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Journal Abstract Search

159 related items for PubMed ID: 3706414

  • 1. 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; 24(1):69-82. PubMed ID: 3706414
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  • 2. Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes.
    Datta NS, Wilson GN, Hajra AK.
    N Engl J Med; 1984 Oct 25; 311(17):1080-3. PubMed ID: 6566965
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  • 3. 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 25; 23(4):869-901. PubMed ID: 3515938
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  • 4. Aberration in de novo ether lipid biosynthesis in peroxisomal disorders.
    van den Bosch H, Schalkwijk CG, Schrakamp G, Wanders RJ, Schutgens RB, Schram AW, Tager JM.
    Prog Clin Biol Res; 1988 Apr 25; 282():139-50. PubMed ID: 3071794
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  • 8. [Diagnosis of Zellweger's cerebrohepatorenal syndrome].
    Schutgens RB, Heymans HS, Purvis R, Wanders RJ, Schrakamp G, van den Bosch H.
    Tijdschr Kindergeneeskd; 1984 Dec 25; 52(6):231-8. PubMed ID: 6528320
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  • 11. The role of peroxisomes in glycerol ether lipid metabolism.
    Hajra AK, Horie S, Webber KO.
    Prog Clin Biol Res; 1988 Dec 25; 282():99-116. PubMed ID: 3071810
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  • 12. Plasmalogen biosynthesis in the diagnosis of peroxisomal disorders.
    Kremser K, Roscher A.
    J Clin Chem Clin Biochem; 1989 May 25; 27(5):315-7. PubMed ID: 2760566
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  • 13. 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 25; 125(3):524-35. PubMed ID: 2879480
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  • 14. Zellweger syndrome knockout mouse models challenge putative peroxisomal beta-oxidation involvement in docosahexaenoic acid (22:6n-3) biosynthesis.
    Infante JP, Huszagh VA.
    Mol Genet Metab; 2001 Jan 25; 72(1):1-7. PubMed ID: 11161822
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  • 15. Properties of the enzymes catalyzing the biosynthesis of lysophosphatidate and its ether analog in cultured fibroblasts from Zellweger syndrome patients and normal controls.
    Webber KO, Datta NS, Hajra AK.
    Arch Biochem Biophys; 1987 May 01; 254(2):611-20. PubMed ID: 3646870
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  • 16. Analysis of very long-chain fatty acids and plasmalogen in the erythrocyte membrane: a simple method for the detection of peroxisomal disorders and discrimination between adrenoleukodystrophy and Zellweger syndrome.
    Tanaka K, Nishizawa K, Yamamoto H, Naruto T, Izeki E, Taga T, Shimada M, Saeki Y.
    Neuropediatrics; 1990 Aug 01; 21(3):119-23. PubMed ID: 2234315
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  • 17. [Retinopathy in Zellweger's cerebrohepatorenal syndrome. The electrophysiological aspects].
    Stănescu-Segall B.
    Oftalmologia; 1996 Aug 01; 40(4):357-60. PubMed ID: 8962865
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  • 18. [The contribution of peroxisomes to lipid metabolism].
    Kramar R.
    J Clin Chem Clin Biochem; 1986 Feb 01; 24(2):109-18. PubMed ID: 3711795
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  • 19. Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome.
    Heymans HS, vd Bosch H, Schutgens RB, Tegelaers WH, Walther JU, Müller-Höcker J, Borst P.
    Eur J Pediatr; 1984 Apr 01; 142(1):10-5. PubMed ID: 6714253
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  • 20. [Zellweger syndrome. Reports on two new cases].
    Cáceres-Marzal C, Vaquerizo-Madrid J, Girós M, Ruiz F, Roels F.
    Rev Neurol; 1984 Apr 01; 36(11):1030-4. PubMed ID: 12808498
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