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Jacques Young

Showing results (191-200 of 208) with videos related to

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European Journal of Endocrinology|April 15, 2026
Risk of bone overstimulation in long-term PTH(1-34) therapy for hypoparathyroidismRebecca Fischler, Anne-Lise Lecoq, Pascal Houillier, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 2014
The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patientsSéverine Marcos, Julie Sarfati, Chrystel Leroy, et al.
The Journal of Clinical Endocrinology and Metabolism|July 26, 2013
One-year progression-free survival of therapy-naive patients with malignant pheochromocytoma and paragangliomaSégolène Hescot, Sophie Leboulleux, Laurence Amar, et al.
Human Molecular Genetics|July 10, 2012
An ancient founder mutation in PROKR2 impairs human reproductionMagdalena Avbelj Stefanija, Marc Jeanpierre, Gerasimos P Sykiotis, et al.
Clinical Chemistry|December 6, 2021
Galaxy Is a Suitable Bioinformatics Platform for the Molecular Diagnosis of Human Genetic Disorders Using High-Throughput Sequencing Data Analysis: Five Years of Experience in a Clinical LaboratoryKenneth Chappell, Bruno Francou, Christophe Habib, et al.
The Journal of Clinical Endocrinology and Metabolism|January 30, 2014
Ketoconazole in Cushing's disease: is it worth a try?Frederic Castinetti, Laurence Guignat, Pauline Giraud, et al.
Orphanet Journal of Rare Diseases|March 22, 2017
Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism, Corin Badiu, Marco Bonomi, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadismHichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, et al.
The Journal of Clinical Endocrinology and Metabolism|March 31, 2015
Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National SurveyClaire Bouvattier, Laure Esterle, Peggy Renoult-Pierre, et al.
JCI Insight|September 22, 2017
Adrenal GIPR expression and chromosome 19q13 microduplications in GIP-dependent Cushing's syndromeAnne-Lise Lecoq, Constantine A Stratakis, Say Viengchareun, et al.
Pageof 21

Showing results (191-200 of 208) with videos related to

Sort By:
Pageof 21
European Journal of Endocrinology|April 15, 2026
Risk of bone overstimulation in long-term PTH(1-34) therapy for hypoparathyroidismRebecca Fischler, Anne-Lise Lecoq, Pascal Houillier, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 2014
The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patientsSéverine Marcos, Julie Sarfati, Chrystel Leroy, et al.
The Journal of Clinical Endocrinology and Metabolism|July 26, 2013
One-year progression-free survival of therapy-naive patients with malignant pheochromocytoma and paragangliomaSégolène Hescot, Sophie Leboulleux, Laurence Amar, et al.
Human Molecular Genetics|July 10, 2012
An ancient founder mutation in PROKR2 impairs human reproductionMagdalena Avbelj Stefanija, Marc Jeanpierre, Gerasimos P Sykiotis, et al.
Clinical Chemistry|December 6, 2021
Galaxy Is a Suitable Bioinformatics Platform for the Molecular Diagnosis of Human Genetic Disorders Using High-Throughput Sequencing Data Analysis: Five Years of Experience in a Clinical LaboratoryKenneth Chappell, Bruno Francou, Christophe Habib, et al.
The Journal of Clinical Endocrinology and Metabolism|January 30, 2014
Ketoconazole in Cushing's disease: is it worth a try?Frederic Castinetti, Laurence Guignat, Pauline Giraud, et al.
Orphanet Journal of Rare Diseases|March 22, 2017
Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism, Corin Badiu, Marco Bonomi, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadismHichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, et al.
The Journal of Clinical Endocrinology and Metabolism|March 31, 2015
Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National SurveyClaire Bouvattier, Laure Esterle, Peggy Renoult-Pierre, et al.
JCI Insight|September 22, 2017
Adrenal GIPR expression and chromosome 19q13 microduplications in GIP-dependent Cushing's syndromeAnne-Lise Lecoq, Constantine A Stratakis, Say Viengchareun, et al.
Pageof 21