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European Journal of Endocrinology
|
October 3, 2015
Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty
Dominique 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 Study
Tifenn 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 children
Sarah 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 Success
Marie 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 deficiency
James 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 variants
Karine 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 Families
Margot 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 trajectory
Maithe 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 pathogenic
Clémence Delcour, Carole Harbulot, Leila Drira, et al.
Annales D'Endocrinologie
|
January 18, 2018
SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook
Yves Reznik, Pascal Barat, Jérôme Bertherat, et al.
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Search research articles
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Showing results (61-70 of 91) with videos related to
Sort By:
Page
of 10
European Journal of Endocrinology
|
October 3, 2015
Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty
Dominique 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 Study
Tifenn 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 children
Sarah 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 Success
Marie 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 deficiency
James 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 variants
Karine 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 Families
Margot 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 trajectory
Maithe 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 pathogenic
Clémence Delcour, Carole Harbulot, Leila Drira, et al.
Annales D'Endocrinologie
|
January 18, 2018
SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook
Yves Reznik, Pascal Barat, Jérôme Bertherat, et al.
Page
of 10