SEARCH

SEARCH BY CITATION

References

  • 1
    Beutler, E. (1997) Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations. Lancet, 349, 296 297.
  • 2
    Beutler, E., Gelbert, T., West, C., Lee, P., Adams, M., Blackstone, R., Pockros, P., Kosty, M., Venditti, C.P., Phatak, P.D., Seese, N.K., Chorney, K.A., Ten Elshof, A.E., Gerhard, G.S., Chorney, M. (1996) Mutation analysis in hereditary hemochromatosis. Blood Cells and Molecular Diseases, 22, 187 194.
  • 3
    Burt, M.J., Halliday, J.W., Powell, L.W. (1993) Iron and coronary heart disease. British Medical Journal, 307, 575 576.
  • 4
    Corti, M.C., Gaziano, M., Hennekens, C.H. (1997) Iron status and risk of cardiovascular disease. Annals of Epidemiology, 7, 62 68.
  • 5
    Dabbagh, A.J., Shwaery, G.T., Keaney, J.F.Jr, Frei, B. (1997) Effect of iron overload and iron deficiency on atherosclerosis in the hypercholesterolemic rabbit. Arteriosclerosis, Thrombosis and Vascular Biology, 17, 2638 2645.
  • 6
    Feder, J.N., Gnirke, A., Thomas, W., Tsuchihashi, Z., Ruddy, D.A., Basava, A., Dormishian, F., Domingo, R.Jr, Ellis, M.C., Fullan, A., Hinton, L.M., Jones, N.L., Kimmel, B.E., Kronmal, G.S., Lauer, P., Lee, V.K., Loeb, D.B., Mapa, F.A., McClelland, E., Meyer, N.C., Mintier, G.A., Moeller, N., Moore, T., Morikang, E., Prass, C.E., Quintane, L., Starnes, S.M., Schatzman, R.C., Brunke, K.J., Drayna, D.T., Risch, N.J., Bacon, B.R., Wolff, R.K. (1996) A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nature Genetics, 13, 399 408.
  • 7
    Figueiredo, M.S., Baffa, O., Barbieri-Neto, J., Zago, M.A. (1993) Liver injury and generation of hydroxyl free radicals in experimental secondary hemochromatosis. Research in Experimental Medicine , 193, 27 37.
  • 8
    Kiechl, S., Aichner, F., Gerstenbrand, F., Egger, G., Mair, A., Rungger, G., Spogler, F., Jarosch, E., Oberhollenzer, F., Willeit, J. (1994) Body iron stores and presence of carotid atherosclerosis. Arteriosclerosis and Thrombosis, 14, 1625 1630.
  • 9
    Kiechl, S., Willeit, J., Egger, G., Poewe, W., Oberhollenzer, F. (1997) Body iron stores and the risk of carotid atherosclerosis: prospective results from the Bruneck Study. Circulation, 96, 3300 3307.
  • 10
    Lauffer, R.B. (1991) Iron stores and the international variation in mortality from coronary artery disease. Medical Hypotheses, 35, 96 102.
  • 11
    Martinez, P.A., Biron, C., Blanc, F., Masmejean, C., Jeanjean, P., Michel, H., Schved, J. (1997) Compound heterozygotes for haemochromatosis gene mutations: may they help to understand the pathophysiology of the disease? Blood Cells and Molecular Diseases, 23, 269 276.
  • 12
    Merryweather-Clarke, A.T., Pointon, J.J., Shearman, J.D., Robson, K.J.H. (1997) Global prevalence of putative haemochromatosis mutations. Journal of Medical Genetics, 34, 275 278.
  • 13
    Meyers, D.G. (1996) The iron hypothesis: does iron cause atherosclerosis? Clinical Cardiology, 19, 925 929.
  • 14
    Morrison, H.I., Semenciw, R.M., Mao, Y., Wigle, D.T. (1994) Serum iron and risk of fatal acute myocardial infarction. Epidemiology, 5, 243 246.
  • 15
    Roberts, A.G., Whatley, S.D., Morgan, R.R., Worwood, M., Elder, G.H. (1997) Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda. Lancet, 349, 321 323.
  • 16
    Salonen, J.T., Korpela, H., Hyyssonen, K., Porkkala, E., Tuomainen, T.P., Belcher, J.D., Jacobs, D.R., Salonen, R. (1995) Lowering of body iron stores by blood letting and oxidation resistance of serum lipoproteins: a randomized cross-over trial in male smokers. Journal of Internal Medicine, 237, 161 168.
  • 17
    Salonen, J.T., Nyyssonen, K., Korpela, H., Tuomilehto, J., Seppanen, R., Salonen, R. (1992) High stored iron levels are associated with excessive risk of myocardial infarction in eastern Finnish men. Circulation, 86, 803 811.
  • 18
    Sampietro, M., Piperno, A., Lupica, L., Arosio, C., Vergani, A., Corbetta, N., Malosio, I., Mattioli, M., Fracanzani, A.L., Cappellini, M.D., Fiorelli, G., Fargioni, S. (1998) High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda. Hepatology, 27, 181 184.
  • 19
    Sempos, C.T., Looker, A.C., Gillum, R.F. (1996) Iron and heart disease: the epidemiologic data. Nutrition Reviews, 54, 73 84.
  • 20
    Witte, D.L., Crosby, W.H., Edwards, C.Q., Fairbanks, V.F., Mitros, F.A. (1996) Practice parameter for hereditary hemochromatosis. Clinica Chimica Acta, 245, 139 200.