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Showing results (371-380 of 375) with videos related to

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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.
Annales D'Endocrinologie|April 7, 2004
[Therapeutic strategies in somatotroph adenomas with extrasellar extension: role of the medical approach, a consensus study of the French Acromegaly Registry]Ph Jaquet, Ch Cortet-Rudelli, G Sassolas, et al.
The Journal of Clinical Endocrinology and Metabolism|December 23, 2004
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutationsSophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino, 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 Frailty & Aging|November 25, 2016
MACVIA-LR (Fighting Chronic Diseases for Active and Healthy Ageing in Languedoc-Roussillon): A Success Story of the European Innovation Partnership on Active and Healthy AgeingJ Bousquet, R Bourret, T Camuzat, et al.
Pageof 38

Showing results (371-380 of 375) with videos related to

Sort By:
Pageof 38
You have reached the last page of results.This site can display upto 375 results.
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.
Annales D'Endocrinologie|April 7, 2004
[Therapeutic strategies in somatotroph adenomas with extrasellar extension: role of the medical approach, a consensus study of the French Acromegaly Registry]Ph Jaquet, Ch Cortet-Rudelli, G Sassolas, et al.
The Journal of Clinical Endocrinology and Metabolism|December 23, 2004
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutationsSophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino, 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 Frailty & Aging|November 25, 2016
MACVIA-LR (Fighting Chronic Diseases for Active and Healthy Ageing in Languedoc-Roussillon): A Success Story of the European Innovation Partnership on Active and Healthy AgeingJ Bousquet, R Bourret, T Camuzat, et al.
Pageof 38