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Journal Abstract Search

219 related items for PubMed ID: 3819771

  • 1. Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts.
    Wanders RJ, Schutgens RB, Schrakamp G, Tager JM, Van den Bosch H, Moser AB, Moser HW.
    J Neurol Sci; 1987 Feb; 77(2-3):331-40. PubMed ID: 3819771
    [Abstract] [Full Text] [Related]

  • 2. Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.
    Singh I, Moser AE, Goldfischer S, Moser HW.
    Proc Natl Acad Sci U S A; 1984 Jul; 81(13):4203-7. PubMed ID: 6588384
    [Abstract] [Full Text] [Related]

  • 3. Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders.
    Wanders RJ, van Roermund CW, van Wijland MJ, Heikoop J, Schutgens RB, Schram AW, Tager JM, van den Bosch H, Poll-Thé BT, Saudubray JM.
    Clin Chim Acta; 1987 Jul 15; 166(2-3):255-63. PubMed ID: 2441904
    [Abstract] [Full Text] [Related]

  • 4. Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome.
    Heymans HS, vd Bosch H, Schutgens RB, Tegelaers WH, Walther JU, Müller-Höcker J, Borst P.
    Eur J Pediatr; 1984 Apr 15; 142(1):10-5. PubMed ID: 6714253
    [Abstract] [Full Text] [Related]

  • 5. Plasmalogen deficiency in cultured skin fibroblasts from neonatal adrenoleukodystrophy.
    Sakai T, Antoku Y, Goto I.
    Exp Neurol; 1986 Oct 15; 94(1):149-54. PubMed ID: 3758277
    [Abstract] [Full Text] [Related]

  • 6. Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy.
    Chen WW, Watkins PA, Osumi T, Hashimoto T, Moser HW.
    Proc Natl Acad Sci U S A; 1987 Mar 15; 84(5):1425-8. PubMed ID: 3469675
    [Abstract] [Full Text] [Related]

  • 7. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
    Aubourg P, Kremser K, Roland MO, Rocchiccioli F, Singh I.
    Pediatr Res; 1993 Sep 15; 34(3):270-6. PubMed ID: 7510868
    [Abstract] [Full Text] [Related]

  • 8. Very long chain fatty acids in genetic peroxisomal disease fibroblasts: differences between the cerebro-hepato-renal (Zellweger) syndrome and adrenoleukodystrophy variants.
    Molzer B, Korschinsky M, Bernheimer H, Schmid R, Wolf C, Roscher A.
    Clin Chim Acta; 1986 Nov 30; 161(1):81-90. PubMed ID: 3815856
    [Abstract] [Full Text] [Related]

  • 9. Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies.
    Schutgens RB, Wanders RJ, Nijenhuis A, van den Hoek CM, Heymans HS, Schrakamp G, Bleeker-Wagemakers EM, Delleman JW, Schram AW, Tager JM.
    Enzyme; 1987 Nov 30; 38(1-4):161-76. PubMed ID: 3440444
    [Abstract] [Full Text] [Related]

  • 10. Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors.
    Schrakamp G, Schalkwijk CG, Schutgens RB, Wanders RJ, Tager JM, van den Bosch H.
    J Lipid Res; 1988 Mar 30; 29(3):325-34. PubMed ID: 3379344
    [Abstract] [Full Text] [Related]

  • 11. Peroxisomal disorders.
    Gordon N.
    Brain Dev; 1987 Mar 30; 9(6):571-5. PubMed ID: 3328519
    [Abstract] [Full Text] [Related]

  • 12. Biochemical abnormalities in rhizomelic chondrodysplasia punctata.
    Hoefler G, Hoefler S, Watkins PA, Chen WW, Moser A, Baldwin V, McGillivary B, Charrow J, Friedman JM, Rutledge L.
    J Pediatr; 1988 May 30; 112(5):726-33. PubMed ID: 2452243
    [Abstract] [Full Text] [Related]

  • 13. 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 May 30; 11(4):358-71. PubMed ID: 2468817
    [Abstract] [Full Text] [Related]

  • 14. Adrenoleukodystrophy. The chain shortening of erucic acid (22:1(n-9)) and adrenic acid (22:4(n-6)) is deficient in neonatal adrenoleukodystrophy and normal in X-linked adrenoleukodistrophy skin fibroblasts.
    Christensen E, Grønn M, Hagve TA, Kase BF, Christophersen BO.
    Biochim Biophys Acta; 1989 Mar 14; 1002(1):79-83. PubMed ID: 2538146
    [Abstract] [Full Text] [Related]

  • 15. [Peroxisomal disorders; newer concept and recent studies].
    Kamoshita S.
    Nihon Rinsho; 1990 Mar 14; 48(3):629-38. PubMed ID: 2192101
    [No Abstract] [Full Text] [Related]

  • 16. Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophy.
    Vamecq J, Draye JP, Van Hoof F, Misson JP, Evrard P, Verellen G, Eyssen HJ, Van Eldere J, Schutgens RB, Wanders RJ.
    Am J Pathol; 1986 Dec 14; 125(3):524-35. PubMed ID: 2879480
    [Abstract] [Full Text] [Related]

  • 17. 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 14; 29(5):397-408. PubMed ID: 2427264
    [Abstract] [Full Text] [Related]

  • 18. Plasmalogen biosynthesis in the diagnosis of peroxisomal disorders.
    Kremser K, Roscher A.
    J Clin Chem Clin Biochem; 1989 May 14; 27(5):315-7. PubMed ID: 2760566
    [Abstract] [Full Text] [Related]

  • 19. X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters.
    Wanders RJ, van Roermund CW, van Wijland MJ, Nijenhuis AA, Tromp A, Schutgens RB, Brouwer-Kelder EM, Schram AW, Tager JM, van den Bosch H.
    Clin Chim Acta; 1987 Jun 15; 165(2-3):321-9. PubMed ID: 3652454
    [Abstract] [Full Text] [Related]

  • 20. The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detection.
    Roscher A, Molzer B, Bernheimer H, Stöckler S, Mutz I, Paltauf F.
    Pediatr Res; 1985 Sep 15; 19(9):930-3. PubMed ID: 4047762
    [Abstract] [Full Text] [Related]

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