong-Kyu Jin2 1 Guri, Republic of Korea, 2Seoul, Republic of Korea P2-d1-1037
Review of the clinical scoring systems in Silver-Russell Syndrome and development of modified diagnostic criteria to guide molecular genetic testing Renuka P. Dias1, Peter Nightingale1, Gail Kirby1, Susan Price2, Fiona MacDonald1, Timothy Barrett1, Eamonn Maher1 1 Birmingham, UK, 2Northampton, UK P2-d1-1038
Long-term effects of cow milk feeding in infancy on metabolic health Alevtina Durmashkina1, Elena F. Lukushkina1, Olga Netrebenko2 1 Nizhny Novgorod, Russian Federation, 2Moscow, Russian Federation P2-d1-1039
Poster Sessions P2
Prader-Willi syndrome: influence of the genotype on the mental performances Adriana Franzese, Enza Mozzillo, Eugenio Zito, Roberta Ida Ferrentino, Eleanna De Nitto, Paola Iaccarino Idelson, Sara Mobilia, Carmela Bravaccio, Valentina Fattorusso Naples, Italy
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Puberty and Gonads 4
Session title: Chairs:
Berthold Hauffa, Essen, Germany Nicos Skordis, Nicosia, Cyprus
P2-d1-1040
A new variant in the human luteinizing hormone receptor causing Leydig cell hypoplasia: functional characterisation Paolo Duminuco1, Alessandra Vottero2, Valeria Vezzoli1, Roberta Minari2, Elisa Pignatti3, Manuela Simoni3, Sergio Bernasconi2, Luca Persani1,4, Marco Bonomi1 1 Cusano Milanino, Italy, 2Parma, Italy, 3Modena, Italy, 4Milan, Italy
174
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-1041
Hyperandrogenaemia is associated with insulin resistance independently of adiposity in young polycystic ovary syndrome patients Alice Albu, Lavinia Antonie, Lavinia Stejareanu, Suzana Florea, Simona Fica Bucharest, Romania P2-d1-1042
Lack of functional compensatory activity of the seminiferous tubules remaining testis in monorchid boys Romina P. Grinspon, Carolina Habib, María G. Ropelato, María G. Ballerini, Patricia Bedecarrás, Silvia Gottlieb, Rodolfo A. Rey Buenos Aires, Argentina P2-d1-1043
Correlation between total testosterone and free testosterone with anti-Mullerian hormone and clinical features of hyperandrogaenism in adolescent girls Polina S. Bogdanova, Maria A. Kareva, Irina S. Yarovaya, Alexander V. Ilyin, Olga A. Zlotnikova, Valentina A. Peterkova Moscow, Russian Federation P2-d1-1044
Relationship between fetal weight and maternal nutritional status, serum concentrations of insulin, leptin and adiponectin during normal gestation Maria F. Borges, Sandra B. Mangucci Callegari, Heloisa Marcelino Cunha Palhares, Elisabete A. Mantovani Rodrigues Resende, Beatriz Pires Ferreira Uberaba, Brazil P2-d1-1045
Testicular functions in regularly blood-transfused thalassaemia major patients Sukumarn Siripunthana, Rottanat Rugpolmuang, Darin Sosothikul, Vichit Supornsilchai Bangkok, Thailand P2-d1-1046
Should patients with Down syndrome be screened for testicular microlithiasis? Ayse Nurcan Cebeci, Ayca Dilruba Aslanger, Mustafa Ozdemir Kocaeli, Turkey P2-d1-1047
Primary ovarian insufficiency in an adolescent exposed to in utero chemotherapy Jan M. Foote1,2 1 Des Moines, USA, 2Iowa City, USA P2-d1-1048
High prevalence of polycystic ovarian syndrome adolescents with type 1 diabetes mellitus: is there a difference according to NIH and Rotterdam criteria? Ana Colmenares, Kanetee Busiah, Nadia Tubiana-Rufi, Claire Levy-Marchal, Christine Delcroix, Paul Jacquin, Delphine Martin, Lila Benadjaoud, Evelyne Jacqz Aigrain, Kathleen Laborde, Elisabeth Thibaud, Jean-Jacques Robert, Dinane Samara-Boustani, Michel Polak Paris, France Prospective study of ovarian function secondary to fetal ovarian cyst Catherine Pienkowski, Sophie Cataix, Audrey Cartault, Marie Bournez, Luana Carfagna, Ouardia Bouali, Sofia Mouttalib, Julie Vial, Christiane Baunin, Emilie Berard, Maithe Tauber, Philippe Galinier Toulouse, France P2-d1-1050
Clinical follow-up of ovarian cysts in childhood and adolescence: a multicentre study Banu Kucukemre Aydin1, Nurcin Saka1, Firdevs Bas1, Gul Yesiltepe Mutlu2, Filiz Cizmeci2, Sukru Hatun2, Belma Haliloglu1, Serap Turan1, Abdullah Bereket1, Digdem Bezen3, Filiz Tutunculer3, Pinar İsguven1, Nihal Memioglu1, Tulay Guran1, Nurcan Cebeci2, Oya Ercan1, Sukran Poyrazoglu1, Ruveyde Bundak1, Feyza Darendeliler1 1 Istanbul, Turkey, 2Kocaeli, Turkey, 3Edirne, Turkey
9th Joint Meeting of Paediatric Endocrinology 2013
175
Poster Sessions P2
P2-d1-1049
Poster sessions | P2
P2-d1-1051
Phenotypic and cytogenetic findings in girls with “Y” sequences in their karyotypes Ana Keselman, Johanna Acosta, Maria E. Escobar de Lazzari, Graciela Del Rey, Luis Zuccardi, Marcela Venara, Andrea Arcari, Martín Boukhair, Alicia Martinez, Ignacio Bergadá, Mirta Gryngarten Buenos Aires, Argentina
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2 Puberty and Gonads 5
Session title: Chairs:
Matti Hero, Helsinki, Finland Grete Teilmann, Copenhagen, Denmark
P2-d2-1052
Hypogonadotropic hypogonadism and the gene for fibroblast growth factor receptor 1 – successful pregnancy through gonadotropin therapy and intracytoplasmic sperm injection Naoko Sato1, Yasuhiro Naiki1, Reiko Horikawa1, Toshiaki Tanaka1, Tsutomu Ogata2 1 Tokyo, Japan, 2Hamamatsu, Japan P2-d2-1053
Girls with McCune Albright syndrome: is there a place for unilateral ovarian surgery during childhood? Carmen Capito, Maud Bidet, Dinane Samara-Boustani, Graziella Pinto, Elisabeth Thibaud, Sabine Sarnacki, Michel Polak Paris, France P2-d2-1054
The management of prepubertal gynaecomastia in two monozygotic twins with Peutz Jeghers syndrome: from aromatase inhibitors to radical mastectomy Tiziana Romano, Anna Grandone, Francesco De Francesco, Enrica Emanuela Cascone, Francesco Di Mauro, Giuseppe Andrea Ferraro, Emanuele Miraglia Del Giudice, Laura Perrone Naples, Italy P2-d2-1055
Various endocrine disorders in children with 45,XY,der(13;14)(q10;q10) karyotype Byung Ho Choi, Cheol-Woo Ko Daegu, Republic of Korea P2-d2-1056
Lower cortisol response after OGTT related to glucocorticoid sensitivity Aristotle Panayiotopoulos1, Divya Khurana1, Amrit Bhangoo2, Steven Ghanny3, Svetlana Ten1 1 Brooklyn, USA, 2Long Beach, USA, 3Hackensack, USA P2-d2-1057
Clitoromegaly in a 3-year-old child: first presentation of a neurocutaneous syndrome? Zacharoula Karabouta, Israel Rousso, Fani Athanassiadou-Piperopoulou Thessaloniki, Greece
Poster Sessions P2
P2-d2-1058
Clinical and molecular characterization of children with idiopathic hypogonadotropic hypogonadism Miao Qin, Xiu Chun Gong, Zhan Qi Beijing, China P2-d2-1059
Girls with central precocious puberty during 5 years after completion of long-term treatment with GnRH agonist Marta Snajderova, Daniela Zemkova, Vera Lanska, Leos Teslik Prague, Czech Republic
176
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d2-1060
The cut-off point of sex hormone in simply identifying central precocious puberty and isolated premature thelarche in girls Linqi Chen, Rongrong Xie, Haiying Wu, Fengyun Wang, Xiuli Chen Suzhou, China P2-d2-1061
Body mass index evaluation in girls with idiopathic central precocious puberty during and after treatment with GnRH analogs Andrea J. Arcari, Analía V. Freire, María G. Ballerini, María G. Ropelato, Ignacio Bergadá, María E. Escobar, Mirta G. Gryngarten Buenos Aires, Argentina P2-d2-1062
Age at menarche in girls with coeliac disease Mimouna Bessahraoui, Karim Bouziane Nedjadi, Sakina Niar, Malika Naceur, Amel Zennaki, Ghazalia Boudraa, Mahmoud Touhami Oran, Algeria P2-d2-1063
Increased leptin levels in girls with premature thelarche Bumin Dundar1, Ozlem Sangun2, Ozgur Pirgon2 1 Izmir, Turkey, 2Isparta, Turkey
Session date:
Saturday 21 September (d3),12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3
Session title: Chairs:
Puberty and Gonads 6 A. Kemal Topaloglu, Adana, Turkey Edna Majaliwa, Dar es Salaam, United Republic of Tanzania
P2-d3-1064
Idiopathic central precocious puberty is more prevalent than it is believed to be in boys Ayfer Alikasifoglu, Dogus Vuralli, Nazli Gonc, Huseyin Demirbilek, Alev Ozon, Nurgun Kandemir Ankara, Turkey P2-d3-1065 Pelvic ultrasonography in the diagnosis of isolated premature thelarche
Beata Wikiera, Julita Nocon-Bohusz, Jolanta Bieniasz, Aleksander Basiak, Anna Noczynska Wroclaw, Poland P2-d3-1066
Profiles of pubertal markers in relation to clinical pubertal development in representative cohorts of healthy lean and obese children Antje Körner, Roland Pfäffle, Kathrin Dittrich, Madlen Neef, Antje Berthold, Isabel Wagner, Wieland Kiess, Jürgen Kratzsch Leipzig, Germany Precocious puberty and gynaecomastia in a boy affected by a contiguous gene syndrome caused by a chromosome 19p deletion including STK11 Laura Guazzarotti1, Silvia Mauri1, Mariangela Petruzzi1, Elena Freri1, Michela Malacarne2, Chiara Mameli1, Alessandra Gazzarri1, Federica Occhipinti1, Lucia Angelini1, Lucia Perroni2, Taneli Raivio3, Gian Vincenzo Zuccotti1 1 Milan, Italy, 2Genoa, Italy, 3Helsinki, Finland P2-d3-1068
Physiological estrogen replacement therapy with transdermal patches in girls with hypogonadism: a clinical observational study Ensio Norjavaara1, Berit Kriström2, Carina Ankarberg-Lindgren1 1 Gothenburg, Sweden, 2Umeå, Sweden
9th Joint Meeting of Paediatric Endocrinology 2013
177
Poster Sessions P2
P2-d3-1067
Poster sessions | P2
P2-d3-1069
The effect of extremely adverse critical life events in childhood on age at menarche in a developing country Beatrice Odongkara1, Tereza Piloya Were2, Mworozi Edison2, Thomas Ngwiri3, Paul Laigong3, Ze’ev Hochberg4 1 Gulu, Uganda, 2Kampala, Uganda, 3Nairobi, Kenya, 4Haifa, Israel P2-d3-1070
Testosterone therapy in males with Duchenne muscular dystrophy Christel M. Keefe, Brenda Wong, Jane Khoury, Lindsey Hornung, Cuixia Tian, Lauren Miller, Meilan M. Rutter Cincinnati, USA P2-d3-1071
Serum INSL3 concentrations increase during male puberty in the Mongolian population of East Asia Naishi Li1,2, Fengying Gong1, Yufeng Li1, Dianxi Zhang1, Huijuan Zhu1, Ming Li1, Hui Pan1 1 Beijing, China, 2Groningen, Netherlands P2-d3-1072
Genetic variants of estrogen receptor beta may cause gynaecomastia in adolescents Erdal Eren1, Tuba Edgunlu2, Huseyin Anil Korkmaz3, Esra Deniz Papatya Cakir4, Korcan Demir5, Sevim Karakas Celik6, Esin Sakallı Cetin2 1 Sanliurfa, Turkey, 2Mugla, Turkey, 3Izmir, Turkey, 4Mersin, Turkey, 5Gaziantep, Turkey, 6Zonguldak, Turkey P2-d3-1073
Puberty in Chilean boys shows earlier onset of testicular enlargement Ximena Gaete, Roberto García, Joel Riquelme, Ethel Codner Santiago, Chile P2-d3-1074
Isolated early telarche: is it related with ovarian hyperandrogenism? Gulgun Asar, Sukran Darcan, Petek Bayindir, Damla Goksen Izmir, Turkey P2-d3-1075
Evaluating the efficacy of treatment with a GnRH analogue in patients with central precocious puberty Havva Nur Peltek Kendirci, Sebahat Yılmaz Ağladıoğlu, Veysel Nijat Baş, Aşan Onder, Semra Çetinkaya, Zehra Aycan Ankara, Turkey
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Puberty and Gonads 7
Poster Sessions P2
Session title: Chairs:
Mariangela Cisternino, Pavia, Italy Alfonso Vargas, New Orleans, USA
P2-d1-1076
Androgen profile and anti-Mullerian hormone levels in girls with premature adrenarche Preneet C. Brar1, Mohammed Attaelmannan2, Veeramac Prasad1, Meredith Wilkes1, Raphael David1 1 New York, USA, 2Valencia, USA P2-d1-1077
The selected mutations in KISS1R gene in patients with GnRH-dependent precocious puberty Beata Wikiera, Przemyslaw Leszczynski, Karolina Kwiatkowska, Julita Nocon-Bohusz, Anna Noczynska, Robert Smigiel Wroclaw, Poland
178
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-1078
Pubertal pathways and the relationship to anthropometric changes in childhood: results from a prospective JUSAD study Bratimirka M. Jelenkovic1, Brankica M. Vasic1, Ivana Novakovic2, Milena Radicev2 1 Zajecar, Serbia, 2Belgrade, Serbia P2-d1-1079
The value of breast and pelvic ultrasonography for the diagnosis of precocious puberty Banu Kucukemre Aydin, Alev Kadioglu, Gamze Asker Kaya, Esra Devecioglu, Firdevs Bas, Sukran Poyrazoglu, Nurcin Saka, Ruveyde Bundak, Gulbin Gokcay, Feyza Darendeliler Istanbul, Turkey P2-d1-1080
Clinical presentation and etiology of central precocious puberty in Vietnamese children Bui Phuong Thao, Vũ Chí Dũng, Nguyen Ngoc Khanh, Can Thi Bich Ngoc, Nguyen Thi Hoan Hanoi, Vietnam P2-d1-1081
Epidemiologic study on current pubertal development in Chinese school-aged children Mingqiang Zhu, Jun-Fen Fu Hangzhou, China P2-d1-1082
Prepubertal diagnosis of congenital hypogonadotropic hypogonadism by whole-exome sequencing in a neonate with microphallus and cryptorchidism Cheng Xu1,2, Mariarosaria Lang-Muritano3, Daniele Cassatella1, Andrew Dwyer1, Franziska Phan-Hug1, Michael Hauschild1, Gerasimos Sykiotis1, Brian J. Stevenson1, Moosa Mohammadi4, Nelly Pitteloud1 1 Lausanne, Switzerland, 2Shanghai, China, 3Zurich, Switzerland, 4New York, USA P2-d1-1083
Secular trends in growth and sexual maturation among Russian adolescents Oleg Sergeyev1,2, Thuy Lam3, Jane S. Burns3, Paige L. Williams3, Russ Hauser3, Susan A. Korrick3, Boris Revich4, Mary M. Lee5 1 Chapaevsk, Russian Federation, 2Samara, Russian Federation, 3Boston, USA, 4Moscow, Russian Federation, 5Worcester, USA P2-d1-1084
Asymptomatic precocious puberty in children; clinical and laboratory characteristics Byung Ho Choi1, Eun Hee Hong2, Cheol Woo Ko1 1 Daegu, Republic of Korea, 2Kumi, Republic of Korea P2-d1-1085
Age at menarche in chronic diseases: coeliac disease, type 1 diabetes mellitus and growth hormone deficiency Silvia Sordelli, Claudia Banzato, Paolo Cavarzere, Claudia Anita Piona, Orsiol Pepaj, Luigi Benini, Franco Antoniazzi, Claudio Maffeis, Rossella Gaudino Verona, Italy P2-d1-1086
Clinical and laboratory characteristics of bone age advancement in prepubertal children Hae Soon Kim, Hye Ah Lee, Young Ju Kim, Hwayoung Lee, Hye Sun Gwak, Sujin Cho, Eun Hee Ha, Hyesook Park Seoul, Republic of Korea
Poster Sessions P2
P2-d1-1087
Early pubarche and anti-Mullerian hormone Ozlem Korkmaz, Damla Goksen, Samim Ozen, Sukran Darcan Izmir, Turkey
9th Joint Meeting of Paediatric Endocrinology 2013
179
Poster sessions | P2
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2
Session title: Puberty and Gonads 8 Chairs: Richard Stanhope, London, UK Maria Pia Guarneri, Milan, Italy P2-d2-1088
Evaluation of puberty and fertility in French galactosaemic patients Isabelle Flechtner1, Magali Viaud1, Maud Bidet1, Florence Coeugniet2, Alix Mollet-Boudjemline3, Philippe Labrune3, Pascale De Lonlay1, Elisabeth Thibaud1, Michel Polak1 1 Paris, France, 2Reims, France, 3Clamart, France P2-d2-1089
Cytokine profile in girls with early or precocious puberty Ji Won Koh, Jae-Sik Jeon, Jaekyung Kim, Jeesuk Yu Cheonan, Republic of Korea P2-d2-1090
Effects of aromatase inhibitors therapy in boys with short stature Seniha Kiremitci, Betul Ersoy Manisa, Turkey P2-d2-1091
McCune-Albright syndrome: clinical presentation and progression of symptoms in children Suzanne Ngo Um, Delphine Zenaty, Mariza Vivanco, Dinane Samara Boustani, Graziella Pinto, Christian Pauwels, Elisabeth Thibaud, Maud Bidet, Michel Polak, Jean Claude Carel, Juliane Legér Paris, France P2-d2-1092
Hypothalamic pituitary testicular axis maturation among lean and overweight boys Siva Prakash, Iram Shabir, Nandita Gupta, Ariachery C. Ammini New Delhi, India P2-d2-1093
Precocious puberty in Turner syndrome Mi Sun Chang1, Se Hyun Maeng1, Sung Yoon Cho1, Yu Jin Jung1, Young Bae Shon2, Dong-Kyu Jin1 1 Seoul, Republic of Korea, 2Suwon, Republic of Korea P2-d2-1094
Let´s simplify the diagnosis of precocious puberty Mauro Scharf Pinto, Myrna P. Campagnoli, Jaime L.L. Rocha Curitiba, Brazil P2-d2-1095
The relationship between serum vitamin D levels and precocious puberty in children Hwal Rim Jeong, Haesang Lee, Jin Soon Hwang Suwon, Republic of Korea
Poster Sessions P2
P2-d2-1096
Changes of the predicted adult height after gonadotropin-releasing hormone agonist treatment in girls with idiopathic true precocious puberty Se Young Kim1, Eun Young Kim2 1 Seongnam, Republic of Korea, 2Gwangju, Republic of Korea P2-d2-1097
Near-final height and time of menarche in girls with idiopathic central precocious puberty after gonadotropin-releasing hormone agonist treatment Yong Hyuk Kim1, Jae Wook Bae2, Sochung Chung3, Ye Jin Kim3, Ah Reum Kwon3, Jung Min Ahn3, Hyun Wook Chae3, Ho-Seong Kim3 1 Wonju, Republic of Korea, 2Sunchang-gun, Republic of Korea, 3Seoul, Republic of Korea P2-d2-1098
Outcomes of pubertal development as a function of pubertal onset age Alina German, Ze’ev Hochberg Haifa, Israel
180
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1 Sex Differentiation 3
Session title: Chairs:
Annette Richter-Unruh, Essen, Germany Louise A. Metherell, London, UK
P2-d1-1099
Turner syndrome karyotypes without a short arm (p) pair are associated with more severe dysmorphism and ENT morbidity Emma-Jane Gault, Malcolm D.C. Donaldson Glasgow, UK P2-d1-1100
Childhood androgen treatment effects on body composition and bone density in boys with Klinefelter syndrome: results of a two-year, placebo-controlled clinical trial Judith Ross1,2, Harvey Kushner1, Martha Bardsley1,2 1 Philadelphia, USA, 2Wilmington, USA P2-d1-1101
Major determinants and prediction of height development in Turner syndrome patients treated with recombinant human growth hormone Teresa Genoni, Moira Gianninoto, Silvia Laura Carla Meroni, Alessandra di Lascio, Ilaria Colombo, Gianni Russo Milan, Italy P2-d1-1102
Secular trends on birth parameters and pubertal timing in girls with Ullrich-Turner syndrome Joachim Woelfle1, Anders Lindberg2, Ferah Aydin2, Helmuth Doerr3, Bettina Gohlke1 1 Bonn, Germany, 2Sollentuna, Sweden, 3Erlangen, Germany P2-d1-1103
Liver function test abnormalities begin early in life in Turner syndrome Jose M. Jimenez-Vega, Philippe Backeljauw, Jane Khoury, Sarah Lawson, Iris Gutmark-Little Cincinnati, USA P2-d1-1104
What features predict the development of cholesteatoma in Turner syndrome? David B.N. Lim, Emma-Jane Gault, Haytham Kubba, M. Simon C. Morrissey, Malcolm D.C. Donaldson Glasgow, UK P2-d1-1105
The outcome of prenatal identification of a sex chromosome abnormality Angela K. Lucas-Herald1, Fiona Cann2, Clare Durajczyk2, Lorna Crawford1, Ruth McGowan2, S. Faisal Ahmed1 1 Glasgow, UK, 2Aberdeen, UK A rare cause of delayed puberty Pierluigi Marzuillo, Anna Grandone, Maria L. Cavaliere, Rita Genesio, Mariasole Conte, Francesco Capuano, Emanuele Miraglia del Giudice, Laura Perrone Naples, Italy P2-d1-1107
Dynamics of parameters of bone remodeling in girls with Turner syndrome on the background of treatment with recombinant growth hormone Nataly Volevodz1, Oleg Malievsky2, Valentina Peterkova1 1 Moscow, Russian Federation, 2Ufa, Russian Federation P2-d1-1108
A 45,X male patient with 7q distal deletion and rearrangement with SRY gene translocation; a case report Aysenur Ökten, Gülay Karagüzel Trabzon, Turkey
9th Joint Meeting of Paediatric Endocrinology 2013
181
Poster Sessions P2
P2-d1-1106
Poster sessions | P2
P2-d1-1109
Turner syndrome: epidemiological study in Tunis Leïla Essaddam, Sarra Ben Jemaa, Saloua Makni, Nadia Mattoussi, Monia Khemiri, Sihem Barsaoui, Khedija Boussetta, Lamia Ben Jemaa, Zohra Fitouri, Saayda Ben Becher Tunis, Tunisia P2-d1-1110
Cardiovascular and renal anomalies in Turner syndrome Ouidad Baz1, Samia Sakher1, Mourad Semrouni1, Samir Ayat2 1 Algiers, Algeria, 2Bab El Oued, Algeria
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2
Session title: Sex Differentiation 4 Chairs: Richard Sharpe, Edinburgh, UK Edna Roche, Dublin, Ireland P2-d2-1111
A de novo novel heterozygous deletion mutation in steroidogenic factor 1 in a 46,XY patient with primary adrenal failure and splenic hypoplasia/aplasia Hua-Mei Ma, Zhe Su, Yan-Hong Li, Min-Lian Du Guangzhou, China P2-d2-1112
Measurement of ano-genital distance in healthy children at 4 years Ana Cristina Rodríguez-Dehli1, Isolina Riaño-Galán1, Ana Fernández-Somoano2, Adonina Tardon2 1 Avilés, Spain, 2Oviedo, Spain P2-d2-1113
Extreme phenotypic variability of two siblings with 46,XY DSD and a disrupting frame shift mutation in exon 4 of the NR5A1 gene Ralf Werner1, Ralf Lünstedt1, Dagmar Struve1, Tim Strom2, Olaf Hiort1 1 Lübeck, Germany, 2Munich, Germany P2-d2-1114
Comparison of clinical features between individuals with partial and mixed gonadal dysgenesis Juliana G.R. Andrade, Ana Paula Santos, Juliana De Paulo, Gil Guerra-Junior, Andréa T. Maciel-Guerra Campinas, Brazil P2-d2-1115
Stigmatisation of children and adolescents with DSD in medical settings Heino F. L. Meyer-Bahlburg, Jananne Khuri, Maria I. New New York, USA
Poster Sessions P2
P2-d2-1116
Clinical and hormonal variations associated with androgen receptor gene mutation Zeynep Sıklar, Vehap Topcu, Pınar Kocaay, Merih Berberoğlu, Bülent Hacıhamdioğlu, Şenay Savaş Erdeve, Hatice Ilgın Ruhi, Ajlan Tükün, Gönül Öçal Ankara, Turkey P2-d2-1117
The role of anti-Mullerian and inhibin B hormones in the elevation of 46 XY disorders of sex development Isis Ghaly, Mona Hasan Hafez, Fatma El Mougy El Mougy, Soha Abdel Dayem, Abeer Atef, Manal Kandil, Ashraf Galal, Alaa Abd Al Hamid P2-d2-1118
Disorders of gonadal differentiation: histological evaluation, gender assignment and surgical approach Nadezda Raygorodskaya1, Dmitry Morozov2, Nina Bolotova1 1 Saratov, Russian Federation, 2Moskow, Russian Federation
182
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d2-1119
Persistent Müllerian duct syndrome: a novel mutation in anti-Müllerian hormone gene Alexandra Chatzi1, Konstantina Kosta1, Kyriaki Tsiroukidou1, Jean-Yves Picard2, Yves Morel3, Maria Papagianni1 1 Thessaloniki, Greece, 2Clamart, France, 3Bron Cedex, France P2-d2-1120
Mutation analysis for androgen receptor gene in patients with suspected androgen insensitivity syndrome Iram Shabir, Madan L. Khurana, Marumudi Eunice, Rajesh Khadgawat, Rima Dada, Ariachery C. Ammini New Delhi, India P2-d2-1121
A case of SOX 9 mutation without campomelic or acampomelic dysplasia Friederike Denzer, Christian Denzer, Walter Just, Martin Wabitsch Ulm, Germany P2-d2-1122
Effective treatment with low dose dihydrotestosterone gel on three Chinese boys with 5-alphareductase II deficiency Yuet-Ling Tung, Pik-To Cheung Hong Kong, Hong Kong
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3
Session title: Chairs:
Sex Differentiation 5 Laura Gaspari, Montpellier, France Hala Al Shaikh, Muscat, Oman
P2-d3-1123
Pubertal virilisation of a 46,XY female adolescent without adrenal insufficiency due to a novel heterozygous mutation in steroidogenic factor-1 Zeynep Siklar, Gönül Öcal, Serdar Ceylaner, Emine Camtosun, Pınar Kocaay, Gülnur Göllü, Ayşe Sertçelik, Merih Berberoglu Ankara, Turkey P2-d3-1124
SRD5A2 gene mutation can lead to sex development disorder: a case of a Turkish patient with 46,XY Mehmet Boyraz1, Korkut Ulucan2, Teoman Akcay2, Arzu Akcay2, Necati Taskin2 1 Ankara, Turkey, 2Istanbul, Turkey P2-d3-1125
P2-d3-1126
A novel mutation of the aromatase gene (CYP19A1) in 46,XX two siblings cases of assigned with different gender Samim Ozen, Tahir Atik, Ozlem Korkmaz, Huseyin Onay, Damla Goksen, Ferda Ozkinay, Ozgur Cogulu, Sukran Darcan Izmir, Turkey P2-d3-1127
Disorders of sex development: a review of 139 cases Chourouk Mansour, Meriem Chabah, Farida Jennane, Hicham Sibai Casablanca, Morocco
9th Joint Meeting of Paediatric Endocrinology 2013
183
Poster Sessions P2
A case of disorder of sex development that showed bilateral testicular development with extremely low population of a 46,XY lineage Risa Nomura1, Kentaro Miyai1, Michiyo Okada1, Michiko Kajiwara1, Makoto Ono1, Tsutomu Ogata1,2, Shuki Mizutani1, Kenichi Kashimada1 1 Tokyo, Japan, 2Hamamatsu, Japan
Poster sessions | P2
P2-d3-1128
Patients with 45X/46XY lie within the broad spectrum of Turner syndrome: experience from one clinical centre Aneta Gawlik, Halla Kaminska, Lukasz Machnica, Grzegorz Kudela, Tomasz Koszutski, Ewa Malecka-Tendera Katowice, Poland P2-d3-1129
Bilateral inguinal haernia in a 3-week-old girl: an unusual presentation of XY-DSD caused by 17α-hydroxylase/17,20-lyase deficiency and practical recommendations for diagnostic workup Ulrich J. Fuchs, Michaela F. Hartmann, Stefan A. Wudy Giessen, Germany P2-d3-1130
Adolescent with Frasier syndrome – WT1 mutation as a cause of 46, XY DSD and progressive nephropathy Carla Costa, Helena Pinto, Cintia Castro-Correia, Estevão Costa, Manuel Fontoura Porto, Portugal P2-d3-1131
A rare case of siblings with partial androgen insensitivity syndrome diagnosed following gynaecomastia and the successful management of gynaecomastia using tamoxifen Reiko Saito1, Yukiyo Yamamoto1, Motohide Gotoh1, Shunsuke Araki1, Kubo Kazuyasu1, Rinko Kawagoe1, Yasusada Kawada1, Koichi Kusuhara1, Maki Igarashi2, Fumiko Kato2, Maki Fukami2 1 Kitakyu-city, Japan, 2Tokyo, Japan P2-d3-1132
Analysis of 5α-reductase type 2 and androgen receptor gene in Korean patients with ambiguous genitalia Yong Hyuk Kim1, Duk Hee Kim2, Ah Reum Kwon2, Ye Jin Kim2, Jung Min Ahn2, Jin Woo Jeong2, Hyun Wook Chae2, Ho-Seong Kim2 1 Wonju, Republic of Korea, 2Seoul, Republic of Korea P2-d3-1133
Absent visualisation of a hypoplastic uterus in a 16-year-old with complete 46 XY gonadal dysgenesis (Swyer syndrome) Hector M. Granados, Priya Phulwani Hartford, USA P2-d3-1134
Poster Sessions P2
Penile agenesis: case report and management in a limited resources country Foued Abdelaziz Guelma, Algeria
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1
Session title: Chairs:
Thyroid 4 Shohei Harada, Tokyo, Japan Mariella Valenzise, Messina, Italy
P2-d1-1135
Predictors for thyroid carcinoma in Israel: a national cohort of 1,624,310 adolescents followed for up to 40 years
Alon Farfel1,2, Jeremy Kark3, Estela Derazne2, Dorit Tzur2, Micha Barchana3, Liora Lazar1,4, Arnon Afek2,3,4, Ari Shamiss2,4
Petah Tikva, Israel, 2Tel Hashomer, Israel, 3Jerusalem, Israel, 4Ramat Aviv, Israel
1
P2-d1-1136
Congenital central hypothyroidism associated to multiple pituitary hormone deficiency has an impaired thyroid function similar to congenital primary hypothyroidism due to ectopic or eutopic thyroid Débora Braslavsky, Ana Keselman, Ana Chiesa, Ignacio Bergadá Buenos Aires, Argentina
184
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-1137
Comparison between liquid L-thyroxine solution and tablet in congenital hypothyroidism Maria C. Vigone, Elena Peroni, Lorenzo A. Bassi, Marianna Di Frenna, Arianna Passoni, Clara Pozzi, Stefano Mora, Giovanna Weber Milan, Italy P2-d1-1138
Family satisfaction in an endocrine nurse specialist led congenital hypothyroid service Peter Laing, Dinesh Giri, Zoe Yung, Julie Green, Swathi Upadrasta, Joanne Blair, Poonam Dharmaraj, Urmi Das, Renuka Ramakrishnan, Mohammed Didi Liverpool, UK P2-d1-1139
Pitfalls in the diagnosis of congenital hypothyroidism Ilaria Bettocchi, Antonella Cantasano, Milva Bal, Angela Rizzello, Anna Lisa Martini, Rita Sciutti, Laura Mazzanti, Alessandra Cassio Bologna, Italy P2-d1-1140
Fibroblast growth factor 21: a biomarker of mitochondrial diseases is increased in congenital hyperthyroidism and Hashimoto disease between endocrine diseases Shuichi Yatsuga, Yasutoshi Koga Kurume, Japan P2-d1-1141
Can an endocrine nurse specialist led service for congenital hypothyroidism deliver care in accordance with internationally accepted recommendations? Dinesh Giri, Peter Laing, Zoe Yung, Anne Haddick, Julie Green, Joanne Blair, Urmi Das, Poonam Dharmaraj, Renuka Ramakrishnan, Mohammed Didi Liverpool, UK P2-d1-1142
Health-related quality of life in 10-year-old children with congenital hypothyroidism diagnosed by neonatal screening: the need for implementing patient reported outcomes in clinical practice Liesbeth van der Sluijs Veer1, Jan Pieter Marchal1, Marlies J. E. Kempers2, Heleen Maurice-Stam1, Thomas Vulsma1, A. S. Paul van Trotsenburg1, Martha A. Grootenhuis1 1 Amsterdam, Netherlands, 2Nijmegen, Netherlands P2-d1-1143
Allan-Herndon-Dudley syndrome caused by a novel MCT8/SLC16A2 mutation in a Turkish family Omer Faruk Aydin1, Cengiz Kara1, Julie Jones2, Tim C. Wood2, Melanie M. May2, Michael J. Friez2, Charles E. Schwartz2 1 Samsun, Turkey, 2Greenwood, USA P2-d1-1144
Interstitial deletion of the long arm of chromosome 2 in IgA deficiency and Graves disease Tokuo Mukai, Masaru Shirai, Aiko Aoyama, Emi Ishibazawa, Mitsumaro Nii, Yoichiro Yoshida, Takashi Sato, Genya Taketazu, Hiroshi Sakata, Junichi Oki Asahikawa, Japan P2-d1-1145
Poster Sessions P2
Copy number determination of hypothyroidism genes by MLPA analysis in patients with hypothyroidism and thyroid hypoplasia Annalisa Nicoletti, Alessandra Cassio, Ilaria Bettocchi, Soara Menabò, Angela Rizzello, Giuseppe A. Cangemi, Laura Mazzanti, Lilia Baldazzi Bologna, Italy P2-d1-1146
A novel NKX2.1 mutation in a family with congenital hypothyroidism Christos Shammas1, Vassos Neocleous1, Leonidas A. Phylactou1, Eleni Tsoka Gennata2 1 Nicosia, Cyprus, 2Athens, Greece
9th Joint Meeting of Paediatric Endocrinology 2013
185
Poster sessions | P2
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2
Session title: Chairs:
Thyroid 5 Antonella Olivieri, Rome, Italy Maurizio Delvecchio, San Giovanni Rotondo, Italy
P2-d2-1147
Prevalence of renal and cardiac abnormalities in children with congenital hypothyroidism Olcay Evliyaoglu, Manolya Kara, Bahar Ozcabi, Sibel Lacinel, Ayse Eroglu, Ibrahim Adaletli, Oya Ercan Istanbul, Turkey P2-d2-1148
Three cases of congenital central hypothyroidism in two families with TSH and prolactin deficiency caused by IGSF1 mutation Kazuteru Kitsuda1,2, Nobuo Matsuura3, Kiyomi Abe4, Shigeyuki Ohtsu1, Noriyuki Takubo1, Mayumi Kazahari1, Keiko Shibayama1, Yukifumi Yokota2, Satoshi Narumi4, Tomonobu Hasegawa4, Masahiro Ishii1 1 Kitasato, Japan, 2Hashimoto, Japan, 3Matsudo, Chiba, Japan, 4Shinanomachi, Japan P2-d2-1149
Longitudinal study on thyroid function in patients with thalassaemia major: high incidence of central hypothyroidism by 18 years Ashraf Soliman1, Mohamed Yassin1, Fawzia Al Yafei1, Lolwa Alnaimi1, Noora Almarri1, Vincenzo De Sanctis2, Aml Sabt1 1 Doha, Qatar, 2Ferrara, Italy P2-d2-1150
Glutathione peroxidase and selenoprotein P levels in children and adolescents with Hashimoto thyroiditis and subclinical hypothyroidism Mitra Nourbakhsh, Zahra Malekpour-Dehkordi, Behnam Chahardoli, Amir Hossein Doustimotlagh, Abolfazl Golestani, Maryam Razzaghy-Azar Tehran, Islamic Republic of Iran P2-d2-1151
Follow-up study of thyroid function after oncologic treatment in children Ruby Philip, Iwona Ben-Skowronek, Elzbieta Sadurska, Agnieszka Zaucha-Prazmo, Agnieszka Brodzisz, Maria Klatka, Sangita Patel Lublin, Poland P2-d2-1152
Vitamin D deficiency in autoimmune thyroiditis Olcay Evliyaoglu, Manolya Kara, Bahar Özcabı, Sibel Lacinel, Oya Ercan Istanbul, Turkey P2-d2-1153
Poster Sessions P2
Resistance to thyroid hormone in two generations with de novo mutation traced to a mutation in ancestral germline – report of the first Croatian family Jasenka Ille1, Pilar Gill Ibáñez2, Anita Spehar Uroic1, Natasa Rojnic Putarek1, Nevena Krnic1, Samuel Refetoff2 1 Zagreb, Croatia, 2Chicago, USA P2-d2-1154
Effects of two years L-thyroxine therapy on bone status in children with idiopathic subclinical hypothyroidism Andrea Esposito, Federica D’Elia, Raffaella Di Mase, Sara Alfano, Ida D’Acunzo, Donatella Capalbo, Mariacarolina Salerno Naples, Italy P2-d2-1155
The occurrence of Evans syndrome during remission of Graves disease Young-Lim Shin Bucheon, Republic of Korea
186
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d2-1156
Diagnostic and predictive value of ultrasound and isotope thyroid scanning, alone and in combination, in infants referred with thyroid stimulating hormone elevation on newborn screening Angela Lucas-Herald1, Jeremy H. Jones1, Morag Attaie1, Sanjay Maroo2, David Neumann3, Therese Bradley1, Joachim Pohlenz4, Malcolm Donaldson1 1 Glasgow, UK, 2Vancouver, Canada, 3Hradec Kralove, Czech Republic, 4Mainz, Germany P2-d2-1157
Personalised replacement therapy with L-thyroxine + L-triiodothyronine in congenital hypothyroidism Ferenc Péter, Ágota Muzsnai Budapest, Hungary P2-d2-1158
Neurodevelopmental outcomes in children with congenital hypothyroidism treated with high-dose initial replacement and close monitoring Paul L. Hofman, Ben Albert, Natasha Heather, Wouldes Trecia, Sarah Mathai, Jose Derraik, Craig Jefferies, Sheryl Tregurtha, Alastair J. Gunn, Wayne S. Cutfield Auckland, New Zealand
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d3
Session title: Chairs:
Thyroid 6 Mirelle Castanet, Rouen, France Maria Cristina Vigone, Milan, Italy
P2-d3-1159
The main features of thyrotoxicosis in prepubertal children Katsiaryna Konchits, Anzhalika Solntsava, Ludmila Viazava Minsk, Belarus P2-d3-1160
Twins with hypothyroidism and Papillon-Lefevre syndrome Amir Babiker, Huda Osman, Muneera J. Alshammari, Maha El Husseini Riyadh, Saudi Arabia P2-d3-1161
The incidence and characteristics of thyroid nodules in congenital hypothyroidism in infants Jeongho Lee, Seo Young Youn, Dong Hwan Lee Seoul, Republic of Korea P2-d3-1162
Long-term outcomes of paediatric Graves disease Ganesh Jevalikar1,2, Julieta Solis1, Margaret Zacharin1 1 Melbourne, Australia, 2Gurgaon, India Establishment of reference ranges for thyrotropin, thyroxine, free thyroxine, triiodothyronine and T-uptake in neonates and infants Maria Lescurat, Gabriela Sobrero, Cintia Tarifa, Cecilia Aguirre, Ivan Collet, Liliana Silvano, Silvia Martin, Mariana Ochetti, Graciela Testa, Mirta Miras, Liliana Muñoz Córdoba, Argentina P2-d3-1164
Clinical utility of thyroid scans in mild neonatal hyperthyrotropinaemia Asaf Oren, Michael Ke Wang, Lori Brnjac, Farid H. Mahmud, Mark R. Palmert Toronto, Canada
9th Joint Meeting of Paediatric Endocrinology 2013
187
Poster Sessions P2
P2-d3-1163
Poster sessions | P2
P2-d3-1165
Familial non-autoimmune hyperthyroidism: activating mutation of thyrotropin receptor gene discovered after three generations of a family Song Hai Lim1,2, Johari Mohd Ali1, Loo Ling Wu1 1 Kuala Lumpur, Malaysia, 2Putrajaya, Malaysia P2-d3-1166
Familial papillary thyroid carcinoma: description of 4 paediatric cases Claudia L. Godoy, Hernan G. Garcia, Clarita E. Ferrada Santiago, Chile P2-d3-1167
A novel MCT8 mutation in a Japanese patient with Allan-Herndon-Dudley Syndrome Sumito Dateki1, Kohei Haraguchi1, Tatsuharu Sato1, Akiko Nakatomi1, Makoto Fujiwara2, Maiko Sakurai2, Noriyuki Namba2, Keiichi Ozono2, Hiroyuki Moriuchi1 1 Nagasaki City, Japan, 2Suita, Japan P2-d3-1168
Bone maturation and growth in children with congenital hypothyroidism detected by neonatal screening: a longitudinal study Verónica G. González, María C. Apezteguía, Analía Morin, Viviana A. Balbi, Luis M. Guimarey, Zulma C. Santucci La Plata, Argentina P2-d3-1169
Severe acquired primary hypothyroidism in children older than 3 years: a retrospective analysis of 43 cases Marianne Becker, Heiko Krude, Dirk Schnabel, Erwin Lankes, Paulina Aleksander, Klemens Raile, Oliver Blankenstein Berlin, Germany P2-d3-1170
Ovarian and thyroid disorders in a group of adolescents with type 1 diabetes Eduard Circo Constanta, Romania
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d1
Session title: Thyroid 7 Chairs: Diet Rustama, Bandung, Indonesia Simonetta Bellone, Novara, Italy P2-d1-1171
Familial dysalbuminemic hyperthyroxinaemia: a reminder to take extended family histories Dipti Deshmukh, Isabelle Hodgson, Charles R. Buchanan, Abbi Lulsegged London, UK
Poster Sessions P2
P2-d1-1172
A case of MCT8 deficiency with a novel mutation in the SLC16A2 gene Erina Ono1, Masamichi Ariga1, Sakiko Oshima1, Mika Hayakawa1, Masayuki Imai1, Yukikatsu Ochiai1, Satoshi Matsushima1, Ichiro Miyata1, Noriyuki Namba2, Keiichi Ozono2, Hiroyuki Ida1 1 Tokyo, Japan, 2Suita, Japan P2-d1-1173
Thyroid nodules in paediatrics: a 4-year prospective study Patricia Papendieck1, Laura Gruñeiro-Papendieck1, Marcela Venara2, Oscar Acha2, Hugo Cozzani2, Fernanda Matteos2, Silvana Maglio2, Ignacio Bergada2, Ana Chiesa2 1 Caba, Argentina, 2Buenos Aires, Argentina
188
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P2
P2-d1-1174
Extra-thyroid congenital abnormalities with thyroid dysgenesis Filiz Mine Cizmecioglu, Elif Ozsu, Gurkan Altun, Bayram Yıldırım, Aysegul Yuksel, Fatih Takavcı, Ahmet Akca, Kadir Babaoglu, Sukru Hatun Kocaeli, Turkey P2-d1-1175
Review of presentation and management of juvenile thyrotoxicosis at a single centre between 2000-2010 Suma Nanjundappa, Talat Mushtaq, Sabah N. Alvi Leeds, UK P2-d1-1176
An adolescent girl with hypothyroid coma due to autoimmune thyroiditis Noora Alhumaidi, Maryam Elali, Aml Sabt, Ashraf Soliman Doha, Qatar P2-d1-1177
Partial pituitary thyroid hormone resistance in a 14-year-old boy: a case report Galyna Soloviova1, Larysa Nifontova1, Vira Yakovenko2 1 Kiev, Ukraine, 2Simferopol, Ukraine P2-d1-1178
Amiodarone-induced thyrotoxicosis: a rare complication in children Celine Marrec1, Patricia Bretones2, Graziella Pinto3, Marie Mansilla4, Dinane Samara Boustani3, Caroline Bonnet5, Gilbert Simonin1, Rachel Reynaud1 1 Marseille Cedex, France, 2Bron, France, 3Paris, France, 4Strasbourg, France, 5Dijon, France P2-d1-1179
Prevalence of permanent congenital hypothyroidism Mahin Hashemipour, Mahmood Ghasemi, Silva Hovsepian, Marjan Mansourian Isfahan, Islamic Republic of Iran P2-d1-1180
The role of thyroid ultrasonography in the etiological investigation of patients with congenital hypothyroidism Maria F. Borges, Nathalie Almeida Sedassari, Luis R. Marquez Ferreira Souza, Anelise Almeida Sedassari, Heloisa M. Cunha Palhares, Beatriz Pires Ferreira Uberaba, Brazil P2-d1-1181
Juvenile hyperthyroidism Said Azzoug, Farida Chentli Algiers, Algeria P2-d1-1182
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P2 (Exhibition Hall)
Session type:
Poster Session P2-d2
Session title: Chairs:
Thyroid 8
Poster Sessions P2
Newborn screening program for congenital hypothyroidism in Montenegro Mira Samardzic, Najdana Gligorovic, Milena Popovic Podgorica, Montenegro
Kanshi Minamitani, Chiba, Japan Ana Chiesa, Buenos Aires, Argentina
P2-d2-1183
A study of iodine organification in transient hypothyroidism with biallelic DUOX2 mutations: organification defect is not an invariable feature Keisuke Nagasaki1, Satoshi Narumi,2, Kiyomi Abe2, Tadashi Asami1, Hidetoshi Sato1, Yohei Ogawa1, Toru Kikuchi1, Tomonobu Hasegawa2, Akihiko Saitoh1 1 Niigata, Japan, 2Tokyo, Japan
9th Joint Meeting of Paediatric Endocrinology 2013
189
Poster sessions | P2
P2-d2-1184
Thyrotoxic hypokalaemic periodic paralysis in a Hispanic teenager Magdalena Dumin, Justin Triemstra, Rahul Bhatia, Carla Minutti Maywood, USA P2-d2-1185
Thyroid function abnormalities in term newborns from Korean mothers with autoimmune thyroid disease So Eun Park1, Sung Yeon Ahn2 1 Seoul, Republic of Korea, 2Chuncheon, Republic of Korea P2-d2-1186
Two novel mutations of the MCT8 gene: clinical and laboratory aspects Caroline De Gouveia Buff Passone, Hamilton Cabral Menezes-Filho, Lygia Spassapan Oliveira, Luciana Felipe Férrer, Suemi Marui, Ester Saraiva Brust, Anderson L. Ribeiro Silva, Hilton Kuperman, Durval Damiani São Paulo, Brazil P2-d2-1187
Continuum of phenotypes in the evaluation of hyperthyroidism in children and adolescents with autoimmune thyroid disease referred to a tertiary care centre: Hashitoxicosis versus Graves disease Ahmet Uçar, Dilek Güneş, Şükran Poyrazoğlu, Ali Satan, Firdevs Baş, Nurçin Saka, Rüveyde Bundak, Feyza Darendeliler Istanbul, Turkey P2-d2-1188
Maternal thyroid function during early pregnancy and neurodevelopmental outcome at 6 years Yasuhiro Naiki, Chie Takahashi, Kengo Miyashita, Satsuki Nishigaki, Yusuke Mizuno, Reiko Horikawa Tokyo, Japan P2-d2-1189
Primary cutaneous amyloidosis in an adolescent with Graves disease: previously unknown association Vijith Reddy Puthi, Nikhil Ganjoo Peterborough, UK P2-d2-1190
Blood coagulation and fibrinolytic activity in children with subclinical hypothyroidism Federica D’Elia, Manuela Cerbone, Sara Alfano, Andrea Esposito, Flavia Barbieri, Nicola Improda, Mariacarolina Salerno Naples, Italy P2-d2-1191
Clinico-pathologic characteristics and treatment of differentiated thyroid cancers in children Sukran Poyrazoglu, Nurcin Saka, Firdevs Bas, Ruveyde Bundak, Feyza Darendeliler Istanbul, Turkey P2-d2-1192
Refetoff syndrome associated to common variable immunodeficiency and psoriasis: a case report Angelo Acquafredda, Flavia Urbano, Maria Felicia Faienza, Clara Zecchino, Anna L.S. Di Giovinazzo, Fabrizia De Palma, Vincenza Luce, Luciano Cavallo Bari, Italy
Poster Sessions P2
P2-d2-1193
What value of capillary TSH on screening should trigger referral for venipuncture in preschool and school-aged children with Down syndrome? Sheena McGowan1, Jeremy Jones1, Kirsty McLaughlin1, Joan MacKenzie1, Kath Leyland1, Patricia Charleton2, Mona Rahim3, Mohamed Mansor4, Malcolm Donaldson1, The Scottish Down Syndrome Screening Group 1 Glasgow, UK, 2Aberdeen, UK, 3Ayrshire, UK, 4Stirling, UK P2-d2-1194
Clinical features of children with congenital hypothyroidism due to thyroglobulin deficiency Mehmet Keskin, Murat Karaoglan, Yilmaz Kor, Ozlem Keskin Gaziantep, Turkey
190
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Adrenals and HPA Axis 8
Session title: P3-d1-1195
The clinical charateristics and genetic analysis of Allgrove syndrome in 3 Chinese cases Wenjing Li, Chunxiu Gong, Di Wu, Bingyan Cao Beijing, China P3-d1-1196
Pregnancy in women with CAH and women at risk of having children with CAH Eunice Marumudi, Bindu Kulshreshtha, Arundhati Sharma, Rajesh Khadgawat, Madan L. Khurana, Ariachery C. Ammini New Delhi, India P3-d1-1197
Pubertal suppression with added growth hormone treatment to protect final height potential in 2 brothers with 11β-hydroxylase deficiency Isabelle D. Hodgson, Dipti Deshmukh, Charles R. Buchanan, Norman F. Taylor London, UK P3-d1-1198
Cyclic hypercortisolism – a case presentation Erwin Lankes, Dirk Schnabel, Heiko Krude Berlin, Germany P3-d1-1199
Congenital adrenal hyperplasia: a review of 91 cases Meryem Chabah, Chourouk Mansour, Farida Jennane, Hicham Sibai Casablanca, Morocco P3-d1-1200
Normal urinary free cortisol as pitfall in diagnosis of Cushing disease in children: alternative workup options Ilana Koren, Gabriel Dickstein Haifa, Israel P3-d1-1201
Behavioural outcome of children with congenital adrenal hyperplasia treated and followed at UKM Medical Centre Arini N.M. Idris1, Viji Chandran2, Zulkifli S.Z. Syed2, Rahmah Rasat2 1 Putrajaya, Malaysia, 2Kuala Lumpur, Malaysia P3-d1-1202
Allgrove syndrome Faiza Boutekdjiret, Said Azzoug, Faiza Belhimer, Farida Chentli Algiers, Algeria Distribution of the most frequent mutations and clinical characteristics among children with 21-hydroxylase deficiency in South-Eastern of Turkey Murat Karaoglan, Mehmet Keskin, Yilmaz Kor, Ozlem Keskin Gaziantep, Turkey P3-d1-1204
A three generation family with low cortisol, CBG deficiency, chronic fatigue and pain, lipomatosis and behavioral alterations Stefania Moia1, Gillian E. Walker1, Marta Roccio1, Roberta Ricotti1, Enza Giglione1, Simonetta Bellone1, Flaminia Fanelli2, Gianni Bona1, Flavia Prodam1 1 Novara, Italy, 2Bologna, Italy
9th Joint Meeting of Paediatric Endocrinology 2013
191
Poster Sessions P3
P3-d1-1203
Poster sessions | P3
P3-d1-1205
Reversible cause of cardiomyopathy in the paediatric age group: family history of ambiguous genitalia is the key of diagnosis Mohammad Ahmad Al-Qahtani Abha, Saudi Arabia
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d2 Adrenals and HPA Axis 9
Session title: P3-d2-1206
Unusual biochemical presentation of 17-alpha hydroxylase/17,20-lyase deficiency in a recent immigrant from Ecuador: a case report Divya Khurana, Aristotle Panayiotopoulos, Svetlana Ten Brooklyn, USA P3-d2-1207
Adrenocortical carcinoma in a child Kiran Bhagoo Parbhoo, Fatima Moosa, Nilesh Lala, Dawn-Lee van der Byl Johannesburg, South Africa P3-d2-1208
A novel microdeletion in NR0B1 (DAX1) gene in a boy with congenital adrenal hypoplasia Aleksandra Rojek1, Maciej Krawczynski1, Aleksander Jamsheer1, Barbara Iwaniszewska2, Ewa Malunowicz3, Marek Niedziela1 1 Poznan, Poland, 2Torun, Poland, 3Warsaw, Poland P3-d2-1209
A case of adrenal insufficiency due to isolated ACTH deficiency met the diagnostic criteria of orthostatic dysregulation Yuichiro Tomita, Hiroyuki Ishiguro, Hiromi Hyodo Kanagawa, Japan P3-d2-1210
Presentation of two brothers with diagnostic problems: P450 oxidoreductase deficiency? Ayla Güven, Suna Hancili Istanbul, Turkey P3-d2-1211
Overweight in Addison disease: a case report Angelo Acquafredda, Fabrizia De Palma, Maria Felicia Faienza, Clara Zecchino, Vincenza Luce, Pasquale Bratta, Paolo Diaferia, Luciano Cavallo Bari, Italy P3-d2-1212
Poster Sessions P3
Adrenal haemorrhage after abdominal blunt trauma in a 5-year-old boy Mesut Parlak1, Ali Erdal Karakaya1, Fatih Tuten1, Ayse Eda Parlak2 1 Kahramanmaras, Turkey, 2Antalya, Turkey P3-d2-1213
Effects of dexamethasone treatment in a 18-year-old boy with congenital adrenal hyperplasia due to 11βhydroxysteroid dehydrogenase type 1 deficiency: case report Beata Sawicka1, Janusz Pomaski1, Tomasz Romer2, Edyta Pietrewicz1, Artur Bossowski1 1 Bialystok, Poland, 2Warsaw, Poland P3-d2-1214
Corticosteroid insufficiency provoking ventricular arrhythmia Amir Babiker, Mohammed Al Ghamdi, Sharifah Al Issa, Nasir A. Al Jurayyan Riyadh, Saudi Arabia
192
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
P3-d2-1215
Cushing syndrome due to multinodular adrenal hyperplasia: case report Yılmaz Kor, Gokhan Soker, Deniz Kor, Fatih Temiz, Bilgin Yuksel Adana, Turkey
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Autoimmune Endocrine Diseases 4
Session title: P3-d1-1216
Prevalence of hypothyroidism and coeliac disease among children with diabetes mellitus Alexey Kiyaev, Konstantin Alexandrov, Olga Kovtun Yekaterinburg, Russian Federation P3-d1-1217
Coincidence of Graves disease and Sjögren syndrome in a 16-year-old girl Katrin Heldt, Gregor Dückers, Susanne Fricke-Otto Krefeld, Germany P3-d1-1218
Polyglandular autoimmune syndrome type II with adrenalitis, thyroiditis and ovarian failure in an adolescent girl Carsten Doeing1, Sebastian Kummer1, Wolfgang Mueller2, Ertan Mayatepek1, Thomas Meissner1 1 Duesseldorf, Germany, 2Moenchengladbach, Germany P3-d1-1219
Basal insulin requirement in children, adolescents and young adults using continuous subcutaneous insulin infusion Junichi Suzuki, Rumi Kuwabara, Masako Habu, Ayako Yoshida, Masako Okuno, Tatsuhiko Urakami Tokyo, Japan P3-d1-1220
A unique case of a patient with acute onset type 1 diabetes mellitus and two other autoimmune illnesses Sarah M. Reynolds, Yelena Nicholson Dayton, USA P3-d1-1221
Prevalence of autoimmune thyroid disease in children and adolescents with type 1 diabetes mellitus from Western Algeria Mimouna Bessahraoui, Karim Bouziane Nedjadi, Malika Naceur, Sakina Niar, Amel Zennaki, Ghazalia Boudraa, Mahmoud Touhami Oran, Algeria Hyponatraemia in a teenager: a rare diagnosis Filipa Correia, Alexandre Fernandes, Teresa Mota, Milagros Garcia, Cíntia Correia, Augusto Ribeiro, Manuel Fontoura Porto, Portugal P3-d1-1223
Difficulties in treatment of polyglandular autoimmune syndrome, type 1 Desislava Yordanova, Elisaveta Stefanova, Krasimira Kazakova, Zdravka Todorova, Mihaela Dimitrova Sofia, Bulgaria
9th Joint Meeting of Paediatric Endocrinology 2013
193
Poster Sessions P3
P3-d1-1222
Poster sessions | P3
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Bone, Growth Plate and Mineral Metabolism 7
Session title: P3-d1-1224
Juvenile hypoparathyroidism Said Azzoug, Faiza Boutekdjiret, Mohamed Bendali, Farida Chentli Algiers, Algeria P3-d1-1225
Tumor-associated FGF-23 induced hypophosphatemic rickets in an 8-year-old boy Marie-Anne Burckhardt, Alexandra Schifferli, Andreas H. Krieg, Daniel Baumhoer, Christoph Rudin, Gabor Szinnai Basel, Switzerland P3-d1-1226
A 5-year-old boy with massive osteolysis and hypophosphatemic rickets Takeshi Sato1, Koji Muroya1, Junko Hanakawa1, Yumi Asakura1, Yukichi Tanaka1, Ryuji Fukuzawa2, Jiro Machida1, Gen Nishimura2, Tomonobu Hasegawa3, Masanori Adachi1 1 Yokohama, Japan, 2Fuchu, Japan, 3Shinjuku, Japan P3-d1-1227
Acute vitamin D intoxication in three children: unproven manufacturing error of unique multivitamin preparation Ahmet Anik, Gönül Catli, Ayhan Abaci, Ceyhun Dizdarer, Ece Bober Izmir, Turkey P3-d1-1228
The management of osteogenesis imperfecta in the South-West part of Romania in different ethnic groups Giorgiana Flavia Brad, Otilia Marginean, Calin Marius Popoiu, Oana Belei, Vlad David, Andreea Dobrescu Timisoara, Romania P3-d1-1229
Evaluation of two different pamidronate treatment protocols in children with osteogenesis imperfecta Fatih Gurbuz, Neslihan Onenli Mungan, Ozden Ozgur, Eda Mengen, Ali Kemal Topaloglu, Bilgin Yuksel Adana, Turkey P3-d1-1230
Caffey disease with R836C COL1A1 mutation: a case report Shan Huang, Yan Liang, Qin Ning, Xiao-Ping Luo Wuhan, China P3-d1-1231
Poster Sessions P3
An unusual presentation of PHEX mutated X-linked hypophosphatemic rickets in a child Sarar Mohamed, Nasir Al-Juryyan, Rana Hasanato, Amir Babiker, Hessah Al-Otibi, Amal Al-Hakamy, Abdelrahman Al-Nemri, Mustafa A.M. Salih Riyadh, Saudi Arabia P3-d1-1232
Novel PHEX gene mutation in a Korean family with X-linked hypophosphatemic rickets Kyoungsoon Cho Seoul, Republic of Korea P3-d1-1233
Bilateral slipped capital femoral epiphysis with vitamin D deficiency and extremely high levels of parathyroid hormone in a 7-year-old boy Yelena S. Nicholson Dayton, USA
194
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
P3-d1-1234
Bone mineral density in Turner syndrome Montasser Nadeem, Edna F. Roche Dublin, Ireland P3-d1-1235
Cinacalcet in management of hypophosphatemic rickets one week after treatment Aristotle Panayiotopoulos1, Divya Khurana1, Amrit Bhangoo2, Svetlana Ten1 1 Brooklyn, USA, 2Long Beach, USA
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d2 Bone, Growth Plate and Mineral Metabolism 8
Session title: P3-d2-1236
A rare case of severe hypocalcaemia in an infant Ramona Stroescu, Teofana Bizerea, Otilia Marginean, Elena Pop, Ioana Micle Timisoara, Romania P3-d2-1237
Cardiac evaluation of paediatric patients with hypophosphatemic rickets Takashi Hamajima, Masako Izawa, Hidenori Tada, Yuki Naruse, Sayaka Mii, Kazushi Yasuda Obu, Japan P3-d2-1238
Vitamin D deficiency and secondary hyperparathyroidism among schoolchildren of Ukraine Vladyslav Povoroznyuk, Oleksandra V. Tyazhka, Nataliya I. Balatska, Tetyana V. Budnik, Inga V. Kubey, Nataliya B. Haliyash Kyiv, Ukraine P3-d2-1239
Urinary calcium to creatinine ratio is valuable in detecting secondary hyperparathyroidism in patients with abnormal vitamin D metabolism Kentaro Miyai1, Toshikazu Onishi1,2, Kenichi Kashimada1,3, Yukihiro Hasegawa1 1 Tokyo, Japan, 2Itami, Japan, 3Tsuchiura, Japan P3-d2-1240
Infantile malignant osteopetrosis: case report Nevenka Slaveska, Marina Krstevska-Konstantinova, Zoran Trajkovski Skopje, The Former Yugoslav Republic of Macedonia P3-d2-1241
Vitamin D deficiency in girls with Turner syndrome Bensalah Meriem, Benaissa Assia, Ouldkablia Samia, Kemali Zahra Algiers, Algeria Vitamin D status in Irish children and adolescents: value of fortification and supplementation Aoife Carroll, Malachi J. Mc Kenna, Ethna O’Shea, Philip Mayne, Eleanor J. Molloy, Nuala P. Murphy Dublin, Ireland P3-d2-1243
Aetiology of hypoparathyroidism in a region of North Africa with high consanguinity Bouferoua Fadila, Mohamed El Mokhtar Khiari Algiers, Algeria P3-d2-1244
Cinacalcet has a limited effect in hyperparathyroidism secondary to X-linked hypophosphatemic rickets: a case report Kaori Kawano, Keisuke Yoshii, Kiyomi Horiuchi, Makiko Osawa Tokyo, Japan
9th Joint Meeting of Paediatric Endocrinology 2013
195
Poster Sessions P3
P3-d2-1242
Poster sessions | P3
P3-d2-1245
Hungry bone treatment in one child with malignant hypercalcaemia due to pareneoplastic syndrome in acute lymphoid leukaemia Alejandra Valencia1, Juan P. Llano1, Juan J. Lammoglia1, Liliana Mejia2 1 Bogota, Colombia, 2Cali, Colombia P3-d2-1246
Refractory hypocalcaemia induced by influenza virus in primary hypoparathyroidism Maria C. Maggio, Giovanni Corsello Palermo, Italy P3-d2-1247
Pseudohypoparathyroidism: case report in paediatrics Liliana Mejia de Beldjenna1, Juan J. Lamoglia2, Audrey Matallana1 1 Cali, Colombia, 2Bogotá, Colombia P3-d2-1248
Risedronate in the ambulatory management of infant and child with osteogenesis imperfecta in a country with difficult access to pamidronate Juan J. Lammoglia1, Laura Forero1, Juan Pablo Llano1, Liliana Mejia2 1 Bogota, Colombia, 2Cali, Colombia
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Endocrine Oncology 2
Session title: P3-d1-1249
Incidence and risk factors for ovarian failure after haematopoietic stem cell transplantation Dorine Bresters, Joyce A.M. Emons, Nardin Nuri, Lynn M. Ball, Wouter J.W. Kollen, Sabine E. Hannema, J. G. Bom van der, Wilma Oostdijk Leiden, Netherlands P3-d1-1250
A rare case of Cushing syndrome by ectopic ACTH Lilian Argentino Pinchiari, Talita Cordeschi, Monica Mota Lima, Luciana Felipe Férrer Aragão, Renata Nobile, Thais Della Manna, Hilton Kuperman, Hamilton Cabral De Menezes Filho, Vaê Dichtchekenian, Louise Cominato, Leandra Steinmetz, Nuvarte Setian, Durval Damiani São Paulo, Brazil P3-d1-1251
Endocrine complications and parameters of metabolic syndrome in survivors of childhood solid tumors Shlomit Shalitin1,2, Elad Laur2, Yacob Goshen1,2, Yael Lebenthal1, Shifra Ash1,2, Isaac Yaniv1,2, Moshe Phillip1,2 1 Petah Tikva, Israel, 2Tel Aviv, Israel
Poster Sessions P3
P3-d1-1252
Birth parameters and neoplasm diseases in children Anna Malczewska, Magdalena Jarzynska, Lukasz Marchwiński, Jerzy Szymocha, Ewa Barg Wroclaw, Poland P3-d1-1253
Evaluation of electrolyte serum levels and inflammatory parameters in children with newly diagnosed acute leukaemias Anna Malczewska, Magdalena Jarzynska, Lukasz Marchwiński, Jerzy Szymocha, Ewa Barg Wroclaw, Poland P3-d1-1254
Ectopic ACTH syndrome in a child, caused by yolk sac tumor Oleg Malievsky, Vladimir Makhonin, Dilara Nurmukhametova, Alexander Arzamascev Ufa, Russian Federation
196
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
P3-d1-1255
Paediatric craniopharyngiomas Nassima Belhadj Aissa, Said Azzoug, Saida Kabour, Saida Fedala, Farida Chentli Algiers, Algeria P3-d1-1256
The first report of cabergoline-induced immune haemolytic anaemia in an adolescent with prolactinoma Bilgin Yuksel, Fatih Gurbuz, Begul Yagcı Kupeli, Yılmaz Kor, Suzan Zorludemir, Serhan Kupeli Adana, Turkey P3-d1-1257
Low level of vitamin D in children with newly diagnosed neoplasm diseases? Ewa Barg, Karolina Galant, Anna Malczewska, Bernarda Kazanowska Wrocław, Poland
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Fat Metabolism, Obesity 13
Session title: P3-d1-1258
Metabolic differences between prepubertal and pubertal obese children Mirjana Kocova, Elena Sukarova-Angelovska, Milica Tanaskoska, Snezana Palchevska Skopje, The Former Yugoslav Republic of Macedonia P3-d1-1259
How early is dyslipidaemia among obese children in the age group of 6 to 18 years among North Indian population? Sangeeta Yadav, T. Aravind Yadav, Smita Kaushik, Mukta Mantan New Delhi, India P3-d1-1260
Is early age at adiposity rebound a risk factor of obesity in pubertal stage? Olga Zagrebaeva, Anzhalika Solntsava, Katerina Konchits Minsk, Belarus P3-d1-1261
Vitamin D deficiency and metabolic syndrome in obese children Irina Nikitina, Anastasia Todieva, Tatiana Karonova Saint Petersburg, Russian Federation P3-d1-1262
Type 2 diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and Prader-Willi like phenotype Stefano Stagi1, Elisabetta Lapi1, Marilena Pantaleo1, Maria Parpagnoli1, Francesco Chiarelli2, Maurizio de Martino1, Salvatore Seminara1 1 Florence, Italy, 2Chieti, Italy P3-d1-1263
Poster Sessions P3
Partial lipodystrophy in a 12-year-old African-American male Divya Khurana, Aristotle Panayiotopoulos, Natalia Marks, Mark Flyer, Svetlana Ten Brooklyn, USA P3-d1-1264
A review of childhood obesity seen at a tertiary Children’s Hospital Azriyanti Anuar1,2, Helen Wolfenden1, Tafadzwa Makaya1, Fiona Ryan1 1 Oxford, UK, 2Kuala Lumpur, Malaysia P3-d1-1265
The role of spontaneous physical activity on obese children´s health Andrea Di Blasio1, Rita Capanna2, Elena Di Pietro3, Elisabetta Modestini3, Francesco Di Donato1, Mario Di Pietro3 1 Chieti, Italy, 2S. Omero, Italy, 3Atri, Italy
9th Joint Meeting of Paediatric Endocrinology 2013
197
Poster sessions | P3
P3-d1-1266
Using cutaneous signs as clinical markers for metabolic complications in a group of overweight and obese children Mirela Mogoi, Iulian Velea, Corina Paul Timisoara, Romania P3-d1-1267
Body composition and links with cardiovascular risk factors in childhood obesity Antonio Alcoba Conde, Javier Caballero-Villarraso, Virginia Moreno-Moral, María D. Cañete-Vázquez,, Diego Rodríguez-Cano, Ramón Cañete Córdoba, Spain P3-d1-1268
Lifestyle programme for healthy living in childhood François P.R. de Villiers Pretoria, South Africa P3-d1-1269
Medical and psychosocial implications of adolescent extreme obesity – acceptance and effects of structured care study – a consortium of the BMBF competence network obesity Annika Bickenbach1, Belinda Lennerz2, Anja Moss2, Alex Geisler3, Reinhard W. Holl2, Rolf Holle4, Wieland Kiess5, Yvonne Mühlig6, Madlen Neef5, Claudia Ose6, Thomas Reinehr3, André Scherag6, Christina M. Teuner4, Barbara Wolters3, Susanna Wiegand1, Johannes Hebebrand6, Martin Wabitsch2 1 Berlin, Germany, 2Ulm, Germany, 3Datteln, Germany, 4München, Germany, 5Leipzig, Germany, 6Essen, Germany P3-d1-1270
Profile of circulating cytokines (IL-1α, IL-β, IL-2, IL-6, TNF-α, IFN-γ) in disturbances of body weight in children: anorexia nervosa vs. obesity Katarzyna Ziora1, Marta Swider2, Joanna Oswiecimska1, Bogdan Mazur1, Pawel Matusik3, Ewa Malecka-Tendera3 1 Zabrze, Poland, 2Ruda Slaska, Poland, 3Katowice, Poland
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d2 Fat Metabolism, Obesity 14
Session title: P3-d2-1271
An example of a nutritional assessment tool Raluca Pop, Ionela Pascanu, Ana Maria Pitea, Oana Marginean Tirgu Mures, Romania P3-d2-1272
Fast-food consumption frequency and the influence on children´s nutritional profile Ana Carolina Vieira Porto, Bianca Araújo Barbosa Pires, Simone Côrtes Coelho Duque de Caxias, Brazil
Poster Sessions P3
P3-d2-1273
School results, self-esteem and quality of life in overweight children aged 11 Christelle Charles, Anne-Marie Bertrand, Sylvain Quinart, Pierre Rohrlich, Veronique Negre Besancon, France P3-d2-1274
Gestational diabetes and obesity Rosaura Leis1, Adriana Rodríguez1, Sabela Fariña1, Concepción M. Aguilera2, Mercedes Gil-Campos3, Gloria Bueno4, Josune Olza2, Nazareth Martinón1, Vanesa Crujeiras1, Lidia Castro1, Rocío Vázquez1, Rafael Tojo1 1 Santiago de Compostela, Spain, 2Granada, Spain, 3Córdoba, Spain, 4Zaragoza, Spain P3-d2-1275
Changes of body composition indicators in pubertal children with alimentary obesity Hanna Mikhno, Angelika Solntsava Minsk, Belarus
198
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
P3-d2-1276
Metabolic syndrome in obese Peruvian adolescents 10 to 16 years of age, attending the Instituto Nacional de Salud del Niño in Lima – Peru Juan Falen Boggio, Luis Rivero Dávila, Lourdes Rodríguez Temoche, Ana Rivero Monteagudo, Martín Rodríguez Cabrera, Carlos Del Águila Villar Lima, Peru P3-d2-1277
Endocrine disorders in a series of Prader-Willi syndrome patients Andreea I. Dobrescu, Adela Chirita-Emandi, Maria Puiu, Corina Pienar, Otilia Marginean Timisoara, Romania P3-d2-1278
Correlation between level of 25(OH)D and body mass index in adolescents in Manado Nanik Rahayu1, Vivekenanda Pateda1,2, Adrian Umboh1 1 Manado, Indonesia, 2Jakarta, Indonesia P3-d2-1279
Maternal child abuse as an unusual cause of exogenous obesity Zerrin Orbak Erzurum, Turkey P3-d2-1280
The importance of weight loss in treating PCOS in an adolescent girl Iliana Christaki, Elpis Vlachopapadopoulou, Irene Kaloumenou, Feneli Karachaliou, Stefanos Michalacos Athens, Greece P3-d2-1281
Carotid intima-media thickness, gender and age distribution in obese children Rada S.P. Petrovic1, Sajic Silvija2, Merkovic Slavica3, Lesovic Snezana4 1 Cacak, Serbia, 2Belgrade, Serbia, 3Kragujevac, Serbia, 4Zlatibor, Serbia P3-d2-1282
Neonatal hypotonia as an indicator for early diagnosis of Prader-Willi syndrome
Maria Chueca, Maria A. Ramos, Sara Berrade, Javier Guibert, Maria E. Yoldi, Alvarez Jorge, Mirentxu Oyarzabal
Pamplona, Spain P3-d2-1283
Comparative assessment of metabolic syndrome incidence in obese adolescents Shahnoza Sh. Azimova, Gulnara N. Rakhimova Tashkent, Uzbekistan P3-d2-1284
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 GH and IGF Physiology and Treatment 7
Session title:
Poster Sessions P3
The prevalence of obesity and overweight in children and adolescents Oleg Malievsky, Nataly Maslova Ufa, Russian Federation
P3-d1-1285
Growth hormone treatment of patients with Fanconi anaemia after haematopoietic cell transplantation Anna Petryk, Lynda E. Polgreen, Bradley S. Miller, Margaret L. MacMillan, John Wagner Minneapolis, USA P3-d1-1286
Analysis of efficacy and security of long-term GH treatment in small for gestational age patients Juan P. Lopez-Siguero1, Noemi A. Fuentes-Bolaños2, Isabel Leiva1, Maria J. Martínez-Aedo1 1 Malaga, Spain, 2Badajoz, Spain
9th Joint Meeting of Paediatric Endocrinology 2013
199
Poster sessions | P3
P3-d1-1287
Final height in Silver-Russell syndrome patients treated with growth hormone Amaia Vela, Anibal Aguayo, Gema Grau, Amaia Rodriguez, Itxaso Rica Barakaldo, Spain P3-d1-1288
Development of antibodies against growth hormone during rhGH therapy in a girl with idiopathic GH deficiency: a case report Cristina Meazza1, Michael Schaab2, Sara Pagani1, Valeria Calcaterra1, Elena Bozzola3, Juergen Kratzsch2, Mauro Bozzola1 1 Pavia, Italy, 2Leipzig, Germany, 3Rome, Italy P3-d1-1289
Long-term metabolic effects of two growth hormone doses in short Japanese children born small for gestational age Reiko Horikawa1, Susumu Yokoya1, Toshiaki Tanaka1, Yoshihisa Ogawa1, Fumiaki Kiyomi1, Anne-Marie Kappelgaard2 1 Tokyo, Japan, 2Søborg, Denmark P3-d1-1290
Investigating growth hormone deficiency: is our practice evolving? Scott T.C. Shepherd, Angela Lucas-Herald, Avril Mason, Phey M. Yeap, Jane McNeilly, Malcolm C. Donaldson, S. Faisal Ahmed, M. Guftar Shaikh Glasgow, UK P3-d1-1291
Effect of zinc supplementation on growth hormone-insulin growth factor axis in short Egyptian children with zinc deficiency Raha Hamza, Amira Hamed, Mahmoud Sallam Cairo, Egypt P3-d1-1292
Optimizing growth hormone therapy by dose titration in short children born small for gestation age Kitaro Kosaka, Satoru Sugimoto, Ikuyo Ito, Hisakazu Nakajima, Hajime Hosoi, Toru Yamamoto Kyoto, Japan P3-d1-1293
Two cases of maternal uniparental disomy of chromosome 14 presenting with scoliosis during growth hormone therapy Hidetoshi Sato, Keisuke Nagasaki, Yohei Ogawa, Toru Kikuchi, Akihiko Saitoh Niigata, Japan P3-d1-1294
Growth and biochemical response in short small for gestational age children during the first year of growth hormone treatment Maria J. Korpal-Szczyrska Gdansk, Poland
Poster Sessions P3
P3-d1-1295
Cardiovascular risk factors in children with growth hormone deficiency: effect of a 12-month GH treatment Stefania De Marco, Valentina Chiavaroli, Chiara De Leonibus, Ilaria Di Giovanni, Tommaso de Giorgis, Francesco Chiarelli, Angelika Mohn Chieti, Italy
200
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d2 GH and IGF Physiology and Treatment 8
Session title: P3-d2-1296
Anthropometric characteristics, clinical findings, and growth hormone responses of children with bioinactive growth hormone Veysel Nijat Baş, Sebahat Yilmaz Agladioglu, Asan Onder, Havva Nur Peletek Kendirci, Semra Çetinkaya, Zehra Aycan Ankara, Turkey P3-d2-1297
Safety profile of biosimilar growth hormone in children María José Rivero, María José Alcázar, Constanza Navarro, María Sanz Fuenlabrada, Spain P3-d2-1298
Growth hormone testing – reducing the need for a second test for the diagnosis of isolated growth ormone deficiency Zain Juma, Renuka P. Dias, Jeremy M.W. Kirk Birmingham, UK P3-d2-1299
Growth hormone therapy and Legg-Calvé-Perthes disease. Casual or causal relation? María José Rivero Martín, Cristina Salvador, María José Alcázar, Constanza Navarro, María Sanz Fuenlabrada, Spain P3-d2-1300
One year treatment with recombinant human growth hormone in a group of children with short stature: results from the DATAC study Amparo Rodriguez1, Maria Dolores Rodriguez-Arnao1, Jose Luis Lechuga2, Angela Dominguez3, Sofia Quinteiro3, Maria Jose Martinez-Aedo4, Cesar Garcia-Rey1, on behalf of the DATAC Group 1 Madrid, Spain, 2Cadiz, Spain, 3Las Palmas de Gran Canaria, Spain, 4Malaga, Spain P3-d2-1301
Growth hormone treatment in a boy with Becker muscular dystrophy Rossella Gaudino1, Claudia Anita Piona1, Grazia Morandi1, Evelina Maines1, Orsiol Pepaj1, Claudia Banzato1, Elena Monti2, Paolo Cavarzere1, Franco Antoniazzi1 1 Verona, Italy, 2Legnago, Italy P3-d2-1302
Somatotrope axis evaluation in a group of patients with Cornelia de Lange syndrome María Del Rosario Alicia Vicente Gabás, Carolina Baquero Montoya, María C. Gil Rodríguez, María Hernández Marcos, María E.T. Rodrigo, Beatriz Puisac Uriol, Inés Bueno Martínez, Juan P. Juste, Jesús M. Garagorri Otero, Feliciano J. Ramos Fuentes, Gloria Bueno Lozano Zaragoza, Spain P3-d2-1303
Poster Sessions P3
Idiopathic growth hormone insensitivity Jason M. Yates1, Mark Harris1, Kerry Buchanan2, Vivian Hwa3, Ron Rosenfeld3, Andrew Cotterill1, Gary Leong1 1 South Brisbane, Australia, 2Brisbane, Australia, 3Portland, USA P3-d2-1304
Neurofibromatosis type I and endocrine disorders Ali El Mehdi Aem Haddam, Nora Soumeya N. Fedala, Djamila D. Meskine, Farida F. Chentli, Naziha Ns Fedala Algiers, Algeria P3-d2-1305
Metabolic impact of GH deficiency in children Nora Soumeya N.S. Haddam, Ali El Mehdi Haddam, Farida Chentli, Naziha Fedala Algiers, Algeria
9th Joint Meeting of Paediatric Endocrinology 2013
201
Poster sessions | P3
P3-d2-1306
Growth hormone deficiency in a girl with Killian Pallister syndrome Elena Sukarova-Angelovska, Mirjana Kocova, Natalija Angelkova Skopje, The Former Yugoslav Republic of Macedonia P3-d2-1307
The efficiency of treatment with growth hormone replacement therapy in children with idiopathic growth hormone deficiency in Albania Adela Shkurti Tirana, Albania
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d3 GH and IGF Physiology and Treatment 9
Session title: P3-d3-1308
Growth hormone treatment in children with cystic fibrosis born small for gestational age Marina Krstevska Konstantinova, Stojka Fustic, Nevenka Slaveska, Lidija Seckova, Aleksandra Jancevska, Zoran Gucev Skopje, The Former Yugoslav Republic of Macedonia P3-d3-1309
Multiple dose trial of long-acting growth hormone (NNC0195-0092) in Japanese and non-Asian healthy subjects Michael Højby Rasmussen, Minna B. Olsen Soborg, Denmark P3-d3-1310
Divergent response to growth hormone therapy in 2 siblings with SHOX haploinsufficiency Guy Massa1, Elfride De Baere2, Geert Mortier3 1 Hasselt, Belgium, 2Ghent, Belgium, 3Antwerp, Belgium P3-d3-1311
Effect of GH treatment on height velocity of children with pycnodystosis Zohreh Karamizadeh, Homa Ilkanipoor, Fereshte Bagheri Shiraz, Islamic Republic of Iran P3-d3-1312
Morphological findings of pituitary in patients with growth hormone deficiency and correlation with height standard deviation score before treatment, 6 months and 12 months after treatment Maria Claudia Schmitt-Lobe, Luana Xavier Guirado, Romulo Pamplona Schramm Blumenau, Brazil
Poster Sessions P3
P3-d3-1313
Paediatric patients diagnosed with small for gestational age, growth hormone deficiency, and idiopathic short stature fulfilling birth weight criteria for SGA status: results from the ANSWER program® Robert Rapaport1, Peter Lee2, Judith Ross3, John Germak4 1 New York, USA, 2Hershey, USA, 3Philadelphia, USA, 4Princeton, USA P3-d3-1314
Switching to Omnitrope® from other recombinant human growth hormone therapies: a retrospective study in an integrated healthcare system Nazia Rashid1, Yi-Lin Wu1, Woehling Heike2, Paul Saenger3, Fima Lifshitz4, Michael Muenzberg2, Matthew Frankel5, Robert Rapaport6 1 Downey, USA, 2Holzkirchen, Germany, 3Bronx, USA, 4Santa Barbara, USA, 5Princeton, USA, 6 New York, USA P3-d3-1315
Efficacy and safety of recombinant human growth hormone therapy for 155 children with short stature Ruimin Chen, Ying Zhang, Xiaohong Yang, Xiangquan Lin Fuzhou, China
202
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
P3-d3-1316
System construction for quality assurance, quality assessment and quality control of clinical medical examination process of short stature with growth hormone replacement therapy using the patient condition adaptive path system and electrical medical record Takanori Motoki1, Ei-Ichi Wake1, Ayako Ozawa1, Erina Ono1, Ken Sakurai1, Yoshihiro Saito1, Toshio Katsunuma1, Takanori Minoura2, Tohru Kobayashi3, Masako Fujiwara1, Ichiro Miyata1, Satoko Tsuru1, Hiroyuki Ida1, PCAPS Study Group 1 Tokyo, Japan, 2Sendai, Japan, 3Toronto, Canada P3-d3-1317
Growth hormone treatment in short stature children born small for gestational age Elisa Guidoni, Renato Scarinci, Marco Lucherini, Giovanna Municchi Siena, Italy P3-d3-1318
Comparison of growth patterns between patients with congenital MPHD and those due to an abnormal delivery Zvi Laron, Hadar Haim, Peal Lilos, Rivka Kauli Petah Tikva, Israel P3-d3-1319
Clinical features and vitamin D levels in paediatric patients with growth hormone deficiency Snijezana Hasanbegovic Sarajevo, Bosnia and Herzegovina
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Glucose Metabolism 15
Session title: P3-d1-1320
Extra-hepatic portal vein obstruction and type 1 diabetes in a child: a co-incidence or causal association? Rakesh Kumar, Devi Dayal Chandigarh, India P3-d1-1321
Helicobacter pylori infection and metabolic control in young type 1 diabetes mellitus patients Lara V. Marçal1, Poliana H. Ueno1, Letícia T. E. Silva1, Jacqueline D. Tibúrcio2, José N. Januário1, Dulciene M. De M. Queiroz1, Ivani N. Silva1 1 Belo Horizonte, Brazil, 2São João Del Rei, Brazil P3-d1-1322
Warts of the fingertips in a paediatric diabetic patient Carla Minutti, Teresa Alesia Maywood, USA Frequency of skin alterations in children and adolescents with type 1 diabetes and insulin pump treatment Sabine E. Hofer, Elisabeth Binder, Dagmar Meraner, Christine Moser, Olga Lange, Elisabeth Steichen Innsbruck, Austria P3-d1-1324
Permanent neonatal diabetes mellitus due to insulin gene mutation in northeast of Thailand: case report Jaturat Petchkul Ubonratchathani, Thailand P3-d1-1325
Clinical and genetic characteristics of diabetes mellitus in adolescents in Siberia Alla Ovsyannikova, Oksana Rymar, Mikhail Voevoda Novosibirsk, Russian Federation
9th Joint Meeting of Paediatric Endocrinology 2013
203
Poster Sessions P3
P3-d1-1323
Poster sessions | P3
P3-d1-1326
Paradoxical hypoglycaemia associated with the use of high dose diazoxide for the treatment of hyperinsulinaemic hypoglycaemia Caroline Ponmani, Hannah Gannon, Khalid Hussain, Senthil Senniappan London, UK P3-d1-1327
Evaluation of DCA Vantage for rapid in-clinic measurement of HbA1c on capillary blood in young patients with type 1 diabetes Houda El Arabi, Dominique Willems, Chritian Mélot, Harry Dorchy Bruxelles, Belgium P3-d1-1328
Hyperinsulinaemic hypoglycaemia associated with a novel mutation in the SCHAD gene Maria V. Karantza1, Evangelos Papakonstantinou1, Arnold W. Strauss2, Angela Hatzaki1, Melpomeni Saklamaki1 1 Athens, Greece, 2Cincinnati, USA P3-d1-1329
Symptomatic cerebral infarction in a child with severe diabetic ketoacidosis Ayla Güven, Suna Hancili, Fatma Dursun, Elif Yüksel Karatoprak, Bülent Taşel Istanbul, Turkey P3-d1-1330
Glycogen storage disease type 0: case report Polina S. Bogdanova, Elena V. Nagaeva, Maria A. Melikian, Ekaterina U. Zakharova, Valentina A. Peterkova Moscow, Russian Federation P3-d1-1331
Treatment with growth hormone for one year in a patient with Fanconi-Bickel syndrome with severe short stature Elsa Puerto, Diego de Sotto, Maria Caimari, M. Dolores Rodrigo, M. Angeles Ruiz, Joan Figuerola Palma de Mallorca, Spain P3-d1-1332
Gut autoimmunity and type 1 diabetes mellitus Zerrin Onal, Semra Gursoy, Atilla Ersen, Hasan Onal, Erdal Adal Istanbul, Turkey
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d2 Glucose Metabolism 16
Session title:
Poster Sessions P3
P3-d2-1333
A diagnostic conundrum: case of diabetes mellitus and deafness in twin boys associated with unusual associations Kamal Weerasinghe, Praveen Jauhari, John Harvey Wrexham, UK P3-d2-1334
Relationship between metabolic control and neurocognitive functions of children with type 1 diabetes mellitus Ozlem Temel, Sibel Tulgar Kınık, Misli Baydogan, Nursel Muratoglu Sahin, Taner Sezer, Fusun Alehan Ankara, Turkey P3-d2-1335
Clinical characteristics, genetics and treatment outcome of 6 patients with congenital hyperinsulinism Huseyin Demirbilek1, Sarah E. Flanagan2, Mehmet Nuri Ozbek1, Riza Taner Baran1, Sian Ellard2, Khalid Hussain2 1 Diyarbakır, Turkey, 2London, UK
204
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
P3-d2-1336
Glibenclamide and repaglinide therapy in two infants with diabetic ketoacidosis and mutation in KCNJ11 gene Maryam Razzaghy-Azar, Mahsa Mohammad Amoli, Ali Talea, Farzaneh Abbasi, Bagher Larijani Tehran, Islamic Republic of Iran P3-d2-1337
Investigation and analysis of the quality of life in children and youth with type 1 diabetes in China Feng Xiong1, Rong Li1, Shun Qing Luo1, Lin Hou2, Ran Xin Chen3, Min Zhu1 1 Chongqing, China, 2WuHan, China, 3Chendu, China P3-d2-1338
Two cases of iliopsoas abscess in adolescents with type 1 diabetes mellitus Vittoria Cauvin, Evelina Maines, Roberto Franceschi, Maria Bellizzi, Annunziata Di Palma Trento, Italy P3-d2-1339
A new de novo mutation in the GCK gene causing MODY2 Alessandro Salina, Concetta Aloi, Nicola Minuto, Sara Bolloli, Marta Marchi, Andrea Accogli, Francesca Lugani, Renata Lorini, Giuseppe d’Annunzio Genoa, Italy P3-d2-1340
Continuous glucose monitoring: our experience in 4 patients with documented or suspect metabolic diseases other than diabetes Albina Tummolo, Federica Ortolani, Maria Pia Natale, Maristella Masciopinto, Sabino Pesce, F. Carella, Cosima Grande, Marcella Vendemiale, Elvira Piccinno, Francesco Papadia Bari, Italy P3-d2-1341
Glycaemic variability assessment in association with physical activity performed by children with type 1 diabetes mellitus during summer camp Nicola Minuto, Annalisa Arrighi, Marta Marchi, Paola Diana, Chiara Russo, Katia Perri, Sara Bolloli, Alessia Omenetti, Luigi Molfetta, Angela Pistorio, Renata Lorini, Giuseppe d’Annunzio Genoa, Italy P3-d2-1342
A case of type 1 diabetes mellitus associated with Turner syndrome Nesibe Akyürek, Mehmet Emre Atabek, Beray Selver Eklioğlu Konya, Turkey P3-d2-1343
Fatal multi-organ failure with onset of diabetes Marcie Drury Brown, David Crudo Winston Salem, USA P3-d2-1344
Dietary habits in children and adolescents with type 1 diabetes using continuous subcutaneous insulin infusion vs. multiple daily injections: a descriptive transverse observational study Andrea E. Scaramuzza, Alessandra Bosetti, Matteo Ferrari, Francesca Platerote, Valentina Comaschi, Francesca Redaelli, Alessandra Gazzarri, Laura De Angelis, Maddalena Macedoni, Elisa Giani, Gian Vincenzo Zuccotti Milan, Italy
Poster Sessions P3
P3-d2-1345
Compliance to treatment among children with type 1 diabetes mellitus: experience in Abakaliki Maryann Ugochi Ibekwe1, Chinwe Flora Ogugua1, Roland Chidi Ibekwe2 1 Abakaliki, Nigeria, 2Enugu, Nigeria
9th Joint Meeting of Paediatric Endocrinology 2013
205
Poster sessions | P3
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d3 Glucose Metabolism 17
Session title: P3-d3-1346
Paediatric hyperglycaemic hyperosmolar non ketotic syndrome: a rare and dangerous diagnosis which has to be known Catherine Piquard Mercier, Ariane Cuny, Agnes Linglart, Pierre Bougnères Kremlin-Bicêtre, France P3-d3-1347
Impact of insulin pump therapy in children and adolescents with type 1 diabetes on long-term metabolic control: a one year follow-up prospective study Nancy Samir Elbarbary Cairo, Egypt P3-d3-1348
Frequency of chronic diabetes complications in children with type 1 diabetes and poor glycaemic control in Ukraine, treated with continuous subcutaneous insulin infusion vs multiple daily insulin injections (results from 3-year follow-up data) Evgenia Globa, Nataliya Zelinskaya, Larisa Nifontova, Nataliya Pogadaeva Kyiv, Ukraine P3-d3-1349
Two families with diabetes mellitus and sensorineural deafness Maha Mohamed Sherif1, Ibtisam Hadeed2, Azizun Nessa1, Sofia A. Rahman1, Ved B. Arya1, Senthil Senniappan1, Mehul Dattani1, Khalid Hussain1 1 London, UK, 2Tripoli, Libyan Arab Jamahiriya P3-d3-1350
Alstrom syndrome: case report of two new cases Vittoria Cauvin, Valentina Viliotti, Roberto Franceschi, Maria Bellizzi, Fiorenza Soli, Francesca Rivieri, Annunziata Di Palma Trento, Italy P3-d3-1351
Glucagon rescue for emergency and surgical rescue in children with congenital hyperinsulinism Juan Javier Lammoglia Bogota, Colombia P3-d3-1352
An infant with transient hypocortisolaemia and hyperinsulinism: a case report Atilla Cayir, Zerrin Orbak, Hakan Doneray, Kadir Tekgunduz, Ibrahim Caner Erzurum, Turkey P3-d3-1353
Poster Sessions P3
Incidence of child immigration and a public awareness campaign in diabetic ketoacidosis debut in Spain Ignacio Diez Lopez, Ainhoa Sarasua Miranda, Isabel Lorente Blazquez, Gaizka Mestraitua Aurrekoetexa, Alfredo Bosque Zabala Vitoria, Spain P3-d3-1354
Uncontrolled diabetes: a difficult mother or a mother in difficulty? Sundeep Sandhu1, Amir Babiker1,2 1 Grimsby, UK, 2Riyadh, Saudi Arabia P3-d3-1355
The level of knowledge on diabetes of children and adolescents with type 1 diabetes mellitus in Uzbekistan Akmaral Tashmanova, Said Ismailov, Gulnara Rakhimova, Anna Alieva Tashkent, Uzbekistan
206
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
P3-d3-1356
Management of a restrictive eating disorder in an adolescent male with insulin dependent diabetes mellitus Betty P. Messazos, Kristen Neville Sydney, Australia P3-d3-1357
The effect of automated bolus calculators on HbA1c in children with type 1 diabetes in Macclesfield Hussain Alsaffar, Thomas Whitby, Surendran Chandrasekaran Macclesfield, UK P3-d3-1358
Clinical study of behavioural problems among children with type 1 diabetes mellitus in Minia governorate, Egypt Basma Abd El Moez Ali, Diaai Ali Mahmoud, Maha Ali Hassen, Haidy Nabil Sedky Minia, Egypt
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1
Session title:
Growth 7
P3-d1-1359
Children of mothers with pre-gestational and gestational diabetes tend to be overweight at age 17 Alon Farfel1,2, Rona Rabinovitz1, Gadi Kampino2, Dorit Tzur2, Estela Derazne2, Tami Laron-Kenet1, Zvi Laron1 1 Petah Tikva, Israel, 2Tel Hashomer, Israel P3-d1-1360
Establishment and validation of a new cut-off concentration for growth hormone stimulation tests in children Isabel Viola Wagner1, Claudia Petzold1, Ruth Gausche1, Mandy Vogel1, Antje Koerner1, Joachim Thiery1, Wieland Kiess1, Christian Gabriel Arsene2, Arne Henrion2, Roland Pfaeffle1, Jürgen Kratzsch1 1 Leipzig, Germany, 2Braunschweig, Germany P3-d1-1361
Do children with 1p36 deletion deserve growth hormone treatment? Panagiota Triantafyllou, Dimitrios Zafeiriou, Athanasios Christoforidis Thessaloniki, Greece P3-d1-1362
Absence or reduction of the physiological catch-up growth after adoption in internationally adopted children exposed to alcohol in utero Raffaele Virdis1, Silvia Cesari1, Rossella Quarta Colosso1, Maria Gugliotta1, Cesare Terzi1, Livia Garavelli2, Maria E. Street1 1 Parma, Italy, 2Reggio Emilia, Italy GH deficiency in patients with Noonan syndrome: growth response to rhGH therapy related to the genotype Francesca Marabotto1, Alexandra Madè1, Lorenzo Andrea Bassi1, Giulia Rossetti1, Giovanni Pieri1, Ilaria Brambilla1, Patrizia Bulzomì1, Paola Riva2, Mariangela Cisternino1 1 Pavia, Italy, 2Milan, Italy P3-d1-1364
The long-term effects of recombinant growth hormone therapy on growth and glucose homeostasis in poorly growing children with inflammatory bowel disease Mabrouka M. Al Towati1, Jarod Wong1, Peter J. Galloway2, Jo C. Blair2, Richard K. Russell1, Paraic McGrogan1, Faisal S. Ahmed1 1 Glasgow, UK, 2Liverpool, UK
9th Joint Meeting of Paediatric Endocrinology 2013
207
Poster Sessions P3
P3-d1-1363
Poster sessions | P3
P3-d1-1365
Sleep pattern and growth hormone secretion during sleep in short children with and without growth hormone deficiency Betul Ersoy, Hikmet Yilmaz, Fatma Taneli, Gonul Dinc Manisa, Turkey P3-d1-1366
Coeliac disease in idiopathic short stature children Robabeh Ghergherehchi, Mandana Rafeey, Nazanin Hazhir Karzar Tabriz, Islamic Republic of Iran P3-d1-1367
Intermittent rhGH treatment as an alternative to rhIGF-I in a boy with GH1 macrodeletion Soraya L. S. Milani, Rodrigo José Custódio, Sonir R.R. Antonini, Ayrton C. Moreira, Carlos E. Martinelli Jr. Ribeirao Preto, Brazil P3-d1-1368
Growth hormone deficiency in a patient with Gitelman syndrome Ebe D’Adamo1, Fiorenzo Lupi1, Ugo Cavallari1, Carlo Poggiani1, Fabio Buzi2 1 Cremona, Italy, 2Mantova, Italy P3-d1-1369
Height and weight at 6 years of age in children born preterm: preliminary results Adriane Cardoso-Demartini, Francisca de Lara, Antonio Carlos Bagatin, Ana Lúcia Sarquis, Daniela C.A. Schimdtke, Regina P.G.V.C. da Silva, Margaret C.S. Boguszewski Curitiba, Brazil P3-d1-1370
The high incidence of oligosymptomatic gastrointestinal tract diseases in children with short stature of different etiology Renata Stawerska, Joanna Smyczyńska, Maciej Hilczer, Sylwia Prymus, Marzena Kolasa-Kicińska, Alina Durko, Andrzej Lewiński, Elżbieta Czkwianianc Lodz, Poland
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d2
Session title:
Growth 8
P3-d2-1371
Racial/ethnic differences in perceived barriers to short stature evaluation and treatment Adda Grimberg, Pamela Cousounis, Terri H. Lipman, Andrew J. Cucchiara, Kenneth R. Ginsburg Philadelphia, USA
Poster Sessions P3
P3-d2-1372
Clinical, biochemical and radiological manifestations of newborns with hypocalcaemia due to vitamin D deficiency Ashraf Soliman1, Hossam Salama1, Emad Shatla1, Safwan Alomar1, Elsaid Bedair2, Aml Sabt1 1 Doha, Qatar, 2Alkhor, Qatar P3-d2-1373
12q subtelomere deletion in a child with delayed psychomotor development, food seeking behavior, obesity, growth retardation and congenital heart defect Mette Madsen1, Else Marie Vestergaard2, Rikke Christensen2, Mariane Rix1 1 Aalborg, Denmark, 2Aarhus, Denmark P3-d2-1374
Linear growth after paediatric liver transplantation Ashraf Soliman, Wail Saleem, Hatem Abdelrahman, Aml Sabt Doha, Qatar
208
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
P3-d2-1375
Three years of growth hormone therapy in children with growth deficiency Corina Galesanu, Andra Iulia Loghin, Luminita Apostu, Didona Ungureanu, Mihail Romeo Galesanu Iasi, Romania P3-d2-1376
Etiologic analysis of 1023 children with short stature in Shanghai China Dijing Zhi, Shuixian Shen, Zhuhui Zhao, Feihong Luo, Rong Ye, Ruoqian Chen, Zhong Lu Shanghai, China P3-d2-1377
Can only local IGF-I hold normal growth during pubertal spurt? Soraya L.S. Milani, Thiago Hirose, Emiliana Ribeiro, Raphael Del R. Liberatore Jr, Francisco J. Paula, Carlos E. Martinelli Jr Ribeirao Preto, Brazil P3-d2-1378
Childhood growth in female patients with congenital hypogonadotropic hypogonadism Matti Hero, Eeva.Maria Laitinen, Varimo Tero, Johanna Tommiska, Taneli Raivio Helsinki, Finland P3-d2-1379
Primary hypertrophic arthritis in differential diagnosis of acromegaly – case report Urszula Wątrobińska1, Elżbieta Moszczyńska1, Mieczysław Szalecki1,2 1 Warsaw, Poland, 2Kielce, Poland P3-d2-1380
Distinctive craniofacial features associated to cone-shaped epiphyses at the phalanges and short stature: trichorhinophangeal syndrome, type I Cristiane Kopacek, Vinicius Freitas de Mattos, José A. Monteiro Flores, Rafael F. Machado Rosa, Patrícia Trevisan, Victória Bernardes Guimarães, Luciana Amorin Beltrão, Mônica Léon Bacil, Samira Hasan Musa, Paulo R. Gazzola Zen Porto Alegre, Brazil P3-d2-1381
A case of Crouzon syndrome associated to growth hormone deficiency Maria F. Tutera, Francesca Simi, Giuseppe Saggese Pisa, Italy P3-d2-1382
The effect of social environment on height and sexualisation process Eduard Circo, Marian Beciu Constanta, Romania
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d3
Session title:
Growth 9
Long-term follow-up of a case with a clinically recognisable genetic cause of short stature-KBG syndrome Korcan Demir1, Mustafa Tekin2,3, Gonul Catli1, Ayca Altincik1, Ayhan Abaci1, Ece Bober1 1 Izmir, Turkey, 2Miami, USA, 3Ankara, Turkey P3-d3-1384
Turner syndrome: results after three years of growth hormone therapy Andra Iulia Loghin, Corina Galesanu, Luminita Apostu, Didona Ungureanu, Mihail Romeo Galesanu Iasi, Romania P3-d3-1385
Growth hormone treatment in an active paediatric Crohn´s disease Jessica Jaillet1, Philippe Rebaud1, Laure Warin1, Michel Chambon1, Michel David2 1 Villefranche sur Saone, France, 2Lyon, France
9th Joint Meeting of Paediatric Endocrinology 2013
209
Poster Sessions P3
P3-d3-1383
Poster sessions | P3
P3-d3-1386
Coeliac disease and GH deficiency: report of two cases Elisa Guidoni, Renato Scarinci, Marco Lucherini, Giovanna Municchi Siena, Italy P3-d3-1387
Rare genetic mutations in patients with dwarfism Cristina G. Matei, Binu S. Anand Bury St Edmunds, UK P3-d3-1388
Abstract has been withdrawn P3-d3-1389
Saizen®-online: a longitudinal observational study on the efficacy and safety of recombinant human growth hormone for paediatric indications Klaus K.P. Hartmann1, René Ramseger2, Saizen®-online Electronic Observational Study Group 1 Frankfurt am Main, Germany, 2Darmstadt, Germany P3-d3-1390
Acute myocardial infarction in a male adolescent receiving the aromatase inhibitor anastrozole: is there a causal relationship? Ana Colmenares1, Nusen Beer2, Roberto Lanes2 1 San Cristobal, Venezuela, 2Caracas, Venezuela P3-d3-1391
AEG (syndrome syndromic microphtalmia type 3): endocrine involvement in a patient with a new mutation Emanuela Scarano, Federica Tamburrino, Annamaria Perri, Benedetta Vestrucci, Monica Guidetti, Laura Mazzanti Bologna, Italy P3-d3-1392
Growth and puberty abnormalities in a 15-year old boy with partial chromosome 15q26.2-qter trisomy coding gene of IGF1 receptor and chromosome 21p-21q21.2 trisomy excluding Down syndrome critical region – case report Edyta Pietrewicz1, Anna Jakubiuk-Tomaszuk2, Janusz Pomaski1, Ewa Jakubowska1, Beata Sawicka1, Artur Bossowski1 1 Bialystok, Poland, 2Białystok, Poland P3-d3-1393
Subjective global assessment of hospitalized children Lívia Silvério da Rocha, Lucianni Reis Nunes da Silva, Simone Cortes Coelho, Mônica Pinheiro Cantalapiedra, Arlete Aguiar de Carvalho Duque de Caxias, Brazil P3-d3-1394
An unusual same karyotype anomaly in a mother and her two daughters with short stature: 46, X, del(x)(p21 pter) Zerrin Orbak, Sener Tasdemir, Avni Kaya Erzurum, Turkey
Poster Sessions P3
P3-d3-1395
Achondroplasia: about thirteen patients Saraoui F. Fatima, Fedala N.S. Nora Soumeya, Chentli F. Farida Algiers, Algeria
210
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Perinatal and Neonatal Endocrinology 3
Session title: P3-d1-1396
Improved head and linear growth at 36 weeks in extremely preterm infants (< 27 weeks) with early intensified parenteral nutrition Maria Heyman, Barbro Diderholm Uppsala, Sweden P3-d1-1397
Transient abnormalities in brain MRI in a newborn with X-linked congenital adrenal hypoplasia Ana Tangari Saredo1, Sandra Verónica Tilitzky1, Karina Kesler1, Graciela Del Rey1, Roxana Stratico1, Viviana Sanchez1, Fabian Vera1, Andrea Grosse1, Felix Riepe2 1 Buenos Aires, Argentina, 2Kiel, Germany P3-d1-1398
Reversible pulmonary hypertension caused by diazoxide therapy in patients with congenital hyperinsulinism Charles Roitsch, Lisa Tran, Paul S. Thornton Fort Worth, USA P3-d1-1399
Anogenital distances in female and male Nigerian newborns, a descriptive study Olumide O. Jarrett1, Omolola O. Ayoola2, Bjourn Jonsson3, Kerstin Albertsson-Wikland4, Martin Ritzen5 1 Ibadan, Nigeria, 2Manchester, UK, 3Uppsala, Sweden, 4Gothenburg, Sweden, 5Stockholm, Sweden P3-d1-1400
The prevalence of congenital hypothyroidism in the Republic of Bashkortostan, Russia: 20 years of neonatal screening Oleg Malievsky, Galina Pechenina, Dilara Nurmukhametova, Marina Klimentieva Ufa, Russian Federation P3-d1-1401
An interesting presentation of septo-optic dyplasia and panhypopituitarism with collapse and liver failure Delith K. Garrick Doncaster, UK P3-d1-1402
Relation of estimated birth brain weight to circulating insulin-like growth factor binding protein-3 in not-life-threatened newborns: an explanatory role for the part of birth body weight not attributable to estimated birth brain weight is recognisable independently of the presence of caesarean section Cesare Terzi1, Raffaele Virdis1, Werner F. Blum2, Sergio Zani1, Marco Riani1, Gabriele Tridenti3, Andrea Cerioli1, Elena Chesi3, Sergio Bernasconi1, Giacomo Banchini3 1 Parma, Italy, 2Giessen, Germany, 3Reggio Emilia, Italy P3-d1-1403
9th Joint Meeting of Paediatric Endocrinology 2013
Poster Sessions P3
SGA and obesity: the importance of detecting metabolic risk backgrounds Ainhoa Sarasua Miranda, Ignacio Diez Lopez, Marta del Hoyo Moracho Vitoria, Spain
211
Poster sessions | P3
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Pituitary and Neuroendocrinology 5
Session title: P3-d1-1404
Fanconi anaemia presents as short stature in Yemenite siblings Sheila Perez, Nouhad Raissouni, Scott Miller, Elka Jacobson-Dickman Brooklyn, USA P3-d1-1405
Late diagnosis of congenital panhypopituitarism Claudia Hernandez, Daniela Cáceres, Verónica Figueroa, Oscar H. Brunetto Buenos Aires, Argentina P3-d1-1406
Rapid onset obesity, endocrine hypertension and ganglioneuroblastoma intermixed: early manifestation of ROHHAD-NET syndrome? Presentation of two cases Federico Baronio, Angelica Marsigli, Diego Rinaldini, Emanuela Zazzetta, Laura Mazzanti, Antonio Balsamo, Andrea Pession Bologna, Italy P3-d1-1407
Severe hypothalamo-pituitary dysfunction accompanied by influenza-associated encephalopathy Hideaki Yagasaki, Kisho Kobayashi, Tomohiro Saitou, Yusuke Goto, Takayuki Komai, Kanji Sugita Yamanashi, Japan P3-d1-1408
Endocrine management of sellar lesions in children Emilio García-García1, Beatriz González-Aguilera1, Patricia Oliva2, Icíar García-Escobar2, José L. Gómez-Llorente2, Jerónimo Momblan2 1 Sevilla, Spain, 2Almería, Spain P3-d1-1409
Clinical characteristics and evolving syndrome of pituitary stalk interruption Ali El Mehdi Aem Haddam, Nora Soumeya Fedala, Djamila Meskine, Farida Chentli, Naziha Fedala Algiers, Algeria P3-d1-1410
Female paediatric and adolescent prolactinomas Lina Akkache, Katia Daffeur, Hadjer Zellagui, Fetta Amel Yaker, Farida Chentli Algiers, Algeria P3-d1-1411
Endocrine disorders after craniopharyngioma treatment in children: a retrospective study Camila Mascaretti Dias, Hilton Kuperman, Rachel Lana Obata Giroto, Lilian Pinchiari, Caroline Kupsch Medrado, Claudilene Battistin, Leandra Steinmetz, Dichtchekenian Vaê, Thais Della Manna, Hamilton Cabral de Menezes Filho, Louise Cominato, Durval Damiani São Paulo, Brazil
Poster Sessions P3
P3-d1-1412
Paediatric male prolactinomas: response to medical treatment Hadjer Zellagui, Lina Akkache, Katia Daffeur, Fetta Amel Yaker, Farida Chentli Algiers, Algeria
212
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d2 Pituitary and Neuroendocrinology 6
Session title: P3-d2-1413
Diabetes insipidus in a premature infant with severe intraventricular haemorrhage Kathryn Jackson, Ghufran Babar, Figen Ugrasbul Kansas City, USA P3-d2-1414
Obesity in patients with childhood pituitary adenomas is unlikely to be related to treatment or hormone replacement therapies Vassilis Tsitourus, Urmi Das, Poonam Dharmaraj, Mohammed Didi, Ajay Singha, Conor Mallucci, Benedetta Pettorini, Shivram Avula, Laurence Abernethy, Joanne C. Blair Liverpool, UK P3-d2-1415
Syndrome of inappropriate antidiuretic hormone secretion: a challenge in diagnosis and therapy Tânia Martins, Carla Costa, Juliana Oliveira, Ana Teixeira, Raquel Martins, Cíntia Castro-Correia, Manuel Fontoura Porto, Portugal P3-d2-1416
Familial hypopituitarism with pituitary stalk interruption syndrome Meriem Haddad, Abderrahim Bey, Soumeya Fedala, Farida Chentli Algiers, Algeria P3-d2-1417
Pituitary stalk tuberculosis: difficult diagnosis Victor Mendoza Rojas, Ernesto Rueda Arenas, Luis Miguel Sosa Avila Bucaramanga, Colombia P3-d2-1418
Phenotypic and evolutionary diabetes insipidus of childhood Nora Soumeya Ns Fedala, Ali El Mehdi Haddam, Farida Chentli, Naziha Fedala Algiers, Algeria P3-d2-1419
Holoprosencephaly and pituitary deficiency Mohamed Bendali, Said Azzoug, Farida Chentli Algiers, Algeria P3-d2-1420
Hypoglycaemia and hepatic failure in an infant with congenital hypopituitarism Juan J. Lammoglia, Laura Forero, Juan P. Llano Linares, Jose F. Vera Bogota, Colombia Neuropsychiatric symptoms in a patient with short stature with delayed diagnosis due to atypical presentation Juan J. Lammoglia1, Laura Forero1, Juan P. Llano Linares1, Liliana Mejia2 1 Bogota, Colombia, 2Cali, Colombia
9th Joint Meeting of Paediatric Endocrinology 2013
213
Poster Sessions P3
P3-d2-1421
Poster sessions | P3
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Puberty and Gonads 9
Session title: P3-d1-1422
Longitudinal evaluation of patients with autonomous ovarian follicular cysts Haruo Mizuno, Yukari Sugiyama, Kohei Aoyama, Shinji Saitoh Nagoya, Japan P3-d1-1423
Evaluation of adolescent girls with hyperandrogenism Bahar Özcabi, Ayse Tekin, Ferıde Tahmıscıoglu Bucak, Oya Ercan, Olcay Evlıyaoglu Istanbul, Turkey P3-d1-1424
Extreme minipuberty presenting with vaginal bleeding in a 5-month-old preterm girl Kathryn Jackson, Ghufran Babar, Figen Ugrasbul Kansas City, USA P3-d1-1425
An unusual case of primary amenorrhea and short stature: ovarian resistance syndrome Enver Simsek, Cigdem Binay, Baran Tokar, Sare Kabukcuoglu Eskisehir, Turkey P3-d1-1426
Van Wyk Grumbach syndrome: case report Aicha Maiz Hadj Ahmed, Faiza Belhemer, Sihem Belahcene, Farida Chentli Algiers, Algeria P3-d1-1427
Mature teratoma in paediatrics: a case report Liliana Mejia de Beldjenna1, Ana Maria Gomez Vasquez1, Audrey Matallana1, Juan J. Lamoglia2 1 Cali, Colombia, 2Bogotá, Colombia P3-d1-1428
Primary ovarian failure and a successful pregnancy Catarina Moniz, Rute Ferreira, Ricardo Fonseca, Filipa Serra, Carlos Vasconcelos, Machado Saraiva Lisboa, Portugal P3-d1-1429
Premature ovarian failure: management in adolescents Egidijab Bielskute, Vijay Kista Reddy, Gumma Aparna, Vijith Reddy Puthi Peterborough, UK P3-d1-1430
Testosterone level and response to HCG stimulation in children with micropenis Tamunopriye Jaja1,2, Abiola Oduwole1 1 Lagos, Nigeria, 2Port Harcourt, Nigeria
Poster Sessions P3
P3-d1-1431
Premature adrenarche: long-term implications Elpis Vlachopapadopoulou, Iliana Christaki, Irene Kaloumenou, Feneli Karachaliou, Aspasia Fotinou, Marina Vakaki, Stefanos Michalacos Athens, Greece P3-d1-1432
Effects of nourishing “Yin”-removing “Fire” Chinese herbs on the gene translation of hypothalamic ghrelin and its receptor in female precocious rats Yu Jian, Yan Yan Sun, Yong Hong Wang, Jing Li, Zhanzhuang Tian Shanghai, China
214
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d2 Puberty and Gonads 10
Session title: P3-d2-1433
Precocious puberty in a familial type 1 neurofibromatosis case caused by a microdeletion on chromosome 17q11.2 Rita Fischetto1, Federica Ortolani1, Maristella Masciopinto1, Leonardo D’Agruma2, Massimo Carella2, Franca Diquonzo1, Francesco Papadia1 1 Bari, Italy, 2San Giovanni Rotondo, Italy P3-d2-1434
Korean environmental health survey (KorEHS) in children and adolescents focusing on puberty Ji Won Koh1, Jaekyung Kim1, Mina Ha1, Hojang Kwon1, Jong-Han Leem2, Hwan-Cheol Kim2, Seung-Do Yu2, Bo-Eun Lee2, Jeesuk Yu1 1 Cheonan, Republic of Korea, 2Incheon, Republic of Korea P3-d2-1435
Hyperandrogenism and aggression; assessment of anxiety – anger scale in the polycystic ovarian syndrome cases Ayça Törel Ergür, Nurper Erberk Özen, Berk Karaoğlu Ankara, Turkey P3-d2-1436
Clinical features of Kallmann syndrome and the importance of smell test(s) and brain magnetic resonance imaging in diagnosis: report of five adolescents Ahmet Anik, Gonul Catli, Ayhan Abaci, Cagdas Guducu, Handan Guleryuz, Adile Oniz, Sule Can, Bumin N. Dundar, Ece Bober Izmir, Turkey P3-d2-1437
The evaluation of GnRH analog treatment on anterior hypophysis hormones in girls with central precocious puberty Havva Nur Peltek Kendirci, Sebahat Yılmaz Ağladıoğlu, Aşan Onder, Veysel Nijat Baş, Semra Çetinkaya, Zehra Aycan Ankara, Turkey P3-d2-1438
Central precocious puberty and hypobetalipoproteinaemia in a boy with Prader-Willi syndrome Feneli Karachaliou, Irene Kaloumenou, Elpis Vlachopapadopoulou, Anastasia Skouma, Aspasia Fotinou, Stefanos Michalacos Athens, Greece P3-d2-1439
Puberty in obese and overweight boys and adolescents 10- and 15-years-old in YUSAD study Bratimirka M. Jelenkovic1, Ivana Novakovic2, Brankica Vasic1 1 Zajecar, Serbia, 2Belgrade, Serbia An unusual case of bilateral galactocele in a male infant Gülay Karagüzel1, Aysenur Ökten1, Sibel Kul1, Güngör Karagüzel2, Mustafa İmamoglu1 1 Trabzon, Turkey, 2Antalya, Turkey P3-d2-1441
Hormonal and metabolic evaluation of adolescents and young adult women assisted since childhood due to premature adrenarche Beatriz Pires Ferreira, Raphael Melo Franciscon, Joana C. Frare, Patricia Naves, Elisabete Aparecida Mantovani Rodrigues Resende, Flavia Alves Ribeiro, Heloisa M. Cunha Palhares, Maria Fátima Borges Uberaba, Brazil P3-d2-1442
Williams and Beuren syndrome: what about endocrine associations? About 2 cases Leïla Essaddam, Rahma Guedri, Nadia Mattoussi, Ahmed Maherzi, Zohra Fitouri, Saayda Ben Becher Tunis, Tunisia
9th Joint Meeting of Paediatric Endocrinology 2013
215
Poster Sessions P3
P3-d2-1440
Poster sessions | P3
P3-d2-1443
Pseudocyesis as a cause of abdomen enlargement in a female adolescent Veselin Škrabić, Željka Vlastelica Split, Croatia
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d3 Puberty and Gonads 11
Session title: P3-d3-1444
Prevalence of genital abnormalities among Uzbek boys in Tashkent city Gulnara Rakhimova, Kamil Gilyazetdinov Tashkent, Uzbekistan P3-d3-1445
Pubertal disorders by acceleration: behaviour in a population during the period from January 2010 to January 2012 Paola Duran Ventura, Silvia Chahin, Adriana lema, Nancy Bernal, Diana Chacon, Juanita Molina, Lorena Peñalosa Bogota, Colombia P3-d3-1446
Sexual development following exposure to topical testosterone during prepubertal age: a case report Jyotsna Keni, Christine Chou, Anna Pawlikowska-Haddal Los Angeles, USA P3-d3-1447
Aromatase excess syndrome in a family from Santo Domingo, Dominican Republic Elbi A. Morla, Rosario Almanzar, Carmen Rosario Santo Domingo, Dominican Republic P3-d3-1448
Central precocious puberty due to hamartoma Natascha Van Der Werf Grohmann, Andreas Krebs, Thomas Kratzin, Alexandra Krause, Karl Otfried Schwab Freiburg, Germany P3-d3-1449
Virginal breast hypertrophy in a 12-year-old girl: a case report Gülay Karagüzel, Sevcan Bilen, Aysenur Ökten, Ümit Naci Karaçal Trabzon, Turkey P3-d3-1450
Congenital intracranial arachnoid cysts and endocrinological outcomes in a young girl Vjosa Mulliqi Kotori, Afrim Kotori Prishtina, Albania
Poster Sessions P3
P3-d3-1451
Precipitous puberty: pathologic correlations with disturbed ovarian function Eduard Circo Constanta, Romania
216
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1 Sex Differentiation 6
Session title: P3-d1-1452
A 14-year-old patient with X chromosome monosomy mosaic karyotype and male Turner phenotype Karolina Kot, Elzbieta Moszczynska, Krystyna Chrzanowska, Mieczyslaw Szalecki Warsaw, Poland P3-d1-1453
Short stature presenting with 45, X/46, XY mosaicism Mehmet Keskin, Murat Karaoglan, Seval Cevik, Murat Sanlı, Ozlem Keskin Gaziantep, Turkey P3-d1-1454
Profile of 46, XY DSD patients attending a tertiary care hospital: age at presentation and social background Iram Shabir, Marumudi Eunice, Madan L. Khurana, Rajesh Khadgawat, Bindu Kulshreshtha, Ariachery C. Ammini New Delhi, India P3-d1-1455
P.ALA65PRO mutation in a case with 5α-reductase deficiency Aysun Bideci, Esra Döğer, Çelik Nurullah, Hamdi Cihan Emeksiz, Özge Yüce, Orhun Mahmut Çamurdan, Peyami Cinaz Ankara, Turkey P3-d1-1456
Expanding the phenotypic spectrum of the 45,X/46,XY karyotype – ovotesticular disorder of sex development Juliana Gabriel Ribeiro de Andrade, Guilherme Guaragna-Filho, Georgette Beatriz de Paula, Leticia Esposito Sewaybricker, Vanessa Brito Campoy Rocha, Gil Guerra-Junior, Andréa Trevas Maciel-Guerra, GIEDDS Campinas, Brazil P3-d1-1457
Topical testosterone treatment in idiopathic micropenis Atilla Buyukgebiz1, Ayhan Abaci2, Ece Bober1,2 1 Istanbul, Turkey, 2Izmir, Turkey P3-d1-1458
Psychosexual outcomes in 3 siblings with 46, XY DSD: impact of nature versus nurture Angela A. Joseph, Iram Shabir, Eunice Marumadi, Reema Dada, Manju Mehta, Ammini C. Ariachery New Delhi, India P3-d1-1459
46 XX DSD: ambiguity lies where? Surabhi Venkata Satya Krishna, Sunil K.L. Kota, Mohd Khan Yousuf, Kirtikumar D. Modi Hyderabad, India
Poster Sessions P3
P3-d1-1460
A rare case of 46 XX ovotesticular syndrome: delayed diagnosis Beray’ Selver Eklioglu, Mehmet Emre Atabek, Akyurek Nesibe, Mesut Piskin Konya, Turkey
9th Joint Meeting of Paediatric Endocrinology 2013
217
Poster sessions | P3
Session date:
Thursday 19 September (d1), 14:20 – 15:20
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d1
Session title:
Thyroid 9
P3-d1-1461
A case with Graves disease who developed agranulocytosis and vasculitis during metimazole treatment Ozlem Kara, Fatma Demirel, Derya Tepe, Nermin Uncu, Abdullah Kocabas, Ihsan Esen, Gokce Gur Ankara, Turkey P3-d1-1462
Prevalence and etiology of congenital hypothyroidism detected through an Argentine neonatal screening program (1997-2010) Ana Elena Chiesa, Laura B. Prieto, Virginia Mendez, Patricia Papendieck, Maria Lujan Calcagno, Laura Gruñeiro Papendieck Buenos Aires, Argentina P3-d1-1463
Assessment of the current iodine status via determination of the frequency of transient congenital hypothyroidism in the Central Black Sea Region of Turkey Figen Gunindi, Cengiz Kara, Ala Ustyol, Murat Aydin Samsun, Turkey P3-d1-1464
Hypothyroidism as the predominant symptom of Albright hereditary osteodystrophy in two children Anna M. Kucharska, Katarzyna Kadziela Warszawa, Poland P3-d1-1465
Acute suppurative thyroiditis in children Veselin Škrabić, Željka Vlastelica, Ivana Unić Split, Croatia P3-d1-1466
Clinical characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase gene Toru Yamamoto1, Yoshiki Katsumi2, Yoshihiro Kajita2, Hisakazu Nakajima1, Kitaro Kosaka1 1 Kyoto, Japan, 2Nantan, Japan P3-d1-1467
Hyperthyroidism in the absence of thyroid stimulating immunoglobulins in a 5-year-old girl Adalbert Raimann, Alexandra Ertl, Gabriele Haeusler Vienna, Austria P3-d1-1468
Graves disease: clinical and therapeutic aspects in 16 paediatric patients Joice Marquez, Talita Cordeschi, Caroline De Gouveia Buff Passone, Daniela Martins Airoldi, Hamilton Cabral Menezes-Filho, Hilton Kuperman, Vaê Dichtchekenian, Durval Damiani São Paulo, Brazil
Poster Sessions P3
P3-d1-1469
Early diagnosed Hashimoto thyroiditis in a context of familial autoimmunity Laure Warin1, Jessica Jaillet1, Claire-Lise Gay2, Edwige Dornier1, Michel David2, Philippe Rebaud1 1 Villefranche sur Saône Cedex, France, 2Lyon, France P3-d1-1470
Diagnosis of papillary carcinoma in paediatric patients with 99mTc scan hyperfunctioning thyroid nodules in a iodine sufficient area Ana Tangari Saredo, Gabriela Benzrihen, Javier Farias, Débora Braslavsky, Horacio Solarz, Verónica Forclaz, Paula Morano, Regina Papazian, Horacio Bignon, Ignacio Bergadá Buenos Aires, Argentina P3-d1-1471
Thyroid function of critically-ill infants in the intensive care setting Siska Mayasari Lubis, Melda Deliana, Bugis Mardina Lubis Medan, Indonesia
218
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P3
Session date:
Friday 20 September (d2), 13:00 – 14:00
Room:
P3 (Exhibition Hall)
Session type:
Poster Session P3-d2
Session title:
Thyroid 10
P3-d2-1472
An evaluation of the effects of carbamazepine on thyroid function tests in childhood epilepsy Mehmet Ibrahim Turan, Atilla Cayir, Huseyin Tan Erzurum, Turkey P3-d2-1473
Follow-up of congenital hypothyroidism: from screening to precocious treatment Maria Cristina Maggio, Patrizia Iona, Mariagrazia I. Mineo, Giovanni Corsello Palermo, Italy P3-d2-1474
One case report of thyrotoxic myopathy and review Gu Yi Beijing, China P3-d2-1475
Congenital hypothyroidism in Palermo: epidemiological data of the screening centre in the years 2010-2012 Maria Crsitina Maggio, Patrizia Iona, Mariagrazia Irene Mineo, Giovanni Corsello Palermo, Italy P3-d2-1476
Hyperthyroidism in children and adolescents with different clinical conditions Natallia Akulevich, Julia Boiko, Yulia Makarava, Irina Khmara Minsk, Belarus P3-d2-1477
Interobserver agreement in detecting goitre by palpation in a school population Ana Muñoz-Serrano1, Abel González-González1, Jose María Tenías-Burillo2, P. Falero-Gallego2, R. Cañete3 1 Ciudad Real, Spain, 2Alcázar de San Juan, Ciudad Real, Spain, 3Córdoba, Spain P3-d2-1478
Is it the thyroid problem? What can endocrinologist do for patients with obesity problems? Y. Miles Yu Orlando, USA P3-d2-1479
Gender- and age-related characteristics of the course of autoimmune thyroiditis in children Natalia Volkova, Anzhalika Solntsava Minsk, Belarus P3-d2-1480
Prevalence of sensorineural hearing loss in patients with congenital hypothyroidism Fatemeh Saffari, Neda Esmailzadehha, Mohammad Hassan Ababafha Qazvin, Islamic Republic of Iran P3-d2-1481
Poster Sessions P3
A comparison of subclinical hypothyroidism and 25-hydroxyvitamin D levels in children using valproic acid Mehmet Ibrahim Turan, Atilla Cayir, Huseyin Tan Erzurum, Turkey P3-d2-1482
Electrocardiographic changes of corrected QT prolongation in hyperthyroidism Phil Soo Oh Chuncheon, Republic of Korea
9th Joint Meeting of Paediatric Endocrinology 2013
219
Poster sessions | P1
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type: Session title:
Poster Session LB1 Adrenals, Bone, Endocrine Oncology
Chairs:
Linda DiMeglio, Indianapolis, USA Maria Felicia Faienza, Bari, Italy
LB1-1489
A patient with primary adrenal insufficiency presenting with persistant hyponatremia Nesibe Andıran, Derya Buluş, Elif Yağlı Ankara, Turkey LB1-1490
Identification and characterisation of a novel mutation (IVS5-2A>G) in the CYP21A2 gene in a patient with classical virilising congenital adrenal hyperplasia with two rares mutation Mirta S. Stivel, Melisa Taboas, Luciana Gomez Acuña, Noemi Buzzakino, Liliana Dain Buenos Aires, Argentina LB1-1491
A longitudinal study of bone biochemical markers in postmenarchal adolescent girls: relationship with gynecological age, body mass index, race/ethnicity, and serum estradiol levels Zeev Harel1, Jason Machan1, Kevin Wolter2, Melanie Gold3, Barbara Cromer4, Ronald Burkman5, Robert Brown6, Ann Bruner7, Susan Coupey2, Paige Hertweck8, Henry Bone9, Christine Johnson9, Anita Nelson10, Sharon Marshall9, Laura Bachrach11 1 Providence, USA, 2New York, USA, 3Pittsburgh, USA, 4Cleveland, USA, 5Springfield, USA, 6 Philadelphia, USA, 7Baltimore, USA, 8Louisville, USA, 9Detroit, USA, 10Torrance, USA, 11Stanford, USA LB1-1492
A novel CLND16 mutation in a large family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis Asma Deeb1, Salima Abood1, Job Simon1, Hormazdiar Dastoor1, Simon H.S. Pearce2, John A. Sayer2 1 AbuDhabi, United Arab Emirates, 2Newcastle Upon Tyne, UK LB1-1493
WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta identify a key WNT ligand regulating bone mass Outi Mäkitie1, Christine Laine1, Kyu Sang Joeng2, Philippe Campeau2, Riku Kiviranta3, Kati Tarkkonen3, Monica Grover2, James Lu2, Minna Pekkinen1, Maija Wessman1, Terhi Heino3, Vappu Nieminen-Pihala3, Tero Laine1, Heikki Kröger4, William Cole5, Anna-Elina Lehesjoki1, Deborah Krakow6, Cynthia Curry7, Daniel Cohn6, Richard Gibbs2, Brendan Lee2 1 Helsinki, Finland, 2Houston, USA, 3Turku, Finland, 4Kuopio, Finland, 5Edmonton, Canada, 6Los Angeles, USA, 7San Francisco, USA LB1-1494
Metabolic profile after treatment in child and adolescent in patients with acute lymphoblastic leukaemia Fernanda Pereira André, Marília Martins Guimarães, Maria Alice Neves Bordallo, Maurício De Pinho Gama Rio de Janeiro, Brazil
Poster Sessions P1
LB1-1495
Ovarian reserve in young woman diagnosed with lymphoblastic leukaemia during childhood and adolescence Maria I. Hernandez, Paulina M. Merino, Jeanette Linares, German Iñiguez, Alejandra Avila, Rosita Moreno, Nimia Vallejos, Veronica Oyarce, Paola Kobalan, Gabriel Cavada, Pamela Silva, Ethel Codner Santiago, Chile
220
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type:
Poster Session LB2 Fat Metabolism, Obesity
Session title:
Chairs: Gianpaolo De Filippo, Le Kremlin-Bicêtre, France Sarah Ehtisham, Manchester, UK LB2-1496
Analysis of the influence of CLOCK 3111 T/C SNP on the presence of obesity and duration of sleep in children Nayara Paula Bermudes Giovaninni1, Jeanne Teixeira Bessa Fuly1, Thais Coutinho Nicola1, Leonardo Iezzi Moraes1, Alexander Augusto Lima Jorge2, Ericka Barbosa Trarbach2, Everlayny Fiorot Costalonga1 1 Vila Velha, Brazil, 2Sao Paulo, Brazil LB2-1497
Association study of polymorphisms in FTO with childhood overweight and obesity Chun Lin Wang, Wei Fen Zhu, Li Liang, Yi Min Zhu Hangzhou, China LB2-1498
Circulating lipoprotein-associated phospholipase a2 levels are elevated in obese children Sophia D. Sakka, Panagiota Pervanidou, Natalia Lazopoulou, Christina Kaminioti, Christina Kanaka-Gantenbein, George P. Chrousos, Ioannis Papassotiriou Athens, Greece LB2-1499
Internalising and externalising symptoms in obese children: associations with daily salivary cortisol concentrations Panagiota Pervanidou, Despoina Bastaki, Giorgos Chouliaras, Katerina Papanicolaou, Christina Kanaka-Gantenbein, George P. Chrousos Athens, Greece LB2-1500
Interrelations between serum N-terminal pro B-type natriuretic peptide levels and early cardiovascular risk factors and echocardiographic parameters in obese adolescents Mehmet Boyraz1, Özgür Pirgon2 1 Ankara, Turkey, 2Isparta, Turkey LB2-1501
Long-term treatment of n-3 polyunsaturated fatty acids in obese children with non-alcoholic fatty liver disease Mehmet Boyraz1, Ozgur Pirgon2, Bumin Dundar3, Ferhat Cekmez1, Mustafa Akcam2 1 Ankara, Turkey, 2Isparta, Turkey, 3Izmir, Turkey LB2-1502
Paediatric providers are poor at identifying severe obesity in young children Cassandra Brady1, Todd Lingren1, Stephanie Kennebeck1, Imre Solti1,2, Nancy A. Crimmins1 1 Cincinnati, USA, 2Seattle, USA Plasma obtained from prepubertal severely obese children modifies insulin stimulated nitric oxide bioavailability in cultured human umbilical vein endothelial cells Tommaso de Giorgis, Sara Di Silvestre, Angelika Mohn, Natalia Di Pietro, M. Loredana Marcovecchio, Vincenzo Cordone, Michela Toro, Valentina Chiavaroli, Giuseppina Bologna, Assunta Pandolfi, Francesco Chiarelli Chieti, Italy LB2-1504
The effect of childhood obesity on cardiac functions Abdurrahman Uner, Murat Doğan, Zerrin Epcecan, Serdar Epcecan Van, Turkey
9th Joint Meeting of Paediatric Endocrinology 2013
221
Poster Sessions P1
LB2-1503
Poster sessions | P1
LB2-1505
The new effect of growth differentiation factor 5 on 3T3-L1 preadipocyte differentiation Zhou Pei, Feihong Luo Shanghai, China
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type: Session title:
Poster Session LB3 Glucose Metabolism
Chairs:
Kenneth Jones, San Diego, USA Alex Dost, Jena, Germany
LB3-1506
Abstract has been withdrawn LB3-1507
Are paediatric patients attending their annual diabetic retinopathy screening? Lisa Li, Alice Rogan, Rajesh Jayaraman Birmingham, UK LB3-1508
Diabetes mellitus type 1 and 25(OH)vitamin D levels in children and adolescents Olga Slavcheva, Maia Konstantinova, Adelina Tsakova, Radka Savova, Margarita Arshinkova, Nelly Tomova Sofia, Bulgaria LB3-1509
European research network in diabetes and endocrinology David B. Dunger1, Mehul Dattani2, Irene Netchine3, Janina Karres2, Paolo Tomasi2 1 Cambridge, UK, 2London, UK, 3Paris, France LB3-1510
Glycaemic variability in type 1 diabetes: which indicators to use? Sophie Guilmin-Crépon1, Julien Schroedt1, Erwan Scornet1, Véronique Sulmont2, Anne-Sophie Salmon3, Claire Le Tallec4, Régis Coutant5, Fabienne Dalla-Vale6, Chantal Stuckens7, Hélène Bony-Trifunovic8, Hélène Crosnier9, François Kurtz10, Jean-Claude Carel1, Corinne Alberti1, Nadia Tubiana-Rufi1 1 Paris, France, 2Annemasse, France, 3Reims, France, 4Toulouse, France, 5Angers, France, 6Montpellier, France, 7Lille, France, 8Amiens, France, 9Poissy, France, 10Saint Avold, France LB3-1511
Insulin independence after foetal haematopoietic stem cells allotransplantation in patients with type 1 diabetes Farzaneh Abbasi, Mahsa M. Amoli, Bagher Larijani Tehran, Islamic Republic of Iran
Poster Sessions P1
LB3-1512
Insulin resistance in adolescent girls with PCOS Slavica R. Markovic1, Zoran Igrutinovic1, Gordana Kostic1, Rada Petrovic2, Zorica Raskovic1, Jelena Tanaskovic-Nestorovic1 1 Kragujevac, Serbia, 2Cacak, Serbia LB3-1513
NGAL: an early marker of diabetic nephropathy? Nektaria Papadopoulou, Chrysanthi Skevaki, Ioanna Kosteria, Melpomeni Peppa, Ioannis Papassotiriou, George Chrousos, Christina Kanaka-Gantenbein Athens, Greece LB3-1514
Screening for coeliac disease in children diagnosed with diabetes mellitus Karen Waldon, Rajesh Jayaraman Birmingham, UK
222
9th Joint Meeting of Paediatric Endocrinology 2013
poster sessions | P1
LB3-1515
Screening glucose disorders in cystic fibrosis: continuous subcutaneous glucose monitoring compared to oral glucose tolerance test Marta Santalha1, Teresa Borges2, Telma Barbosa2, Brigida Amaral2, Luís Ribeiro2, Maria João Oliveira2, Helena Cardoso2, Ana Paula Silva2, Cármen Cardoso2, Vírgilio Senra2, Herculano Rocha2 1 Guimarães, Portugal, 2Porto, Portugal LB3-1516
Structured feedback in the development of the first educational smartphone application (Pumps4Kids) for insulin pump education Colin Patrick Hawkes1, Peter C. Hindmarsh2, Nuala P. Murphy3, Marian McCarthy1, Stephen M.P. O’Riordan1 1 Cork, Ireland, 2London, UK, 3Dublin, Ireland LB3-1517
Testosterone levels and lack of hypogonadism in male adolescents and adults with type 1 diabetes Joel Riquelme, Anita Rocha, Daniela Martínez, Patricia López, Germán Iñiguez, Nestor Soto, Ethel Codner Santiago, Chile LB3-1518
Transient expressive aphasia and quadriparesis in a patient treated for severe diabetic ketoacidosis Noor Shafina Mohd Nor1, Muhammad Yazid Jalaludin2, Vanessa Lee Wan Mun2, Fatimah Harun2 1 Selangor, Malaysia, 2Kuala Lumpur, Malaysia
Session date:
Saturday 21 September (d3), 12:45 – 13:45
Room:
P1 (Exhibition Hall)
Session type:
Poster Session LB4 Pituitary, Growth, Thyroid
Session title: Chairs:
Malcolm Donaldson, Glasgow, UK Jennifer Miller, Chicago, USA
LB4-1519
CUL7, OBSL1 and CCDC8 modulate alternative splicing of exon 11 of the insulin receptor gene Daniel Hanson, Graeme CM Black, Peter E. Clayton Manchester, UK LB4-1520
Growth proportions, obesity and hypertension in children: what is the relation? Daniele Gasparini Marcato1, Jéssica Dutra Sampaio1, Eduardo Roberty Badiani Alves1, Julyanna Silva Araujo de Jesus1, Thais Coutinho Nicola1, Leonardo Iezzi De Moraes1, Nayara Paula Bermudes Giovaninni1, Jeanne Teixeira Bessa Fuly1, Everlayny Fiorot Costalonga1,2 1 Vila Velha, Brazil, 2Vitória-ES, Brazil Long-term safety and effectiveness of daily and once-weekly growth hormone treatment in paediatric patients Young-Jun Rhie1, Choong Ho Shin2, Il Tae Hwang2, Sochung Chung2, Min-Ho Jung2, Jae Hyun Kim2, Hyun-Wook Chae2 1 Ansan-si, Korea, Republic of, 2Seoul, Korea, Republic of LB4-1522
Short stature likely caused by biologically inactive growth hormone: auxologic, laboratory and recombinant human growth hormone treatment aspects of a collection of 19 patients followed in the period of 1996-2013 Fernanda Figueira Jorge, Julienne Angela Ramires Carvalho, Suzana Nesi França, Rosana Marques Pereira, Luiz De Lacerda Curitiba, Brazil
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LB4-1521
Poster sessions | P1
LB4-1523
Mild traumatic brain injury and immediate hypopituitarism in children Alcinda Aranha Nigri, Sandro Blasi Esposito, Rodrigo Rejtman Guimarães, David Gonçalves Nordon Sorocaba, Brazil LB4-1524
Cavernous sinus sampling and cytology is helpful in pituitary surgery of difficult paediatric Cushing´s disease Patricia A. Crock1, Dieter K. Ludecke2, Joerg Flitsch2, Ulrich Grzyska2, Wolfgang Saeger2 1 New Lambton Heights, Australia, 2Hamburg, Germany LB4-1525
Early over-treatment in congenital hypothyroidism is more harmful for eventual cognitive outcome than early under-treatment Jacoba J. Bongers-Schokking, Sabine M.P.F. de Muinck Keizer-Schrama Rotterdam, Netherlands LB4-1526
Monitoring of iodine deficiency in central Siberia according to the results of neonatal TSHscreening Irina V. Osokina, Darya E. Osokina Krasnoyarsk, Russian Federation LB4-1527
Natural history of TSH receptor mutations gene: insights from long-term follow-up of affected children Yardena Tenenbaum Rakover1, Shlomo Almashanu2, Hamed Hag-Daud3, Samuell Refetoff4, Danni Bercovich5 1 Afula, Israel, 2Tel Aviv, Israel, 3Um-El Fahem, Israel, 4Chicago, USA, 5Tel Hai, Israel LB4-1528
Poster Sessions P1
Somatic mutations/rearrangements in 33 hot thyroid nodules in children Marek Niedziela1, Markus Eszlinger2, Eva Typlt2, Sandra Huth2, Holger Jäschke2, Jörg Schaarschmidt2, Knuth Krohn2, Ralf Paschke2 1 Poznan, Poland, 2Leipzig, Germany
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general information
Scientific Information Abstract Book and USB-stick
Accepted abstracts are published in the meeting Abstract Book, as a supplement to Hormone Research in Paediatrics. The abstract book is available on the Meeting website in PDF. In addition, a USB-stick version of all abstracts is given to delegates on a first-come first-served basis. Please collect the USB-stick at the Novo Nordisk exhibition booth by using the voucher received in the Meeting bag. Certificate of Attendance
A Certificate of Attendance is available from Saturday 21 September at the Registration Area. CME Credits
The ‘Serono Symposia International Foundation’ (or) ‘Joint Meeting of Paediatric Endocrinology 2013’ is accredited by the European Accreditation Council for Continuing Medical Education (EACCME) to provide the following CME activity for medical specialists. The EACCME is an institution of the European Union of Medical Specialists (UEMS), www.uems.net. The ‘Joint Meeting of Paediatric Endocrinology 2013’ is designated for a maximum of (or ‘for up to’) 18 hours of European external CME credits. Each medical specialist should claim only those hours of credit that he/she actually spent in the educational activity. Through an agreement between the European Union of Medical Specialists and the American Medical Association, physicians may convert EACCME credits to an equivalent number of AMA PRA Category 1 Credits™. Information on the process to convert EACCME credit to AMA credit can be found at www.ama-assn.org/go/internationalcme. Live educational activities, occurring outside of Canada, recognized by the UEMS-EACCME for ECMEC credits are deemed to be Accredited Group Learning Activities (Section 1) as defined by the Maintenance of Certification Program of The Royal College of Physicians and Surgeons of Canada The CME accreditation is valid for the main meeting programme only and does not cover the company-sponsored symposia. ISO 9001 Certification:
Serono Symposia International Foundation has received the ISO 9001 Certification of Quality Management Systems. This Quality certification requires all participants to fill in a scientific questionnaire and to evaluate the overall quality of the event. Questionnaires will be distributed in the meeting bag onsite. Disclosure Statement
The intent of this disclosure statement is not to prevent speakers, with significant financial or other relationships, from making a presentation, but rather to provide the audience with the information necessary to determine whether a speakers’ interest or relationships influence the presentation with regard to exposition or conclusion. Finally, all faculty are required to identify to the audience any use of a product or service that is either investigational or without FDA/EMEA-approved product labelling.
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In compliance with the Continuing Medical Education (CME) guidelines of the European Accreditation Council for Continuing Medical Education (EACCME) and the main European accrediting bodies, it is essential to ensure balance, independence, objectivity and scientific rigor in educational activities. All faculty members participating are required to disclose to the activity audience, any significant financial interest or other relationship with the manufacturer(s) of any commercial product(s) and/or provider(s) of commercial services discussed in an educational presentation and with any commercial supporters of the activity. Significant financial interest or other relationship may include: grants, research support, status as an employee, consultant, major stockholder, member of a speakers’ bureau, etc.
general information
Please note that at the 9th Joint Meeting of Paediatric Endocrinology in Milan, the presenter will show a slide with disclosure information in the beginning of his/her lecture. The disclosure statements are also listed online on the Meeting website at www.jointmeeting2013.org Joint Meeting President Poster Awards
The Joint Meeting President Poster Awards are voted by members of the Joint Programme Organising Committee after the last poster session and are given to five presenting authors (among 50 nominees). The winners will be announced by the President at the Joint Meeting President Poster Award Session prior to the Closing Ceremony. The voting criteria will be based on the scientific content and style of poster presentation. The Awards consist of an official Joint Meeting Award Diploma, a Presidential gift and a place in the official listing on the society website among Joint Meeting Award Winners in the following year. Meet the Expert Handout
A leaflet including handouts for the Meet the Expert Sessions are given to all registered delegates in their meeting bag. A printer friendly PDF version will be available on the Joint Meeting website at www.jointmeeting2013.org after the meeting. Speakers’ Support Centre
The Speakers’ Support Centre (SSC) is located on level 2. All speakers giving a presentation are requested to validate their presentation in the SSC a minimum of two hours before the session starts or the day before if it is a morning session. Presentations received after this deadline cannot be guaranteed optimal audiovisual support. The SSC is open the following hours: Wednesday Thursday Friday Saturday Sunday
18 September 19 September 20 September 21 September 22 September
14:00–18:00 07:30–19:00 07:00–18:00 07:00–18:00 07:00–12:30
Travel Grants
Joint Meeting Travel Grants can be collected at the cashier desk in the registration area the following opening hours: Saturday Sunday
21 September 22 September
10:00–18:00 09:00–12:00
To collect your travel grant it is mandatory to bring the documents requested in your acceptance letter. Yearbook of Paediatric Endocrinology
The Yearbook is given to all delegates. Please collect the Yearbook at the ESPE Society exhibition booth using the voucher received together with your name badge.
Future ESPE Meetings
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A future meeting area is located in the Exhibition Hall. Please visit this area and pick up information about future ESPE meetings as well as other meetings within the field of Endocrinology. Remember to mark your calendar for future ESPE meetings: ESPE 2014 ESPE 2015 ESPE 2016 10th Joint Meeting 2017
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Dublin, Ireland Barcelona, Spain Paris, France Washington, USA
9th Joint Meeting of Paediatric Endocrinology 2013
18–20 September 2014 1–3 October 2015 10–13 September 2016 September 2017
floor plan of the meeting venue
Floor Plan of the Meeting Venue
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SPEAKERS’ SUPPORT CENTRE CENTRE HOSPITALITY SUITES
OSPITALITY SUITES
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FAMILY ROOM office 10 PRAYER ROOM office14
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MILY ROOM office 10 LEVEL 0
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commercial exhibition
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Commercial Exhibition
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commercial exhibition
An exhibition of related products, services and technologies is being held concurrently with the meeting. This provides delegates with an excellent opportunity to interact with industry and to familiarise themselves with the latest advances in technology and therapeutics. The exhibition opening hours are as follows: Thursday Friday Saturday
19 September 20 September 22 September
09:45–20:00 08:30–18:00 08:30–17:15
The following companies will be exhibiting their products during the meeting and welcome you to their stand. Please see page 228 for the floor plan. Platinum Sponsors
Stand Number
Eli Lilly and Company Ferring Pharmaceuticals Ipsen Merck Serono S.A. Novo Nordisk A/S Pfizer Endocrine Care Sandoz International GmbH
01 www.lilly.com 03 www.ferring.com 08 www.ipsen.com 05 www.merckserono.net 06 www.novonordisk.com 07 www.pfizer.com 04 www.sandoz.com
Other Exhibitors
Stand Number
Alexion Pharma International
02c
Alstrom Syndrome UK
17
European Society for Paediatric Endocrinology (ESPE)
05a
ESPE 2014 - Dublin Ireland
20
Growth Analyser
18
Immunodiagnostic Systems (IDS)
14
IPWSO 09 ISPAD 02e Medtronic 24 Nestlé Nutrition S.A
02a
PC PAL
11
Pediatric Endocrine Society
21
PROLOR Biotech
22
Serono Symposia International Foundation
02d
S Karger
19
SonicBone Medical
23
The Endocrine Society
10
The International Classification of Pediatric Endocrine Diagnosis (ICPED)
18a
Visiana 13 15
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Wisepress Medical Bookshop
commercial exhibition
Platinum Sponsors Eli Lilly and Company Stand 01 Eli Lilly and Company is a global partner in support of healthcare professionals and those whose lives are affected by diabetes, growth disorders and growth hormone deficiency. Not only has Lilly been a global leader in diabetes care since we introduced the world’s first commercial insulin in 1923, we have also been committed for more than 25 years to our work around recombinant human growth hormone. Today, we remain at the forefront of medical and delivery device innovation that helps children and adults manage their diseases. In addition to drug therapy we believe in taking a personal approach and a commitment to providing personal solutions including educational tools, resources and support programs that help overcome barriers to success and fit into everyday lives. As a result of this, we continue to research and collaborate to bring forward innovative therapies and dynamic solutions to make lives better. We welcome you to the Joint Meeting and look forward to seeing you at the Lilly booth. Eli Lilly and Company Lilly Corporate Center Indianapolis, IN 46285 USA Telephone: +1 317 276 3233 Fax: +1 317 276 6900 Website: www.lilly.com
Ferring Pharmaceuticals Stand 03 Endocrinology is a core therapeutic area for Ferring Pharmaceuticals. We have been supplying therapeutic and diagnostic hormones for many years, and are committed to future developments in this field. Ferring is a leader in needle-free technology. Please come to the Ferring stand to learn more about our easy-to-use needle-free devices for the administration of growth hormone. With global headquarters in Switzerland, Ferring is a major supporter of education in Paediatric Endocrinology, being the exclusive sponsor of the annual ESPE Summer School and Winter School meetings. Ferring has also hosted 7 International Paediatric Endocrinology Symposia to date. Please visit www.ferring.com for further information about Ferring.
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Ferring International Center S.A. Chemin de la Vergognausaz 50 1162 Saint-Prex Switzerland
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Ipsen Stand 08 Ipsen is a global specialty-driven pharmaceutical company with total sales exceeding €1.2 billion in 2012. Ipsen’s ambition is to become a leader in specialty healthcare solutions for targeted debilitating diseases. Its development strategy is supported by four franchises: neurology, endocrinology and uro-oncology. Moreover, the Group has an active policy of partnerships. R&D is focused on innovative and differentiated technological patient driven platforms, peptides and toxins. In 2012, R&D expenditure totaled close to €250 million, representing more than 20% of Group sales. The Group has total worldwide staff of close to 4,900 employees. Ipsen’s shares are traded on segment A of Euronext Paris (stock code: IPN, ISIN code: FR0010259150) and eligible to the “Service de Règlement Différé” (“SRD”). The Group is part of the SBF 120 index. Ipsen has implemented a Sponsored Level I American Depositary Receipt (ADR) program, which trade on the over-the-counter market in the United States under the symbol IPSEY. For more information on Ipsen, visit www.ipsen.com. Ipsen Pharma 65 quai Georges Gorse 92100 Boulogne Billancourt cedex France Telephone: +33 1 58 33 50 00 Fax: +33 1 58 33 50 01 Website: www.ipsen.com
Merck Serono S.A. Stand 05 Merck Serono is the biopharmaceutical division of Merck KGaA. With headquarters in Darmstadt, Germany, Merck Serono offers leading brands in 150 countries to help patients with cancer, multiple sclerosis, infertility, endocrine and metabolic disorders as well as cardiovascular diseases. In the United States and Canada, EMD Serono operates as a separately incorporated subsidiary of Merck Serono. Merck Serono discovers, develops, manufactures and markets prescription medicines of both chemical and biological origin in specialist indications. We have an enduring commitment to deliver novel therapies in our core focus areas of neurology, oncology, immune-oncology, and immunology. Merck is a leading pharmaceutical, chemical and life science company with total revenues of €11.2 billion in 2012, a history that began in 1668, and a future shaped by approx. 39,000 employees in 66 countries. Its success is characterised by innovations from entrepreneurial employees. Merck’s operating activities come under the umbrella of Merck KGaA, in which the Merck family holds an approximately 70% interest and free shareholders own the remaining approximately 30%. In 1917 the U.S. subsidiary Merck & Co. was expropriated and has been an independent company ever since. For more information, please visit www.merckserono.com or www.merckgroup.com
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Merck Serono Frankfurter Strasse 250 64293 Darmstadt Germany Website: www.merckserono.com
commercial exhibition
Novo Nordisk A/S Stand 06 Novo Nordisk is a global healthcare company with 90 years of innovation and leadership in diabetes care. The company also has leading positions within haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 35,000 employees in 75 countries, and markets its products in 180 countries. Novo Nordisk manufactures and markets pharmaceutical products and services that make a significant difference to patients, the medical profession and society. With over 40 years of innovation and achievement in growth hormone therapy in children and adults, Novo Nordisk offers easy to use delivery systems as well as comprehensive programmes and services to support everyone involved with growth hormone treatment. Please visit the Novo Nordisk exhibit for the latest information on growth hormone disorders as well as on our treatment options. Novo Nordisk Health Care AG Thurgauerstrasse 36/38 8050 Zurich Switzerland Telephone: +41 43 222 43 00 Fax: +41 43 222 44 04 Email:
[email protected] Website: www.novonordisk.com
Pfizer Endocrine Care Stand 07 Pfizer is the world’s largest research-based pharmaceutical company. Our goal is to discover, develop, manufacture and deliver quality, effective prescription medicines to treat and help prevent disease. Pfizer has an excellent heritage in endocrinology and is highly committed to its endocrine product portfolio. The company has an active Investigator-Initiated Research program supporting advances in medical and scientific knowledge, and supports medical education through provision of post-graduate education programs. The Pfizer team looks forward to welcoming you to the Pfizer Endocrine Care booth where you will have the opportunity to discuss latest developments. We also hope you will be able to attend our Satellite Symposium: Personalised medicine promises to enhance patient care and clinical outcomes in a wide range of therapeutic fields. For this promise to be fulfilled, the principles of personalisation must be translated into clinical practice in Endocrinology. Practical application of personalised medicine in paediatric and adolescent endocrinology, 18:00–19:30, Friday 20 September, Space 1+2, Milano Congressi. Pfizer Endocrine Care wishes you an interesting and enjoyable meeting.
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Pfizer Endocrine Care Pfizer Ltd Walton Oaks, Dorking Road Walton-on-the-Hill, Tadworth Surrey, KT20 7NS United Kingdom Website: www.pfizer.com
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commercial exhibition
Sandoz International GmbH Stand 04 Sandoz is a Novartis company with a reputation for quality. Present in 140 countries, our broad portfolio of affordable, high-quality medicines is accessible to 90% of the world’s population. Sandoz Biopharmaceuticals, a specialised global business unit within Sandoz develops, produces and markets high-quality biopharmaceutical medicines. Sandoz International GmbH Industriestrasse 25, 83607 Holzkirchen Germany Telephone: +49 802 44 76 0 Fax:+49 802 44 76 25 99 Email:
[email protected] Website: www.sandoz.com
Exhibitors Alexion Pharma International Stand 02c Alexion is focused on serving patients with severe and ultra-rare disorders through lifetransforming therapies. We developed and market a treatment for ultra-rare and life-threatening disorders caused by chronic uncontrolled complement activation, and are developing other innovative product candidates, including an enzyme replacement therapy for hypophosphatasia (HPP), a severe multisystem metabolic disorder. Alexion Pharma International Avenue du Tribunal Fédéral 34 1005 Lausanne Switzerland Telephone: + 41 (0) 21 318 40 00 Fax: + 41 (0) 21 318 40 01 Email:
[email protected] Website: www.alxn.com
Alstom Syndrome UK Stand 17 Representing EU WABB (Wolfram, Alstrom and Bardet Biedl syndromes) as a 7th framework EU grant was received to raise awareness of these rare diseases.
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Alstrom Syndrome UK Kay Parkinson, Founder and Director Telephone: +44 1803 524238 Fax: +44 798 524 38 34 Email:
[email protected] Website: www.alstrom.org.uk . EURORDIS Patient Organisation 2013
commercial exhibition
European Society for Paediatric Endocrinology (ESPE) Stand 05a The European Society for Paediatric Endocrinology (ESPE) is a truly international membership organisation, committed to serving its members and the scientific community with the aim to promote the highest levels of knowledge, research, education and clinical practice of paediatric endocrinology and metabolism throughout the world. ESPE Euro House, 22 Apex Court Woodlands, Bradley Stoke Bristol BS3 4JT UK Telephone: +44 (0) 145 46 42 246 Fax: +44 (0) 145 46 42 222 Email:
[email protected] Website: www.eurospe.org
ESPE 2014 – Dublin Ireland Stand 20 Dublin, host city to ESPE 2014, capital city of the emerald isle of Ireland. Effortlessly combining the traditional with the modern, the historic with the contemporary, and the dynamic with the famous Irish hospitality. The host venue, Convention Centre Dublin, a stunning iconic building designed by Pritzker award winning architect Kevin Roche is located on the banks of the River Liffey. Dublin is an exciting and inspirational city, eager to extend a warm welcome to you. Dublin Convention Bureau Fáilte Ireland Áras Fáilte 88-95 Amiens Street Dublin 1 www.dublinconventionbureau.com www.visitdublin.com www.failteireland.ie
Growth Analyser Stand 18 Growth Analyser BV develops effective software programmes for paediatricians, researchers, patients and parents to document, monitor and analyse growth and development of children and adolescents ( 50,000 children followed in iNCGS / NCGS since 19851. NutropinAq Pen Liquid formulation, prefilled cartridge2
References *. Before and after GH treatment. N Engl J Med 1999; 341: 1206-16 1. Bell et. al. J Clin Endocrinol Metab. 2010 Jan;95(1):167-77. 2. SmPC
Before prescribing, please refer to your local product information as registration congresses only.
Floor Plan Exhibition Author Index
Submitted to AIFA on 7.6.2013
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The Grant for Growth Innovation (GGI) The Grant for Growth Innovation (GGI) award has been established to support innovative projects for the advancement of science and medical research in the field of growth. The GGI will allow close collaboration between researchers in academia and industry leading innovative research projects in the field of growth.
Researchers leading research projects that have the potential to advance understanding in the field of growth are invited to apply for the first GGI that will total up to 400,000 Euros. Applications will be evaluated by a Scientific Steering Committee, according to five criteria: innovative research, scientific rationale, feasibility, practical utility and relevance to clinical practice. Potential research topics which could be funded through the GGI include: ■ ■ ■ ■ ■ ■ ■
Innovative translational research that could potentially improve patients’ lives The impact of nutrition on growth The metabolic impact of growth disorders Techniques in diagnosis and follow up on growth disorders Extremes in growth disorders Identification of biomarkers in patients with growth disorders Studies elucidating the long-term metabolic impact of the “GH-IGF axis” activity
The first award grantees will be announced at the 53rd European Society for Paediatric Endocrinology (ESPE) meeting in Dublin in September 2014. For further information about how to apply for the grant, please visit www.grantforgrowthinnovation.org Applications will be accepted from May 1st until December 1st 2013.
MER130216_ANZ_GGI_125x234.indd 1
Tells you what you want to know
27.05.13 11:33
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Merck Serono
Novo Nordisk® sponsored Satellite Symposium at the 9th Joint Meeting of Paediatric Endocrinology
Optim misiing therapy in n childre en with h growth dissord ders frrom m dia agnosiss to adult heig ght: casse sttudy deb bate Chaired by David Dunger, Cambridge, UK, and Susumu Yokoya, Tokyo, Japan
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Floor Plan Exhibition Author Index
ESPE Research Fellowship Grant Programme for more than 20 years. Come and visit us at our exhibit and learn more about the programme.
© 2013 Novo Nordisk Health Care AG Thurgauerstrasse 36/38 CH-8050 Zurich, Switzerland www.novonordisk.com
13-1546 Program Ad DR.indd 1
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5/28/13 10:01 AM
A lifetime commitment
25 years in Endocrinology Individualised Treatment – Our focus for the future
Specialty Care Endocrine
Date of Preparation: April 2013 EBT/GEN/13/43
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To find out more, visit us at the Pfizer booth
a Novartis company
Sandoz Biopharmaceuticals Pioneering the Future Visit booth 4 to learn more about our vision and products
Floor Plan Exhibition Author Index
www.sandoz.com
Date of preparation: July 2013 HQ/OMN/13-0005l
10100182 Pragram ad V2a.indd 1
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30/07/2013 10:32
Visit the Karger booth and profit from a 30% discount on these and many more titles The latest volumes in the book series Endocrine Development Vol. 25 Endocrine Development
The Ghrelin System
Editor: P.-E. Mullis Vol. 25
The
Ghrelin System Editors
A. Benso F.F. Casanueva E. Ghigo nata R. Granata
Editors: Benso, A. (Turin); Casanueva, F.F. (Santiago de Compostela); Ghigo, E.; Granata, R. (Turin) VIII + 172 p., 16 fig., 2 in color, 4 tab., hard cover, 2013 CHF 180.– / EUR 150.– / USD 212.00 ISBN 978–3–8055–9908–5 Vol. 24
Endocrine Development Editor: P.-E. Mullis Vol. 24
Hormone Resistance and Hypersensitivity
Hormone Resistance and Hypersensitivity From Genetics to Clinical Management
From Genetics to Clinical Management
Editors
M. Maghnie S. Loche M. Cappa L. Ghizzoni R. Lorini
Editors: Maghnie, M. (Genoa); Loche, S. (Cagliari); Cappa, M. (Rome); Ghizzoni, L. (Turin); Lorini, R. (Genoa) VIII + 160 p., 26 fig., 7 in color, 10 tab., hard cover, 2013 CHF 168.– / EUR 140 .– / USD 198.00 ISBN 978–3–318–02267–4
Endocrine Development Editor: P.-E. Mullis Vol. 23
Developmental Biology of GH Secretion, Growth and Treatment Editor
P.-E. Mullis
Vol. 23
Developmental Biology of GH Secretion, Growth and Treatment Editor: Mullis, P.-E. (Bern) VIII + 126 p., 22 fig., 1 in color, 10 tab., hard cover, 2012 CHF 156.– / EUR 130.– / USD 184.00 ISBN 978–3–318–02244–5
4th revised and extended edition of this indispensable reference tool
M.B. Ranke . P.-E. Mullis
Diagnostics of Endocrine Function in Children and Adolescents 4th, revised and extended edition
P. Fischer-Posovszky C.E. Flück O. Fricke H. Frisch A. Grüters H.P. Haber M.F. Hartmann P.-M. Holterhus J.W. Honour K. Hussain R.J. Johnston H. Krude M. Lassmann P.-E. Mullis
A. Neu A.L. Ogilvy-Stuart A.V. Pandey L. Perry M. Polak M.B. Ranke T. Reinehr C. Reiners S. Riedl S. Rosberg M.O. Savage E. Schoenau V. Valayannopoulos M. Wabitsch W.H.B. Wallace J.C.K. Wells S.A. Wudy
4th, revised and extended edition
Editors: Ranke, M.B. (Tübingen); Mullis, P.-E. (Bern) XII + 536 p., 109 fig., 80 tab., hard cover, 2011 CHF 180.– / EUR 133.50 / USD 180.00 ISBN 978–3–8055–9414–1 Prices subject to change EUR price for Germany, USD price for USA only
KI13696
K. Albertsson-Wikland J. Allgrove M.G. Bianchetti W.F. Blum C. Böttcher P.M. Crofton P. Czernichow P. de Lonlay S. Ehehalt M.W. Elmlinger J. Farahati P. Ferrari
Diagnostics of Endocrine Function in Children and Adolescents
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Editors
As the of ficial airline network for the 9th Joint Meeting of Paediatric Endocrinology, we’d like to thank you for choosing the Star Alliance network and hope that all goes really well for you here today. Whilst you concentrate on the day’s events, we hope you’ll consider us the nex t time you need to attend a conference. With over 21,900 flights a day to 1,329 airpor ts across 194 countries, our 27 member airlines will extend a wide choice of flights to any future conference you’re planning to attend. And no matter which of those airlines’ frequent flyer programmes you belong to, you can earn and redeem miles across all of them.
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So the nex t time you want to concentrate all your energies on your conference, we hope you’ll decide to leave the travel arrangements to us.
staralliance.com Information correct as at 11/2012
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file name: Conventions_Plus_WelCome_message_234x125_1
ESPE Advert 125x234mm_Layout 1 10/07/2013 15:48 Page 1
Join ESPE today! Member benefits include… Reduced registration fees for annual meeting Subscription to Hormone Research in Paediatrics Web-based directory of ESPE members
Visit the ESPE Connect stand to join the Society, meet Council members and find out more about all ESPE’s programmes and activities, such as: Summer School Winter School
Research Fellowship Clinical Fellowship
Access to grants,
Sabbatical Leave Programme
Regular news updates
Young Investigator Awards
awards and fellowships
Visiting Scholarship Science School
Visit the ESPE stand in the exhibition hall,
www.eurospe.org 9th Joint Meeting of Paediatric Endocrinology 2013
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or go to the ESPE website
author index
Author Index Numbers refer to abstract numbers or session numbers.
Floor Plan Exhibition Author Index
A
Ababafha, Mohammad Hassan P3-d2-1480 Abaci, Ayhan P1-d1-454, P1-d2-365, P2-d2-706, P3-d1-1227*, P3-d1-1457, P3-d2-1436, P3-d3-1383 Abali, Saygin P1-d2-464*, P2-d1-742, P2-d1-849, P2-d1-884, P2-d3-715*, P2-d3-803 Abbasi, Farzaneh LB3-1511*, P3-d2-1336 Abbondanza, Ciro P2-d1-960 Abbot, Vimmi P2-d2-639* Abd Al Hamid, Alaa P2-d2-1117 Abd El-Aziz, Sherin P1-d1-446 Abdalrahaman, Naiemh P1-d2-303* Abdel Dayem, Soha P2-d2-1117 Abdel Rahman, Rania P1-d1-446 Abdelaziz, Foued P2-d3-1134* Abdelrahman, Hatem P3-d2-1374 Abe, Kiyomi FC19-229*, P2-d2-1148, P2-d2-1183 Abe, Takayuki FC19-229 Abe, Yuki P1-d1-283* Abernethy, Laurence P3-d2-1414 Abid, Noina P2-d1-739 Abood, Salima LB1-1492 Abrams, B. P2-d1-1004 Abreu, Ana FC4-138 Abu-Amero, Khalid P2-d3-713 Abu-Libdeh, Abdulsalam P2-d1-1001* Accili, Domenico P1-d1-473 Accogli, Andrea P1-d2-301*, P2-d1-919*, P3-d2-1339 Acerini, Carlo FC3-135, P2-d1-953 Acerno, Stefania FC2-129 Aceto, Gabriella P2-d1-727 Acha, Oscar P2-d1-1173 Achermann, John P2-d2-634 Ackerman, Kathryn P2-d1-1012* Acosta, Johanna P2-d1-1051* Acosta, Wilson P2-d1-743 Acquafredda, Angelo P2-d2-1192*, P3-d2-1211* Adachi, Hiroyuki P1-d2-605*, P2-d1-998
Adachi, Masanori FC19-229, P1-d1-504, P1-d3-404, P3-d1-1226 Adal, Erdal P1-d3-609, P2-d1-729, P2-d1-888*, P2-d3-948*, P3-d1-1332 Adaletli, Ibrahim P2-d2-1147 Adami, Nicole P1-d3-561 Adams, Judith P1-d2-294 Addor, Marie-Claude P2-d1-995 Aerts, Isabelle P2-d1-691, P2-d1-738 Afek, Arnon P2-d1-1135 Afenjar, Alexandra P1-d1-511 Affinita, Maria Carmen P2-d1-684 Agarwal, Anjoo P2-d2-699 Agarwal, Meenal WG3-97 Aglony, Marlene P1-d1-235, P1-d2-325, P2-d1-920 Agostoni, Carlo SAT7 Aguayo, Anibal P1-d1-591, P2-d3-904, P3-d1-1287 Aguilera, Concepción FC15-204, P1-d1-354, P3-d2-1274 Aguirre, Alvaro P2-d1-743, P2-d1-750 Aguirre, Andrea P2-d1-743* Aguirre, Cecilia P2-d1-622, P2-d3-1163 Agwu, Chizo P2-d2-677* Ahlsson, Fredrik P1-d2-357* Ahmad, Noman P2-d1-728* Ahmadi, Firooz P1-d1-318, P2-d2-753 Ahmed, S. Faisal FC7-156, FC8-166, P1-d2-303, P1-d2-585, P1-d2-586, P2-d1-1105, P2-d1-690, P2-d3-983, P3-d1-1290, P3-d1-1364, S12, S12-48*, WG6-114*, WG6-117 Ahmed, Sarra P2-d1-621 Ahmid, Mahjouba P2-d2-827* Ahn, Jung Min P2-d2-1097, P2-d3-1132 Ahn, Sung Yeon P2-d2-1185 Aigrain, Yves P1-d2-581 Aimaretti, Gianluca P2-d1-816 Airoldi, Daniela P3-d1-1468 Ajami, Gholamhossein P1-d2-298 Akani, Nwadiuto P2-d1-723 Akca, Ahmet P2-d1-1174 Akcam, Mustafa LB2-1501
* Presenting author
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9th Joint Meeting of Paediatric Endocrinology 2013
Akcay, Arzu P2-d1-782, P2-d3-1124 Akcay, Teoman P2-d1-782, P2-d2-862*, P2-d3-1124 Akçurin, Sema P1-d2-552, P2-d1-722 Akdag, Mehmet P2-d2-791 Akin, Leyla P2-d1-1006, P2-d1-787, P2-d2-698 Akin, Mehmet P2-d1-719 Akin, Mustafa P1-d1-500, P2-d1-1006 Akinci, Aysehan P1-d2-364* Akkache, Lina P2-d1-1018, P2-d2-1026*, P3-d1-1410*, P3-d2-1412 Akkurt, Ilker P1-d2-256 Aksionava, Elena P1-d3-371 Aksu, Mehmet P1-d2-359*, P2-d2-928, P2-d3-776 Akulevich, Natallia FC10-179, P3-d2-1476* Akyürek, Nesibe P2-d2-760, P2-d2-865, P3-d2-1342* Al Ghamdi, Mohammed P3-d2-1214 Al Issa, Sharifah P3-d2-1214 Al Jurayyan, Nasir P3-d2-1214 Al Oum, Muna P1-d1-420 Al Yafei, Fawzia P2-d2-1149 Alajbegovic, Salem P2-d1-916 Alam, Syeda P2-d1-850 Alatzoglou, Kyriaki S. P1-d1-507* Albala, Cecilia P1-d3-372, P2-d2-757, P2-d2-894 Albert, Ben P2-d2-1158 Alberti, Corinne LB3-1510, P1-d2-487 Albertsson-Wikland, Kerstin FC3-133*, P1-d2-302, P1-d2-392, P1-d2-479*, P1-d2-548, P1-d3-558, P2-d2-835, P2-d2-836, P2-d2-971, P2-d3-974, P2-d3-981, P3-d1-1399 Albisu Aparicio, Marian P1-d1-310, P2-d3-804 Albu, Alice P2-d1-1041 Alcázar Villar, María José P2-d3-717*, P3-d2-1297, P3-d2-1299 Alcoba Conde, Antonio P3-d1-1267 Alehan, Fusun P3-d2-1334 Aleksander, Paulina P1-d2-603*, P1-d3-612, P2-d3-1169
Alesia, Teresa P3-d1-1322 Alessio, Paola P1-d1-385, P1-d1-505 Alexandrou, Andreas P2-d2-864 Alexandrov, Konstantin P3-d1-1216 Alexiu, Florin P2-d2-800 Alfano, Sara P1-d1-592, P2-d2-1154, P2-d2-1190 Al-Hakamy, Amal P3-d1-1231 Alhumaidi, Noora P2-d1-1176* Ali, Basma P3-d3-1358* Alieva, Anna P3-d3-1355 Alikasifoglu, Ayfer P2-d2-1022, P2-d3-1064 Alimova, Nasiba WG3-95 Alioglu, Bülent P2-d3-766 Al-Juryyan, Nasir P2-d2-935, P3-d1-1231 Alkhaldi, Hisham P2-d3-713 Alkhawari, Mona FC8-166 Alkuraya, Fowzan FC10-174 Allain-Launay, Emma FC2-128 Allegri, Anna E.M. P2-d1-1014 Allen, David P1-d2-363, P1-d3-378 Allen, Janet P1-d2-431 Allgrove, Jeremy FC12-187, P2-d1-671, SAT3 Allvin, Kerstin P1-d2-355 Alm, Bernt P2-d2-700 Almanzar, Rosario P3-d3-1447 Almarri, Noora P2-d2-1149 Almashanu, Shlomo LB4-1527 Almeida, Ana P2-d2-681* Almqvist-Tangen, Gerd P2-d2-700 Almutair, Angham FC10-174 Alnaimi, Lolwa P2-d2-1149 Al-Nemri, Abdelrahman P2-d2-935, P3-d1-1231 Aloi, Concetta P2-d2-899, P2-d3-946, P3-d2-1339 Alomar, Safwan P3-d2-1372 Alonso, Daniel P2-d2-869 Alonso, Guillermo P2-d2-635* Alonso, Milagros P2-d1-853, P2-d1-886, P2-d2-869, P2-d2-930* Al-Otibi, Hessah P2-d2-935, P3-d1-1231 Alp, Hayrullah P2-d2-865 Al-Qahtani, Mohammad P3-d1-1205* Alsaffar, Hussain P3-d3-1357* Alsaif, Ramlah P2-d3-945* Alshammari, Muneera P2-d3-1160 Altieri, Elena P1-d3-369 Altincik, Ayca P3-d3-1383
AlTowati, Mabrouka P3-d1-1364* Altun, Gurkan P2-d1-1174 Álvarez Escolá, Cristina FC19-232 Alvarez, Flor P2-d1-780 Alvarez, M. Angeles P2-d1-851, P2-d1-886 Álvarez, María P2-d1-853, P2-d2-930 Alves, Eduardo Roberty LB4-1520 Alvi, Sabah P2-d1-1175 Al-Zubedi, Hiba P2-d2-704 Amano, Naoko FC18-226, FC19-229, FC3-134, P1-d1-243*, P1-d1-504 Amaral, Brigida LB3-1515 Amaral, Daniela P2-d2-754 Amaral, Diego P2-d1-629 Amaro, Andrea P1-d1-239 Amemiya, Shin P1-d2-460 Amin, Rakesh FC9-170, P2-d1-671 Amirhakimi, Gholamhossein P1-d2-298 Amitzi, Leanne P1-d1-391, P2-d2-828 Ammerpohl, Ole FC8-165 Ammini, Ariachery P2-d2-1092*, P2-d2-1120, P3-d1-1196, P3-d1-1454 Amoli, Mahsa M. LB3-1511 Amorin Beltrão, Luciana P3-d2-1380 Amselem, Serge P1-d1-511 Anabwani, Gabriel P2-d1-950 Anand, Binu P3-d3-1387 Ananieva-Jordanova, Rossi P1-d1-278 Anazawa, Akira P1-d3-268 Anckaert, Ellen P2-d2-795 Anderson, Jemma P1-d1-276*, P2-d2-679* Anderson, Richard FC8-162 Andersson, Björn P1-d2-302, P2-d2-836*, P2-d2-971 Andiran, Nesibe LB1-1489 Andoniadou, Cynthia FC10-174 Andonova, Silvia P2-d2-1032 Andrade, Juliana P2-d2-1114 André, Fernanda LB1-1494* Angelini, Lucia P2-d3-1067 Angelkova, Natalija P3-d2-1306 Angulo, Mario FC6-151* Angulo, Moris P1-d2-358 Aniel-Quiroga, M.Angeles P1-d1-591 Anik, Ahmet P1-d2-365, P2-d2-706*, P3-d1-1227, P3-d2-1436*
Ankarberg-Lindgren, Carina P1-d3-564*, P2-d3-1068 Antolini, Laura P2-d1-668 Antón-Gamero, Montserrat P1-d1-423 Antoniazzi, Franco P1-d2-549, P1-d3-561, P2-d1-1085, P3-d2-1301 Antonie, Lavinia P2-d1-1041 Antonini, Sonir FC13-192, FC13-193, FC20-1486*, P3-d1-1367 Anuar, Azriyanti P3-d1-1264* Anzilotti, Giulia P2-d3-847 Aoyama, Aiko P2-d1-1144 Aoyama, Kohei P3-d1-1422 Aparna, Gumma P3-d1-1429 Apezteguía, María P2-d3-1168 Apostolov, Yevgenly P1-d1-386, P2-d1-620 Apostu, Luminita P3-d2-1375, P3-d3-1384 Aragão, Luciana P3-d1-1250 Aragones, Gemma P1-d1-313 Arai, Hirokazu P1-d2-605 Araki, Shunsuke P2-d3-1131 Aranda, Mario P2-d3-880 Araújo, Amélia FC13-192 Arbelaez, Ana Maria P1-d3-442 Arcari, Andrea P1-d3-563, P2-d1-1051, P2-d2-1061* Argandoña, Felipe P1-d1-567 Argente, Jesús FC15-207, FC17-218, FC17-219, FC17-221, P1-d1-308, P1-d1-311, P1-d1-347*, P1-d1-566, P1-d2-360, P1-d3-333, PL4-5*, SAT1 Argente-Arizón, Pilar FC15-207, FC17-221, P1-d1-308 Ariachery, Ammini P3-d1-1458 Ariga, Masamichi P2-d1-1172 Arilla-Ferreiro, Eduardo P1-d1-311 Arisaka, Osamu P1-d1-494 Arlorio, Marco P1-d3-379 Arlt, Wiebke FC8-166, FC9-170, FC9-172, P1-d3-267, SAT4, WG6-118 Armaou, Marianna P2-d3-812 Armougon, Aurélie P2-d1-736 Armstrong, Gregory P1-d2-515 Arner, Peter S8-35* Arnhold, Ivo FC3-134, P1-d1-469, P1-d1-472, P1-d1-506, P1-d2-482, P2-d1-952 Arnoux, Jean-Baptiste NP1-69 Aronsson, Stefan P1-d2-479, P1-d2-548, P1-d3-558
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
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Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Aroyo, Ani P2-d2-1023*, P2-d2-1032*, P2-d3-644 Arpesella, Marisa P1-d3-331 Arrighi, Annalisa P3-d2-1341 Arrigo, Teresa P2-d2-1025 Arroyo Díez, Francisco P2-d1-922 Arsac, Pascaline P1-d1-470 Arsene, Christian P3-d1-1360 Arshinkova, Margarita LB3-1508 Arslanian, Silva P1-d3-438 Arslanoglu, Sertaç P1-d2-519 Artan, Sevilhan P2-d1-662 Arveiler, Benoit P1-d2-329 Arya, Ved FC11-183, FC11-185, P2-d1-850*, P3-d3-1349 Arzamascev, Alexander P3-d1-1254 Asai, Masato FC20-1484 Asakura, Yumi FC19-229, P1-d1-504, P3-d1-1226 Asami, Tadashi P2-d2-1183 Asar, Gulgun P2-d3-1074 Asci, Ali P1-d2-552 Asenjo, Sylvia P2-d3-880 Asensio Llorente, Marino P1-d1-238 Ash, Shifra P3-d1-1251 Ashworth, Michael FC11-185 Askenas, Meik FC6-152 Asker Kaya, Gamze P2-d1-1079 Aslanger, Ayca Dilruba P2-d1-1046 Aso, Keiko P1-d1-237* Asselta, Rosanna P1-d2-434 Assia, Benaissa P3-d2-1241 Atabek, Mehmet Emre P2-d2-760*, P2-d2-865*, P3-d2-1342, P3-d1-1460 Atay, Zeynep P1-d2-464, P2-d1-742, P2-d1-849, P2-d1-884, P2-d3-715, P2-d3-803* Atef, Abeer P2-d2-1117 Athanassiadou-Piperopoulou, Fani P2-d2-1057, P2-d2-798 Athanassiou-Metaxa, Miranda P2-d2-702 Atik, Tahir P2-d3-1126 Attaelmannan, Mohammed P2-d1-1076 Attaie, Morag P2-d2-1156 Auchus, Richard P2-d1-624 Audí Parera, Laura P1-d1-291*, P1-d3-265, P1-d1-310, P2-d3-804 Auger, Julie P2-d1-1000* Augoulea, Areti P2-d2-864 Auriol, Françoise P1-d2-329
Avalos, Carolina P1-d1-235, P1-d2-325, P2-d1-920 Avatapalle, Bindu FC11-182, FC11-184* Avbelj Stefanija, Magdalena P2-d3-773* Avdjieva, Daniela P2-d2-1032 Aversa, Tommaso P1-d3-271, P2-d2-834 Avila, Alejandra LB1-1495 Avula, Shivram P3-d2-1414 Awadalla, Shokery P2-d1-744*, P2-d1-788* Ayabe, Tadayuki P2-d1-818* Ayalon, Itay FC9-173* Ayat, Samir P2-d1-1110 Aycan, Zehra P2-d1-817, P2-d3-1075, P2-d3-643, P3-d2-1296, P3-d2-1437 Aydin, Ferah P1-d3-409, P2-d1-1102 Aydin, Murat P3-d1-1463 Aydin, Omer Faruk P2-d1-1143 Aye, Tandy P1-d2-428*, P1-d3-442 Aymé, Ségolène P1-d1-422 Ayoola, Omolola P3-d1-1399 Ayyavoo, Ahila P1-d1-524, P1-d1-525 Azaretzky, Miriam P1-d3-373, P2-d2-755 Azcona, Cristina P1-d2-323* Azimova, Shahnoza P3-d2-1283* Aziz, Qadeer FC11-183 Azocar, Marta P1-d1-471, P1-d2-296 Azzi, Salah P1-d1-387, S6-30 Azzolini, Claudio P1-d1-420 Azzolini, Sara P2-d1-956 Azzoug, Said P2-d1-1181*, P2-d1-735, P2-d2-1029, P3-d1-1202, P3-d1-1224*, P3-d1-1255, P3-d2-1419 B
Babaoglu, Kadir P2-d1-1174 Babar, Ghufran P3-d1-1424, P3-d2-1413 Babiker, Amir P2-d2-935, P2-d3-1160*, P3-d1-1231, P3-d2-1214*, P3-d3-1354 Bacchelli, Chiara FC10-174 Bacchetta, Justine P1-d1-470 Bacher, H. Peter P1-d3-554 Bachrach, Laura LB1-1491 Backeljauw, Philippe P1-d2-394, P1-d2-395*, P2-d1-1103 Badiel, Marisol FC6-151 Bae, Jae Wook P2-d2-1097 Bae, Yoon Ju P1-d1-390
* Presenting author
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9th Joint Meeting of Paediatric Endocrinology 2013
Baek, Joon Woo P1-d3-556, P2-d1-892 Bagatin, Antonio Carlos P3-d1-1369 Bagheri, Fereshte P3-d3-1311 Baglin, James FC14-201 Bahadir, Sevgi P1-d1-280 Bahillo-Curieses, Pilar P2-d1-955, P2-d2-634 Bahlmann, Hagen P2-d2-861 Bailez, Marcela FC8-163 Baizhumanov, Adil P2-d1-813, P2-d1-814 Bak, Beata FC10-176 Bakker, Nienke P1-d3-411* Bal, Milva P2-d1-1139, P2-d3-976* Balatska, Nataliya P3-d2-1238 Balbi, Viviana P2-d3-1168 Balci, Ali P2-d1-693 Baldazzi, Lilia P2-d1-1145*, P2-d1-619, P2-d3-649 Baldinotti, Fulvia P1-d2-588 Baldoli, Cristina FC2-129 Balestri, Eleonora P2-d1-882 Baleva, Dilyana P1-d2-356 Balkir, Ferat P2-d2-926 Ball, Lynn P3-d1-1249 Ballarini, Elisa P2-d1-694 Ballerini, María G. P1-d1-239*, P1-d3-413*, P1-d3-563, P2-d3-982, P2-d1-1042, P2-d2-1061 Balsamo, Antonio FC8-166, P1-d1-594, P2-d1-619, P2-d3-648, P2-d3-649*, P2-d3-810*, P3-d1-1406 Balsamo, Claudia P2-d2-896 Baltacioglu, Feyyaz P2-d1-663 Baltaretsou, Elisabeta P2-d3-812 Bancalari, Rodrigo P1-d1-235, P1-d2-325, P2-d1-920 Banchini, Giacomo P1-d1-498*, P3-d1-1402 Bando, Hironori S15-58 Banecka, Bozena P2-d1-669 Banerjee, Indi FC11-181, FC11-182 Banerjee, Indraneel FC11-184, P2-d1-1002 Banerjee, Kausik P2-d1-671 Bang, Peter FC7-161*, P2-d2-825, SAT9 Bankenstein, Oliver P1-d3-612 Banzato, Claudia P2-d1-1085, P3-d2-1301 Baptista, Maria P1-d2-253 Baquedano, Eva P1-d1-347 Baquedano, Maria Sonia FC9-168*
Baquero Montoya, Carolina P3-d2-1302 Bar Ilan, Ahuva FC16-215 Baran, Riza P2-d1-686, P3-d2-1335 Baranowski, Elizabeth P2-d2-634* Barbaro, Daniele P2-d1-956 Barbetti, Fabrizio P1-d1-473* Barbieri, Flavia P2-d2-1190 Barbosa, Telma LB3-1515 Barchana, Micha P2-d1-1135 Bardadin, Krzysztof P1-d2-599 Bardsley, Martha P2-d1-1100 Barg, Ewa P1-d3-406, P3-d1-1252*, P3-d1-1253, P3-d1-1257* Baricco, Marta P2-d1-988 Bar-Iilan, Ahuva P1-d1-391 Barisic, Ingeborg P1-d2-259, P2-d3-914 Barnea-Goraly, Naama P1-d3-442 Barnes, Michael FC4-141 Barnes, Nicole P1-d2-515 Baron, Jeffrey FC2-127, P2-d2-972, PL9-9* Baron, Sabine P1-d2-580 Baronio, Federico P1-d2-402, P2-d1-694, P2-d3-648*, P3-d1-1406* Barreiro, Jesús P2-d1-951 Barreno-Sardiña, Guillermo P1-d2-435 Barrera, Antonio P2-d2-902 Barrett, Timothy FC9-170, P1-d1-422*, P2-d1-1037, S3, S3-20*, Barrio, Raquel P2-d1-851, P2-d1-853, P2-d1-886, P2-d2-869, P2-d2-930 Barrios, Vicente FC15-207, FC17-221, P1-d1-308, P1-d1-311*, P1-d2-360, P1-d3-333* Barsaoui, Sihem P2-d1-1109 Barthlen, Winfried P2-d2-861, P2-d2-934, P2-d3-914 Bartucci, Andrea P1-d2-360* Bartus, Bela P2-d2-863 Bas, Firdevs P1-d1-352, P2-d1-1050, P2-d1-1079, P2-d2-1187, P2-d2-1191, P2-d3-652, P2-d3-771* Bas, Veysel Nijat P2-d3-643*, P2-d1-817, P2-d3-1075, P3-d2-1296*, P3-d2-143 Basiak, Aleksander P2-d3-1065 Bassi, Lorenzo P1-d2-547, P2-d1-1137, P2-d1-996, P2-d3-716, P3-d1-1363
Bassols, Judit FC14-198*, FC14-199, FC15-209, FC17-216, P1-d2-321*, P1-d3-376, P2-d2-636 Bastaki, Despoina LB2-1499 Bastug, Osman P1-d1-500 Bath, Louise P2-d2-827 Battaglia, Cristina P1-d2-434 Battaglia, Teresa P2-d2-695 Battaglino, Roseila P2-d1-668, P2-d2-675, P2-d2-676 Battelino, Tadej P1-d2-457, P1-d3-334, P1-d3-367, P2-d1-687, P2-d2-829, P2-d3-772, P2-d3-773, SAT8 Battistin, Claudilene P3-d1-1411 Bau, Anne-Madeleine P1-d2-328, P1-d3-555 Bauer, Jana-Leonie FC7-159, P2-d3-845 Baumhoer, Daniel P3-d1-1225 Baunin, Christiane P2-d1-1049 Baur, Isabel P2-d1-958 Bauters, Melissa FC13-195 Baydogan, Misli P3-d2-1334 Bayhan, Asuman P2-d3-806 Bayindir, Petek P2-d3-1074 Baz, Ouidad P2-d1-1110* Bazan, Maria P2-d2-763* Beardsley, Elaine P2-d1-925 Beauloye, Véronique P1-d2-250, P1-d2-401, P2-d3-708 Beccaria, Luciano P1-d2-258 Bechtold, Susanne FC6-152 Beciu, Marian P3-d2-1382* Beck, Roy P1-d3-442 Becker, Bettina FC7-159, P2-d3-845 Becker, Marianne P2-d3-1169* Beckers, Dominique FC4-138, P1-d2-250, P1-d2-401 Beck-Nielsen, Signe P2-d1-689* Beck-Peccoz, Paolo P2-d1-1020, WG5-106* Bedair, Elsaid P3-d2-1372 Bedecarrás, Patricia P2-d1-1042 Bedrosian, Camille FC20-1488 Beer, Nusen P3-d3-1390 Behret, Fabian P1-d1-448 Belahcene, Sihem P3-d1-1426 Belei, Oana P2-d3-808, P3-d1-1228 Belgorosky, Alicia FC8-163, FC9-168, P1-d3-267, P1-d3-562, P1-d3-610, P2-d2-632 Belhadj Aissa, Nassima P3-d1-1255*
Belhimer, Faiza P2-d1-735, P3-d1-1202, P3-d1-1426 Bellanné-Chantelot, Christine P2-d3-914 Bellini, Francesca P2-d2-896 Bellizzi, Maria P3-d2-1338, P3-d3-1350 Bellone, Simonetta P1-d1-348, P1-d3-369, P1-d3-379, P2-d1-816*, P3-d1-1204 Beltrami, Nadia FC1-123, P1-d2-490 Beltrand, Jacques P1-d1-502 Ben Ari, Tal P1-d3-441 Ben Becher, Saayda P2-d1-1109, P3-d2-1442 Ben Jemaa, Lamia P2-d1-1109 Ben Jemaa, Sarra P2-d1-1109 Benabbad, Imane P2-d1-738 Benadjaoud, Lila P2-d1-1048 Ben-Ami, Michal P2-d3-807 Benary, Doreen P2-d3-807 Bendali, Mohamed P3-d1-1224, P3-d2-1419* Bendlova, Bela P1-d3-340 Benedetti, Andrea P1-d2-461 Benevento, Danila P2-d1-889, P2-d2-761 Benini, Luigi P2-d1-1085 Benitez-Aguirre, Paul P1-d3-443 Benito-Sanz, Sara P2-d1-955, P2-d2-969 Benkerrou, Malika P1-d2-487 Bennie, Marion P2-d1-752 Benoit, Melissa Anne S19 Ben-Shachar, Shay FC9-173 Ben-Skowronek, Iwona P1-d1-590*, P1-d3-406, P2-d1-669*, P2-d1-986, P2-d2-1151 Benyi, Emelie P1-d2-484* Benzrihen, Gabriela P3-d1-1470 Berard, Emilie P2-d1-1049 Berard, Laurence P1-d1-387 Berberoglu, Merih P2-d2-1116, P2-d3-1123 Bercovich, Danni LB4-1527 Bereket, Abdullah P1-d2-300, P1-d2-464, P2-d1-1050, P2-d1-742, P2-d1-849, P2-d1-884, P2-d3-715, P2-d3-803 Berensztein, Esperanza FC8-163* Bergadá, Ignacio P1-d1-239, P1-d3-270, P1-d3-413, P1-d3-563, P2-d1-1051, P2-d1-1136, P2-d1-1173, P2-d2-1061, P2-d3-982, P3-d1-1470
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
255
Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Bergamaschi, Silvia P2-d1-1020 Bergman, Stefan P2-d2-700 Berini, Jenny P1-d2-399 Bermudo, Francisco P2-d1-745 Bernal, Nancy P3-d3-1445 Bernard, Daniel FC10-176 Bernardes Guimarães, Victória P3-d2-1380 Bernasconi, Sergio FC5-145, P1-d1-498, P2-d1-1040, P2-d1-956, P3-d1-1402 Bernlohr, David P1-d2-324 Berrade, Sara P2-d2-703*, P3-d2-1282 Bertelloni, Silvano FC8-166 Bertherat, Jerôme FC1-122 Berthold, Antje P2-d3-1066 Bertholt, María P2-d1-785 Bertok, Sara P2-d1-687 Bertrand, Anne-Marie FC6-155, P3-d2-1273 Bervoets, Liene P2-d1-779 Bessahraoui, Mimouna P2-d2-1062*, P3-d1-1221* Bessenay, Lucie FC12-187 Besser, Rachel FC14-200* Bettendorf, Markus P1-d2-604 Bettocchi, Ilaria P2-d1-1139*, P2-d1-1145, P2-d3-976 Beux, Sheila P2-d1-988 Bey, Abderrahim P3-d2-1416 Bezen, Digdem P2-d1-1050 Bezlepkina, Olga P2-d2-832 Bhangoo, Amrit P1-d1-386, P2-d1-620, P2-d2-1056, P3-d1-1235 Bhatia, Rahul P2-d2-1184 Bhatia, Vijaylakshmi P2-d2-699*, WG3-97 Bianchi, Maria Luisa SAT3 Biassoni, Lorenzo P1-d2-426, P2-d1-859 Bickenbach, Annika P1-d2-328, P3-d1-1269* Bidad, Katayoon P2-d2-789 Bideci, Aysun P2-d3-770, P2-d3-944, P3-d1-1455* Bidet, Maud P1-d1-533*, P2-d2-1053, P2-d2-1088, P2-d2-1091 Bielitz, Julia P1-d1-318, P2-d2-753 Bielskute, Egidijab P3-d1-1429* Bieniasz, Jolanta P2-d3-1065 Bieri, Andreas P1-d2-485* Biermasz, Nienke FC10-177 Bieth, Eric P1-d2-329 Bignon, Horacio P3-d1-1470 Bilen, Sevcan P3-d3-1449 Binay, Cigdem P2-d1-662, P2-d2-641*, P3-d1-1425 Binder, Elisabeth P3-d1-1323
Binder, Gerhard FC7-159*, P1-d2-545, P1-d2-604, P2-d3-845, SAT6 Bircan, Iffet P1-d2-552, P2-d2-791* Birkebæk, Niels P1-d1-281, P2-d1-666*, P2-d1-724* Birkholz-Walerzak, Dorota P1-d3-406 Bisacchi, Nicoletta P2-d3-810 Bishop, Jonathan P2-d3-983 Bistritzer, Tzvi FC3-137 Bizerea, Teofana P1-d1-452, P3-d2-1236 Bizzarri, Carla P1-d2-255, P2-d1-889*, P2-d2-1031 Bjerknes, Robert P1-d1-474 Black, Corri P2-d1-752 Black, Graeme LB4-1519 Blair, Jo C. P2-d3-839, P3-d1-1364 Blair, Joanne P1-d1-244*, P2-d1-1138, P2-d1-1141, P2-d1-630, P2-d2-931, P3-d2-1414* Blaise, Annick FC5-147 Blanco, Estela P1-d3-372, P2-d2-757, P2-d2-894 Blanco, Miguel P1-d1-380 Blankenstein, Oliver P1-d2-463*, P1-d2-603, P2-d3-1169 Blaschek, Astrid FC6-152 Blazewicz, Anna P2-d1-986 Blethen, Sandra P1-d2-400 Blokh, Sofya P2-d2-633* Bloomfield, Frank P1-d1-524 Blouin, Jean-Louis P2-d2-927 Blum, Samantha P1-d2-394 Blum, Werner FC10-179, P1-d1-498, P1-d3-407, P2-d1-1011, P2-d2-831, P3-d1-1402 Boal, Rachel P2-d1-690 Bober, Ece P1-d1-454, P1-d2-365, P2-d2-706, P3-d1-1227, P3-d1-1457, P3-d2-1436, P3-d3-1383 Bocchini, Sarah P1-d2-465, P2-d1-659* Bodzenta-Lukaszyk, Anna P1-d1-596 Boettcher, Claudia FC18-227* Bogdanova, Polina P2-d1-1043*, P3-d1-1330* Bogolubov, Sergey P2-d1-658 Bogova, Elena P1-d2-327* Boguszewski, Margaret P1-d1-389*, P3-d1-1369* Böhles, Hansjosef P1-d1-349
* Presenting author
256
9th Joint Meeting of Paediatric Endocrinology 2013
Boiani, Arianna P1-d1-385, P1-d2-255*, P1-d2-465, P2-d1-889 Boiko, Julia P3-d2-1476 Bojesen, Anders FC1-125 Bokelmann, Jessica P1-d1-418 Bolli, Geremia B. S5, S5-26* Bolloli, Sara P2-d2-897, P2-d3-874, P2-d3-946*, P3-d2-1339*, P3-d2-1341 Bologna, Giuseppina LB2-1503 Bolotova, Nina P2-d2-1118 Bolte, Lilian P1-d1-235, P1-d2-325, P2-d1-920 Bolten, Margarete P2-d3-768 Bom van der, J. P3-d1-1249 Bomanji, Jamshed P1-d2-426, P2-d1-859 Bona, Gianni P1-d1-348, P1-d3-369, P1-d3-379, P2-d1-816, P3-d1-1204 Bondy, Carolyn WG5-109* Bone, Henry LB1-1491 Boner, Attilio P1-d2-549 Bonfanti, Riccardo P2-d1-668, P2-d2-675, P2-d2-676 Bonfig, Walter P2-d1-625* Bongers-Schokking, Jacoba LB4-1525* Bongiovanni, Marzia P2-d1-889 Bonillo, Antonio P2-d3-775 Bonnefond, Amélie FC6-155 Bonnet, Caroline P2-d1-1178 Bonomelli, Irene P1-d1-569, P1-d3-331 Bonomi, Marco FC10-177, P1-d2-547, P2-d1-1040* Bonura, Clara P2-d1-668, P2-d2-675, P2-d2-676* Bony-Trifunovic, Hélène LB3-1510, P1-d2-581 Boomsma, Dorret I. P1-d1-595 Boquete, Hugo P1-d3-373, P2-d2-755* Borba, Vanessa P2-d2-794* Bordallo, Ana Paula P1-d2-322 Bordallo, Maria Alice LB1-1494, P1-d2-322 Bordoni, Roberta P1-d2-434 Borges Polli, Janaina P2-d2-962 Borges, Marcos Antonio P1-d2-322 Borges, Maria P2-d1-1044*, P2-d1-1180*, P2-d2-866, P3-d2-1441 Borges, Teresa LB3-1515* Boros, Erika P2-d3-708 Borschiver, Clarice P1-d2-322 Bosetti, Alessandra P1-d1-540, P3-d2-1344 Bosley, Thomas P2-d3-713
author index
Braslavsky, Débora P1-d3-413, P2-d1-1136*, P2-d3-982, P3-d1-1470 Bratanic, Nevenka P1-d3-334 Bratanic, Nina P1-d3-367*, P2-d1-687 Bratina, Nataša P1-d2-457, P1-d3-334, P1-d3-367, P2-d3-773 Bratta, Pasquale P3-d2-1211 Braun, Regina P1-d1-448 Brauner, Raja P1-d2-580 Bravaccio, Carmela P2-d1-1039 Brehar, Andreea-Cristiana P2-d2-800 Brenner, Herrmann P1-d1-528 Bressiani, Marina FC13-194 Bresters, Dorine P3-d1-1249 Bretones, Patricia P2-d1-1178 Breukhoven, Petra FC16-212 Brigati, Giorgia P2-d3-718 Bright, George FC16-214* Brilli, Richard P1-d1-449 Brioude, Frederic FC5-147*, P1-d1-387, S6-30 Brito, Vinicius FC4-138, P1-d1-506 Brixen, Kim P2-d1-689 Brnjac, Lori P2-d3-1164 Brodzisz, Agnieszka P2-d2-1151 Broomhead, Sarah P2-d2-677 Brosse, Aurelie FC1-124 Brown, Robert LB1-1491 Bruel, Montserrat FC14-199 Brueton, Louise P1-d1-511 Brufani, Claudia P1-d2-465, P2-d1-999 Brugger, Markus FC5-148 Brugières, Laurence P2-d1-691, P2-d1-738 Bruner, Ann LB1-1491 Brunet, Ernest FC19-228 Brunetti, Giacomina FC2-130, P1-d1-316*, P2-d1-727 Brunetto, Oscar P2-d1-629, P3-d1-1405 Bruno, Claudio P2-d3-718 Bruno, Maria P2-d2-763 Brusgaard, Klaus P2-d1-689 Brust, Ester P2-d2-1186 Bruzzi, Patrizia P1-d1-350, P2-d1-737*, P2-d1-741, P2-d1-749, P2-d1-882* Bryce, Jillian FC8-166, WG6-117* Bryer, Paul P2-d2-797 Bryk, Kristina P1-d1-574 Bucak, Feride Tahmiscioglu P3-d1-1423
Buchanan, Charles R. P1-d2-516, P2-d1-1171, P2-d2-639, P3-d1-1197 Buchanan, Kerry P3-d2-1303 Buchfelder, Michael P2-d1-665 Buck, Cecília P2-d3-949 Budnik, Tetyana P3-d2-1238 Bueno Lozano, Gloria P3-d2-1302* Bueno Martínez, Inés P3-d2-1302 Bueno, Gloria P1-d1-354, P3-d2-1274 Buffet, Alexandre P1-d2-329 Bui, Thao P2-d2-893, P2-d3-879, P2-d3-939 Bullock, Jemima P2-d1-883 Bulus, Derya LB1-1489* Bulwer, Chloe P1-d2-517* Bulzomì, Patrizia P2-d3-716, P3-d1-1363 Bunch, Trevor P1-d2-584 Bundak, Rüveyde P1-d1-352, P2-d1-1050, P2-d1-1079, P2-d2-1187, P2-d2-1191, P2-d3-652, P2-d3-771 Burckhardt, Marie-Anne P3-d1-1225* Burgos-Ramos, Emma P1-d1-311, P1-d3-333 Burke, Derek FC10-174 Burkman, Ronald LB1-1491 Burns, Jane P2-d1-1083 Burrai, Carlo P2-d1-956 Burrows, Raquel P1-d3-372, P2-d2-757, P2-d2-894* Burundukov, Ella FC4-139 Busiah, Kanetee FC6-155*, P2-d1-1000, P2-d1-1048* Bustos, Mayra P2-d1-780 Bustos, Paulina P2-d3-880* Butler, Gary P1-d1-468*, S1-11, S1-14, S1-15 Butyhina, Viktoria P1-d1-497* Buysse, Wesley P1-d2-250* Buyukgebiz, Atilla P3-d1-1457* Buzi, Fabio P3-d1-1368 Buzzakino, Noemi LB1-1490 C
Caballero-Villarraso, Javier P3-d1-1267 Cabanas, Paloma P2-d1-951 Cabral de Menezes Filho, Hamilton P3-d1-1411 Cabrera, Claudia FC4-141 Cabrera, Martín Rodríguez P3-d2-1276 Cabrol, Sylvie P1-d1-511, P1-d2-580 Cáceres, Daniela P3-d1-1405 Cafiero, Giulia P2-d1-999
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
257
Floor Plan Exhibition Author Index
Bosque Zabala, Alfredo P3-d3-1353 Bossowska, Anna P1-d1-596, P1-d2-599 Bossowski, Artur P1-d1-596*, P1-d2-599*, P1-d3-406, P3-d2-1213, P3-d3-1392 Boto, Leonor P1-d1-245 Bouali, Ouardia P2-d1-1049 Bouchoucha, Nadia P1-d2-581* Boudraa, Ghazalia P2-d2-1062, P3-d1-1221 Bougnères, Pierre FC12-187, P1-d1-529, P2-d1-751, P3-d3-1346 Boukhair, Martín P2-d1-1051 Bourdeaut, Franck P2-d1-738 Bourguignon, Jean-Pierre P1-d2-579 Bournez, Marie P2-d1-1049 Boussetta, Khedija P2-d1-1109 Boustani, Dinane Samara P2-d1-1178 Boutekdjiret, Faiza P3-d1-1202*, P3-d1-1224 Bouvattier, Claire FC1-122, P1-d1-529, P1-d2-580, WG6-118 Bouziane Nedjadi, Karim P2-d2-1062, P3-d1-1221 Bowlby, Deborah P2-d3-840 Boyanovsky, Adriana P2-d3-979 Boyko, Valentina P2-d3-807 Boyraz, Mehmet LB2-1500*, LB2-1501, P2-d1-782, P2-d2-862, P2-d3-1124* Boz, Adil P2-d1-722 Bozlak, Serdar P2-d3-652 Bozzola, Elena P3-d1-1288 Bozzola, Mauro P3-d1-1288 Brachet, Cécile P1-d1-387, P1-d2-401, P2-d3-708 Brad, Giorgiana Flavia P2-d3-808, P3-d1-1228* Bradley, Karin P1-d2-362, P1-d3-336 Bradley, Therese P2-d2-1156 Brady, Cassandra LB2-1502* Brain, Caroline P2-d2-631 Brambilla, Alice P1-d1-569 Brambilla, Ilaria P1-d2-547, P3-d1-1363 Brambilla, Paolo P2-d1-668* Brandalise, Silvia FC13-192, FC13-193, FC20-1486 Brandi, Maria-Luisa P2-d1-683 Brandt, Marcus FC17-217 Brandt, Stephanie P1-d1-528* Brannsether, Bente P1-d1-474 Brar, Preneet P2-d1-1076*, P2-d2-901*
Floor Plan Exhibition Author Index
author index
Caimari, Maria P3-d1-1331 Caine, Louise FC11-184, P2-d1-1002 Caiulo, Silvana P1-d1-598 Cakir, Meltem Didem P2-d2-1022* Calais, Flávia P1-d2-577* Calandra, Erika P2-d2-695 Calcagno, María De Luján P1-d3-373, P2-d2-755, P3-d1-1462 Calcaterra, Valeria P1-d1-569, P1-d3-331*, P3-d1-1288 Caldwell, Karen P1-d2-431 Calhoun, Peter P1-d2-431 Callegari, Sandra P2-d1-1044 Callens, Nina FC8-167 Cama, Alessandro P1-d2-366 Camacho-Hubner, Cecilia P2-d1-824 Camargo, Kenny Yelena P1-d3-270 Camats, Núria P1-d3-265* Cambiaso, Paola P1-d2-252*, P1-d2-255, P2-d2-1031 Cameron, Fergus FC6-154, P1-d3-436, P1-d3-440, P1-d3-443 Campagnoli, Myrna P2-d2-1094 Campbell, Daniel FC18-225 Campeau, Philippe LB1-1493 Campi, Irene FC10-177 Campino, Carmen P1-d1-235, P1-d2-325, P1-d3-377, P2-d1-920 Campos, Clara P1-d1-566 Campos-Barros, Angel P1-d2-435*, P2-d3-844* Campoy, Cristina P1-d2-323 Camtosun, Emine P2-d3-1123 Çamurdan, Orhun P2-d3-770*, P2-d3-944, P3-d1-1455 Can, Ngoc P2-d2-893*, P2-d3-879, P2-d3-939* Can, Sule P3-d2-1436 Candela, Gilberto P2-d2-1030, P2-d2-870 Canelles, Sandra P1-d3-333 Caner, Ibrahim P2-d2-926, P3-d3-1352 Cañete-Vázquez, María D. P1-d1-491, P2-d1-745, P3-d1-1267* Cañete, Ramón P1-d1-491, P2-d1-745, P3-d1-1267, P3-d2-1477 Cangemi, Giuseppe P2-d1-1145 Cann, Fiona P2-d1-1105 Cannalire, Giuseppe P2-d1-1019, P2-d1-1021
Cano, Francisco P1-d1-471, P1-d2-296* Canpolat, Cengiz P2-d1-742 Cantalapiedra, Mônica P3-d3-1393 Cantamessa, Gloria P1-d1-569 Cantasano, Antonella P2-d1-1139, P2-d3-976 Canton, Ana P1-d1-469*, P1-d1-506 Cao, Bing P2-d2-937 Cao, Bingyan P3-d1-1195 Cao, Xu FC2-126 Cao, Yingting P1-d1-353 Capalbo, Donatella P1-d2-588, P1-d3-410, P2-d2-1154 Capanna, Rita P1-d2-366, P3-d1-1265 Capito, Carmen P2-d2-1053* Cappa, Marco FC1-123, P1-d1-275, P1-d1-505, P1-d2-252, P1-d2-255, P1-d2-465, P1-d2-490, P1-d3-415, P2-d1-659, P2-d1-889, P2-d1-999, P2-d2-1031, P2-d2-761 Caprio, Sonia S8-37* Capuano, Francesco P1-d1-312, P2-d1-1106, P2-d1-684, P2-d1-960 Caragheorgheopol, Andra P2-d2-800 Carbone, Claudia P1-d1-316 Carcavilla, Atilano P1-d1-477* Cardani, Roberta P1-d1-420 Cardinale, Giuliana P2-d1-956 Cardinalli, Izilda FC13-193 Cardoso, Cármen LB3-1515 Cardoso, Helena LB3-1515 Cardoso-Demartini, Adriane P3-d1-1369 Carducci, Chiara P2-d2-761, P2-d3-874 Carel, Jean-Claude LB3-1510, P1-d2-487, P2-d2-1091, PL4-4, S1, S1-11, S1-12*, S1-14, S1-15 Carella, Francesca P1-d1-450, P3-d2-1340 Carella, Massimo P2-d3-842, P3-d2-1433 Carey, Dennis P1-d1-246 Carfagna, Luana P2-d1-1049 Carla, Chilelli P1-d3-610 Carloni, Laura P1-d2-297 Carmichael, Polly FC4-143, P2-d1-883 Carolan, Eirin P1-d3-338 Caron, Philippe FC1-122 Carrasco, Nancy P1-d3-611
* Presenting author
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9th Joint Meeting of Paediatric Endocrinology 2013
Carrascosa Lezcano, Antonio P1-d1-238, P1-d1-310, P1-d3-265, P2-d3-804 Carré, Aurore FC19-230 Carreras-Badosa, Gemma FC14-198, FC14-199*, FC15-209, FC17-216, P1-d2-321 Carrilho, Alexandre José P1-d3-270 Carroll, Aoife P3-d2-1242* Carroll, Rona FC4-138 Cartault, Audrey P2-d1-1049 Cartigny, Maryse FC1-122 Caruso, Silvia P2-d1-734 Caruso-Nicoletti, Manuela P1-d2-434 Carvajal, Cristian P1-d1-235, P1-d2-325, P1-d3-377, P2-d1-920 Carvalho, Cecilia P1-d2-322 Carvalho, Julienne LB4-1522 Carvalho, Luciani P1-d1-506, P2-d1-952 Casano- Sancho, Paula P1-d1-388* Cascone, Enrica E. P1-d1-312, P2-d1-628, P2-d1-684 Cascone, Enrica P2-d2-1054 Casey, Angela P1-d1-534, P2-d1-821 Cassatella, Daniele P2-d1-1082, P2-d1-995 Cassio, Alessandra P2-d1-1139, P2-d1-1145, P2-d3-976 Cassorla, Fernando P1-d1-382*, P1-d1-419, P1-d1-492, P1-d1-495, P1-d1-567, P1-d3-445 Castagno, Matteo P1-d3-369, P2-d1-816 Castanet, Mireille P2-d1-736* Castaño, Luis P1-d1-591, P2-d3-904 Castellaneta, Stefania P1-d1-450 Castelnuovo, Paolo P1-d2-399 Castro, Andrea P1-d1-419, P1-d1-567*, P1-d3-445 Castro, Juan José P1-d1-492, P1-d1-495 Castro, Laura Cecilia P2-d3-979* Castro, Lidia P1-d1-354, P3-d2-1274 Castro, Magdalena P2-d3-875 Castro, Margaret FC13-192, FC13-193, FC20-1486 Castro-Correia, Cíntia P2-d3-1130, P3-d2-1415
Castro-Feijoo, Lidia P2-d1-951* Castro-González, David FC15-207, FC17-221, P1-d1-308 Cataix, Sophie P2-d1-1049 Catalina, Contreras FC6-151 Catena, Maria Ausilia P2-d2-870 Catherine, Peters P1-d1-245 Catli, Gönül P1-d1-454*, P1-d2-365*, P2-d2-706, P3-d1-1227, P3-d2-1436, P3-d3-1383 Cato, Allison P1-d3-442 Cauvin, Vittoria P2-d3-911, P3-d2-1338*, P3-d3-1350* Cavada, Gabriel LB1-1495, P2-d2-902 Cavaliere, Maria L. P2-d1-1106 Cavallari, Ugo P3-d1-1368 Cavalli, Loredana P2-d1-683 Cavallo, Luciano FC2-130, P1-d1-316, P2-d1-1016, P2-d1-727, P2-d2-1192, P3-d2-1211 Cavarzere, Paolo P1-d2-549, P1-d3-561, P2-d1-1085, P3-d2-1301 Cavé, Hélène FC6-155, P2-d1-1000 Cayir, Atilla P2-d1-721, P2-d3-714, P3-d2-1472*, P3-d2-1481*, P3-d3-1352 Ceballos, María P1-d1-471, P1-d2-296 Cebeci, Ayse Nurcan P1-d3-335*, P2-d1-1046*, P2-d1-663, P2-d2-860 Cebeci, Nurcan P2-d1-1050 Cebrià Romeo, Judith P1-d1-315 Cechinel, Julio P1-d1-472 Cekmez, Ferhat LB2-1501 Celebi Bitkin, Eda P2-d1-782 Celebi, Serdar P2-d3-938 Celik, Tanju P2-d1-693 Cendrós Carreras, JosepMaria P1-d2-400 Cengiz, Ali Bulent P2-d2-1022 Cengiz, Eda P1-d2-430 Cerbone, Manuela P1-d1-592*, P2-d2-1190 Cerioli, Andrea P1-d1-498, P3-d1-1402 Ceroni, Federica P2-d1-734 Cesari, Silvia P3-d1-1362* Cesur, Yasar P1-d2-359, P2-d2-928, P2-d3-776 Cetin, Irene SAT7
Çetinkaya, Semra P2-d1-817, P2-d3-1075, P2-d3-643, P3-d2-1296, P3-d2-1437 Cevik, Seval P3-d1-1453 Ceyhan, Mehmet P2-d2-1022 Ceylaner, Serdar P2-d3-1123 Chabah, Meryem P2-d3-1127, P3-d1-1199* Chabre, Olivier FC1-122 Chacon, Diana P3-d3-1445 Chae, Hyun-Wook LB4-1521, P2-d2-1097, P2-d3-1132 Chagin, Andrei S12-47 Chahardoli, Behnam P2-d2-1150 Chahin, Silvia P3-d3-1445 Chahla, Rossana P2-d2-763 Chaila, Zulema P2-d2-763 Chaler, Eduardo P1-d3-610* Chalumeau, Martin MTE9:1, MTE9:2 Chambon, Michel P3-d3-1385 Chan, Albert P1-d1-424 Chan, Li FC18-222, FC18-225*, FC20-1484 Chandler, Kate P1-d2-294 Chandran, Viji P3-d1-1201 Chandrasekaran, Surendran P3-d3-1357 Chang, Mi Sun P2-d2-1093* Chang, Young Pyo P2-d2-972 Chanoine, Jean-Pierre P1-d2-486, WG3-91* Chanudet, Estelle FC10-174 Chaplin, John P1-d2-392* Charalambous, Marika FC7-157* Chardon, Laurence P1-d1-470 Charles, Christelle P3-d2-1273 Charleton, Patricia P2-d2-1193 Charmandari, Evangelia FC18-223, FC8-164*, P1-d1-245, P1-d1-476, P1-d3-260, P1-d3-266, P1-d3-269, YB2 Chatelain, Pierre FC16-211, FC7-158, FC8-166, P2-d2-830*, SAT2, WG6-118 Chatterjee, Krishna FC10-177 Chatterjee, Sudip P2-d3-947* Chatzi, Alexandra P2-d2-1119 Chaussain, Catherine FC2-128 Chaves, Evelyne P2-d2-866 Chaychenko, Tetyana P2-d3-805* Chemaitilly, Wassim P1-d2-515* Chen, Hong-Shan P1-d2-396, P1-d3-559, P2-d1-1013* Chen, Lei P1-d2-430 Chen, Linqi P2-d2-1060* Chen, Malka FC4-139
Chen, Ming P2-d1-624* Chen, Qiu-Li P1-d2-396 Chen, Ran P3-d2-1337 Chen, Ruimin P3-d3-1315* Chen, Ruoqian P3-d2-1376 Chen, Xiuli P2-d2-1060 Chen, Xue P1-d3-370 Cheng, Peiyao P1-d3-442 Cheng, Ruoqian P2-d2-903 Cheng, Tina P1-d1-246 Cheng, Xinran P2-d1-1008* Chentli, Farida P2-d1-1018, P2-d1-1181, P2-d1-735, P2-d2-1026, P2-d2-1029, P3-d1-1202, P3-d1-1224, P3-d1-1255, P3-d1-1409, P3-d1-1410, P3-d1-1426, P3-d2-1304, P3-d2-1305, P3-d2-1412, P3-d2-1416, P3-d2-1418, P3-d2-1419 Cherchi, Gabriella P2-d1-619 Chernyak, Irina P2-d2-682 Chesi, Elena P3-d1-1402 Cheung, Pik-To P2-d2-1122 Chevenne, Didier P1-d1-502 Chiang, Sheng-Fong P1-d1-501 Chiarelli, Francesco FC5-149, LB2-1503, P1-d1-343, P1-d2-366, P1-d3-374, P2-d1-746, P3-d1-1262, P3-d1-1295 Chiarotti, Flavia P1-d2-606 Chiavaroli, Valentina FC5-149*, LB2-1503, P1-d1-343, P1-d3-374, P2-d1-746, P3-d1-1295 Chidanandaswamy, Rajesh P2-d1-1002 Chiera, Fernanda P2-d2-870 Chiesa, Ana P2-d1-1136, P2-d1-1173, P3-d1-1462* Chikulaeva, Olga P2-d1-813, P2-d2-832 Child, Christopher P1-d3-407, P2-d1-1011*, P2-d2-831* Chirico, Valeria P2-d2-1025* Chirita-Emandi, Adela P3-d2-1277 Chistousova, Galina P2-d2-633 Chitra, Surya P1-d3-557 Chiumello, Giuseppe FC1-123, P1-d1-594, P1-d2-258, P1-d2-399, P1-d2-434, P2-d1-1021, P2-d1-668, P2-d2-675, P2-d2-676 Chivu, Olivia P2-d3-708 Cho, Kyoung Soon P1-d1-475, P1-d2-458, P1-d2-483, P2-d1-777, P3-d1-1232* Cho, Sujin P2-d1-1086 Cho, Sung Yoon P2-d1-1003, P2-d1-1036*, P2-d2-1093
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
259
Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Cho, Won Kyoung P1-d1-475, P1-d2-458, P1-d2-483, P2-d1-777 Cho, Yoon Hi P1-d3-443* Choi, Byung P2-d2-1055* Choi, Jin-Ho P1-d1-234, P1-d3-618, P2-d1-731, P2-d1-887 Choi, Yun Jung P1-d1-475* Chong, W.K. P2-d1-883 Choong, Catherine P2-d3-841 Chou, Christine P3-d3-1446 Chouliaras, Giorgos LB2-1499 Chowen, Julie FC15-207, FC17-221*, P1-d1-308*, P1-d1-311, P1-d1-347, PL4-5 Christaki, Iliana P3-d1-1431, P3-d2-1280* Christensen, Rikke P3-d2-1373 Christesen, Henrik P1-d3-444* Christin-Maitre, Sophie FC1-122 Christoforidis, Athanasios P2-d1-994*, P2-d2-702*, P3-d1-1361 Chrousos, George FC18-223, FC8-164, LB2-1498, LB2-1499, LB3-1513, P1-d2-257, P1-d2-541, P1-d3-260, P1-d3-263, P1-d3-266, P1-d3-269 Chrysis, Dionisios P1-d2-484, S12-47 Chrzanowska, Krystyna P3-d1-1452 Chueca, Maria P2-d2-703, P3-d2-1282* Chugunov, Igor P2-d1-658* Chung, Sochung LB4-1521, P2-d2-1097 Chung, Woo Yeong P1-d2-488* Chun-I., Wu FC10-175 Cianfarani, Stefano P1-d1-385, P1-d1-505, P1-d2-255, P1-d3-415, P2-d1-889, P2-d1-999, S1, S1-11*, S1-14, S1-15, YB1 Ciccarelli, Maria FC2-130, P1-d1-316 Ciechanowska, Marta P2-d1-917, P2-d3-942 Ciftci, Ergin P2-d2-1022 Cilingir, Oguz P2-d1-662, P2-d2-641 Cinaz, Peyami P2-d3-770, P2-d3-944*, P3-d1-1455 Cinek, Ondrej FC10-179, P2-d2-895 Cioffi, Daniela P2-d1-956 Circo, Eduard P2-d3-1170*, P3-d2-1382, P3-d3-1451*
Cirillo, Grazia P1-d1-312, P2-d1-960 Cisternino, Mariangela P1-d2-399, P1-d2-547*, P2-d1-996, P2-d3-716*, P3-d1-1363 Cizmeci, Filiz P2-d1-1050 Çizmecioglu, Filiz Mine P1-d2-299, P2-d1-1174*, P2-d3-806 Claahsen-van der Grinten, Hedi P2-d1-657, WG6-118 Clark, Adrian FC18-222, FC18-224, FC18-225, FC20-1484 Clark, Chris P2-d1-883 Clark, Karen P1-d2-515 Clarke, Hannah P1-d2-306 Clarke, Iain FC6-150 Clayton, Peter FC11-181, FC11-182, FC11-184, FC16-211, FC7-158, LB4-1519, P2-d1-1002, P2-d2-830, S1-11, S1-14, S1-15 Clayton-Smith, Jill P1-d2-294 Cleemann, Line P1-d1-277* Cleland, Jeffrey FC16-214 Clément, Florencia P2-d3-982* Clemente León, María P1-d1-310 Clèries, Ramón P1-d1-503 Clisby, Holly P2-d1-883 Coccioli, Maria P2-d1-956 Cochat, Pierre P1-d1-470 Cocho, José Ángel FC19-228 Cochrane, Katherine P2-d1-921 Codazzi, Alessia P2-d3-716 Codner, Ethel LB1-1495, LB3-1517, P1-d1-419, P1-d2-543, P1-d3-445, P2-d3-1073, S16, S16-60*, WG4-101* Cody, Declan P1-d3-338* Coelho, Simone P3-d2-1272*, P3-d3-1393* Coeli-Lacchini, Fernanda P1-d2-253, P1-d3-270 Coeugniet, Florence P2-d2-1088 Cogulu, Ozgur P2-d3-1126 Cohen, Enzo P1-d1-511 Cohen, Pinchas CPE2-74*, SAT1 Cohen-Kettenis, Peggy S2, S2-17*, WG6-118 Cohn, Daniel LB1-1493 Cohn, Richard P1-d2-304, P2-d1-688 Colajacomo, Mauro P2-d1-659
* Presenting author
260
9th Joint Meeting of Paediatric Endocrinology 2013
Colao, Annamaria MTE3:1, MTE3:2 Colares Neto, Guido P2-d2-696* Colclough, Kevin P2-d1-852 Cole, Tim P1-d1-468 Cole, William LB1-1493 Coles, Rebecca P1-d1-278 Colle, Michel P1-d2-580, P2-d2-829 Collet, Ivan P2-d1-622, P2-d3-1163 Collett-Solberg, Paulo P1-d2-322* Collin, Philippe P2-d2-762 Collingwood, Catherine P1-d1-244, P2-d1-630 Collins, James P1-d2-394 Collot, Nathalie P1-d1-511 Colman, Peter P1-d3-436 Colmenares, Ana P2-d1-1048, P3-d3-1390* Colombo, Carlo P1-d1-473 Colombo, Ilaria P2-d1-1101, P2-d3-647 Colucci, Silvia P1-d1-316 Comaschi, Valentina P3-d2-1344 Combie, Michael P1-d3-440 Cominato, Louise P3-d1-1250, P3-d1-1411 Connor, Ellen P1-d2-363, P1-d3-378 Conte, Mariasole P1-d1-312*, P2-d1-1106, P2-d1-684, P2-d1-960 Conwell, Louise P2-d1-857 Cools, Martine FC8-165, FC8-166, FC8-167*, P1-d2-250, P2-d3-708 Cooper, Andrew P2-d3-984 Corbetta, Carlo P1-d1-598, P1-d2-254, P1-d2-606* Cordeschi, Talita P3-d1-1250, P3-d1-1468 Cordone, Vincenzo LB2-1503 Cormack, Barbara P1-d1-524 Cormier-Daire, Valerie WG1-85* Corona, Alberto M. P2-d1-628 Correa, Fernanda P1-d1-506* Corrêa, Pedro H. P2-d2-696 Correa-Burrows, Paulina P1-d3-372*, P2-d2-757*, P2-d2-894 Correia, Cíntia P3-d1-1222 Correia, Filipa P3-d1-1222* Corrias, Andrea FC1-123, P1-d1-594, P1-d2-258, P1-d2-600, P2-d1-737 Corrigan, Michelle P1-d3-338
Corsello, Giovanni P3-d2-1246*, P3-d2-1473, P3-d2-1475 Corvalan, Camila P1-d3-341, P1-d3-375 Cosgrove, Karen FC11-181, FC11-182, FC11-184 Coskun, Kenan P2-d1-663 Costa Neto, Luciane FC13-194 Costa, Carla P2-d3-1130*, P3-d2-1415 Costa, Elaine Maria P1-d2-583, P1-d3-270 Costa, Estevão P2-d3-1130 Costa, Silvia P1-d1-506 Costalonga, Everlayny LB2-1496*, LB4-1520*, P1-d1-506, P1-d2-482 Coste, Joël S1, S1-13* Cotterill, Andrew P1-d3-443, P2-d1-1017, P2-d3-841, P3-d2-1303 Couch, Robert P2-d2-867 Counts, Debra P2-d3-840 Couper, Jennifer P1-d1-345, P1-d2-433*, P1-d3-443, P2-d2-679 Couper, Jenny P1-d1-276 Coupey, Susan LB1-1491 Couriel, Jonathan P1-d1-244, P2-d1-630 Cousounis, Pamela P3-d2-1371 Coutant, Régis FC12-187, LB3-1510, P1-d2-580 Cowell, Chris P1-d2-304 Cowley, Michael P1-d1-531 Cox, Kathryn P1-d2-586* Cox, Rachel P1-d2-362, P1-d3-336 Cozzani, Hugo P2-d1-1173 Craen, Margarita P1-d2-250 Craig, Maria P1-d1-424, P1-d2-603, P1-d3-443, P2-d2-893, P2-d3-939 Cramers, Nicole P2-d1-959 Crane, Janet FC2-126* Crawford, Lorna P2-d1-1105 Cresta, Nicoletta P2-d1-628*, P2-d1-684* Crimmins, Nancy LB2-1502 Crinò, Antonino FC1-123, P1-d1-594, P1-d2-258, P1-d2-465, P2-d1-659 Crispel, Yonatan FC5-144 Crock, Patricia LB4-1524* Cromer, Barbara LB1-1491 Crosnier, Hélène LB3-1510, P1-d1-533 Crowne, Elizabeth P1-d1-383, P1-d1-467, P1-d2-362, P1-d2-520, P1-d3-336 Crudo, David P3-d2-1343
Crujeiras, Vanesa P1-d1-354, P3-d2-1274 Cucchiara, Andrew P3-d2-1371 Cukier, Priscilla FC4-138 Cummings, Elizabeth P1-d2-486 Cun, Yueshuang P2-d2-968 Cunha, Sarah Baccarini P1-d2-577 Cuny, Ariane P1-d1-529*, P3-d3-1346 Curry, Cynthia LB1-1493 Curtis, Vanessa P1-d2-363 Cuscó, Ivon PL4-5 Custódio, Rodrigo P3-d1-1367 Cusumano, Janine P1-d1-424 Cutfield, Wayne P1-d1-524*, P1-d1-525*, P2-d2-1158, PL3-3*, SAT5 Cutler Jr., Gordon P2-d1-1011 Czarnocka, Barbara P1-d2-599 Czernichow, Paul FC6-155, P2-d1-819* Czkwianianc, Elzbieta P3-d1-1370 D
da Rocha, Lívia P3-d3-1393 Da Rocha, Simao FC7-157 da Silva, Lucianni P3-d3-1393 da Silva, Regina P3-d1-1369 Dabadghao, Preeti WG3-97, WG4-102* Dabrowska, Milena P1-d1-596 Dacheva, Daniela P2-d2-1023 Dacou-Voutetakis, Catherine P1-d2-541, P1-d3-263 D’Acunzo, Ida P2-d2-1154 Dada, Reema P3-d1-1458 Dada, Rima P2-d2-1120 D’Adamo, Ebe P1-d2-366, P3-d1-1368* D’Addato, Olinda P2-d1-727 Daescu, Camelia P2-d3-808 Daffeur, Katia P2-d1-1018*, P2-d2-1026, P3-d1-1410, P3-d2-1412 Dagmar, Lallemand P2-d3-768* D’Agruma, Leonardo P3-d2-1433 Dahan, Sonia P2-d1-1000 Dahlgren, Jovanna P1-d2-355*, P2-d2-700, P2-d2-971, P2-d2-973* Dain, Liliana LB1-1490 D’Alberton, Franco P2-d3-810 Dallal, Marina P2-d3-949 Dallar Bilge, Yildiz P2-d3-766 Dalla-Vale, Fabienne LB3-1510 Dalton, R. P1-d3-443 d’Alva, Catarina P2-d1-954
Damia, Chiara Maria P2-d1-1019*, P2-d1-1021 Damiani, Durval P2-d2-1186, P2-d2-697, P2-d2-756, P3-d1-1250, P3-d1-1411, P3-d1-1468 Damilano, Cecilia P. P2-d1-1004 Damir, Mohamed P1-d2-487 Dang, Duong P2-d3-879 Daniela, Friebe P1-d1-318 Danilenko, Nina P1-d3-371 Dannemann, Almut P1-d2-328 d‘Annunzio, Giuseppe P1-d2-301, P2-d1-919, P2-d2-897*, P2-d3-874*, P2-d3-946, P3-d2-1339, P3-d2-1341 Daoud, Ghania P2-d1-691 Darcan, Sukran P2-d1-1087, P2-d3-1074*, P2-d3-1126 D‘Arcy, Bronwyn P1-d1-276, P2-d2-679 Darendeliler, Feyza FC8-166, P1-d1-352, P2-d1-1050, P2-d1-1079, P2-d2-1187, P2-d2-1191, P2-d3-652, P2-d3-771 Das, Urmi P2-d1-1138, P2-d1-1141, P2-d2-931, P3-d2-1414 Das, Vineeta WG3-97 Das, Vinita P2-d2-699 Daskas, Nikolaos P1-d1-383*, P1-d2-520* Dastamani, Antonia P1-d2-541 Dastoor, Hormazdiar LB1-1492 Dastot, Florence P1-d1-511 Dateki, Sumito P2-d3-1167* Dattani, Mehul T. FC10-174, FC10-175, FC10-177, LB3-1509, P1-d1-242, P1-d1-245, P1-d1-507, P2-d1-1010, P2-d1-621, P2-d2-631, P2-d2-634, P3-d3-1349, S15-56*, YB2 Datz, Nicolin P1-d2-462 Dauber, Andrew FC4-138 David, Michel P2-d1-1009, P3-d1-1469, P3-d3-1385 David, Raphael P2-d1-1076 David, Vlad P3-d1-1228 Davies, Peter P1-d1-476*, SAT2 Dávila, Luis Rivero P3-d2-1276 Davis, Elizabeth P1-d3-443 Dayal, Devi P3-d1-1320 De Andrea, Maurilio P1-d2-600 De Angelis, Diego P1-d1-505 De Angelis, Laura P3-d2-1344 de Arriba, Antonio P2-d1-989* De Baere, Elfride P3-d3-1310
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
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Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
De Beaufort, Carine FC8-165 De Bellis, Gianluca P1-d2-434 de Boer, Suzan FC5-146 de Carvalho, Arlete P3-d3-1393 de Carvalho, Luciane P1-d3-270* de Castro, Margaret P1-d3-270 De Cuypere, Griet FC8-167 De Djob, Louis WG3-98 De Filippo, Gianpaolo P2-d1-751* De Francesco, Francesco P2-d2-1054 De Franco, Elisa P1-d1-454 de Giorgis, Tommaso FC5-149, LB2-1503*, P1-d1-343, P1-d3-374*, P2-d1-746, P3-d1-1295 De Guchtenaere, Ann P2-d2-795 De Kerdanet, Marc FC6-155, P1-d2-580, P2-d1-819 De la Cruz Moreno, Jesús P2-d2-678, P2-d2-966 de la Puente, Romina P2-d1-629 De Lacerda, Luiz FC13-194, LB4-1522 de Lara, Francisca P3-d1-1369 De Leon, Diva P2-d1-1004 De Leonibus, Chiara FC16211*, FC7-158, P2-d1-746, P3-d1-1295 De Lonlay, Pascale NP1-69, P2-d2-1088 De Luca, Alessandro P2-d2-899 De Luca, Filippo P1-d1-592, P1-d3-271, P2-d2-1030, P2-d2-834, P2-d2-870, P2-d3-649 De Marco, Stefania FC5-149, P1-d3-374, P3-d1-1295* de Martino, Maurizio P2-d1-683, P2-d3-709, P2-d3-842, P2-d3-846, P2-d3-847, P3-d1-1262 de Mattos, Vinicius P3-d2-1380 de Mello, Maricilda P1-d2-253 De Muinck Keizer- Schrama, Sabine LB4-1525, P1-d3-564b De Nitto, Eleanna P1-d1-346, P2-d1-1039 De Palma, Fabrizia P2-d2-1192, P3-d2-1211 De Paoli, Anita P1-d2-254 de Paula, Georgette Beatriz P3-d1-1456 De Paulo, Juliana P2-d2-1114 De Ridder, Maria FC16-212 de Rijke, Yolanda P2-d1-656 de Roux, Nicolas PL4-4*, YB3 de Sanctis, Luisa P2-d1-988*
De Sanctis, Vincenzo FC12188, P2-d2-1149 De Schepper, Jean P1-d2-250, P1-d2-401, P1-d3-414, P2-d2-795, P2-d3-708 de Sotto, Diego P3-d1-1331 de Steenwinkel, Florentien P2-d3-707* De Toro Codes, Marta P2-d2-966* de Villiers, François P3-d1-1268* De Vries, Liat FC4-140, FC6-155, P1-d2-249*, P2-d1-858 de Vries, Martine FC9-172 De Waele, Kathleen P1-d2-250, P1-d2-401, P2-d3-708 De Witte, Wouter P2-d3-769 de Zegher, Francis FC14-198, FC14-199, FC15-209, FC4-138, P1-d1-388, P1-d1-535, P1-d2-321, P1-d2-361, P1-d3-339, P1-d3-376, P2-d2-636, WG4-104, WG4-99* Deal, Cheri P1-d2-247, P2-d1-1011 Dealberti, Prisca P2-d1-1009 Deardorff, Matthew FC20-1483 Debatin, Klaus-Michael FC15-205, P1-d1-349 Debode, Patrick P2-d2-795 DeBoer, Mark P1-d1-307*, P1-d3-332* Dechaume, Aurélie FC6-155 Decker, Ralph P2-d2-971* Deeb, Asma LB1-1492*, P2-d3-975* Degenhardt, Franziska P1-d1-349 Deghmoun, Samia P1-d1-502 Dehez, Marion P1-d2-400* Deiana, Maria Grazia P1-d1-473 Deillon, Eva P2-d1-990* Dejner, Aleksandra P1-d3-616 Del Águila Villar, Carlos P3-d2-1276 del Hoyo Moracho, Marta P3-d1-1403 Del Rey, Graciela P1-d1-538*, P2-d1-1051, P3-d1-1397 del Río Navarro, Blanca Estela P2-d1-778 Delabar, Jean-Maurice FC19-230 Deladoey, Johnny FC6-153*, P1-d2-247, S4, S4-25* Delcroix, Christine P2-d1-1048
* Presenting author
262
9th Joint Meeting of Paediatric Endocrinology 2013
Delemarre-van de Waal, Henriette P1-d2-326, P1-d2-546* Delgado, Iris P1-d2-296 D’Elia, Federica P2-d2-1154, P2-d2-1190* Deliana, Melda P3-d1-1471 Delis, Dimitris P2-d2-900 Della Casa Alberighi, Ornella P2-d3-874 Della Manna, Thais P3-d1-1411 Delonlay, Pascale P1-d1-533 Delucchi, Angela P1-d2-296 Delvecchio, Maurizio FC1-123, P1-d1-316, P1-d1-594, P2-d1-1016*, P2-d1-727 Demir, Haci Ahmet P2-d2-1024 Demir, Korcan P1-d2-519*, P2-d3-1072, P3-d3-1383* Demirbilek, Huseyin P2-d1-686, P2-d3-1064, P3-d2-1335* Demirci, Serpil P1-d2-602 Demirel, Fatma P1-d2-403, P2-d1-915*, P2-d2-1024, P3-d1-1461 Demirkol, Demet P2-d2-928 den Brinker, Marieke P2-d3-708 Denzer, Christian P2-d1-1034*, P2-d2-1121 Denzer, Friederike P2-d2-1121* Deodati, Annalisa P1-d3-415* Derazne, Estela P2-d1-1135, P3-d1-1359 Derraik, Jose P1-d1-524, P1-d1-525, P2-d2-1158 Desai, Meena P1-d1-390 Deschenes, Georges FC2-128 Deshmukh, Dipti P2-d1-1171*, P3-d1-1197 Désirée, Christelle FC6-155, P2-d1-1000 Desloovere, An FC8-166, P1-d2-250 Desrosiers, Paul FC16-214 Destenaves, Benoit FC16-211, FC7-158, P2-d2-830 DeToro-Codes, Marta P2-d2-678* Deubzer, Beate P1-d2-545* Devecioglu, Esra P2-d1-1079 Devriendt, Koenraad P2-d1-959 Dewailly, Didier FC1-122 Dharmalingam, Mala P1-d1-390 Dharmaraj, Poonam P1-d1-244, P2-d1-1138, P2-d1-1141, P2-d2-931, P3-d2-1414
Dhondt, Karlien P1-d2-250 Di Bitonto, Pierpaolo P2-d3913 Di Blasio, Andrea P3-d1-1265* Di Candia, Stefania FC1-123, P1-d2-258, P1-d2-399, P1-d2-434* Di Donato, Francesco P3-d1-1265 Di Donato, Iolanda P1-d1-592 Di Frenna, Marianna P1-d1-598, P2-d1-1137 Di Giovanni, Ilaria P3-d1-1295 Di Giovinazzo, Anna L.S. P2-d2-1192 Di Iorgi, Natascia P1-d2-490, P2-d1-1014, P2-d1-734, P2-d2-695, P2-d3-718* Di Lascio, Alessandra P2-d1-1101, P2-d3-647, P2-d3-650 Di Lauro, Roberto S4, S4-23* Di Mase, Raffaella P1-d1-592, P2-d2-1154 Di Mauro, Francesco P1-d1-312, P2-d1-628, P2-d1-684, P2-d2-1054 Di Palma, Annunziata P3-d2-1338, P3-d3-1350 Di Pietro, Elena P3-d1-1265 Di Pietro, Mario P3-d1-1265 Di Pietro, Natalia LB2-1503 Di Silvestre, Sara LB2-1503 Diaferia, Paolo P3-d2-1211 Diana, Paola P3-d2-1341 Dias, Camila P3-d1-1411 Dias, Renuka FC9-170, P2-d1-1037*, P3-d2-1298 Diaz Naderi, Ruben P1-d1-315 Díaz, Francisca FC17-218, FC17-221, P1-d1-308 Díaz, Marta FC14-198, P1-d1-313, P1-d1-388, P1-d1-535, P1-d2-361, P1-d3-339, P1-d3-376*, P2-d2-636 Díaz-Roldán, Ferran FC14-198, FC14-199, FC17-216, P1-d2-321 Diceglie, Cecilia P1-d2-434 Dichtchekenian, Vaê P2-d2-697, P3-d1-1250, P3-d1-1468 Dicken, Bryan P2-d2-867 Dickstein, Gabriel P3-d1-1200 Diderholm, Barbro P1-d2-357, P3-d1-1396 Didi, Mohammed P1-d1-244, P2-d1-1138, P2-d1-1141, P2-d1-630, P2-d2-931, P3-d2-1414
Diez Lopez, Ignacio P2-d2-799, P3-d1-1403, P3-d3-1353* Dilek, Coban P1-d1-500 Dimitri, Paul P2-d1-661 Dimitriadou, Meropi P2-d2-702 Dimitrova, Mihaela P2-d3-651, P3-d1-1223 Dimoula, Maria P2-d3-812 Dinc, Gonul P3-d1-1365 Dinc, Oktay P2-d2-791 Diquonzo, Franca P3-d2-1433 Dirlewanger, Mirjam P2-d2-927, P2-d3-940* D‘Isa, Gabriela P1-d3-610 Dittrich, Kathrin P1-d1-318, P2-d1-747, P2-d2-753, P2-d3-1066 Dizdarer, Ceyhun P1-d2-519, P3-d1-1227 Djermane, Adel P2-d1-991 Dobie, Ross FC7-156* Dobrescu, Andreea P2-d3-808, P3-d1-1228, P3-d2-1277* Doeing, Carsten P2-d2-965, P3-d1-1218* Doerfer, Juergen P1-d1-451 Doerr, Helmuth P2-d1-1102 Dogan, Melike P1-d2-602 Dogan, Murat LB2-1504* Dohle, Gert R. P1-d3-564b Döger, Esra P2-d3-770, P2-d3-944, P3-d1-1455 Dolan, Lawrence P1-d1-351 Dolezal-Oltarzewska, Katarzyna P2-d2-640* Dolhain, Radboud P2-d3-707 Domené, Horacio P1-d1-380, P1-d1-384, P1-d3-413 Domenice, Sorahia P1-d2-583, P1-d3-270 Dominguez, Angela P3-d2-1300 Domínguez, María Mercedes P2-d1-989 Donaghue, Kim P1-d1-424, P1-d3-443, S18, S18-67* Donaldson, Malcolm FC19231, P1-d2-544, P1-d2-607, P2-d1-1099, P2-d1-1104, P2-d2-1156, P2-d2-1193, P2-d2-827, P2-d3-877, P2-d3-984, P3-d1-1290 Donati, Simone P1-d1-420 Doneray, Hakan P2-d2-926*, P2-d3-985*, P3-d3-1352 Dong, Li FC20-1487 Donghi, Valentina FC2-129 Dongmo, Félicitée WG3-98 Donnelly, Sharon P2-d3-984 Dorchy, Harry P1-d3-437, P3-d1-1327
Dornier, Edwige P3-d1-1469 Dörr, Helmuth-G. P1-d2-604*, P2-d2-638, YB3 Dos Santos, Sophie FC19-233 Dost, Axel FC6-152 Dotis, John P2-d1-994 Dötsch, Jörg P1-d2-604 Dougher, Carly P2-d1-855 Douglas, Thomas P2-d1-670 Doustimotlagh, Amir Hossein P2-d2-1150 Dowling, Kate P1-d1-276, P1-d2-433 Doz, François P2-d1-691, P2-d1-738 Dracopoulou-Vabouli, Maria P1-d2-541, P2-d2-868 Driscoll, Dan S6-29* Drop, Stenvert FC8-166, P2-d1-1011 Droz, Ivaine P2-d3-940 Drui, Delphine FC1-122 Drummond, Kate P2-d1-925 Drummond, Russel P1-d2-303 Drunat, Séverine FC6-155 Drury Brown, Marcie P3-d2-1343* du Preez, Marguerite P1-d2-426, P2-d1-859 Du, Min-Lian P1-d2-396, P1-d3-559, P2-d1-1013, P2-d2-1111, P2-d2-642 Dubuis, Jean-Michel P2-d1-990 Dückers, Gregor P3-d1-1217 Dufour, Christelle P2-d1-691, P2-d1-738 Dumic, Katja Kubat P1-d2-259*, P2-d3-914 Dumic, Miroslav P1-d2-259 Dumin, Magdalena P2-d2-1184* Duminuco, Paolo P1-d2-547, P2-d1-1040 Dumitrescu, CristinaPatricia P2-d2-800 Duncan, Emma P2-d1-857 Dundar, Bumin LB2-1501, P1-d2-602, P2-d2-1063*, P3-d2-1436 Dundar, Nihal P1-d2-602 Dung Chi, Vu P1-d2-578 Dung, Vu P2-d1-1080 Dunger, David FC3-135, LB3-1509*, P1-d2-398, P1-d2-431, P1-d3-410, P1-d3-443, P2-d1-953 Dunkel, Leo FC14-202, FC14-203, FC4-141, FC7-160, P1-d1-466*, P2-d1-997 Dunne, Mark FC11-181, FC11-182, FC11-184
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
263
Floor Plan Exhibition Author Index
author index
author index
Dunstheimer, Désirée P1-d1-570 Dupuy, Corinne FC19-230 Duque, Yeray P1-d1-591 Durajczyk, Clare P2-d1-1105 Duran Ventura, Paola P3-d3-1445* Duran, Ibrahim P1-d2-481 Durazo, Ramon P2-d3-905 Durko, Alina P3-d1-1370 Durmashkina, Alevtina P2-d1-1038* Durmaz, Erdem P1-d2-552* Durr, Alexandra PL4-4 Dursun, Fatma P1-d1-530*, P3-d1-1329 Dusatkova, Lenka P1-d3-340* Dušátkova, Petra FC10-179*, P1-d1-278, P1-d2-429, P2-d1-993, P2-d2-895 Dutailly, Pascale P1-d2-395, P1-d3-405, P2-d2-825 Dwyer, Andrew P2-d1-1082, P2-d1-995 Dzivite-Krisane, Iveta P2-d3-802, P2-d3-809 Dzodan, Bojana P2-d1-687
Floor Plan Exhibition Author Index
E
Ebensperger, Mauricio P1-d1-567 Eblé, Andrée FC16-210 Economou, Marina P2-d2-702 Ecosse, Emmanuel FC19-233 Eddiry, Sanaa P1-d2-329* Edgunlu, Tuba P2-d1-924, P2-d3-1072 Edison, Mworozi P2-d3-1069 Edouard, Thomas P2-d3-711* Edwards, Christine P1-d3-337 Efraimidou, Smaragda P2-d3-765 Ehtisham, Sarah FC11-184, P2-d1-1002, P2-d2-634 Eickhoff, Jens P1-d3-378 Eke, Gracia P2-d1-723 El Arabi, Houda P1-d3-437*, P3-d1-1327* El Husseini, Maha P2-d3-1160 El Kholy, Mohamed P1-d1-291 El Mehdi Haddam, Ali P3-d2-1305, P3-d2-1418 El Mougy, Fatma El Mougy P2-d2-1117 Elali, Maryam P2-d1-1176 Elawwa, Ahmed FC12-188 Elbarbary, Nancy P2-d2-932*, P3-d3-1347* Elcioglu, Nursel P2-d2-963 Elder, Deborah P2-d3-878 Eleutheriou, Eirini P2-d2-868 Elfers, Clinton P1-d2-320
Elgadi, Aziz FC15-206*, P1-d1-353* Elhaj Burrani, Huda P1-d2-544* Elias, Adriana P2-d2-763 Elie, Caroline FC6-155, P2-d1-691, P2-d1-738 Elkiran, Özlem P1-d2-364 Ellaith, Mona FC8-166 Ellard, Sian FC11-183, FC11-185, FC14-200, P1-d1-454, P2-d1-849, P2-d1-850, P2-d1-852, P2-d2-860, P2-d2-893, P2-d2-932, P2-d3-877, P2-d3-879, P2-d3-909, P2-d3-939, P3-d2-1335 Elleri, Daniela P1-d2-431* El-Morsi, Doaa P1-d1-446 Elsedfy, Heba P1-d1-291, P1-d1-390 Elsharkawy, Ashraf P1-d1-446* Elson, Ruth P1-d2-362, P1-d3-336 Emeksiz, Hamdi Cihan P2-d3-770, P2-d3-944, P3-d1-1455 Eminson, Jane P2-d2-677 Emir, Suna P2-d2-1024 Emons, Joyce P3-d1-1249 Endoh, Akira P1-d1-527 Endozo, Raymond P1-d2-426, P2-d1-859 Enes, Patricia P2-d1-851, P2-d1-853*, P2-d1-886, P2-d2-869*, P2-d2-930 Engelsberger, Ilse P1-d2-462 Engiz, Ozlem P2-d3-766* Engler-Schmidt, Charlotte P2-d3-872 Enlund, Eveliina FC15-204 Enriori, Pablo P1-d1-531 Eom, Tae Min P1-d2-488 Epcecan, Serdar LB2-1504 Epcecan, Zerrin LB2-1504 Er, Anil P2-d3-770 Erberk Özen, Nurper P3-d2-1435 Ercan, Oya P1-d3-609, P2-d1-1050, P2-d2-1147, P2-d2-1152, P2-d3-938*, P3-d1-1423 Eren, Erdal P2-d1-924*, P2-d3-1072* Ergen, Arzu P1-d2-359, P2-d3-776 Ergin, Merve P2-d1-817 Erkekoglu, Pinar P1-d2-552 Ernert, Andrea P1-d2-328, P1-d3-555 Eroglu, Ayse P2-d2-1147
* Presenting author
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9th Joint Meeting of Paediatric Endocrinology 2013
Ersen, Atilla P1-d3-609, P2-d1-888, P3-d1-1332 Ersen, Huriye P2-d3-948 Ersoy, Betul P2-d2-1090, P3-d1-1365* Ersu, Refika P2-d1-884 Ertl, Alexandra P3-d1-1467 Ertl, Diana-Alexandra P1-d2-480* Escobar de Lazzari, Maria E. P2-d1-1051 Escobar, María P1-d3-563, P2-d2-632, P2-d2-1061 Esen, Ihsan P1-d2-403*, P2-d1-915, P3-d1-1461 Esmailzadehha, Neda P2-d1-685, P3-d2-1480 Espada, Mercedes P1-d1-591 Espiner, Eric FC3-132 Espinosa, Armando P2-d1-780 Esposito, Andrea P2-d2-1154*, P2-d2-1190 Esposito, Sandra LB4-1523, P2-d1-816 Esposito, Susanna P2-d1-1020 Essaddam, Leïla P2-d1-1109*, P3-d2-1442* Esteban-Marfil, Victoria P2-d2-678, P2-d2-966 Esterle, Laure FC1-122*, FC2-128 Estrugo, Andrés P1-d1-567 Eszlinger, Markus LB4-1528 Eugster, Erica P1-d1-574, P1-d3-557 Eunice, Marumudi P2-d2-1120, P3-d1-1454 Even, Lea P1-d2-302* Evliyaoglu, Olcay P2-d2-1147*, P2-d2-1152*, P3-d1-1423 Ewin, Anna Maria P1-d2-544 Expósito-Montes, Juan F. P2-d2-678 Eyal, Ori FC9-173, P2-d1-627 Ezquieta, Begoña P1-d1-477 F
Fabrizi, Emanuele P2-d1-999 Fadeel, Bengt S12-47 Fadila, Bouferoua P3-d2-1243* Fagerholm, Rainer FC10-178 Faienza, Maria Felicia FC2-130*, P1-d1-316, P2-d1-727*, P2-d1-1016, P2-d2-1192, P3-d2-1211 Faisal, Ahmed P2-d1-957, P2-d2-827 Falcini, Fernanda P2-d1-683 Falen Boggio, Juan P3-d2-1276* Falero-Gallego, P. P3-d2-1477
Fanelli, Flaminia P2-d1-619, P3-d1-1204 Fanelli, Marina P1-d2-583* Fang, Jianpei P2-d3-977 Faraci, Maura P2-d1-734 Fardella, Carlos P1-d1-235, P1-d3-377, P2-d1-920 Farfel, Alon P2-d1-1135*, P3-d1-1359* Farias, Javier P3-d1-1470 Farida, Chentli P3-d3-1395 Fariña, Sabela P3-d2-1274 Farmer, Amy P1-d1-422 Farooqi, I. FC20-1484 Farpour-Lambert, Nathalie P2-d3-768, P2-d3-940 Farquharson, Colin FC7-156 Fatima, Saraoui P3-d3-1395* Fattorusso, Valentina P2-d1-1039 Faussat, Anne-Marie FC5-147 Faustino, Vince P1-d2-430 Fauth, Christine P2-d1-959 Favalli, Valeria P2-d1-668, P2-d2-675*, P2-d2-676 Fazzini, Cristina P1-d3-415 Fedala, Naziha P3-d1-1409, P3-d2-1304, P3-d2-1305, P3-d2-1418 Fedala, Nora Soumeya P3-d2-1304, P3-d2-1418* Fedala, Saida P3-d1-1255 Fedala, Soumeya P3-d2-1416 Fedatto, Paola FC13-192, FC13-193 Feilbelmann, Taciana P2-d2-866 Felikman, Yana FC16-215 Felius, Abraham P1-d2-326 Fenchel, Matthew P2-d3-878 Feng, Ling P2-d2-796 Feng, Yueying FC17-220 Ferguson-Smith, Anne FC7-157 Ferket, Peter FC20-1484 Fernandes, Alexandre P3-d1-1222 Fernandez Ramos, Concepcion P2-d1-781 Fernandez, Aroa P1-d3-339 Fernández, Juan P1-d3-265 Fernández, María FC13-197 Fernández-Cancio, Mónica P1-d3-265, P1-d1-291 Fernández-Real, José M. FC14-198, FC17-216, FC17-219 Fernández-Somoano, Ana P2-d2-764, P2-d2-1112 Ferrada, Clarita P2-d3-1166 Ferrández-Longás, Ángel P2-d1-989
Ferrarello, Maria Piera P2-d1-1019, P2-d1-1021 Ferrari, Mara P2-d1-956 Ferrari, Matteo P3-d2-1344 Ferraro, Giuseppe P2-d2-1054 Ferreira, Beatriz P2-d1-1044, P2-d1-1180, P2-d2-866*, P3-d2-1441* Ferreira, Rute P3-d1-1428 Ferrentino, Roberta Ida P2-d1-1039 Férrer, Luciana P2-d2-697, P2-d2-1186 Ferretti, Patrizia P1-d1-466 Ferro, Giusy P2-d1-668, P2-d2-676 Fertipreserve, Group FC1-124 Festen, Dederieke P1-d3-411 Fetuga, Bolanle P2-d3-974*, P2-d3-981* Fica, Simona P2-d1-1041 Ficociello, Carmine P2-d1-684 Fidani, Liana P2-d2-702 Fidani, Styliani P2-d3-765 Fideleff, Gabriel P1-d3-373, P2-d2-755 Fideleff, Hugo P1-d3-373*, P2-d2-755 Fierabracci, Alessandra P1-d1-275 Figueroa Barrón, Mireya P2-d1-778 Figueroa, Verónica P2-d1-629, P3-d1-1405 Figuerola, Joan P3-d1-1331 Filho, Hamilton P3-d1-1250 Filizola, Rosalia P2-d2-794 Fima, Eyal FC16-215, P1-d1-391, P2-d2-828 Finelli, Palma P2-d1-996 Finkielstain, Gabriela Paula P1-d3-270, P2-d3-982 Fintini, Danilo P1-d2-465*, P2-d1-659, P2-d1-999* Fiorentino, Bruno P1-d3-405*, P2-d3-843 Fiori, Rossana P1-d1-385, P2-d2-761 Fiorito, Cristina P2-d1-816 Fischer, Philip FC12-189 Fischer-Posovszky, Pamela FC15-204*, FC15-205*, P1-d1-349 Fischer-Rosinsky, Antje FC17-217 Fischetto, Rita FC2-130, P2-d2-899, P3-d2-1433* Fisher, Victoria P2-d2-827 Fissore, Maria P2-d1-988 Fitas, Ana P2-d2-681 Fitouri, Zohra P2-d1-1109, P3-d2-1442
Flanagan, Sarah E. FC11-183, FC11-185, FC14-200, P1-d1-454, P2-d1-850, P2-d2-860, P2-d2-862, P2-d2-932, P2-d3-877, P2-d3-879, P2-d3-909, P3-d2-1335 Flechtner, Isabelle FC6-155, P2-d2-1088* Flechtner-Mors, Marion P2-d1-1034 Flint, Amanda P1-d3-438 Flitsch, Joerg LB4-1524 Florea, Suzana P2-d1-1041 Flores, José A. P3-d2-1380 Flores, Raquel FC17-218, FC17-219, P1-d1-566, PL4-5 Flores, Yolotzin P2-d1-780 Flórez, Martha P1-d1-567 Flück, Christa E. FC16-210, P1-d2-485, P1-d2-581, P1-d3-265, SAT4, WG6-112* Flyer, Mark P3-d1-1263 Foley, Niamh P1-d3-338 Fonseca, Ricardo P3-d1-1428 Fontenele, Eveline P1-d2-482, P2-d1-954* Fontoura, Manuel P2-d3-1130, P3-d1-1222, P3-d2-1415 Foote, Jan P2-d1-1047* Forclaz, Verónica P3-d1-1470 Ford, George WG3-96* Forero Torres, Carolina P1-d1-310, P2-d3-804 Forero, Laura P3-d2-1248, P3-d2-1420, P3-d2-1421 Foster, John P1-d2-303 Fotinou, Aspasia P3-d1-1431, P3-d2-1438 Fotis, Lampros P2-d2-826 Fox, Larry P1-d3-442 Frago, Laura P1-d1-347 Fragoso, Maria Candida FC20-1486 Fraige Filho, Fadlo P2-d3-949 França, Marcela P1-d1-506, P2-d1-952 França, Suzana LB4-1522 Francavilla, Ruggiero P1-d1-450, P2-d1-1016 France, Annick P1-d2-401, P2-d3-708 Franceschi, Roberto P1-d1-285, P1-d2-297, P2-d3-911, P3-d2-1338, P3-d3-1350 Franchini, Simone P1-d1-343 Franciscon, Priscila P2-d2-866 Franciscon, Raphael P3-d2-1441 Franckx, Hilde P2-d2-795 Francois, G. P1-d2-250
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
265
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author index
Floor Plan Exhibition Author Index
author index
François, Inge P1-d2-250, P1-d2-401 Frankel, Matthew P3-d3-1314 Franzese, Adriana P1-d1-346*, P2-d1-1039* Franzoni, Alessandra P2-d1-619 Frare, Joana P3-d2-1441 Freemont, Anthony P1-d2-294 Freiberg, Clemens FC6-152 Freire, Analía P1-d3-413, P1-d3-563*, P2-d2-1061 Freitas de Mattos, Vinicius P2-d2-962 Freitas, Marcela FC4-142 Freri, Elena P2-d3-1067 Frerichs, Carley P2-d1-670* Frezza, Elda P2-d3-913 Fricke-Otto, Susanne P3-d1-1217 Friebe, Daniela P2-d1-747, P2-d2-753 Friez, Michael P2-d1-1143 Friis-Hansen, Lennart P1-d3-444 Frilander, Mikko PL4-5 Friszer, Stéphanie P1-d1-511 Froguel, Philippe FC6-155 Fröhlich-Reiterer, Elke FC6-152, P1-d1-349 Frohnert, Brigitte P1-d2-324* Frontino, Giulio P2-d1-668, P2-d2-675, P2-d2-676 Frühbeck, Gema P1-d3-333 Frühwald, Michael P1-d1-570 Frye, Joseph FC2-126 Fu, Jun-Fen FC17-220, P1-d3-370, P2-d1-1081 Fuchs, Ulrich P2-d3-1129* Fuente-Martín, Esther FC15-207, FC17-221, P1-d1-308 Fuentes-Bolaños, Noemi P2-d1-922*, P3-d1-1286 Fujimaru, Rika P1-d2-432 Fujimoto, Masanobu P2-d1-815*, P2-d2-637 Fujita, Keinosuke P2-d1-725 Fujiwara, Ikuma P1-d2-432 Fujiwara, Makoto P1-d2-513*, P2-d3-1167, P3-d3-1316 Fukami, Maki FC9-171, MTE1:1, MTE1:2, P1-d1-283, P1-d1-290, P1-d1-527, P1-d2-578, P1-d2-582, P1-d3-262, P2-d1-626, P2-d1-818, P2-d3-1131 Fuke, Tomoko P1-d1-523*, P1-d1-527 Fukuda, Chiyoko P2-d1-725 Fukuzawa, Ryuji FC18-226, P1-d1-572, P3-d1-1226
Fuly, Jeanne LB2-1496, LB4-1520 Funari, Mariana FC3-134, P1-d2-482 Fuqua, John FC16-214 Furcas, Maria P1-d1-272 Furdela, Viktoriya P1-d2-427* Furioli, Jean P1-d1-511 Furman, Andrzej P1-d2-300 Furmaniak, Jadwiga P1-d1-278 Fusco, Concetta P2-d1-889 Fustic, Stojka P3-d3-1308 G
Gabriel, Liana P1-d2-358* Gabrielli, Liliana P2-d2-896 Gadian, David P2-d1-883 Gaete, Ximena P1-d1-382, P2-d2-1033*, P2-d3-1073* Gagliardi, Priscila FC4-138 Gahagan, Sheila P1-d3-372, P2-d2-757, P2-d2-894 Gailite, Jurgita P2-d3-802*, P2-d3-809* Gajjar, Amar P1-d2-515 Galal, Ashraf P2-d2-1117 Galán Gómez, Enrique P2-d1-922 Galant, Karolina P3-d1-1257 Galazka, Andrew SAT2 Galbis, Lilian P1-d1-477 Galcheva, Sonya P1-d2-356*, P2-d1-852, P2-d3-769 Galera, Rafael P2-d3-775 Galesanu, Corina P3-d2-1375*, P3-d3-1384 Galesanu, Mihail Romeo P3-d2-1375, P3-d3-1384 Gali, Christina P1-d3-615 Galinier, Philippe P2-d1-1049 Gallardo, Pedro P1-d1-382 Gallardo, Vivian P2-d2-902* Gallarotti, Federica P2-d1-956 Galler, Angela P2-d2-863* Galli-Tsinopoulou, Assimina P2-d3-765 Gallo, Francesco P2-d1-956 Galloway, Peter J. P3-d1-1364 Gama, Maurício LB1-1494 Gambineri, Alessandra P2-d1-619 Gan, Hoong-Wei FC13-196*, P1-d2-517 Gandrud, Laura P2-d1-720 Ganjoo, Nikhil P2-d2-1189* Gannon, Hannah P3-d1-1326 Ganta, Rajesh P1-d1-351 Garagorri Otero, Jesús M. P1-d2-323, P3-d2-1302 Garavelli, Livia P1-d1-498, P3-d1-1362
* Presenting author
266
9th Joint Meeting of Paediatric Endocrinology 2013
Garbetta, Gisella P2-d1-1019, P2-d1-1021 Garcia Barcina, Maria P2-d1-781 García, Hernán P1-d1-235, P1-d2-325*, P1-d3-377, P2-d1-920, P2-d2-1033, P2-d3-1166 García, Laura FC19-228 Garcia, Lorena P1-d1-235, P1-d2-325 García, Marta FC19-232* Garcia, Milagros P3-d1-1222 García, Roberto P2-d3-875, P2-d3-1073 García-Escobar, Icíar P2-d3-775, P3-d1-1408 García-García, Emilio P2-d3-775*, P3-d1-1408* García-Martínez, Elena P1-d1-423 García-Miñáur, Sixto P1-d1-477 Garcia-Rey, Cesar P3-d2-1300 Garcia-Rudaz, Maria P1-d1-531* Gardovska, Dace P2-d3-802, P2-d3-809 Garfias, Carolina P2-d2-902 Garg, Sumedha FC20-1484 Gargantini, Luigi FC1-123, P1-d1-594, P1-d2-258, P1-d2-399 Garibay, Nayely P2-d1-780* Garmendia, Maria Luisa P1-d3-341, P1-d3-375 Garrè, Maria P2-d2-695 Garrick, Delith P3-d1-1401* Garten, Antje P1-d1-309, P1-d3-368, P2-d1-732 Gascón, Félix P2-d1-745 Gaßner, Birgit FC3-132 Gastaldi, Roberto P2-d1-1014 Gaston, Veronique P1-d2-329 Gaston-Massuet, Carles FC10-175* Gatti, Davide FC2-131, P1-d1-285 Gattorno, Marco P1-d1-272 Gat-Yablonski, Galia P1-d1-286* Gaudino, Rossella P1-d2-549, P1-d3-561, P2-d1-1085, P3-d2-1301 Gault, Emma-Jane P2-d1-1099*, P2-d1-1104*, P2-d3-984 Gausche, Ruth P3-d1-1360 Gavan, Michal P1-d3-441 Gawlik, Aneta P1-d3-616*, P2-d3-1128* Gawlik, Tomasz P1-d3-616
Gay, Claire-Lise P1-d2-580, P3-d1-1469 Gaya, Daniel P2-d1-957 Gayo-Escribano, Miriam P2-d1-955, P2-d2-969 Gazolla, Fernanda P1-d2-322 Gazzarri, Alessandra P2-d3-1067, P3-d2-1344 Gazzola Zen, Paulo P2-d2-962, P3-d2-1380 Gebahrdt, Ursel P1-d1-508, P2-d1-1015 Gedik, Hakan P2-d2-928 Geer, Eliza FC18-223 Geffner, Mitchell P2-d3-840* Geiger, Kathrin P2-d2-1028 Geisler, Alex P3-d1-1269 Gelander, Lars P1-d2-479, P1-d2-548, P1-d3-558 Genesio, Rita P2-d1-1106 Genin, Emmanuelle PL4-4 Gennero, Isabelle P2-d3-711 Genoni, Giulia P1-d3-369, P2-d1-816 Genoni, Teresa P2-d1-1101*, P2-d3-647, P2-d3-650 Genovesi, Simonetta P2-d1-668 Gent, Roger P1-d1-276 Geoffroy, Louis FC6-153 Georgiou, George FC1-121, FC15-208, P1-d1-314 Gérard, Bénédicte FC6-155 Gerasimidis, Konstantinos P1-d3-337, P2-d1-957 Germak, John P1-d2-393, P2-d3-839, P3-d3-1313 German, Alina P2-d2-1098* Germani, Daniela P1-d3-415 Gertosio, Chiara P1-d1-569 Gerver, Willem P2-d1-959 Gesing, Julia P1-d1-318, P2-d1-747, P2-d2-753* Gessi, Alessandra P1-d2-434 Gevers, Evelien FC7-160, P1-d1-242*, P2-d1-621* Ghaly, Isis P2-d2-1117 Ghanny, Bryan P1-d1-386*, P2-d1-620* Ghanny, Steven P1-d1-386, P2-d1-620, P2-d2-1056 Gharavi, Ali G. P1-d1-575 Ghasemi, Mahmood P2-d1-1179 Ghataore, Lea P2-d2-639 Ghergherehchi, Robabeh P3-d1-1366* Gherlan, Iuliana P2-d2-800* Ghirardello, Stefano P1-d1-598, P1-d2-606 Ghizzoni, Lucia CPE1-72*
Giaccardi, Marta P2-d1-1014, P2-d1-734, P2-d2-695*, P2-d3-718 Giacomozzi, Claudio P1-d3-415 Gialetti, Sara P2-d3-874 Giani, Elisa P3-d2-1344 Giannini, Cosimo FC5-149, P1-d1-343*, P1-d2-366, P1-d3-374, P2-d1-746 Gianninoto, Moira P2-d1-1101, P2-d3-647*, P2-d3-650 Giardino, Ida S18, S18-65* Giavoli, Claudia P2-d1-1020* Gibbs, Richard LB1-1493 Gibson, Brenda P1-d2-544 Gies, Inge P1-d2-250, P1-d2-401, P2-d2-795*, P2-d3-708* Giglio, Sabrina P2-d3-846, P2-d3-847 Giglione, Enza P1-d3-369, P3-d1-1204 Gil Rodríguez, María C. P3-d2-1302 Gil, Silvia P1-d3-562 Gilbert, Clare P1-d2-426, P2-d1-859, P2-d3-906, P2-d3-910* Gil-Campos, Mercedes P1-d1-354, P3-d2-1274 Gill, John FC4-138 Gilyazetdinov, Kamil P3-d3-1444 Gimenez, María P2-d2-635 Gimenez-Roqueplo, AnnePaule S10, S10-41* Ginsburg, Kenneth P3-d2-1371 Giovaninni, Nayara Paula LB2-1496, LB4-1520 Giray, Belma P1-d2-552 Giri, Dinesh P2-d1-1138, P2-d1-1141*, P2-d1-630*, P2-d2-931 Giroto, Rachel P3-d1-1411 Gispert-Saüch, Montserrat P1-d2-321 Giuliani, Francesca P2-d1-988 Giurcaneanu, Mihaela P2-d2-800 Giussani, Marco P2-d1-668 Glaser, Tamar FC4-139 Gleeson, Sean P1-d1-449 Gleiss, Andreas P1-d2-480 Gligorovic, Najdana P2-d1-1182 Globa, Evgenia P3-d3-1348* Glybyna, Tatyana P2-d3-646 Godoy, Claudia P1-d3-445, P2-d3-1166* Gohlke, Bettina P1-d2-601, P2-d1-1102
Goischke, Alexandra P2-d1-691 Gokcay, Gulbin P2-d1-1079 Gokdemir, Yasemin P2-d1-884 Gokoglu, Sonay P1-d1-500 Goksen, Damla P2-d1-1087*, P2-d3-1074, P2-d3-1126 Golanov, Andrey P2-d2-1027 Gold, Melanie LB1-1491 Golestani, Abolfazl P2-d2-1150 Göllü, Gülnur P2-d3-1123 Golmayo, Luz P2-d2-930 Gomes, Debora FC20-1486 Gomez Acuña, Luciana LB1-1490 Gomez Vasquez, Ana Maria P3-d1-1427 Gómez-Ambrosi, Javier P1-d3-333 Gómez-Chaparro, José L. P1-d1-491 Gómez-Llorente, José P2-d3-775, P3-d1-1408 Gómez-Núñez, Ana P1-d2-435, P2-d3-844 Gomila-Borja, Antoni FC15-209 Gonc, Nazli P2-d2-1022, P2-d3-1064 Gonçalves, Fabrícia P1-d3-270 Gong, Chun P2-d2-937 Gong, Chunxiu P1-d2-456, P2-d1-1007, P2-d1-856, P2-d1-885, P2-d3-912, P3-d1-1195 Gong, Fengying P2-d3-1071 Gong, Xiu P2-d2-1058 González Briceño, Laura P2-d1-691*, P2-d1-738* González de Buitrago Amigo, Jesus P2-d1-922 González, Antía P1-d1-354 González, Claudio P1-d3-373, P2-d2-755 González, Isabel FC19-232 González, Laura P1-d3-341, P1-d3-375 Gonzalez, Maria P2-d2-964 González, Verónica P2-d3-1168* González-Aguilera, Beatriz P3-d1-1408 González-Casado, Isabel P1-d2-435, P2-d1-955 González-González, Abel P3-d2-1477 González-Zorzano, Eduardo P1-d2-323 Gopalakrishnan, Vignesh WG3-97 Gopal-Kothandapani, Jaya Sujatha P1-d2-294*
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
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author index
Floor Plan Exhibition Author Index
author index
Gopal-Kothandapani, Jaya P2-d1-1002* Gordon, Catherine P2-d1-786, WG4-105* Gordon, Derak P1-d2-303 Gorelyshev, Sergey P2-d2-1027 Gorski, Theresa P2-d1-732* Goshen, Yacob P3-d1-1251 Gosney, Elahu P1-d1-347 Goto, Masahiro P2-d3-881 Goto, Yusuke P3-d1-1407 Gotoh, Motohide P2-d3-1131 Gotthardt, Martin P1-d3-444 Gottlieb, Silvia P2-d1-1042 Graiff, Olga P2-d2-763 Gram, Jeppe P2-d1-689 Granados, Hector P2-d3-1133* Grande, Cosima P3-d2-1340 Grandone, Anna P1-d1-312, P2-d1-1106, P2-d1-628, P2-d1-684, P2-d1-960*, P2-d2-1054 Grano, Maria FC2-130, P1-d1-316 Grant, Struan NP2-71* Grasemann, Corinna P1-d1-522* Grasemann, Hartmut P1-d1-522 Grasso, Valeria P1-d1-473 Grau, Gema P1-d1-591*, P3-d1-1287 Gravholt, Claus H. MTE6:1, MTE6:2 Gravholt, Claus FC1-125*, P1-d1-277, WG5-111* Gray-Donald, Katherine P1-d2-461 Graziadio, Carla P2-d2-962 Graziano, Claudio P2-d1-694 Greaves, Ronda FC14-201 Greco, Donatella FC1-123 Green, Andrew P2-d3-909 Green, Daniel P1-d2-515 Green, Julie P2-d1-1138, P2-d1-1141, P2-d2-931* Greenberg, Cheryl FC20-1488*, SAT3 Greening, James P2-d1-1010 Greggio, Nella P1-d1-594 Gregory, John SAT5 Gregory, Louise C. P1-d1-507, P2-d1-1010* Griffin, Aliesha FC9-169 Grill, Jacques P2-d1-691, P2-d1-738 Grimberg, Adda P3-d2-1371* Grimbly, Chelsey P2-d2-867* Grinspon, Romina P2-d1-1042*, P2-d3-982 Grob, Francisca P2-d2-1033
Grohmann, Natascha P3-d3-1448* Grootenhuis, Martha A. P1-d3-613, P2-d1-1142 Grošelj, Urh P1-d3-334*, P1-d3-367, P2-d3-773 Grosse, Andrea P3-d1-1397 Grossfeld, Paul P2-d2-704 Grossi, Armando P1-d1-275*, P2-d2-761 Groth, Kristina SAT2 Grötsch, Helga P1-d1-573 Grötzinger, Joachim P1-d2-256 Grover, Monica LB1-1493 Grozdanova, Radoslava P2-d2-1032, P2-d3-644 Grubic, Zorana P1-d2-259 Grugni, Graziano FC1-123*, FC2-131, P1-d1-316, P1-d1-594, P1-d2-258*, P1-d2-399, P1-d2-465 Grulich-Henn, Jürgen P1-d1-421, P1-d1-451, P1-d2-462 Gruñeiro-Papendieck, Laura P2-d1-1173, P3-d1-1462 Grüters, Annette FC17-217 Grybek, Virginie FC12-190 Gryngarten, Mirta P1-d3-563, P2-d1-1051, P2-d2-1061 Grzyska, Ulrich LB4-1524 Gu, Yufen P1-d3-559 Guaragna-Filho, Guilherme P3-d1-1456 Guarducci, Silvia P2-d3-847 Guarneri, Maria Pia P2-d2-834 Guasti, Leo FC18-224 Guasti, Leonardo P1-d1-466 Guazzarotti, Laura P1-d1-540*, P2-d3-1067* Gucev, Zoran P1-d1-575*, P3-d3-1308 Guducu, Cagdas P3-d2-1436 Guedri, Rahma P3-d2-1442 Guemazi, Fatiha P1-d2-487 Güemes, María FC19-228, P2-d2-631* Guercio, Gabriela FC8-163 Guereca, Gabriela P2-d1-1012 Guerra-Júnior, Gil P1-d2-253, P1-d2-577, P2-d2-1114, P3-d1-1456 Guerrero, Julio FC19-232 Guerrero-Fernández, Julio P1-d2-435 Guerrot, Anne-Marie P1-d1-511 Gugliotta, Maria P3-d1-1362 Guibert, Javier P3-d2-1282 Guidetti, Monica P3-d3-1391
* Presenting author
268
9th Joint Meeting of Paediatric Endocrinology 2013
Guidoni, Elisa P3-d3-1317*, P3-d3-1386* Guillén-Navarro, Encarna P1-d1-477 Guilmin-Crépon, Sophie LB3-1510* Guimarães, Marília LB1-1494 Guimarães, Rodrigo LB4-1523 Guimarey, Luis P2-d3-1168 Guirado, Luana P3-d3-1312 Gul, Mehmet P2-d3-985 Guleryuz, Handan P1-d1-454, P3-d2-1436 Gullì, Mariolina FC5-145 Gunawan, I. Made P2-d1-992 Günes, Dilek P2-d2-1187 Günes, Tamer P2-d2-698 Gunindi, Figen P3-d1-1463 Gunn, Alastair P2-d2-1158 Guo, Shujuan P2-d2-968 Guo, Xirong FC17-220 Gupta, Nandita P2-d2-1092 Gur, Gokce P3-d1-1461 Güran, Tülay FC8-166, P1-d2-464, P2-d1-1050, P2-d1-742, P2-d1-849, P2-d1-884, P2-d3-715, P2-d3-803 Gurbuz, Fatih P1-d1-241*, P2-d2-701, P3-d1-1229, P3-d1-1256* Gürbüz, Sibel P1-d2-364 Gurka, Matthew P1-d1-307 Gursoy, Semra P3-d1-1332 Gussinyer Canadell, Miquel P1-d1-238* Gustafsson, Jan P1-d3-560 Gut, Robert P1-d2-393 Gutiérrez, Armand FC17-218, PL4-5 Gutmark-Little, Iris P2-d1-1103 Güven, Ayla P1-d1-530, P1-d3-335, P2-d1-663*, P2-d2-860*, P3-d1-1329, P3-d2-1210 Guy, Rachel FC16-215 Guzy, Serge P2-d2-828 Guzzetti, Chiara P1-d2-490* Gwak, Hye Sun P2-d1-1086 H
Ha, Eun Hee P2-d1-1086 Ha, Mina P3-d2-1434 Haberland, Holger P2-d1-1034, P2-d2-863 Habib, Carolina P2-d1-1042 Habisch, Hansjörg FC15-205 Habu, Masako P2-d1-674, P3-d1-1219 Hacihamdioglu, Bülent P2-d2-1116
Haddad, Meriem P3-d2-1416* Haddam, Ali El Mehdi P3-d1-1409*, P3-d2-1304* Haddam, Nora Soumeya P3-d2-1305* Haddick, Anne P2-d1-1141 Hadeed, Ibtisam P3-d3-1349 Hadziselimovic, Faruk FC1-120*, P1-d2-587* Hadziselimovic, Nils FC1-120, P1-d2-587 Haeusler, Gabriele P1-d2-480, P3-d1-1467 Hafez, Mona P2-d2-1117* Hag-Daud, Hamed LB4-1527 Hahn, Gabriele P2-d2-1028 Hahn, Seung Hoon P1-d1-475 Hahn, Wendy P1-d2-324 Haim, Hadar P3-d3-1318 Hainer, Vojtech P1-d3-340 Hakanen, Tiina FC3-136 Hakonarson, Hakon FC20-1483, FC20-1487 Hale, Daniel P1-d2-395 Haliloglu, Belma P1-d2-464, P2-d1-1050, P2-d1-742, P2-d1-849*, P2-d1-884*, P2-d3-715, P2-d3-803 Haliyash, Nataliya P3-d2-1238 Halley, Dicky P1-d2-301 Halvadzhiyan, Irina P2-d1-852 Hamad, Muddathir P2-d3-713* Hamajima, Naoki P2-d1-815 Hamajima, Takashi P3-d2-1237* Hämäläinen, Anu-Maaria P1-d1-274 Hamed, Amira P3-d1-1291 Hamilton, Jill P1-d1-455 Hamm, Michaela P1-d2-601* Hammes, Hans P. S18, S18-66* Hamza, Raha P3-d1-1291* Han, Heon-Seok P1-d1-416* Hanakawa, Junko P3-d1-1226 Hanaki, Keiichi P2-d1-815, P2-d2-637 Hanas, Ragnar MTE2:1, MTE2:2 Hancili, Suna P3-d1-1329*, P3-d2-1210* Handke, Daniela FC17-217 Hannema, Sabine FC3-132*, P1-d2-326*, P1-d2-478, P1-d2-546, P3-d1-1249 Hannila, Marja-Leena FC14-203 Hanoch-Levi, Adi P2-d1-730 Hanson, Daniel LB4-1519* Haqq, Andrea P2-d2-867 Haraguchi, Kohei P2-d3-1167 Haramaras, Ilias P2-d3-812* Harasymczuk, Jerzy P1-d2-599
Harel, Zeev LB1-1491* Harju, Samuli P2-d1-997 Harjunmaa, Ulla FC3-136 Harmatz, Paul FC20-1488 Harmer, Steve FC11-183 Harris, Mark P2-d1-1017, P2-d1-857, P2-d3-841, P3-d2-1303 Harris, Richard P2-d1-820 Hart, Gili FC16-215, P1-d1-391*, P2-d2-828* Hartmann, Klaus P2-d1-958*, P3-d3-1389* Hartmann, Michaela FC18-227, FC5-148, P1-d2-248, P2-d3-1129 Harun, Fatimah LB3-1518 Harvey, John P3-d2-1333 Hasan Musa, Samira P2-d2-962, P3-d2-1380 Hasanato, Rana P2-d2-935, P3-d1-1231 Hasanbegovic, Snijezana P3-d3-1319* Hasegawa, Satomi P1-d3-268 Hasegawa, Tomonobu FC12-191, FC18-226, FC3-134, FC9-171, P1-d1-240, P1-d1-243, P1-d1-284, P1-d1-504, P1-d1-523, P1-d1-572, P1-d3-404, P2-d2-1148, P2-d2-1183, P2-d2-831, P3-d1-1226, S4-24 Hasegawa, Yukihiro P1-d1-237, P1-d1-504, P1-d1-532, P1-d1-572, P1-d1-593, P1-d2-578, P2-d3-881, P3-d2-1239 Hashemipour, Mahin P2-d1-1179* Hassani, Yasmine FC19-233 Hasselmann, Caroline P1-d2-247* Hassen, Maha P3-d3-1358 Hatipoglu, Nihal P1-d1-500*, P2-d1-1006, P2-d1-787* Hattersley, Andrew FC14-200, P1-d1-454 Hatun, Sükrü P1-d2-299, P2-d1-1050, P2-d1-1174, P2-d3-806 Hatzaki, Angela P3-d1-1328 Hauffa, Berthold P1-d1-522, P1-d2-462 Haupt, Riccardo P2-d1-734 Hauschild, Michael P2-d11082, P2-d1-990, P2-d1-995* Hauser, Russ P2-d1-1083 Hawkes, Colin LB3-1516 Hayakawa, Mika P2-d1-1172 Hayasaka, Kiyoshi P2-d3-881
Hayashi, Mie P1-d1-243 Hazebroek, Frans W.J. P1-d3-564b Hazes, Johanna P2-d3-707 Hazhir Karzar, Nazanin P3-d1-1366 He, Guoping P2-d2-929 He, Zhanwen P2-d3-977 Heath, Karen P2-d1-955*, P2-d2-969*, SAT6 Heather, Natasha P2-d2-1158 Hebebrand, Johannes FC17-217, P3-d1-1269 Heffernan, Emmeline P2-d1-739* Heidemann, Peter P1-d1-570 Heidtmann, Bettina P1-d1-418, P2-d3-872 Heike, Woehling P3-d3-1314 Heiman, Julia P1-d1-574 Heino, Terhi LB1-1493 Heinrich, Juan P1-d1-380 Heinrichs, Claudine P1-d1-387 Heinze, Matthias P1-d3-409 Heldt, Katrin P3-d1-1217* Hellström, Ann FC3-133 Helms, Peter J. P2-d1-752 Helvacioglu, Didem P2-d1-742* Hemi, Rina P2-d1-623 Henderson, Mélanie FC6-153, P1-d2-461* Hennum, Jesse P2-d1-720 Henrion, Arne P3-d1-1360 Heo, Sun-Hee P1-d3-618 Heredia, Claudia P2-d1-951 Hermanns, Pia FC19-231*, P1-d3-614* Hernandez Cadena, Leticia P2-d1-778 Hernández Marcos, María P3-d2-1302 Hernandez, Arturo FC7-157 Hernandez, Claudia P2-d1-629*, P3-d1-1405* Hernandez, Maria Isabel P2-d3-875 Hernandez, Maria LB1-1495* Hero, Matti P3-d2-1378* Herpy, James P1-d1-347 Herrlich, Susan P1-d1-448 Herrmann, Ralf P1-d1-522 Hershey, Tamara P1-d3-442 Herskovits, Oren FC16-215, P1-d1-391, P2-d2-828 Hertweck, Paige LB1-1491 Hertz, Jens Michael FC1-125 Heslegrave, Amanda FC11-183 Hey-Hadavi, Judith P2-d3-840 Heyman, Maria P3-d1-1396*
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
269
Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Hilczer, Maciej P1-d3-406, P1-d3-412, P2-d3-838*, P3-d1-1370 Hill, Nathan P1-d1-245 Hinchey, Louise P1-d2-426, P2-d1-859, P2-d3-906, P2-d3-910 Hindmarsh, Peter FC11-180, LB3-1516, P1-d1-245, P2-d1-621, P2-d2-631 Hines, Melissa S2, S2-19* Hinney, Anke FC17-217 Hiort, Olaf FC8-165, FC8-166, P1-d1-573, P2-d2-1113, WG6-119* Hirose, Shinichi P1-d2-295 Hirose, Thiago P3-d2-1377 Hirschhorn, Joel FC20-1484, FC4-138 Hitoglou-Makedou, Areti P2-d2-798 Hladnik, Uros P1-d1-594 Hlavaty, Petr P1-d3-340 Ho, Caroline FC20-1484 Ho, Chung Shun FC14-201 Ho, Cindy Weili P2-d3-941 Hoan, Nguyen P2-d1-1080 Hochberg, Ze‘ev FC5-144*, P1-d2-257, P1-d2-302, P2-d2-1098, P2-d3-1069, WG3-90*, YB2 Hodgson, Isabelle P2-d1-1171, P3-d1-1197* Hodgson, Maria Isabel P2-d2-898 Hoebeke, Piet FC8-167 Hoertenhuber, Thomas P1-d2-462 Hoey, Hilary P1-d2-398 Hoeybye, Charlotte P2-d2-829 Hofbauer, Lorenz P2-d2-1028 Hofer, Sabine P3-d1-1323* Hoffmann, Anika P1-d1-508, P2-d1-1015 Hofman, Paul P1-d1-524, P1-d1-525, P2-d2-1158* Hogan, Andrew P1-d3-338 Hogler, Wolfgang FC12-187 Hokken-Koelega, Anita FC16-212, P1-d1-509, P1-d2-397, P1-d3-411, P2-d2-762, P2-d3-707, S1-11, S1-14, S1-15 Holder, Martin P1-d1-451 Holl, Reinhard FC6-152, P1-d1-418, P1-d1-421, P1-d2-462, P2-d1-1034, P2-d2-863, P2-d3-872, P3-d1-1269, S5, S5-28* Hollay, Erik P2-d2-895 Holle, Rolf P3-d1-1269 Holm, Kirsten P1-d1-277
Holm, Tara P2-d2-964 Holmes, William P1-d2-585 Holmgren, Anton P1-d2-479, P1-d2-548*, P1-d3-558* Holt, Victoria FC4-143 Holter, Benjamin P1-d1-468 Holterhus, Paul-Martin FC8-165, FC8-166, P1-d1-418*, P1-d2-256, P1-d3-264 Homayon, Mojtaba P2-d3-774* Homma, Keiko FC9-171, P1-d1-240*, P1-d1-243 Hoppmann, Julia P2-d1-665* Hori, Naoaki P1-d1-284 Horikawa, Reiko P1-d1-523, P1-d2-578, P1-d3-404, P2-d1-890, P2-d2-1052, P2-d2-1188, P3-d1-1289* Horiuchi, Kiyomi P3-d2-1244 Horn, Paul P1-d2-394 Hornig, Nadine FC8-165*, P1-d3-264 Hornung, Lindsey P1-d1-351, P2-d1-820, P2-d3-1070 Horodnicka-Jozwa, Anita P1-d3-406 Horovitz, Michal P1-d2-249 Horowitz, Michael P1-d2-433 Horvat, Milena P2-d3-772 Horvath, Tamas L. S13-51* Hosoi, Hajime P1-d3-342, P3-d1-1292 Hosokawa, Yuki P1-d2-432 Høst, Christian P2-d1-724 Hotsubo, Tomoyuki FC10-176 Hou, Lele P2-d3-977 Hou, Lin P3-d2-1337 Houari, Zineddine P1-d2-487 Hougaard, David P1-d1-281 Houghton, Jayne P2-d2-926, P2-d3-877, P2-d3-879 Houlier, Marine FC19-230 Houtzager, Bregje A. P1-d3-613 Hovatta, Outi WG5-108* Hovendal, Claus P1-d3-444 Hovorka, Roman P1-d2-431 Hovsepian, Silva P2-d1-1179 Howard, Caoimhe P2-d3-909* Howard, Sasha FC4-141* Howell, Jonathan P2-d1-820 Hoyer-Kuhn, Heike P1-d1-282*, P1-d2-481 Hu, Shengyong P1-d2-394 Huang, Fengyang P2-d1-778* Huang, Ke P1-d3-370 Huang, Shan P1-d1-425*, P3-d1-1230* Huang, Yu-Hsiu P1-d1-501 Hudson, Melissa P1-d2-515 Huebner, Angela P2-d2-1028*, P2-d3-712
* Presenting author
270
9th Joint Meeting of Paediatric Endocrinology 2013
Hughes, Beverley FC9-172 Hughes, Claire FC18-222, FC18-225, P2-d2-634 Hughes, Ian P2-d3-841* Hughes, Ieuan FC3-135, FC8-166, P1-d2-584, P2-d1-953 Huh, Rimm P2-d1-1003* Hui, Yuen Ching P2-d3-876 Huijbregts, Lukas PL4-4 Huke, Verena FC5-148 Humayun, Khadija P2-d1-1010 Humphriss, Eric FC16-214 Hunt, Linda P1-d2-362, P1-d3-336 Hunt, Rodney FC14-201 Huot, Céline P1-d2-247 Husebye, Eystein S. P2-d1-673 Husebye, Eystein P1-d1-277 Hussain, Ishrat P2-d1-784 Hussain, Khalid FC11-180, FC11-183, FC11-185, MTE4:1, MTE4:2, P1-d2-426*, P1-d2-463, P1-d3-439, P2-d1-850, P2-d1-852, P2-d1-859, P2-d1-883, P2-d3-877, P2-d3-906, P2-d3-910, P2-d3-944, P3-d1-1326, P3-d2-1335, P3-d3-1349 Huth, Sandra LB4-1528 Hwa, Vivian FC16-215, P3-d2-1303 Hwang, Il Tae LB4-1521, P2-d1-726 Hwang, Jin Soon P1-d3-553, P2-d2-1095 Hyodo, Hiromi P3-d2-1209 Hysenaj, Gerald P2-d1-849 I
Iaccarino Idelson, Paola P1-d1-346, P2-d1-1039 Ibacache, María P1-d2-296 Ibáñez, Lourdes FC14-198, FC14-199, FC15-209, P1-d1-313, P1-d1-388, P1-d1-535*, P1-d2-321, P1-d2-361, P1-d3-339, P1-d3-376, P2-d2-636, WG4-99, WG4-104* Ibáñez, Pilar Gill P2-d2-1153 Ibba, Anastasia P1-d2-490 Ibekwe, Maryann P3-d2-1345* Ibekwe, Roland P3-d2-1345 Ichikawa, Go P1-d1-494* Ichikawa, Junko P1-d1-494 Ida, Hiroyuki P2-d1-1172, P3-d3-1316 Ida, Shinobu P1-d2-578 Idelevich, Anna P1-d1-286
Idkowiak, Jan FC9-170*, FC9-172 Idris, Arini P3-d1-1201* Iezzi, Maria Laura P2-d1-741* Ifflaender, Sascha P2-d2-1028 Igaki, Junko P2-d3-881 Igarashi, Maki P1-d2-578*, P2-d3-1131 Iglesias, Ainhoa FC19-228* Ignaccolo, Giovanna P2-d3-911 Igrutinovic, Zoran LB3-1512 Iguchi, Genzo S15-58 Ihe, Chibuzor P1-d2-516* Ikeda, Kazushige FC9-171, P1-d1-240 Ikelaar, Nadine A. P1-d3-613 Ilgin Ruhi, Hatice P2-d2-1116 Ilkanipoor, Homa P3-d3-1311* Ilkhanipoor, Homa P1-d2-298 Ille, Jasenka P2-d2-1153* Ilonen, Jorma P1-d1-274 Ilyin, Alexander P2-d1-1043 Imai, Kazuhide P1-d1-243 Imai, Masayuki P2-d1-1172 Imamoglu, Mustafa P3-d2-1440 Improda, Nicola P1-d2-588*, P2-d2-1190 Inada, Nahoko P2-d1-725 Iñiguez, Germán LB1-1495, LB3-1517, P1-d1-382, P1-d1-419, P1-d1-492*, P1-d1-495*, P1-d2-543 Iñiguez, German P1-d3-445 Inokuchi, Mikako FC12-191 Inzaghi, Elena P1-d1-385 Iona, Patrizia P3-d2-1473, P3-d2-1475 Iotova, Violeta P1-d2-356, P2-d1-733, P2-d1-852*, P2-d3-769 Irarrazabal, Carlos P1-d1-471, P1-d2-296 Isabel, Pinto P1-d1-477 Isguven, Pinar P2-d1-1050 Isguven, Sukriye P2-d2-963* Ishibazawa, Emi P2-d1-1144 Ishiguro, Hiroyuki P3-d2-1209 Ishii, Masahiro P2-d2-1148, P2-d3-811 Ishii, Tomohiro FC12-191, FC18-226, FC19-229, MTE8:1, MTE8:2, P1-d1-240, P1-d1-243, P1-d1-504 Ishizawa, Michiyasu P1-d2-295 Ishizu, Katsura FC12-186 Ishizu, Katura FC10-176 Ismail, Heba P2-d1-921 Ismailov, Said P3-d3-1355 Isnard, Myriam FC12-187 Isojima, Tsuyoshi P1-d1-289, P1-d2-295* Israel, Shoshana FC9-173
Ito, Ikuyo P3-d1-1292 Ito, Junko P1-d2-521* Ito, Kimiko P1-d1-593 Ito, Mari P2-d3-811 Iughetti, Lorenzo P1-d1-350*, P1-d1-594*, P1-d2-258, P1-d2-399, P2-d1-737, P2-d1-741, P2-d1-749, P2-d1-882, P2-d1-956 Ivanov, Krasimir P2-d1-733 Ivanova, Olga P2-d2-633 Ivarsson, Sten P1-d2-398 Iwaniszewska, Barbara P3-d2-1208 Iwasaki, Yasumasa FC12-191 Izawa, Masako P3-d2-1237 Izumi, Yoichi P2-d3-908 J
Jääskeläinen, Jarmo P1-d1-236 Jackowski, Tomasz P1-d3-406 Jackson, B. P2-d1-1004 Jackson, Jessica P2-d1-883 Jackson, Kathryn P2-d3-943, P3-d1-1424*, P3-d2-1413* Jacobson-Dickman, Elka P3-d1-1404* Jacquier, Sandrine PL4-4 Jacquin, Paul P2-d1-1048 Jacqz Aigrain, Evelyne P2-d1-1048 Jahnukainen, Kirsi CPE4-79*, P1-d1-293 Jaillet, Jessica P2-d1-1009, P3-d1-1469, P3-d3-1385* Jaime, Sánchez-Pozo P1-d1-477 Jaja, Tamunopriye P3-d1-1430* Jakubiuk-Tomaszuk, Anna P3-d3-1392 Jakubowska, Ewa P3-d3-1392 Jalaludin, Muhammad Yazid LB3-1518 James, Chela FC11-183 Jamsheer, Aleksander P3-d2-1208 Janchevska, Aleksandra P1-d1-575, P3-d3-1308 Janel, Nathalie FC19-230 Janssen, Joop FC10-177 Janssen, Sofie P1-d2-579 Januário, José P3-d1-1321 Janus, Magdalena P2-d2-970 Jaramillo, Enrique FC6-151 Jaron, Ranit P2-d1-1001 Jarrett, Olumide P3-d1-1399* Jarzynska, Magdalena P3-d1-1252, P3-d1-1253 Jäschke, Holger LB4-1528 Jasim, Seema FC7-156 Jasper, Héctor P1-d1-380, P1-d1-384, P1-d3-413 Jauhari, Praveen P3-d2-1333
Jaworski, Maciej P2-d1-667 Jayaraman, Rajesh LB3-1507, LB3-1514 Jee, Youn Hee P2-d2-972* Jeelani, Owase P1-d2-517 Jefferies, Craig P2-d2-1158 Jelenkovic, Bratimirka P2-d1-1078*, P3-d2-1439* Jennane, Farida FC6-155, P2-d3-1127, P3-d1-1199 Jensen, Rikke P1-d2-398 Jeon, Jae-Sik P2-d2-1089 Jeong, Hwal Rim P2-d2-1095* Jeong, Jin Woo P2-d3-1132 Jesus, Julyanna LB4-1520 Jetha, Mary P2-d2-867 Jevalikar, Ganesh P1-d1-568*, P2-d3-1162* Jeznach, Marta P1-d1-596 Ji, Chenbo FC17-220 Ji, Hyi-Jeong P1-d1-390 Jian, Yu P3-d1-1432* Jiang, Jipu WG6-117 Jiménez-Chillarón, Josep P1-d1-315 Jimenez-Vega, Jose P2-d1-1103*, P2-d1-720* Jin, Dong-Kyu P2-d1-1003, P2-d1-1036, P2-d2-1093 Jin, Hye Young P1-d3-618 Joachim, Maria FC20-1484 Joel, Dipesalema P2-d1-950* Joeng, Kyu Sang LB1-1493 Johnson, Christine LB1-1491 Johnson, María Cecilia P1-d1-492, P1-d1-495 Johnson, Stephanie P2-d1-1017, P2-d1-857* Johnston, Robert P2-d1-739 Johnston, Zoe FC8-162 Joki, Henna P1-d1-293* Jones, Jeremy FC19-231, P1-d2-607, P2-d2-1156, P2-d2-1193 Jones, Julie P2-d1-1143 Jones, Kenneth P2-d2-704 Jones, Timothy P1-d3-443 Jonsson, Björn P1-d2-392, P1-d3-560, P2-d1-822, P2-d2-835, P2-d3-974, P2-d3-981 Jonsson, Bjourn P3-d1-1399 Jonsson, Peter P1-d3-410 Joo Turoni, Claudio P2-d2-763 Jordan, Faron FC16-213* Jordanova, Desislava P2-d3-651 Jorge, Alexander A.L. FC3-134, LB2-1496, MTE12:1, MTE12:2, P1-d1-469, P1-d1-472, P1-d1-506, P1-d2-482, P2-d1-952, P2-d1-954, P2-d3-949
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
271
Floor Plan Exhibition Author Index
author index
author index
Jorge, Alvarez P3-d2-1282 Jorge, Fernanda LB4-1522 Josefson, Jami FC13-195* Joseph, Angela P3-d1-1458* Joshi, Kriti WG3-97* Joshi, Sarita P2-d1-820 Joustra, Sjoerd FC10-177* Joyce, Caroline P2-d3-909 Juan, López-Alvarenga P2-d1-780 Julia, Madarina P2-d1-992* Júlíusson, Pétur P1-d1-474*, P2-d3-839 Juma, Zain P3-d2-1298* Jung, Ana FC3-134 Jung, In Ah P1-d2-483*, P2-d1-777* Jung, Min Ho LB4-1521, P1-d1-475, P1-d2-458, P1-d2-483, P2-d1-777 Jung, You Jin P2-d1-1003 Jung, Yu Jin P2-d2-1093 Jürimäe, Jaak P2-d3-710 Jürimäe, Toivo P2-d3-710 Just, Walter P2-d2-1121 Juste, Juan P3-d2-1302 Juul, Anders S11, S11-44*
Floor Plan Exhibition Author Index
K
Kabour, Saida P3-d1-1255 Kabukcuoglu, Sare P3-d1-1425 Kadioglu, Alev P2-d1-1079 Kadziela, Katarzyna P3-d1-1464 Kagami, Masayo P1-d1-523, P1-d1-527, P2-d1-626, S6-31* Kahill, Laurie P2-d3-878 Kain, Juliana P1-d3-341, P1-d3-375 Kaiser, Ursula FC4-138 Kajita, Yoshihiro P3-d1-1466 Kajiwara, Michiko P2-d3-1125 Kakee, Naoko P2-d1-818 Kakleas, Kostas P2-d3-812 Kalaca, Sibel P1-d2-299 Kalapurackal, Mila Ann FC2-129* Kalchev, Kalin P2-d1-733 Kalicka-Kasperczyk, Anna P2-d1-664, P2-d2-640 Kalina, Maria P1-d3-406, P2-d3-837 Kalina-Faska, Barbara P1-d3-406, P2-d3-837 Kalitsi, Jennifer P1-d2-516 Kalogerakou, Kleanthi P1-d3-615 Kaloumenou, Irene P1-d3-615, P3-d1-1431, P3-d2-1280, P3-d2-1438 Kamali Sarvestani, Eskandar P1-d1-273
Kamboj, Manmohan P1-d1-449* Kamekawa, Daisuke P2-d3-811 Kamenicky, Peter FC2-128 Kaminioti, Christina LB2-1498 Kaminska, Halla P2-d3-1128 Kämpe, Olle S14, S14-54* Kampino, Gadi P3-d1-1359 Kamrath, Clemens P1-d2-248* Kamrath, Heidi P2-d1-720 Kanaka-Gantenbein, Christina LB2-1498, LB2-1499, LB3-1513* Kandemir, Nurgun P2-d2-1022, P2-d3-1064 Kandil, Manal P2-d2-1117 Kanety, Hana P2-d1-623 Kaneva, Rada P2-d2-1023 Känsäkoski, Johanna FC10-178 Kant, Sarina FC3-132, FC9-172, P1-d2-326, P1-d2-478 Kanumakala, Shankar P2-d2-829 Kanzaki, Susumu P2-d1-815, P2-d2-637 Kaoru, Konishi P1-d3-268 Kaparos, Georgios P2-d2-864 Kapelari, Klaus FC12-187, P1-d2-305 Kapellen, Thomas P1-d1-418, P2-d3-872* Kapoor, Ritika FC11-183, P2-d1-883 Kappelgaard, Anne-Marie P3-d1-1289 Kaprova, Jana P2-d1-993 Kara, Ates P2-d2-1022 Kara, Cengiz P2-d1-1143*, P3-d1-1463* Kara, Manolya P2-d2-1147, P2-d2-1152 Kara, Ozlem P1-d2-403, P2-d1-915, P2-d2-1024, P3-d1-1461 Kara, Setenay P1-d1-449 Karabocuoglu, Metin P2-d3-938 Karabouta, Zacharoula P2-d2-1057*, P2-d2-798* Karaca, Züleyha P1-d2-256 Karaçal, Ümit Naci P3-d3-1449 Karachaliou, Feneli P1-d3-615, P3-d1-1431, P3-d2-1280, P3-d2-1438* Karadag Oncel, Eda P2-d2-1022 Karadag, Bulent P2-d1-884 Karagedik, Hande P1-d2-359, P2-d3-776
* Presenting author
272
9th Joint Meeting of Paediatric Endocrinology 2013
Karagüzel, Gülay P1-d1-280*, P2-d1-1108, P3-d2-1440, P3-d3-1449* Karagüzel, Güngör P3-d2-1440 Karakas Celik, Sevim P2-d3-1072 Karakaya, Ali Erdal P3-d2-1212 Karakoc, Fazilet P2-d1-884 Karakurt, Cemsit P1-d2-364 Karalok, Zeynep P2-d2-791 Karamifar, Hamdollah P1-d2-298* Karamizadeh, Zohreh P1-d1-273, P1-d2-298, P2-d2-705, P3-d3-1311 Karantza, Maria P3-d1-1328* Karaoglan, Murat P2-d2-1194, P3-d1-1203*, P3-d1-1453 Karaoglu, Berk P3-d2-1435 Karavanaki, Kyriaki P2-d2-864*, P2-d3-812 Karayianni, Christina P2-d3-812 Kareva, Maria P2-d1-1043, P2-d1-658, P2-d2-633, P2-d3-646 Karga, Helen P1-d1-496 Karges, Beate P1-d2-604 Kariyawasam, Dulanjalee FC19-230 Kark, Jeremy P2-d1-1135 Karlsson, Ann-Katrine P1-d2-355 Karmanov, Maxim P2-d2-1027 Karonova, Tatiana P3-d1-1261 Karpathios, Themistoklis P1-d3-263 Karra, Efthimia P1-d3-439 Karres, Janina LB3-1509 Karvela, Alexia FC1-121, FC15-208, P1-d1-314* Kashimada, Kenichi P1-d3-261, P1-d3-268, P2-d3-1125, P3-d2-1239 Kasia, Tessa FC10-174 Kassai, Behrouz P1-d1-470 Käßner, Franziska P1-d1-309*, P1-d3-368* Katam, Kishore P2-d2-699 Kato, Chii P2-d3-811 Kato, Fumiko P2-d3-1131 Katoh-Fukui, Yuko P1-d1-290* Katsikis, Ilias P1-d2-541 Katsumi, Yoshiki P3-d1-1466 Katsunuma, Toshio P3-d3-1316 Katz, Michelle P2-d1-855* Katz, Stuart P2-d2-901 Katzman, Debra P1-d2-306 Katzos, George P2-d2-702 Kauli, Rivka P3-d3-1318 Kaunisto, Kari FC10-178 Kaunisto, Mari FC10-178
Kaushik, Smita P3-d1-1259 Kawada, Yasusada P2-d3-1131 Kawagoe, Rinko P2-d3-1131 Kawai, Masanobu P1-d2-513 Kawakita, Rie P1-d2-432 Kawano, Atsuko P2-d1-987 Kawano, Kaori P3-d2-1244* Kawashima, Minae P1-d1-289 Kawashima, Yuki P2-d1-815, P2-d2-637* Kaya Kiliç, Fatma P1-d2-519 Kaya, Avni P3-d3-1394 Kazahari, Mayumi P2-d2-1148, P2-d3-811 Kazakova, Krasimira P2-d3-651, P3-d1-1223 Kazanowska, Bernarda P3-d1-1257 Kazantzidou, Eirini P2-d2-702 Kazuyasu, Kubo P2-d3-1131 Ke Wang, Michael P2-d3-1164 Kedji, Leila P2-d1-991 Kedzia, Andrzej P1-d3-406 Keefe, Christel P2-d3-1070* Kelberman, Dan FC10-174 Kelestimur, Fahrettin P1-d2-256 Keller, Marion P1-d1-533 Kelnar, Christopher J. FC8-162, YB3 Kemal Topaloglu, Ali P1-d1-241, P2-d2-701, P3-d1-1229 Kempers, Marlies J. E. P2-d1-1142 Kendirci, Mustafa P2-d2-698* Keni, Jyotsna P3-d3-1446 Kennebeck, Stephanie LB2-1502 Keogh, Julia FC20-1484 Kerlan, Véronique FC1-122 Kern, Sonja P2-d2-638 Kershaw, Melanie P2-d2-677 Keselman, Ana P1-d3-413, P2-d1-1051, P2-d1-1136, P2-d3-982 Keser, Alev P2-d3-806* Keski-Filppula, Riikka FC10-178 Keskin, Mehmet P2-d2-1194*, P3-d1-1203, P3-d1-1453* Keskin, Ozlem P2-d2-1194, P3-d1-1203, P3-d1-1453 Kesler, Karina P3-d1-1397 Kesraoui, Mourad P2-d2-1029* Keupp, Katharina P1-d1-282 Khadgawat, Rajesh P1-d1-390, P2-d2-1120, P3-d1-1196, P3-d1-1454 Khadilkar, Vaman P1-d1-390 Khadr, Sophie FC4-143* Khairi, Ranna P1-d2-584
Khan, Khalid P2-d2-964 Khan, Muhammad P1-d3-337* Khanh, Nguyen P2-d1-1080 Khatchadourian, Karine P1-d2-251* Khemiri, Monia P2-d1-1109 Khiari, Mohamed El Mokhtar P3-d2-1243 Khmara, Irina P3-d2-1476 Khoury, Jane P1-d1-351, P2-d1-1103, P2-d1-820, P2-d3-1070 Khurana, Divya P2-d1-673, P2-d2-1056, P3-d1-1235, P3-d1-1263*, P3-d2-1206* Khurana, Madan P2-d1-784, P2-d2-1120, P3-d1-1196, P3-d1-1454 Khuri, Jananne P2-d2-1115 Ki, Chang-Seok P2-d1-1003, P2-d1-1036 Kiess, Wieland P1-d1-309, P1-d1-318, P1-d3-368, P2-d1-665, P2-d1-732, P2-d1-747, P2-d2-753, P2-d3-1066, P3-d1-1269, P3-d1-1360 Kiewert, Cordula P1-d1-522 Kikuchi, Akira P2-d3-908 Kikuchi, Toru P2-d2-1183, P3-d1-1293 Kilian, Agnieszka P1-d3-406 Kim, Duk Hee P2-d3-1132 Kim, Eun Young P2-d2-1096 Kim, Gu-Hwan P1-d1-234, P1-d3-618, P2-d1-731, P2-d1-887 Kim, Hae Soon P2-d1-1086* Kim, Ho-Seong P1-d1-476, P2-d2-1097, P2-d3-1132 Kim, Hwan-Cheol P3-d2-1434 Kim, Ja Hye P1-d1-234, P1-d3-618, P2-d1-731*, P2-d1-887* Kim, Jae Hyun LB4-1521 Kim, Jaekyung P2-d2-1089, P3-d2-1434 Kim, Jae-Min P1-d1-234 Kim, Ju-Hyun P1-d1-234, P1-d3-618 Kim, Se Young P2-d2-1096* Kim, Shin Hee P1-d1-475, P1-d2-483, P2-d1-777 Kim, Shin-Hye P2-d2-759 Kim, Su Jin P2-d1-1003 Kim, Ye Jin P2-d2-1097, P2-d3-1132 Kim, Yong Hyuk P2-d2-1097*, P2-d3-1132* Kim, Yoo-Mi P1-d1-234*, P1-d3-618*, P2-d1-731, P2-d1-887
Kim, Young Ju P2-d1-1086 King, Gareth FC16-213 King, Mary-Claire P2-d1-1001 Kingswell, Robin P2-d3-843 Kinik, Sibel Tulgar P3-d2-1334* Kinmond, Sheena P2-d3-984 Kinoshita, Eiichi P2-d2-833 Kionke, Janina P1-d2-601 Kirby, Bradley P2-d1-752 Kirby, Gail P2-d1-1037 Kirchhoff, Esther P2-d3-768 Kirel, Birgul P2-d1-662 Kiremitci, Seniha P2-d2-1090* Kirillova, Inara P2-d3-802, P2-d3-809 Kirk, Jeremy FC9-170, P1-d1-476, P1-d1-534, P1-d2-398, P2-d1-821*, P3-d2-1298 Kista Reddy, Vijay P3-d1-1429 Kitagawa, Teruo P1-d3-268 Kitanaka, Sachiko P1-d1-289, P1-d2-295 Kitaoka, Taichi P1-d1-289, P1-d2-513 Kitsuda, Kazuteru P2-d2-1148*, P2-d3-811 Kiviranta, Panu FC14-203* Kiviranta, Riku LB1-1493 Kiyaev, Alexey P3-d1-1216* Kiyomi, Fumiaki P3-d1-1289 Kizilocak, Hande P2-d1-782 Kizilok, Hande P2-d2-862 Kizu, Rika P1-d1-243 Klammt, Jurgen P2-d2-967 Klancar, Gašper P1-d3-334, P1-d3-367 Klatka, Maria P2-d1-986*, P2-d2-1151 Klee, Dirk P2-d2-934 Klee, Kristi P2-d1-925 Klee, Philippe P2-d2-927* Klein, David P1-d1-351* Klein, Karen P1-d3-554 Kleintjens, Joris SAT5 Kleta, Robert FC10-174 Kletter, Gad FC16-214, P1-d3-557* Klibanski, Anne P1-d2-306 Kliesch, Sabine P1-d2-550 Klimentieva, Marina P3-d1-1400 Klouwer, Femke P1-d3-613 Knauth, Burkhild P1-d2-462 Kneppo, Carolin P1-d2-604 Knip, Mikael P1-d1-274, PL2-2* Knoll, Christian P1-d2-319 Ko, Cheol-Woo P2-d2-1055 Kobalan, Paola LB1-1495 Kobayashi, Kisho P1-d1-537, P3-d1-1407
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
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Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Kobayashi, Masao P2-d1-674 Kobayashi, Tohru P3-d3-1316 Kobez, Tatiana P2-d2-793 Koc, Nevra P1-d2-403 Koca, Cemile P2-d1-817 Koca, Tugba P1-d2-602 Kocaay, Pinar P2-d2-1116, P2-d3-1123 Kocabas, Abdullah P3-d1-1461 Kochavi, Beigitte P2-d1-730 Kochi, Cristiane FC4-138 Kochova, Elena P2-d2-967 Kociemba, Anna P2-d2-970 Kocova, Mirjana P2-d2-967*, P3-d1-1258*, P3-d2-1306 Kodama, Hiroko P2-d3-908 Koenig, Wolfgang P1-d1-528 Koga, Yasutoshi P2-d1-1140 Koh, Ji Won P2-d2-1089, P3-d2-1434 Köhler, Birgit WG6-118* Kojima, Yoshiyuki P1-d2-578 Kok, Fernando FC4-142 Koki, Paul WG3-98 Kolasa-Kicinska, Marzena P3-d1-1370 Kolesinska, Zofia FC8-166* Kolev, Nikola P2-d1-733 Koleva, Reni P2-d2-1032 Kollen, Wouter P3-d1-1249 Kollman, Craig P1-d2-431, P1-d3-442 Kolouskova, Stanislava P1-d1-278, P2-d1-993 Koltin, Dror P1-d1-455 Koltowska-Häggström, Maria P1-d3-409, P1-d3-410 Komai, Takayuki P3-d1-1407 Konchits, Katerina P3-d1-1260 Konchits, Katsiaryna P2-d3-1159* Kondoh, Tatsuro P1-d1-523 Kondratyeva, Elena P2-d2-682 Konrad, Katja P1-d1-421, P1-d2-462* Konstantakopoulos, Sotiris P2-d2-826, P2-d2-868, P2-d2-900 Konstantinova, Maia LB3-1508 Kool, Pille P1-d1-274 Kopacek, Cristiane P2-d2-962*, P3-d2-1380* Kopchick, John P1-d1-347 Kopylova, Irina P2-d3-646* Kor, Deniz P3-d2-1215 Kor, Yilmaz P2-d2-1194, P3-d1-1203, P3-d1-1256, P3-d2-1215* Korbonits, Marta P1-d2-517, S10, S10-42* Koren, Ilana FC9-173, P3-d1-1200*
Koren-Morag, Nira FC3-137 Korkmaz, Huseyin P1-d2-519, P2-d3-1072 Korkmaz, Ozlem P2-d1-1087, P2-d3-1126 Körner, Antje P1-d1-309, P1-d1-318, P1-d3-368, P2-d1-747, P2-d2-753, P2-d3-1066*, P3-d1-1360 Korpal-Szczyrska, Maria P1-d3-406, P3-d1-1294* Korrick, Susan P2-d1-1083 Kosaka, Kitaro P1-d3-342, P3-d1-1292*, P3-d1-1466 Kosar, Ugur P2-d3-766 Kosta, Konstantina P2-d2-1119 Kostalova, Ludmila P1-d1-476 Kosteria, Ioanna LB3-1513 Kostic, Gordana LB3-1512 Kostova, Antoaneta P2-d3-644* Kostrova, Irina P2-d2-633 Koszutski, Tomasz P2-d3-1128 Kot, Karolina P2-d3-645, P3-d1-1452* Kota, Sunil P3-d1-1459 Kotan, Leman Damla P1-d1-241 Kotanidou, Eleni P2-d3-765* Kotnik, Primož P1-d2-457*, P2-d3-772*, P2-d3-773 Kotori, Afrim P3-d3-1450 Kotori, Vjosa P3-d3-1450* Kotsani, Eleni P2-d3-812 Kovac, Jernej P2-d3-772 Kovalenko, Svetlana P2-d1-813, P2-d1-814 Koves, Ildiko P2-d1-921*, P2-d1-925* Kovtun, Olga P3-d1-1216 Kowalczyk, Julia FC18-222, FC18-224*, FC7-160 Koyama, Yuhei FC9-171*, P1-d1-240 Krakow, Deborah LB1-1493 Krasin, Matthew P1-d2-515 Kratzin, Thomas P3-d3-1448 Kratzsch, Jürgen P1-d3-368, P2-d3-1066, P3-d1-1288, P3-d1-1360* Krause, Alexandra P3-d3-1448 Krawczynski, Maciej P3-d2-1208 Kreatsa, Maria P2-d2-864 Krebs, Andreas P1-d1-451, P3-d3-1448 Krieg, Andreas P3-d1-1225 Kriegler, Julia WG6-115* Krishna Prasad, Hemchand P1-d1-453, P1-d1-534* Krishna, Surabhi P3-d1-1459* Kristensen, Kurt P1-d1-281* Kristiansen, Hege P1-d1-474
* Presenting author
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Kriström, Berit P1-d2-302, P1-d2-392, P2-d2-829, P2-d2-835, P2-d2-836, P2-d2-971, P2-d3-1068 Kritas, Stamatiki P1-d2-433 Krnic, Nevena P2-d2-1153, P2-d3-914 Kröger, Heikki LB1-1493 Krohn, Knuth LB4-1528 Krone, Nils FC9-169, MTE10:1, MTE10:2, P1-d3-267, P2-d1-624, P2-d2-634 Krstevska-Konstantinova, Marina P1-d1-575, P3-d2-1240, P3-d3-1308* Krude, Heiko CPE3-77*, FC17-217, P1-d1-512, P1-d2-328, P1-d2-603, P1-d3-555, P2-d3-1169, P3-d1-1198 Krukowska-Andrzejczyk, Barbara P2-d3-837* Kržišnik, Ciril FC10-179, P2-d3-772 Kuba, Valesca P2-d2-756* Kubba, Haytham P2-d1-1104 Kubey, Inga P3-d2-1238 Kubota, Takuo P1-d2-513 Kucharska, Anna P1-d3-617*, P3-d1-1464* Kucukemre Aydin, Banu P2-d1-1050*, P2-d1-1079* Kudela, Grzegorz P2-d3-1128 Kuehnen, Peter FC17-217*, P1-d2-463, P1-d3-555 Kuhn, Jean-Marc FC1-122 Kuhn, Michaela FC3-132 Kuiri-Hänninen, Tanja FC14-202*, FC14-203 Kul, Sibel P3-d2-1440 Kullberg, Joel P1-d2-355 Kulle, Alexandra FC8-165, P1-d2-256, P1-d3-264* Kulshreshtha, Bindu P3-d1-1196, P3-d1-1454 Kumar, Rakesh P3-d1-1320* Kumaran, Anitha P2-d1-883*, P2-d3-910 Kumareswaran, Kavita P1-d2-431 Kume, Tuncay P1-d2-365, P2-d2-706 Kummer, Sebastian P2-d2-965*, P3-d1-1218 Kumorowicz-Czoch, Malgorzata P1-d3-614 Kun, Larry P1-d2-515 Kunaeva, Olga P2-d2-633 Kunert, Marlene P1-d1-573 Kunesova, Marie P1-d3-340 Kupeli, Serhan P3-d1-1256
Kuperberg Bar-Niv, Maayan P2-d1-858 Kuperman, Hilton P2-d2-1186, P2-d2-697, P3-d1-1250, P3-d1-1411*, P3-d1-1468 Kuppens, Renske P1-d3-411, P2-d2-762* Kuroda, Yukiko P2-d1-987 Kurosawa, Kenji P2-d1-987 Kurtoglu, Selim P1-d1-500, P1-d2-256, P2-d1-1006*, P2-d1-787 Kurtz, François LB3-1510 Kuru, Lutfi Ihsan P1-d3-335 Kuryan, Ranita P1-d1-246* Kušec, Vesna P1-d2-259 Kushner, Harvey P2-d1-1100 Kusuhara, Koichi P2-d3-1131 Kutlay, Ozden P2-d1-662, P2-d2-641 Kuwabara, Remi P2-d1-674 Kuwabara, Rumi P3-d1-1219 Kwiatkowska, Karolina P2-d1-1077 Kwon, Ah Reum P2-d2-1097, P2-d3-1132 Kwon, Hojang P3-d2-1434 Kwong, Pandina P2-d2-639 Kyriakou, Andreas P2-d1-655 L
La Rosa, Mariangela P2-d2-1025 Labarta, José Ignacio P2-d1-989 Laborde, Kathleen P2-d1-1048 Labrune, Philippe P2-d2-1088 Lachlan, Katherine FC8-166 Lacinel, Sibel P2-d2-1147, P2-d2-1152 Lacombe, Chantal P1-d1-511 Ladaki, Christini P2-d2-973 Ladjouze, Asmahane P2-d1-991* Lafeber, Harrie P1-d1-499 Laffel, Lori P2-d1-855 Lafferty, Antony P1-d2-257* LaFranchi, Stephen WG3-96 Lahermo, Päivi FC10-178 Lahr, Georgia P1-d1-349 Laigong, Paul P2-d3-1069 Laine, Christine LB1-1493 Laine, Tero LB1-1493 Laing, Peter P2-d1-1138*, P2-d1-1141, P2-d1-630 Laitala-Leinonen, Tiina P1-d1-293 Laitinen, Eeva-Maria P3-d2-1378 Lakka, Timo P1-d1-236 Lala, Nilesh P3-d2-1207 Lam, Bich P1-d1-387*
Lam, Jessica FC10-176 Lam, Thuy P2-d1-1083 Lamas, Adelaida P2-d1-851 Lambrinoudaki, Irene P2-d2-864 Lammert, Eckhard P2-d2-934 Lammoglia, Juan P3-d2-1245, P3-d2-1248, P3-d2-1420, P3-d2-1421*, P3-d3-1351*, P3-d1-1427, P3-d2-1247 Lancaster, Gill P1-d1-244, P2-d1-630 Landmann, Eva FC5-148* Landreh, Luise P1-d1-536* Lanes, Roberto P3-d3-1390 Lange, Olga P3-d1-1323 Lang-Muritano, Mariarosaria P2-d1-1082 Lankes, Erwin P1-d1-512, P2-d3-1169, P3-d1-1198* Lanocha, Magdalena P2-d2-970 Lanska, Vera P2-d2-1059 Lapi, Elisabetta P2-d3-842*, P2-d3-846, P2-d3-847*, P3-d1-1262 Lara Moctezuma, Luis P1-d1-310 Laraba, Abdennour P2-d1-991 Lardone, Cecilia P1-d1-419, P1-d1-567 Larijani, Bagher LB3-1511, P3-d2-1336 Larizza, Daniela P1-d1-569*, P1-d3-331 Larizza, Lidia P2-d1-996 Laron, Zvi P3-d1-1359, P3-d3-1318* Laron-Kenet, Tami P3-d1-1359 Larsen, Lois P1-d3-554 Lasecki, Mateusz P1-d1-589 Lateva, Mina P2-d3-769* Latronico, Ana FC4-138, FC8-164, FC20-1486, FC4-142, S11, S11-46* Lätt, Evelin P2-d3-710 Laue, Sandy P2-d1-732 Lauga-Tunina, Una P2-d3-802, P2-d3-809 Laur, Elad P3-d1-1251 Lausch, Ekkehart P2-d2-965 Lavanderos, Sergio P1-d1-235, P1-d2-325 Lawrence, Sarah P1-d2-486* Lawrenz, Barbara P1-d2-545 Lawson, Elizabeth P1-d2-395 Lawson, Sarah P2-d1-1103 Lazar, Liora FC4-140, P2-d1-1135, P2-d1-858 Lazopoulou, Natalia LB2-1498 Lazzarotto, Tiziana P2-d2-896 Lazzati, Juan P1-d3-562, P1-d3-610
Lazzeroni, Pietro P1-d1-245, P2-d1-621 Le Bouc, Yves FC5-147, P1-d1-387, S6-30 Le Jule, Marilyne FC5-147 Le Stunff, Catherine FC20-1485 Le Tallec, Claire FC6-155, LB3-1510 Le, Phuong P1-d3-262 Leal, Letícia FC13-193 Leal, Leticia FC20-1486 Lebenthal, Yael FC4-140*, P1-d2-249, P2-d1-858*, P3-d1-1251 Lebid, Igor P2-d2-793 Lebl, Jan FC10-179, P1-d1-278, P1-d1-292, P1-d1-476, P1-d2-429, P2-d1-993, P2-d2-831, P2-d2-895 Lebrethon, Marie-Christine P1-d2-401 Lechuga, Jose Luis P3-d2-1300 Lecka-Ambroziak, Agnieszka P1-d3-408*, P2-d3-645 Lecointre, Claudine P1-d2-580 Lee, Beom Hee P1-d1-234, P1-d3-618, P2-d1-731, P2-d1-887 Lee, Bo-Eun P3-d2-1434 Lee, Brendan LB1-1493 Lee, Byung Churl P1-d1-475 Lee, Dong Hwan P2-d3-1161 Lee, Hae Sang P1-d3-553 Lee, Haesang P2-d2-1095 Lee, Hwayoung P2-d1-1086 Lee, Hye Ah P2-d1-1086 Lee, Jeongho P2-d3-1161* Lee, Kee-Hyoung P1-d3-556*, P2-d1-892 Lee, Kun Song P2-d2-972 Lee, Mary P2-d1-1083 Lee, Peter P1-d2-393, P1-d3-554*, P2-d3-839*, P3-d3-1313 Lee, Young Ah P1-d1-287*, P2-d1-740* Lee, Yung Seng P2-d3-941* Leelarathna, Lalantha P1-d2-431 Leem, Jong-Han P3-d2-1434 Legendre, Marie P1-d1-511* Lèger, Aubene FC19-228 Léger, Juliane PL4-4, CPE3-76*, FC19-233, P1-d1-511, P1-d2-580, P2-d2-1091 Legrand, Julie P1-d3-405 Lehesjoki, Anna-Elina LB1-1493 Leipert, Jenny P1-d1-309 Leis, Rosaura P1-d1-354*, P2-d1-951, P3-d2-1274*
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
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Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Leiva Gea, Ana P1-d1-417 Leiva Gea, Isabel P1-d1-417* Leiva, Isabel P3-d1-1286 Lejeune, Herve FC1-124 Lejona Martinez de Lecea, Begoña P2-d1-781 Lek, Ngee P2-d3-876 Leka, Sofia PL4-4 Lem, Annemieke P1-d2-397 Lema, Adriana P3-d3-1445 Lemos-Marini, Sofia P1-d2-253 Lennerz, Belinda P1-d1-349*, P1-d2-319*, P3-d1-1269 Lenzi, Lorenzo P2-d3-911 Léon Bacil, Mônica P2-d2-962, P3-d2-1380 Leon, Maria P2-d3-804 Leone, Cláudio P2-d2-756 Leong, Gary P2-d1-1017, P3-d2-1303 Lerín, Carles P1-d1-315 Lerner-Geva, Liat P2-d3-807 Lescai, Francesco FC10-174 Leschek, Ellen P2-d2-972 Lescurat, Maria P2-d1-622, P2-d3-1163 Leszczynski, Przemyslaw P2-d1-1077 Leu, Michael P2-d1-925 Levin, Amnon FC3-137 Levine, Michael FC20-1483*, FC20-1487* Levitsky, Lynne P2-d3-840 Lev-Vaisler, Tali P1-d3-554 Levy, Hannah P2-d3-906 Levy, Miles P2-d1-1010 Levy-Lahad, Efrat P2-d1-1001 Lévy-Marchal, Claire P1-d1-502, P2-d1-1048 Levy-Shraga, Yael P2-d1-623*, P2-d1-730, P2-d3-807 Lewinski, Andrzej P1-d3-412, P2-d3-838, P3-d1-1370 Lewis, Jeff P1-d1-449 Leyland, Kath P2-d2-1193 Li, Cheng-Fang P1-d1-501 Li, Dong FC20-1483 Li, Dongfang P2-d3-977 Li, Jing P3-d1-1432 Li, Lisa LB3-1507* Li, Ming P2-d3-1071 Li, Naishi P2-d3-1071* Li, Rong P3-d2-1337 Li, Wenjing P3-d1-1195* Li, Yan-Hong P1-d1-288, P1-d2-396, P1-d3-559*, P2-d2-1111, P2-d2-642 Li, Yufeng P2-d3-1071 Li, Zhenghong P1-d2-515 Liang, Li LB2-1497, P1-d3-370 Liang, Liyang P2-d3-977
Liang, Yan P1-d1-425, P3-d1-1230 Liao, Lihong P1-d1-526 Liberatore Jr, Raphael P3-d2-1377 Libman, Ingrid P1-d3-438 Libretto, Tina P2-d3-877 Lichte, Kai P1-d1-451 Lichtenberger, Lydia FC19-233* Lido, Andria P2-d1-952* Liese, Johannes FC20-1488 Lieu, Phuong P2-d1-1004 Lifshitz, Fima P3-d3-1314 Lilienthal, Eggert P2-d3-872 Lilos, Peal P3-d3-1318 Lim, David P2-d1-1104 Lim, Jung Sub P1-d3-553* Lim, Pei Kwee P2-d3-876* Lim, Song Hai P2-d3-1165* Lim, Soo Ting P2-d3-876 Lim, Yvonne Yijuan P2-d3-941 Lima, Monica P3-d1-1250 Lima, Roberto P2-d2-794 Limbert, Catarina P2-d2-681, P2-d2-754* Limor, Rona P2-d1-627 Lin, Ashleigh FC6-154 Lin, Hu P1-d3-370* Lin, Xiangquan P3-d3-1315 Linares, Jeannette P1-d3-341*, P1-d3-375*, P2-d2-1033, LB1-1495 Lindberg, Anders P1-d1-389, P1-d3-409, P2-d1-1102, P2-d1-824 Lindi, Virpi P1-d1-236 Lindsay, Robert P1-d2-303 Linglart, Agnès FC12-187, FC12-190, FC20-1485, FC2-128, P3-d3-1346 Lingren, Todd LB2-1502 Linhart, Kirsten FC20-1484 Lionetti, Paolo P2-d3-709 Lipiäinen, Ludmila FC3-136 Lipman, Terri P3-d2-1371 Lippert, Hans P1-d2-319 Lira, Régia FC13-193 Lisa, Lidka FC8-166 Lista, Mary P1-d1-346 Liu, Hao-Chuan P1-d1-501 Liu, Jiayan P2-d1-624 Liu, Wei-Shih P1-d1-522 Llano Linares, Juan P3-d2-1420, P3-d2-1421 Llano, Juan P3-d2-1245, P3-d2-1248 Lljuhhina, Jelena P2-d1-957 Lo Presti, Donatella P2-d3-874 Lo Russo, Monica P2-d3-709 Lo, Fu-Sung P1-d1-501 Lo, Ming-Yu P1-d1-501 Lo, Sin Ting P2-d2-762
* Presenting author
276
9th Joint Meeting of Paediatric Endocrinology 2013
Loche, Sandro P1-d1-476, P1-d2-490 Löffler, Dennis P2-d1-747 Logan, Chad P1-d1-528 Logan, Karen P1-d1-245*, P2-d1-621 Loghin, Andra Iulia P3-d2-1375, P3-d3-1384* Lohse, Judith P2-d3-712 Loidi, Lourdes P2-d1-951 Loke, Kah-Yin P2-d3-941 Lombardo, Fortunato P2-d2-1030*, P2-d2-834, P2-d2-870* Lonero, Antonella P2-d1-1016 Long, Eric P1-d2-324 Longhi, Silvia FC2-131*, P1-d1-285, P1-d2-297* Longui, Carlos FC4-138 Looijenga, Leendert FC5-146 Lopes, Lurdes P2-d2-681, P2-d2-754 López de Heredia, Miguel P1-d1-422, P1-d1-503* López Siguero, Juan Pedro P1-d1-417, P1-d1-477, P3-d1-1286* López, Patricia LB3-1517, P1-d1-419, P1-d3-445, P1-d1-567, P1-d2-543 López, Raúl P2-d1-780 Lopez-Barea, Juan L. P1-d1-491 López-Bermejo, Abel WG4-99, FC14-198, FC14-199, FC15-209, FC17-216, P1-d2-361, P1-d1-388, P1-d1-535, P1-d2-321, P1-d3-339, P1-d3-376, P2-d2-636, WG4-104 Lorente Blazquez, Isabel P2-d2-799, P3-d3-1353 Lorenz, Norbert P2-d2-1028 Lorenz-Depiereux, Bettina P1-d2-305 Lorenzini, Françoise P1-d2-329 Lorini, Renata P1-d2-301, P2-d1-919, P2-d2-897, P2-d3-874, P2-d3-946, P3-d2-1339, P3-d2-1341 Lorrain, Marie-Pierre P2-d1-691 Losa, Laura P1-d2-547, P2-d1-996*, P2-d3-716 Lösch-Binder, Martina P1-d1-448 Losekoot, Monique FC3-132, FC9-172, P1-d2-326, P1-d2-478* Loureiro, Carolina P1-d2-325, P2-d1-920* Lovato, Luigi P1-d1-565 Lu, James LB1-1493
Lu, Junying P1-d2-518 Lu, Wei P2-d2-903 Lu, Yung-Hsiu P1-d1-501 Lu, Zhong P3-d2-1376 Lubis, Bugis P3-d1-1471 Lubis, Siska P3-d1-1471* Lucaccioni, Laura P2-d1-749 Lucas-Herald, Angela P2-d1-1105*, P2-d2-1156*, P3-d1-1290 Luce, Vincenza P2-d2-1192, P3-d2-1211 Lucena, Roberto P2-d2-794 Lucherini, Marco P3-d3-1317, P3-d3-1386 Luciano, Bernardi P1-d3-331 Luczay, Andrea P1-d1-476 Ludecke, Dieter LB4-1524 Lugani, Francesca P3-d2-1339 Lukushkina, Elena P2-d1-1038 Lulsegged, Abbi P2-d1-1171 Lund, Carina P1-d2-551 Lundberg, Elena P2-d2-835* Lundgren, Maria P1-d2-357 Lundin, Karolina P1-d2-551 Lünstedt, Ralf P2-d2-1113 Luo, Bonin P2-d1-1013 Luo, Feihong LB2-1505, P2-d2-903*, P3-d2-1376 Luo, Shun P3-d2-1337 Luo, Xiangyang P2-d3-977 Luo, Xiao-Ping P1-d1-425 Luo, Xiaoping P1-d1-526 Luo, Xiao-Ping P3-d1-1230 Lupi, Fiorenzo P3-d1-1368 Lusa, Lara P2-d3-773 Luzuriaga Tomás, Maria P2-d1-785* Lyczkowska, Anna P1-d2-599 M
Ma, Hua-Mei P1-d1-288*, P1-d2-396, P1-d3-559, P2-d2-1111*, P2-d2-642 Ma, Yaping P1-d2-518 Maasalu, Katre P2-d3-710 Mabikwa, Vincent P2-d1-950 Mabulac, Marichu P2-d2-933* Macarulla Arenaza, M.T. P2-d2-799 MacDonald, Fiona P2-d1-1037 Macedo, Delanie FC4-138* Macedoni, Maddalena P1-d1-540, P3-d2-1344 Maceiras, Mercedes FC8-163, P1-d3-267, P1-d3-562, P1-d3-610 Machado Rosa, Rafael P2-d2-962, P3-d2-1380 Machado, Aline P1-d3-270 Machan, Jason LB1-1491 Machida, Jiro P3-d1-1226
Machnica, Lukasz P2-d3-1128 Maciel-Guerra, Andréa P1-d2-577, P2-d2-1114*, P3-d1-1456 Mackay, Deborah FC14-200, P2-d2-862 MacKenzie, Joan P2-d2-1193 MacMillan, Margaret P3-d1-1285 Macrae, Mhairi P1-d2-585 MacRae, Vicky FC7-156 Madè, Alexandra P1-d2-547, P3-d1-1363 Madeira, Isabel P1-d2-322 Madeo, Simona P1-d1-350, P2-d1-737, P2-d1-882 Madjinca, Sabrina FC9-168 Madsen, Mette P3-d2-1373* Maeng, Se Hyun P2-d1-1003, P2-d2-1093 Maes, Marc P2-d3-708, S1-11, S1-14, S1-15 Mäestu, Jarek P2-d3-710 Maffei, Pietro P1-d1-422 Maffeis, Claudio P2-d1-1085 Maftei, Oana P1-d1-276, P2-d2-679 Magdelaine, Corine P2-d3-711 Maggio, Maria C. P3-d2-1246, P3-d2-1473*, P3-d2-1475* Maghnie, Mohamad MTE7:1, MTE7:2, P1-d1-507, P1-d2-490, P2-d1-1014, P2-d1-734, P2-d2-695, P2-d3-718, S19, SAT1 Maglio, Silvana P2-d1-1173 Magnani, Alessandra P1-d1-272 Magrassi, Silvia P2-d3-716 Mahadevan, Shriraam P1-d1-390 Maher, Eamonn P2-d1-1037 Maherzi, Ahmed P3-d2-1442 Mahler, Birgitte P1-d3-564 Mahmoud, Diaai P3-d3-1358 Mahmud, Farid P2-d3-1164 Mai, Knut P1-d2-328 Maines, Evelina P1-d2-549, P1-d3-561*, P3-d2-1301, P3-d2-1338 Mairon, Nicole P2-d1-819 Maisonobe, Pascal P2-d2-825 Maiz Hadj Ahmed, Aicha P3-d1-1426* Majewski, Jacek P1-d2-247 Majzoub, Joseph FC20-1484* Makarava, Yulia P3-d2-1476 Makay, Balahan P2-d2-706 Makaya, Tafadzwa P2-d1-661, P3-d1-1264 Makhanda, Jerry P2-d1-950
Makhonin, Vladimir P3-d1-1254 Makishima, Makoto P1-d2-295 Mäkitie, Outi LB1-1493*, MTE11:1, MTE11:2, P2-d1-997, WG1-82*, YB1 Makni, Saloua P2-d1-1109 Maksimov, Georgy P2-d1-813, P2-d1-814 Malacarne, Michela P2-d3-1067 Malaquias, Alexsandra P1-d2-482* Malczewska, Anna P3-d1-1252, P3-d1-1253*, P3-d1-1257 Malecka-Tendera, Ewa P1-d3-406, P1-d3-616, P2-d3-1128, P2-d3-837, P3-d1-1270 Malekpour-Dehkordi, Zahra P2-d2-1150 Malievsky, Oleg P2-d1-1005*, P2-d1-1107, P2-d2-633, P3-d1-1254*, P3-d1-1400, P3-d2-1284 Malikova, Jana FC10-179 Mallone, Roberto S14, S14-53* Mallucci, Conor P3-d2-1414 Malmusi, Giovanni P2-d1-749 Malo, Joseph P1-d2-428 Maltoni, Giulio P1-d2-402, P1-d2-431, P2-d2-896*, P2-d3-911* Malunowicz, Ewa P3-d2-1208 Malvezzi, Anna Chiara P1-d1-569 Mameli, Chiara P2-d3-1067 Mamkin, Andrey P2-d1-673* Mammarella, Sandra P1-d2-366 Mancini, M. Grazia P1-d2-301 Manco, Melania P2-d1-999 Mangano, Eleonora P1-d2-434 Manger, Thomas P1-d2-319 Mangiantini, Francesca P2-d3-709* Manna, Thais P2-d2-697, P3-d1-1250 Manoni, Cristina P2-d3-846 Mansilla, Marie P2-d1-1178 Mansor, Mohamed FC19-231, P2-d2-1193 Mansour, Chourouk P2-d3-1127*, P3-d1-1199 Mansourian, Marjan P2-d1-1179 Mantan, Mukta P3-d1-1259 Mäntyselkä, Aino P1-d1-236* Marabotto, Francesca P3-d1-1363* Marazan, Monica P1-d1-452 Marazza, Matteo P1-d1-420
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
277
Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Marc, Janja P2-d1-687 Marçal, Lara P3-d1-1321* Marcato, Daniele LB4-1520 Marchal, Jan Pieter P1-d3-613*, P2-d1-1142* Marchi, Marta P2-d3-946, P3-d2-1339, P3-d2-1341 Marchwinski, Lukasz P3-d1-1252, P3-d1-1253 Marco Antonio, David FC13-192 Marcos, Ascensión P1-d2-323 Marcos, Maria Victoria P1-d1-535 Marcovecchio, M. Loredana FC5-149, LB2-1503, P1-d1-343, P1-d2-366*, P1-d3-374, P2-d1-746*, YB3 Marcus, Claude FC15-206, FC20-1484, P1-d1-353 Marelli, Susan P2-d1-692 Marginean, Oana P3-d2-1271 Marginean, Otilia P1-d1-452, P2-d3-808*, P3-d1-1228, P3-d2-1236, P3-d2-1277 Maria, Veronica Elena P2-d1-923 Mariana, Costanzo FC8-163 Marini, Joan P1-d1-282 Marini, Romana P1-d2-252, P1-d2-255, P2-d2-1031* Marinkovic, Maja P2-d2-704* Marino, Roxana FC8-163, P1-d3-267, P2-d2-632* Marion, Vincent S3, S3-22* Maris, Ioana P2-d3-909 Märkl, Bruno P1-d1-570 Markou, Athina P1-d3-260 Markovic, Slavica LB3-1512* Marks, Natalia P3-d1-1263 Marmiroli, Nelson FC5-145 Marolda, Agostina P1-d3-369 Maroo, Sanjay P2-d2-1156 Marquard, Jan P2-d2-934 Marques Pereira, Rosana FC13-194* Marques, Filipa P2-d2-754 Marquez, Joice P3-d1-1468 Marrec, Celine P2-d1-1178* Marsciani, Alberto P2-d1-737 Marshall, Kristina P2-d1-783* Marshall, Sharon LB1-1491 Marsigli, Angelica P2-d3-648, P2-d3-649, P3-d1-1406 Marsolo, Keith P1-d1-351 Marta, Diaz FC6-151 Mårtensson, Anton FC3-133 Marti, Amelia P1-d2-323 Martin, Ayelen FC13-197* Martin, David WG3-94* Martin, Delphine P2-d1-1048
Martin, Dieter P1-d1-390 Martin, James P1-d2-433 Martin, Regina P2-d2-696 Martín, Silvia P2-d1-622, P2-d3-979, P2-d3-1163 Martin, Xavier P2-d3-768 Martinelli Jr, Carlos FC13-192, FC13-193, FC20-1486, P3-d1-1367, P3-d2-1377 Martinerie, Laetitia P1-d2-580* Martinet, Danielle P2-d1-995 Martínez Moya, Gabriela P2-d2-966 Martínez, Alicia P1-d1-380*, P1-d3-413, P2-d1-1051, P2-d3-982 Martínez, Daniela LB3-1517, P1-d1-419*, P1-d3-445, P1-d1-567 Martínez, José P1-d2-323 Martinez, Rosa P2-d3-904 Martínez-Aedo, Maria P3-d1-1286, P3-d2-1300 Martínez-Aguayo, Alejandro P1-d1-235*, P1-d2-325, P1-d3-377*, P2-d1-920 Martinez-Barbera, Juan Pedro FC10-174, FC10-175, P1-d1-507 Martínez-Moya, Gabriela P2-d2-678 Martín-Frías, María P2-d1-851*, P2-d1-853, P2-d2-869, P2-d1-886*, P2-d2-930 Martini, Alberto P1-d1-272 Martini, Anna Lisa P1-d2-402, P2-d1-1139, P2-d1-619, P2-d3-810, P2-d3-911 Martinón, Nazareth P1-d1-354, P3-d2-1274 Martin-Pena, Mercè FC19-230 Martins, Raquel P3-d2-1415 Martins, Tânia P3-d2-1415* Martorana, Davide P1-d2-356 Martos, Rosario P2-d1-745 Martos-Moreno, Gabriel FC17-218, FC17-219, P1-d1-566*, P1-d2-360, PL4-5 Martul, Pedro P1-d1-591 Marui, Suemi P2-d2-1186 Maruka, Katia P2-d3-716 Marumudi, Eunice P3-d1-1196*, P3-d1-1458 Marzelli, Matthew P1-d3-442 Marzuillo, Pierluigi P2-d1-1106* Masarwi, Majdi P1-d1-286 Maschan, Alexey P1-d1-279
* Presenting author
278
9th Joint Meeting of Paediatric Endocrinology 2013
Masciopinto, Maristella P1-d1-450, P2-d2-899, P3-d2-1340, P3-d2-1433 Maslova, Nataly P3-d2-1284* Mason, Avril P2-d1-957*, P2-d3-983*, P3-d1-1290 Mason, Rebecca S7, S7-34* Massa, Guy P1-d2-401, P2-d1-779*, P3-d3-1310* Massa, Ornella P1-d1-473 Mastellaro, Maria FC13-192, FC13-193, FC20-1486 Mastriani, Silvana P2-d1-668 Masue, Michiya P2-d1-998 Matallana, Audrey P2-d2-680*, P3-d1-1427, P3-d2-1247 Matarazzo, Patrizia P1-d3-415, P2-d2-834 Matei, Cristina P3-d3-1387* Mathai, Sarah P1-d1-524, P1-d1-525, P2-d2-1158 Mathó, Cecilia FC13-197 Matsigou, Eirini FC15-208 Matsubara, Keiko P1-d1-523, P1-d1-527, P2-d1-626* Matsubara, Yohei P1-d3-261 Matsui, Akira P2-d1-818 Matsumoto, Naomichi P1-d2-489 Matsunaga, Regina P1-d3-270 Matsuo, Kensuke P1-d3-342 Matsushima, Satoshi P2-d1-1172 Matsuura, Hiroki P1-d1-243 Matsuura, Nobuo P2-d2-1148 Matteos, Fernanda P2-d1-1173 Matthews, David P1-d1-245 Mattoussi, Nadia P2-d1-1109, P3-d2-1442 Matucci-Cerinic, Marco P2-d1-683 Matusik, Pawel P3-d1-1270 Mauras, Nelly P1-d3-442, P1-d3-554 Mauri, Silvia P1-d1-540*, P2-d3-1067 Maurice-Stam, Heleen P2-d1-1142 May, Melanie P2-d1-1143 Mayatepek, Ertan P2-d2-934, P2-d2-965, P3-d1-1218 Mayayo, Esteban P2-d1-989 Mayenburg, Adine P1-d1-276, P2-d2-679 Mayerhofer, Artur P1-d1-536 Mayne, Philip P3-d2-1242 Mayol, Lluís P1-d2-321 Mazaika, Paul P1-d3-442 Mazej, Darja P2-d3-772 Mazen, Inas FC8-166 Mazerkina, Nadezhda P2-d2-1027*
Mazicioglu, Mumtaz P1-d1-500, P2-d1-1006 Mazor-Aronovitch, Kineret FC3-137, P2-d3-807 Mazur, Bogdan P3-d1-1270 Mazur, Tom WG6-116* Mazzanti, Laura P1-d1-565*, P1-d1-571, P1-d2-402, P2-d1-1139, P2-d1-1145, P2-d1-694, P2-d2-834, P2-d3-649, P2-d3-810, P2-d3-976, P3-d1-1406, P3-d3-1391 Mazzarella, Giuseppe P1-d1-346 Mc Carthy, Anthony P2-d1-739 Mc Kenna, Malachi P3-d2-1242 McCabe, Mark FC10-174, FC10-175, P1-d1-507, P2-d1-1010 Mccafferty, Susan P1-d1-422 McCarthy, Marian LB3-1516 McComb, Christie P1-d2-303 McCrea, Kathryn P2-d2-677 McElreavey, Ken S9, S9-39*, WG6-113* McGowan, Ruth P2-d1-1105 McGowan, Sheena P2-d3-984, P2-d2-1193* McGown, Ivan P2-d1-857 McGrogan, Paraic P2-d3-983, P3-d1-1364 McGuire, Troy P2-d1-925 McIvor, Jane P2-d1-783 McKay, Gerard P1-d2-303 McLaughlin, Kirsty P2-d2-1193 McLay, James S. P2-d1-752 McMahon, Ann P2-d1-1004, P2-d1-1004* McMillan, Martin P1-d2-585, P2-d3-983 McNeil, Ethel P2-d2-827 McNeilly, Jane P2-d1-690*, P2-d3-983, P3-d1-1290 McTavish, Lindsay P2-d3-873 Meazza, Cristina P3-d1-1288* Medaglini, Stefania FC2-129 Medrado, Caroline P3-d1-1411 Mehta, Manju P3-d1-1458 Meimaridou, Eirini FC18-224 Meissner, Thomas P1-d1-421, P1-d2-462, P2-d2-934, P2-d2-965, P3-d1-1218 Mejia de Beldjenna, Liliana P2-d2-680, P3-d1-1427*, P3-d2-1245, P3-d2-1247*, P3-d2-1248*, P3-d2-1421 Melamed, Philippa FC5-144 Melikian, Maria P3-d1-1330 Meloni, Antonella P1-d1-272* Mélot, Christian P1-d3-437, P3-d1-1327
Memioglu, Nihal P2-d1-1050 Menabò, Soara P2-d1-1145, P2-d1-619*, P2-d3-649 Menargues, Angel P1-d2-400 Mendez, Mariana P2-d2-635 Mendez, Virginia P3-d1-1462 Mendonca, Berenice PL6-7*, FC4-138, P1-d3-270, P1-d1-469, P1-d1-506, P1-d2-482, P1-d2-583, P2-d1-952, P2-d1-954 Mendoza Rojas, Victor P3-d2-1417* Mendoza, Carolina P2-d2-898* Menezes-Filho, Hamilton P2-d2-697, P2-d2-1186, P3-d1-1468 Meng, Xi P1-d2-456, P2-d1-856*, P2-d2-937, P2-d3-912* Meng, Zhe P2-d3-977* Mengen, Eda P1-d1-241, P2-d2-701*, P3-d1-1229 Menghi, Ilaria P2-d2-761 Meraner, Dagmar P3-d1-1323 Mercader, Josep M. FC17-216 Merchant, Thomas P1-d2-515 Mercolini, Federico P1-d2-297 Meredith, Suzanne P1-d1-242 Mericq, Verónica P1-d1-492, P1-d1-495, P1-d3-375, P2-d3-875 Meriem, Bensalah P3-d2-1241* Merino, Paulina LB1-1495, P1-d1-419, P1-d2-543, P1-d3-445* Mermejo, Livia FC20-1486, P1-d3-270 Meroni, Silvia P2-d3-647, P2-d3-650, P2-d1-1101 Meschi, Franco P2-d1-668, P2-d2-675, P2-d2-676 Meskine, Djamila P3-d1-1409, P3-d2-1304 Messazos, Betty P3-d3-1356* Messina, Giovanni P2-d1-727 Messina, Maria Francesca P2-d2-834 Mestraitua Aurrekoetexa, Gaizka P3-d3-1353 Metherell, Louise FC18-222, FC18-224, FC18-225, FC4-141, FC7-160, NP2-70*, P1-d1-241 Metz, Chantal FC6-155 Metzger, Daniel FC20-1487, P1-d2-251, P1-d2-486 Meusers, Michael P2-d2-863 Meyer-Bahlburg, Heino P2-d2-1115* Meyerovitch, Joseph FC4-140 Mibu, Kazuhiro P2-d3-811
Michael, Zitzmann P1-d2-550 Michalacos, Stefanos P1-d3-615, P3-d1-1431, P3-d2-1280, P3-d2-1438 Michalczyk, Aneta P2-d1-669 Michelatto, Débora P1-d2-253* Michl, Joseph P1-d1-386, P2-d1-620 Michon, Jean P2-d1-691, P2-d1-738 Micle, Ioana P1-d1-452, P3-d2-1236 Mii, Sayaka P3-d2-1237 Mikhailova, Svetlana P1-d1-279 Mikhno, Hanna P3-d2-1275* Mikolajczak, Agata P2-d1-823 Mikos, Hanna P2-d1-672 Mikos, Marcin P2-d1-672 Milagro, Fermín P1-d2-323 Milani, Soraya P3-d1-1367*, P3-d2-1377* Milenkovic, Tatjana P2-d3-654 Miles, Harriet FC8-166, P1-d2-584 Miletta, Maria FC16-210*, P1-d2-485 Militaru, Andreea P2-d3-808 Miller, Bradley P1-d2-395, P2-d2-964, P3-d1-1285 Miller, Karen P1-d2-306 Miller, Lauren P2-d3-1070 Miller, Scott P3-d1-1404 Milovanovic, Ivana P1-d1-502* Mimoun, Emmanuelle P2-d3-711 Minard, Veronique P2-d1-691 Minari, Roberta P2-d1-1040, P2-d1-956* Mineo, Mariagrazia P3-d2-1473, P3-d2-1475 Minoura, Takanori P3-d3-1316 Minuto, Nicola P2-d2-897, P3-d2-1339, P3-d2-1341* Minutti, Carla P2-d2-1184, P2-d3-905*, P3-d1-1322* Mirabelli, Silvestro P1-d3-271, P2-d3-649 Miraglia Del Giudice, Emanuele P1-d1-312, P2-d1-628, P2-d1-960, P2-d2-1054 Miranda, América P2-d1-780 Miranda, Gorka P1-d1-591 Miras, Mirta P2-d1-622, P2-d3-1163, P2-d3-979 Mishra, T.K. P2-d1-854, P2-d3-978 Misra, Madhusmita P1-d2-306*, P2-d1-1012 Mitanchez, Delphine P2-d1-1000 Mitchell, Rod FC8-162*
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
279
Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Mitev, Vanio P2-d2-1023 Mitkova, Atanaska P2-d2-1023 Mito, Naomi P1-d2-521 Mitrovic, Katarina P2-d3-654* Mitsui, Toshikatsu FC12-191* Mitui, Toshikata P1-d1-284 Miura, Kohji P1-d2-489, P1-d2-513 Miwa, Kumiko P1-d1-381 Miwa, Masayuki FC9-171, P1-d1-240 Miyahara, Naoki P2-d2-637 Miyai, Kentaro P1-d3-261, P2-d3-1125, P3-d2-1239* Miyako, Kenichi P2-d1-987* Miyashita, Kengo P2-d1-890, P2-d2-1188 Miyata, Ichiro P2-d1-1172, P3-d3-1316 Miyazaki, Toru PL5-6*, WG2-88* Miyoshi, Tatsuya P1-d1-532*, P1-d1-593 Miyoshi, Yoko P1-d1-523, P1-d2-489* Mizuno, Haruo P3-d1-1422* Mizuno, Kentaro P1-d2-578 Mizuno, Seiji P1-d1-523 Mizuno, Yusuke P2-d1-890, P2-d2-1188 Mizutani, Shuki P1-d3-261, P1-d3-268, P2-d3-1125 Mlynarski, Wojciech P1-d1-422 Moayeri, Hashmat P2-d2-789* Mobilia, Sara P2-d1-1039 Mochizuki, Hiroshi P1-d1-243 Mochizuki, Takahiro P2-d1-725* Moctezuma, Luis P2-d3-804 Modan-Moses, Dalit FC9-173, P2-d1-730*, P2-d3-807 Modestini, Elisabetta P3-d1-1265 Modi, Kirtikumar P3-d1-1459 Mogoi, Mirela P2-d3-848, P3-d1-1266* Mohamed, Sarar P2-d2-935*, P2-d3-713, P3-d1-1231* Mohammad Amoli, Mahsa P3-d2-1336 Mohammadi, Moosa P2-d1-1082 Mohd Ali, Johari P2-d3-1165 Mohd Nor, Noor Shafina LB3-1518* Mohn, Angelika FC5-149, LB2-1503, P1-d1-343, P1-d2-366, P1-d3-374, P2-d1-746, P3-d1-1295 Mohnike, Klaus P2-d2-861
Mohnike, Wolfgang P1-d2-463, P2-d2-861 Moia, Stefania P1-d1-348, P1-d3-379, P3-d1-1204* Moleres, Adriana P1-d2-323 Molfetta, Luigi P3-d2-1341 Molina, Juanita P3-d3-1445 Molina, María Antonia FC19-232 Molina-Hazan, Vered P2-d1-623 Molinas, Catherine P1-d2-329 Møller, Bjarne P1-d1-281 Mollet-Boudjemline, Alix P2-d2-1088 Molloy, Eleanor P3-d2-1242 Molz, Esther FC6-152, P2-d2-863 Momblan, Jerónimo P2-d3-775, P3-d1-1408 Mongan, Nigel P1-d2-584 Moniuszko, Marcin P1-d1-596 Moniz, Catarina P3-d1-1428* Monlleó, Isabella L. P1-d2-577 Monsonego-Ornan, Efrat P1-d1-286 Monstrey, Stan FC8-167 Montanini, Luisa FC5-145 Monteagudo, Ana Rivero P3-d2-1276 Monteiro, Alexandra P1-d2-322 Montenegro, Luciana FC4-138, FC4-142* Montero, Francisco P2-d2-680 Monti, Elena P1-d3-561, P3-d2-1301 Montinaro, Raffaele P2-d1-956 Montravers, Françoise NP1-69* Monzani, Alice P1-d3-369 Moore, Wayne FC16-214 Moosa, Fatima P3-d2-1207 Mora, Stefano P1-d2-434, P2-d1-1137, P2-d1-692, P2-d3-650, P2-d3-716 Morabito, Lorena P1-d1-346 Moraes, Leonardo LB2-1496, LB4-1520 Moraes, Maria Elisabete P2-d1-954 Morales, Rosario P2-d1-745 Morana, Giovanni NP1-68* Morandi, Grazia P1-d2-549*, P1-d3-561, P3-d2-1301 Morano, Paula P3-d1-1470 Morehart, Paula P1-d2-394 Moreira, Ayrton FC20-1486, P3-d1-1367 Morel, Yves FC1-124, P1-d2-254, P1-d2-580, P2-d2-1119
* Presenting author
280
9th Joint Meeting of Paediatric Endocrinology 2013
Moreno Villamil, Esperanza P2-d3-804* Moreno, José Carlos FC19-228 Moreno, José FC19-232 Moreno, Rosita LB1-1495 Moreno-Moral, Virginia P3-d1-1267 Moreno-Navarrete, Jose FC14-198 Moreno-Villamil, Esperanza P1-d1-310* Morgan, Kate P1-d2-426, P2-d1-859, P2-d3-906, P2-d3-910 Morikawa, Syuntarou FC10-176*, FC12-186 Morin, Analía P2-d3-1168 Morio, Tomohiro P2-d1-674 Moritani, Maki P1-d2-460 Moriuchi, Hiroyuki P2-d3-1167 Morla, Elbi P3-d3-1447* Morozov, Dmitry P2-d2-1118 Morrissey, M. Simon P2-d1-1104 Morsellino, Vera P2-d1-734* Mortier, Geert P3-d3-1310 Mosca, Fabio P1-d1-598, P1-d2-606 Moschcovich, Laura FC16-215* Moser, Christine P3-d1-1323 Moss, Anja P1-d2-320, P1-d1-528, P3-d1-1269 Moss, Celia FC9-170 Moszczynska, Elzbieta P2-d3-645*, P3-d1-1452, P3-d2-1379 Mota, Teresa P3-d1-1222 Motoki, Takanori P3-d3-1316* Motor, Sedat P2-d1-693 Motoyama, Kahoko P2-d3-908 Motta, Claudia P1-d1-473 Motte, Emmanuelle FC12-190*, FC20-1485* Mouly, Céline P2-d3-711 Mourelatou, Rosa FC1-121* Mousavy, Neda FC10-175 Mouttalib, Sofia P2-d1-1049 Mozzillo, Enza P1-d1-346, P2-d1-1039 Mrozinski, Bartlomiej P2-d2-970 Mueller, Jonathan FC9-172 Mueller, Thomas FC3-132 Mueller, Wolfgang P3-d1-1218 Muenzberg, Michael P3-d3-1314 Mughal, M. P1-d2-294 Mühlig, Yvonne P3-d1-1269 Mukai, Tokuo P2-d1-1144* Müller, Carsten P2-d2-861 Müller, Ferenc FC9-169
Müller, Hermann P1-d1-508*, P2-d1-1015* Mullis, Primus S1-15, FC16-210, P1-d2-485, P1-d3-265, S1-11, S1-14 Municchi, Giovanna P2-d1-956, P3-d3-1317, P3-d3-1386 Muniz, Bruna P1-d2-322 Muñoz, Liliana P2-d1-622, P2-d3-1163, P2-d3-979 Muñoz-Calvo, María Teresa P1-d2-360 Muñoz-Serrano, Ana P3-d2-1477* Murakami, Nobuyuki P2-d1-626 Murata, Mitsuru FC9-171, P1-d1-240 Murko, Simona P2-d3-772 Muroya, Koji FC19-229, P1-d1-243, P1-d1-504, P1-d1-523, P1-d2-578, P2-d1-987, P3-d1-1226 Murphy, Dianne P2-d1-1004 Murphy, Nuala LB3-1516, P2-d3-909, P3-d2-1242 Murray, Philip P2-d2-631, P2-d2-634 Murri, Virginia P1-d2-549, P1-d3-561 Mushimoto, Yuichi P2-d1-987 Mushtaq, Talat P2-d1-1175 Musio, Alessandra P2-d1-1021* Musolino, Gianluca P1-d1-420 Mussa, Alessandro P1-d2-258, P1-d2-600* Muto, Takashi P1-d1-494 Muzsnai, Ágota P2-d2-1157 Muzumdar, Radhika P1-d3-611 Myers, Rebecca S19 N
Naceur, Malika P2-d2-1062, P3-d1-1221 Nadeem, Montasser P3-d1-1234* Nagaeva, Elena P2-d1-814, P2-d2-832*, P3-d1-1330 Nagai, Toshiro P1-d1-523, P2-d1-626 Nagaki, Shigeru P1-d1-381* Nagasaki, Keisuke FC12-191, FC19-229, P1-d1-283, P1-d1-504, P2-d2-1183*, P3-d1-1293 Nagata, Eiko P1-d2-582 Naiki, Yasuhiro P2-d1-890, P2-d2-1052, P2-d2-1188* Nakajima, Hisakazu P1-d3-342, P3-d1-1292, P3-d1-1466 Nakajima, Keisuke P1-d3-261
Nakamura, Akie FC10-176, FC12-186* Nakano, Yukiko P2-d2-833 Nakashima, Shinichi P1-d2-582* Nakatomi, Akiko P2-d3-1167 Näke, Andrea P2-d2-863 Nam, Hyo-Kyoung P1-d3-556, P2-d1-892 Namba, Noriyuki P1-d1-289, P1-d2-489, P1-d2-513, P2-d1-1172, P2-d3-1167 Nanjundappa, Suma P2-d1-1175* Napoli, Flavia P2-d2-695 Nardelli, Jeannette PL4-4 Narumi, Satoshi FC12-191, FC19-229, P1-d1-243, P1-d1-284, P2-d2-1148, P2-d2-1183, S4, S4-24* Naruse, Yuki P3-d2-1237 Natale, Clelia P1-d1-346 Natale, Maria Pia P2-d2-899, P3-d2-1340 Nathwani, Nisha FC18-222 Naud-Saudreau, Catherine P1-d1-511 Naugolny, Larisa FC3-137 Nava, Michela P2-d1-668 Navarro Moreno, Constanza P2-d3-717 Navarro Olivos, Efraín P2-d1-778 Navarro, Constanza P3-d2-1297, P3-d2-1299 Navarro, Victor FC4-138 Naveau, Elise P1-d2-579 Naves, Patricia P3-d2-1441 Nazim, Joanna P2-d1-917 Nchingane, Seeletso P2-d1-950 Neder, Luciano FC13-192, FC13-193 Neef, Madlen P2-d3-1066, P3-d1-1269 Neely, E. Kirk P1-d3-557 Negre, Veronique P3-d2-1273* Negrete, Alejandro P2-d2-763 Neild, Peter P1-d2-428 Nelson, Anita LB1-1491 Neocleous, Vassos P2-d1-1146, P2-d1-655 Nesi França, Suzana FC13-194 Nesibe, Akyurek P3-d1-1460 Ness, Kirsten P1-d2-515 Nessa, Azizun FC11-183*, P2-d1-850, P3-d3-1349 Netchine, Irene FC5-147, LB3-1509, P1-d1-387, S6-30* Netrebenko, Olga P2-d1-1038 Netzer, Christian P1-d1-282 Neu, Andreas P1-d1-448
Neumann, David P2-d2-1156, P2-d2-895 Neville, Kristen P1-d2-304*, P2-d1-688*, P3-d3-1356 New, Maria P1-d2-259, P2-d2-1115 Newbury-Ecob, Ruth P1-d1-467 Newfield, Ronald P2-d3-840 Newland, Paul P1-d1-244, P2-d1-630 Ngo Um, Suzanne P2-d2-1091*, WG3-98* Ngoc, Can P2-d1-1080 Nguyen, Dat P2-d2-893, P2-d3-879, P2-d3-939 Nguyen, Ha P1-d3-262 Nguyen, Hoan P2-d2-893, P2-d3-879, P2-d3-939 Nguyen, Khanh P2-d2-893, P2-d3-879, P2-d3-939 Nguyen, Liem P1-d3-262, P2-d3-879 Nguyen, Thanh P1-d1-317 Ngwiri, Thomas P2-d3-1069 Ni, Guichen P2-d3-907 Niar, Sakina P2-d2-1062, P3-d1-1221 Nicholson, Yelena P2-d2-797*, P3-d1-1220, P3-d1-1233* Nicola, Juan P1-d3-611 Nicola, Thais LB2-1496, LB4-1520 Nicolaides, Nicolas FC18-223*, P1-d3-266* Nicoletti, Annalisa P2-d1-1145, P2-d3-649 Nicolino, Marc P1-d1-470*, P1-d1-476 Nicoll, Nicky S19 Niculescu, Elena Carmen P2-d1-923 Niedziela, Marek FC8-166, LB4-1528*, P2-d1-672*, P2-d2-970, P3-d2-1208 Nieminen-Pihala, Vappu LB1-1493 Nierop, Andreas P1-d2-479, P1-d2-548, P1-d3-558 Niez, Philippe P2-d1-961 Nifontova, Larisa P2-d1-1177, P3-d3-1348 Nightingale, Peter P2-d1-1037 Nigri, Alcinda LB4-1523* Nihoul-Fekete, Claire P1-d2-580 Nii, Mitsumaro P2-d1-1144 Nikitina, Irina P3-d1-1261* Niklasson, Aimon FC3-133, P1-d2-479, P1-d2-548, P1-d3-558 Nikolaides, Nicolas P1-d3-269
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
281
Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Nilsson, Ola FC2-127*, P1-d2-484, WG1-80* Nimri, Revital FC6-155 Ning, Qin P1-d1-425, P3-d1-1230 Niranjan, Usha P2-d1-661* Nishi, Mirian P1-d2-482 Nishigaki, Satsuki P2-d1-890, P2-d2-1188 Nishigaki, Toshinori P2-d1-725 Nishimura, Gen P3-d1-1226 Nishimura, Rei P2-d1-815, P2-d2-637 Nishina, Noriko P1-d1-532, P1-d1-572* Nissen, Peter P2-d1-724 Nitta, Akihisa P1-d1-494 Niu, Dau-Ming P1-d1-501* Nivot, Sylvie P1-d1-511 Nivot-Adamiak, Sylvie FC6-155 Njuieyon, Falucar P1-d1-502 Nobile, Renata P2-d2-697, P3-d1-1250 Nobili, Valerio P1-d1-385 Nocon-Bohusz, Julita P2-d1-1077, P2-d3-1065 Noczynska, Anna P1-d3-406, P2-d1-1077, P2-d3-1065 Nodale, Marianna P1-d2-431 Noel, Sekoni FC4-138 Noisa, Parinya P1-d2-551 Noli, Serena P2-d1-1014, P2-d1-734, P2-d2-695, P2-d3-718 Nomura, Risa P2-d3-1125* Noordam, Cees P1-d3-444 Nora Soumeya, Fedala P3-d3-1395 Nordenstrom, Anna FC8-166, WG6-118 Nordon, David LB4-1523 Norek, Berenika P1-d3-616 Norgren, Svante P1-d1-476 Norjavaara, Ensio P1-d3-564, P2-d3-1068* Norris, Jill S14, S14-55* Northam, Elisabeth FC6-154*, P1-d3-440* Nose, Osamu P2-d2-833 Notini, Amanda FC5-146 Nourbakhsh, Mitra P2-d21150* Novakovic, Ivana P2-d1-1078, P3-d2-1439 Novoselova, Mariia P2-d1-891 Novoselova, Tatiana FC18-225, FC20-1484 Numakura, Chikahiko P1-d1-523, P1-d1-572, P2-d3-881 Nummi, Tapio FC3-136
Nunes, Virginia P1-d1-422, P1-d1-503 Núñez Estévez, Manuela P2-d1-922 Nuñez Rodriguez, Javier P2-d1-781* Nuñez, Anai P1-d1-238 Nuri, Nardin P3-d1-1249 Nurmio, Mirja P1-d1-293 Nurmukhametova, Dilara P3-d1-1254, P3-d1-1400 Nurullah, Çelik P2-d3-770, P2-d3-944, P3-d1-1455 Nuthalapati, Nikhil FC20-1484 Nuti, Amith P2-d2-936* O
O’Meara, Celia P1-d2-426 O’Rahilly, Stephen FC20-1484 Obara-Moszynska, Monika P2-d2-970* Obeid, Joyce P1-d1-317 Obermannova, Barbora FC10179, P1-d2-429*, P2-d1-993* Oberwinkler, Heike FC3-132 Ocak, Ilhan P2-d3-938 Öçal, Gönül P2-d2-1116, P2-d3-1123 Ocaranza, Paula P1-d1-382 Occhipinti, Federica P1-d1-540, P2-d3-1067 Ochetti, Mariana P2-d1-622, P2-d3-1163 Ochiai, Yukikatsu P2-d1-1172 O›Connell, Jean P1-d3-338 O›Connell, Michele P1-d3-436 O›Connell, Susan P2-d3-909 Odén, Anders FC3-133 Odongkara, Beatrice P2-d3-1069* Oduwole, Abiola P3-d1-1430, WG3-93* Oflaz, Hüseyin P1-d1-352 Oftedal, Bergithe P1-d1-277 Ogata, Tsutomu FC9-171, P1-d1-523, P1-d1-527, P1-d2-578, P1-d2-582, P2-d1-626, P2-d2-1052, P2-d3-1125 Ogawa, Eishin P2-d3-908 Ogawa, Masamichi P2-d2-833 Ogawa, Yohei P2-d2-1183, P3-d1-1293 Ogawa, Yoshihisa P3-d1-1289 Oghabian, Ali PL4-5 Ogugua, Chinwe P3-d2-1345 Ogunlesi, Tinuade P2-d3-974, P2-d3-981 Oguz, Deniz P2-d3-944 Oh, Phil Soo P3-d2-1482* Oh, Seung Hwan P1-d2-488 Ohishi, Akira P1-d2-582
* Presenting author
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9th Joint Meeting of Paediatric Endocrinology 2013
Ohta, Masanori P1-d1-537* Ohtsu, Shigeyuki P2-d2-1148 Ohyama, Kenji P1-d1-537 Oikonomou, Eleni FC15-208*, P1-d1-314 Ojeda, Sergio P1-d1-531 Okada, Michiyo P2-d3-1125 Okayama, Yoshiki P2-d2-637 Okdemir, Deniz P2-d1-1006, P2-d1-787 Oki, Junichi P2-d1-1144 Okorokov, Pavel P2-d2-790 Oktem, Faruk P1-d2-359, P2-d3-776 Ökten, Aysenur P1-d1-280, P2-d1-1108*, P3-d2-1440*, P3-d3-1449 Okuno, Masako P3-d1-1219 Okuno, Misako P2-d1-674* Olchowy, Cyprian P1-d1-589 Olds, Tim P1-d1-276 Olds, Timothy P2-d2-679 Oleynik, Oksana P2-d1-891 Oliva, Maria P1-d1-450* Oliva, Patricia P2-d3-775, P3-d1-1408 Oliveira, Juliana P3-d2-1415 Oliveira, Laura P2-d2-754 Oliveira, Lygia P2-d2-1186 Oliveira, Maria João LB3-1515 Oliver-Petit, Isabelle FC5-147 Olivieri, Antonella P1-d2-606 Olivieri, Irene P2-d3-718 Olsen, Minna P3-d3-1309 Olsen, Oystein P1-d2-426, P2-d1-859 Olza, Josune P1-d1-354, P3-d2-1274 Omenetti, Alessia P3-d2-1341 Omer, Hala P2-d2-935 Onal, Hasan P1-d3-609*, P2-d1-888, P2-d3-938, P2-d3-948, P3-d1-1332 Onal, Zerrin P1-d3-609, P2-d1-888, P3-d1-1332* Onay, Huseyin P2-d3-1126 Onder, Asan P2-d1-817*, P2-d3-1075, P3-d2-1296, P3-d2-1437 O’Neil, Donna FC9-170 O’Neill, Luke P1-d3-338 Onenli Mungan, Neslihan P2-d2-701, P3-d1-1229 Ong, Ken S11, YB3, FC3-135, P2-d1-953, S11-45*, WG4-100* Onishi, Toshikazu P3-d2-1239 Oniz, Adile P3-d2-1436 Ono, Erina P2-d1-1172*, P3-d3-1316 Ono, Makoto P1-d3-261, P2-d3-1125
Oomen, Petra P1-d1-509 Oommen, Prasad P2-d2-965 Oostdijk, Wilma FC10-177, FC3-132, FC9-172*, P1-d2-326, P1-d2-478, P3-d1-1249* Oosterhuis, J. Wolter P2-d1-733 Opas, Evan FC20-1487 O‘Rahilly, Stephen S13-50* Orbach, Daniel P2-d1-691, P2-d1-738 Orbak, Zerrin P2-d3-985, P3-d3-1352*, P3-d3-1394* Oren, Asaf P2-d1-627, P2-d3-1164* O‘Riordan, Stephen LB3-1516*, P2-d3-909 Orlova, Elizaveta P1-d1-279, P2-d1-658, P2-d2-1027 Ortega, Francisco J. FC17-216 Ortiz, Maria P2-d3-904 Ortolani, Federica P1-d1-450, P2-d2-899*, P2-d3-913, P3-d2-1340*, P3-d2-1433 Oruc, Elif P2-d3-985 Osawa, Makiko P1-d1-381, P3-d2-1244 Ose, Claudia P3-d1-1269 O’Shea, Donal P1-d3-338 O’Shea, Ethna P3-d2-1242 Oshima, Sakiko P2-d1-1172 Osimani, Sara P2-d1-1019, P2-d1-1021 Osiniri, Inés P1-d2-321 Osman, Huda P2-d3-1160 Osman, Mohamed P2-d2-935 Osokina, Darya LB4-1526 Osokina, Irina LB4-1526* Østergaard, John FC1-125 Oswiecimska, Joanna P2-d1-823*, P3-d1-1270* Otero, Patricia P1-d1-239 Oto, Yuji P1-d2-578, P2-d1-626 Otonkoski, Timo P2-d2-934 Otto, Aline P1-d1-506, P2-d1-952 Ouarezki, Yasmine P2-d1-991 Outsu, Shigeyuki P2-d3-811 Oveisi, Sonia P2-d1-685 Ovsyannikova, Alla P3-d1-1325* Owens, Gay P1-d3-557 Oyakawa, Yoko P2-d2-869 Oyarce, Veronica LB1-1495 Oyarzabal, Mirentxu P2-d2-703, P3-d2-1282 Oz, Fahrettin P1-d1-352 Ozawa, Ayako P3-d3-1316 Ozbek, Mehmet P2-d1-686*, P3-d2-1335 Özcabi, Bahar P2-d2-1152, P3-d1-1423*, P2-d2-1147
Özcan, Alper P2-d2-698 Ozdem, Sebahat P2-d1-722, P2-d2-791 Ozdemir, Mustafa P2-d1-1046 Ozen, Samim P2-d1-1087, P2-d3-1126* Ozgen, Ilker P1-d2-359, P2-d2-928*, P2-d3-776* Ozgur, Ozden P2-d2-701, P3-d1-1229 Ozhan, Bayram P2-d1-719* Ozkan, Behzat P1-d2-519, P2-d1-721, P2-d3-714 Ozkan, Ozalkan P2-d1-721 Ozkinay, Ferda P2-d3-1126 Ozon, Alev P2-d2-1022, P2-d3-1064 Ozono, Keiichi P1-d1-289, P1-d2-489, P1-d2-513, P1-d3-404, P2-d1-1172, P2-d3-1167 Ozsen, Ahu P1-d2-300 Ozsu, Elif P1-d2-299, P2-d1-1174 Özsu, Elif P2-d3-806 Ozturk, Oznur P2-d1-787 P
Pacciani, Enzo P2-d1-659 Pacquement, Hélène P2-d1-691, P2-d1-738 Padidela, Raja FC11-181, FC11-182, FC11-184, P1-d2-294, P2-d1-1002 Padoan, Giovanni P1-d2-399 Paetow, Ulrich P1-d1-349 Pagani, Sara P3-d1-1288 Palandi de Mello, Maricilda P1-d2-577 Palau-Collazo, Miladys P1-d2-430* Palchevska, Snezana P3-d1-1258 Palestini, Nicola P1-d2-600 Palhares, Heloisa P2-d1-1044, P2-d1-1180, P3-d2-1441 Palmert, Mark CPE1-73*, P1-d1-522, P1-d2-486, P2-d3-1164 Pampanini, Valentina P1-d1-385* Pan, Hui P2-d3-1071 Panariello, Angela P2-d1-956 Panayiotopoulos, Aristotle P1-d1-386, P2-d1-620, P2-d1-673, P2-d2-1056*, P3-d1-1235*, P3-d1-1263, P3-d2-1206 Pandey, Amit P1-d2-581, P1-d3-265 Pando, Rakefet P1-d1-286 Pandolfi, Assunta LB2-1503
Panei, Pietro P1-d3-415 Panepucci, Rodrigo FC13-192 Panidis, Dimitrios P1-d2-541 Pankratova, Maria P2-d1-813, P2-d1-814* Pannagasayanan, Anitha P1-d1-453 Pantaleo, Marilena P2-d3-846, P2-d3-847, P3-d1-1262 Pantsulaia, Natia P1-d1-386 Papachristou, Fotios P2-d1-994 Papadia, Francesco FC2-130, P1-d1-450, P2-d2-899, P3-d2-1340, P3-d2-1433 Papadopoulou, Alexsandra P2-d2-826 Papadopoulou, Konstantina P2-d2-868, P2-d2-900 Papadopoulou, Nektaria LB3-1513 Papadopoulou-Alataki, Efimia P2-d3-765 Papagianni, Maria P2-d2-1119* Papakonstantinou, Evangelos P3-d1-1328 Papandreou, Dimitrios P2-d2-798 Papanicolaou, Katerina LB2-1499 Papassotiriou, Ioannis LB2-1498, LB3-1513 Papatya Cakir, Esra P2-d3-1072 Papazian, Regina P3-d1-1470 Papendieck, Patricia P2-d1-1173*, P3-d1-1462 Pappa, Aliki P1-d1-314 Paquis, Véronique P1-d1-422 Parajes, Silvia FC9-169*, P1-d3-267*, P2-d2-634 Parbhoo, Kiran P3-d2-1207* Parent, Anne-Simone P1-d2-579* Paret, Gidi P2-d1-623 Paris, Carolyn P2-d1-921, P2-d1-925 Park, Hyesook P2-d1-1086 Park, Mi-Jung P2-d2-759* Park, Sangshin P2-d2-759 Park, So Eun P2-d2-1185* Park, So Hyun P1-d1-475, P1-d2-458*, P1-d2-483, P2-d1-777 Parkinson, Kay P1-d1-422 Parks, John FC10-179 Parlak, Ayse Eda P3-d2-1212 Parlak, Mesut P2-d1-722*, P3-d2-1212* Parpagnoli, Maria P2-d1-956, P3-d1-1262 Parshina, Evgenia P2-d1-813, P2-d1-814 Partyka, Malgorzata P2-d1-986
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
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author index
Floor Plan Exhibition Author Index
author index
Pascanu, Ionela P3-d2-1271 Paschke, Ralf LB4-1528 Paschoini, Marina P2-d2-866 Pashova, Shina P2-d2-1023, P2-d2-1032, P2-d3-644 Pasqualini, Natalia P2-d2-632 Pasqualini, Titania P2-d2-635 Pass, Chloe FC7-156 Passone, Caroline P2-d2-1186*, P2-d2-697, P3-d1-1468* Passoni, Arianna P2-d1-1137 Pateda, Vivekenanda P3-d2-1278 Patel, Chirag P1-d1-511 Patel, Leena FC11-184, P2-d1-1002 Patel, Payal P2-d2-901 Patel, Sangita P2-d2-1151 Patera, Ippolita P2-d1-889 Paterson, Wendy P2-d3-984 Patianna, Viviana Dora P2-d1-749, P2-d1-751 Paul, Corina P2-d3-848*, P3-d1-1266 Paula, Francisco P3-d2-1377 Paumard-Hernández, Beatriz P2-d1-955, P2-d2-969 Pauwels, Christian P2-d2-1091 Pawelec da Silva, Alessandra P2-d2-962 Pawlikowska-Haddal, Anna P3-d3-1446* Pawlus, Aleksander P1-d1-589 Peak, Matthew P1-d1-244, P2-d1-630 Pearce, Simon LB1-1492 Pechatnicova, Natalya P1-d1-279 Pechenina, Galina P3-d1-1400* Pecoraro, Maria P1-d3-271 Pedersen, Anders FC1-125 Pedersen, Birgitte P2-d3-839 Pedicelli, Stefania P1-d1-505*, P1-d2-252 Pedrosa, Denise P1-d2-253 Peet, Aleksandr P1-d1-274* Pehrson, Nils-Gunnar FC3-133 Pei, Zhou LB2-1505* Peker, Selçuk P2-d1-663 Pekkinen, Minna LB1-1493 Pela, Ivana P2-d3-709 Pelliza, Constanza P2-d3-979 Peltek Kendirci, Havva Nur P2-d1-817, P2-d3-1075*, P3-d2-1296, P3-d2-1437* Pena, Alexia P1-d1-276, P1-d1-345, P2-d2-679 Peña, Verónica P1-d1-495 Peñalosa, Lorena P3-d3-1445 Penke, Melanie P2-d1-732 Pennisi, Patricia FC13-197
Pentinat Pelegrin, Thais P1-d1-315 Pepaj, Orsiol P2-d1-1085, P3-d2-1301 Peppa, Melpomeni LB3-1513 Peral de Bruno, Maria P2-d2-763 Perano, Shiree P1-d2-433 Perchard, Reena P2-d1-671* Pereira, Alberto FC10-177, FC3-132 Pereira, Rosana LB4-1522* Pereira, Sabrina FC6-155 Pereyra, Mónica P2-d1-750 Perez de Nanclares, Guiomar P2-d2-703 Perez Garrido, Natalia FC8-163, P1-d3-267, P2-d2-632 Pérez Ontiveros, José Alfredo P2-d1-778 Perez, Miriam P1-d2-361 Perez, Sheila P3-d1-1404 Pérez-Aytés, Antonio P1-d1-477 Perez-Bravo, Francisco P1-d3-445 Pérez-Jurado, Luis FC17-218, FC17-219, P1-d1-566, PL4-5 Perianes-Cachero, Arancha P1-d1-311 Peroni, Elena P2-d1-1137 Perri, Annamaria P1-d1-565, P1-d1-571, P3-d3-1391 Perri, Katia P3-d2-1341 Perrone, Laura P1-d1-312, P1-d3-415, P2-d1-1106, P2-d1-628, P2-d1-684, P2-d1-956, P2-d1-960, P2-d2-1054 Perroni, Lucia P2-d3-1067 Perry, Colin P1-d2-303, P2-d2-827 Persani, Luca FC10-177, P1-d2-547, P2-d1-1040 Persky, Rebecca P2-d1-786 Peruzzi, Sonia P2-d1-1016 Pervanidou, Panagiota LB2-1498, LB2-1499* Pesce, Sabino P1-d1-450, P3-d2-1340 Pession, Andrea P2-d3-648, P2-d3-976, P3-d1-1406 Petchkul, Jaturat P3-d1-1324* Péter, Ferenc P2-d2-1157* Peterkova, Valentina P1-d2-327, P2-d1-1043, P2-d1-1107, P2-d1-813, P2-d1-814, P2-d2-790, P2-d2-832, P3-d1-1330 Peters, Catherine FC18-222, P1-d1-242, P2-d2-631
* Presenting author
284
9th Joint Meeting of Paediatric Endocrinology 2013
Petersen, Henrik P1-d3-444 Petkovic, Vibor FC16-210, P1-d2-485 Petri, Antonella P2-d1-816 Petriczko, Elzbieta P1-d3-406* Petroli, Reginaldo José P1-d2-577 Petrova, Chaika P2-d1-852 Petrovic, Rada LB3-1512, P3-d2-1281* Petruzelkova, Lenka P1-d1-278* Petruzzi, Mariangela P1-d1-540, P2-d3-1067 Petryk, Anna P3-d1-1285* Pettifor, John FC12-189, WG3-94 Pettorini, Benedetta P3-d2-1414 Petzold, Claudia P3-d1-1360 Petzold-Quinque, Stefanie P2-d1-732 Pfäffle, Roland FC10-179, P2-d3-1066, P2-d1-665, P2-d2-829*, P2-d2-967, P3-d1-1360, S1-11, S1-14, S1-15 Phadke, Shubha WG3-97 Phan-Hug, Franziska FC10-178, P2-d1-1082, P2-d1-990, P2-d1-995 Phedonos, Alexia P2-d1-655 Philibert, Pascal P1-d3-263 Philip, Ruby P2-d2-1151* Philippi, Valeska P1-d2-257 Phillip, Moshe FC4-140, FC6-155, P1-d1-286, P1-d2-249, P1-d3-441, P2-d1-858, P3-d1-1251, SAT8 Phulwani, Priya P2-d3-1133 Phylactou, Leonidas P2-d1-1146, P2-d1-655 Piacente, Laura FC2-130 Piaditis, Geoarge P1-d3-260 Pianovski, Mara FC13-194 Piazza, Michele P1-d2-549 Picard, Jean-Yves P2-d2-1119 Piccini, Barbara P2-d3-911 Piccinno, Elvira P1-d1-450, P2-d2-899, P2-d3-913*, P3-d2-1340 Piekarski, Robert P2-d1-669 Pienar, Corina P3-d2-1277 Pienkowski, Catherine P1-d2-580, P2-d1-1049*, WG6-118 Pierce, Lisa P2-d1-1012 Pieri, Giovanni P2-d1-996, P2-d3-716, P3-d1-1363 Pierro, Agostino P1-d2-426, P2-d1-859 Pieterse, D. Jaco P2-d2-639
author index
Pokrovska, Tzveta P1-d2-607* Polak, Michel FC19-230*, FC6-155, P1-d1-511, P1-d1-533, P1-d2-581, P2-d1-1000, P2-d1-1048, P2-d1-691, P2-d1-738, P2-d1-819, P2-d2-1053, P2-d2-1088, P2-d2-1091, P2-d2-825, YB2 Polat, Seher P1-d2-256* Polgreen, Lynda P3-d1-1285 Polychroni, Ioanna P2-d2-826 Pomaski, Janusz P3-d2-1213, P3-d3-1392 Pombo, Manuel P2-d1-951 Ponmani, Caroline P3-d1-1326* Poon, Myra P1-d1-424* Pop, Elena P3-d2-1236 Pop, Raluca P3-d2-1271* Popalisky, Jean P2-d1-925 Popko, Katarzyna P1-d3-617 Popoiu, Calin Marius P3-d11228 Popovic, Jadranka P2-d3-943 Popovic, Milena P2-d1-1182 Porcaro, Federica P2-d2-1030, P2-d2-870 Pörksen, Sven P1-d3-444 Portillo Baquedano, M.P. P2-d2-799 Porto, Ana Carolina P3-d2-1272 Possner, Mike SAT7 Pouvreau, Nathalie FC6-155, P2-d1-1000 Povoroznyuk, Vladyslav P3-d2-1238* Powell, Micheal P1-d2-517 Powell, Mike P1-d1-278 Poyrazoglu, Sükran P1-d1-352, P2-d1-1050, P2-d1-1079, P2-d2-1187*, P2-d2-1191*, P2-d3-652, P2-d3-771 Pozo, Jesús P1-d2-360 Pozzi, Clara P2-d1-1137 Pozzobon, Gabriella P2-d1-1019, P2-d1-1021 Prado, Xochitl P2-d1-780 Prado-Carro, Ana María P2-d3-844 Prakash, Siva P2-d2-1092 Prandstraller, Daniela P1-d1-565 Prasad, Rathi FC18-222*, FC18-224 Prasad, Veeramac P2-d1-1076 Prats-Puig, Anna FC14-198, FC14-199, FC15-209*, FC17-216*, P1-d2-321 Praz, Francoise FC5-147
Predieri, Barbara P1-d1-350, P1-d1-594, P2-d1-737, P2-d1-741, P2-d1-749*, P2-d1-882 Premsler, Thomas FC3-132 Prentice, Philippa FC3-135*, P2-d1-953* Pribilincova, Zuzana FC10-179 Pricci, Flavia P1-d3-415 Price, Susan P2-d1-1037 Prickett, Timothy FC3-132 Prié, Dominique FC2-128 Prieto, Laura P3-d1-1462 Printza, Nikoleta P2-d1-994 Prior, Julia P2-d1-821 Procopiuc, Camelia P2-d2-800 Prodam, Flavia P1-d1-348, P1-d3-369*, P1-d3-379, P2-d1-816, P3-d1-1204 Profka, Eriselda P2-d1-1020 Proietti Pannunzi, Laura P1-d1-473 Proos, Lemm P1-d3-560* Proverbio, Maria Carla P1-d2-434 Pruhova, Stepanka P1-d2-429, P2-d2-895* Pryce, Rebekah P2-d2-936 Prycki, Pawel P2-d2-970 Prymus, Sylwia P3-d1-1370 Puebla-Jiménez, Lilian P1-d1-311 Puerto, Elsa P3-d1-1331* Puget, Stéphanie P2-d1-691, P2-d1-738 Puglianiello, Antonella P1-d3-415 Pugliese-Pires, Patricia P1-d1-472 Pui, Ching-Hon P1-d2-515 Puisac Uriol, Beatriz P3-d2-1302 Puiu, Alexandra Oltea P2-d1-923 Puiu, Ileana P2-d1-923* Puiu, Maria P3-d2-1277 Pupo, Joyce P2-d2-697 Purge, Priit P2-d3-710 Puthi, Vijith P2-d1-783, P2-d2-1189, P3-d1-1429 Putman, Melissa P2-d1-786 Pyda, Malgorzata P2-d2-970 Pyra, Eileen S19 Pyrzak, Beata P1-d3-406, P1-d3-617 Pys-Spychala, Magdalena P2-d1-823 Q
Qi, Zhan P2-d2-1058 Qin, Miao P2-d2-1058* Qiu, Tao FC2-126
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
285
Floor Plan Exhibition Author Index
Pietrangiolillo, Zaira P1-d1-350 Pietrewicz, Edyta P1-d3-406, P3-d2-1213, P3-d3-1392* Pignatti, Elisa P2-d1-1040 Pijnenburg, Marielle P2-d1-656 Piketty, Marie P2-d1-691 Pilia, Sabrina P1-d2-490 Pilotta, Alba P1-d1-594, P1-d2-399 Piloya Were, Tereza P2-d3-1069 Pilpel, Nurit P2-d3-871 Pina, Rosa P2-d2-754 Pinchiari, Lilian P2-d2-697*, P3-d1-1250*, P3-d1-1411 Pinhas-Hamiel, Orit P2-d1623, P2-d1-730, P2-d3-807*, P2-d3-871*, SAT8, YB1 Pinheiro, Daniel P2-d1-954 Pinheiro, Suellen P1-d2-322 Pini, Alessandro P2-d1-692 Pinto, Graziella P2-d1-1178, P2-d1-819, P2-d2-1053, P2-d2-1091 Pinto, Helena P2-d3-1130 Pinto, Heyde Francine FC13-194 Pinzer, Thomas P2-d2-1028 Piona, Claudia Anita P2-d1-1085, P3-d2-1301* Pipman, Viviana P1-d1-538 Piquard Mercier, Catherine P2-d1-751, P3-d3-1346* Piraino, Basilia P2-d2-1025 Pires, Bianca P3-d2-1272 Pirgon, Özgür LB2-1500 Pirgon, Ozgur LB2-1501*, P1-d2-602, P2-d2-1063 Pisi, Giovanna FC5-145 Piskin, Mesut P3-d1-1460 Pistorio, Angela P2-d1-1014, P2-d1-919, P2-d2-897, P3-d2-1341 Pitea, Ana Maria P3-d2-1271 Pitea, Marco P2-d3-650* Pitkin, Janne FC14-201 Pitteloud, Nelly FC10-178, P2-d1-1082, P2-d1-990, P2-d1-995, S15-57* Platerote, Francesca P3-d2-1344 Plotton, Ingrid FC1-124*, P1-d1-470 Pludowska, Pawel P2-d1-667 Plywacz, Dagmara P2-d1-823 Pnueli, Lilach FC5-144 Podkrajšek, Katarina P2-d3-654 Pogadaeva, Nataliya P3-d3-1348 Poggiani, Carlo P3-d1-1368 Pohlenz, Joachim FC19-231, P1-d3-614, P2-d2-1156
author index
Quarta Colosso, Rossella P3-d1-1362 Quattrin, Teresa FC16-214 Quedas, Elisangela FC3-134 Queipo Ortuño, Mª Isabel P1-d1-417 Queipo, Gloria P2-d1-780 Queiroz, Dulciene P3-d1-1321 Quester, Wulf P1-d1-418 Quezado, Rosana P1-d3-270 Quigley, Charmian P1-d1-574*, P1-d3-407*, P2-d1-1011, P2-d2-831, SAT6 Quinart, Sylvain P3-d2-1273 Quince, Christopher P1-d3-337 Quinteiro, Celsa P2-d1-951 Quinteiro, Sofia P3-d2-1300 Quiroz, Luisa P1-d2-296
Floor Plan Exhibition Author Index
R
Rabbone, Ivana P2-d3-874, P2-d3-911 Rabinovitz, Rona P3-d1-1359 Rabska-Pietrzak, Barbara P2-d2-970 Rachdi, Latif FC19-230 Rachmiel, Marianna FC3-137* Radetti, Giorgio FC10-177, FC1-123, FC2-131, P1-d1-285*, P1-d2-297, P1-d2-490, P2-d1-956 Radicev, Milena P2-d1-1078 Radicioni, Antonio P2-d1-956 Rafeey, Mandana P3-d1-1366 Raffeeq, Parakkal P2-d2-677 Ragusa, Letizia FC1-123, P1-d1-594, P1-d2-258 Rahayu, Leni P2-d1-992 Rahayu, Nanik P3-d2-1278* Rahiala, Eero P2-d1-1035 Rahim, Mona P2-d2-1193 Rahman, Nishat P1-d1-468 Rahman, Sofia FC11-183, P1-d3-439*, P2-d1-850, P3-d3-1349 Raile, Klemens FC6-152*, P1-d1-418, P1-d1-421*, P2-d3-1169 Raimann, Adalbert P3-d1-1467* Raissouni, Nouhad P3-d1-1404 Raivio, Taneli FC10-178*, P1-d2-551*, P2-d3-1067, P3-d2-1378 Rajicic, Natasa P2-d3-840 Rakhimova, Gulnara P3-d21283, P3-d3-1355, P3-d3-1444*, WG3-95* Rakover, Yardena LB4-1527* Ramachandrappa, Shwetha FC20-1484
Ramakrishnan, Renuka P2-d1-1138, P2-d1-1141, P2-d2-931 Ramalho, Fernando FC20-1486 Ramalho, Leandra FC13-193, FC20-1486 Ramanathan, Visali FC20-1484 Ramesh, Venkataraman P2-d2-699 Rami-Merhar, Birgit P1-d1-418, P2-d3-872 Ramirez de Carvalho, Julienne Angela FC13-194 Ramírez, Fernando P2-d1-780 Ramirez, Pablo FC8-163, P1-d3-267, P2-d2-632 Ramistella, Vincenzo P2-d2-1030 Ramji, Siddharth P2-d1-854, P2-d3-978 Ramon-Krauel, Marta P1-d1-315*, P2-d3-844 Ramos Fuentes, Feliciano P3-d2-1302 Ramos, Maria P3-d2-1282 Rampi, Gabriela P2-d1-629 Rampling, Dyanne FC11-185 Ramseger, René P2-d1-958, P3-d3-1389 Ranchin, Bruno P1-d1-470 Ranke, Michael P2-d1-824* Rapaport, Robert P3-d3-1313*, P3-d3-1314 Rapini, Novella P1-d2-252 Rasat, Rahmah P3-d1-1201 Raschetti, Roberto P1-d3-331 Rashid, Nazia P3-d3-1314* Raskovic, Zorica LB3-1512 Rasmussen, Lars P1-d3-444 Rasmussen, Michael P3-d3-1309* Raubenheimer, David PL8-8 Rauch, Lindsey P1-d1-449 Ravussin, Eric P1-d1-313 Raygorodskaya, Nadezda P2-d2-1118* Rayner, Christopher P1-d2-433 Razzaghy-Azar, Maryam P2-d2-1150, P3-d2-1336* Rebaud, Philippe P2-d1-1009, P3-d1-1469, P3-d3-1385 Redaelli, Francesca P3-d2-1344 Reeder, Scott P1-d2-363, P1-d3-378 Rees Smith, Bernard P1-d1-278 Refetoff, Samuel P2-d2-1153, LB4-1527 Regensteiner, Judith S13-52* Rehm, Jennifer P1-d2-363*, P1-d3-378
* Presenting author
286
9th Joint Meeting of Paediatric Endocrinology 2013
Reinehr, Thomas P1-d3-264, P1-d3-409*, P3-d1-1269, S16, S16-59* Reiner, Barry P1-d2-395 Reisch, Nicole WG6-118 Reiss, Allan P1-d3-442 Remaley, Alan P2-d2-972 Ren, An P2-d2-929 Rendina, Domenico P2-d1-751 Renes, Judith FC16-212*, P1-d2-397 Renoult-Pierre, Peggy FC1-122 Repaske, David P1-d1-449 Reschke, Felix P2-d3-712* Resende, Elisabete P2-d1-1044, P3-d2-1441 Revich, Boris P2-d1-1083 Rey, Rodolfo P2-d1-1042, P2-d3-982, S9, S9-40* Reyes, Marcela P1-d3-372, P2-d2-757, P2-d2-894 Reynaud, Rachel P2-d1-1178 Reynolds, Sarah P3-d1-1220* Rezzuto, Martina P1-d2-588 Rhie, Young Jun P1-d3-556, P2-d1-892*, LB4-1521* Rhodes, Erinn P2-d1-786* Rhodes, Simon P2-d1-1010 Riani, Marco P1-d1-498, P3-d1-1402 Riaño-Galán, Isolina P2-d2-1112, P2-d2-764* Ribeiro de Andrade, Juliana P3-d1-1456* Ribeiro, Augusto P3-d1-1222 Ribeiro, Emiliana P3-d2-1377 Ribeiro, Flavia P3-d2-1441 Ribeiro, Luís LB3-1515 Ribera, Rodrigo P2-d1-750* Rica, Itxaso P1-d1-591, P2-d3-904*, P3-d1-1287 Ricci, Franco P2-d1-683* Riccio, Andrea P2-d3-842 Richmond, Eric P1-d2-257 Richter-Unruh, Annette WG6-118 Ricordi, Camillo PL1-1* Ricotti, Roberta P1-d1-348, P1-d3-369, P3-d1-1204 Ridder, Maria P1-d3-411 Ridderstråle, Martin FC20-1484 Riepe, Felix P1-d1-245, P1-d1-418, P1-d1-575, P1-d2-256, P1-d3-264, P2-d1-619, P3-d1-1397 Riera, Francisca P1-d3-377 Riera-Pérez, Elena FC15-209 Rigamonti, Andrea P2-d1-668, P2-d2-675, P2-d2-676 Rigby, Lindsey FC11-182, FC11-184, P2-d1-1002
Rigoli, Luciana P2-d2-1025 Rinaldi, Manuela P1-d1-312 Rinaldini, Diego P2-d1-619, P2-d3-649, P2-d3-810, P3-d1-1406 Riquelme, Joel LB3-1517*, P2-d3-1073 Ritzen, Martin P3-d1-1399 Riu, Carmen P1-d3-562* Riva, Paola P3-d1-1363 Rivarola, Marco FC8-163, FC9-168, P1-d3-267, P1-d3-562, P1-d3-610, P2-d2-632 Rivera-Vega, Michelle P1-d3-438* Rivero Martín, María José P2-d3-717, P3-d2-1297*, P3-d2-1299* Rivieri, Francesca P3-d3-1350 Rix, Mariane P3-d2-1373 Rizzello, Angela P1-d1-571, P2-d1-1139, P2-d1-1145, P2-d3-648 Roach, Jennifer P2-d2-827 Robert, Jean-Jacques P2-d1-1048 Roberts, Amy E. S17, S17-64* Robison, Leslie L. S1, S1-16*, P1-d2-515 Roccio, Marta P1-d1-348, P1-d3-379*, P3-d1-1204 Rocco, Carlos P2-d2-632 Rocek, Miloslav P1-d1-292 Rocha, Anita LB3-1517 Rocha, Herculano LB3-1515 Rocha, Jaime P2-d2-1094 Rocha, Vanessa P3-d1-1456 Roche, Edna FC4-143, P1-d2-398, P3-d1-1234 Rodd, Celia P1-d2-486 Rodie, Martina FC8-166, P1-d2-585*, WG6-117 Rodrigo, Mª Dolores P3-d1-1331 Rodrigo, María P3-d2-1302 Rodrigues, Nadia Cristina P1-d2-322 Rodrigues, Tânia FC4-138 Rodrigues, Tatiane P1-d1-469 Rodríguez González, Ana P2-d1-922 Rodríguez Rivera, Victor P2-d2-799 Rodríguez Santiago, Benjamín FC17-218 Rodríguez, Adriana P3-d2-1274 Rodríguez, Amaia P1-d3-333, P3-d1-1287 Rodriguez, Amparo P3-d21300*
Rodríguez, Fernando P1-d1-567 Rodriguez, María P1-d3-413 Rodriguez, William P2-d1-1004 Rodriguez-Arnao, Maria Dolores P3-d2-1300 Rodriguez-Buritica, David P1-d3-611 Rodríguez-Cano, Diego P3-d1-1267 Rodríguez-Dehli, Ana Cristina P2-d2-764, P2-d2-1112* Roelants, Mathieu P1-d1-474 Roelfsema, Ferdinand FC3-132 Roenneberg, Till P1-d3-555 Rofani, Cristina P1-d1-473 Rogan, Alice LB3-1507 Roggen, Inge P2-d2-795 Rogol, Alan P1-d2-257, WG5-110* Rohayem, Julia P1-d2-550* Rohrlich, Pierre P3-d2-1273 Roitsch, Charles P3-d1-1398 Roja-Gil, Andrea P1-d1-314 Rojek, Aleksandra P3-d2-1208* Rojnic Putarek, Natasa P2-d21153, P2-d3-914* Rojo, Angelica P1-d2-296 Rollo, Alessandra P1-d2-490, P2-d2-896, P2-d3-911 Romanisio, Giulia P2-d1-919 Romano, Tiziana P2-d2-1054* Romer, Tomasz P3-d2-1213 Romero, Patricio P2-d2-1033 Rooman, Raoul P1-d3-414, P2-d3-708 Ropelato, María Gabriela P1-d1-239, P1-d1-380, P1-d3-413, P1-d3-563, P2-d1-1042, P2-d2-1061, P2-d3-982 Ros, Purificación FC19-232 Rosario, Carmen P3-d3-1447 Rosário, Frederico P2-d2-754 Rose, Ian P1-d3-267 Rose, Sophie P1-d1-511 Rose, Susan P2-d1-820* Roselli, Teresa P2-d3-913 Rosenbauer, Joachim P2-d1-1034 Rosenberg, Carla P1-d1-469, P1-d1-506 Rosenberg, Moshe FC4-139 Rosenfeld, Ron FC16-215, P1-d3-407, P2-d1-1011, P3-d2-1303 Ros-Miquel, Montserrat FC15-209 Rosolowsky, Elizabeth P2-d2-867
Ros-Pérez, Purificación FC15-207*, P1-d1-308 Ross, Judith P1-d2-393*, P1-d3-407, P2-d1-1100*, P2-d2-831, P2-d3-839, P3-d3-1313, WG5-107* Rossano, Veronica P2-d3-913 Rossello, Fernando FC5-146 Rossello, Stefano P2-d3-913 Rossetti, Giulia P1-d2-547, P2-d1-996, P2-d3-716, P3-d1-1363 Rossi, Andrea P2-d1-1014 Rossi, Giovanni P2-d1-919 Rossignol, Sylvie FC5-147, S6-30 Rossodivita, Aurora P2-d1-659, P2-d1-737, P2-d1-956 Roswall, Josefine P2-d2-700* Roth, Christian P1-d2-320* Rothe, Karin P1-d2-463 Rothenbacher, Dietrich P1-d1-528 Rothenbuhler, Anya FC12-187*, FC2-128 Rotondi, Daniela P1-d2-606 Rotteveel, Joost P1-d1-499* Roussey, Gwenaelle FC2-128 Rousso, Israel P2-d2-1057, P2-d2-798 Roux-Lombard, Pascale P2-d3-940 Roviglione, Barbara P2-d1-1014*, P2-d1-734, P2-d2-695, P2-d3-718 Rubinshtein, Marina P2-d1-623 Rubio-Cabezas, Oscar P1-d1-423* Rudin, Christoph P3-d1-1225 Rudloff, Silvia FC5-148 Rudzinski, Andrzej P2-d1-917 Rueda Arenas, Ernesto P3-d2-1417 Rueda, Carmen P2-d1-989 Ruedy, Katrina P1-d3-442 Rugpolmuang, Rottanat P2-d1-1045 Ruibal, Gabriela P1-d3-373, P2-d2-755 Ruivenkamp, Claudia FC3-132 Ruiz, Mª Angeles P3-d1-1331 Ruiz, Maite P2-d2-703 Ruiz-González, Maria D. P1-d1-491* Ruiz-López, Ana P1-d1-347 Rumié, Hanna P2-d2-898 Rumsby, Gill P2-d2-639 Ruperez, Azahara FC15-204 Rusak, Malgorzata P1-d1-596 Russell, Richard P2-d3-983, P3-d1-1364 Russo, Chiara P3-d2-1341
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
287
Floor Plan Exhibition Author Index
author index
author index
Russo, Gianni P2-d1-1101, P2-d1-619, P2-d3-647, P2-d3-650 Russo, Silvia P2-d1-996 Russo, Vincenzo FC6-150, P1-d1-568 Rustogi, Deepika P2-d1-854*, P2-d3-978* Rutigliano, Vincenzo P2-d1-1016 Rutter, Meilan P1-d2-394*, P2-d3-1070 Ryan, Fiona P3-d1-1264 Rymar, Oksana P3-d1-1325
Floor Plan Exhibition Author Index
S
Säämänen, Anna-Marja P1-d1-293 Saar, Meeli P2-d3-710 Saari, Antti FC14-203, P2-d1-997* Saba, Jorge P2-d2-902 Sabin, Matthew FC6-150, P1-d1-568, P2-d3-767 Sabt, Aml FC12-188, P2-d1-1176, P2-d2-1149, P3-d2-1372*, P3-d2-1374* Sacco, Michele FC1-123 Saccomandi, Marina P2-d1-741 Sachdev, Pooja P2-d1-661 Sacks, David B. P2-d2-972 Sadurska, Elzbieta P2-d2-1151 Saeger, Wolfgang LB4-1524 Saenger, Paul P1-d1-390*, P1-d2-358, P1-d3-611*, P3-d3-1314 Sáez, Katia P2-d3-880 Saffari, Fatemeh P2-d1-685*, P3-d2-1480* Sagastibeltza, Amaia P2-d2-703 Saggese, Giuseppe P2-d3-980, P3-d2-1381 Sagmeister, Susanne P1-d2-480 Saha, Marja-Terttu FC3-136, P2-d1-997 Sahakitrungruang, Taninee P2-d1-660* Sahin, Nursel Muratoglu P3-d2-1334 Sainte-Rose, Christian P2-d1-691, P2-d1-738 Saint-Martin, Cecile P2-d3-914 Sairenchi, Toshimi P1-d1-494 Saito, Reiko P2-d3-1131* Saito, Yoshihiro P3-d3-1316 Saitoh, Akihiko P2-d2-1183, P3-d1-1293 Saitoh, Shinji P3-d1-1422 Saito-Hakoda, Akiko P1-d2-432 Saitou, Tomohiro P3-d1-1407 Saji, Tsutomu P1-d1-237
Saka, Nurçin P1-d1-352, P2-d1-1050, P2-d1-1079, P2-d2-1187, P2-d2-1191, P2-d3-652, P2-d3-771 Sakalli Cetin, Esin P2-d3-1072 Sakarya, Nil P1-d1-280 Sakata, Hiroshi P2-d1-1144 Sakher, Samia P2-d1-1110 Saki, Forough P1-d1-273*, P2-d2-705* Sakka, Sophia LB2-1498* Saklamaki, Melpomeni P3-d1-1328 Sakurai, Ken P3-d3-1316 Sakurai, Maiko P2-d3-1167 Salama, Hossam P3-d2-1372 Salamanca Fresno, Luis P1-d2-435 Salazar, Teresa P1-d1-471 Saleem, Wail P3-d2-1374 Salerno, Mariacarolina P1-d1-592, P1-d2-588, P2-d1-956, P2-d2-1154, P2-d2-1190 Salih, Mustafa P2-d3-713, P3-d1-1231 Salina, Alessandro P2-d3-946, P3-d2-1339 Salinaro, Ivan P2-d3-913 Sallai, Agnes FC10-179 Sallam, Mahmoud P3-d1-1291 Salles, Jean Pierre P1-d2-329, P2-d3-711 Salmon, Anne-Sophie LB3-1510 Salo, Matti FC3-136 Salpietro, Carmelo P2-d2-1025 Salvador, Cristina P3-d2-1299 Salvatoni, Alessandro P1-d1-420*, P1-d1-594, P1-d2-254, P1-d2-258, P1-d2-399*, P1-d2-434 Salvatore, Alessia P2-d1-741 Salzano, Giuseppina P1-d3-271, P2-d2-1030, P2-d2-870 Samaan, M. Constantine P1-d1-317* Samara-Boustani, Dinane P1-d2-581, P2-d1-1048, P2-d2-1053, P2-d2-1091 Samardzic, Mira P2-d1-1182* Samia, Ouldkablia P3-d2-1241 Samoylova, Julia P2-d1-891* Sampaio, Jéssica LB4-1520 Samuels, Mark P1-d2-247 Sánchez del Pozo, Jaime P2-d1-955 Sanchez Gonzalez, Elena P2-d1-781 Sanchez, Viviana P3-d1-1397 Sánchez-Garrido, Miguel Ángel FC15-207, P1-d1-308
* Presenting author
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9th Joint Meeting of Paediatric Endocrinology 2013
Sanchez-Infantes, David P1-d1-313*, P1-d3-376 Sandhu, Sundeep P3-d3-1354* Sandrini, Romolo FC13-194 Sang, Yanmei P2-d3-907* Sangaralingam, Thangavelu P1-d1-453 Sangun, Ozlem P1-d2-602*, P2-d1-693*, P2-d2-1063 Sankilampi, Ulla FC14-202, FC14-203, P2-d1-997 Sanli, Murat P3-d1-1453 Sanna-Cherchi, Simone P1-d1-575 Sano, Shinichiro P1-d1-523, P1-d1-527*, P1-d2-582 Santalha, Marta LB3-1515 Santanera, Arianna P1-d2-600 Santen, Gijs FC3-132, P1-d2-478 Santidrian, Valeria P2-d1-629 Santomé, Luis P1-d1-477 Santos, Ana Paula P2-d2-1114 Santos, Maria P2-d2-754 Santos-Simarro, Fernando P2-d1-955, P2-d2-969 Santucci, Zulma P2-d3-1168 Sanyal, Debmalya P2-d3-947 Sanz Fernández, María P2-d3-717 Sanz, María P3-d2-1297, P3-d2-1299 Sanz, Nuria P1-d3-339* Saporiti, Anna P1-d1-420 Sarafoglou, Kyriakie P2-d2-964* Saraiva, Machado P3-d1-1428 Sarasua Miranda, Ainhoa P2-d2-799*, P3-d1-1403*, P3-d3-1353 Sardar, Colette P2-d3-984* Saritas, Umit A. P2-d3-948 Sarnacki, Sabine P2-d2-1053 Sarquis, Ana Lúcia P3-d1-1369 Sartorio, Alessandro FC1-123, P1-d2-258 Sas, Theo SAT1 Sasaki, Atsuko P1-d1-243 Sasaki, Goro FC19-229 Satake, Eiichiro P1-d2-582 Satan, Ali P2-d2-1187 Sato, Hidetoshi P2-d2-1183, P3-d1-1293* Sato, Mari P1-d1-237 Sato, Naoko P2-d2-1052* Sato, Seiji P1-d1-523 Sato, Takashi P2-d1-1144 Sato, Takeshi P3-d1-1226* Sato, Tatsuharu P2-d3-1167 Sato, Yasuhiro P2-d3-908*
Savage, Martin CPE2-75*, FC7-160, P2-d3-843*, SAT4, SAT9 Savas Erdeve, Senay P2-d2-1116 Sävendahl, Lars FC3-133, P1-d2-484, P2-d3-839, S1, S1-11, S1-14*, S1-15, S12-47 Savic, Ivanka S2, S2-18* Savov, Alexei P2-d2-1032 Savova, Radka LB3-1508 Sawicka, Beata P1-d1-596, P3-d2-1213*, P3-d3-1392 Sawnani, Hemant P1-d2-394 Say, Jemma P2-d1-671 Sayer, John LB1-1492 Scaglia, Paula P1-d1-380, P1-d1-384, P1-d3-413 Scalco, Renata P1-d1-472*, P1-d2-482 Scalini, Perla P2-d3-842 Scanlon, John P2-d2-677 Scaramuzza, Andrea P3-d2-1344* Scarano, Emanuela P1-d1-565, P1-d1-571, P2-d1-694*, P3-d3-1391* Scarinci, Renato P3-d3-1317, P3-d3-1386 Schaab, Michael P3-d1-1288 Schaarschmidt, Jörg LB4-1528 Schachter Davidov, Anita P2-d1-627*, FC9-173 Schagen, Sebastian P1-d2-546 Schaper, Joerg P2-d2-965 Scharf Pinto, Mauro P2-d2-1094* Scharf, Rebecca P1-d3-332 Scharfmann, Raphaël FC6-155, FC19-230 Scherag, André P3-d1-1269 Scherer, Philipp S8-36* Schiaffini, Riccardo P1-d2-252 Schifferli, Alexandra P3-d1-1225 Schimdtke, Daniela P3-d1-1369 Schleifer, Kristin P1-d2-428 Schleifer, Nicole P1-d2-428 Schmid, Gordian P1-d1-309, P1-d3-368 Schmidt, Heinrich P1-d2-604 Schmidt-Trucksaess, Arno P1-d1-451 Schmitt-Lobe, Maria Claudia P3-d3-1312* Schnabel, Dirk P1-d1-512, P2-d3-1169, P3-d1-1198 Schneider, Angelika P1-d1-448 Schneider, Pascale P2-d1-736 Schober, Edith P1-d1-421, P2-d1-1034, P2-d2-863
Schoemaker, Marieke FC3-135, P2-d1-953 Schoenau, Eckhard P1-d1-282, P1-d2-481 Schoenmakers, Nadia FC10-177 Schott, Dina P2-d1-959* Schramm, Romulo P3-d3-1312 Schrander-Stumpel, Constance P2-d1-959 Schreiner, Felix P1-d2-601 Schröder, Carmen P2-d2-861 Schroedt, Julien LB3-1510 Schuck, Ellen P2-d2-829 Schulga, John FC19-231 Schündeln, Michael P1-d1-522 Schuster, Susanne P2-d1-732 Schuster, Tobias P1-d1-570 Schwab, Karl Otfried P1-d1-451*, P3-d3-1448 Schwartz, Charles P2-d1-1143 Schwarz, Hans Peter P2-d1-625 Schweizer, Roland FC7-159, P1-d1-448*, P2-d3-845* Schwitzgebel, Valérie P2-d2-927, P2-d3-940 Scipione, Mirella P1-d1-571, P1-d2-402, P2-d2-896 Scirè, Giuseppe P1-d1-505 Sciutti, Rita P2-d1-1139 Scornet, Erwan LB3-1510 Scott, Amanda P2-d1-1017* Scratch, Shannon P1-d3-440 Scrideli, Carlos FC13-192*, FC13-193*, FC20-1486 Sdogou, Triantafyllia P2-d3-812 Sebastiani, Giorgia P1-d1-535, P1-d2-361* Sebire, Neil P1-d1-242 Seckova, Lidija P3-d3-1308 Sedassari, Anelise P2-d1-1180 Sedassari, Nathalie P2-d1-1180 Sedej, Katarina P2-d3-773 Sedky, Haidy P3-d3-1358 Sedlackova, Barbora P1-d3-340 Segaloff, Deborah FC8-164 Seidinger, Ana FC13-192, FC13-193 Selver Eklioglu, Beray P2-d2-760, P2-d2-865, P3-d1-1460*, P3-d2-1342 Seminara, Manuela P2-d1-996 Seminara, Salvatore P2-d1-683, P2-d3-709, P2-d3-842, P2-d3-846, P2-d3-847, P3-d1-1262 Semler, Oliver P1-d1-282, P1-d2-481* Sempach, Robert P2-d3-768 Semrouni, Mourad P2-d1-1110 Senatore, Laura P2-d1-1020
Senatorova, Ganna P2-d3-805 Senniappan, Senthil FC11-180*, FC11-185*, P1-d2-426, P2-d1-850, P2-d1-859, P3-d1-1326, P3-d3-1349 Senra, Vírgilio LB3-1515 Sentchordi, Lucía FC19-232 Seppä, Satu P2-d1-1035* Sepúlveda, Carolina P2-d2-902, P2-d3-875 Ser, Nicole FC6-155 Sergeyev, Oleg P2-d1-1083* Serra, Elisa P2-d3-810 Serra, Filipa P3-d1-1428 Serra-Juhé, Clara FC17-218*, FC17-219* Serrano Barral, Araceli P2-d3-717 Sertçelik, Ayse P2-d3-1123 Sertedaki, Amalia FC18-223, FC8-164, P1-d3-260*, P1-d3-263, P1-d3-266, P1-d3-269* Setian, Nuvarte P2-d2-697, P3-d1-1250 Settas, Nikolaos P1-d2-541* Severino, Maria Savina P2-d1-1014 Sewaybricker, Leticia P3-d1-1456 Sezer, Taner P3-d2-1334 Shabir, Iram P2-d1-784, P2-d2-1092, P2-d2-1120*, P3-d1-1454*, P3-d1-1458 Shackleton, Cedric FC9-169, FC9-170 Shah, Arti P2-d3-878* Shah, Pratik FC11-185, P1-d1-242, P1-d2-426, P2-d1-859*, P2-d3-906*, P2-d3-910 Shahar, Ron P1-d1-286 Shahroodi, Parisa P2-d1-685 Shaikh, Guftar S19, P1-d2-303, P1-d2-607 Shaikh, Mohamed P1-d3-337, P1-d2-544, P2-d1-690, P2-d2-827, P3-d1-1290 Shakiba, Alimohammmad P1-d2-298 Shalet, Stephen FC16-213 Shalitin, Shlomit P1-d3-441*, P2-d1-858, P3-d1-1251*, WG1-81* Shamiss, Ari P2-d1-1135 Shammas, Christos P2-d11146, P2-d1-655 Sharma, Arundhati P3-d1-1196 Sharma, Atul P1-d2-486 Sharpe, Richard FC8-162, S9, S9-38*
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
289
Floor Plan Exhibition Author Index
author index
Floor Plan Exhibition Author Index
author index
Sharples, Peta P1-d2-520 Shatla, Emad P3-d2-1372 Shavrikova, Elena P2-d1-1011 Shaw, Nick S7, S7-33*, SAT3 Shen, Shuixian P2-d2-903, P3-d2-1376 Shen, Yuan FC20-1484 Shepherd, Maggie FC14-200 Shepherd, Scott FC19-231, P3-d1-1290* Sherif, Maha FC11-183, P2-d1-850, P3-d3-1349* Shi, Chunmei FC17-220 Shi, Yanqin FC11-182* Shibata, Ayako P1-d1-240 Shibata, Hironori FC12-191, P1-d1-284* Shibayama, Keiko P2-d2-1148 Shields, Beverley FC14-200 Shimizu, Nobuko P1-d1-240 Shin, Choong Ho LB4-1521, P1-d1-287, P2-d1-740 Shin, Young-Lim P2-d2-1155* Shinohara, Hiroyuki P1-d1-593* Shirai, Masaru P2-d1-1144 Shiraishi, Masahisa P2-d1-626 Shiryaeva, Tatiana P2-d1-813, P2-d1-814, P2-d2-832 Shkurti, Adela P3-d3-1307* Shmoish, Michael FC5-144 Shon, Young Bae P2-d2-1093 Shore, Richard FC13-195 Short, John P1-d1-468 Shtaif, Biana P1-d1-286 Shu, Na P2-d1-1008 Sibai, Hicham P2-d3-1127, P3-d1-1199 Sicsic, Aude P1-d2-395, P2-d3-843 Siddique, Jamila P2-d3-984 Siemensma, Elbrich P1-d3-411, P2-d2-762 Siepl, E. Christine P1-d1-390 Sierra, Cristina P1-d3-339 Sifianou, Popi P1-d1-496* Siklar, Zeynep P2-d2-1116*, P2-d3-1123* Silva, Adriana P2-d2-866 Silva, Ana Paula LB3-1515 Silva, Anderson P2-d2-1186 Silva, Cicero P1-d2-430 Silva, Ivani P3-d1-1321 Silva, Letícia P3-d1-1321 Silva, Pamela LB1-1495 Silva, Rosana P1-d2-583, P1-d3-270 Silvano, Liliana P2-d1-622*, P2-d3-1163 Silve, Caroline FC12-190, FC20-1485, FC2-128
Silveira, Letícia FC4-142, FC8-164 Silverman, Lawrence P1-d3-557, P2-d3-840 Silvestri, Michela P2-d1-919 Silvija, Sajic P3-d2-1281 Simeonov, Emil P2-d3-651 Simi, Francesca P2-d3-980*, P3-d2-1381 Simi, Paolo P1-d2-588 Simidrea, Ioan P2-d3-808 Simon, Albane FC6-155 Simon, Dominique P1-d2-487*, P2-d1-819 Simon, Job LB1-1492 Simoni, Manuela P2-d1-1040 Simonin, Gilbert P2-d1-1178 Simpson, Helen P1-d3-410 Simpson, Stephen PL8-8* Simsek, Betül P2-d3-766 Simsek, Enver P2-d1-662*, P2-d2-641, P3-d1-1425* Sinai, Tali P2-d2-792*, P2-d3-801* Sinclair, Graham P1-d2-251 Singer, Sigal P2-d3-871 Singha, Ajay P3-d2-1414 Siniawski, Andrzej P2-d2-970 Sinnott, Richard P1-d1-422, WG6-117 Sinopidis, Xenophon FC1-121 Širca Campa, Andreja P2-d3-773 Siripunthana, Sukumarn P2-d1-1045 Siviero-Miachon, Adriana Aparecida P1-d1-384, P1-d2-577 Skae, Mars FC11-181, FC11-182, FC11-184, P2-d1-1002 Skakkebæk, Anne FC1-125 Skakkebæk, Niels PL10-10* Skalicka, Veronika P1-d1-292 Skevaki, Chrysanthi LB3-1513 Sklar, Charles P1-d2-515 Skogstrand, Kristin P1-d1-281 Skordis, Nicos P2-d1-655 Skouma, Anastasia P3-d2-1438 Škrabic, Veselin P1-d2-259, P3-d1-1465*, P3-d2-1443* Skwirut-Carlsson, Christine FC7-161 Slaibe, Lissete P2-d2-898 Slater, Olga P1-d1-242 Slattery, Meghan P2-d1-1012 Slavcheva, Olga LB3-1508* Slaveska, Nevenka P3-d2-1240*, P3-d3-1308 Slavica, Merkovic P3-d2-1281 Slowikowska-Hilczer, Jolante WG6-118
* Presenting author
290
9th Joint Meeting of Paediatric Endocrinology 2013
Smerieri, Arianna FC5-145 Smigiel, Robert P2-d1-1077 Smyczynska, Joanna P1-d3-406, P1-d3-412*, P2-d3-838, P3-d1-1370 Snajderova, Marta P2-d2-1059* Snezana, Lesovic P3-d2-1281 Soardi, Fernanda P1-d2-253, P1-d2-577 Sobrero, Gabriela P2-d1-622, P2-d3-1163* Sobrier, Marie-Laure P1-d1-511 Söder, Olle P1-d1-536, P1-d2-398, YB2, FC8-166 Soejima, Hidenobu P2-d1-998 Sogno Valin, Paola P1-d2-434 Sohn, Young Bae P2-d1-1003 Sojar, Valentin P1-d3-367 Soker, Gokhan P3-d2-1215 Sokol, Sergei Y. FC10-175 Solarz, Horacio P3-d1-1470 Soldano, Lucia P2-d1-727 Soleyan, Aude P1-d1-511 Soli, Fiorenza P3-d3-1350 Soliman, Ashraf FC12-188*, P2-d1-1176, P2-d2-1149*, P3-d2-1372, P3-d2-1374 Solis, Julieta P2-d3-1162 Solntsava, Angelika P1-d1-497, P3-d2-1275 Solntsava, Anzhalika P1-d3-371, P2-d3-1159, P3-d1-1260, P3-d2-1479 Solovyova, Galina P2-d2-793, P2-d1-1177* Solti, Imre LB2-1502 Song, Young-Hwan P2-d2-759 Sood, Beena P2-d1-1004 Sordelli, Silvia P2-d1-1085* Sørensen, Jesper P1-d1-281 Sørensen, Karina FC1-125 Sorge, Roberto P1-d3-415 Soriano Rodríguez, Pilar FC15-209 Soriguer, Federico P1-d1-417 Sorter, Michael P1-d1-351 Sosa Avila, Luis Miguel P3-d2-1417 Sosothikul, Darin P2-d1-1045 Soto, Nestor LB3-1517 Souberbielle, Jean-Claude P2-d1-691 Soucek, Ondrej P1-d1-292* Souchon, Pierre-François FC2-128 Soumeya Fedala, Nora P3-d1-1409 Sourani, Maria P2-d3-812 Souto, Ana P2-d2-764 Souza, Luis P2-d1-1180 Sowden, Jane FC10-174
author index
Stevens, Adam FC11-181*, FC11-182, FC16-211, FC7-158*, P2-d2-830 Stevens, Michael P1-d2-362, P1-d3-336 Stevenson, Brian P2-d1-1082 Stier, Bernhard P1-d1-451 Stimjanin, Ena P2-d1-916 Stimjanin-Koldzo, Diana P2-d1-916* Stingl, Katarina P1-d2-259 Stipancic, Gordana FC10-179 Stivel, Mirta LB1-1490 Stobbe, Heike P2-d2-967 Stoeva, Iva P2-d2-1023, P2-d2-1032, P2-d3-644 Stone, Janet P1-d1-383 Stone, Peter P1-d1-524 Stoppa, Sophie P2-d1-990, P2-d1-995 Storr, Helen FC18-222, FC4-141, FC7-160* Stoyanov, George P1-d1-476 Straetemans, Saartje P1-d3-414* Stratico, Roxana P3-d1-1397 Strauch, Konstantin FC5-148 Strauss, Arnold P3-d1-1328 Street, Maria FC5-145*, P1-d2-356, P2-d1-737, P3-d1-1362 Strele, Ieva P2-d3-802, P2-d3-809 Strochlic, David FC20-1484 Stroescu, Ramona P1-d1-452*, P3-d2-1236* Stroh, Christine P1-d2-319 Strom, Tim P1-d2-305, P2-d2-1113 Struve, Dagmar P1-d1-573, P2-d2-1113 Stuckens, Chantal FC6-155, LB3-1510 Stuji, Yoshikazu P1-d2-578 Su, Chang P2-d1-885* Su, Zhe P1-d1-288, P1-d2-396, P1-d3-559, P2-d2-1111, P2-d2-642* Suárez, Martha P1-d3-373, P2-d2-755 Suazo, Cristian P1-d1-471 Subburayalu, Saranya P1-d1-453 Subtil, Sandra FC9-170 Such, Kamila P1-d3-616 Sugihara, Shigetaka P1-d2-460 Sugimoto, Satoru P1-d3-342*, P3-d1-1292 Sugita, Kanji P1-d1-537, P3-d1-1407 Sugiyama, Yukari P3-d1-1422
Suh, Byung Kyu P1-d1-475, P1-d2-458, P1-d2-483, P2-d1-777 Sukalo, Alexandr P1-d3-371 Sukarova-Angelovska, Elena P2-d2-967, P3-d1-1258, P3-d2-1306* Sulmont, Véronique FC6-155, LB3-1510 Sultan, Charles P1-d3-263, WG6-118 Sumnik, Zdenek P1-d1-278, P1-d1-292, P1-d2-429, P2-d1-993, P2-d2-895 Sun, Pei-Chen P2-d1-752* Sun, Yan Yan P3-d1-1432 Sundaram, Janani P1-d1-453* Sundernathan, Tulika P1-d1-345 Supornsilchai, Vichit P2-d1-1045* Suwanai, Ayuko P1-d1-572 Suyama, Noriko P2-d3-811 Suzuki, Eri P1-d1-593 Suzuki, Erina P1-d2-578 Suzuki, Junichi P2-d1-674, P3-d1-1219* Suzuki, Makoto FC18-226 Suzumura, Hiroshi P1-d1-494 Svechnikov, Konstantin P1-d1-536 Svensson, Per-Arne P1-d2-355 Swerdlow, Anthony S1, S1-11, S1-14, S1-15* Swider, Marta P3-d1-1270 Swiercz, Anna P2-d1-667 Switnicki, Michal FC1-125 Swolin-Eide, Diana P2-d2-836 Syed, Zulkifli P3-d1-1201 Sykiotis, Gerasimos P2-d1-1082 Szalecki, Mieczyslaw P1-d3-406, P1-d3-408, P2-d1-667*, P2-d3-645, P3-d1-1452, P3-d2-1379 Szarras-Capnik, Maria WG6-118 Szczesniak, Rhonda P2-d3-878 Szewczyk, Leszek P1-d3-406 Szinnai, Gabor P3-d1-1225 Sztefko, Krystyna P2-d1-917 Szymlak, Agnieszka P2-d1-823 Szymocha, Jerzy P3-d1-1252, P3-d1-1253 T
Ta, Van P1-d3-262 Tabin, René P2-d1-990 Tabitha, Randell P2-d1-670 Taboada, Giselle P1-d3-270 Taboas, Melisa LB1-1490* Tachibana, Nao P2-d3-881
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
291
Floor Plan Exhibition Author Index
Sozaeva, Leila P1-d1-279* Spadoni, Emanuela P1-d1-507 Spadoni, Gian Luigi P1-d1-505, P1-d2-252 Spehar Uroic, Anita P2-d2-1153 Spencer, Suzanne P2-d1-925 Sperling, Mark P1-d2-395 Spica Russotto, Valeria P1-d2-399 Spiliotis, Bessie FC1-121, FC15-208, P1-d1-314 Spinelli, Roberta P1-d2-434 Spinnler, Katrin P1-d1-536 Spinola de Castro, Angela Maria P1-d2-577 Spinola-Castro, Angela P1-d1-384* Spinozzi, Emiliano FC2-131 Spoudeas, Helen FC13-196, P1-d2-517, P2-d2-631 Spranger, Joachim FC17-217, P1-d2-328 Srivastava, Deo Kumar P1-d2-515 Stagi, Stefano P2-d1-683, P2-d3-709, P2-d3-842, P2-d3-846*, P2-d3-847, P3-d1-1262* Stamatelopoulos, Kimon P2-d2-864 Stamogiannou, Lela P2-d2-826 Stark, Christina P1-d2-481 Starzyk, Jerzy P2-d1-664, P2-d1-917, P2-d2-640, P2-d3-942* Stawerska, Renata P1-d3-412, P2-d3-838, P3-d1-1370* Stechova, Katerina P1-d1-278 Stefanova, Elisaveta P2-d3-651, P3-d1-1223 Steichen, Elisabeth P3-d1-1323 Steichen-Gersdorf, Elisabeth P1-d2-305* Stein, Daniel P2-d1-730 Steinmetz, Leandra P3-d11250, P3-d1-1411 Stejareanu, Lavinia P2-d1-1041* Stella, Lenira P2-d3-949* Stelmach, Malgorzata P2-d1-917, P2-d3-942 Stelmaszczyk- Emmel, Anna P1-d3-617 Stenerson, Matthew P1-d2-428 Stephens, Jacqueline P1-d1-313 Stephens, Kathryn P1-d1-449 Sterkenburg, Anthe P1-d1-508, P2-d1-1015 Stern, Eve P1-d2-517 Stern, Naftali P2-d1-627
Floor Plan Exhibition Author Index
author index
Tada, Hidenori P3-d2-1237 Tadokoro-Cuccaro, Rieko FC8-166, P1-d2-584* Tafi, Luca P2-d1-956 Tagliabue, Claudia P2-d1-1020 Tajima, Terutaka P1-d1-593 Tajima, Toshihiro FC10-176, FC12-186, P1-d3-404* Takada, Fumio P1-d2-582 Takagi, Masaki P1-d1-504*, P1-d1-593, P2-d3-881 Takahashi, Chie P2-d1-890*, P2-d2-1188 Takahashi, Ikuko P1-d2-605, P2-d1-998* Takahashi, Tsutomu P1-d2-605, P2-d1-998 Takahashi, Yutaka S15-58* Takakuwa, Satoshi P1-d2-578 Takasawa, Kei P1-d1-240, P1-d3-261 Takavci, Fatih P2-d1-1174 Takazawa, Kei P1-d2-578 Takeda, Ryojun P2-d3-881* Takehara, Kenji P2-d1-818 Taketazu, Genya P2-d1-1144 Taketomo, Carol P2-d1-1004 Takishima, Shigeru P1-d3-261* Takubo, Noriyuki P2-d2-1148, P2-d3-811* Takubo, Yumiko P2-d3-811 Talea, Ali P3-d2-1336 Tal-Pony, Limor P2-d2-792, P2-d3-801 Tamada, Izumi P1-d1-243 Tamborlane, William P1-d2-430, P1-d3-442 Tamburrino, Federica P1-d1-565, P1-d1-571*, P3-d3-1391 Tamura, Mayuko P1-d1-289* Tan, Huseyin P2-d3-714, P3-d2-1472, P3-d2-1481 Tanaka, Toshiaki P1-d3-404, P2-d2-1052, P2-d2-833*, P3-d1-1289 Tanaka, Yukichi P3-d1-1226 Tanaka, Yuko P2-d1-725 Tanaskoska, Milica P3-d1-1258 Tanaskovic-Nestorovic, Jelena LB3-1512 Taneli, Fatma P3-d1-1365 Tang, Fang P2-d1-1008 Tangari Saredo, Ana P3-d1-1397*, P3-d1-1470* Taniguchi, Yuko P1-d1-243 Tannert, Astrid P1-d1-309 Tapia, Alejandra P1-d3-377 Tarasenko, Nataliya P2-d2-682 Tardon, Adonina P2-d2-1112, P2-d2-764 Tardy, Véronique FC1-122
Tarifa, Cintia P2-d1-622, P2-d3-1163 Tarkkonen, Kati LB1-1493 Tartaglia, Marco S17, S17-62* Tartuci, Juliana P1-d1-384 Tasdemir, Sener P3-d3-1394 Tasel, Bülent P3-d1-1329 Tashmanova, Akmaral P3-d3-1355* Tasic, Velibor P1-d1-575 Taskin, Necati P2-d1-782, P2-d3-1124 Tata, Brooke PL4-4 Tatsi, Christina P1-d1-386 Tau, Cristina P1-d3-610 Tauber, Maithe FC5-147, P1-d2-329, P2-d1-1049 Tawfik, Sameh P2-d3-877* Tayfun, Meltem P2-d2-1024* Taylor, Angela FC9-169, FC9-170, FC9-172, P1-d3-267, P2-d2-634 Taylor, Michael P1-d2-394 Taylor, Norman P2-d2-639, P3-d1-1197 Teixeira, Ana P3-d2-1415 Teixeira, Virginia P1-d3-270 Tekgunduz, Kadir P2-d2-926, P3-d3-1352 Tekin, Ayse P3-d1-1423 Tekin, Mustafa P3-d3-1383 Teli, Aikaterini P2-d2-702 Temel, Ozlem P3-d2-1334 Temiz, Fatih P3-d2-1215 Temoche, Lourdes Rodríguez P3-d2-1276 Temple, Karen FC14-200 ten Dam, Monique P1-d2-326 Ten, Svetlana P1-d1-386, P2-d1-620, P2-d1-673, P2-d2-1056, P3-d1-1235, P3-d1-1263, P3-d2-1206 Tena-Sempere, Manuel FC15-207, P1-d1-308 Tenenbaum, Ariel P2-d1-858 Tenenbaum-Rakover, Yardena FC9-173 Tenhola, Sirpa P2-d1-1035 Tenías-Burillo, Jose María P3-d2-1477 Tepe, Derya P1-d2-403, P2-d1-915, P2-d2-1024, P3-d1-1461* Terek, Demet P1-d2-519 Tero, Varimo P3-d2-1378 Terzi, Cesare P1-d1-498, P3-d1-1362, P3-d1-1402* Teslik, Leos P2-d2-1059 Testa, Graciela P2-d3-1163 Teuner, Christina P3-d1-1269 Tews, Daniel FC15-205
* Presenting author
292
9th Joint Meeting of Paediatric Endocrinology 2013
Tfayli, Hala WG2-89*, WG4-103* Thabit, Hood P1-d2-431 Thacher, Tom FC12-189* Thankamony, Ajay P1-d2-398*, P1-d3-410*, SAT5 Thao, Bui P2-d1-1080* Theintz, Gérald-Edouard P2-d1-990 Théret, Claire FC2-128* Thibaud, Elisabeth P1-d2-580, P2-d1-1048, P2-d2-1053, P2-d2-1088, P2-d2-1091 Thibaud, Nathalie FC5-147, P1-d1-387 Thiery, Joachim P3-d1-1360 Thim, Signe P2-d1-724 Thiry-Counson, Geneviève P1-d2-401 Thodberg, Hans Henrik WG3-94 Thomas, Alison FC11-183 Thomas, Muriel P1-d2-401* Thompson, Iain FC4-138 Thon, Angelika P1-d1-421 Thornton, Paul P1-d1-493*, P2-d1-1004, P3-d1-1398* Thyagiarajan, Manigandan P1-d2-362, P1-d3-336 Thyen, Ute WG6-118 Tian, Cuixia P2-d3-1070 Tian, Zhanzhuang P3-d1-1432 Tibúrcio, Jacqueline P3-d1-1321 Tieder, Joel P2-d1-925 Tilitzky, Sandra P3-d1-1397 Tillmann, Vallo P1-d1-274, P1-d1-422, P2-d3-710* Timmons, Brian P1-d1-317 Tinker, Andrew FC11-183 Tiryaki, Tugrul P2-d3-643 Titman, Andrew P1-d1-244, P2-d1-630 Tittel, Bettina P2-d2-1028 Tlif, Asiet P2-d2-682* Todieva, Anastasia P3-d1-1261 Todorova, Zdravka P2-d3-651*, P3-d1-1223 Todorovic, Sladjana P2-d3-654 Toglia, Rossana P1-d1-569 Tojo, Rafael P1-d1-354, P3-d2-1274 Tokar, Baran P3-d1-1425 Tokunaga, Katsushi P1-d1-289 Toledo, Karen P2-d3-880 Tolle, Michael P2-d1-950 Tomasi, Paolo LB3-1509 Tomita, Yuichiro P3-d2-1209* Tommiska, Johanna FC10-178, P3-d2-1378 Tomova, Nelly LB3-1508
author index
Tsalikian, Eva P1-d3-442 Tsekoura, Efstathia FC1-121 Tsentidis, Charalambos P2-d3-812 Tsiroukidou, Kyriaki P2-d2-1119 Tsitourus, Vassilis P3-d2-1414 T’Sjoen, Guy FC8-167 Tsoka Gennata, Eleni P2-d1-1146* Tsouvalas, Emmanouil P2-d2-864 Tsuchiya, Takayoshi P2-d1-626 Tsuji, Atsumi P1-d3-268* Tsuru, Satoko P3-d3-1316 Tubiana-Rufi, Nadia FC6-155, LB3-1510, P2-d1-1048 Tucci Jr., Silvio FC13-192, FC13-193 Tucci, Silvio FC20-1486 Tugrul Kabasakal, Melike P1-d1-352 Tükün, Ajlan P2-d2-1116 Tuluc, Florin FC20-1487 Tummers-de Lind van Wijngaarden, Roderick P1-d3-411 Tummolo, Albina FC2-130, P1-d1-450, P2-d1-956, P2-d2-899, P2-d3-913, P3-d2-1340 Tung, Yuet-Ling P2-d2-1122* Turan, Mehmet P2-d1-721*, P2-d3-714*, P3-d2-1472, P3-d2-1481 Turan, Serap P1-d2-300*, P1-d2-464, P2-d1-1050, P2-d1-742, P2-d1-849, P2-d1-884, P2-d3-715, P2-d3-803 Turchetta, Attilio P2-d1-999 Turchetti, Daniela P2-d1-694 Turhan, Murat P2-d2-791 Türkyilmaz, Zafer P2-d3-944 Tuten, Fatih P3-d2-1212 Tutera, Maria P2-d3-980, P3-d2-1381* Tutunculer, Filiz P2-d1-1050 Tuuri, Timo P1-d2-551 Tuvemo, Torsten P1-d2-392, P1-d3-560 Tyazhka, Oleksandra P3-d2-1238 Typlt, Eva LB4-1528 Tyrawa, Katarzyna P2-d1-664, P2-d2-640 Tzur, Dorit P2-d1-1135, P3-d1-1359 U
Uauy, Ricardo P1-d3-341
Ubertini, Graziamaria P1-d2-255, P2-d2-761* Uçar, Ahmet P1-d1-352*, P2-d2-1187, P2-d3-652*, P2-d3-771 Uchida, Noboru FC18-226* Udhane, Sameer P1-d3-265 Uematsu, Ayumi FC18-226 Ueno, Poliana P3-d1-1321 Ugarte, Francisca P1-d1-471*, P1-d2-296, P2-d2-902 Ugrasbul, Figen P2-d3-943*, P3-d1-1424, P3-d2-1413 Uitterlinden, André FC3-132, FC9-172, P1-d2-326, P1-d2-478 Ulman, Mira FC4-139 Ulucan, Korkut P2-d1-782*, P2-d2-862, P2-d3-1124 Umboh, Adrian P3-d2-1278 Umur, Özge P2-d3-652, P2-d3-771 Unal, Sule P2-d1-693 Unanue, Nancy P2-d3-875 Uncu, Nermin P3-d1-1461 Uner, Abdurrahman LB2-1504 Ungaro, Carla P1-d2-588 Ungureanu, Didona P3-d2-1375, P3-d3-1384 Unic, Ivana P3-d1-1465 Unsal, Erbil P2-d2-706 Unuvar, Tolga P2-d1-729* Upadrasta, Swathi P2-d1-1138, P2-d2-931 Urakami, Tatsuhiko P2-d1-674, P3-d1-1219 Urano, Fumihiko S3, S3-21* Urbach, Stacey P1-d1-455 Urbano, Flavia P2-d2-1192 Urbón López de Linares, Lidia P2-d1-785 Urda, Antonio P1-d1-417 Urmi, Das P1-d1-244 Urrutia, Inés P2-d3-904 Ustyol, Ala P3-d1-1463 Usui, Takeshi P2-d2-637 Utsal, Liina P2-d3-710 Uygur, Turkan P2-d1-729 Uzun, Gulbahar P2-d2-791 V
Vaê, Dichtchekenian P3-d1-1411 Vago, Tarcisio P1-d1-540 Vahcic, Mitja P2-d3-772 Vaiani, Elisa P1-d3-562 Vail, Andy FC11-184 Vaivre-Douret, Laurence FC6-155 Vakaki, Marina P1-d3-615, P2-d2-864, P3-d1-1431 Valdes, Carolina P2-d3-875*
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
293
Floor Plan Exhibition Author Index
Tone, Luiz FC13-192, FC13-193, FC20-1486 Tonelli, Carlos P1-d1-472 Tonev, Anton P2-d1-733 Toni, Sonia P2-d3-874 Topcu, Vehap P2-d2-1116 Toppari, Jorma P1-d1-293 Törel Ergür, Ayça P3-d2-1435* Torelli, Cataldo P2-d3-913 Toro, Michela LB2-1503 Torpiano, John P1-d1-242 Torre, Riccardo P1-d3-415 Torres Alcántara, Saúl P2-d1-778 Torres, Andy P1-d1-492 Torres, Ernesto P1-d1-495 Torun, Emel P1-d2-359, P2-d3-776 Tosca, Maria Angela P2-d1-919 Toscano, Inés FC19-232 Toscano, Vincenzo P1-d1-473 Touhami, Mahmoud P2-d2-1062, P3-d1-1221 Toumba, Meropi P2-d1-655* Touraine, Philippe FC1-122 Tournaye, Herman CPE4-78* Tournis, Symeon P2-d2-868 Tovar-Larrucea, Juan P1-d2-435 Townsend, Caroline P1-d2-426, P2-d1-859 Trabarch, Ericka FC4-142 Traggiai, Elisabetta P1-d1-272 Trajkovski, Zoran P3-d2-1240 Tran, Khanh P1-d3-262 Tran, Lisa P1-d1-493, P3-d1-1398 Trarbach, Ericka LB2-1496, P2-d1-954 Trebusak Podkrajsek, Katarina P1-d3-334, P2-d1-687* Trecia, Wouldes P2-d2-1158 Tregurtha, Sheryl P2-d2-1158 Trendafilow, Maria P2-d1-958 Trettene, Adolfo P1-d1-420, P1-d2-254* Trevisan, Patrícia P2-d2-962, P3-d2-1380 Triantafyllou, Panagiota P2-d1-994, P2-d2-702, P3-d1-1361* Tridenti, Gabriele P1-d1-498, P3-d1-1402 Triemstra, Justin P2-d2-1184 Trifirò, Giuliana P1-d2-399, P2-d1-692* Trivedi, Shamita P2-d3-905 Trolle, Birgitta P2-d1-666 Trolle, Christian P1-d1-277 Trunin, Yury P2-d2-1027 Tsakova, Adelina LB3-1508
Floor Plan Exhibition Author Index
author index
Valdevenito, Raúl P1-d1-567 Valencia, Alejandra P3-d2-1245* Valenzise, Mariella P2-d2-834 Valle, Miguel P2-d1-745* Vallée, Marc FC20-1488 Vallejos, Nimia LB1-1495 Valteau-Couanet, Dominique P2-d1-691, P2-d1-738 Van Aken, Sara P1-d2-250 van Alfen-van der Velden, Janielle P2-d1-657 van Beijsterveldt, Toos C. P1-d1-595 Van Brakel, Jocelyn P1-d3-564b* van Buuren, Stef P1-d1-468 van de Crommert, Viviane P2-d1-657* van de Lagemaat, Monique P1-d1-499 Van Den Abbeele, Thierry FC19-233 van den Akker, Erica P2-d1-656, P2-d3-653 van den Driesche, Sander FC8-162 van der Byl, Dawn-Lee P3-d2-1207 van der Kaay, Danielle P2-d3-653* van der Linde, Annelieke P2-d1-657 van der Sluijs Veer, Liesbeth P2-d1-1142 van der Steen, Manouk P1-d2-397* van der Veer, Eline P1-d1-499 van der Wielen, Michiel P1-d2-478 van der Zwan, Yvonne FC5-146*, FC8-166 van Donkelaar, Eva L. P2-d1-745 van Duyvenvoorde, Hermine FC3-132, P1-d2-478 Van Helvoirt, Maria P2-d2-795 Van Hoecke, Eline FC8-167 van Iersel, Laura P1-d1-509* van Leeuwen, Leonie P2-d1-656 van Santen, Hanneke P1-d1-509 van Tol, Eric FC3-135, P2-d1-953 van Trotsenburg, A.S. Paul FC10-177, P1-d1-509, P1-d1-595, P1-d3-613, P2-d1-1142 Van Vliet, Guy P1-d2-247
van Weissenbruch, Mirjam P1-d1-499 Vanbesien, Jesse P2-d2-795 VanderMeulen, John P1-d1-476 Vandoni, Matteo P1-d3-331 Vannier, Jean Pierre P2-d1-736 VanSchuyver, Marisa P2-d2-797 Varewijck, Aimée FC10-177 Vargha-Khadem, Fareneh P2-d1-883 Varol, Emine P2-d2-861* Vasanwala, Rashida P2-d1-918*, P2-d3-876 Vasconcelos, Carlos P3-d1-1428 Vasic, Brankica P2-d1-1078, P3-d2-1439 Vasques, Gabriela FC3-134* Vasquez, Leticia P2-d3-875 Vasyukova, Olga P2-d2-790* Vatankulu, Ferhat P2-d2-698 Vaxillaire, Martine FC6-155 Vazeou, Andriani P2-d2-826, P2-d2-868, P2-d2-900* Vázquez, Angeles P2-d3-775 Vázquez, Rocío P1-d1-354, P3-d2-1274 Vázquez-Ruíz, Monserrat FC14-199 Vcelak, Josef P1-d3-340 Vcelakova, Jana P1-d1-278 Veijola, Riitta FC10-178 Vela, Amaia P1-d1-591, P3-d1-1287* Velagic, Zinka P1-d2-457 Velander, Clara P2-d2-973 Velásquez Rodríguez, Ana María P2-d2-636*, P2-d3-844 Velea, Iulian P3-d1-1266 Velea, Puiu Iulian P2-d3-848 Venara, Marcela FC13-197, P2-d1-1051, P2-d1-1173 Vendemiale, Marcella P1-d1-450, P2-d2-899, P2-d3-913, P3-d2-1340 Vendrell, Teresa P1-d1-477 Venta Obaya, Rafael P2-d2-764 Ventura, Annamaria FC2-130, P1-d1-316 Vera, Fabian P3-d1-1397 Vera, Jose P3-d2-1420* Verhorstert, Kim P1-d3-613 Verkauskiene, Rasa FC10-179 Verkerk, Annemieke FC3-132, FC9-172, P1-d2-326, P1-d2-478 Verlinde, Franciska P1-d2-401 Verma, Bhupendra PL4-5 Vervoort, Jacques P2-d1-953 Vestergaard, Else Marie P3-d2-1373
* Presenting author
294
9th Joint Meeting of Paediatric Endocrinology 2013
Vestrucci, Benedetta P1-d1-565, P1-d1-571, P2-d3-648, P3-d3-1391 Vetter, Celine P1-d3-555 Vezzoli, Valeria P2-d1-1040 Vial, Julie P2-d1-1049 Viaud, Magali P2-d2-1088 Viazava, Liudmila P1-d3-371*, P2-d3-1159 Vicente Gabás, María Del Rosario Alicia P3-d2-1302 Vidal-Puig, Antonio WG2-86 Vigone, Maria Cristina P1-d1-598*, P1-d2-606, P2-d1-1137* Vijzelaar, Raymon FC9-170 Viliotti, Valentina P3-d3-1350 Villanueva, Soledad P2-d2-902 Villarroel, Claudio P1-d2-543* Vincens, Monique FC19-228 Viner, Russell FC4-143 Virdis, Raffaele P1-d1-498, P3-d1-1362, P3-d1-1402 Viterbo, Gisela P1-d3-610 Vivanco, Mariza P2-d2-1091 Vivi, Giulia P1-d1-594 Vlachaki, Efthimia P2-d2-702 Vlachopapadopoulou, Elpis P1-d3-615*, P3-d1-1431*, P3-d2-1280, P3-d2-1438 Vladoiu, Suzana P2-d2-800 Vlastelica, Željka P3-d1-1465, P3-d2-1443 Vockley, Jerry FC20-1488 Voevoda, Mikhail P3-d1-1325 Vogel, Ida P2-d1-666 Vogel, Mandy P3-d1-1360 Vogel, Markus P2-d2-965 Vogelgesang, Silke P2-d2-861 Volevodz, Natalya P1-d2-327, P2-d1-1107* Volkening, Lisa P2-d1-855 Völkl, Thomas P2-d2-638* Volkova, Natalia P3-d2-1479* von Schnurbein, Julia P1-d2-320 Voorend-van den Bergen, Sandra P2-d1-656 Vorontsova, Maria P2-d1-813*, P2-d1-814 Voss, Egbert P1-d2-604 Voto, Andrea P2-d1-1019, P2-d1-1021 Vottero, Alessandra P2-d1-1040, P2-d1-956 Voutetakis, Antonis P1-d3-263* Voutilainen, Raimo P2-d1-1035 Vu, Dung P1-d3-262*, P2-d2-893, P2-d3-879*, P2-d3-939 Vu-Hong, Thuy-Ai P1-d1-387 Vukovic, Rade P2-d3-654
Vulsma, Thomas P2-d1-1142 Vuorela, Nina FC3-136* Vuralli, Dogus P2-d3-1064* W
Wabitsch, Martin FC15-204, FC15-205, P1-d1-309, P1-d1-349, P1-d1-528, P1-d2-319, P1-d2-320, P1-d2-604, P1-d3-368, P2-d1-1034, P2-d2-1121, P3-d1-1269, WG2-87*, YB1 Wagner, Isabel P1-d1-318*, P2-d1-665, P2-d1-747*, P2-d2-753, P2-d3-1066, P3-d1-1360 Wagner, John P3-d1-1285 Wagner, Verena P1-d1-418 Waguespack, Steven S10, S10-43* Wajnrajch, Michael P2-d3-840 Wake, Ei-Ichi P3-d3-1316 Wakui, Masatoshi P1-d1-240 Walczak, Mieczyslaw P1-d3-406 Waldon, Karen LB3-1514* Waldthausen, Ursula P1-d1-570* Walker, Gillian P1-d1-348*, P1-d3-379, P3-d1-1204 Walker, Jan P1-d2-304, P2-d1-688 Walker, Lisa P2-d1-883 Wallace, Hamish FC8-162 Wallentin, Mikkel FC1-125 Walsh, Tom P2-d1-1001 Wan Mun, Vanessa Lee LB3-1518 Wang, Chun Lin LB2-1497* Wang, Fengyun P2-d2-1060 Wang, Qing P1-d2-518 Wang, Yong Hong P3-d1-1432 Wani, Sumayya P2-d1-784* Ward, Leanne S12, S12-49*, WG1-84* Warin, Laure P2-d1-1009*, P3-d1-1469*, P3-d3-1385 Warman, Diana P1-d3-267 Warman, Matthew WG1-83* Wasniewska, Malgorzata P1-d1-594, P1-d3-271*, P1-d1-592, P2-d1-956, P2-d2-834*, P2-d3-649 Watabe, Yoshiyuki P1-d1-494 Watanabe, Jun FC18-226 Watrobinska, Urszula P3-d2-1379* Watt, John WG6-117 Webb, Emma FC10-174*
Weber, Giovanna FC2-129, P1-d1-598, P1-d2-606, P2-d1-1019, P2-d1-1021, P2-d1-1137, S7, S7-32* Weber, Karin P1-d2-545 Weck, Melanie P1-d1-528 Wedrychowicz, Anna P2-d2-640, P2-d3-942 Weerasinghe, Kamal P3-d2-1333* Wehtje, Henrik P1-d2-484 Wei, Christina P1-d2-362*, P1-d3-336* Wei, Huiqin P2-d3-907 Wei, Li P2-d2-937* Wei, Yan P2-d1-1008 Weill, Jacques P2-d1-961* Weinel, Pamela P2-d1-1004 Weiner, Rudolf P1-d2-319 Weinhandel, Gudrun P1-d1-349 Weintrob, Naomi FC8-166, FC9-173, P2-d1-627 Weinzimer, Stuart P1-d2-430, P1-d3-442 Weise, Martina FC2-127 Wejaphikul, Karn P2-d1-660 Welsh, Michelle P1-d2-585, P1-d2-586 Welters, Alena P2-d2-934* Welzel, Maik FC8-165, P1-d3-264 Wemeau, Jean Louis FC19-228 Werner, Ralf FC8-165, P1-d1-573*, P2-d2-1113* Werther, George FC6-150, FC6-154 Wessel, Theda P1-d1-512* Wessman, Maija LB1-1493 Westrupp, Elizabeth P1-d3-440 Wharton, Gerold P2-d1-1004 Whitby, Thomas P3-d3-1357 White, Anne P1-d1-242 White, Chris P1-d2-304, P2-d1-688 White, Mary P1-d1-539, P1-d3-436*, P2-d3-767* White, Neil S5, S5-27*, P1-d3-442* White, Stefan FC5-146 Whittle, Andrew WG2-86* Whyte, Michael P2-d2-705 Wiegand, Susanna P1-d2-328*, P1-d2-462, P1-d3-555*, P3-d1-1269 Wieland, Ilse P2-d2-861 Wierzbicka, Elzbieta P2-d1-667 Wiesemann, Claudia WG6-118 Wikiera, Beata P1-d3-406, P2-d1-1077*, P2-d3-1065* Wilhelm, Franziska P1-d1-309, P1-d3-368
Wilinska, Malgorzata P1-d2-431 Wilke, Martina P1-d2-301 Wilkes, Meredith P2-d1-1076 Willems, Dominique P1-d3-437, P3-d1-1327 Willemsen, Ruben P2-d1-656* Williams, Georgina P1-d1-467* Williams, Paige P2-d1-1083 Wilson, Darrell P1-d2-428 Wilson, Jenny P1-d1-531 Wilson, Robert P1-d2-259 Wilton, Patrick P2-d1-822* Wiltshire, Esko P1-d1-345*, P2-d3-873* Winkler, Karl P1-d1-451 Wisniowiecka, Magdalena P1-d1-590 Wit, Jan FC3-132, FC9-172, FC10-177, P1-d2-326, P1-d2-478 Witchel, Selma S16, S16-61* Witteveen, Emma P1-d3-613 Woehrl, Jan P1-d1-451 Woelfle, Joachim P1-d1-421, P1-d2-601, P2-d1-1102*, P2-d2-825*, SAT9 Wojcik, Malgorzata P2-d1-664*, P2-d1-917*, P2-d2-640 Wolfenden, Helen P3-d1-1264 Wolff, Stephanie P1-d2-319 Wolfgram, Peter P1-d2-363, P1-d3-378* Wölfle, Joachim P1-d2-462, P2-d1-1034 Wollmann, Hartmut P1-d1-389, P1-d3-410, P2-d1-824 Wollnik, Bernd P1-d1-282 Wolter, Kevin LB1-1491 Wolters, Barbara P3-d1-1269 Woltersdorf, Wolf P1-d1-383, P1-d2-520 Wong, Brenda P1-d2-394, P2-d3-1070 Wong, Jarod P3-d1-1364 Wong, Sze Choong P1-d1-510* Wood, Tim P2-d1-1143 Wright, Charlotte P1-d1-468 Wu, Di P1-d2-456*, P2-d1-1007*, P2-d2-937, P3-d1-1195 Wu, Haiying P2-d2-1060 Wu, Loo Ling P2-d3-1165 Wu, Wei P1-d1-425, P1-d3-370 Wu, Yi-Lin P3-d3-1314 Wu, Yujun P2-d3-907 Wudy, Stefan FC18-227, FC5-148, P1-d2-248, P2-d1-665, P2-d3-1129 Würth, Bettina P2-d2-795
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
295
Floor Plan Exhibition Author Index
author index
author index
Wysocka-Lukasik, Beata P2-d1-669 X
Xatzipsalti, Maria P2-d2-826*, P2-d2-868*, P2-d2-900 Xi, Li P2-d2-903 Xian, Lingling FC2-126 Xie, Fang P2-d2-968 Xie, Rongrong P2-d2-1060 Xie, Wangang P1-d3-554 Xie, Xuemei P1-d1-526* Xing, Xuenong P2-d2-929 Xing, Yan P2-d2-929 Xiong, Feng P2-d2-968, P3-d2-1337* Xiong, Hui P1-d2-396* Xu, Cheng P2-d1-1082* Xu, Xiaoqin FC17-220* Xu, Zhuangjian P1-d2-518* Xu, Zidi P2-d3-907
Floor Plan Exhibition Author Index
Y
Yadav, Sangeeta P2-d1-854, P2-d3-978, P3-d1-1259 Yadav, T. Aravind P3-d1-1259* Yagasaki, Hideaki P1-d1-537, P3-d1-1407* Yagci Kupeli, Begul P3-d1-1256 Yagli, Elif LB1-1489 Yaker, Fetta Amel P2-d1-1018, P2-d1-735*, P2-d2-1026, P2-d2-1029, P3-d1-1410, P3-d2-1412 Yakovenko, Vira P2-d1-1177, P2-d2-793* Yalcin, Koray P2-d1-888 Yamada, Shiro P1-d1-243 Yamada, Shozo P1-d2-521 Yamaguchi, Rie P1-d2-582 Yamamoto, Keiko P1-d1-289, P1-d2-513 Yamamoto, Toru P3-d1-1292, P3-d1-1466* Yamamoto, Yukiyo P2-d3-1131 Yaman, Selçuk P1-d1-280 Yamaoka, Yui FC18-226 Yamazawa, Kazuki P1-d1-523 Yan, Jie P2-d3-907 Yan, Li P2-d1-1008 Yang, Chia-Feng P1-d1-501 Yang, Fan P2-d2-796* Yang, Qiulan P1-d2-456 Yang, Ruey-Bing FC3-132 Yang, Sei Won P1-d1-287, P2-d1-740 Yang, Seung P2-d1-726* Yang, Wenli P2-d3-907 Yang, Xiaohong P3-d3-1315 Yaniv, Isaac P3-d1-1251 Yanovski, Jack P2-d2-972 Yap, Fabian P2-d3-876
Yarhere, Iroro P1-d3-612*, P2-d1-723* Yarovaya, Irina P2-d1-1043, P2-d3-646 Yassin, Mohamed FC12-188, P2-d2-1149 Yasuda, Kazushi P3-d2-1237 Yates, Jason P3-d2-1303* Yatsuga, Shuichi P2-d1-1140* Yau, Steven FC6-150*, P1-d1-568 Yazarli, Esra P2-d3-766 Ye, Rong P2-d2-903, P3-d2-1376 Ye, Shandong P2-d2-929 Yeap, Phey P3-d1-1290 Yelmo, Rosa P2-d1-851, P2-d1-853, P2-d1-886, P2-d2-930 Yen, Lilly P2-d1-1004 Yeshayahu, Yonatan P1-d1-455* Yesiltepe Mutlu, Gul P1-d2299*, P2-d3-806, P2-d1-1050 Yeste Fernández, Diego P1-d1238, P1-d1-310, P2-d3-804 Yetkin, Ilhan P2-d1-924 Yi, Gu P3-d2-1474* Yildirim, Bayram P2-d1-1174 Yildiz, Metin P1-d1-530, P2-d2-963 Yilmaz Agladioglu, Sebahat P2-d1-817, P2-d3-1075, P2-d3-643, P3-d2-1296, P3-d2-1437 Yilmaz, Hikmet P3-d1-1365 Yilmaz, Yasin P2-d3-771 Yizmeyian, Anahi P2-d2-902 Yokota, Ichiro P1-d2-460* Yokota, Yukifumi P2-d2-1148, P2-d3-811 Yokoya, Susumu P1-d2-521, P1-d3-404, P2-d1-818, P3-d1-1289 Yokoyama, Misako P2-d3-811 Yoldi, Maria P3-d2-1282 Yoo, Han-Wook P1-d1-234, P1-d3-618, P2-d1-731, P2-d1-887, S17, S17-63* Yoon, Young Ahn P2-d1-1036 Yordanova, Desislava P3-d11223* Yordanova, Galina P2-d1-733* Yorifuji, Tohru FC10-176, P1-d2-432* Yoshida, Ayako P2-d1-674, P3-d1-1219 Yoshida, Hideki P1-d1-289 Yoshida, Makoto P1-d1-284 Yoshida, Yoichiro P2-d1-1144 Yoshihashi, Hiroshi P2-d3-881 Yoshii, Keisuke P3-d2-1244 Yoshimura, Kazuko P1-d2-295
* Presenting author
296
9th Joint Meeting of Paediatric Endocrinology 2013
Yotov, Yoto P1-d2-356 Youn, Seo Young P2-d3-1161 Young, Jacques FC1-122 Yousuf, Mohd P3-d1-1459 Yturriaga, Rafael P1-d1-566 Yu, Jae Hong P1-d1-416 Yu, Jeesuk P2-d2-1089*, P3-d2-1434* Yu, Seung-Do P3-d2-1434 Yüce, Özge P2-d3-770, P2-d3-944, P3-d1-1455 Yuen, Tony P1-d2-259 Yüksel Karatoprak, Elif P3-d1-1329 Yuksel, Aysegul P2-d3-806, P1-d2-299, P2-d1-1174 Yuksel, Bilgin P1-d1-241, P2-d2-701, P3-d1-1229*, P3-d1-1256, P3-d2-1215 Yuksel, Zafer P2-d1-662, P2-d2-641 Yunes, José FC13-192, FC13-193, FC20-1486 Yung, Zoe P2-d1-1138, P2-d1-1141, P2-d1-630 Yusipovich, Alexander P2-d1-813, P2-d1-814 Z
Zabel, Bernhard P1-d1-282 Zabransky, Markus P2-d2-829 Zacharin, Margaret FC14-201*, P1-d1-510, P1-d1-539*, P1-d1-568, P2-d3-1162, P2-d3-767, WG3-92* Zadik, Zvi FC4-139 Zafeiriou, Dimitrios P3-d1-1361 Zagotta, Ivana FC15-205 Zagrebaeva, Olga P3-d1-1260* Zahra, Kemali P3-d2-1241 Zaidman, Veronica P1-d3-610 Zak, Monika P1-d2-358 Zak, Teresa P1-d1-589 Žakelj, Martina P1-d2-457 Zakharova, Ekaterina P3-d1-1330 Zaleska-Dorobisz, Urszula P1-d1-589* Zaman, Farasat S12, S12-47* Zammitt, Nicola P2-d2-827 Zamproni, Ilaria P1-d2-434 Zamrazilova, Hana P1-d3-340 Zandwijken, Gladys P1-d1-509 Zangen, David P2-d1-1001 Zani, Sergio P1-d1-498, P3-d1-1402 Zanotti, Martina P2-d3-976 Zare, Elham P2-d1-748* Zaucha-Prazmo, Agnieszka P2-d2-1151
author index
Zoli, Matteo P2-d3-648 Zorludemir, Suzan P3-d1-1256 Zuccardi, Luis P2-d1-1051 Zucchini, Stefano P1-d2-402*, P1-d2-490, P2-d2-896, P2-d3-911 Zuccotti, Gian Vincenzo P1-d1-540, P2-d3-1067, P3-d2-1344 Zukerman-Levin, Nehama FC9-173 Zumbrunn, Andrea P2-d3-768 Zung, Amnon FC4-139*, P1-d1-511 Zupancic, Mirjana P2-d3-772 Zwaveling-Soonawala, Nitash P1-d1-595* Zygmunt-Górska, Agata P2-d1-664
* Presenting author 9th Joint Meeting of Paediatric Endocrinology 2013
297
Floor Plan Exhibition Author Index
Zazzetta, Emanuela P2-d3-648, P2-d3-976, P3-d1-1406 Zdravkovic, Dragan P2-d3-654 Zecchino, Clara P2-d2-1192, P3-d2-1211 Zelante, Leopoldo P2-d3-842 Zelinskaya, Nataliya P3-d3-1348 Zellagui, Hadjer P2-d1-1018, P2-d2-1026, P3-d1-1410, P3-d2-1412* Zemkova, Dana P1-d1-292 Zemkova, Daniela P2-d1-993, P2-d2-1059 Zenaty, Delphine P2-d2-1091 Zenker, Martin P2-d2-861 Zennaki, Amel P2-d2-1062, P3-d1-1221 Zennaro, Maria-Christina P2-d1-1009 Zerah, Michel P2-d1-691, P2-d1-738 Zerbini, Gianpaolo P2-d2-675 Zeybek, Umit P1-d2-359, P2-d3-776 Zhang, Dianxi P2-d3-1071 Zhang, Lina P2-d3-977 Zhang, Meihui P1-d1-526 Zhang, Meilin FC8-164 Zhang, Miaoying P2-d2-903 Zhang, Rong FC20-1484 Zhang, Ying P3-d3-1315 Zhao, Jinling P1-d2-518 Zhao, Luo FC2-126 Zhao, Zhuhui P2-d2-903, P3-d2-1376 Zhi, Dijing P3-d2-1376* Zhou, Shaoxia FC15-205 Zhu, Cheng P2-d3-907 Zhu, Huijuan P2-d3-1071 Zhu, Jie P2-d2-929* Zhu, Min P2-d2-968*, P3-d2-1337 Zhu, Mingqiang P2-d1-1007, P2-d1-1081* Zhu, Wei Fen LB2-1497 Zhu, Yi Min LB2-1497 Zieschang, Juergen P2-d1-819 Zilmer, Mihkel P2-d3-710 Zimmer, Klaus-Peter FC18-227 Zimmerman, Donald FC13-195, MTE5:1, MTE5:2 Zimmerman, Jerry P2-d1-925 Zimmermann, Alan P1-d3-407, P2-d1-1011, P2-d2-831 Ziora, Katarzyna P1-d3-406, P2-d1-823, P3-d1-1270 Zirilli, Giuseppina P1-d3-271, P2-d2-1030 Zito, Eugenio P1-d1-346, P2-d1-1039, P2-d3-874 Zlotnikova, Olga P2-d1-1043
Notes
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9th Joint Meeting of Paediatric Endocrinology 2013
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Notes
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9th Joint Meeting of Paediatric Endocrinology 2013