15 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 30244162 | Reduced phenotypic expression in genetic hemochromatosis with time: Role of exposure to non-genetic modifiers. | 2019 Jan | 1 |
2 | 26474245 | The role of genetic factors in patients with hepatocellular carcinoma and iron overload - a prospective series of 234 patients. | 2016 May | 1 |
3 | 22728873 | The hemochromatosis proteins HFE, TfR2, and HJV form a membrane-associated protein complex for hepcidin regulation. | 2012 Nov | 1 |
4 | 21354231 | Hemochromatosis gene and nonalcoholic fatty liver disease: a systematic review and meta-analysis. | 2011 Nov | 1 |
5 | 19931264 | HFE genotype, parenchymal iron accumulation, and liver fibrosis in patients with nonalcoholic fatty liver disease. | 2010 Mar | 1 |
6 | 16979952 | The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis. | 2006 Nov | 1 |
7 | 17101320 | Roles of iron and HFE mutations on severity and response to therapy during retreatment of advanced chronic hepatitis C. | 2006 Nov | 1 |
8 | 16234052 | Phenotype variation in C282Y homozygotes for the hemochromatosis gene. | 2005 Oct | 2 |
9 | 12948285 | Heterozygosity for the Cys282Tyr mutation in the HFE gene and the risk of colorectal cancer (Netherlands). | 2003 Aug | 1 |
10 | 15017658 | Natural history of the C282Y homozygote for the hemochromatosis gene (HFE) with a normal serum ferritin level. | 2003 Sep | 1 |
11 | 11874997 | A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation. | 2002 Mar | 1 |
12 | 11984516 | Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene. | 2002 May | 1 |
13 | 10930379 | Two novel nonsense mutations of HFE gene in five unrelated italian patients with hemochromatosis. | 2000 Aug | 1 |
14 | 9922318 | Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives. | 1999 Feb | 1 |
15 | 10348824 | A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote. | 1999 Jun | 1 |