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: 10 mar. 2026. , 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 2026 mar. 10 ] -
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 2026 mar. 10 ] - Primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 (HTP/Men 1): Increment of bone mineral density after parathyroidectomy
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- AIP ad P27/KIP1 gne vriants are not associated ptuitary aenoma penotypes in a large MEN1 family
- Sindrome hereditária caracterizada por micropênis, hipoandrogenismo e níveis séricos altos de gonadotrofinas devido a distúrbio primário nas células de leydig, associada a testículos de tamanho normal e ausência de ambiguidade genital: uma provável nova entidade clínica
- Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female
- Missense mutation in the lh receptor gene causas leydig cell hypoplasia
- A differential diagnosis of inherited endocrine tumors and their tumor counterparts
- Hugt frequency of hirschprung in a large family C620R-ret mutated family
- Peptide hormone receptor defects leading to abnormal phenotypes
- Hypercalcitoninemia is not pathognomonic of medullary thyroid carcinoma
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