Scientific Programme, ePosters & Abstracts
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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
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
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
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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