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174 related items for PubMed ID: 6754447

  • 1. 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]

  • 2. Defects in synthesis, phosphorylation, and maturation of acid alpha-glucosidase in glycogenosis type II.
    Reuser AJ, Kroos M, Oude Elferink RP, Tager JM.
    J Biol Chem; 1985 Jul 15; 260(14):8336-41. PubMed ID: 3159730
    [Abstract] [Full Text] [Related]

  • 3. [Characterization of alpha-glucosidase in skin fibroblasts in the diagnosis of glycogenosis type 2 (Pompe disease)].
    Braulke T, Sandig KR.
    Kinderarztl Prax; 1984 Aug 15; 52(8):377-82. PubMed ID: 6384623
    [No Abstract] [Full Text] [Related]

  • 4. Immunochemical studies of human acid alpha-1,4-glucosidase in type II glycogenosis.
    Bienvenu J, Mathieu M.
    Enzyme; 1981 Aug 15; 26(4):182-90. PubMed ID: 7018896
    [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 15; 155(1):178-89. PubMed ID: 6237928
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 15; 24(1):90-4. PubMed ID: 2970619
    [Abstract] [Full Text] [Related]

  • 8. [Immunochemical study of acid alpha-1,4-glucosidase in 7 patients with type II glycogenosis].
    Bienvenu J, Mathieu M, Collombel C, Baltassat P, Divry P, Dorche C, Cotte J.
    Pediatrie; 1979 Sep 15; 34(6):659-76. PubMed ID: 388338
    [No Abstract] [Full Text] [Related]

  • 9. Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease).
    Steckel F, Gieselmann V, Waheed A, Hasilik A, von Figura K, Oude Elferink R, Kalsbeek R, Tager JM.
    FEBS Lett; 1982 Dec 13; 150(1):69-76. PubMed ID: 6761145
    [Abstract] [Full Text] [Related]

  • 10. 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 13; 19(1):55-63. PubMed ID: 7006871
    [Abstract] [Full Text] [Related]

  • 11. Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.
    Beratis NG, LaBadie GU, Hirschhorn K.
    J Clin Invest; 1978 Dec 13; 62(6):1264-74. PubMed ID: 34626
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. 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]

  • 14. Clinical diversity in glycogenosis type II. Biosynthesis and in situ localization of acid alpha-glucosidase in mutant fibroblasts.
    Reuser AJ, Kroos M, Willemsen R, Swallow D, Tager JM, Galjaard H.
    J Clin Invest; 1987 Jun 14; 79(6):1689-99. PubMed ID: 3108320
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Subcellular distribution of acid alpha-glucosidase in fibroblasts and of antigenically cross-reactive material in Pompe's disease fibroblasts.
    Iwamasa T, Nashiro K, Ohshita T, Matsuda I.
    Histochem J; 1986 Aug 15; 18(11-12):613-24. PubMed ID: 3549635
    [Abstract] [Full Text] [Related]

  • 17. Methods for analysis of acid alpha-1,4-glucosidase activity in single hybrid cells.
    Reuser AJ, Jongkind JF, Galjaard H.
    J Histochem Cytochem; 1976 Apr 15; 24(4):578-86. PubMed ID: 1063791
    [Abstract] [Full Text] [Related]

  • 18. A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studies.
    Loonen MC, Busch HF, Koster JF, Martin JJ, Niermeijer MF, Schram AW, Brouwer-Kelder B, Mekes W, Slee RG, Tager JM.
    Neurology; 1981 Oct 15; 31(10):1209-16. PubMed ID: 6810200
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 53(2):185-92. PubMed ID: 2688540
    [Abstract] [Full Text] [Related]

  • 20. Diagnosis of Pompe's disease using leukocyte preparations. Kinetic and immunological studies of 1,4-alpha-glucosidase in human fetal and adult tissues and cultured cells.
    Shin YS, Endres W, Unterreithmeier J, Rieth M, Schaub J.
    Clin Chim Acta; 1985 May 15; 148(1):9-19. PubMed ID: 3891151
    [Abstract] [Full Text] [Related]

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