Associated Papers
Genetic variants underlying precancerous conditions of hepatocellular carcinoma.
Guerrero JJG et al.
International Journal of Cancer, 2026
Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients.
Sokkar MF et al.
Biochemical Genetics, 2025
Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y.
Barton JC et al.
Plos One, 2022
Iron overload and cirrhosis in referred HFE p.C282Y homozygotes with normal transferrin saturation and elevated serum ferritin.
Adams PC et al.
Canadian Liver Journal, 2020
Effect of the A736V TMPRSS6 polymorphism on the penetrance and clinical expression of hereditary hemochromatosis.
Valenti L et al.
Journal of Hepatology, 2012
Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosis.
Hattori A et al.
Blood Cells, Molecules & Diseases, 2012
Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload.
de Lima Santos PC et al.
Genetic Testing and Molecular Biomarkers, 2010
Analysis of nucleotide variations in genes of iron management in patients of Parkinson's disease and other movement disorders.
Castiglioni E et al.
Parkinson's Disease, 2010
Hepcidin mutation in a beta-thalassemia major patient with persistent severe iron overload despite chelation therapy.
Duca L et al.
Internal and Emergency Medicine, 2010
HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants.
Barton JC et al.
American Journal of Hematology, 2009
Relative contribution of iron genes, dysmetabolism and hepatitis C virus (HCV) in the pathogenesis of altered iron regulation in HCV chronic hepatitis.
Valenti L et al.
Haematologica, 2007
Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele.
Biasiotto G et al.
Blood Cells, Molecules & Diseases, 0
Iron overload is not the same everywhere: Particularities of iron-metabolism gene mutations in Brazil and a proposal for the investigation and management of iron overload in this population.
de Melo Campos P et al.
Hematology, Transfusion and Cell Therapy, 0
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