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Journal Abstract Search

196 related items for PubMed ID: 3369447

  • 21. Erythrocyte uroporphyrinogen decarboxylase activity in porphyria cutanea tarda: a study of 40 consecutive patients.
    Held JL, Sassa S, Kappas A, Harber LC.
    J Invest Dermatol; 1989 Sep; 93(3):332-4. PubMed ID: 2768832
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  • 22. Reduced substrate affinity for human erythrocyte uroporphyrinogen decarboxylase constitutes the inherent biochemical defect in porphyria cutanea tarda.
    Mukerji SK, Pimstone NR.
    Biochem Biophys Res Commun; 1985 Mar 15; 127(2):517-25. PubMed ID: 3977935
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  • 23. The enzymatic defects in porphyria cutanea tarda and variegate porphyria.
    Kushner JP.
    Acta Derm Venereol Suppl (Stockh); 1982 Mar 15; 100():51-6. PubMed ID: 6962633
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  • 24. Uroporphyrinogen decarboxylase deficiency in hepatoerythropoietic porphyria: further evidence for genetic heterogeneity.
    Kószó F, Elder GH, Roberts A, Simon N.
    Br J Dermatol; 1990 Mar 15; 122(3):365-70. PubMed ID: 2322500
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  • 25. Uroporphyrinogen decarboxylase deficiency in experimental chronic hepatic porphyria.
    von Tiepermann R, Koss G, Doss M.
    Hoppe Seylers Z Physiol Chem; 1980 Aug 15; 361(8):1217-22. PubMed ID: 7409755
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  • 26. Decreased hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda.
    Felsher BF, Carpio NM, Engleking DW, Nunn AT.
    N Engl J Med; 1982 Apr 01; 306(13):766-9. PubMed ID: 7062951
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  • 35. Immunoreactive uroporphyrinogen decarboxylase in the liver in porphyria cutanea tarda.
    Elder GH, Urquhart AJ, De Salamanca RE, Munoz JJ, Bonkovsky HL.
    Lancet; 1985 Aug 03; 2(8449):229-33. PubMed ID: 2862415
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  • 36. [Hereditary uroporphyrinogen decarboxylase deficiency in porphyria cutanea tarda caused by hormonal contraceptives].
    Doss M.
    Dtsch Med Wochenschr; 1983 Dec 02; 108(48):1857-8. PubMed ID: 6641540
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  • 38. Hereditary uroporphyrinogen-decarboxylase deficiency predisposing porphyria cutanea tarda (chronic hepatic porphyria) in females after oral contraceptive medication.
    Sixel-Dietrich F, Doss M.
    Arch Dermatol Res; 1985 Dec 02; 278(1):13-6. PubMed ID: 4096525
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  • 39. Development of chronic hepatic porphyria (porphyria cutanea tarda) with inherited uroporphyrinogen decarboxylase deficiency under exposure to dioxin.
    Doss M, Sauer H, von Tiepermann R, Colombi AM.
    Int J Biochem; 1984 Dec 02; 16(4):369-73. PubMed ID: 6714509
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  • 40. Mutations in familial porphyria cutanea tarda: two novel and two previously described for hepatoerythropoietic porphyria.
    Mendez M, Rossetti MV, De Siervi A, del Carmen Batlle AM, Parera V.
    Hum Mutat; 2000 Sep 02; 16(3):269-70. PubMed ID: 10980536
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