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

Frederic Castinetti

Showing results (81-90 of 133) with videos related to

Pageof 14
Sort By:
Anticancer Research|April 30, 2014
Contemporary review of large adrenal tumors in a tertiary referral centerDiane Mege, David Taieb, Aoife Lowery, et al.
Endocrine|May 11, 2020
MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectivesVincent Amodru, David Taieb, Carole Guerin, et al.
Annales D'Endocrinologie|June 9, 2026
Redefining the role of surgery in hypophysitis: our experience, and a literature reviewLéa Miquel, Benoit Testud, Nicolas Sahakian, et al.
European Journal of Endocrinology|September 29, 2021
Acromegaly in remission: a view from the partnerRachel Fourneaux, Marie Vermalle, Frederique Albarel, et al.
European Journal of Endocrinology|February 16, 2018
Significant prevalence of <i>NR3C1</i> mutations in incidentally discovered bilateral adrenal hyperplasia: results of the French MUTA-GR StudyGéraldine Vitellius, Séverine Trabado, Christine Hoeffel, et al.
Journal of Clinical Hypertension (Greenwich, Conn.)|August 22, 2025
Primary Aldosteronism and Long-Term Cardiovascular Complications: Comparison of Medical Versus Surgical TreatmentSofia Benameur, Julien Bertolino, Laura Bonnaud, et al.
The Lancet. Diabetes & Endocrinology|May 21, 2022
Osilodrostat for the treatment of Cushing's disease: efficacy, stability, and persistence - Authors' replyMaria Fleseriu, Frederic Castinetti, Mônica Gadelha, et al.
Human Molecular Genetics|August 11, 2022
Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and manHironori Bando, Michelle L Brinkmeier, Frederic Castinetti, et al.
The Journal of Clinical Endocrinology and Metabolism|September 23, 2024
Deciphering the Presentation and Etiologies of Hypophysitis Highlights the Need for Repeated Systematical InvestigationLea Miquel, Benoit Testud, Frederique Albarel, et al.
European Journal of Endocrinology|October 6, 2022
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiencyRachel Fourneaux, Rachel Reynaud, Gregory Mougel, et al.
Pageof 14

Showing results (81-90 of 133) with videos related to

Sort By:
Pageof 14
Anticancer Research|April 30, 2014
Contemporary review of large adrenal tumors in a tertiary referral centerDiane Mege, David Taieb, Aoife Lowery, et al.
Endocrine|May 11, 2020
MEN2-related pheochromocytoma: current state of knowledge, specific characteristics in MEN2B, and perspectivesVincent Amodru, David Taieb, Carole Guerin, et al.
Annales D'Endocrinologie|June 9, 2026
Redefining the role of surgery in hypophysitis: our experience, and a literature reviewLéa Miquel, Benoit Testud, Nicolas Sahakian, et al.
European Journal of Endocrinology|September 29, 2021
Acromegaly in remission: a view from the partnerRachel Fourneaux, Marie Vermalle, Frederique Albarel, et al.
European Journal of Endocrinology|February 16, 2018
Significant prevalence of <i>NR3C1</i> mutations in incidentally discovered bilateral adrenal hyperplasia: results of the French MUTA-GR StudyGéraldine Vitellius, Séverine Trabado, Christine Hoeffel, et al.
Journal of Clinical Hypertension (Greenwich, Conn.)|August 22, 2025
Primary Aldosteronism and Long-Term Cardiovascular Complications: Comparison of Medical Versus Surgical TreatmentSofia Benameur, Julien Bertolino, Laura Bonnaud, et al.
The Lancet. Diabetes & Endocrinology|May 21, 2022
Osilodrostat for the treatment of Cushing's disease: efficacy, stability, and persistence - Authors' replyMaria Fleseriu, Frederic Castinetti, Mônica Gadelha, et al.
Human Molecular Genetics|August 11, 2022
Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and manHironori Bando, Michelle L Brinkmeier, Frederic Castinetti, et al.
The Journal of Clinical Endocrinology and Metabolism|September 23, 2024
Deciphering the Presentation and Etiologies of Hypophysitis Highlights the Need for Repeated Systematical InvestigationLea Miquel, Benoit Testud, Frederique Albarel, et al.
European Journal of Endocrinology|October 6, 2022
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiencyRachel Fourneaux, Rachel Reynaud, Gregory Mougel, et al.
Pageof 14