A rare case of porphyria cutanea tarda in a patient with a homozygous hereditary hemochromatosis gene H63D mutation in the setting of hereditary hemochromatosis. [PDF]
Banta J, Collins J, Kobayashi T.
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Dermatologic manifestations of hereditary hemochromatosis: A systematic review. [PDF]
Akbarialiabad H+3 more
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Hereditary hemochromatosis types 1, 2, and 3 [PDF]
Dorothy H. Crawford
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Iron Overload in Histidine-to-Aspartic Acid Substitution at 63 (H63D) Gene Heterozygous Hereditary Hemochromatosis With Erythrocytosis: A Case Report. [PDF]
Abeyagunawardena I+4 more
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Low ceruloplasmin levels exacerbate retinal degeneration in a hereditary hemochromatosis model.
Anderson BD+4 more
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Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis. [PDF]
Zhang W+17 more
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Long-term outcomes and trends in liver transplantation for hereditary hemochromatosis in the United States. [PDF]
Lymberopoulos P+11 more
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