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Showing page 1 of results 1 - 10 of about 31 pages

100% match
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Non-Isolated Central Precocious Puberty: Prevalence of Brain Lesions and Other Associated Disorders | ESPE2018
Selmen Wannes; Maleh Monique El; Roux Nicolas De; Delphine Zenaty; Dominique Simon; Laetitia Martinerie; Caroline Storey; George
http://abstracts.eurospe.org/hrp/0089/hrp0089rfc9.5.htm
Published: 2018-08-28

86% match
9 hit(s)
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Early Determinants of Thyroid Function Outcome in Children with Congenital Hypothyroidism and a Normally Located Thyroid Gland: A Regional Cohort Study | ESPE2018
Carole Saba; Sophie Guilmin-Crepon; Delphine Zenaty; Laetitia Martinerie; Anne Paulsen; Dominique Simon; Sophie Dos Santos; Jere
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p248.htm
Published: 2018-08-28

36% match
6 hit(s)
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Arbitrary Cutoffs Lead to Underestimation of Metabolic Abnormalities in Obese Children: The Value of Age- and Sex-adjusted Normative Values | ESPE2016
Gonod Adele Carlier; Ahlam Azar; Nathalie Lecomte; Perrod Melanie Amouyal; Manon Prevot; Adeline Jacques; Crepon Sophie Guilmin;
http://abstracts.eurospe.org/hrp/0086/hrp0086p2-p527.htm
Published: 2016-08-19

18% match
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Factors Affecting Loss to Follow-Up for Patients with Chronic Endocrine Conditions During the Pediatric Period: A Cohort Study at a Reference Center for Rare Diseases | ESPE2019
Laura Atger-Lallier; Sophie Guilmin-Crepon; Priscilla Boizeau; Delphine Zenaty; Dominique Simon; Anne Paulsen; Laetitia Martiner
http://abstracts.eurospe.org/hrp/0092/hrp0092RFC3.2
Published: 2019-08-22

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Mutations in the DEAH-box RNA Helicase DHX37 are a Frequent Cause of 46,XY Gonadal Dysgenesis and 46,XY Testicular Regression Syndrome | ESPE2019
Ken McElreavey; Anne Jorgensen; Caroline Eozenou; Tiphanie Merel; Joelle Bignon-Topalovic; Daisy Tan; Denis Houzelstein; Federic
http://abstracts.eurospe.org/hrp/0092/hrp0092FC10.3
Published: 2019-08-22

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Factors Affecting Loss to Follow-Up for Patients with Chronic Endocrine Conditions During the Pediatric Period: A Cohort Study at a Reference Center for Rare Diseases | ESPE2019
Laura Atger-Lallier; Sophie Guilmin-Crepon; Priscilla Boizeau; Delphine Zenaty; Dominique Simon; Anne Paulsen; Laetitia Martiner
http://abstracts.eurospe.org/hrp/0092/hrp0092rfc3.2.html
Published: 2019-08-22

18% match
3 hit(s)
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Mutations in the DEAH-box RNA Helicase DHX37 are a Frequent Cause of 46,XY Gonadal Dysgenesis and 46,XY Testicular Regression Syndrome | ESPE2019
Ken McElreavey; Anne Jorgensen; Caroline Eozenou; Tiphanie Merel; Joelle Bignon-Topalovic; Daisy Tan; Denis Houzelstein; Federic
http://abstracts.eurospe.org/hrp/0092/hrp0092fc10.3.html
Published: 2019-08-22

18% match
3 hit(s)
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Neonatal Monitoring of Newborns Born from Mothers with Graves' Disease: Results of a Retrospective Monocentric Study | ESPE2018
Cecile Dumaine; Sophie Guilmin Crepon; Justine Pages; Didier Chevenne; Jonathan Rosenblatt; Caroline Storey; Laetitia Martinerie
http://abstracts.eurospe.org/hrp/0089/hrp0089p2-p382.htm
Published: 2018-08-28

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3 hit(s)
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Does X-Chromosome Gene Dosage Determine Growth and Phenotypic Features in Turner Syndrome with 45,X/46,XX Mosaicism on Standard Karyotyping? A Cross-Sectional Analysis of the French National Rare Disease Network Database | ESPE2018
Elodie Fiot; Delphine Zenaty; Paul Pick; Patricia Boizeau; Jeremy Haignere; Santos Sophie Dos; Sophie Christin-Maitre; Jean-Clau
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p159.htm
Published: 2018-08-28

18% match
3 hit(s)
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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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