Screening for Hemochromatosis: High Prevalence and Low Morbidity in an Unselected Population of 65,238 Persons
Tóm tắt
Từ khóa
Tài liệu tham khảo
Powell LW, 2000, Haemochromatosis in the new millennium. J Hepatol, 32, 48
Bacon BR, 1999, Hoofnagle JH. Molecular medicine and hemochromatosis: at the crossroads. Gastroenterology, 116, 193
Niederau C, 1994, Epidemiology, clinical spectrum and prognosis of hemochromatosis. Adv Exp Med Biol, 356, 293
Niederau C, 1994, Clinical spectrum and management of haemochromatosis. Baillieres Clin Haematol, 7, 881, 10.1016/S0950-3536(05)80129-5
Witte DL, 1996, Practice guideline development task force of the College of American Pathologists. Hereditary hemochromatosis. Clin Chim Acta, 245, 139
Phatak PD, 1994, Cost- effectiveness of screening for hereditary hemochromatosis. Arch Intern Med, 154, 769
Wiggers P, 1991, Screening for haemochromatosis: prevalence among Danish blood donors. J Intern Med, 230, 265
Siedel J, 1984, AACC meeting abstract. Clin Chem, 30, 975
Kalbfleisch JD, 1980, New York:Wiley, p. 10
Adams P, 2000, EASL International Consensus Conference on Haemochromatosis. J Hepatol, 33, 485
Bassett ML, 1986, Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis. Hepatology, 6, 24
Niederau C, 1998, Screening for hemochromatosis and iron deficiency in employees and primary care patients in Western Germany. Ann Intern Med, 128, 337
McDonnell SM, 1999, Population-based screening for hemochromatosis using phenotypic and DNA testing among employees of health maintenance organizations in Springfield, Missouri. Am J Med, 107, 30
Mueller RF, 1998, Edinburgh: Churchill Livingstone, p. 113
Bell H, 2000, Excessive oral iron intake may lead to secondary hemochromatosis even in HFE C282Y mutation negative subjects. Scand J Gastroenterol, 35, 1301
Cardoso EM, 1998, HFE mutations in patients with hereditary haemochromatosis in Sweden. J Intern Med, 243, 203