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Yves Morel

Showing results (71-80 of 83) with videos related to

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Hormone Research in Paediatrics|February 14, 2015
Inadequate cortisol response to the tetracosactide (Synacthen®) test in non-classic congenital adrenal hyperplasia: an exception to the rule?Athanasia Stoupa, Laura González-Briceño, Graziella Pinto, et al.
European Journal of Endocrinology|January 13, 2012
Impaired puberty, fertility, and final stature in 45,X/46,XY mixed gonadal dysgenetic patients raised as boysLaetitia Martinerie, Yves Morel, Claire-Lise Gay, et al.
The Journal of Clinical Investigation|December 20, 2022
Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonationCécily Lucas, Kay-Sara Sauter, Michael Steigert, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2019
Exposure to Glucocorticoids in the First Part of Fetal Life is Associated with Insulin Secretory Defect in Adult HumansJean-Pierre Riveline, Baz Baz, Jean-Louis Nguewa, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2020
Preoperative Topical Estrogen Treatment vs Placebo in 244 Children With Midshaft and Posterior HypospadiasDaniela Gorduza, Ingrid Plotton, Laurent Remontet, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2009
Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family membersMaud Bidet, Christine Bellanné-Chantelot, Marie-Béatrice Galand-Portier, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 2, 2022
Clinical, biochemical, and biomolecular aspects of congenital adrenal hyperplasia in a group of Cameroonian children and adolescentsSuzanne Sap Ngo Um, Ritha Mbono Betoko, Isabelle Mekone, et al.
European Journal of Endocrinology|May 1, 2016
NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defectsFlorence Roucher-Boulez, Delphine Mallet-Motak, Dinane Samara-Boustani, et al.
Annales D'Endocrinologie|October 10, 2025
Rare causes of pediatric primary adrenal insufficiency: Data from a large nationwide Tunisian cohortRania Khalfallah, Fakhri Kallabi, Delphine Mallet, et al.
The Journal of Clinical Endocrinology and Metabolism|December 5, 2013
Novel associations in disorders of sex development: findings from the I-DSD RegistryKathryn Cox, Jillian Bryce, Jipu Jiang, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Hormone Research in Paediatrics|February 14, 2015
Inadequate cortisol response to the tetracosactide (Synacthen®) test in non-classic congenital adrenal hyperplasia: an exception to the rule?Athanasia Stoupa, Laura González-Briceño, Graziella Pinto, et al.
European Journal of Endocrinology|January 13, 2012
Impaired puberty, fertility, and final stature in 45,X/46,XY mixed gonadal dysgenetic patients raised as boysLaetitia Martinerie, Yves Morel, Claire-Lise Gay, et al.
The Journal of Clinical Investigation|December 20, 2022
Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonationCécily Lucas, Kay-Sara Sauter, Michael Steigert, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2019
Exposure to Glucocorticoids in the First Part of Fetal Life is Associated with Insulin Secretory Defect in Adult HumansJean-Pierre Riveline, Baz Baz, Jean-Louis Nguewa, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2020
Preoperative Topical Estrogen Treatment vs Placebo in 244 Children With Midshaft and Posterior HypospadiasDaniela Gorduza, Ingrid Plotton, Laurent Remontet, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2009
Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family membersMaud Bidet, Christine Bellanné-Chantelot, Marie-Béatrice Galand-Portier, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 2, 2022
Clinical, biochemical, and biomolecular aspects of congenital adrenal hyperplasia in a group of Cameroonian children and adolescentsSuzanne Sap Ngo Um, Ritha Mbono Betoko, Isabelle Mekone, et al.
European Journal of Endocrinology|May 1, 2016
NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defectsFlorence Roucher-Boulez, Delphine Mallet-Motak, Dinane Samara-Boustani, et al.
Annales D'Endocrinologie|October 10, 2025
Rare causes of pediatric primary adrenal insufficiency: Data from a large nationwide Tunisian cohortRania Khalfallah, Fakhri Kallabi, Delphine Mallet, et al.
The Journal of Clinical Endocrinology and Metabolism|December 5, 2013
Novel associations in disorders of sex development: findings from the I-DSD RegistryKathryn Cox, Jillian Bryce, Jipu Jiang, et al.
Pageof 9