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214 related items for PubMed ID: 3515938

  • 1. 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; 23(4):869-901. PubMed ID: 3515938
    [Abstract] [Full Text] [Related]

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

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

  • 4. 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]

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

  • 6. [Neonatal adrenoleukodystrophy. Apropos of 3 cases in siblings].
    Sarda H, Henry V, Le Loc'h H, Aubourg P, Poll-The BT, Saudubray JM.
    Ann Pediatr (Paris); 1989 Apr; 36(4):233-6. PubMed ID: 2662877
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Diagnosis of peroxisomal disorders with neurological involvement.
    Molzer B.
    Padiatr Padol; 1993 May 03; 28(1):43-8. PubMed ID: 8446428
    [Abstract] [Full Text] [Related]

  • 9. Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.
    Wilson GN, Holmes RG, Custer J, Lipkowitz JL, Stover J, Datta N, Hajra A.
    Am J Med Genet; 1986 May 03; 24(1):69-82. PubMed ID: 3706414
    [Abstract] [Full Text] [Related]

  • 10. 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 03; 125(3):524-35. PubMed ID: 2879480
    [Abstract] [Full Text] [Related]

  • 11. History of the cerebrohepatorenal syndrome of Zellweger and other peroxisomal disorders.
    Zellweger H, Maertens P, Superneau D, Wertelecki W.
    South Med J; 1988 Mar 03; 81(3):357-64. PubMed ID: 2450404
    [Abstract] [Full Text] [Related]

  • 12. Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders.
    Martinez M.
    Brain Res; 1992 Jun 26; 583(1-2):171-82. PubMed ID: 1504825
    [Abstract] [Full Text] [Related]

  • 13. 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 26; 39(1):44-7. PubMed ID: 2462697
    [Abstract] [Full Text] [Related]

  • 14. 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 26; 177(1):107-18. PubMed ID: 3776884
    [Abstract] [Full Text] [Related]

  • 15. Cerebrohepatorenal syndrome of Zellweger: a peroxisomal deficiency disorder. Case report and review.
    Kaplan M, Eidelman AI, Shapira Y, Collins J, Goldfischer S.
    Isr J Med Sci; 1988 Jun 26; 24(6):319-24. PubMed ID: 3042692
    [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 26; 77(2-3):331-40. PubMed ID: 3819771
    [Abstract] [Full Text] [Related]

  • 17. [Endocrine disease in adrenoleukodystrophy].
    Girard S, Bruckert E, Turpin G.
    Ann Med Interne (Paris); 2001 Feb 26; 152(1):15-26. PubMed ID: 11240421
    [Abstract] [Full Text] [Related]

  • 18. Ocular histopathologic and biochemical studies of the cerebrohepatorenal syndrome (Zellweger's syndrome) and its relationship to neonatal adrenoleukodystrophy.
    Cohen SM, Brown FR, Martyn L, Moser HW, Chen W, Kistenmacher M, Punnett H, de la Cruz ZC, Chan NR, Green WR.
    Am J Ophthalmol; 1983 Oct 26; 96(4):488-501. PubMed ID: 6624831
    [Abstract] [Full Text] [Related]

  • 19. 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 26; 70(2):172-7. PubMed ID: 2408988
    [Abstract] [Full Text] [Related]

  • 20. Clinical approach to inherited peroxisomal disorders: a series of 27 patients.
    Baumgartner MR, Poll-The BT, Verhoeven NM, Jakobs C, Espeel M, Roels F, Rabier D, Levade T, Rolland MO, Martinez M, Wanders RJ, Saudubray JM.
    Ann Neurol; 1998 Nov 26; 44(5):720-30. PubMed ID: 9818927
    [Abstract] [Full Text] [Related]

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