Genetic Iron Overload

Sheldon J.H. Haemochromatosis. London: Oxford University Press, 1935

Simon M. , Brissot P. The genetics of haemochromatosis. J Hepatol 1988; 6: 116–24.

Lombard M. , Bomford A. , Poison R. , Williams R. Differential expression of the transferrin receptor in liver and gut in hereditary haemochromatosis. Gut 1988; 29: A725.

Fracanzani A.L. , Fargion S. , Romano R. , Piperno A. , Arosio P. , Ruggeri G. , Ronchi G. , Fiorelli G. Immuno-histochemical evidence for a lack of ferritin in duodenal absorptive epithelial cells in idiopathic haemochromatosis. Gastroenterology 1989; 96: 1071–8.

Silver M.M. , Beverley D.W. , Valberg L.S. , Cutz E. , Phillips M.J. , Shaheed W.A. Perinatal haemochromatosis: clinical, morphologic and quantitative iron studies. Am J Pathol 1987; 128: 538–51.

Herrick A.L. , Mclnnes G.T. , MacSween R.N.M. , Goldberg A. Idiopathic haemochromatosis in a young female with amenorrhoea. J R Soc Med 1989; 82: 556–8.

Beaumont C. , Simon M. , Fauchet R. , Hespel J.P. , Brissot P. , Genetet B. , Bourel M. Serum ferritin as a possible marker of the haemochromatosis allele. N Engl J Med 1979; 301: 174

Simon M. Secondary iron overload and the haemochromatosis allele. Br J Haematol 1987; 60: 1–5.

Fellows I.W. , Stewart M. , Jeffcoate W.J. , Smith P.G. , Toghill P.S. Hepatocellular carcinoma in primary haemochromatosis in the absence of cirrhosis. Gut 1988; 29: 1603–6.

Bomford A. , Williams R. Long term results of venesection therapy in idiopathic haemochromatosis. Q J Med XLV 1976; 180: 611–23

Edwards C.Q. , Griffen L.M. , Goldgar D. , Drummond C. , Skolnick M.H. , Kushner J.P. Prevalence of haemochromatosis among 11 065 presumably healthy blood donors. N Engl J Med 1988; 318: 1355–62.