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	Provedor de dados BJMBR (1) Autor Alves,M.A.V.R. (1) Costa,F.F. (1) Perícole,F.V. (1) Saad,S.T.O. (1) Palavra-chave Anemia (1) Chronic renal insufficiency (1) HFE (1) Iron metabolism (1) Tipo do documento Info:eu-repo/semantics/other (1) Ano 2005 (1) País Brazil (1) Idioma Inglês (1)		Ordenar por:  Relevância Autor Título Ano Registros recuperados: 1 Primeira ... 1 ... Última Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patients BJMBR Perícole,F.V.; Alves,M.A.V.R.; Saad,S.T.O.; Costa,F.F.. Patients with chronic renal insufficiency (CRI) have reduced hemoglobin levels, mostly as a result of decreased kidney production of erythropoietin, but the relation between renal insufficiency and the magnitude of hemoglobin reduction has not been well defined. Hereditary hemochromatosis is an inherited disorder of iron metabolism. The importance of the association of hemochromatosis with treatment for anemia among patients with CRI has not been well described. We analyzed the frequency of the C282Y and H63D mutations in the HFE gene in 201 Brazilian individuals with CRI undergoing hemodialysis. The analysis of the effects of HFE mutations on iron metabolism and anemia with biochemical parameters was possible in 118 patients of this study (hemoglobin,... Tipo: Info:eu-repo/semantics/other Palavras-chave: HFE; Chronic renal insufficiency; Anemia; Iron metabolism. Ano: 2005 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2005000900005 Registros recuperados: 1 Primeira ... 1 ... Última

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