Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (2010)
- Autores:
- Autores USP: MENDONÇA, BERENICE BILHARINHO DE - FM ; BACHEGA, TÂNIA APARECIDA SARTORI SANCHEZ - FM
- Unidade: FM
- Assuntos: FARMACOGENÉTICA; HIPERPLASIA SUPRARRENAL CONGÊNITA; HIDROXILASE (DEFICIÊNCIA); RESUMOS (EVENTOS)
- Idioma: Inglês
- Imprenta:
- Fonte:
- Nome do evento: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP"
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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: 19 set. 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 set. 19 ] -
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 set. 19 ] - Síndromes hiperandrogênicas
- Classic congenital adrenal hyperplasia and its impact on reproduction
- Quality of life in a large cohort of adult Brazilian patients with 46,XX and 46,XY disorders of sex development from a single tertiary centre
- Weight-adjusted neonatal 17OH-progesterone cutoff levels improve the efficiency of newborn screening for congenital adrenal hyperplasia
- Modulatory effect of BclI GR gene polymorphisms on the obesity phenotype in Brazilian patients with Cushing's disease
- Clonality analysis and expression of ACTH and androgen receptors in giant myelolipomas
- Long-Term dexamethasone treatment is not associated with obesity and or metabolic syndrome in adult patients with classical forms of 21-hydroxylase deficiency
- Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia
- The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene
- Adrenal crisis and mortality rate in adrenal insufficiency and congenital adrenal hyperplasia
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