The significance of haemochromatosis gene mutations in the general population: implications for screening. - Wikidata - wikimedia - TriplyDB

The significance of haemochromatosis gene mutations in the general population: implications for screening.

The significance of haemochromatosis gene mutations in the general population: implications for screening.

http://www.wikidata.org/entity/Q35353437

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Pathophysiology of hereditary hemochromatosis Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance Hepatocellular carcinoma and the penetrance of HFE C282Y mutations: a cross sectional study Hemochromatosis gene in leukemia and lymphoma Genetic predisposition to iron overload: prevalence and phenotypic expression of hemochromatosis-associated HFE-C282Y gene mutation Modifying factors of the HFE hemochromatosis phenotype Genetic susceptibility to lead poisoning Incidence of liver disease in people with HFE mutations.Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins.Nucleotide-binding oligomerization domain containing 1 (NOD1) haplotypes and single nucleotide polymorphisms modify susceptibility to inflammatory bowel diseases in a New Zealand caucasian population: a case-control study.HFE gene mutations increase the risk of coronary heart disease in women.Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH).IMPDH1 promoter mutations in a patient exhibiting azathioprine resistance.Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis.Public health aspects of genetic screening for hereditary haemochromatosis in Australia.Hereditary hemochromatosis: perspectives of public health, medical genetics, and primary care.Prevalent iron metabolism gene variants associated with increased brain ferritin iron in healthy older men.Mutations in the hereditary haemochromatosis gene HFE in professional endurance athletes.Population screening for haemochromatosis.HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?Haemochromatosis gene mutations in idiopathic dilated cardiomyopathy.Iron nutrition in the UK: getting the balance right.A diagnostic approach to hemochromatosis Haplotype Analysis of Hemochromatosis Gene Polymorphisms in Chronic Hepatitis C Virus Infection: A Case Control Study.Single nucleotide polymorphism in the tumor necrosis factor-alpha gene affects inflammatory bowel diseases risk HFE gene variants affect iron in the brain.Iron neurochemistry in Alzheimer's disease and Parkinson's disease: targets for therapeutics.Clinical penetrance in hereditary hemochromatosis: estimates of the cumulative incidence of severe liver disease among HFE C282Y homozygotes.Hemochromatosis gene mutations may affect the survival of patients with myelodysplastic syndrome.Tumor necrosis factor receptor superfamily, member 1B haplotypes increase or decrease the risk of inflammatory bowel diseases in a New Zealand caucasian population.Screening in liver disease.HFE based re-evaluation of heterozygous hemochromatosis.Iron-related gene variants and brain iron in multiple sclerosis and healthy individuals.Mice lacking liver-specific β-catenin develop steatohepatitis and fibrosis after iron overload.Opinion of the Scientific Panel on Dietetic products, nutrition and allergies [NDA] related to the Tolerable Upper Intake Level of Iron The role of HFE genotype in macrophage phenotype.Using iron studies to predict HFE mutations in New Zealand: implications for laboratory testing.Influence of haemochromatosis gene mutations on treatment outcomes in patients with hepatitis C.

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P2860

The significance of haemochromatosis gene mutations in the general population: implications for screening.

http://www.wikidata.org/entity/Q35353437

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1998 nî lūn-bûn

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P2860

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

Global prevalence of putative haemochromatosis mutations

Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis.

Screening for hemochromatosis.

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis.

Genetic linkage between hereditary hemochromatosis and HLA

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients

Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene.

The genetics of hemochromatosis.

Hemochromatosis screening in asymptomatic ambulatory men 30 years of age and older.

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