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Journal Abstract Search

268 related items for PubMed ID: 2879480

  • 1. 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; 125(3):524-35. PubMed ID: 2879480
    [Abstract] [Full Text] [Related]

  • 2. Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities.
    Goldfischer S, Collins J, Rapin I, Neumann P, Neglia W, Spiro AJ, Ishii T, Roels F, Vamecq J, Van Hoof F.
    J Pediatr; 1986 Jan; 108(1):25-32. PubMed ID: 2868085
    [Abstract] [Full Text] [Related]

  • 3. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).
    Poll-The BT, Roels F, Ogier H, Scotto J, Vamecq J, Schutgens RB, Wanders RJ, van Roermund CW, van Wijland MJ, Schram AW.
    Am J Hum Genet; 1988 Mar; 42(3):422-34. PubMed ID: 2894756
    [Abstract] [Full Text] [Related]

  • 4. 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; 34(3):270-6. PubMed ID: 7510868
    [Abstract] [Full Text] [Related]

  • 5. 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; 84(5):1425-8. PubMed ID: 3469675
    [Abstract] [Full Text] [Related]

  • 6. Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: plasma changes and skin fibroblast phytanic acid oxidase.
    Poulos A, Sharp P, Fellenberg AJ, Danks DM.
    Hum Genet; 1985 Mar; 70(2):172-7. PubMed ID: 2408988
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy.
    Lazo O, Contreras M, Hashmi M, Stanley W, Irazu C, Singh I.
    Proc Natl Acad Sci U S A; 1988 Oct; 85(20):7647-51. PubMed ID: 3174658
    [Abstract] [Full Text] [Related]

  • 9. Deficient activities and proteins of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome.
    Suzuki Y, Orii T, Mori M, Tatibana M, Hashimoto T.
    Clin Chim Acta; 1986 Apr 30; 156(2):191-6. PubMed ID: 3519003
    [Abstract] [Full Text] [Related]

  • 10. Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.
    Schutgens RB, Wanders RJ, Heymans HS, Schram AW, Tager JM, Schrakamp G, van den Bosch H.
    J Inherit Metab Dis; 1987 Apr 30; 10 Suppl 1():33-45. PubMed ID: 3119940
    [Abstract] [Full Text] [Related]

  • 11. 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 30; 81(13):4203-7. PubMed ID: 6588384
    [Abstract] [Full Text] [Related]

  • 12. Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: cytochemical and morphometric data.
    Roels F, Pauwels M, Poll-Thé BT, Scotto J, Ogier H, Aubourg P, Saudubray JM.
    Virchows Arch A Pathol Anat Histopathol; 1988 Jul 30; 413(4):275-85. PubMed ID: 3140473
    [Abstract] [Full Text] [Related]

  • 13. Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders.
    Hughes JL, Crane DI, Robertson E, Poulos A.
    Virchows Arch A Pathol Anat Histopathol; 1993 Jul 30; 423(6):459-68. PubMed ID: 7507276
    [Abstract] [Full Text] [Related]

  • 14. Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.
    Kelley RI, Moser HW.
    Am J Med Genet; 1984 Dec 30; 19(4):791-5. PubMed ID: 6517102
    [Abstract] [Full Text] [Related]

  • 15. Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes.
    Kelley RI, Datta NS, Dobyns WB, Hajra AK, Moser AB, Noetzel MJ, Zackai EH, Moser HW.
    Am J Med Genet; 1986 Apr 30; 23(4):869-901. PubMed ID: 3515938
    [Abstract] [Full Text] [Related]

  • 16. [Peroxisomes and neurologic diseases].
    Sereni C, Paturneau-Jouas M.
    Rev Neurol (Paris); 1989 Apr 30; 145(5):341-9. PubMed ID: 2472665
    [Abstract] [Full Text] [Related]

  • 17. Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.
    Schram AW, Goldfischer S, van Roermund CW, Brouwer-Kelder EM, Collins J, Hashimoto T, Heymans HS, van den Bosch H, Schutgens RB, Tager JM.
    Proc Natl Acad Sci U S A; 1987 Apr 30; 84(8):2494-6. PubMed ID: 2882519
    [Abstract] [Full Text] [Related]

  • 18. Peroxisomal beta-oxidation of polyunsaturated long chain fatty acids in human fibroblasts. The polyunsaturated and the saturated long chain fatty acids are retroconverted by the same acyl-CoA oxidase.
    Christensen E, Woldseth B, Hagve TA, Poll-The BT, Wanders RJ, Sprecher H, Stokke O, Christophersen BO.
    Scand J Clin Lab Invest Suppl; 1993 Apr 30; 215():61-74. PubMed ID: 8327852
    [Abstract] [Full Text] [Related]

  • 19. [Clinical biochemical and genetic aspects of peroxisome-deficient disorders].
    Suzuki Y.
    No To Hattatsu; 1992 Mar 30; 24(2):194-7. PubMed ID: 1373633
    [Abstract] [Full Text] [Related]

  • 20. 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]

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