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Philippe Touraine

Showing results (101-110 of 156) with videos related to

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European Journal of Endocrinology|March 7, 2024
Impact of exenatide on weight loss and eating behavior in adults with craniopharyngioma-related obesity: the CRANIOEXE randomized placebo-controlled trialBlandine Gatta-Cherifi, Kamel Mohammedi, Tanguy Cariou, et al.
Human Genetics|October 14, 2021
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing lossFarid Ullah, Waqar Rauf, Kamal Khan, et al.
European Journal of Endocrinology|November 21, 2014
Ovarian macrocysts and gonadotrope-ovarian axis disruption in premenopausal women receiving mitotane for adrenocortical carcinoma or Cushing's diseaseSylvie Salenave, Valérie Bernard, Christine Do Cao, et al.
Human Mutation|September 22, 2016
An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the LiteratureJustine Lerat, Laurence Jonard, Natalie Loundon, et al.
Journal of Assisted Reproduction and Genetics|November 3, 2023
NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insightsPénélope Jordan, Camille Verebi, Sandrine Perol, et al.
European Journal of Endocrinology|April 9, 2008
Impact of total cumulative glucocorticoid dose on bone mineral density in patients with 21-hydroxylase deficiencyZeina Chakhtoura, Anne Bachelot, Dinane Samara-Boustani, et al.
Neuro-Oncology|March 11, 2024
Very long-term outcomes of pediatric patients treated for optic pathway gliomas: A longitudinal cohort studyAlice Morin, Rodrigue Allodji, Dulanjalee Kariyawasam, et al.
Frontiers in Endocrinology|October 26, 2023
Identifying patient-related predictors of permanent growth hormone deficiencyVeronica Mericq, German Iñiguez, Graziella Pinto, et al.
European Journal of Endocrinology|April 29, 2006
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failurePaul Laissue, Sophie Christin-Maitre, Philippe Touraine, 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.
Pageof 16

Showing results (101-110 of 156) with videos related to

Sort By:
Pageof 16
European Journal of Endocrinology|March 7, 2024
Impact of exenatide on weight loss and eating behavior in adults with craniopharyngioma-related obesity: the CRANIOEXE randomized placebo-controlled trialBlandine Gatta-Cherifi, Kamel Mohammedi, Tanguy Cariou, et al.
Human Genetics|October 14, 2021
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing lossFarid Ullah, Waqar Rauf, Kamal Khan, et al.
European Journal of Endocrinology|November 21, 2014
Ovarian macrocysts and gonadotrope-ovarian axis disruption in premenopausal women receiving mitotane for adrenocortical carcinoma or Cushing's diseaseSylvie Salenave, Valérie Bernard, Christine Do Cao, et al.
Human Mutation|September 22, 2016
An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the LiteratureJustine Lerat, Laurence Jonard, Natalie Loundon, et al.
Journal of Assisted Reproduction and Genetics|November 3, 2023
NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insightsPénélope Jordan, Camille Verebi, Sandrine Perol, et al.
European Journal of Endocrinology|April 9, 2008
Impact of total cumulative glucocorticoid dose on bone mineral density in patients with 21-hydroxylase deficiencyZeina Chakhtoura, Anne Bachelot, Dinane Samara-Boustani, et al.
Neuro-Oncology|March 11, 2024
Very long-term outcomes of pediatric patients treated for optic pathway gliomas: A longitudinal cohort studyAlice Morin, Rodrigue Allodji, Dulanjalee Kariyawasam, et al.
Frontiers in Endocrinology|October 26, 2023
Identifying patient-related predictors of permanent growth hormone deficiencyVeronica Mericq, German Iñiguez, Graziella Pinto, et al.
European Journal of Endocrinology|April 29, 2006
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failurePaul Laissue, Sophie Christin-Maitre, Philippe Touraine, 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.
Pageof 16