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156 related items for PubMed ID: 7957386

  • 1. Clinical and biochemical characteristics of peroxisomal disorders: an update.
    Wanders RJ, Barth PG, Schutgens RB, Tager JM.
    Eur J Pediatr; 1994; 153(7 Suppl 1):S44-8. PubMed ID: 7957386
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  • 2. [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; 104(21):665-70. PubMed ID: 1282286
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  • 4. [Zellweger syndrome, neonatal adrenoleukodystrophy or infantile Refsum's disease in a case with generalized peroxisome defect?].
    Schmitt K, Molzer B, Stöckler S, Tulzer G, Tulzer W.
    Wien Klin Wochenschr; 1993; 105(11):320-2. PubMed ID: 7687405
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  • 6. Peroxisomal disorders in neurology.
    Wanders RJ, Heymans HS, Schutgens RB, Barth PG, van den Bosch H, Tager JM.
    J Neurol Sci; 1988 Dec; 88(1-3):1-39. PubMed ID: 3066850
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  • 7. 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 Dec; 38(1-4):161-76. PubMed ID: 3440444
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  • 9. Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata.
    Schutgens RB, Bouman IW, Nijenhuis AA, Wanders RJ, Frumau ME.
    Clin Chem; 1993 Aug; 39(8):1632-7. PubMed ID: 8353949
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  • 11. Diagnosis of peroxisomal disorders with neurological involvement.
    Molzer B.
    Padiatr Padol; 1993 Aug; 28(1):43-8. PubMed ID: 8446428
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  • 14. [Peroxisomes and neurologic diseases].
    Sereni C, Paturneau-Jouas M.
    Rev Neurol (Paris); 1989 Aug; 145(5):341-9. PubMed ID: 2472665
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  • 15. An improved method for quantification of very long chain fatty acids in plasma.
    Vallance H, Applegarth D.
    Clin Biochem; 1994 Jun; 27(3):183-6. PubMed ID: 7522996
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  • 16. Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction.
    Poulos A, Sharp P, Fellenberg AJ, Johnson DW.
    Eur J Pediatr; 1988 Feb; 147(2):143-7. PubMed ID: 2452737
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  • 17. Studies on the degradation of [U-3H]-phytanic acid and [U-3H]-pristanic acid in cultured fibroblasts from children with peroxisomal disorders.
    Kase BF, Björkhem I.
    Scand J Clin Lab Invest; 1996 May; 56(3):211-7. PubMed ID: 8761525
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  • 19. Fatty acid composition of human myelin proteolipid protein in peroxisomal disorders.
    Bizzozero OA, Zuñiga G, Lees MB.
    J Neurochem; 1991 Mar; 56(3):872-8. PubMed ID: 1704424
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  • 20. 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; 88(6):1873-9. PubMed ID: 1752949
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