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Results 1-10 of 22 (Search time: 0.054 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 | 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 | New mutation in the CASR gene in a family with familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT) | RODRIGUES, Luiza Souza; CAU, Ana Carolina Arias; BUSSMANN, Luciane Zgoda; BASTIDA, Gabriela; BRUNETTO, Oscar H.; CORREA, Pedro Henrique Silveira; MARTIN, Regina Matsunaga |
| 2011 | Transitory increase in creatinine levels after parathyroidectomy: evidence of another action of the parathyroid glands? | MONTENEGRO, Fabio M.; BRANDAO, Lenine G.; FERREIRA, Gustavo F.; LOURENCO JR., Delmar M.; MARTIN, Regina M.; CUNHA-NETO, Malebranche B.; HELOU, Claudia B.; TOLEDO, Sergio A.; CORDEIRO, Anoi C.; IANHEZ, Luiz E. |
| 2011 | Os interferentes endócrinos ambientais precisam receber a atenção dos endocrinologistas brasileiros | BACHEGA, Tania A. S. Sanchez; VERRESCHI, Ieda T.; FRADE, Elaine M. Costa; D'ABRONZO, Francisco Homero; LAZARETTI-CASTRO, Marise |
| 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. |
| 2011 | Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism | BENEDUZZI, Daiane; IYER, Anita K.; TRARBACH, Ericka Barbosa; SILVEIRA-NETO, Acacio P.; SILVEIRA, Leticia G.; TUSSET, Cintia; YIP, Kathleen; MENDONCA, Berenice B.; MELLON, Pamela L.; LATRONICO, Ana Claudia |
| 2011 | Clinical and molecular aspects of congenital isolated hypogonadotropic hypogonadism | TUSSET, Cintia; TRARBACH, Ericka B.; SILVEIRA, Leticia Ferreira Gontijo; BENEDUZZI, Daiane; MONTENEGRO, Luciana; LATRONICO, Ana Claudia |