Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort (2011)
- Authors:
- USP affiliated authors: CASTRO, MARGARET DE - FMRP ; MONTENEGRO, LUCIANA RIBEIRO - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Schools: FMRP; FM
- Subject: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Place of publication: Chevy Chase
- Date published: 2011
- Source:
- Título do periódico: Endocrine Reviews
- ISSN: 0163-769X
- Volume/Número/Paginação/Ano: v. 32, suppl. 3, res. P3-707, 2011
- Conference title: International Pituitary Congress
-
ABNT
SILVEIRA, Letícia F. G. et al. Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort. Endocrine Reviews. Chevy Chase: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 04 jul. 2022. , 2011 -
APA
Silveira, L. F. G., Teles, M. G., Abreu, A. P., Montenegro, L. R., Tusset, C., Beneduzzi, D., et al. (2011). Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort. Endocrine Reviews. Chevy Chase: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Silveira LFG, Teles MG, Abreu AP, Montenegro LR, Tusset C, Beneduzzi D, Castro M de, Costa EMF, Lofrano-Porto A, Baptista MTM, Garmes HM, Guerra-Júnior G, Mendonça BB de, Latronico AC, Trarbach EB. Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort. Endocrine Reviews. 2011 ; 32[citado 2022 jul. 04 ] -
Vancouver
Silveira LFG, Teles MG, Abreu AP, Montenegro LR, Tusset C, Beneduzzi D, Castro M de, Costa EMF, Lofrano-Porto A, Baptista MTM, Garmes HM, Guerra-Júnior G, Mendonça BB de, Latronico AC, Trarbach EB. Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort. Endocrine Reviews. 2011 ; 32[citado 2022 jul. 04 ] - Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome
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- Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients
- 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
- Clinical and molecular analysis of TAC3 and TACR3 genes in Brazilian patients with isolated hypogonadotropic hypogonadism
- Novel mutations (P.G6R and P.R511W) in IGF1R gene in children born small for gestational age (SGA) without catch-up growth
- 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: Comparison between cyproterone and ketoconazole therapies
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