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Hepatitis C virus and porphyria cutanea tarda: Lehninger principles of biochemistry. Role of complement in porphyrininduced photosensitivity. Hemkcromatose I stimulation of collagen biosynthesis in human skin fibroblasts.

Acute intermittent porphyria: case report and review of the literature

Liver involvement in porphyria. Low-dose oral chloroquine in patients with porphyria cutanea tarda and low-moderate iron overload. Inborn errors of metabolism around time of birth.

The long evolution of the disease is emphasised, since the patient presented tratamsnto liver cirrhosis 25 years ago, this long survival is probably due to alcohol abstention and intensive phlebotomies.

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Urine and faecal porphyrin profiles by reversed-phase high-performance liquid chromatography in the porphyrias. Malina L, Chlumsky J. Please enter a hemocromztose username and password and try again. Light microscopy, electron microscopy, immunohistochemical and immunofluorescence analysis.

Molecular aspects of the inherited porphyrias. HFE genotype in patients with hemochromatosis and other liver diseases. Haemophilia, hepatitis and porphyria. Alcoholic beverages in acute porphyria.

Biochemical diagnosis of the cutaneous porphyrias: Influence of chloroquine on the porphyrin metabolism. Histochemistry of the skin in erythropoietic protoporphyria.

Cutaneous changes in the porphyrias: Genetic diseases of sphingolipid metabolism: Porphyria cutanea tarda associated with the acquired immune deficiency syndrome. Porphyria cutanea tarda and hepatitis C viral infection. J Hepatol ; Immunoreactive uroporphyrinogen decarboxylase in the liver in tratajento cutanea tarda. Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: Hepatitis C virus antibodies and liver disease in patients with porphyria cutanea tarda.

Porphyria cutanea tarda

The development and prognosis of chronic intoxication by tetrachlorodibenzo-p-dioxin in men. Results of in vitro and in vivo studies.

All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Sign up for a FREE trial. Dramatic resolution of skin lesions associated with porphyria cutanea tarda after interferon-alpha therapy in a case of chronic hepatitis C.

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Porphyrin-binding effect of cholestyramine. Co-inheritance of mutations in the uroporphyrinogen decarboxylase and hemochromatosis genes accelerates the onset of porphyria cutanea tarda.

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Uroporphyria induced by 5-aminolevulinic acid in Ahrd SWR mice. Sixel-Dietrich F, Hemocromatkse M. Treatment of inborn errors of metabolism.

Ergebnisse bei der Behandlung der Porphyria cutanea tarda mit Aderlass und Resorchin. Microscopic and fine structural aspects of porphyrias. Methylmalonic and propionic acidaemias: Fakan F, Chlumska A. Activation of complement by nm light in serum from porphyria cutanea tarda.

Nat Genet ; N Eng J Med. Observations on the pathogenesis, complications and treatment of diabetes in cases of haemochromatosis.