High prevalence of adrenal insufficiency in adults with childhood onset growth hormone deficiency without PROP1 or HESX1 mutations (2004)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: GLÂNDUALAS SUPRA-RENAIS; MUTAÇÃO GENÉTICA; GLÂNDULA PITUITÁRIA (FISIOPATOLOGIA); IMAGEM POR RESSONÂNCIA MAGNÉTICA; HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA); RESUMOS (CONGRESSOS)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of pediatric endocrinology and metabolism
- ISSN: 0334-018X
- Volume/Número/Paginação/Ano: v. 17, n. suppl.5, p. 1343, res. Miniposter 10, 2004
- Conference titles: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP)
-
ABNT
MARCHISOTTI, F. G. et al. High prevalence of adrenal insufficiency in adults with childhood onset growth hormone deficiency without PROP1 or HESX1 mutations. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 09 maio 2024. , 2004 -
APA
Marchisotti, F. G., Berger, K., Carvalho, L. R., Arnhold, I. J. P., & Mendonça, B. B. (2004). High prevalence of adrenal insufficiency in adults with childhood onset growth hormone deficiency without PROP1 or HESX1 mutations. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Marchisotti FG, Berger K, Carvalho LR, Arnhold IJP, Mendonça BB. High prevalence of adrenal insufficiency in adults with childhood onset growth hormone deficiency without PROP1 or HESX1 mutations. Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1343.[citado 2024 maio 09 ] -
Vancouver
Marchisotti FG, Berger K, Carvalho LR, Arnhold IJP, Mendonça BB. High prevalence of adrenal insufficiency in adults with childhood onset growth hormone deficiency without PROP1 or HESX1 mutations. Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1343.[citado 2024 maio 09 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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