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Journal Abstract Search

348 related items for PubMed ID: 7176294

  • 1. Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids.
    Brown FR, McAdams AJ, Cummins JW, Konkol R, Singh I, Moser AB, Moser HW.
    Johns Hopkins Med J; 1982 Dec; 151(6):344-51. PubMed ID: 7176294
    [No Abstract] [Full Text] [Related]

  • 2. The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis.
    Moser AE, Singh I, Brown FR, Solish GI, Kelley RI, Benke PJ, Moser HW.
    N Engl J Med; 1984 May 03; 310(18):1141-6. PubMed ID: 6709009
    [Abstract] [Full Text] [Related]

  • 3. Very long chain fatty acids in genetic peroxisomal disease fibroblasts: differences between the cerebro-hepato-renal (Zellweger) syndrome and adrenoleukodystrophy variants.
    Molzer B, Korschinsky M, Bernheimer H, Schmid R, Wolf C, Roscher A.
    Clin Chim Acta; 1986 Nov 30; 161(1):81-90. PubMed ID: 3815856
    [Abstract] [Full Text] [Related]

  • 4. Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.
    Singh I, Moser AE, Goldfischer S, Moser HW.
    Proc Natl Acad Sci U S A; 1984 Jul 30; 81(13):4203-7. PubMed ID: 6588384
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Adrenoleukodystrophy: survey of 303 cases: biochemistry, diagnosis, and therapy.
    Moser HW, Moser AE, Singh I, O'Neill BP.
    Ann Neurol; 1984 Dec 30; 16(6):628-41. PubMed ID: 6524872
    [Abstract] [Full Text] [Related]

  • 7. Neonatal-onset adrenoleukodystrophy in a girl.
    Haas JE, Johnson ES, Farrell DL.
    Ann Neurol; 1982 Nov 30; 12(5):449-57. PubMed ID: 6295256
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. An adult case of adrenoleukodystrophy with features of olivo-ponto-cerebellar atrophy: II. Lipid biochemical studies.
    Taketomi T, Hara A, Kitazawa N, Takada K, Nakamura H.
    Jpn J Exp Med; 1987 Feb 30; 57(1):59-70. PubMed ID: 3476777
    [Abstract] [Full Text] [Related]

  • 10. The peroxisome: nervous system role of a previously underrated organelle. The 1987 Robert Wartenberg lecture.
    Moser HW.
    Neurology; 1988 Oct 30; 38(10):1617-27. PubMed ID: 2458548
    [No Abstract] [Full Text] [Related]

  • 11. Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: plasma changes and skin fibroblast phytanic acid oxidase.
    Poulos A, Sharp P, Fellenberg AJ, Danks DM.
    Hum Genet; 1985 Oct 30; 70(2):172-7. PubMed ID: 2408988
    [Abstract] [Full Text] [Related]

  • 12. [Adrenoleukodystrophy: the significance of peroxisomal disease in adult neurology].
    Gold R, Hunneman DH, Kappos L, Hanefeld F.
    Nervenarzt; 1990 Feb 30; 61(2):77-82. PubMed ID: 2320193
    [No Abstract] [Full Text] [Related]

  • 13. Schilder's myelinoclastic diffuse sclerosis.
    Poser CM, Goutières F, Carpentier MA, Aicardi J.
    Pediatrics; 1986 Jan 30; 77(1):107-12. PubMed ID: 3940347
    [Abstract] [Full Text] [Related]

  • 14. [Two adult cases of adrenoleukodystrophy with clinical features of striatonigral degeneration--a probable variant of adrenoleukodystrophy].
    Sano M, Yokota T, Kushi Y, Handa S, Tsukagoshi H.
    Rinsho Shinkeigaku; 1988 Sep 30; 28(9):996-1003. PubMed ID: 3246111
    [No Abstract] [Full Text] [Related]

  • 15. Adrenoleukodystrophy.
    Lenard HG.
    Neuropediatrics; 1984 Sep 30; 15 Suppl():16-9. PubMed ID: 6100794
    [Abstract] [Full Text] [Related]

  • 16. [Liver pathologies due to peroxisome disorders].
    Lovisetto P, Raviolo P.
    Recenti Prog Med; 1994 Feb 30; 85(2):134-41. PubMed ID: 8184191
    [Abstract] [Full Text] [Related]

  • 17. [Adrenoleukodystrophy and adrenomyeloneuropathy].
    Masson C.
    Presse Med; 1986 Jun 07; 15(23):1091-3. PubMed ID: 2942890
    [Abstract] [Full Text] [Related]

  • 18. Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.
    Kelley RI, Moser HW.
    Am J Med Genet; 1984 Dec 07; 19(4):791-5. PubMed ID: 6517102
    [Abstract] [Full Text] [Related]

  • 19. Adrenoleukodystrophy.
    O'Neill BP, Moser HW.
    Can J Neurol Sci; 1982 Nov 07; 9(4):449-52. PubMed ID: 6758925
    [No Abstract] [Full Text] [Related]

  • 20. Plasma polyenoic very-long-chain fatty acids in peroxisomal disease: biochemical discrimination of Zellweger's syndrome from other phenotypes.
    Poulos A, Sharp P, Johnson D.
    Neurology; 1989 Jan 07; 39(1):44-7. PubMed ID: 2462697
    [Abstract] [Full Text] [Related]

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