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Rachel Reynaud

Showing results (61-70 of 91) with videos related to

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European Journal of Endocrinology|October 3, 2015
Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious pubertyDominique Simon, Ibrahima Ba, Nancy Mekhail, et al.
The Journal of Clinical Endocrinology and Metabolism|April 7, 2025
Inhibin B and AMH for Diagnosis of Hypogonadotropic Hypogonadism in Boys Under One Year of Age: A Case-Control StudyTifenn Gueguen, Laetitia Martinerie, Sarah Castets, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 27, 2024
Diagnosis and management of congenital hypopituitarism in childrenSarah Castets, Cécile Thomas-Teinturier, Carine Villanueva, et al.
The Journal of Clinical Endocrinology and Metabolism|October 4, 2016
mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic SuccessMarie Szymanowski, Maria Salomon Estebanez, Raja Padidela, et al.
The Journal of Clinical Endocrinology and Metabolism|June 2, 2005
Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiencyJames P G Turton, Rachel Reynaud, Ameeta Mehta, et al.
European Journal of Endocrinology|February 12, 2025
Phenotype and genotype of 23 patients with hypopituitarism and pathogenic GLI2 variantsKarine Aouchiche, Camille Charmensat, Pertuit Morgane, et al.
The Journal of Urology|May 4, 2018
Family History is Underestimated in Children with Isolated Hypospadias: A French Multicenter Report of 88 FamiliesMargot Ollivier, Francoise Paris, Pascal Philibert, et al.
Orphanet Journal of Rare Diseases|February 5, 2026
Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectoryMaithe Tauber, Gwenaelle Diene, Pascale Fichaux-Bourin, et al.
Hormone Research in Paediatrics|April 8, 2026
MKRN3 variants in central precocious puberty as an example of the complexity to classify missense variants in imprinted genes as pathogenicClémence Delcour, Carole Harbulot, Leila Drira, et al.
Annales D'Endocrinologie|January 18, 2018
SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbookYves Reznik, Pascal Barat, Jérôme Bertherat, et al.
Pageof 10

Showing results (61-70 of 91) with videos related to

Sort By:
Pageof 10
European Journal of Endocrinology|October 3, 2015
Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious pubertyDominique Simon, Ibrahima Ba, Nancy Mekhail, et al.
The Journal of Clinical Endocrinology and Metabolism|April 7, 2025
Inhibin B and AMH for Diagnosis of Hypogonadotropic Hypogonadism in Boys Under One Year of Age: A Case-Control StudyTifenn Gueguen, Laetitia Martinerie, Sarah Castets, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 27, 2024
Diagnosis and management of congenital hypopituitarism in childrenSarah Castets, Cécile Thomas-Teinturier, Carine Villanueva, et al.
The Journal of Clinical Endocrinology and Metabolism|October 4, 2016
mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic SuccessMarie Szymanowski, Maria Salomon Estebanez, Raja Padidela, et al.
The Journal of Clinical Endocrinology and Metabolism|June 2, 2005
Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiencyJames P G Turton, Rachel Reynaud, Ameeta Mehta, et al.
European Journal of Endocrinology|February 12, 2025
Phenotype and genotype of 23 patients with hypopituitarism and pathogenic GLI2 variantsKarine Aouchiche, Camille Charmensat, Pertuit Morgane, et al.
The Journal of Urology|May 4, 2018
Family History is Underestimated in Children with Isolated Hypospadias: A French Multicenter Report of 88 FamiliesMargot Ollivier, Francoise Paris, Pascal Philibert, et al.
Orphanet Journal of Rare Diseases|February 5, 2026
Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectoryMaithe Tauber, Gwenaelle Diene, Pascale Fichaux-Bourin, et al.
Hormone Research in Paediatrics|April 8, 2026
MKRN3 variants in central precocious puberty as an example of the complexity to classify missense variants in imprinted genes as pathogenicClémence Delcour, Carole Harbulot, Leila Drira, et al.
Annales D'Endocrinologie|January 18, 2018
SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbookYves Reznik, Pascal Barat, Jérôme Bertherat, et al.
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