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Philippe Touraine

Showing results (141-150 of 156) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|April 12, 2024
Lessons From Prospective Longitudinal Follow-up of a French APECED CohortLinda Humbert, Emmanuelle Proust-Lemoine, Sylvain Dubucquoi, et al.
Annales D'Endocrinologie|August 14, 2023
Position statement on the diagnosis and management of acromegaly: The French National Diagnosis and Treatment Protocol (NDTP)Thierry Brue, Haïfa Rahabi, Abdoulaye Barry, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2013
Study of anti-Müllerian hormone and its relation to the subsequent probability of pregnancy in 112 patients with systemic lupus erythematosus, exposed or not to cyclophosphamideNathalie Morel, Anne Bachelot, Zeina Chakhtoura, 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.
Endocrine Connections|October 13, 2022
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centresLuca Persani, Martine Cools, Stamatina Ioakim, et al.
Annals of Neurology|May 14, 2020
GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency SyndromeA Reghan Foley, Yaqun Zou, James E Dunford, et al.
The Journal of Clinical Endocrinology and Metabolism|February 22, 2023
Assessment of Puberty and Hypothalamic-Pituitary-Gonadal Axis Function After Childhood Brain Tumor TreatmentManon Rosimont, Dulanjalee Kariyawasam, Dinane Samara-Boustani, et al.
European Journal of Endocrinology|May 6, 2022
Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patientsLucas Bouys, Anna Vaczlavik, Anne Jouinot, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 2021
High Prevalence of Early Endocrine Disorders After Childhood Brain Tumors in a Large CohortLaura Gabriela González Briceño, Dulanjalee Kariyawasam, Dinane Samara-Boustani, et al.
Human Mutation|July 22, 2008
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndromeDiane Beysen, Sarah De Jaegere, David Amor, et al.
Pageof 16

Showing results (141-150 of 156) with videos related to

Sort By:
Pageof 16
The Journal of Clinical Endocrinology and Metabolism|April 12, 2024
Lessons From Prospective Longitudinal Follow-up of a French APECED CohortLinda Humbert, Emmanuelle Proust-Lemoine, Sylvain Dubucquoi, et al.
Annales D'Endocrinologie|August 14, 2023
Position statement on the diagnosis and management of acromegaly: The French National Diagnosis and Treatment Protocol (NDTP)Thierry Brue, Haïfa Rahabi, Abdoulaye Barry, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2013
Study of anti-Müllerian hormone and its relation to the subsequent probability of pregnancy in 112 patients with systemic lupus erythematosus, exposed or not to cyclophosphamideNathalie Morel, Anne Bachelot, Zeina Chakhtoura, 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.
Endocrine Connections|October 13, 2022
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centresLuca Persani, Martine Cools, Stamatina Ioakim, et al.
Annals of Neurology|May 14, 2020
GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency SyndromeA Reghan Foley, Yaqun Zou, James E Dunford, et al.
The Journal of Clinical Endocrinology and Metabolism|February 22, 2023
Assessment of Puberty and Hypothalamic-Pituitary-Gonadal Axis Function After Childhood Brain Tumor TreatmentManon Rosimont, Dulanjalee Kariyawasam, Dinane Samara-Boustani, et al.
European Journal of Endocrinology|May 6, 2022
Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patientsLucas Bouys, Anna Vaczlavik, Anne Jouinot, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 2021
High Prevalence of Early Endocrine Disorders After Childhood Brain Tumors in a Large CohortLaura Gabriela González Briceño, Dulanjalee Kariyawasam, Dinane Samara-Boustani, et al.
Human Mutation|July 22, 2008
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndromeDiane Beysen, Sarah De Jaegere, David Amor, et al.
Pageof 16