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

Anne Bachelot

Showing results (91-100 of 102) with videos related to

Pageof 11
Sort By:
European Journal of Endocrinology|May 5, 2009
Phenotyping and genetic studies of 357 consecutive patients presenting with premature ovarian failureAnne Bachelot, Agnès Rouxel, Nathalie Massin, et al.
Gene|June 28, 2024
Revisiting GDF9 variants in primary ovarian insufficiency: A shift from dominant to recessive pathogenicity?Pénélope Jordan, Camille Verebi, Bérénice Hervé, et al.
The Journal of Clinical Endocrinology and Metabolism|June 21, 2013
Primary adrenal insufficiency due to bilateral adrenal hemorrhage-adrenal infarction in the antiphospholipid syndrome: long-term outcome of 16 patientsIsolde Ramon, Alexis Mathian, Anne Bachelot, et al.
Fertility and Sterility|February 4, 2022
Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of familiesAlexandre Rouen, Eli Rogers, Véronique Kerlan, et al.
Clinical Genetics|April 1, 2024
Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiologyPénélope Jordan, Camille Verebi, Bérénice Hervé, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|July 4, 2026
Early Metabolic Risk in Childhood Brain Cancer Survivors with Childhood-Onset Growth Hormone DeficiencyAlice Casiraghi, Olivier Pollé, Clément Bailly, et al.
Annales D'Endocrinologie|March 7, 2024
Position statement on the diagnosis and management of congenital pituitary deficiency in adults: The French National Diagnosis and Treatment Protocol (NDTP)Sarah Castets, Frédérique Albarel, Anne Bachelot, 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.
Endocrine Connections|January 6, 2023
Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in FranceEstelle Bonnet, Mathias Winter, Delphine Mallet, et al.
Annales D'Endocrinologie|September 11, 2021
Position statement on the diagnosis and management of premature/primary ovarian insufficiency (except Turner Syndrome)Sophie Christin-Maitre, Maria Givony, Frédérique Albarel, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
European Journal of Endocrinology|May 5, 2009
Phenotyping and genetic studies of 357 consecutive patients presenting with premature ovarian failureAnne Bachelot, Agnès Rouxel, Nathalie Massin, et al.
Gene|June 28, 2024
Revisiting GDF9 variants in primary ovarian insufficiency: A shift from dominant to recessive pathogenicity?Pénélope Jordan, Camille Verebi, Bérénice Hervé, et al.
The Journal of Clinical Endocrinology and Metabolism|June 21, 2013
Primary adrenal insufficiency due to bilateral adrenal hemorrhage-adrenal infarction in the antiphospholipid syndrome: long-term outcome of 16 patientsIsolde Ramon, Alexis Mathian, Anne Bachelot, et al.
Fertility and Sterility|February 4, 2022
Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of familiesAlexandre Rouen, Eli Rogers, Véronique Kerlan, et al.
Clinical Genetics|April 1, 2024
Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiologyPénélope Jordan, Camille Verebi, Bérénice Hervé, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|July 4, 2026
Early Metabolic Risk in Childhood Brain Cancer Survivors with Childhood-Onset Growth Hormone DeficiencyAlice Casiraghi, Olivier Pollé, Clément Bailly, et al.
Annales D'Endocrinologie|March 7, 2024
Position statement on the diagnosis and management of congenital pituitary deficiency in adults: The French National Diagnosis and Treatment Protocol (NDTP)Sarah Castets, Frédérique Albarel, Anne Bachelot, 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.
Endocrine Connections|January 6, 2023
Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in FranceEstelle Bonnet, Mathias Winter, Delphine Mallet, et al.
Annales D'Endocrinologie|September 11, 2021
Position statement on the diagnosis and management of premature/primary ovarian insufficiency (except Turner Syndrome)Sophie Christin-Maitre, Maria Givony, Frédérique Albarel, et al.
Pageof 11