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S Vallette

Showing results (1-10 of 10) with videos related to

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Clinical Genetics|August 28, 2007
Of old and new diseases: genetics of pituitary ACTH excess (Cushing) and deficiencyJ Drouin, S Bilodeau, S Vallette
Annales D'Endocrinologie|January 1, 1997
[Congenital multiple anterior pituitary hormone deficiencies. An approach of pituitary ontogenesis]T Brue, S Vallette, I Pellegrini-Bouiller, et al.
Annales D'Endocrinologie|October 16, 1999
[Transcription factors of the anterior pituitary and combined hypopituitarism]S Vallette, I Pellegrini-Bouiller, P Jaquet, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 2, 2002
Pseudotumor of the pituitary due to PROP-1 deletionC Teinturier, S Vallette, C Adamsbaum, et al.
Molecular Endocrinology (Baltimore, Md.)|February 27, 2001
Combined pituitary hormone deficiency due to the F135C human Pit-1 (pituitary-specific factor 1) gene mutation: functional and structural correlatesS Vallette-Kasic, I Pellegrini-Bouiller, F Sampieri, et al.
Annales D'Endocrinologie|September 6, 2000
[Pituitary development and pathology of transcription factors]A Barlier, S Vallette-Kasic, M Manavela, et al.
La Revue De Medecine Interne|January 1, 1997
[Cushing syndrome disclosing bronchial neuroendocrine carcinoma: value of scintigraphy with octreotide]S Vallette, P Disdier, I Morange-Ramos, et al.
European Journal of Endocrinology|December 22, 2000
Markers of tumor invasion are major predictive factors for the long-term outcome of corticotroph microadenomas treated by transsphenoidal adenomectomyS Vallette-Kasic, H Dufour, M Mugnier, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiencyS Vallette-Kasic, A Barlier, C Teinturier, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2011
Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutationsC Couture, A Saveanu, A Barlier, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Clinical Genetics|August 28, 2007
Of old and new diseases: genetics of pituitary ACTH excess (Cushing) and deficiencyJ Drouin, S Bilodeau, S Vallette
Annales D'Endocrinologie|January 1, 1997
[Congenital multiple anterior pituitary hormone deficiencies. An approach of pituitary ontogenesis]T Brue, S Vallette, I Pellegrini-Bouiller, et al.
Annales D'Endocrinologie|October 16, 1999
[Transcription factors of the anterior pituitary and combined hypopituitarism]S Vallette, I Pellegrini-Bouiller, P Jaquet, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 2, 2002
Pseudotumor of the pituitary due to PROP-1 deletionC Teinturier, S Vallette, C Adamsbaum, et al.
Molecular Endocrinology (Baltimore, Md.)|February 27, 2001
Combined pituitary hormone deficiency due to the F135C human Pit-1 (pituitary-specific factor 1) gene mutation: functional and structural correlatesS Vallette-Kasic, I Pellegrini-Bouiller, F Sampieri, et al.
Annales D'Endocrinologie|September 6, 2000
[Pituitary development and pathology of transcription factors]A Barlier, S Vallette-Kasic, M Manavela, et al.
La Revue De Medecine Interne|January 1, 1997
[Cushing syndrome disclosing bronchial neuroendocrine carcinoma: value of scintigraphy with octreotide]S Vallette, P Disdier, I Morange-Ramos, et al.
European Journal of Endocrinology|December 22, 2000
Markers of tumor invasion are major predictive factors for the long-term outcome of corticotroph microadenomas treated by transsphenoidal adenomectomyS Vallette-Kasic, H Dufour, M Mugnier, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiencyS Vallette-Kasic, A Barlier, C Teinturier, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2011
Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutationsC Couture, A Saveanu, A Barlier, et al.
Pageof 1