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Showing page 1 of results 1 - 10 of about 12 pages

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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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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

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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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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

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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

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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

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BOREALIN Mutations in Thyroid Dysgenesis Reveal a New Function of this Protein in Cell Adhesion and Migration | ESPE2016
Aurore Carre; Athanasia Stoupa; Dulanjalee Karyiawasam; Manelle Gueriouz; Cyrille Ramond; Sebastien Gaujoux; Nicolas Glaser; Jul
http://abstracts.eurospe.org/hrp/0086/hrp0086ha2.htm
Published: 2016-08-19

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Adult Height after Growth Hormone Treatment and its Association with X Chromosome Dosage in Turner Syndrome: a Cross-Sectional Database Analysis of the French National Rare Disease Network | ESPE2015
Elodie Fiot; Delphine Zenaty; Priscilla Boizeau; Jeremie Haignere; Sophie Dos Santos; Juliane Leger; Syndrome Study Group French
http://abstracts.eurospe.org/hrp/0084/hrp0084p1-141.htm
Published: 2015-08-26

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X Chromosome Gene Dosage and the Risk of Developing Congenital and Acquired Traits in Turner Syndrome: a Cross-Sectional Database Analysis of the French National Rare Disease Network | ESPE2015
Delphine Zenaty; Elodie Fiot; Priscilla Boizeau; Jeremie Haignere; Sophie Dos Santos; Jean Claude Carel; Juliane Leger; Turner S
http://abstracts.eurospe.org/hrp/0084/hrp0084fc5.4.htm
Published: 2015-08-26

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Triiodothyronine-Predominant Graves' Disease (T3-P-GD): Description and Management in Childhood | ESPE2014
Julie Harvengt; Priscilla Boizeau; Delphine Zenaty; Anne Paulsen; Dominique Simon; Sophie Guilmin Crepon; Corinne Alberti; Jean-
http://abstracts.eurospe.org/hrp/0082/hrp0082p1-d2-251.htm
Published: 2014-08-28

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