Clinical and biochemical expression of the genetic abnormality in idiopathic hemochromatosis
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
Reference18 articles.
1. Idiopathic hemochromatosis. Demonstration of recessive transmission and early detection by family HLA typing;Simon;N Engl J Med,1977
2. Pedigree analysis of the linkage between HLA and hemochromatosis, genetic epidemiology;Kravitz,1978
3. Genetics of hemochromatosis;Motulsky;N Engl J Med,1979
4. Idiopathic haemochromatosis: an autosomal recessive disease;Saddi;Clin Genet,1974
5. Histocompatibility antigens as markers of abnormal iron metabolism in patients with idiopathic haemochromatosis and their relatives;Bomford;Lancet,1977
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1. Liver Affection in Iron Overload Studied with Serum Ferritin and Serum Aminotransferases;Acta Medica Scandinavica;2009-04-24
2. Evaluation of Liver Iron Content by Computed Tomography: Its Value in the Follow-Up of Treatment in Patients with Idiopathic Hemochromatosis;Hepatology;2007-09-21
3. Circadian variations of transferrin saturation levels in iron-overloaded patients: implications for the screening of C282Y-linked haemochromatosis;British Journal of Haematology;2003-01
4. Biochemical expression of heterozygous hereditary hemochromatosis;European Journal of Internal Medicine;2000-12
5. Population Screening for Haemochromatosis: Expectations Based on a Study of Relatives of Symptomatic Probands;Journal of Medical Screening;1996-12
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