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Journal Abstract Search

314 related items for PubMed ID: 6391315

  • 1. [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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  • 2. 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 Sep 15; 28(3):245-55. PubMed ID: 6440527
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  • 3. [A retrospective study of six patients with late-onset Pompe disease].
    Saux A, Laforet P, Pagès AM, Figarella-Branger D, Pellissier JF, Pagès M, Labauge P.
    Rev Neurol (Paris); 2008 Apr 15; 164(4):336-42. PubMed ID: 18439925
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  • 10. 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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  • 13. Enzyme replacement therapy in late-onset Pompe's disease: a three-year follow-up.
    Winkel LP, Van den Hout JM, Kamphoven JH, Disseldorp JA, Remmerswaal M, Arts WF, Loonen MC, Vulto AG, Van Doorn PA, De Jong G, Hop W, Smit GP, Shapira SK, Boer MA, van Diggelen OP, Reuser AJ, Van der Ploeg AT.
    Ann Neurol; 2004 Apr 15; 55(4):495-502. PubMed ID: 15048888
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  • 16. 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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