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Journal Abstract Search

181 related items for PubMed ID: 3140473

  • 1. 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; 413(4):275-85. PubMed ID: 3140473
    [Abstract] [Full Text] [Related]

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  • 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. 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 Mar; 423(6):459-68. PubMed ID: 7507276
    [Abstract] [Full Text] [Related]

  • 5. Stereological analysis of peroxisomes and mitochondria in intestinal epithelium of patients with peroxisomal deficiency disorders: Zellweger's syndrome and neonatal-onset adrenoleukodystrophy.
    Black VH, Cornacchia L.
    Am J Anat; 1986 Sep; 177(1):107-18. PubMed ID: 3776884
    [Abstract] [Full Text] [Related]

  • 6. Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies.
    Goldfischer S, Collins J, Rapin I, Coltoff-Schiller B, Chang CH, Nigro M, Black VH, Javitt NB, Moser HW, Lazarow PB.
    Science; 1985 Jan 04; 227(4682):67-70. PubMed ID: 3964959
    [Abstract] [Full Text] [Related]

  • 7. 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 04; 125(3):524-35. PubMed ID: 2879480
    [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 04; 84(5):1425-8. PubMed ID: 3469675
    [Abstract] [Full Text] [Related]

  • 9. Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity.
    Naidu S, Hoefler G, Watkins PA, Chen WW, Moser AB, Hoefler S, Rance NE, Powers JM, Beard M, Green WR.
    Neurology; 1988 Jul 04; 38(7):1100-7. PubMed ID: 3386829
    [Abstract] [Full Text] [Related]

  • 10. Hepatic peroxisomes are deficient in infantile refsum disease: a cytochemical study of 4 cases.
    Roels F, Cornelis A, Poll-The BT, Aubourg P, Ogier H, Scotto J, Saudubray JM.
    Am J Med Genet; 1986 Oct 04; 25(2):257-71. PubMed ID: 2430454
    [Abstract] [Full Text] [Related]

  • 11. Adrenoleukodystrophy, cerebrohepatorenal syndrome (Zellweger syndrome), and peroxisomes.
    Applegarth DA, Dimmick JE.
    Pediatr Pathol; 1985 Oct 04; 3(2-4):377-8. PubMed ID: 4095031
    [No Abstract] [Full Text] [Related]

  • 12. Peroxisomes in cirrhosis of the human liver: a cytochemical, ultrastructural and quantitative study.
    De Craemer D, Pauwels M, Roels F.
    Hepatology; 1993 Mar 04; 17(3):404-10. PubMed ID: 8444413
    [Abstract] [Full Text] [Related]

  • 13. Zellweger syndrome amniocytes: morphological appearance and a simple sedimentation method for prenatal diagnosis.
    Lazarow PB, Small GM, Santos M, Shio H, Moser A, Moser H, Esterman A, Black V, Dancis J.
    Pediatr Res; 1988 Jul 04; 24(1):63-7. PubMed ID: 3412850
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 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. 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 30; 77(2-3):331-40. PubMed ID: 3819771
    [Abstract] [Full Text] [Related]

  • 17. Peroxisomal disorders in children: immunohistochemistry and neuropathology.
    Kamei A, Houdou S, Takashima S, Suzuki Y, Becker LE, Armstrong DL.
    J Pediatr; 1993 Apr 30; 122(4):573-9. PubMed ID: 8463903
    [Abstract] [Full Text] [Related]

  • 18. Alterations of hepatocellular peroxisomes in patients with cancer. Catalase cytochemistry and morphometry.
    De Craemer D, Pauwels M, Hautekeete M, Roels F.
    Cancer; 1993 Jun 15; 71(12):3851-8. PubMed ID: 7685235
    [Abstract] [Full Text] [Related]

  • 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 Jun 15; 11(4):358-71. PubMed ID: 2468817
    [Abstract] [Full Text] [Related]

  • 20. Neonatal adrenoleukodystrophy.
    Aubourg P, Scotto J, Rocchiccioli F, Feldmann-Pautrat D, Robain O.
    J Neurol Neurosurg Psychiatry; 1986 Jan 15; 49(1):77-86. PubMed ID: 2420940
    [Abstract] [Full Text] [Related]

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