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- W1968212597 abstract "Australian and New Zealand Journal of MedicineVolume 24, Issue 6 p. 711-716 Genetic haemochromatosis – preventable rust J. K. Olynyk, Corresponding Author J. K. Olynyk Senior Lecturer and Head of Gastroenterology, Fremantle Hospital, Fremantle, WA.*Senior Lecturer and Head of Gastroenterology, Fremantle Hospital, PO Box 480, Fremantle 6160, WA, Australia.Search for more papers by this author J. K. Olynyk, Corresponding Author J. K. Olynyk Senior Lecturer and Head of Gastroenterology, Fremantle Hospital, Fremantle, WA.*Senior Lecturer and Head of Gastroenterology, Fremantle Hospital, PO Box 480, Fremantle 6160, WA, Australia.Search for more papers by this author First published: December 1994 https://doi.org/10.1111/j.1445-5994.1994.tb01789.xCitations: 2AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Trousseau A. Clinique Med de l'Hotel de Paris, 2nd ed. 1865; 2: 663–98. 2 Troisier M. Diabete Sucre. Bull Soc Anat Paris 1871; 44: 231–5. 3 Green R, Charlton R, Seftel H, et al. Body iron excretion in man. A collaborative study. Am J Med 1968; 45: 336–53. 4 Tavill AS, Bacon BR. Haemochromatosis: Iron metabolism and the iron overload syndromes. In: D Zakin, TD Boyer (Eds.). Hepatology: A textbook of liver disease, 2nd ed. Philadelphia : WB Saunders; 1990, 1273–99. 5 Nichols GN, Bacon BR. Hereditary haemochromatosis: pathogenesis and clinical features of a common disease. Am J Gastroenterol 1989; 84: 851–62. 6 Kostinas J, Portmann B, Lombard M, Williams R. Persistent iron overload 4 years after inadvertent transplantation of a haemochromatic liver in a patient with primary biliary cirrhosis. J Hepatol 1992; 16: 351–4. 7 Bacon BR. Haemochromatosis: diagnosis and management. Res Staff Phys 1991; 37: 21–7. 8 Simon M, Brissot P. The genetics of haemochromatosis. J Hepatol 1988; 6: 116–24. 9 Basset ML, Halliday JW, Powell LW. HLA typing in idiopathic haemochromatosis: Distinction between homozygotes and heter-ozygotes with biochemical expression. Hepatology 1981; 1: 120–6. 10 Leggett BA, Halliday JW, Brown NN, Bryant S, Powell LW. Prevalence of haemochromatosis amongst asymptomatic Australians. Br J Haematol 1990; 74: 525–30. 11 Jazwinska EC, Lee SC, Webb SI, Halliday JW, Powell LW. Localisation of the haemochromatosis gene close to D65105. Am J Human Genetics 1993; 53: 347–52. 12 Bassett ML, Halliday JW, Bryant S, Dent O, Powell LW. Screening for haemochromatosis. In: LR Weintraub, CQ Edwards and M Krikker (Eds.). Proceedings of the First International Conference on Haemochromatosis. Ann NY Acad Sci 1988; 526: 274–89. 13 Phelps G, Chapman I, Hall P, Braund W, MacKinnon M. Prevalence of genetic haemochromatosis among diabetic patients. Lancet 1989; i: 233–4. 14 Olynyk J, Hall P, Ahern M, Kwiatek R, Mackinnon M. Screening for genetic haemochromatosis in a rheumatology clinic. Aust NZ J Med 1994; 24: 22–5. 15 Adams PC. Intrafamilial variation in hereditary haemochromatosis. Dig Dis Sci 1992; 37: 361–3. 16 Adams PC, Kertesz AE, Valberg LS. Clinical presentation of haemochromatosis: a changing scene. Am J Med 1991; 90: 445–9. 17 Adams PC, Speechley M, Kertesz AE. Long-term survival analysis in hereditary haemochromatosis. Gastroenterology 1991; 101: 368–72. 18 Edwards CG, Cartwright GE, Skolnick ME, Amos DB. Homozygosity for haemochromatosis: Clinical manifestations. Ann Intern Med 1980; 93: 519–25. 19 Niederau C, Fischer R, Sonnenberg A, Stremmel W, Tram-pisch H, Strohmeyer G. Survival and causes of death in cirrhotic and in noncirrhotic patients with primary haemochromatosis. N Engl J Med 1985; 313: 1256–62. 20 Powell LW, Halliday JW. Idiopathic haemochromatosis. In: A Jacobs, M Worwood (Eds.). Iron in biochemistry and medicine II. London and New York : Academic Press, 1980, pp 461–98. 21 Huaux JP, Geubel A, Koch MC et al The arthritis of haemochromatosis. A review of 25 cases with special reference to chondrocalcinosis, and a comparison with patients with primary hyperparathyroidism and controls. Clin Rheumatol 1986; 5: 317–24. 22 Bacon BR, Britton RS. The pathology of hepatic iron overload: A free radical-mediated process. Hepatology 1990; 11: 127–37. 23 Britton RS, Edling JE, Grisham MB, Bacon BR. Hepatic DNA damage in rats with chronic dietary iron overload. In: Proceedings of the Third International Conference on Haemochromatosis; 1991, p 4. 24 Nordenson I, Ritter B, Beckman A, Beckman L. Idiopathic haemochromatosis and chromosomal damage. Human Heredity 1992; 42: 143–5. 25 Saudek CD. Haemochromatosis and diabetes. Baillieres Clin Endocrin Metab 1992; 6: 807–17. 26 Bielby J, Olynyk J, Chin S et al. Transferrin index: an alternative method for calculating the iron saturation of transferrin. Clinical Chemistry 1992; 38: 2078–81. 27 Bassett ML, Halliday JW, Ferris RA, Powell LW. Diagnosis of haemochromatosis in young subjects: Predictive accuracy of biochemical screening tests. Gastroenterology 1984; 87: 628–33. 28 Olynyk J, O'Neill R, Britton RS, Bacon BR. Determination of hepatic iron concentration in fresh and paraffin-embedded tissue: diagnostic implications. Gastroenterology 1994; 106: 674–7. 29 Bassett ML, Halliday JW, Powell LW. Value of iron measurement in early haemochromatosis and determination of the critical iron level associated with fibrosis. Hepatology 1986; 6: 24–9. 30 Summers KM, Halliday JW, Powell LW. Identification of homozygous haemochromatosis subjects by measurement of hepatic iron index. Hepatology 1990; 12: 20–5. 31 Olynyk J, Hall P, Sallie R, Reed W, Shilkin K, Mackinnon M. Computerized measurement of iron in liver biopsies: comparison with biochemical iron measurement. Hepatology 1990; 12: 26–30. 32 Bonkovsky HL, Slaker DP, Bills ED, Wolf DC. Usefulness and limitations of laboratory and hepatic imaging studies in iron storage disease. Gastroenterology 1990; 99: 1079–91. 33 Sallie RW, Reed WD, Shilkin KB. Confirmation of the efficacy of hepatic tissue iron index in differentiating genetic haemochromatosis from alcoholic liver disease complicated by alcoholic haemosiderosis. Gut 1991; 32: 207–10. 34 Olynyk J, Luxon BA, Jeffrey GP, Reed WD, Bacon BR. Predicting phlebotomy requirements in the treatment of iron overload. ] Gastroenterol Hepatol 1994; 9: A84. 35 Adams PC, Kertesz AE, Valberg LS. Rate of iron reaccumula-tion following iron depletion in hereditary haemochromatosis. Implications for venesection therapy. J Clin Gastroenterol 1993; 16: 207–10. 36 Adams PC, Speechley M, Kertesz AE. Long-term survival analysis in hereditary haemochromatosis. Gastroenterology 1991; 101: 368–72. 37 Cundy T, Butler J, Bomford A, Williams R. Reversibility of hypogonadotropic hypogonadism associated with genetic haemochromatosis. Clin Endocrinol 1993; 38: 617–20. Citing Literature Volume24, Issue6December 1994Pages 711-716 ReferencesRelatedInformation" @default.
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