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Christine Cortet-Rudelli

Showing results (21-30 of 26) with videos related to

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Clinical Endocrinology|October 24, 2020
Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohortNicolas Jullien, Alexandru Saveanu, Julia Vergier, et al.
Plos Genetics|August 29, 2012
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndromeNaresh Kumar Hanchate, Paolo Giacobini, Pierre Lhuillier, et al.
European Journal of Endocrinology|January 17, 2013
Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysisThomas Cuny, Morgane Pertuit, Mona Sahnoun-Fathallah, et al.
Endocrine-Related Cancer|February 1, 2012
Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindredsMaria A Tichomirowa, Misu Lee, Anne Barlier, et al.
The Journal of Clinical Endocrinology and Metabolism|January 30, 2024
Beyond MEN1, When to Think About MEN4? Retrospective Study on 5600 Patients in the French Population and Literature ReviewBenjamin Chevalier, Lucie Coppin, Pauline Romanet, et al.
Acta Neuropathologica|February 13, 2013
A new prognostic clinicopathological classification of pituitary adenomas: a multicentric case-control study of 410 patients with 8 years post-operative follow-upJacqueline Trouillas, Pascal Roy, Nathalie Sturm, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Clinical Endocrinology|October 24, 2020
Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohortNicolas Jullien, Alexandru Saveanu, Julia Vergier, et al.
Plos Genetics|August 29, 2012
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndromeNaresh Kumar Hanchate, Paolo Giacobini, Pierre Lhuillier, et al.
European Journal of Endocrinology|January 17, 2013
Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysisThomas Cuny, Morgane Pertuit, Mona Sahnoun-Fathallah, et al.
Endocrine-Related Cancer|February 1, 2012
Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindredsMaria A Tichomirowa, Misu Lee, Anne Barlier, et al.
The Journal of Clinical Endocrinology and Metabolism|January 30, 2024
Beyond MEN1, When to Think About MEN4? Retrospective Study on 5600 Patients in the French Population and Literature ReviewBenjamin Chevalier, Lucie Coppin, Pauline Romanet, et al.
Acta Neuropathologica|February 13, 2013
A new prognostic clinicopathological classification of pituitary adenomas: a multicentric case-control study of 410 patients with 8 years post-operative follow-upJacqueline Trouillas, Pascal Roy, Nathalie Sturm, et al.
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