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Journal Abstract Search

176 related items for PubMed ID: 2760566

  • 1. Plasmalogen biosynthesis in the diagnosis of peroxisomal disorders.
    Kremser K, Roscher A.
    J Clin Chem Clin Biochem; 1989 May; 27(5):315-7. PubMed ID: 2760566
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  • 2. 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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  • 5. 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; 19(9):930-3. PubMed ID: 4047762
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  • 7. 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; 321():545-58. PubMed ID: 2183242
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  • 9. [Peroxisomes and neurologic diseases].
    Sereni C, Paturneau-Jouas M.
    Rev Neurol (Paris); 1989 Sep; 145(5):341-9. PubMed ID: 2472665
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  • 10. Rhizomelic chondrodysplasia punctata: another peroxisomal disorder.
    Heymans HS, Oorthuys JW, Nelck G, Wanders RJ, Schutgens RB.
    N Engl J Med; 1985 Jul 18; 313(3):187-8. PubMed ID: 4010717
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  • 11. Peroxisomal disorders: clinical commentary and future prospects.
    Wilson GN, Holmes RD, Hajra AK.
    Am J Med Genet; 1988 Jul 18; 30(3):771-92. PubMed ID: 2461077
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  • 12. 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 18; 77(2-3):331-40. PubMed ID: 3819771
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  • 13. Diagnosis of peroxisomal disorders with neurological involvement.
    Molzer B.
    Padiatr Padol; 1993 Feb 18; 28(1):43-8. PubMed ID: 8446428
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  • 14. 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 Feb 18; 38(1-4):161-76. PubMed ID: 3440444
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  • 15. Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.
    Heikoop JC, van Roermund CW, Just WW, Ofman R, Schutgens RB, Heymans HS, Wanders RJ, Tager JM.
    J Clin Invest; 1990 Jul 18; 86(1):126-30. PubMed ID: 2365812
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  • 16. Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency.
    Barr DG, Kirk JM, al Howasi M, Wanders RJ, Schutgens RB.
    Arch Dis Child; 1993 Mar 18; 68(3):415-7. PubMed ID: 8466247
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  • 18. Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochemical studies on peroxisomes in human amniocytes.
    Suzuki Y, Shimozawa N, Kawabata I, Yajima S, Inoue K, Uchida Y, Izai K, Tomatsu S, Kondo N, Orii T.
    Brain Dev; 1994 Mar 18; 16(1):27-31. PubMed ID: 8059925
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  • 20. 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 18; 39(1):13-25. PubMed ID: 1705185
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