A large brazilian genealogy presenting familial medullary thyroid carcinoma (FMTC), C620R ret mutation and hirchprung disease (HSCR): Total thyroidectomy at early MTC stages (2008)
- Authors:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Subjects: PROTO-ONCOGENES; CARCINOMA MEDULAR
- Language: Inglês
- Imprenta:
- Source:
- Título: Arquivos Brasileiros de Endocrinologia e Metabologia
- ISSN: 0004-2730
- Volume/Número/Paginação/Ano: v. 52, supl. 6, parte II, p. S1161, res. PO-1080, 2008
- Conference titles: International Congress of Endocrinology
-
ABNT
AZEVEDO, J. A. et al. A large brazilian genealogy presenting familial medullary thyroid carcinoma (FMTC), C620R ret mutation and hirchprung disease (HSCR): Total thyroidectomy at early MTC stages. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 06 out. 2024. , 2008 -
APA
Azevedo, J. A., Lourenço Junior, D. M., Toledo, R. A., Quedas, E., Toledo, S. P. A., Ezabella, M. C. L., et al. (2008). A large brazilian genealogy presenting familial medullary thyroid carcinoma (FMTC), C620R ret mutation and hirchprung disease (HSCR): Total thyroidectomy at early MTC stages. Arquivos Brasileiros de Endocrinologia e Metabologia. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Azevedo JA, Lourenço Junior DM, Toledo RA, Quedas E, Toledo SPA, Ezabella MCL, Nunes AB, Tavares MR. A large brazilian genealogy presenting familial medullary thyroid carcinoma (FMTC), C620R ret mutation and hirchprung disease (HSCR): Total thyroidectomy at early MTC stages. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S1161.[citado 2024 out. 06 ] -
Vancouver
Azevedo JA, Lourenço Junior DM, Toledo RA, Quedas E, Toledo SPA, Ezabella MCL, Nunes AB, Tavares MR. A large brazilian genealogy presenting familial medullary thyroid carcinoma (FMTC), C620R ret mutation and hirchprung disease (HSCR): Total thyroidectomy at early MTC stages. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52 S1161.[citado 2024 out. 06 ] - Molecular analysis of p53 vhl and ret genes in pheochromocytoma
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- Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene
- Lit/lit mice release growth hormone (GH) in response to GH releasing peptide-2 (GHRP-2) administration
- Impact of RET proto-oncogene analysis on the clinical management of multiple endocrine neoplasia type 2
- A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas
- Neoplasia endócrina múltipla
- Rastreamento de mutações no gene ret em indivíduos com baixa idade, sob risco para neoplasia endócrina múltipla, tipo 2 (NEM-2)
- Hugt frequency of hirschprung in a large family C620R-ret mutated family
- Peptide hormone receptor defects leading to abnormal phenotypes
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