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Journal Abstract Search

230 related items for PubMed ID: 1373633

  • 21. [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; 105(11):320-2. PubMed ID: 7687405
    [Abstract] [Full Text] [Related]

  • 22. Accumulation and defective beta-oxidation of very long chain fatty acids in Zellweger's syndrome, adrenoleukodystrophy and Refsum's disease variants.
    Poulos A, Singh H, Paton B, Sharp P, Derwas N.
    Clin Genet; 1986 May; 29(5):397-408. PubMed ID: 2427264
    [Abstract] [Full Text] [Related]

  • 23. 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; 146(5):477-83. PubMed ID: 2445576
    [Abstract] [Full Text] [Related]

  • 24. Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups.
    Moser AB, Rasmussen M, Naidu S, Watkins PA, McGuinness M, Hajra AK, Chen G, Raymond G, Liu A, Gordon D.
    J Pediatr; 1995 Jul; 127(1):13-22. PubMed ID: 7541833
    [Abstract] [Full Text] [Related]

  • 25. Molecular species of phosphatidylcholine containing very long chain fatty acids in human brain: enrichment in X-linked adrenoleukodystrophy brain and diseases of peroxisome biogenesis brain.
    Sharp P, Johnson D, Poulos A.
    J Neurochem; 1991 Jan; 56(1):30-7. PubMed ID: 1702833
    [Abstract] [Full Text] [Related]

  • 26. Metabolism of branched chain fatty acids in peroxisomal disorders.
    Singh H, Usher S, Johnson D, Poulos A.
    J Inherit Metab Dis; 1990 Jan; 13(3):387-9. PubMed ID: 1700192
    [No Abstract] [Full Text] [Related]

  • 27. Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins.
    Wanders RJ, Schutgens RB, Schrakamp G, van den Bosch H, Tager JM, Schram AW, Hashimoto T, Poll-Thé BT, Saudubrau JM.
    Eur J Pediatr; 1986 Aug; 145(3):172-5. PubMed ID: 2429839
    [Abstract] [Full Text] [Related]

  • 28. 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; 81(6):1710-5. PubMed ID: 2454948
    [Abstract] [Full Text] [Related]

  • 29. Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency.
    Abe Y, Honsho M, Nakanishi H, Taguchi R, Fujiki Y.
    Biochim Biophys Acta; 2014 Apr 04; 1841(4):610-9. PubMed ID: 24418004
    [Abstract] [Full Text] [Related]

  • 30. Immunochemical and biochemical studies of fatty acid oxidation in fibroblasts of Zellweger and X-linked adrenoleukodystrophy patients.
    Reubsaet FA, Veerkamp JH, Brückwilder ML, Trijbels JM, Hashimoto T, Monnens LA.
    Biochim Biophys Acta; 1991 Jun 03; 1083(3):305-9. PubMed ID: 2049396
    [Abstract] [Full Text] [Related]

  • 31. 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 03; 39(1):13-25. PubMed ID: 1705185
    [Abstract] [Full Text] [Related]

  • 32. Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders.
    Hughes JL, Crane DI, Robertson E, Poulos A.
    Virchows Arch A Pathol Anat Histopathol; 1993 Jan 03; 423(6):459-68. PubMed ID: 7507276
    [Abstract] [Full Text] [Related]

  • 33. 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 Jan 03; 52(2-3):77-81. PubMed ID: 7540307
    [Abstract] [Full Text] [Related]

  • 34. Complementation analysis of peroxisomal disorders and classical Refsum.
    Poll-The BT, Skjeldal OH, Stokke O, Demaugre F, Saudubray JM.
    Prog Clin Biol Res; 1990 Jan 03; 321():537-43. PubMed ID: 1691507
    [No Abstract] [Full Text] [Related]

  • 35. A comparative study of straight chain and branched chain fatty acid oxidation in skin fibroblasts from patients with peroxisomal disorders.
    Singh H, Usher S, Johnson D, Poulos A.
    J Lipid Res; 1990 Feb 03; 31(2):217-25. PubMed ID: 1691260
    [Abstract] [Full Text] [Related]

  • 36. 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]

  • 37. Localization of nervonic acid beta-oxidation in human and rodent peroxisomes: impaired oxidation in Zellweger syndrome and X-linked adrenoleukodystrophy.
    Sandhir R, Khan M, Chahal A, Singh I.
    J Lipid Res; 1998 Nov 03; 39(11):2161-71. PubMed ID: 9799802
    [Abstract] [Full Text] [Related]

  • 38. Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damage.
    Hoefler G, Paschke E, Hoefler S, Moser AB, Moser HW.
    J Clin Invest; 1991 Dec 03; 88(6):1873-9. PubMed ID: 1752949
    [Abstract] [Full Text] [Related]

  • 39. Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders.
    Wendland M, Subramani S.
    J Clin Invest; 1993 Nov 03; 92(5):2462-8. PubMed ID: 7693762
    [Abstract] [Full Text] [Related]

  • 40. 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 Nov 03; 321():545-58. PubMed ID: 2183242
    [Abstract] [Full Text] [Related]

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