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Journal Abstract Search

148 related items for PubMed ID: 3379344

  • 1. 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; 29(3):325-34. PubMed ID: 3379344
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  • 2. Aberration in de novo ether lipid biosynthesis in peroxisomal disorders.
    van den Bosch H, Schalkwijk CG, Schrakamp G, Wanders RJ, Schutgens RB, Schram AW, Tager JM.
    Prog Clin Biol Res; 1988 Mar; 282():139-50. PubMed ID: 3071794
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  • 3. The cerebro-hepato-renal (Zellweger) syndrome. Impaired de novo biosynthesis of plasmalogens in cultured skin fibroblasts.
    Schrakamp G, Schutgens RB, Wanders RJ, Heymans HS, Tager JM, Van den Bosch H.
    Biochim Biophys Acta; 1985 Jan 09; 833(1):170-4. PubMed ID: 3967038
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  • 5. 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 Jan 09; 38(1-4):161-76. PubMed ID: 3440444
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  • 6. Glyceryl ethers in peroxisomal disease.
    Poulos A, Bankier A, Beckman K, Johnson D, Robertson EF, Sharp P, Sheffield L, Singh H, Usher S, Wise G.
    Clin Genet; 1991 Jan 09; 39(1):13-25. PubMed ID: 1705185
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  • 8. 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 09; 112(5):726-33. PubMed ID: 2452243
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  • 11. 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
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  • 14. Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damage.
    Hoefler G, Paschke E, Hoefler S, Moser AB, Moser HW.
    J Clin Invest; 1991 Dec 15; 88(6):1873-9. PubMed ID: 1752949
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  • 16. Inherited disorders of fatty alcohol metabolism.
    Rizzo WB.
    Mol Genet Metab; 1998 Oct 15; 65(2):63-73. PubMed ID: 9787098
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  • 17. 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
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  • 18. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.
    Tager JM, Brul S, Wiemer EA, Strijland A, Van Driel R, Schutgens RB, Van den Bosch H, Wanders RJ, Westerveld A.
    Prog Clin Biol Res; 1990 Sep 15; 321():545-58. PubMed ID: 2183242
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  • 19. Cholesterol biosynthesis in dermal fibroblasts from patients with metabolic disorders of peroxisomal origin.
    Malle E, Oettl K, Sattler W, Hoefler G, Kostner GM.
    Eur J Clin Invest; 1995 Jan 15; 25(1):59-67. PubMed ID: 7705389
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  • 20. Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency.
    Barr DG, Kirk JM, al Howasi M, Wanders RJ, Schutgens RB.
    Arch Dis Child; 1993 Mar 15; 68(3):415-7. PubMed ID: 8466247
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