Screening for haemochromatosis—producing or preventing illness?
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference13 articles.
1. Hemochromatosis mutations in the general population: iron overload progression rate;Andersen;Blood,2004
2. Genetic exceptionalism in medicine: clarifying the differences between genetic and nongenetic tests;Green;Ann Intern Med,2003
3. Penetrance of the 845G to A (C282Y) HFE hereditary haemochromatosis mutation in the USA;Beutler;Lancet,2002
4. Non-invasive prediction of cirrhosis in C282Y-linked hemochromatosis;Beaton;Hepatology,2002
5. Disease-related conditions in relatives of patients with hemochromatosis;Bulaj;N Engl J Med,2000
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1. Effects of Excess Iron on the Retina: Insights From Clinical Cases and Animal Models of Iron Disorders;Frontiers in Neuroscience;2022-02-03
2. Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis;Human Molecular Genetics;2014-02-20
3. Hereditary Hemochromatosis: Pathophysiology, Diagnosis, and Management;Critical Care Nursing Clinics of North America;2008-06
4. Asymptomatic individuals at genetic risk of haemochromatosis take appropriate steps to prevent disease related to iron overload;Liver International;2008-02-15
5. Clinical Manifestations of Hemochromatosis inHFEC282Y Homozygotes Identified by Screening;Canadian Journal of Gastroenterology;2008
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