Refining hormonal diagnosis of type II 3'beta'-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 (2005)
- Authors:
- USP affiliated authors: ELIAS, LUCILA LEICO KAGOHARA - FMRP ; MOREIRA, AYRTON CUSTODIO - FMRP ; MENDONCA, BERENICE BILHARINHO DE - FM ; CASTRO, MARGARET DE - FMRP
- Unidades: FMRP; FM
- Subjects: ENDOCRINOLOGIA; HORMÔNIOS
- Language: Inglês
- Imprenta:
- Publisher place: Chevy Chase
- Date published: 2005
- Source:
- Título do periódico: Journal of Clinical Endocrinology & Metabolism
- ISSN: 0021-972X
- Volume/Número/Paginação/Ano: v. 90, n. 3, p. 1287-1293, 2005
-
ABNT
MERMEJO, Lívia Mara et al. Refining hormonal diagnosis of type II 3'beta'-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2. Journal of Clinical Endocrinology & Metabolism, v. 90, n. 3, p. 1287-1293, 2005Tradução . . Acesso em: 18 abr. 2024. -
APA
Mermejo, L. M., Elias, L. L. K., Marui, S., Moreira, A. C., Mendonça, B. B. de, & Castro, M. de. (2005). Refining hormonal diagnosis of type II 3'beta'-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2. Journal of Clinical Endocrinology & Metabolism, 90( 3), 1287-1293. -
NLM
Mermejo LM, Elias LLK, Marui S, Moreira AC, Mendonça BB de, Castro M de. Refining hormonal diagnosis of type II 3'beta'-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2. Journal of Clinical Endocrinology & Metabolism. 2005 ; 90( 3): 1287-1293.[citado 2024 abr. 18 ] -
Vancouver
Mermejo LM, Elias LLK, Marui S, Moreira AC, Mendonça BB de, Castro M de. Refining hormonal diagnosis of type II 3'beta'-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2. Journal of Clinical Endocrinology & Metabolism. 2005 ; 90( 3): 1287-1293.[citado 2024 abr. 18 ] - Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency
- Insuficiência adrenal primária no adulto: 150 anos depois de Addison
- Endocrine disorders in pediatric: onset langerhans cell histiocytosis
- Hiperplasia adrenal congênita (HAC) por deficiência da enzima 3'beta'-hidroxiesteróide desidrogenase (3'beta'HSD): análise bioquímica e genética
- Hiperplasia adrenal congênita (HAC) por deficiência da 3'beta'-hidroxisteroide desidrogenase (3'beta'HSD): análise e bioquímica e genética
- Sensibilidade aos glicocorticóides (GC) em indivíduos normais
- A dose-response study of salivary cortisol after dexamethasone suppression test in Cushing's disease and its potential use in the differential diagnosis of Cushing's syndrome
- Glucocorticoid sensitivity in young healthy individuals: in vitro and in vivo studies
- Salivary cortisol response to overnight dexamethasone suppression test in the differential diagnosis of cushing syndrome
- Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
