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International Journal of Pediatric Endocrinology
|
September 25, 2012
Fulvestrant treatment of precocious puberty in girls with McCune-Albright syndrome
Emily K Sims, Sally Garnett, Franco Guzman, et al.
Fertility and Sterility
|
December 18, 2010
Predominant Sertoli cell deficiency in a 46,XY disorders of sex development patient with a new NR5A1/SF-1 mutation transmitted by his unaffected father
Pascal Philibert, Michel Polak, Ana Colmenares, et al.
Journal of the Society for Gynecologic Investigation
|
February 8, 2005
Association between androgen receptor gene CAG repeat polymorphism and plasma testosterone levels in postmenopausal women
Ilma Simoni Brum, Poli Mara Spritzer, Françoise Paris, et al.
Experimental Neurology
|
November 28, 2006
Mild surfection of neural cells, especially motoneurons, in primary culture and cell lines
Clovis Rakotoarivelo, Didier Petite, Jan de Weille, et al.
European Journal of Endocrinology
|
April 29, 2010
Bone mineral density acquisition in peripubertal female rhythmic gymnasts is directly associated with plasma IGF1/IGF-binding protein 3 ratio
Laurent Maïmoun, Olivier Coste, Florence Galtier, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 5, 2009
Mother-to-son transmission of a luteinizing hormone receptor activating mutation in a prepubertal child with testotoxicosis
Marumudi Eunice, Pascal Philibert, Bindu Kulshreshtha, et al.
Human Reproduction (Oxford, England)
|
August 27, 2011
Prenatal environmental risk factors for genital malformations in a population of 1442 French male newborns: a nested case-control study
Laura Gaspari, Françoise Paris, Claire Jandel, et al.
Journal of Sports Sciences
|
December 13, 2007
Effect of antioxidants and exercise on bone metabolism
Laurent Maïmoun, David Simar, Corinne Caillaud, et al.
Journal of Molecular Endocrinology
|
May 15, 2007
Coexpression of Wilms' tumor suppressor 1 (WT1) and androgen receptor (AR) in the genital tract of human male embryos and regulation of AR promoter activity by WT1
Birgit Köhler, Anne-Lise Delezoide, Brigitte Boizet-Bonhoure, et al.
European Journal of Endocrinology
|
June 12, 2004
An N-terminal WT1 mutation (P181S) in an XY patient with ambiguous genitalia, normal testosterone production, absence of kidney disease and associated heart defect: enlarging the phenotypic spectrum of WT1 defects
Birgit Köhler, Catherine Pienkowski, Françoise Audran, et al.
Page
of 16
Search research articles
Search
Showing results (71-80 of 157) with videos related to
Sort By:
Page
of 16
International Journal of Pediatric Endocrinology
|
September 25, 2012
Fulvestrant treatment of precocious puberty in girls with McCune-Albright syndrome
Emily K Sims, Sally Garnett, Franco Guzman, et al.
Fertility and Sterility
|
December 18, 2010
Predominant Sertoli cell deficiency in a 46,XY disorders of sex development patient with a new NR5A1/SF-1 mutation transmitted by his unaffected father
Pascal Philibert, Michel Polak, Ana Colmenares, et al.
Journal of the Society for Gynecologic Investigation
|
February 8, 2005
Association between androgen receptor gene CAG repeat polymorphism and plasma testosterone levels in postmenopausal women
Ilma Simoni Brum, Poli Mara Spritzer, Françoise Paris, et al.
Experimental Neurology
|
November 28, 2006
Mild surfection of neural cells, especially motoneurons, in primary culture and cell lines
Clovis Rakotoarivelo, Didier Petite, Jan de Weille, et al.
European Journal of Endocrinology
|
April 29, 2010
Bone mineral density acquisition in peripubertal female rhythmic gymnasts is directly associated with plasma IGF1/IGF-binding protein 3 ratio
Laurent Maïmoun, Olivier Coste, Florence Galtier, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 5, 2009
Mother-to-son transmission of a luteinizing hormone receptor activating mutation in a prepubertal child with testotoxicosis
Marumudi Eunice, Pascal Philibert, Bindu Kulshreshtha, et al.
Human Reproduction (Oxford, England)
|
August 27, 2011
Prenatal environmental risk factors for genital malformations in a population of 1442 French male newborns: a nested case-control study
Laura Gaspari, Françoise Paris, Claire Jandel, et al.
Journal of Sports Sciences
|
December 13, 2007
Effect of antioxidants and exercise on bone metabolism
Laurent Maïmoun, David Simar, Corinne Caillaud, et al.
Journal of Molecular Endocrinology
|
May 15, 2007
Coexpression of Wilms' tumor suppressor 1 (WT1) and androgen receptor (AR) in the genital tract of human male embryos and regulation of AR promoter activity by WT1
Birgit Köhler, Anne-Lise Delezoide, Brigitte Boizet-Bonhoure, et al.
European Journal of Endocrinology
|
June 12, 2004
An N-terminal WT1 mutation (P181S) in an XY patient with ambiguous genitalia, normal testosterone production, absence of kidney disease and associated heart defect: enlarging the phenotypic spectrum of WT1 defects
Birgit Köhler, Catherine Pienkowski, Françoise Audran, et al.
Page
of 16