ESPE Abstracts Search

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Fetal and Post-Natal Growth are Impaired in Children with Deletions of the GH1 Gene: Description of a Cohort of 14 Patients | ESPE2019
Elsa Darvish; Marie Legendre; Irene Netchine; Serge Amselem; Frederic Brioude
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-257
Published: 2019-08-22

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Lessons From a Patient Carrying Both an 11p Paternal Duplication and 15q Deletion, Illustrating the Roles of IGF2 and IGF1R in Growth Regulation | ESPE2019
Frederic Brioude; Sandra Chantot- Bastaraud; Sandra Whalen; Irene Netchine; Eloise Giabicani
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-218
Published: 2019-08-22

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Clinical Characteristics, Puberty Pattern and Adult or Near-adult-height Data in a Group of Patients with Growth Failure due to Severe Primary IGF-1 Deficiency (GROWPATI Study) | ESPE2019
Athanasia Stoupa; Christine Lorraud; Isabelle Flechtner; Magali Viaud; Graziella Pinto; Dinane Samara-Boustani; Caroline Thalass
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-80
Published: 2019-08-22

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Increasing Knowledge in IGF1R Defects: Lessons from 20 New Patients | ESPE2019
Eloïse Giabicani; Marjorie Willems; Virginie Steunou; Sandra Chantot-Bastaraud; Sylvie Rossignol; Bouc Yves Le; Irène Netchine
http://abstracts.eurospe.org/hrp/0092/hrp0092FC12.1
Published: 2019-08-22

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Silver Russell and Beckwith-Wiedemann Syndromes: Mosaic Distribution of Epigenetic Anomalies | ESPE2018
Aurelie Pham; Eloise Giabicani; Virginie Steunou; Irene Netchine; Frederic Brioude
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p180.htm
Published: 2018-08-28

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Clinical and Preliminary Molecular Description of a Cohort of Patients with Growth Retardation due to Severe Primary IGF1 Deficiency (GROWPATI Study) | ESPE2018
Athanasia Stoupa; Magali Viaud; Isabelle Flechtner; Graziella Pinto; Dinane Samara-Boustani; Caroline Thalassinos; Laura Gabriel
http://abstracts.eurospe.org/hrp/0089/hrp0089p2-p207.htm
Published: 2018-08-28