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Journal Abstract Search

311 related items for PubMed ID: 11831056

  • 1. [Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria].
    Doss MO, Gross U, Puy H, Doss M, Kühnel A, Jacob K, Deybach JC, Nordmann Y.
    Med Klin (Munich); 2002 Jan 15; 97(1):1-5. PubMed ID: 11831056
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  • 5. Hereditary coproporphyria in Germany: clinical-biochemical studies in 53 patients.
    Kühnel A, Gross U, Doss MO.
    Clin Biochem; 2000 Aug 15; 33(6):465-73. PubMed ID: 11074238
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  • 8. Erythropoietic and hepatic porphyrias.
    Gross U, Hoffmann GF, Doss MO.
    J Inherit Metab Dis; 2000 Nov 15; 23(7):641-61. PubMed ID: 11117426
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  • 10. Red-cell uroporphyrinogen decarboxylase activity in porphyria cutanea tarda and in other forms of porphyria.
    Felsher BF, Norris ME, Shih JC.
    N Engl J Med; 1978 Nov 16; 299(20):1095-8. PubMed ID: 703786
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  • 18. 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 Nov 16; 16(4):369-73. PubMed ID: 6714509
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  • 19. Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase.
    Elder GH, Sheppard DM, De Salamanca RE, Olmos A.
    Clin Sci (Lond); 1980 Jun 16; 58(6):477-84. PubMed ID: 7428280
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  • 20. Erythrocyte uroporphyrinogen decarboxylase activity: diagnostic value and relationship with clinical features in hereditary porphyria cutanea tarda.
    Camagna A, Del Duca P, Petrinelli P, Borelli LG, Ciancio L, Cipollone L, Misasi G, Manfredi MR, Dionisi S, de Martinis C.
    Am J Med Sci; 1998 Jan 16; 315(1):59-62. PubMed ID: 9427577
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