Síndromes hiperandrogênicas (2022)
- Authors:
- USP affiliated authors: BACHEGA, TÂNIA APARECIDA SARTORI SANCHEZ - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: HIRSUTISMO; SÍNDROME DO OVÁRIO POLICÍSTICO
- Language: Português
- Imprenta:
- Publisher: Atheneu
- Publisher place: Rio de Janeiro
- Date published: 2022
- ISBN: 9786555862980
- Source:
- Título: Endocrinologia e Metabologia
-
ABNT
COSTA, Fernanda Cavalieri et al. Síndromes hiperandrogênicas. Endocrinologia e Metabologia. Tradução . Rio de Janeiro: Atheneu, 2022. . . Acesso em: 27 dez. 2025. -
APA
Costa, F. C., Bachega, T. A. S. S., Mendonca, B. B. de, & Gomes, L. G. (2022). Síndromes hiperandrogênicas. In Endocrinologia e Metabologia. Rio de Janeiro: Atheneu. -
NLM
Costa FC, Bachega TASS, Mendonca BB de, Gomes LG. Síndromes hiperandrogênicas. In: Endocrinologia e Metabologia. Rio de Janeiro: Atheneu; 2022. [citado 2025 dez. 27 ] -
Vancouver
Costa FC, Bachega TASS, Mendonca BB de, Gomes LG. Síndromes hiperandrogênicas. In: Endocrinologia e Metabologia. Rio de Janeiro: Atheneu; 2022. [citado 2025 dez. 27 ] - 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
- Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening
- 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
- 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
- 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
- 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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