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Catherine Pienkowski

Showing results (11-20 of 44) with videos related to

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Journal of the Endocrine Society|July 14, 2021
Physical and Reported Subjective Health Status in 222 Individuals with XY Disorder of Sex DevelopmentXin Li Gong, Klemens Raile, Jolanta Slowikowska-Hilczer, et al.
The Journal of Urology|August 30, 2008
Aberrant expression of ovary determining gene FOXL2 in the testis and juvenile granulosa cell tumor in childrenNicolas Kalfa, Marc Fellous, Brigitte Boizet-Bonhoure, et al.
Journal of Cellular and Molecular Medicine|June 11, 2020
Peroxisome proliferator-activated receptor gamma-ligand-binding domain mutations associated with familial partial lipodystrophy type 3 disrupt human trophoblast fusion and fibroblast migrationHussein Shoaito, Sabine Chauveau, Camille Gosseaume, et al.
Psychoneuroendocrinology|January 11, 2020
Psychosocial well-being and quality of life in women with Turner syndromeAriane Liedmeier, David Jendryczko, Hedi Claahsen van der Grinten, et al.
Journal of Pediatric Surgery|September 9, 2009
Ovarian torsion. Management and ovarian prognosis: a report of 45 casesPhilippe Galinier, Luana Carfagna, Martine Delsol, et al.
Hormone Research in Paediatrics|April 17, 2010
Unusual virilization in girls with juvenile granulosa cell tumors of the ovary is related to intratumoral aromatase deficiencyNicolas Kalfa, Geri Méduri, Pascal Philibert, 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 mutationsNicolas Kalfa, Maki Fukami, Pascal Philibert, et al.
Science Immunology|January 28, 2018
<i>TLR7</i> escapes X chromosome inactivation in immune cellsMélanie Souyris, Claire Cenac, Pascal Azar, et al.
Human Genetics|February 24, 2026
Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomaliesAdeline Jacquinet, Lydie Flasse, Manon Dohet, et al.
Human Genetics|April 13, 2026
Correction: Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomaliesAdeline Jacquinet, Lydie Flasse, Manon Dohet, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Journal of the Endocrine Society|July 14, 2021
Physical and Reported Subjective Health Status in 222 Individuals with XY Disorder of Sex DevelopmentXin Li Gong, Klemens Raile, Jolanta Slowikowska-Hilczer, et al.
The Journal of Urology|August 30, 2008
Aberrant expression of ovary determining gene FOXL2 in the testis and juvenile granulosa cell tumor in childrenNicolas Kalfa, Marc Fellous, Brigitte Boizet-Bonhoure, et al.
Journal of Cellular and Molecular Medicine|June 11, 2020
Peroxisome proliferator-activated receptor gamma-ligand-binding domain mutations associated with familial partial lipodystrophy type 3 disrupt human trophoblast fusion and fibroblast migrationHussein Shoaito, Sabine Chauveau, Camille Gosseaume, et al.
Psychoneuroendocrinology|January 11, 2020
Psychosocial well-being and quality of life in women with Turner syndromeAriane Liedmeier, David Jendryczko, Hedi Claahsen van der Grinten, et al.
Journal of Pediatric Surgery|September 9, 2009
Ovarian torsion. Management and ovarian prognosis: a report of 45 casesPhilippe Galinier, Luana Carfagna, Martine Delsol, et al.
Hormone Research in Paediatrics|April 17, 2010
Unusual virilization in girls with juvenile granulosa cell tumors of the ovary is related to intratumoral aromatase deficiencyNicolas Kalfa, Geri Méduri, Pascal Philibert, 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 mutationsNicolas Kalfa, Maki Fukami, Pascal Philibert, et al.
Science Immunology|January 28, 2018
<i>TLR7</i> escapes X chromosome inactivation in immune cellsMélanie Souyris, Claire Cenac, Pascal Azar, et al.
Human Genetics|February 24, 2026
Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomaliesAdeline Jacquinet, Lydie Flasse, Manon Dohet, et al.
Human Genetics|April 13, 2026
Correction: Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomaliesAdeline Jacquinet, Lydie Flasse, Manon Dohet, et al.
Pageof 5