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Blood, 2009
Abstract In a remarkable study in this issue of Blood, Lok and colleagues describe the genotypic and phenotypic characteristics of hereditary hemochromatosis in 42 cases in 8 distinct families of Asian origin ...
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Abstract In a remarkable study in this issue of Blood, Lok and colleagues describe the genotypic and phenotypic characteristics of hereditary hemochromatosis in 42 cases in 8 distinct families of Asian origin ...
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Postgraduate Medicine, 1973
The variable criteria used in diagnosing hemochromatosis have resulted in considerable confusion in the literature. How does one separate the alcoholic with cirrhosis and secondary iron overload from the patient with “familial hemochromatosis” who happens to drink too much? And if phlebotomy is the way to treat hemochromatosis, why not use this therapy
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The variable criteria used in diagnosing hemochromatosis have resulted in considerable confusion in the literature. How does one separate the alcoholic with cirrhosis and secondary iron overload from the patient with “familial hemochromatosis” who happens to drink too much? And if phlebotomy is the way to treat hemochromatosis, why not use this therapy
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The Detection of Iron Overload
New England Journal of Medicine, 1982Human physiology is such that few people accumulate excess iron. Indeed, normal persons are able to control the accumulation of body iron despite ingestion of up to 5 to 10 times the normal amount.1 There are, however, two disorders in which large amounts of iron accumulate in the parenchymal cells.
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