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Journal Abstract Search

197 related items for PubMed ID: 3152090

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  • 4. [Pompe's disease or glycogen storage disease].
    Vanto T, Salmi TT, Kalimo H, Lang H, Näntö V, Berlin M, Penttinen R.
    Duodecim; 1982; 98(9):709-16. PubMed ID: 7049663
    [No Abstract] [Full Text] [Related]

  • 5. Morphological changes in muscle tissue of patients with infantile Pompe's disease receiving enzyme replacement therapy.
    Winkel LP, Kamphoven JH, van den Hout HJ, Severijnen LA, van Doorn PA, Reuser AJ, van der Ploeg AT.
    Muscle Nerve; 2003 Jun; 27(6):743-51. PubMed ID: 12766987
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  • 6. Glycogen storage in multiple muscles of old GSD-II mice can be rapidly cleared after a single intravenous injection with a modified adenoviral vector expressing hGAA.
    Xu F, Ding E, Migone F, Serra D, Schneider A, Chen YT, Amalfitano A.
    J Gene Med; 2005 Feb; 7(2):171-8. PubMed ID: 15515143
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  • 7. 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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  • 8. [Mitigated adult forms of acid maltase deficiency (Pompe's disease). Morphologic and pathobiochemical studies].
    Pongratz D, Hübner G, Deufel T, Wieland OH.
    Klin Wochenschr; 1983 Aug 01; 61(15):743-50. PubMed ID: 6413751
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  • 9. Bone marrow transplantation for Pompé's disease.
    Hoogerbrugge PM, Wagemaker G, van Bekkum DW, Reuser AJ, vd Ploeg AT.
    N Engl J Med; 1986 Jul 03; 315(1):65-6. PubMed ID: 3086726
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  • 10. Correlation of acid alpha-glucosidase and glycogen content in skin fibroblasts with age of onset in Pompe disease.
    Umapathysivam K, Hopwood JJ, Meikle PJ.
    Clin Chim Acta; 2005 Nov 03; 361(1-2):191-8. PubMed ID: 15993875
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  • 11. Glycogenosis type II: identification and expression of three novel mutations in the acid alpha-glucosidase gene causing the infantile form of the disease.
    Montalvo AL, Cariati R, Deganuto M, Guerci V, Garcia R, Ciana G, Bembi B, Pittis MG.
    Mol Genet Metab; 2004 Mar 03; 81(3):203-8. PubMed ID: 14972326
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  • 12. Complete correction of acid alpha-glucosidase deficiency in Pompe disease fibroblasts in vitro, and lysosomally targeted expression in neonatal rat cardiac and skeletal muscle.
    Pauly DF, Johns DC, Matelis LA, Lawrence JH, Byrne BJ, Kessler PD.
    Gene Ther; 1998 Apr 03; 5(4):473-80. PubMed ID: 9614571
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  • 13. [Lysosomal glycogen storage disease without acid maltase deficiency(Danon disease)].
    Ohno K.
    Ryoikibetsu Shokogun Shirizu; 2000 Apr 03; (29 Pt 4):491-2. PubMed ID: 11032005
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  • 14. [Ichthyosiform scaling in alpha-1,4-glucosidase deficiency].
    Gebhart W, Mainitz M, Jurecka W, Niebauer G, Paschke E, Stöckler S, Sluga E.
    Hautarzt; 1988 Apr 03; 39(4):228-32. PubMed ID: 3290163
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  • 15. [Treatment of Pompe's disease with recombinant enzymes].
    Van Hove JL.
    Verh K Acad Geneeskd Belg; 1998 Apr 03; 60(4):347-57. PubMed ID: 9883081
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  • 16. Tissue alpha-glucosidase activity and glycogen content in patients with generalized glycogenosis.
    Steinitz K, Rutenberg A.
    Isr J Med Sci; 1967 Apr 03; 3(3):411-21. PubMed ID: 4951241
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  • 18. 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 03; 13(4):173-6. PubMed ID: 6818487
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  • 19. [Childhood acid maltase deficiency. A case report].
    Higashi Y, Shirabe T, Yasuda T, Inoue S, Sawayama T.
    Rinsho Shinkeigaku; 1988 Jan 03; 28(1):83-91. PubMed ID: 3133150
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  • 20. Infantile acid maltase deficiency. II. Muscle fiber hypertrophy and the ultrastructure of end-stage fibers.
    Griffin JL.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984 Jan 03; 45(1):37-50. PubMed ID: 6199886
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