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Journal Abstract Search

236 related items for PubMed ID: 1691507

  • 1. 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]

  • 2. 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]

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

  • 4. 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]

  • 5. 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]

  • 6. 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]

  • 7. [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 Jul; 104(21):665-70. PubMed ID: 1282286
    [Abstract] [Full Text] [Related]

  • 8. [Zellweger syndrome and other peroxisomal disorders: I. Clinical characteristics of a recently discovered group of diseases].
    Heymans HS, Wanders RJ, Schutgens RB, van den Bosch H, Tager JM, Barth PG.
    Ned Tijdschr Geneeskd; 1990 Mar 31; 134(13):634-9. PubMed ID: 1690863
    [No Abstract] [Full Text] [Related]

  • 9. 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 Mar 31; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

  • 10. [Peroxisomal disorders; newer concept and recent studies].
    Kamoshita S.
    Nihon Rinsho; 1990 Mar 31; 48(3):629-38. PubMed ID: 2192101
    [No Abstract] [Full Text] [Related]

  • 11. 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 31; 146(5):477-83. PubMed ID: 2445576
    [Abstract] [Full Text] [Related]

  • 12. Diagnosis of peroxisomal disorders with neurological involvement.
    Molzer B.
    Padiatr Padol; 1993 Sep 31; 28(1):43-8. PubMed ID: 8446428
    [Abstract] [Full Text] [Related]

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  • 14. [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 Sep 31; 105(11):320-2. PubMed ID: 7687405
    [Abstract] [Full Text] [Related]

  • 15. Peroxisomal disorders. Neurodevelopmental and biochemical aspects.
    Brown FR, Voigt R, Singh AK, Singh I.
    Am J Dis Child; 1993 Jun 31; 147(6):617-26. PubMed ID: 7685145
    [Abstract] [Full Text] [Related]

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  • 17. Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.
    Slawecki ML, Dodt G, Steinberg S, Moser AB, Moser HW, Gould SJ.
    J Cell Sci; 1995 May 31; 108 ( Pt 5)():1817-29. PubMed ID: 7544797
    [Abstract] [Full Text] [Related]

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  • 19. 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 May 31; 11(4):358-71. PubMed ID: 2468817
    [Abstract] [Full Text] [Related]

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