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Journal Abstract Search

175 related items for PubMed ID: 2482247

  • 1. In situ genetic complementation analysis of cells with generalized peroxisomal dysfunction.
    Singh AK, Kulvatunyou N, Singh I, Stanley WS.
    Hum Hered; 1989; 39(5):298-301. PubMed ID: 2482247
    [Abstract] [Full Text] [Related]

  • 2. Complementation analysis of peroxisomal disorders and classical Refsum.
    Poll-The BT, Skjeldal OH, Stokke O, Demaugre F, Saudubray JM.
    Prog Clin Biol Res; 1990; 321():537-43. PubMed ID: 1691507
    [No Abstract] [Full Text] [Related]

  • 3. Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients.
    Roscher AA, Hoefler S, Hoefler G, Paschke E, Paltauf F, Moser A, Moser H.
    Pediatr Res; 1989 Jul; 26(1):67-72. PubMed ID: 2475849
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  • 4. 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 Jul; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

  • 5. [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 Jul; 105(11):320-2. PubMed ID: 7687405
    [Abstract] [Full Text] [Related]

  • 6. 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; 39(1):44-7. PubMed ID: 2462697
    [Abstract] [Full Text] [Related]

  • 7. Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.
    Poll-The BT, Saudubray JM, Ogier HA, Odièvre M, Scotto JM, Monnens L, Govaerts LC, Roels F, Cornelis A, Schutgens RB.
    Eur J Pediatr; 1987 Sep; 146(5):477-83. PubMed ID: 2445576
    [Abstract] [Full Text] [Related]

  • 8. Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
    Brul S, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, van den Bosch H, Tager JM.
    J Clin Invest; 1988 Jun; 81(6):1710-5. PubMed ID: 2454948
    [Abstract] [Full Text] [Related]

  • 9. [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 Jun; 104(21):665-70. PubMed ID: 1282286
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  • 13. [Function and diseases of peroxisomes].
    Wehr H, Zaremba J.
    Neurol Neurochir Pol; 1991 Jun; 25(6):769-74. PubMed ID: 1725818
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  • 17. Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.
    Kelley RI, Moser HW.
    Am J Med Genet; 1984 Dec; 19(4):791-5. PubMed ID: 6517102
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  • 18. 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 Dec; 11(4):358-71. PubMed ID: 2468817
    [Abstract] [Full Text] [Related]

  • 19. Refsum's disease, adrenoleucodystrophy, and the Zellweger syndrome.
    Stokke O, Skrede S, Ek J, Björkhem I.
    Scand J Clin Lab Invest; 1984 Sep; 44(5):463-4. PubMed ID: 6207587
    [No Abstract] [Full Text] [Related]

  • 20. Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders.
    Hughes JL, Poulos A, Robertson E, Chow CW, Sheffield LJ, Christodoulou J, Carter RF.
    Virchows Arch A Pathol Anat Histopathol; 1990 Sep; 416(3):255-64. PubMed ID: 1689088
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