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Journal Abstract Search

240 related items for PubMed ID: 3519003

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  • 3. 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; 84(8):2494-6. PubMed ID: 2882519
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  • 5. 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
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  • 6. 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
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  • 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 30; 34(3):270-6. PubMed ID: 7510868
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  • 8. 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 30; 108(1):25-32. PubMed ID: 2868085
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  • 14. Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.
    Suzuki Y, Shimozawa N, Yajima S, Tomatsu S, Kondo N, Nakada Y, Akaboshi S, Lai M, Tanabe Y, Hashimoto T.
    Am J Hum Genet; 1994 Jan 30; 54(1):36-43. PubMed ID: 8279468
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  • 15. Individual peroxisomal beta-oxidation enzymes.
    Hashimoto T.
    Ann N Y Acad Sci; 1982 Jan 30; 386():5-12. PubMed ID: 6953852
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  • 17. Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder.
    Suzuki Y, Shimozawa N, Orii T, Igarashi N, Kono N, Hashimoto T.
    Clin Chim Acta; 1988 Feb 29; 172(1):65-76. PubMed ID: 2452040
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  • 18. Significance of catalase in peroxisomal fatty acyl-CoA beta-oxidation.
    Hashimoto F, Hayashi H.
    Biochim Biophys Acta; 1987 Sep 04; 921(1):142-50. PubMed ID: 2887206
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  • 19. Immunochemical and biochemical studies of fatty acid oxidation in fibroblasts of Zellweger and X-linked adrenoleukodystrophy patients.
    Reubsaet FA, Veerkamp JH, Brückwilder ML, Trijbels JM, Hashimoto T, Monnens LA.
    Biochim Biophys Acta; 1991 Jun 03; 1083(3):305-9. PubMed ID: 2049396
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