Screening blood donors for hereditary hemochromatosis: Decision analysis model based on a 30-year database
- 31 July 1995
- journal article
- Published by Elsevier BV in Gastroenterology
- Vol. 109 (1), 177-188
- https://doi.org/10.1016/0016-5085(95)90283-x
Abstract
No abstract availableThis publication has 33 references indexed in Scilit:
- Prevalence of abnormal iron studies in heterozygotes for hereditary hemochromatosis: An analysis of 255 heterozygotesAmerican Journal of Hematology, 1994
- Screening for haemochromatosis: prevalence among Danish blood donorsJournal of Internal Medicine, 1991
- Screening for haemochromatosis: Influence of analytical imprecision, diagnostic limit and prevalence on test validityScandinavian Journal of Clinical and Laboratory Investigation, 1991
- Phenotypic expression of the HLA linked iron-loading gene in males over the age of 40 years: a population study using serial serum ferritin estimationsJournal of Internal Medicine, 1990
- Usefulness of Biochemical Screening of Diabetic Patients for HemochromatosisDiabetes Care, 1990
- Prevalence of HemochromatosisNew England Journal of Medicine, 1988
- Cardiac Abnormalities in Primary HemochromatosisAnnals of the New York Academy of Sciences, 1988
- Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood DonorsNew England Journal of Medicine, 1988
- Survival and Causes of Death in Cirrhotic and in Noncirrhotic Patients with Primary HemochromatosisNew England Journal of Medicine, 1985
- Serum Ferritin as a Possible Marker of the Hemochromatosis AlleleNew England Journal of Medicine, 1979