Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (2010)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; BACHEGA, TÂNIA APARECIDA SARTORI SANCHEZ - FM
- Unidade: FM
- Subjects: FARMACOGENÉTICA; HIPERPLASIA SUPRARRENAL CONGÊNITA; HIDROXILASE (DEFICIÊNCIA); RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP"
-
ABNT
MOREIRA, R P P et al. Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 04 maio 2024. , 2010 -
APA
Moreira, R. P. P., Kaupert, L. C., Gomes, L. G., Madureira, G., Mendonça, B. B. de, & Bachega, T. A. S. S. (2010). Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Moreira RPP, Kaupert LC, Gomes LG, Madureira G, Mendonça BB de, Bachega TASS. Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics. 2010 ; 65 S70.[citado 2024 maio 04 ] -
Vancouver
Moreira RPP, Kaupert LC, Gomes LG, Madureira G, Mendonça BB de, Bachega TASS. Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics. 2010 ; 65 S70.[citado 2024 maio 04 ] - Síndromes hiperandrogênicas
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- Modulatory effect of BclI GR gene polymorphisms on the obesity phenotype in Brazilian patients with Cushing's disease
- Gender identity and sexual orientation in adult patients with classical virilizing congenital adrenal hyperplasia (CAH)
- Overexpression of 5 alfa-reductase type 2 in genital skin contributes to higher degree of external genitalia virilization in CAH females
- Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency
- The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene
- Impact of Glucocorticoid Receptor Gene Polymorphisms on Lipid Profile of Children and Adolescents with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
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