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Pubmed for Handhelds

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Journal Abstract Search

186 related items for PubMed ID: 4710876

  • 21. Intermittent acute porphyria--demonstration of a genetic defect in porphobilinogen metabolism.
    Meyer UA, Strand LJ, Doss M, Rees AC, Marver HS.
    N Engl J Med; 1972 Jun 15; 286(24):1277-82. PubMed ID: 5024458
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  • 22. [Clinically important disorders of heme synthesis].
    Stich W.
    Hamatol Bluttransfus; 1972 Jun 15; 10():393-9. PubMed ID: 4668006
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  • 29. Inhibition of uroporphyrinogen I synthase activity and depression of microsomal heme and cytochrome P-450 in rat liver by bilirubin.
    Kohashi M, Tse J, Piper WN.
    Life Sci; 1984 Jan 09; 34(2):193-6. PubMed ID: 6694518
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  • 30. The effect of drugs on 5-aminolaevulinate synthetase and other enzymes in the pathway of liver haem biosynthesis.
    De Matteis F.
    Basic Life Sci; 1975 Jan 09; 6():185-205. PubMed ID: 1098646
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  • 31. Hepatic porphyrias: new findings on the nature of metabolic defects.
    Meyer UA.
    Prog Liver Dis; 1976 Jan 09; 5():280-93. PubMed ID: 775544
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  • 32. Studies on hepatic -aminolevulinic acid synthetase.
    Patton GM, Beattie DS.
    J Biol Chem; 1973 Jun 25; 248(12):4467-74. PubMed ID: 4711614
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  • 38. Acute intermittent porphyria in The Netherlands. Heterogeneity of the enzyme porphobilinogen deaminase.
    Wilson JH, De Rooy FW, Te Velde K.
    Neth J Med; 1986 Jun 25; 29(11):393-9. PubMed ID: 3808142
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