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Journal Abstract Search

346 related items for PubMed ID: 2960768

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  • 2. [Biochemical diagnosis of glycogenosis type II (acid maltase deficiency) (author's transl)].
    Pilz H, Goebel HH, Stefan H, Seidel D, Kohlschütter A.
    J Clin Chem Clin Biochem; 1977 Dec; 15(12):705-8. PubMed ID: 342670
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  • 3. [Pompe's disease or glycogen storage disease].
    Vanto T, Salmi TT, Kalimo H, Lang H, Näntö V, Berlin M, Penttinen R.
    Duodecim; 1982 Dec; 98(9):709-16. PubMed ID: 7049663
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  • 5. Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle cultures.
    Meola G, Scarpini E, Manfredi L, Velicogna M, Pellegrini G, Redi CA, Scarlato G.
    Basic Appl Histochem; 1984 Dec; 28(3):245-55. PubMed ID: 6440527
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  • 8. 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
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  • 9. Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methods.
    Ninomiya N, Iwamasa T, Matsuda I, Nonaka I.
    J Inherit Metab Dis; 1983 Jul; 6(3):131-2. PubMed ID: 6422147
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  • 11. Tissue alpha-glucosidase activity and glycogen content in patients with generalized glycogenosis.
    Steinitz K, Rutenberg A.
    Isr J Med Sci; 1967 Jul; 3(3):411-21. PubMed ID: 4951241
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  • 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; 79(6):1689-99. PubMed ID: 3108320
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