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Journal Abstract Search

346 related items for PubMed ID: 2960768

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  • 26. Properties of the alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease).
    Soyama K, Ono E, Shimada N, Tanaka K, Oya N.
    Clin Chim Acta; 1977 Aug 01; 78(3):473-8. PubMed ID: 267530
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  • 27. [Lysosomal glycogen storage disease without acid maltase deficiency(Danon disease)].
    Ohno K.
    Ryoikibetsu Shokogun Shirizu; 2000 Aug 01; (29 Pt 4):491-2. PubMed ID: 11032005
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  • 28. Immunochemical studies of human acid alpha-1,4-glucosidase in type II glycogenosis.
    Bienvenu J, Mathieu M.
    Enzyme; 1981 Aug 01; 26(4):182-90. PubMed ID: 7018896
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  • 29. [Childhood acid maltase deficiency. A case report].
    Higashi Y, Shirabe T, Yasuda T, Inoue S, Sawayama T.
    Rinsho Shinkeigaku; 1988 Jan 01; 28(1):83-91. PubMed ID: 3133150
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  • 30. Physico-chemical and immunological properties of acid alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease).
    Koster JF, Slee RG, Van der Klei-Van Moorsel JM, Rietra PJ, Lucas CJ.
    Clin Chim Acta; 1976 Apr 01; 68(1):49-58. PubMed ID: 4245
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  • 38. [Clinical, biochemical, morphological and electrophysiological studies of glycogenosis Type II in childhood with double deficiency of enzymes (author's transl)].
    Lück R, Platt D, Lange RH, Kunze K.
    Z Kinderheilkd; 1975 Jul 01; 120(1):19-28. PubMed ID: 125955
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  • 39. [Glycogenosis type II (Pompe's disease) associated with alpha-amylase and hyaluronidase deficiency].
    Platt D, Platt M.
    Dtsch Med Wochenschr; 1969 Jul 04; 94(27):1414-6. PubMed ID: 5254590
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  • 40. Subcellular fractionation studies on hepatic tissue from a patient with Pompe's disease (type II glycogen-storage disease).
    Peters TJ, Jenkins W, Dubowitz V.
    Clin Sci (Lond); 1980 Jul 04; 59(1):7-12. PubMed ID: 7009026
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