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151 related items for PubMed ID: 3065462

  • 1. Prospect for enzyme therapy in glycogenosis II variants: a study on cultured muscle cells.
    van der Ploeg AT, Bolhuis PA, Wolterman RA, Visser JW, Loonen MC, Busch HF, Reuser AJ.
    J Neurol; 1988 Sep; 235(7):392-6. PubMed ID: 3065462
    [Abstract] [Full Text] [Related]

  • 2. Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscle.
    Van der Ploeg AT, Loonen MC, Bolhuis PA, Busch HM, Reuser AJ, Galjaard H.
    Pediatr Res; 1988 Jul; 24(1):90-4. PubMed ID: 2970619
    [Abstract] [Full Text] [Related]

  • 3. Bovine generalised glycogenosis type II. Uptake of lysosomal alpha-glucosidase by cultured skeletal muscle and reversal of glycogen accumulation.
    Di Marco PN, Howell JM, Dorling PR.
    FEBS Lett; 1985 Oct 14; 190(2):301-4. PubMed ID: 3899727
    [Abstract] [Full Text] [Related]

  • 4. Bovine glycogenosis type II. Biochemical and morphological characteristics of skeletal muscle in culture.
    Di Marco PN, Howell JM, Dorling PR.
    Neuropathol Appl Neurobiol; 1984 Oct 14; 10(5):379-95. PubMed ID: 6395034
    [Abstract] [Full Text] [Related]

  • 5. Uptake and stability of human and bovine acid alpha-glucosidase in cultured fibroblasts and skeletal muscle cells from glycogenosis type II patients.
    Reuser AJ, Kroos MA, Ponne NJ, Wolterman RA, Loonen MC, Busch HF, Visser WJ, Bolhuis PA.
    Exp Cell Res; 1984 Nov 14; 155(1):178-89. PubMed ID: 6237928
    [Abstract] [Full Text] [Related]

  • 6. An investigation of the possible influence of neutral alpha-glucosidases on the clinical heterogeneity of glycogenosis type II.
    Van der Ploeg AT, Kroos MA, Swallow DM, Reuser AJ.
    Ann Hum Genet; 1989 May 14; 53(2):185-92. PubMed ID: 2688540
    [Abstract] [Full Text] [Related]

  • 7. Breakdown of lysosomal glycogen in cultured fibroblasts from glycogenosis type II patients after uptake of acid alpha-glucosidase.
    van der Ploeg AT, Kroos M, van Dongen JM, Visser WJ, Bolhuis PA, Loonen MC, Reuser AJ.
    J Neurol Sci; 1987 Jul 14; 79(3):327-36. PubMed ID: 3302116
    [Abstract] [Full Text] [Related]

  • 8. Adult forms of glycogenosis type II. A defect in an early stage of acid alpha-glucosidase realization.
    Reuser AJ, Kroos M.
    FEBS Lett; 1982 Sep 20; 146(2):361-4. PubMed ID: 6754447
    [Abstract] [Full Text] [Related]

  • 9. Rat heart perfusion as model system for enzyme replacement therapy in glycogenosis type II.
    van der Ploeg AT, van der Kraaij AM, Willemsen R, Kroos MA, Loonen MC, Koster JF, Reuser AJ.
    Pediatr Res; 1990 Oct 20; 28(4):344-7. PubMed ID: 2235132
    [Abstract] [Full Text] [Related]

  • 10. Severe course of glycogen storage disease type II (Pompe's disease) without development of cardiomegalia.
    Ullrich K, Gröbe H, Korinthenberg R, von Bassewitz DB.
    Pathol Res Pract; 1986 Oct 20; 181(5):627-32. PubMed ID: 2947052
    [Abstract] [Full Text] [Related]

  • 11. Adult glycogenosis type II (Pompe's disease): morphological abnormalities in muscle and skin biopsies compared with acid alpha-glucosidase activity.
    Wierzba-Bobrowicz T, Lewandowska E, Lugowska A, Rola R, Stepień T, Ryglewicz D, Pasennik E.
    Folia Neuropathol; 2007 Oct 20; 45(4):179-86. PubMed ID: 18176891
    [Abstract] [Full Text] [Related]

  • 12. Immunochemical studies of human acid alpha-1,4-glucosidase in type II glycogenosis.
    Bienvenu J, Mathieu M.
    Enzyme; 1981 Oct 20; 26(4):182-90. PubMed ID: 7018896
    [Abstract] [Full Text] [Related]

  • 13. Skeletal-muscle alpha-glucosidases in bovine generalized glycogenosis type II.
    Dorling PR, Howell JM, Gawthorne JM.
    Biochem J; 1981 Aug 15; 198(2):409-12. PubMed ID: 7034730
    [Abstract] [Full Text] [Related]

  • 14. Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency).
    Loonen MC, Schram AW, Koster JF, Niermeijer MF, Busch HF, Martin JJ, Brouwer-Kelder B, Mekes W, Slee RG, Tager JM.
    Clin Genet; 1981 Jan 15; 19(1):55-63. PubMed ID: 7006871
    [Abstract] [Full Text] [Related]

  • 15. Biochemical, immunological, and cell genetic studies in glycogenosis type II.
    Reuser AJ, Koster JF, Hoogeveen A, Galjaard H.
    Am J Hum Genet; 1978 Mar 15; 30(2):132-43. PubMed ID: 350041
    [Abstract] [Full Text] [Related]

  • 16. Uncommon case of type II glycogenosis.
    de Barsy T, Ferrière G, Fernandez-Alvarez E.
    Acta Neuropathol; 1979 Aug 15; 47(3):245-7. PubMed ID: 384741
    [Abstract] [Full Text] [Related]

  • 17. Enzyme replacement in Pompe disease with an alpha-glucosidase-low density lipoprotein complex.
    Williams JC, Murray AK.
    Birth Defects Orig Artic Ser; 1980 Aug 15; 16(1):415-23. PubMed ID: 7004520
    [No Abstract] [Full Text] [Related]

  • 18. [Cardiomuscular lysosomal glycogenosis in adults without known enzyme deficiency. A cause of familial myocardiopathy and lysosomal glycogen overload with normal acid maltase].
    Bru P, Pellissier JF, Gatau-Pelanchon J, Faugère G, de Barsy T, Levy S, Gérard R.
    Arch Mal Coeur Vaiss; 1988 Jan 15; 81(1):109-14. PubMed ID: 3130016
    [Abstract] [Full Text] [Related]

  • 19. Recombinant human acid alpha-glucosidase corrects acid alpha-glucosidase-deficient human fibroblasts, quail fibroblasts, and quail myoblasts.
    Yang HW, Kikuchi T, Hagiwara Y, Mizutani M, Chen YT, Van Hove JL.
    Pediatr Res; 1998 Mar 15; 43(3):374-80. PubMed ID: 9505277
    [Abstract] [Full Text] [Related]

  • 20. Adenovirus-mediated transfer of the acid alpha-glucosidase gene into fibroblasts, myoblasts and myotubes from patients with glycogen storage disease type II leads to high level expression of enzyme and corrects glycogen accumulation.
    Nicolino MP, Puech JP, Kremer EJ, Reuser AJ, Mbebi C, Verdière-Sahuqué M, Kahn A, Poenaru L.
    Hum Mol Genet; 1998 Oct 15; 7(11):1695-702. PubMed ID: 9736771
    [Abstract] [Full Text] [Related]

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