Improvement of hyperandrogenism and decrease of glucocorticoid dose with aging in female with 21-hydroxylase deficiency (2006)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: ANDRÓGENOS (ANÁLISE); HIDROXILASE (DEFICIÊNCIA); MULHERES; RESUMOS (CONGRESSOS)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Program & Abstracts
- Conference titles: Annual Meeting of the Endocrine Society's
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ABNT
ADMONI, Sharon N.; BRENLHA, Enecy M. L.; UETI, Rosy C.; et al. Improvement of hyperandrogenism and decrease of glucocorticoid dose with aging in female with 21-hydroxylase deficiency. Anais.. Boston: [s.n.], 2006. -
APA
Admoni, S. N., Brenlha, E. M. L., Ueti, R. C., Madureira, G., Billerbeck, A. E. C., Arnhold, I. J. P., et al. (2006). Improvement of hyperandrogenism and decrease of glucocorticoid dose with aging in female with 21-hydroxylase deficiency. In Program & Abstracts. Boston. -
NLM
Admoni SN, Brenlha EML, Ueti RC, Madureira G, Billerbeck AEC, Arnhold IJP, Mendonça BB de, Bachega TASS. Improvement of hyperandrogenism and decrease of glucocorticoid dose with aging in female with 21-hydroxylase deficiency. Program & Abstracts. 2006 ; -
Vancouver
Admoni SN, Brenlha EML, Ueti RC, Madureira G, Billerbeck AEC, Arnhold IJP, Mendonça BB de, Bachega TASS. Improvement of hyperandrogenism and decrease of glucocorticoid dose with aging in female with 21-hydroxylase deficiency. Program & Abstracts. 2006 ; - 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
- Mutations in the SRY, DAX1, SF1 and WNT4 genes in brazilian sex-reversed patients
- Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty
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