Showing results (151-160 of 339) with videos related to
Sort By:
Pageof 34
Molecular and Cellular Endocrinology|April 8, 2014
Characterization of a novel CYP19A1 (aromatase) R192H mutation causing virilization of a 46,XX newborn, undervirilization of the 46,XY brother, but no virilization of the mother during pregnanciesNadia Bouchoucha, Dinane Samara-Boustani, Amit V Pandey, et al.The Journal of Clinical Endocrinology and Metabolism|July 16, 2019
Treatment of Children With GH in the United States and Europe: Long-Term Follow-Up From NordiNet® IOS and ANSWER ProgramLars Sävendahl, Michel Polak, Philippe Backeljauw, et al.Diabetologia|January 31, 2014
Dyrk1a haploinsufficiency induces diabetes in mice through decreased pancreatic beta cell massLatif Rachdi, Dulanjalee Kariyawasam, Fanny Guez, et al.Bone Reports|April 4, 2022
Growth charts in FGFR2- and FGFR3-related faciocraniosynostosesCaroline Ea, Quentin Hennocq, Arnaud Picard, et al.BMJ Paediatrics Open|May 16, 2020
Growth hormone treatment in Prader-Willi syndrome patients: systematic review and meta-analysisCaroline de Gouveia Buff Passone, Ruth Rocha Franco, Simone Sakura Ito, et al.Journal of the Endocrine Society|September 22, 2025
Comparative Outcomes of GH Treatment in Pediatric Idiopathic Short Stature and GH DeficiencyMoshe Phillip, M Jennifer Abuzzahab, Alberto Pietropoli, et al.The Journal of Clinical Endocrinology and Metabolism|October 21, 2004
PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformationsSylvia Sura Trueba, Joëlle Augé, Géraldine Mattei, et al.Diabetes|September 28, 2004
Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patientsMartine Vaxillaire, Céline Populaire, Kanetee Busiah, et al.Molecular Metabolism|February 24, 2018
Modeling human pancreatic beta cell dedifferentiationMarc Diedisheim, Masaya Oshima, Olivier Albagli, et al.European Journal of Pediatrics|October 4, 2007
What's new in metabolic and genetic hypoglycaemias: diagnosis and managementVassili Valayannopoulos, Stéphane Romano, Karine Mention, et al.Pageof 34