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Showing page 1 of results 1 - 10 of about 14 pages

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Extreme Short Stature and Neurological Impairment in a 17-Year-Old Male with Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation | ESPE2019
Hussein Majdoub; Serge Amselem; Dani Bercovich; Shoshana Rath; Yardena Tenenbaum-Rakover
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-200
Published: 2019-08-22

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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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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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Extreme Short Stature and Neurological Impairment in a 17-Year-Old Male with Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation | ESPE2019
Hussein Majdoub; Serge Amselem; Dani Bercovich; Shoshana Rath; Yardena Tenenbaum-Rakover
http://abstracts.eurospe.org/hrp/0092/hrp0092p3-200.html
Published: 2019-08-22

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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.html
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.html
Published: 2019-08-22

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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

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Contribution of Functionally Assessed GHRHR Mutations to Idiopathic Isolated Growth Hormone Deficiency in a Cohort of 312 Unrelated Patients | ESPE2018
Enzo Cohen; Sabrina Belkacem; Soumeya Fedala; Nathalie Collot; Eliane Khallouf; Florence Dastot; Michel Polak; Philippe Duquesno
http://abstracts.eurospe.org/hrp/0089/hrp0089fc9.2.htm
Published: 2018-08-28

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Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance - Identification of New Variants and Impact on the Inheritance Pattern | ESPE2016
Marie Legendre; Florence Dastot; Nathalie Collot; Philippe Duquesnoy; Enzo Cohen; Marie-Laure Sobrier; Paola Adiceam; Donald And
http://abstracts.eurospe.org/hrp/0086/hrp0086rfc14.2.htm
Published: 2016-08-19

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Important Contribution of GH, GHRHR and GHSR Mutations in Isolated Growth Hormone Deficiency with a Normal Location of the Posterior Pituitary -Functional Characterization of New Variants | ESPE2016
Enzo Cohen; Marie-Laure Sobrier; Florence Dastot; Nathalie Collot; Sophie Rose; Aude Soleyan; Marie-Pierre Vie-Luton; Philippe D
http://abstracts.eurospe.org/hrp/0086/hrp0086rfc14.1.htm
Published: 2016-08-19

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