These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

136 related items for PubMed ID: 8484962

  • 1. Complementation analysis of patients with intact peroxisomes and impaired peroxisomal beta-oxidation.
    McGuinness MC, Moser AB, Poll-The BT, Watkins PA.
    Biochem Med Metab Biol; 1993 Apr; 49(2):228-42. PubMed ID: 8484962
    [Abstract] [Full Text] [Related]

  • 2. Peroxisomal bifunctional enzyme deficiency.
    Watkins PA, Chen WW, Harris CJ, Hoefler G, Hoefler S, Blake DC, Balfe A, Kelley RI, Moser AB, Beard ME.
    J Clin Invest; 1989 Mar; 83(3):771-7. PubMed ID: 2921319
    [Abstract] [Full Text] [Related]

  • 3. Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects.
    Paton BC, Sharp PC, Crane DI, Poulos A.
    J Clin Invest; 1996 Feb 01; 97(3):681-8. PubMed ID: 8609223
    [Abstract] [Full Text] [Related]

  • 4. Molecular analysis of peroxisomal beta-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect.
    Guerroui S, Aubourg P, Chen WW, Hashimoto T, Scotto J.
    Biochem Biophys Res Commun; 1989 May 30; 161(1):242-51. PubMed ID: 2471528
    [Abstract] [Full Text] [Related]

  • 5. A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities.
    Wanders RJ, van Roermund CW, Schelen A, Schutgens RB, Tager JM, Stephenson JB, Clayton PT.
    J Inherit Metab Dis; 1990 May 30; 13(3):375-9. PubMed ID: 2122104
    [No Abstract] [Full Text] [Related]

  • 6. Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme protein.
    van Grunsven EG, van Roermund CW, Denis S, Wanders RJ.
    Biochem Biophys Res Commun; 1997 Jun 09; 235(1):176-9. PubMed ID: 9196058
    [Abstract] [Full Text] [Related]

  • 7. 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 09; 34(3):270-6. PubMed ID: 7510868
    [Abstract] [Full Text] [Related]

  • 8. 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 09; 84(5):1425-8. PubMed ID: 3469675
    [Abstract] [Full Text] [Related]

  • 9. Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome.
    Tager JM, Van der Beek WA, Wanders RJ, Hashimoto T, Heymans HS, Van den Bosch H, Schutgens RB, Schram AW.
    Biochem Biophys Res Commun; 1985 Feb 15; 126(3):1269-75. PubMed ID: 3977916
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Biochemical findings in a series of Australian patients with isolated defects in peroxisomal beta-oxidation.
    Paton BC, Sharp PC, Poulos A.
    Ann N Y Acad Sci; 1996 Dec 27; 804():750-1. PubMed ID: 8993614
    [No Abstract] [Full Text] [Related]

  • 13. Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency.
    van Grunsven EG, van Berkel E, Ijlst L, Vreken P, de Klerk JB, Adamski J, Lemonde H, Clayton PT, Cuebas DA, Wanders RJ.
    Proc Natl Acad Sci U S A; 1998 Mar 03; 95(5):2128-33. PubMed ID: 9482850
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies.
    Watkins PA, McGuinness MC, Raymond GV, Hicks BA, Sisk JM, Moser AB, Moser HW.
    Ann Neurol; 1995 Sep 03; 38(3):472-7. PubMed ID: 7668838
    [Abstract] [Full Text] [Related]

  • 16. Peroxisomal disorders: overview.
    Moser HW, Moser AB.
    Ann N Y Acad Sci; 1996 Dec 27; 804():427-41. PubMed ID: 8993562
    [No Abstract] [Full Text] [Related]

  • 17. D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.
    Suzuki Y, Jiang LL, Souri M, Miyazawa S, Fukuda S, Zhang Z, Une M, Shimozawa N, Kondo N, Orii T, Hashimoto T.
    Am J Hum Genet; 1997 Nov 27; 61(5):1153-62. PubMed ID: 9345094
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Peroxisomes and beta-oxidation of long-chain unsaturated carboxylic acids.
    Hiltunen JK.
    Scand J Clin Lab Invest Suppl; 1991 Apr 30; 204():33-46. PubMed ID: 2042025
    [Abstract] [Full Text] [Related]

  • 20. Isolated defect of peroxisomal beta-oxidation in a 16-year-old patient.
    Santer R, Claviez A, Oldigs HD, Schaub J, Schutgens RB, Wanders RJ.
    Eur J Pediatr; 1993 Apr 30; 152(4):339-42. PubMed ID: 8482286
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.