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Journal Abstract Search

109 related items for PubMed ID: 2192101

  • 1. [Peroxisomal disorders; newer concept and recent studies].
    Kamoshita S.
    Nihon Rinsho; 1990 Mar; 48(3):629-38. PubMed ID: 2192101
    [No Abstract] [Full Text] [Related]

  • 2. Adrenoleukodystrophy and Zellweger syndrome.
    Moser HW, Moser AB, Chen WW, Watkins PA.
    Prog Clin Biol Res; 1990 Mar; 321():511-35. PubMed ID: 2183241
    [No Abstract] [Full Text] [Related]

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

  • 4. Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders.
    Molzer B, Kainz-Korschinsky M, Sundt-Heller R, Bernheimer H.
    J Clin Chem Clin Biochem; 1989 May; 27(5):309-14. PubMed ID: 2474624
    [Abstract] [Full Text] [Related]

  • 5. [Peroxisome disorders].
    Hashimoto T, Kamijo K, Suzuki Y.
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):817-20. PubMed ID: 3270898
    [No Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 Feb; 11(4):358-71. PubMed ID: 2468817
    [Abstract] [Full Text] [Related]

  • 8. [Peroxisomes and neurological disorders].
    Suzuki Y, Yamaguchi S, Orii T.
    No To Shinkei; 1990 Jul; 42(7):611-9. PubMed ID: 2223257
    [No Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. The deficient degradation of synthetic 2- and 3-methyl-branched fatty acids in fibroblasts from patients with peroxisomal disorders.
    Van Veldhoven PP, Huang S, Eyssen HJ, Mannaerts GP.
    J Inherit Metab Dis; 1993 Jul; 16(2):381-91. PubMed ID: 7692128
    [Abstract] [Full Text] [Related]

  • 11. Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders.
    Poll-The BT, Skjeldal OH, Stokke O, Poulos A, Demaugre F, Saudubray JM.
    Hum Genet; 1989 Jan; 81(2):175-81. PubMed ID: 2463966
    [Abstract] [Full Text] [Related]

  • 12. Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patients.
    Mihalik SJ, Moser HW, Watkins PA, Danks DM, Poulos A, Rhead WJ.
    Pediatr Res; 1989 May; 25(5):548-52. PubMed ID: 2717271
    [Abstract] [Full Text] [Related]

  • 13. Peroxisomal disorders.
    Gordon N.
    Brain Dev; 1987 May; 9(6):571-5. PubMed ID: 3328519
    [Abstract] [Full Text] [Related]

  • 14. 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 May; 10 Suppl 1():33-45. PubMed ID: 3119940
    [Abstract] [Full Text] [Related]

  • 15. [Peroxisomal disorders in neurology].
    Orii T, Hashimoto T.
    No To Hattatsu; 1992 Mar; 24(2):174-5. PubMed ID: 1567653
    [Abstract] [Full Text] [Related]

  • 16. [Peroxisomes--in search of their function in man].
    Monnens L, Trijbels F, Govaerts L.
    Tijdschr Kindergeneeskd; 1985 Aug; 53(4):129-36. PubMed ID: 3909510
    [Abstract] [Full Text] [Related]

  • 17. [Biochemistry of peroxisome and peroxisomal diseases].
    Vamecq J, Poll-The BT, Saudubray JM.
    Ann Biol Clin (Paris); 1988 Aug; 46(4):233-58. PubMed ID: 3389578
    [No Abstract] [Full Text] [Related]

  • 18. Adrenoleukodystrophy and other peroxisomal disorders that affect the nervous system, including new observations on L-pipecolic acid oxidase in primates.
    Moser HW, Mihalik SJ, Watkins PA.
    Brain Dev; 1989 Aug; 11(2):80-90. PubMed ID: 2653074
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Biochemical abnormalities in rhizomelic chondrodysplasia punctata.
    Hoefler G, Hoefler S, Watkins PA, Chen WW, Moser A, Baldwin V, McGillivary B, Charrow J, Friedman JM, Rutledge L.
    J Pediatr; 1988 May; 112(5):726-33. PubMed ID: 2452243
    [Abstract] [Full Text] [Related]

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