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Journal Abstract Search

180 related items for PubMed ID: 2450404

  • 21. Polarizing inclusions in some organs of children with congenital peroxisomal diseases (Zellweger's, Refsum's, chondrodysplasia punctata (rhizomelic form), X-linked adrenoleukodystrophy).
    Kerckaert I, Dingemans KP, Heymans HS, Vamecq J, Roels F.
    J Inherit Metab Dis; 1988; 11(4):372-86. PubMed ID: 2468818
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  • 25. Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometry.
    Clayton PT, Lake BD, Hall NA, Shortland DB, Carruthers RA, Lawson AM.
    Eur J Pediatr; 1987 Mar; 146(2):166-73. PubMed ID: 2436918
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  • 26. Peroxisomal disorders: clinical commentary and future prospects.
    Wilson GN, Holmes RD, Hajra AK.
    Am J Med Genet; 1988 Jul; 30(3):771-92. PubMed ID: 2461077
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  • 27. Formation of a novel arachidonic acid metabolite in peroxisomes.
    Gordon JA, Heller SK, Rhead WJ, Watkins PA, Spector AA.
    Prostaglandins Leukot Essent Fatty Acids; 1995 Jul; 52(2-3):77-81. PubMed ID: 7540307
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  • 28. Peroxisomal disorders. A review of a recently recognized group of clinical entities.
    Talwar D, Swaiman KF.
    Clin Pediatr (Phila); 1987 Oct; 26(10):497-504. PubMed ID: 2443295
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  • 29. 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 Oct; 11(4):358-71. PubMed ID: 2468817
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  • 30. [Retinopathy in Zellweger's cerebrohepatorenal syndrome. The electrophysiological aspects].
    Stănescu-Segall B.
    Oftalmologia; 1996 Oct; 40(4):357-60. PubMed ID: 8962865
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  • 31. 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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  • 32. Clinical recognition of patients affected by a peroxisomal disorder: a retrospective study in 40 patients.
    Theil AC, Schutgens RB, Wanders RJ, Heymans HS.
    Eur J Pediatr; 1992 Feb; 151(2):117-20. PubMed ID: 1371465
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  • 33. [Peroxisomes and neurologic diseases].
    Sereni C, Paturneau-Jouas M.
    Rev Neurol (Paris); 1989 Feb; 145(5):341-9. PubMed ID: 2472665
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  • 34. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
    Aubourg P, Kremser K, Roland MO, Rocchiccioli F, Singh I.
    Pediatr Res; 1993 Sep; 34(3):270-6. PubMed ID: 7510868
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  • 35. Biochemical abnormalities in rhizomelic chondrodysplasia punctata.
    Hoefler G, Hoefler S, Watkins PA, Chen WW, Moser A, Baldwin V, McGillivary B, Charrow J, Friedman JM, Rutledge L.
    J Pediatr; 1988 May; 112(5):726-33. PubMed ID: 2452243
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  • 36. New approaches in peroxisomal disorders.
    Moser HW.
    Dev Neurosci; 1987 May; 9(1):1-18. PubMed ID: 3297624
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  • 37. Peroxisomal disorders.
    Aubourg P, Wanders R.
    Handb Clin Neurol; 2013 May; 113():1593-609. PubMed ID: 23622381
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  • 38. Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.
    Yajima S, Suzuki Y, Shimozawa N, Yamaguchi S, Orii T, Fujiki Y, Osumi T, Hashimoto T, Moser HW.
    Hum Genet; 1992 Mar; 88(5):491-9. PubMed ID: 1372585
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  • 39. Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation.
    Shimozawa N, Nagase T, Takemoto Y, Ohura T, Suzuki Y, Kondo N.
    Am J Med Genet A; 2003 Jul 01; 120A(1):40-3. PubMed ID: 12794690
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  • 40. Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders.
    Wanders RJ, Waterham HR.
    Clin Genet; 2005 Feb 01; 67(2):107-33. PubMed ID: 15679822
    [Abstract] [Full Text] [Related]

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