Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate (2004)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidades: FM
- Subjects: CORTISOL (APLICAÇÕES TERAPÊUTICAS); HORMÔNIOS (DEFICIÊNCIA); TERAPIAS COMPLEMENTARES; HIPERPLASIA SUPRARRENAL CONGÊNITA
- Language: Inglês
- Imprenta:
- Publisher: International Society of Endocrinology
- Place of publication: Lisboa
- Date published: 2004
- Source:
- Título do periódico: Program and Abstracts
- Conference title: International Congress of Endocrinology
-
ABNT
PARENTE, E.; MARQUEZINE, E.; RODRIGUES, a.; et al. Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. Anais.. Lisboa: International Society of Endocrinology, 2004. -
APA
Parente, E., Marquezine, E., Rodrigues, a., Maureira, G., Brenlha, E. M., Ueti, R., et al. (2004). Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. In Program and Abstracts. Lisboa: International Society of Endocrinology. -
NLM
Parente E, Marquezine E, Rodrigues a., Maureira G, Brenlha EM, Ueti R, Arnhold I, Mendonca BB, Bachega TAS. Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. Program and Abstracts. 2004 ; -
Vancouver
Parente E, Marquezine E, Rodrigues a., Maureira G, Brenlha EM, Ueti R, Arnhold I, Mendonca BB, Bachega TAS. Final heigth in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency treated with cortisone acetate. Program and Abstracts. 2004 ; - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Crescimento linear e estatura final em crianças com tumores adrenais predominantemente virilizantes
- Absense of inactivating mutations and deletions of DAX1 gene in SRY negative 46,XX sex-reversed patients
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
- Heterogeneidade clínica e molecular do hipogonadismo hipogonadotrófico (HH): importância da avaliação do sistema olfatório no diagnóstico diferencial
- Number of CAG repeats in Exon 1 of androgen receptor gene is not related to gender identity in adult patients with male psudohermaphroditism and male transexualism
- Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitibity syndrome in a brazilian cohort: five novel mutations in the androgen receptor gene
- Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Reavaliação na idade adulta do diagnóstico da deficiência de GH (DGH) determinado na infância
- Missense mutation a300v in the DAX1 gene in a Brazilian male with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism
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