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Journal of Pediatric Surgery
|
July 20, 2010
Ovarian germ cell tumors in children. Management, survival and ovarian prognosis. A report of 75 cases
Charlotte Vaysse, Martine Delsol, Luana Carfagna, et al.
European Journal of Endocrinology
|
January 13, 2012
Impaired puberty, fertility, and final stature in 45,X/46,XY mixed gonadal dysgenetic patients raised as boys
Laetitia Martinerie, Yves Morel, Claire-Lise Gay, et al.
Pediatric Endocrinology Reviews : PER
|
June 28, 2019
Karyotype - Phenotype Associations in Patients with Turner Syndrome
Iris D Noordman, Janiëlle Aem van der Velden, Henri Jlm Timmers, et al.
Advances in Experimental Medicine and Biology
|
June 22, 2011
Phenotypic variation of SF1 gene mutations
Pascal Philibert, Françoise Paris, Françoise Audran, et al.
Fertility and Sterility
|
May 26, 2009
Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations
Pascal Philibert, Françoise Audran, Catherine Pienkowski, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
August 11, 2018
Pregnancy outcome in Turner syndrome: A French multi-center study after the 2009 guidelines
Florence Cadoret, Jean Parinaud, Celia Bettiol, et al.
Journal of Gynecology Obstetrics and Human Reproduction
|
May 4, 2019
Clinical practice guidelines for contraception by the French National College of Gynecologists and Obstetricians (CNGOF)
Nathalie Chabbert-Buffet, Henri Marret, Aubert Agostini, et al.
Fertility and Sterility
|
February 4, 2022
Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of families
Alexandre Rouen, Eli Rogers, Véronique Kerlan, et al.
European Journal of Endocrinology
|
February 22, 2023
Perinatal, metabolic, and reproductive features in PPARG-related lipodystrophy
Camille Gosseaume, Thierry Fournier, Isabelle Jéru, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 19, 2025
A recurrent splice variant sheds light on 11beta-hydroxylase deficiency in a unique large cohort
Clément Janot, Delphine Mallet, Alexandre Janin, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Journal of Pediatric Surgery
|
July 20, 2010
Ovarian germ cell tumors in children. Management, survival and ovarian prognosis. A report of 75 cases
Charlotte Vaysse, Martine Delsol, Luana Carfagna, et al.
European Journal of Endocrinology
|
January 13, 2012
Impaired puberty, fertility, and final stature in 45,X/46,XY mixed gonadal dysgenetic patients raised as boys
Laetitia Martinerie, Yves Morel, Claire-Lise Gay, et al.
Pediatric Endocrinology Reviews : PER
|
June 28, 2019
Karyotype - Phenotype Associations in Patients with Turner Syndrome
Iris D Noordman, Janiëlle Aem van der Velden, Henri Jlm Timmers, et al.
Advances in Experimental Medicine and Biology
|
June 22, 2011
Phenotypic variation of SF1 gene mutations
Pascal Philibert, Françoise Paris, Françoise Audran, et al.
Fertility and Sterility
|
May 26, 2009
Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations
Pascal Philibert, Françoise Audran, Catherine Pienkowski, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
August 11, 2018
Pregnancy outcome in Turner syndrome: A French multi-center study after the 2009 guidelines
Florence Cadoret, Jean Parinaud, Celia Bettiol, et al.
Journal of Gynecology Obstetrics and Human Reproduction
|
May 4, 2019
Clinical practice guidelines for contraception by the French National College of Gynecologists and Obstetricians (CNGOF)
Nathalie Chabbert-Buffet, Henri Marret, Aubert Agostini, et al.
Fertility and Sterility
|
February 4, 2022
Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of families
Alexandre Rouen, Eli Rogers, Véronique Kerlan, et al.
European Journal of Endocrinology
|
February 22, 2023
Perinatal, metabolic, and reproductive features in PPARG-related lipodystrophy
Camille Gosseaume, Thierry Fournier, Isabelle Jéru, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 19, 2025
A recurrent splice variant sheds light on 11beta-hydroxylase deficiency in a unique large cohort
Clément Janot, Delphine Mallet, Alexandre Janin, et al.
Page
of 5