Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency (2013)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; BACHEGA, TÂNIA APARECIDA SARTORI SANCHEZ - FM
- Unidade: FM
- DOI: 10.6061/CLINICS/2013(02)OA05
- Subjects: HIDROXILASE (DEFICIÊNCIA); GENÉTICA; ESTUDOS RETROSPECTIVOS; HIPERPLASIAS (DIAGNÓSTICO); RADIOIMUNOENSAIO
- Language: Inglês
- Imprenta:
- Source:
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
GOMES, Larissa G. et al. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, v. 68, n. 2, p. 147-151, 2013Tradução . . Disponível em: https://doi.org/10.6061/CLINICS/2013(02)OA05. Acesso em: 27 fev. 2026. -
APA
Gomes, L. G., Madureira, G., Mendonca, B. B., & Bachega, T. A. S. S. (2013). Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, 68( 2), 147-151. doi:10.6061/CLINICS/2013(02)OA05 -
NLM
Gomes LG, Madureira G, Mendonca BB, Bachega TASS. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinics. 2013 ; 68( 2): 147-151.[citado 2026 fev. 27 ] Available from: https://doi.org/10.6061/CLINICS/2013(02)OA05 -
Vancouver
Gomes LG, Madureira G, Mendonca BB, Bachega TASS. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinics. 2013 ; 68( 2): 147-151.[citado 2026 fev. 27 ] Available from: https://doi.org/10.6061/CLINICS/2013(02)OA05 - 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
Informações sobre o DOI: 10.6061/CLINICS/2013(02)OA05 (Fonte: oaDOI API)
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