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Journal Abstract Search

216 related items for PubMed ID: 2433405

  • 1. Clinical and biochemical heterogeneity in conditions with phytanic acid accumulation.
    Skjeldal OH, Stokke O, Refsum S, Norseth J, Petit H.
    J Neurol Sci; 1987 Jan; 77(1):87-96. PubMed ID: 2433405
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  • 3. Phytanic acid oxidase activity in cultured skin fibroblasts. Diagnostic usefulness and limitations.
    Skjeldal OH, Stokke O, Norseth J, Lie SO.
    Scand J Clin Lab Invest; 1986 May; 46(3):283-7. PubMed ID: 2424078
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  • 4. 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 May; 70(2):172-7. PubMed ID: 2408988
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  • 5. 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
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  • 6. The subcellular localization of phytanic acid oxidase in rat liver.
    Skjeldal OH, Stokke O.
    Biochim Biophys Acta; 1987 Sep 04; 921(1):38-42. PubMed ID: 3620488
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  • 7. Diagnosis of Refsum's disease using [1-14C]phytanic acid as substrate.
    Poulos A.
    Clin Genet; 1981 Oct 04; 20(4):247-53. PubMed ID: 6174257
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  • 8. Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?
    Poulos A, Sharp P, Whiting M.
    Clin Genet; 1984 Dec 04; 26(6):579-86. PubMed ID: 6209040
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  • 11. Patterns of Refsum's disease. Phytanic acid oxidase deficiency.
    Poulos A, Pollard AC, Mitchell JD, Wise G, Mortimer G.
    Arch Dis Child; 1984 Mar 04; 59(3):222-9. PubMed ID: 6201142
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  • 12. [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 04; 104(21):665-70. PubMed ID: 1282286
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  • 14. Neurological disorders and phytanic acid metabolism.
    Skjeldal OH, Nyberg-Hansen R, Stokke O.
    Acta Neurol Scand; 1988 Oct 04; 78(4):324-8. PubMed ID: 3223227
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  • 15. Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease.
    Wanders RJ, Heymans HS, Schutgens RB, Poll-Thé BT, Saudubray JM, Tager JM, Schrakamp G, van den Bosch H.
    J Neurol Sci; 1988 Apr 04; 84(2-3):147-55. PubMed ID: 2454298
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  • 16. Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders.
    ten Brink HJ, Schor DS, Kok RM, Poll-The BT, Wanders RJ, Jakobs C.
    J Lipid Res; 1992 Oct 04; 33(10):1449-57. PubMed ID: 1385561
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  • 19. Refsum's disease: a peroxisomal disorder affecting phytanic acid alpha-oxidation.
    Wierzbicki AS, Lloyd MD, Schofield CJ, Feher MD, Gibberd FB.
    J Neurochem; 2002 Mar 04; 80(5):727-35. PubMed ID: 11948235
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  • 20. 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 04; 27(5):309-14. PubMed ID: 2474624
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