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Rachel Reynaud

Showing results (31-40 of 91) with videos related to

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La Revue Du Praticien|April 2, 2020
[Levothyrox crisis]Xavier Bertagna, Philippe Bouchard, Andre Grimaldi, et al.
European Journal of Endocrinology|January 7, 2016
MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiencyFrederic Castinetti, Rachel Reynaud, Alexandru Saveanu, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2005
An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domainRachel Reynaud, Anne Barlier, Sophie Vallette-Kasic, et al.
Annales D'Endocrinologie|May 8, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
Frontiers in Endocrinology|March 9, 2023
A novel <i>TBX19</i> gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical originThéo Charnay, Gregory Mougel, Cyril Amouroux, et al.
Annales D'Endocrinologie|March 21, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studiesRachel Reynaud, Molka Chadli-Chaieb, Sophie Vallette-Kasic, et al.
Scientific Reports|July 2, 2025
Identification of autoantibodies against HIF1a in patients with anorexia nervosa and their potential role in hepatic cytolysisAhmad Joshkon, Charlotte Reytier, Daniel Bertin, et al.
Molecular Endocrinology (Baltimore, Md.)|March 20, 2004
Activin inhibits pituitary prolactin expression and cell growth through Smads, Pit-1 and meninAnnie Lacerte, Eun-Hye Lee, Rachel Reynaud, 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 10

Showing results (31-40 of 91) with videos related to

Sort By:
Pageof 10
La Revue Du Praticien|April 2, 2020
[Levothyrox crisis]Xavier Bertagna, Philippe Bouchard, Andre Grimaldi, et al.
European Journal of Endocrinology|January 7, 2016
MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiencyFrederic Castinetti, Rachel Reynaud, Alexandru Saveanu, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2005
An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domainRachel Reynaud, Anne Barlier, Sophie Vallette-Kasic, et al.
Annales D'Endocrinologie|May 8, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
Frontiers in Endocrinology|March 9, 2023
A novel <i>TBX19</i> gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical originThéo Charnay, Gregory Mougel, Cyril Amouroux, et al.
Annales D'Endocrinologie|March 21, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studiesRachel Reynaud, Molka Chadli-Chaieb, Sophie Vallette-Kasic, et al.
Scientific Reports|July 2, 2025
Identification of autoantibodies against HIF1a in patients with anorexia nervosa and their potential role in hepatic cytolysisAhmad Joshkon, Charlotte Reytier, Daniel Bertin, et al.
Molecular Endocrinology (Baltimore, Md.)|March 20, 2004
Activin inhibits pituitary prolactin expression and cell growth through Smads, Pit-1 and meninAnnie Lacerte, Eun-Hye Lee, Rachel Reynaud, 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 10