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Diagnosis and treatment of hereditary hemochromatosis: an update.

Diagnosis and treatment of hereditary hemochromatosis: an update.

http://www.wikidata.org/entity/Q38132275

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Management of human factors engineering-associated hemochromatosis: A 2015 update Pathophysiological consequences and benefits of HFE mutations: 20 years of research.Novel gain of function mutation in the SLC40A1 gene associated with hereditary haemochromatosis type 4.Detection of Endogenous Iron Reduction during Hepatocarcinogenesis at Susceptibility-Weighted MR Imaging: Value for Characterization of Hepatocellular Carcinoma and Dysplastic Nodule in Cirrhotic Liver.The risk of new-onset cancer associated with HFE C282Y and H63D mutations: evidence from 87,028 participants High ferritin levels have major effects on the morphology of erythrocytes in Alzheimer's disease.Hypoxia-inducible factors link iron homeostasis and erythropoiesis.Diagnostic morphology: biophysical indicators for iron-driven inflammatory diseases.Use of magnetic resonance imaging to monitor iron overload Recent advances in hemochromatosis: a 2015 update : a summary of proceedings of the 2014 conference held under the auspices of Hemochromatosis Australia.Optimizing the diagnosis and the treatment of iron overload diseases.How we manage patients with hereditary haemochromatosis.Autopsy relevance determining hemochromatosis: Case report.Glyceronephosphate O-acyltransferase as a hemochromatosis modifier gene: Another iron in the fire?Properties of donated red blood cell components from patients with hereditary hemochromatosis.

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Diagnosis and treatment of hereditary hemochromatosis: an update.

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Diagnosis and treatment of hereditary hemochromatosis: an update.

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Diagnosis and treatment of hereditary hemochromatosis: an update.

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17474124.2013.816114

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Expert Review of Gastroenterology & Hepatology

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Diagnosis and treatment of hereditary hemochromatosis: an update.

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Kris V Kowdley

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P2860

A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload.

Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization

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

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

Severe iron deficiency anemia in transgenic mice expressing liver hepcidin

A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload

Geography of HFE C282Y and H63D mutations

Expression of hepcidin in hereditary hemochromatosis: evidence for a regulation in response to the serum transferrin saturation and to non-transferrin-bound iron

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

Global prevalence of putative haemochromatosis mutations

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