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Journal Abstract Search

173 related items for PubMed ID: 350041

  • 1. Biochemical, immunological, and cell genetic studies in glycogenosis type II.
    Reuser AJ, Koster JF, Hoogeveen A, Galjaard H.
    Am J Hum Genet; 1978 Mar; 30(2):132-43. PubMed ID: 350041
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  • 2. [Characterization of alpha-glucosidase in skin fibroblasts in the diagnosis of glycogenosis type 2 (Pompe disease)].
    Braulke T, Sandig KR.
    Kinderarztl Prax; 1984 Aug; 52(8):377-82. PubMed ID: 6384623
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  • 3. 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
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  • 4. Immunochemical studies of human acid alpha-1,4-glucosidase in type II glycogenosis.
    Bienvenu J, Mathieu M.
    Enzyme; 1981 Sep 20; 26(4):182-90. PubMed ID: 7018896
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  • 6. 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
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  • 8. 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
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  • 11. 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
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