Clinical and molecular analysis of TAC3 and TACR3 genes in Brazilian patients with isolated hypogonadotropic hypogonadism (2011)
- Authors:
- USP affiliated authors: CASTRO, MARGARET DE - FMRP ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidades: FMRP; FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Chevy Chase
- Date published: 2011
- Source:
- Título do periódico: Endocrine Reviews
- ISSN: 0163-769X
- Volume/Número/Paginação/Ano: v. 32, suppl. 3, res. P3-708, 2011
- Conference titles: International Pituitary Congress
-
ABNT
TUSSET, Cintia et al. Clinical and molecular analysis of TAC3 and TACR3 genes in Brazilian patients with isolated hypogonadotropic hypogonadism. Endocrine Reviews. Chevy Chase: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 2011 -
APA
Tusset, C., Trarbach, E., Silveira, L. G., Mendonça, B. B. de, Castro, M. de, Guerra, G., et al. (2011). Clinical and molecular analysis of TAC3 and TACR3 genes in Brazilian patients with isolated hypogonadotropic hypogonadism. Endocrine Reviews. Chevy Chase: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Tusset C, Trarbach E, Silveira LG, Mendonça BB de, Castro M de, Guerra G, Lofrano A, Latronico AC. Clinical and molecular analysis of TAC3 and TACR3 genes in Brazilian patients with isolated hypogonadotropic hypogonadism. Endocrine Reviews. 2011 ; 32[citado 2024 abr. 19 ] -
Vancouver
Tusset C, Trarbach E, Silveira LG, Mendonça BB de, Castro M de, Guerra G, Lofrano A, Latronico AC. Clinical and molecular analysis of TAC3 and TACR3 genes in Brazilian patients with isolated hypogonadotropic hypogonadism. Endocrine Reviews. 2011 ; 32[citado 2024 abr. 19 ] - Hemizygous deletion of FGFR1 gene identified in a patient with congenital normosmic isolated hypogonadotropic hypogonadism by ligation-dependent probe amplification analysis
- Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2
- Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence
- Two novel nonsense mutations of the fibroblast growth factor 8 in patients with congenital isolated hypogonadotropic hypogonadism
- Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole
- Long-term treatment of familial male-limited precocious puberty: Comparison between cyproterone and ketoconazole therapies
- Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients
- Análise da região promotora do gene HESX1 em pacientes com deficiência hormonal hipofisária combinada (DHHC) sem mutações na região codoficadora do HESX1
- Inhibin alfa-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers
- Glucocorticoid receptor structure in ACTH-producing pituitary tumors
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