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 é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by-nc
-
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: 18 abr. 2024. -
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 2024 abr. 18 ] 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 2024 abr. 18 ] Available from: https://doi.org/10.6061/CLINICS/2013(02)OA05 - 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
- 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
- Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Informações sobre o DOI: 10.6061/CLINICS/2013(02)OA05 (Fonte: oaDOI API)
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