Development of chronic hepatic porphyria (porphyria cutanea tarda) with inherited uroporphyrinogen decarboxylase deficiency under exposure to dioxin

This publication has 24 references indexed in Scilit:

• Induction of porphyria in the rat by chronic versus acute exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin
  Biochemical Pharmacology, 1982
• The Enzymatic Defect in Porphyria Cutanea Tarda
  New England Journal of Medicine, 1982
• Decreased Hepatic Uroporphyrinogen Decarboxylase Activity in Porphyria Cutanea Tarda
  New England Journal of Medicine, 1982
• Polychlorobiphenyls that induce δ‐aminolevulinic acid synthetase inhibit uroporphyrinogen decarboxylase in cultured chick embryo liver cells
  FEBS Letters, 1981
• Porphyrogenic effect of chronic treatment with 2,3,7,8-tetrachlorodibenzo-p-dioxin in female rats. Dose-effect relationship following urinary excretion of porphyrins
  Toxicology and Applied Pharmacology, 1981
• Heredit re und nicht-heredit re Form der chronischen hepatischen Porphyrie: Unterschiedliches Verhalten der Uroporphyrinogen-Decarboxylase in Leber und Erythrozyten
  Journal of Molecular Medicine, 1980
• Identification of Two Types of Porphyria Cutanea Tarda by Measurement of Erythrocyte Uroporphyrinogen Decarboxylase
  Clinical Science, 1980
• Pathobiochemical transition of secondary coproporphyrinuria to chronic hepatic porphyria in humans
  Klinische Wochenschrift, 1980
• Assessment of the contribution of chlorinated dibenzo-p-dioxins and dibenzofurans to hexachlorobenzene-induced toxicity, porphyria, changes in mixed function oxygenases, and histopathological changes
  Toxicology and Applied Pharmacology, 1978
• Decreased Activity of Hepatic Uroporphyrinogen Decarboxylase in Sporadic Porphyria Cutanea Tarda
  New England Journal of Medicine, 1978