Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole (2008)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; CASTRO, MARGARET DE - FMRP
- Unidades: FM; FMRP
- DOI: 10.1111/j.1365-2265.2007.03160.x
- Subjects: ENDOCRINOLOGIA; PUBERDADE PRECOCE
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Clinical Endocrinology
- ISSN: 0300-0664
- Volume/Número/Paginação/Ano: v. 69, n. 1, p. 93-98, 2008
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ALMEIDA, Madson Queiroz; BRITO, Vinicius Nahime; LINS, Thereza Selma S.; et al. Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole. Clinical Endocrinology, Oxford, v. 69, n. 1, p. 93-98, 2008. DOI: 10.1111/j.1365-2265.2007.03160.x. -
APA
Almeida, M. Q., Brito, V. N., Lins, T. S. S., Guerra-Júnior, G., Castro, M. de, Antonini, S. R., et al. (2008). Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole. Clinical Endocrinology, 69( 1), 93-98. doi:10.1111/j.1365-2265.2007.03160.x -
NLM
Almeida MQ, Brito VN, Lins TSS, Guerra-Júnior G, Castro M de, Antonini SR, Arnhold IJP, Mendonça BB, Latronico AC. Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole. Clinical Endocrinology. 2008 ; 69( 1): 93-98. -
Vancouver
Almeida MQ, Brito VN, Lins TSS, Guerra-Júnior G, Castro M de, Antonini SR, Arnhold IJP, Mendonça BB, Latronico AC. Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole. Clinical Endocrinology. 2008 ; 69( 1): 93-98. - 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
- Long-term treatment of familial male-limited precocious puberty: Comparison between cyproterone and ketoconazole therapies
- Two novel nonsense mutations of the fibroblast growth factor 8 in patients with congenital isolated hypogonadotropic hypogonadism
- Clinical and molecular analysis of TAC3 and TACR3 genes in Brazilian patients with isolated hypogonadotropic hypogonadism
- 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
- Inhibin alfa-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers
- Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency
Informações sobre o DOI: 10.1111/j.1365-2265.2007.03160.x (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
