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Journal Abstract Search

373 related items for PubMed ID: 7428280

  • 1. 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; 58(6):477-84. PubMed ID: 7428280
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  • 2. Familial porphyria cutanea tarda: the pattern of porphyrins formed from porphobilinogen by hemolysates.
    Alleman MA, Wilson JH, van den Berg JW, Edixhoven-Bosdijk A, van Gastel-Quist LM.
    Clin Chem; 1982 May; 28(5):1144-7. PubMed ID: 7074894
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  • 3. 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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  • 4. An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity.
    Kushner JP, Barbuto AJ, Lee GR.
    J Clin Invest; 1976 Nov 16; 58(5):1089-97. PubMed ID: 993332
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  • 5. Porphyria cutanea tarda in three generations of a single family.
    Benedetto AV, Kushner JP, Taylor JS.
    N Engl J Med; 1978 Feb 16; 298(7):358-62. PubMed ID: 622106
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  • 6. Heterogeneity of familial porphyria cutanea tarda.
    Roberts AG, Elder GH, Newcombe RG, Enriquez de Salamanca R, Munoz JJ.
    J Med Genet; 1988 Oct 16; 25(10):669-76. PubMed ID: 3225822
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  • 9. Defective human erythrocyte uroporphyrinogen decarboxylase in familial porphyria cutanea tarda: the metabolic lesion or the result of endogenous porphyrinemia?
    Mukerji SK, Pimstone NR.
    Biochem Biophys Res Commun; 1988 Jul 15; 154(1):39-46. PubMed ID: 3395340
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