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Jacques Young

Showing results (181-190 of 208) with videos related to

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American Journal of Human Genetics|May 7, 2013
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafnessVeronique Pingault, Virginie Bodereau, Viviane Baral, et al.
International Journal of Cancer|April 23, 2014
SDHB mutations are associated with response to temozolomide in patients with metastatic pheochromocytoma or paragangliomaJulien Hadoux, Judith Favier, Jean-Yves Scoazec, et al.
Diabetes|October 27, 2005
Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5Christine Bellanné-Chantelot, Séverine Clauin, Dominique Chauveau, et al.
The Journal of Clinical Endocrinology and Metabolism|September 19, 2019
Cortisol and Aldosterone Responses to Hypoglycemia and Na Depletion in Women With Non-Classic 21-Hydroxylase DeficiencyPeter Kamenický, Anne Blanchard, Antonin Lamaziere, et al.
Clinical Obesity|July 31, 2025
IMPROVE 2023: The 2nd International Meeting on Pathway-Related Obesity: Vision & EvidenceKarine Clément, Erica L T van den Akker, Jesús Argente, et al.
The Journal of Clinical Endocrinology and Metabolism|December 5, 2022
Efficacy and Safety of Osilodrostat in Paraneoplastic Cushing Syndrome: A Real-World Multicenter Study in FranceAlexandre Dormoy, Magalie Haissaguerre, Géraldine Vitellius, et al.
The Lancet. Diabetes & Endocrinology|May 15, 2025
Surgery for the treatment of arterial hypertension in patients with unilateral adrenal incidentalomas and mild autonomous cortisol secretion (CHIRACIC): a multicentre, open-label, superiority randomised controlled trialAntoine Tabarin, Stéphanie Espiard, Timo Deutschbein, et al.
EMBO Molecular Medicine|May 4, 2016
IGSF10 mutations dysregulate gonadotropin-releasing hormone neuronal migration resulting in delayed pubertySasha R Howard, Leonardo Guasti, Gerard Ruiz-Babot, et al.
Plos Genetics|August 29, 2012
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndromeNaresh Kumar Hanchate, Paolo Giacobini, Pierre Lhuillier, et al.
The Journal of Clinical Endocrinology and Metabolism|August 28, 2013
Molecular screening for a personalized treatment approach in advanced adrenocortical cancerMaria Cristina De Martino, Abir Al Ghuzlan, Sebastien Aubert, et al.
Pageof 21

Showing results (181-190 of 208) with videos related to

Sort By:
Pageof 21
American Journal of Human Genetics|May 7, 2013
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafnessVeronique Pingault, Virginie Bodereau, Viviane Baral, et al.
International Journal of Cancer|April 23, 2014
SDHB mutations are associated with response to temozolomide in patients with metastatic pheochromocytoma or paragangliomaJulien Hadoux, Judith Favier, Jean-Yves Scoazec, et al.
Diabetes|October 27, 2005
Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5Christine Bellanné-Chantelot, Séverine Clauin, Dominique Chauveau, et al.
The Journal of Clinical Endocrinology and Metabolism|September 19, 2019
Cortisol and Aldosterone Responses to Hypoglycemia and Na Depletion in Women With Non-Classic 21-Hydroxylase DeficiencyPeter Kamenický, Anne Blanchard, Antonin Lamaziere, et al.
Clinical Obesity|July 31, 2025
IMPROVE 2023: The 2nd International Meeting on Pathway-Related Obesity: Vision & EvidenceKarine Clément, Erica L T van den Akker, Jesús Argente, et al.
The Journal of Clinical Endocrinology and Metabolism|December 5, 2022
Efficacy and Safety of Osilodrostat in Paraneoplastic Cushing Syndrome: A Real-World Multicenter Study in FranceAlexandre Dormoy, Magalie Haissaguerre, Géraldine Vitellius, et al.
The Lancet. Diabetes & Endocrinology|May 15, 2025
Surgery for the treatment of arterial hypertension in patients with unilateral adrenal incidentalomas and mild autonomous cortisol secretion (CHIRACIC): a multicentre, open-label, superiority randomised controlled trialAntoine Tabarin, Stéphanie Espiard, Timo Deutschbein, et al.
EMBO Molecular Medicine|May 4, 2016
IGSF10 mutations dysregulate gonadotropin-releasing hormone neuronal migration resulting in delayed pubertySasha R Howard, Leonardo Guasti, Gerard Ruiz-Babot, et al.
Plos Genetics|August 29, 2012
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndromeNaresh Kumar Hanchate, Paolo Giacobini, Pierre Lhuillier, et al.
The Journal of Clinical Endocrinology and Metabolism|August 28, 2013
Molecular screening for a personalized treatment approach in advanced adrenocortical cancerMaria Cristina De Martino, Abir Al Ghuzlan, Sebastien Aubert, et al.
Pageof 21