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"
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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: 21 fev. 2026. , 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 2026 fev. 21 ] -
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 2026 fev. 21 ] - Plasma Renin Measurements are Unrelated to Mineralocorticoid Replacement Dose in Patients With Primary Adrenal Insufficiency
- CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia
- Long Term Glucocorticoid Exposition Does Not Play the Major Role in the Development of Obesity and Metabolic Syndrome in Classical Form of 21-Hydroxylase Deficiency
- 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
- Long-term cardio-metabolic outcomes in patients with classical congenital adrenal hyperplasia: is the risk real?
- Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency
- 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
- Fadiga e doenças endócrinas
- Neonatal 17-hydroxyprogesterone levels adjusted according to age at sample collection and birthweight improve the efficacy of congenital adrenal hyperplasia newborn screening
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