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Journal Abstract Search

131 related items for PubMed ID: 6442343

  • 1. Demonstration of acid alpha-glucosidase in different types of Pompe disease by use of an immunochemical method.
    Ninomiya N, Matsuda I, Matsuoka T, Iwamasa T, Nonaka I.
    J Neurol Sci; 1984; 66(2-3):129-39. PubMed ID: 6442343
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  • 3. 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; 6(3):131-2. PubMed ID: 6422147
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  • 5. Comparative investigation of alpha-glucosidase activity in leucocytes and skeletal muscle of patients with Morbus Pompe.
    Didt L, Winkler M, Bührdel P, Bormann M, Böhme HJ, Hofmann E.
    Z Med Lab Diagn; 1988; 29(1):7-11. PubMed ID: 3129881
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  • 6. Glycogenosis type II: the infantile- and late-onset acid maltase deficiency observed in one family.
    Koster JF, Busch HF, Slee RG, Van Weerden TW.
    Clin Chim Acta; 1978 Aug 01; 87(3):451-3. PubMed ID: 28188
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  • 7. Genetic heterogeneity in acid alpha-glucosidase deficiency.
    Beratis NG, LaBadie GU, Hirschhorn K.
    Am J Hum Genet; 1983 Jan 01; 35(1):21-33. PubMed ID: 6401921
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  • 8. [Late infantile form of Pompe's disease. Deficiency of alpha-1,4-glucosidase (acid maltase)].
    Colomer J, Roig M, Campistol J, Rullan G, Fernández-Alvarez E.
    An Esp Pediatr; 1984 Sep 15; 21(3):250-9. PubMed ID: 6391315
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  • 9. Vacuolar myopathy with type 2 A fiber atrophy and type 2 B fiber deficiency. A case of childhood form acid alpha-1,4-glucosidase deficiency.
    Matsuishi T, Terasawa K, Yoshida I, Yano E, Yamashita F, Hidaka T, Ishihara O, Yoshino M, Nonaka I, Kurokawa T, Nakamura Y.
    Neuropediatrics; 1982 Nov 15; 13(4):173-6. PubMed ID: 6818487
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  • 11. Immunohistochemical demonstration of acid alpha-glucosidase in muscle in Pompe's disease.
    Ninomiya N, Matsuda I, Fukuda S, Iwamasa T, Osame M.
    Histochem J; 1983 Jun 15; 15(6):601-4. PubMed ID: 6347982
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  • 13. Targeted disruption of the acid alpha-glucosidase gene in mice causes an illness with critical features of both infantile and adult human glycogen storage disease type II.
    Raben N, Nagaraju K, Lee E, Kessler P, Byrne B, Lee L, LaMarca M, King C, Ward J, Sauer B, Plotz P.
    J Biol Chem; 1998 Jul 24; 273(30):19086-92. PubMed ID: 9668092
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  • 14. A microfluorometric assay of leukocyte alpha-1,4-glucosidase.
    Bakhru-Kishore R, Desjardins L, Kelly S.
    Clin Chim Acta; 1976 Nov 15; 73(1):89-92. PubMed ID: 11906
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  • 15. Immunochemical studies of human acid alpha-1,4-glucosidase in type II glycogenosis.
    Bienvenu J, Mathieu M.
    Enzyme; 1981 Nov 15; 26(4):182-90. PubMed ID: 7018896
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  • 17. [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
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  • 19. [Heterogeneity of glycogenosis with alpha-1,4-glucosidase deficiency: enzymatic studies in three families (author's transl)].
    Bienvenu J, Carrier H, Freycon F, Mathieu M.
    Clin Chim Acta; 1978 Mar 15; 84(3):277-92. PubMed ID: 346265
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