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Possible roles of the hereditary hemochromatosis protein, HFE, in regulating cellular iron homeostasis
(Sociedad de Biología de Chile, 2006)
Hereditary hemochromatosis: An opportunity for gene therapy
(SOCIEDAD BIOLGIA CHILE, 2006)
Levels of body iron should be tightly controlled to prevent the formation of oxygen radicals. lipoperoxidation. genotoxicity, and the production of cytotoxic cytokines, which result in damage to a number of organs. Enterocytes ...
Hereditary hemochromatosis: An opportunity for gene therapy
(Sociedad de Biología de Chile, 2006)
Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis
(Biomed Central Ltd, 2018)
Background: Hereditary hemochromatosis (HH) encompasses a group of autosomal recessive disorders mainly characterized by enhanced intestinal absorption of iron and its accumulation in parenchymal organs. HH diagnosis is ...
Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis
(BioMed Central, 2018)
Abstract
Background
Hereditary hemochromatosis (HH) encompasses a group of autosomal recessive disorders mainly characterized by enhanced intestinal absorption of iron and ...
Hereditary hemochromatosis: an opportunity for gene therapy
(SOCIEDAD DE BIOLOGIA DE CHILE, 2006)
Frequency of hereditary hemochromatosis gene mutations (C282Y and H63D) in hemoglobin S carrier from Brazil.
(Amer Assoc Clinical Chemistry, 2003-06-01)
Frequency of hereditary hemochromatosis gene mutations (C282Y and H63D) in hemoglobin S carrier from Brazil.
(Amer Assoc Clinical Chemistry, 2003-06-01)
Non-HFE hemochromatosis
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2012)
Hereditary hemochromatosis (HH) is an autosomal recessive disorder classically related to HFE mutations. However, since 1996, it is known that HFE mutations explain about 80% of HH cases, with the remaining around 20% ...
Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis
(Faculdade de Medicina / USP, 2009)
BACKGROUND: Approximately one-half of Brazilian patients with hereditary hemochromatosis (HH) are neither homozygous for the C282Y mutation nor compound heterozygous for the H63D and C282Y mutations that are associated ...