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Results 1-10 of 23 (Search time: 0.031 seconds).
| Issue Date | Title | Author(s) |
|---|---|---|
| 2011 | 46,XY DSD due to 17 beta-HSD3 Deficiency and 5 alpha-Reductase Type 2 Deficiency | INACIO, Marlene; SIRCILI, Maria Helena P.; BRITO, Vinicius N.; DOMENICE, Sorahia; OLIVEIRA-JUNIOR, Ari Alves; ARNHOLD, Ivo J. P.; TIBOR, Francisco D.; COSTA, Elaine M. F.; MENDONCA, Berenice B. |
| 2011 | 46,XY Disorders of Sex Development (46,XY DSD) due to Androgen Receptor Defects: Androgen Insensitivity Syndrome | ARNHOLD, Ivo J. P.; MELO, Karla; COSTA, Elaine M. F.; DANILOVIC, Debora; INACIO, Marlene; DOMENICE, Sorahia; MENDONCA, Berenice B. |
| 2011 | MAMLD1 (Mastermind-Like Domain Containing 1) Homozygous Gain-of-Function Missense Mutation Causing 46,XX Disorder of Sex Development in a Virilized Female | BRANDAO, Maira Pontual; COSTA, Elaine Maria Frade; FUKAMI, Maki; GERDULO, Mariza; PEREIRA, Natalia P.; DOMENICE, Sorahia; OGATA, Tsutomu; MENDONCA, Berenice B. |
| 2011 | BUPROPION/NALTREXONE FIXED-DOSE COMBINATION FOR THE TREATMENT OF OBESITY | HALPERN, B.; FARIA, A. M.; HALPERN, A. |
| 2011 | Zona fasciculata 21-hydroxysteroids and precursor-to-product ratios in 21-hydroxylase deficiency: Further characterization of classic and non-classic patients and heterozygote carriers | COSTA-BARBOSA, F. A.; CARVALHO, V. M.; NAKAMURA, O. H.; BACHEGA, T. A. S. S.; VIEIRA, J. G. H.; KATER, C. E. |
| 2011 | Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency | MOREIRA, Ricardo P. P.; JORGE, Alexander A. L.; GOMES, Larissa G.; KAUPERT, Laura C.; MASSUD FILHO, Joao; MENDONCA, Berenice B.; BACHEGA, Tania A. S. S. |
| 2011 | Glucose-dependent insulinotropic peptide receptor overexpression in adrenocortical hyperplasia in MEN1 syndrome without loss of heterozygosity at the 11q13 locus | COSTA, Marcia Helena Soares; DOMENICE, Sorahia; TOLEDO, Rodrigo Almeida; JUNIOR, Delmar Muniz L.; LATRONICO, Ana Claudia; PINTO, Emilia Modolo; TOLEDO, Sergio Pereira Almeida; MENDONCA, Berenice Bilharinho; FRAGOSO, Maria Candida Barisson Villares |
| 2011 | Frequency of genetic polymorphisms of PXR gene in the Brazilian population | MOREIRA, Ricardo P. P.; JORGE, Alexander A. L.; MENDONCA, Berenice B.; BACHEGA, Tania A. S. S. |
| 2011 | A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndrome | SILVA, Thatiana Evilen da; NISHI, Mirian Yumie; COSTA, Elaine Maria Frade; MARTIN, Regina Matsunaga; CARVALHO, Filomena Marino; MENDONCA, Berenice Bilharinho; DOMENICE, Sorahia |
| 2011 | KISS1R Intracellular Trafficking and Degradation: Effect of the Arg386Pro Disease-Associated Mutation | BIANCO, Suzy D. C.; VANDEPAS, Lauren; CORREA-MEDINA, Mayrin; GEREBEN, Balazs; MUKHERJEE, Abir; KUOHUNG, Wendy; CARROLL, Rona; TELES, Milena G.; LATRONICO, Ana Claudia; KAISER, Ursula B. |