Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jacques Young

Showing results (171-180 of 208) with videos related to

Pageof 21
Sort By:
JCI Insight|October 5, 2016
PKA regulatory subunit 1A inactivating mutation induces serotonin signaling in primary pigmented nodular adrenal diseaseZakariae Bram, Estelle Louiset, Bruno Ragazzon, et al.
The Journal of Clinical Endocrinology and Metabolism|November 19, 2025
Real-world osilodrostat effectiveness and safety in non-pituitary Cushing syndromeAntoine Tabarin, Jérôme Bertherat, Bénédicte Decoudier, et al.
The New England Journal of Medicine|November 29, 2013
Intraadrenal corticotropin in bilateral macronodular adrenal hyperplasiaEstelle Louiset, Céline Duparc, Jacques Young, et al.
Human Mutation|December 13, 2006
Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesisCatherine Dodé, Corinne Fouveaut, Geert Mortier, et al.
Nature Reviews. Endocrinology|July 22, 2015
Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatmentUlrich Boehm, Pierre-Marc Bouloux, Mehul T Dattani, et al.
Plos Genetics|October 24, 2006
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2Catherine Dodé, Luis Teixeira, Jacqueline Levilliers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 30, 2020
Pathogenic mosaic variants in congenital hypogonadotropic hypogonadismJames S Acierno, Cheng Xu, Georgios E Papadakis, et al.
European Journal of Endocrinology|February 8, 2024
KDM1A genotyping and expression in 146 sporadic somatotroph pituitary adenomasFanny Chasseloup, Daniela Regazzo, Lucie Tosca, et al.
The Journal of Clinical Endocrinology and Metabolism|September 14, 2021
Response to Letter to the Editor from Soghomonian: "Epicardial and Pericardial Adiposity Without Myocardial Steatosis in Cushing Syndrome"Peter Wolf, Benjamin Marty, Khaoula Bouazizi, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 2021
Epicardial and Pericardial Adiposity Without Myocardial Steatosis in Cushing SyndromePeter Wolf, Benjamin Marty, Khaoula Bouazizi, et al.
Pageof 21

Showing results (171-180 of 208) with videos related to

Sort By:
Pageof 21
JCI Insight|October 5, 2016
PKA regulatory subunit 1A inactivating mutation induces serotonin signaling in primary pigmented nodular adrenal diseaseZakariae Bram, Estelle Louiset, Bruno Ragazzon, et al.
The Journal of Clinical Endocrinology and Metabolism|November 19, 2025
Real-world osilodrostat effectiveness and safety in non-pituitary Cushing syndromeAntoine Tabarin, Jérôme Bertherat, Bénédicte Decoudier, et al.
The New England Journal of Medicine|November 29, 2013
Intraadrenal corticotropin in bilateral macronodular adrenal hyperplasiaEstelle Louiset, Céline Duparc, Jacques Young, et al.
Human Mutation|December 13, 2006
Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesisCatherine Dodé, Corinne Fouveaut, Geert Mortier, et al.
Nature Reviews. Endocrinology|July 22, 2015
Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatmentUlrich Boehm, Pierre-Marc Bouloux, Mehul T Dattani, et al.
Plos Genetics|October 24, 2006
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2Catherine Dodé, Luis Teixeira, Jacqueline Levilliers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 30, 2020
Pathogenic mosaic variants in congenital hypogonadotropic hypogonadismJames S Acierno, Cheng Xu, Georgios E Papadakis, et al.
European Journal of Endocrinology|February 8, 2024
KDM1A genotyping and expression in 146 sporadic somatotroph pituitary adenomasFanny Chasseloup, Daniela Regazzo, Lucie Tosca, et al.
The Journal of Clinical Endocrinology and Metabolism|September 14, 2021
Response to Letter to the Editor from Soghomonian: "Epicardial and Pericardial Adiposity Without Myocardial Steatosis in Cushing Syndrome"Peter Wolf, Benjamin Marty, Khaoula Bouazizi, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 2021
Epicardial and Pericardial Adiposity Without Myocardial Steatosis in Cushing SyndromePeter Wolf, Benjamin Marty, Khaoula Bouazizi, et al.
Pageof 21