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Journal Abstract Search

180 related items for PubMed ID: 2450404

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

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

  • 3. Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies.
    Schutgens RB, Wanders RJ, Nijenhuis A, van den Hoek CM, Heymans HS, Schrakamp G, Bleeker-Wagemakers EM, Delleman JW, Schram AW, Tager JM.
    Enzyme; 1987 Mar; 38(1-4):161-76. PubMed ID: 3440444
    [Abstract] [Full Text] [Related]

  • 4. 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; 108 ( Pt 5)():1817-29. PubMed ID: 7544797
    [Abstract] [Full Text] [Related]

  • 5. More on Zellweger's syndrome, infantile Refsum's disease, and rhizomelic chondrodysplasia punctata.
    Goldfischer SL.
    N Engl J Med; 1986 Sep 18; 315(12):766-7. PubMed ID: 2427949
    [No Abstract] [Full Text] [Related]

  • 6. 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 18; 81(2):175-81. PubMed ID: 2463966
    [Abstract] [Full Text] [Related]

  • 7. The peroxisome and the eye.
    Folz SJ, Trobe JD.
    Surv Ophthalmol; 1991 Jan 18; 35(5):353-68. PubMed ID: 1710072
    [Abstract] [Full Text] [Related]

  • 8. Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
    Brul S, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, van den Bosch H, Tager JM.
    J Clin Invest; 1988 Jun 18; 81(6):1710-5. PubMed ID: 2454948
    [Abstract] [Full Text] [Related]

  • 9. Clinical biochemistry of peroxisomal disorders.
    Kaiser E, Kramar R.
    Clin Chim Acta; 1988 Mar 31; 173(1):57-80. PubMed ID: 3289796
    [Abstract] [Full Text] [Related]

  • 10. Glyceryl ethers in peroxisomal disease.
    Poulos A, Bankier A, Beckman K, Johnson D, Robertson EF, Sharp P, Sheffield L, Singh H, Usher S, Wise G.
    Clin Genet; 1991 Jan 31; 39(1):13-25. PubMed ID: 1705185
    [Abstract] [Full Text] [Related]

  • 11. 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 31; 23(4):869-901. PubMed ID: 3515938
    [Abstract] [Full Text] [Related]

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

  • 13. 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]

  • 14. 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 Jun 26; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

  • 15. Postnatal diagnosis of peroxisomal disorders: a biochemical approach.
    Wanders RJ, Schutgens RB, Barth PG, Tager JM, van den Bosch H.
    Biochimie; 1993 Jun 26; 75(3-4):269-79. PubMed ID: 7685190
    [Abstract] [Full Text] [Related]

  • 16. 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 26; 146(5):477-83. PubMed ID: 2445576
    [Abstract] [Full Text] [Related]

  • 17. [Peroxisomal hereditary diseases].
    Chandoga J, Tomková M, Hlavatá A.
    Bratisl Lek Listy; 1997 Jan 26; 98(1):32-42. PubMed ID: 9264803
    [Abstract] [Full Text] [Related]

  • 18. Prenatal and perinatal diagnosis of peroxisomal disorders.
    Schutgens RB, Schrakamp G, Wanders RJ, Heymans HS, Tager JM, van den Bosch H.
    J Inherit Metab Dis; 1989 Jan 26; 12 Suppl 1():118-34. PubMed ID: 2509803
    [Abstract] [Full Text] [Related]

  • 19. Disorders related to the metabolism of phytanic acid.
    Stokke O, Skjeldal OH, Høie K.
    Scand J Clin Lab Invest Suppl; 1986 Jan 26; 184():3-10. PubMed ID: 2438746
    [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 26; 39(1):44-7. PubMed ID: 2462697
    [Abstract] [Full Text] [Related]

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