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Catherine Pienkowski

Showing results (21-30 of 44) with videos related to

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Bone|September 7, 2021
Low bone mass in Noonan syndrome children correlates with decreased muscle mass and low IGF-1 levelsMarine Delagrange, Vanessa Rousseau, Catie Cessans, et al.
BMC Endocrine Disorders|August 20, 2017
Participation of adults with disorders/differences of sex development (DSD) in the clinical study dsd-LIFE: design, methodology, recruitment, data quality and study populationRobert Röhle, Katharina Gehrmann, Maria Szarras-Czapnik, et al.
Plos One|November 13, 2015
Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial PresentationCéline Bar, Charline Zadro, Gwenaelle Diene, et al.
Human Reproduction (Oxford, England)|November 4, 2022
Persistent Müllerian duct syndrome associated with genetic defects in the regulatory subunit of myosin phosphataseJean-Yves Picard, Gilles Morin, Mojgan Devouassoux-Shisheboran, et al.
The Journal of Clinical Endocrinology and Metabolism|November 7, 2003
Adolescents with partial growth hormone (GH) deficiency develop alterations of body composition after GH discontinuation and require follow-upMaithé Tauber, Béatrice Jouret, Audrey Cartault, et al.
Journal of Pediatric Surgery|October 31, 2008
Fetal ovarian cysts management and ovarian prognosis: a report of 82 casesPhilippe Galinier, Luana Carfagna, Michel Juricic, et al.
The Journal of Clinical Endocrinology and Metabolism|October 6, 2022
Obesity, Overweight, and Pituitary Stalk Interruption Syndrome in Children and Young AdultsGaëlle Nannette, Céline Bar, Gwenaëlle Diene, et al.
European Journal of Endocrinology|October 17, 2018
Noonan syndrome males display Sertoli cell-specific primary testicular insufficiencySophie Moniez, Catherine Pienkowski, Benoit Lepage, et al.
The Journal of Clinical Endocrinology and Metabolism|March 2, 2006
Activating mutations of the stimulatory g protein in juvenile ovarian granulosa cell tumors: a new prognostic factor?Nicolas Kalfa, Aude Ecochard, Catherine Patte, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 22, 2026
Study of the ovarian function and gyneco-obstetrical profile of patients with an HNF1B abnormalityAudrey Cartault, Camille Paret, Charlotte Garczynski, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Bone|September 7, 2021
Low bone mass in Noonan syndrome children correlates with decreased muscle mass and low IGF-1 levelsMarine Delagrange, Vanessa Rousseau, Catie Cessans, et al.
BMC Endocrine Disorders|August 20, 2017
Participation of adults with disorders/differences of sex development (DSD) in the clinical study dsd-LIFE: design, methodology, recruitment, data quality and study populationRobert Röhle, Katharina Gehrmann, Maria Szarras-Czapnik, et al.
Plos One|November 13, 2015
Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial PresentationCéline Bar, Charline Zadro, Gwenaelle Diene, et al.
Human Reproduction (Oxford, England)|November 4, 2022
Persistent Müllerian duct syndrome associated with genetic defects in the regulatory subunit of myosin phosphataseJean-Yves Picard, Gilles Morin, Mojgan Devouassoux-Shisheboran, et al.
The Journal of Clinical Endocrinology and Metabolism|November 7, 2003
Adolescents with partial growth hormone (GH) deficiency develop alterations of body composition after GH discontinuation and require follow-upMaithé Tauber, Béatrice Jouret, Audrey Cartault, et al.
Journal of Pediatric Surgery|October 31, 2008
Fetal ovarian cysts management and ovarian prognosis: a report of 82 casesPhilippe Galinier, Luana Carfagna, Michel Juricic, et al.
The Journal of Clinical Endocrinology and Metabolism|October 6, 2022
Obesity, Overweight, and Pituitary Stalk Interruption Syndrome in Children and Young AdultsGaëlle Nannette, Céline Bar, Gwenaëlle Diene, et al.
European Journal of Endocrinology|October 17, 2018
Noonan syndrome males display Sertoli cell-specific primary testicular insufficiencySophie Moniez, Catherine Pienkowski, Benoit Lepage, et al.
The Journal of Clinical Endocrinology and Metabolism|March 2, 2006
Activating mutations of the stimulatory g protein in juvenile ovarian granulosa cell tumors: a new prognostic factor?Nicolas Kalfa, Aude Ecochard, Catherine Patte, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 22, 2026
Study of the ovarian function and gyneco-obstetrical profile of patients with an HNF1B abnormalityAudrey Cartault, Camille Paret, Charlotte Garczynski, et al.
Pageof 5