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B B Mendonca

Showing results (31-40 of 82) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 1, 1995
Women with steroid 5 alpha-reductase 2 deficiency have normal concentrations of plasma 5 alpha-dihydroprogesterone during the luteal phaseL Milewich, B B Mendonca, I Arnhold, et al.
Clinical Endocrinology|January 29, 2000
Mutations in the type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girlsS Marui, M Castro, A C Latronico, et al.
Journal of Medical Genetics|June 1, 1996
Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjectsC Kwok, C Tyler-Smith, B B Mendonca, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 1, 2001
Adrenal nodules in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: regression after adequate hormonal controlL R Giacaglia, B B Mendonca, G Madureira, et al.
Journal of Endocrinological Investigation|June 15, 2000
Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletionsI J Arnhold, S B Oliveira, M G Osorio, et al.
Biochemistry|February 8, 1994
Natural mutagenesis study of the human steroid 5 alpha-reductase 2 isozymeW C Wigley, J S Prihoda, I Mowszowicz, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|December 23, 2003
Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patientsS Domenice, R V Corrêa, E M F Costa, et al.
Journal of Steroid Biochemistry|December 1, 1987
Male pseudohermaphroditism due to nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency: gender role change and absence of gynecomastia at pubertyB B Mendonca, W Bloise, I J Arnhold, et al.
Revista Do Hospital Das Clinicas|August 12, 1998
Protocol for rapid fetal sex determination in chorionic villus through polimerase chain reactionS Domenice, A E Billerbeck, R O Rocha, et al.
Fertility and Sterility|October 3, 1998
No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failureM B da Fonte Kohek, M C Batista, A J Russell, et al.
Pageof 9

Showing results (31-40 of 82) with videos related to

Sort By:
Pageof 9
The Journal of Clinical Endocrinology and Metabolism|November 1, 1995
Women with steroid 5 alpha-reductase 2 deficiency have normal concentrations of plasma 5 alpha-dihydroprogesterone during the luteal phaseL Milewich, B B Mendonca, I Arnhold, et al.
Clinical Endocrinology|January 29, 2000
Mutations in the type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girlsS Marui, M Castro, A C Latronico, et al.
Journal of Medical Genetics|June 1, 1996
Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjectsC Kwok, C Tyler-Smith, B B Mendonca, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 1, 2001
Adrenal nodules in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: regression after adequate hormonal controlL R Giacaglia, B B Mendonca, G Madureira, et al.
Journal of Endocrinological Investigation|June 15, 2000
Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletionsI J Arnhold, S B Oliveira, M G Osorio, et al.
Biochemistry|February 8, 1994
Natural mutagenesis study of the human steroid 5 alpha-reductase 2 isozymeW C Wigley, J S Prihoda, I Mowszowicz, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|December 23, 2003
Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patientsS Domenice, R V Corrêa, E M F Costa, et al.
Journal of Steroid Biochemistry|December 1, 1987
Male pseudohermaphroditism due to nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency: gender role change and absence of gynecomastia at pubertyB B Mendonca, W Bloise, I J Arnhold, et al.
Revista Do Hospital Das Clinicas|August 12, 1998
Protocol for rapid fetal sex determination in chorionic villus through polimerase chain reactionS Domenice, A E Billerbeck, R O Rocha, et al.
Fertility and Sterility|October 3, 1998
No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failureM B da Fonte Kohek, M C Batista, A J Russell, et al.
Pageof 9