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Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 13, 2009
Effectiveness of anastrozole and cyproterone acetate in two brothers with familial male precocious puberty
Stéphanie Eyssette-Guerreau, Graziella Pinto, Ariane Sultan, et al.
Pediatric Dermatology
|
March 12, 2020
Hypophosphatemic rickets: A rare complication of congenital melanocytic nevus syndrome
Anne Welfringer-Morin, Graziella Pinto, Geneviève Baujat, et al.
European Journal of Endocrinology
|
March 29, 2007
GH deficiency with central precocious puberty: a new rare disorder associated with a developmental defect of the hypothalamic-pituitary area
Asmahane Ladjouze, Sylvie Soskin, Catherine Garel, et al.
Journal of Clinical Medicine
|
November 27, 2021
Diabetes Mellitus in Prader-Willi Syndrome: Natural History during the Transition from Childhood to Adulthood in a Cohort of 39 Patients
Alice Clerc, Muriel Coupaye, Héléna Mosbah, et al.
American Journal of Medical Genetics. Part A
|
November 5, 2019
Sleep-disordered breathing in children with pycnodysostosis
Sonia Khirani, Alessandro Amaddeo, Geneviève Baujat, et al.
Hormone Research
|
December 16, 2006
Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Anne Bachelot, Geneviève Plu-Bureau, Elisabeth Thibaud, et al.
Plos One
|
April 6, 2012
Screening of MAMLD1 mutations in 70 children with 46,XY DSD: identification and functional analysis of two new mutations
Nicolas Kalfa, Maki Fukami, Pascal Philibert, et al.
European Journal of Endocrinology
|
August 14, 2013
Monocentric study of 112 consecutive patients with childhood onset GH deficiency around and after transition
Carine Courtillot, Roselyne Baudoin, Tatiana Du Souich, et al.
European Journal of Endocrinology
|
November 12, 2023
Glucose pattern in children with classical congenital adrenal hyperplasia: evidence from continuous glucose monitoring
Alfonso Galderisi, Dulanjalee Kariyawasam, Athanasia Stoupa, et al.
The New England Journal of Medicine
|
April 25, 2008
Mutations in the iodotyrosine deiodinase gene and hypothyroidism
José C Moreno, Willem Klootwijk, Hans van Toor, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 53) with videos related to
Sort By:
Page
of 6
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 13, 2009
Effectiveness of anastrozole and cyproterone acetate in two brothers with familial male precocious puberty
Stéphanie Eyssette-Guerreau, Graziella Pinto, Ariane Sultan, et al.
Pediatric Dermatology
|
March 12, 2020
Hypophosphatemic rickets: A rare complication of congenital melanocytic nevus syndrome
Anne Welfringer-Morin, Graziella Pinto, Geneviève Baujat, et al.
European Journal of Endocrinology
|
March 29, 2007
GH deficiency with central precocious puberty: a new rare disorder associated with a developmental defect of the hypothalamic-pituitary area
Asmahane Ladjouze, Sylvie Soskin, Catherine Garel, et al.
Journal of Clinical Medicine
|
November 27, 2021
Diabetes Mellitus in Prader-Willi Syndrome: Natural History during the Transition from Childhood to Adulthood in a Cohort of 39 Patients
Alice Clerc, Muriel Coupaye, Héléna Mosbah, et al.
American Journal of Medical Genetics. Part A
|
November 5, 2019
Sleep-disordered breathing in children with pycnodysostosis
Sonia Khirani, Alessandro Amaddeo, Geneviève Baujat, et al.
Hormone Research
|
December 16, 2006
Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Anne Bachelot, Geneviève Plu-Bureau, Elisabeth Thibaud, et al.
Plos One
|
April 6, 2012
Screening of MAMLD1 mutations in 70 children with 46,XY DSD: identification and functional analysis of two new mutations
Nicolas Kalfa, Maki Fukami, Pascal Philibert, et al.
European Journal of Endocrinology
|
August 14, 2013
Monocentric study of 112 consecutive patients with childhood onset GH deficiency around and after transition
Carine Courtillot, Roselyne Baudoin, Tatiana Du Souich, et al.
European Journal of Endocrinology
|
November 12, 2023
Glucose pattern in children with classical congenital adrenal hyperplasia: evidence from continuous glucose monitoring
Alfonso Galderisi, Dulanjalee Kariyawasam, Athanasia Stoupa, et al.
The New England Journal of Medicine
|
April 25, 2008
Mutations in the iodotyrosine deiodinase gene and hypothyroidism
José C Moreno, Willem Klootwijk, Hans van Toor, et al.
Page
of 6