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Journal Abstract Search

350 related items for PubMed ID: 1378993

  • 1. Very long-chain fatty acids in peroxisomal disease.
    Poulos A, Beckman K, Johnson DW, Paton BC, Robinson BS, Sharp P, Usher S, Singh H.
    Adv Exp Med Biol; 1992; 318():331-40. PubMed ID: 1378993
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  • 3. Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders.
    Molzer B, Kainz-Korschinsky M, Sundt-Heller R, Bernheimer H.
    J Clin Chem Clin Biochem; 1989 May; 27(5):309-14. PubMed ID: 2474624
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  • 4. Accumulation and defective beta-oxidation of very long chain fatty acids in Zellweger's syndrome, adrenoleukodystrophy and Refsum's disease variants.
    Poulos A, Singh H, Paton B, Sharp P, Derwas N.
    Clin Genet; 1986 May; 29(5):397-408. PubMed ID: 2427264
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  • 6. Metabolism of saturated and polyunsaturated very-long-chain fatty acids in fibroblasts from patients with defects in peroxisomal beta-oxidation.
    Street JM, Singh H, Poulos A.
    Biochem J; 1990 Aug 01; 269(3):671-7. PubMed ID: 2117919
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  • 7. Plasma polyenoic very-long-chain fatty acids in peroxisomal disease: biochemical discrimination of Zellweger's syndrome from other phenotypes.
    Poulos A, Sharp P, Johnson D.
    Neurology; 1989 Jan 01; 39(1):44-7. PubMed ID: 2462697
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  • 8. [Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers].
    Molzer B, Stöckler S, Bernheimer H.
    Wien Klin Wochenschr; 1992 Jan 01; 104(21):665-70. PubMed ID: 1282286
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  • 9. Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.
    Slawecki ML, Dodt G, Steinberg S, Moser AB, Moser HW, Gould SJ.
    J Cell Sci; 1995 May 01; 108 ( Pt 5)():1817-29. PubMed ID: 7544797
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  • 10. A comparative study of straight chain and branched chain fatty acid oxidation in skin fibroblasts from patients with peroxisomal disorders.
    Singh H, Usher S, Johnson D, Poulos A.
    J Lipid Res; 1990 Feb 01; 31(2):217-25. PubMed ID: 1691260
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  • 11. Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophy.
    Small GM, Santos MJ, Imanaka T, Poulos A, Danks DM, Moser HW, Lazarow PB.
    J Inherit Metab Dis; 1988 Feb 01; 11(4):358-71. PubMed ID: 2468817
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  • 14. Formation of a novel arachidonic acid metabolite in peroxisomes.
    Gordon JA, Heller SK, Rhead WJ, Watkins PA, Spector AA.
    Prostaglandins Leukot Essent Fatty Acids; 1995 Feb 01; 52(2-3):77-81. PubMed ID: 7540307
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  • 15. Ratios for very-long-chain fatty acids in plasma of subjects with peroxisomal disorders, as determined by HPLC and validated by gas chromatography-mass spectrometry.
    Hall NA, Lynes GW, Hjelm NM.
    Clin Chem; 1988 Jun 01; 34(6):1041-5. PubMed ID: 2454167
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  • 17. Fatty acid synthesis from [2-14C]acetate in normal and peroxisome-deficient (Zellweger) fibroblasts.
    Poulos A, Usher S, Paton BC.
    Lipids; 1993 Feb 01; 28(2):97-102. PubMed ID: 8441343
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  • 19. Bile acids in peroxisomal disorders.
    Van Eldere JR, Parmentier GG, Eyssen HJ, Wanders RJ, Schutgens RB, Vamecq J, Van Hoof F, Poll-The BT, Saudubray JM.
    Eur J Clin Invest; 1987 Oct 01; 17(5):386-90. PubMed ID: 2446876
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  • 20. [Clinical biochemical and genetic aspects of peroxisome-deficient disorders].
    Suzuki Y.
    No To Hattatsu; 1992 Mar 01; 24(2):194-7. PubMed ID: 1373633
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