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Catherine Pienkowski

Showing results (31-40 of 44) with videos related to

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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 casesCharlotte 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 boysLaetitia Martinerie, Yves Morel, Claire-Lise Gay, et al.
Pediatric Endocrinology Reviews : PER|June 28, 2019
Karyotype - Phenotype Associations in Patients with Turner SyndromeIris 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 mutationsPascal 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 mutationsPascal 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 guidelinesFlorence 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 familiesAlexandre Rouen, Eli Rogers, Véronique Kerlan, et al.
European Journal of Endocrinology|February 22, 2023
Perinatal, metabolic, and reproductive features in PPARG-related lipodystrophyCamille 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 cohortClément Janot, Delphine Mallet, Alexandre Janin, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Journal of Pediatric Surgery|July 20, 2010
Ovarian germ cell tumors in children. Management, survival and ovarian prognosis. A report of 75 casesCharlotte 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 boysLaetitia Martinerie, Yves Morel, Claire-Lise Gay, et al.
Pediatric Endocrinology Reviews : PER|June 28, 2019
Karyotype - Phenotype Associations in Patients with Turner SyndromeIris 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 mutationsPascal 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 mutationsPascal 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 guidelinesFlorence 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 familiesAlexandre Rouen, Eli Rogers, Véronique Kerlan, et al.
European Journal of Endocrinology|February 22, 2023
Perinatal, metabolic, and reproductive features in PPARG-related lipodystrophyCamille 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 cohortClément Janot, Delphine Mallet, Alexandre Janin, et al.
Pageof 5