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The relevance of early diagnosis is underlined.

Elder GH, Worwood M. Porphyria cutanea tarda and hepatitis C virus and B virus infection: Erythropoietic and hepatic porphyrias. Sheldon and hereditary hemochromatosis: Eur J Clin Invest.

Agents affecting porphyrin formation and secretion: Diabetes mellitus in connection with hereditary disease. Presentation and diagnosis in the s.

If you have hemocromattose Best Practice personal account, your own subscription or have registered for a free trial, log in here: Hemochromatosis genes and other factors contributing to the pathogenesis of porphyria cutanea tarda. Is there a threshold of hepatic iron concentration that leads to cirrhosis in CY Hemochromatosis?. The significance of histologic analysis of skin lesions in porphyria cutanea tarda.

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Bull Soc Fr Derm Syph. Nat Genet ; Treatment of inborn errors of metabolism. Uroporphyrin I stimulation of collagen biosynthesis in human skin fibroblasts.

Recent advances in dermatology. Increased mast cell numbers in the sclerotic skin of Porphyria cutanea tarda. Porphyria cutanea tarda in association with human immunodeficiency virus infection: Services on Demand Journal. Skin morphology in porphyria cutanea tarda does not improve despite clinical remission.

Potential role of increased iron stores in diabetes. Autoantibodies to human cytosol: Dermatology in General medicine. Observations on the pathogenesis, complications and treatment of diabetes in cases of haemochromatosis.

Dabski C, Beutner EH. J Inherit Metab Dis. Carlos Gomes, cj. Inborn errors of metabolism around time of birth. Hepatitis C virus-related autoimmunity in patients with porphyria cutanea tarda.

Porphyria cutanea tarda

Microscopic and fine structural aspects of porphyrias. Porphyria cutanea tarda after allogenic bone marrow transplantation for chronic myelogenous leukemia. Iron storage in porphyria cutanea tarda.

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Alcoholic beverages in acute porphyria. N Engl J Med ; Low-dose oral chloroquine in patients with porphyria cutanea tarda and hemocrkmatose iron overload.

Pathophysiology and clinical features of Wilson disease. The treatment of porphyria cutanea tarda by venesection. HFE genotype in patients with hemochromatosis and other liver diseases.

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Oxidation of uroporphyrinogens by hydroxyl radicals: Malina L, Chlumsky J. The molecular basis of the action of chloroquine in porphyria cutanea tarda. Manual of metabolic paediatrics. Como citar este artigo.

Molecular aspects of the inherited porphyrias.