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Journal Abstract Search

408 related items for PubMed ID: 2947052

  • 1. Severe course of glycogen storage disease type II (Pompe's disease) without development of cardiomegalia.
    Ullrich K, Gröbe H, Korinthenberg R, von Bassewitz DB.
    Pathol Res Pract; 1986 Oct; 181(5):627-32. PubMed ID: 2947052
    [Abstract] [Full Text] [Related]

  • 2. 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 Oct; 45(1):37-50. PubMed ID: 6199886
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. [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; 39(4):228-32. PubMed ID: 3290163
    [Abstract] [Full Text] [Related]

  • 5. [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; 164(4):336-42. PubMed ID: 18439925
    [Abstract] [Full Text] [Related]

  • 6. 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 Apr; 28(3):245-55. PubMed ID: 6440527
    [Abstract] [Full Text] [Related]

  • 7. Glycogen storage disease. Studies related to the mechanism of glycogenosome formation.
    Iwamasa T, Ninomiya N, Fukuda S, Hamada T, Hirashima M, Osame M.
    Pathol Res Pract; 1983 Mar; 176(2-4):236-52. PubMed ID: 6304667
    [Abstract] [Full Text] [Related]

  • 8. Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscle.
    Van der Ploeg AT, Loonen MC, Bolhuis PA, Busch HM, Reuser AJ, Galjaard H.
    Pediatr Res; 1988 Jul; 24(1):90-4. PubMed ID: 2970619
    [Abstract] [Full Text] [Related]

  • 9. 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; 361(1-2):191-8. PubMed ID: 15993875
    [Abstract] [Full Text] [Related]

  • 10. Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form.
    Verloes A, Massin M, Lombet J, Grattagliano B, Soyeur D, Rigo J, Koulischer L, Van Hoof F.
    Am J Med Genet; 1997 Oct 17; 72(2):135-42. PubMed ID: 9382133
    [Abstract] [Full Text] [Related]

  • 11. [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
    [No Abstract] [Full Text] [Related]

  • 12. [Involvement of vascular, mesenchymal and neural structures in a muscle of the patients with Pompe's disease (glycogenosis 2) (electron microscopic study)].
    Jadro-Santel D.
    Acta Med Iugosl; 1976 Mar 01; 30(2):203-14. PubMed ID: 1064289
    [No Abstract] [Full Text] [Related]

  • 13. Glycogen storage disease type II (Pompe's disease): the first biochemical evidence in Thailand.
    Rangdaeng S, Scollard DM, Srichairatanakol S, Sutthachit M, Phornphutkul C.
    J Med Assoc Thai; 1987 Sep 01; 70(9):536-42. PubMed ID: 2960768
    [No Abstract] [Full Text] [Related]

  • 14. [Pompe's disease or glycogen storage disease].
    Vanto T, Salmi TT, Kalimo H, Lang H, Näntö V, Berlin M, Penttinen R.
    Duodecim; 1982 Sep 01; 98(9):709-16. PubMed ID: 7049663
    [No Abstract] [Full Text] [Related]

  • 15. The endocrine glands in Pompe's disease. Report of two cases.
    Hui KS, Williams JC, Borit A, Rosenberg HS.
    Arch Pathol Lab Med; 1985 Oct 01; 109(10):921-5. PubMed ID: 3899054
    [Abstract] [Full Text] [Related]

  • 16. Biochemical genetics of the Lapland dog model of glycogen storage disease type II (acid alpha-glucosidase deficiency).
    Walvoort HC, Slee RG, Sluis KJ, Koster JF, Reuser AJ.
    Am J Med Genet; 1984 Nov 01; 19(3):589-98. PubMed ID: 6391168
    [Abstract] [Full Text] [Related]

  • 17. Infantile acid maltase deficiency. III. Ultrastructure of metachromatic material and glycogen in muscle fibers.
    Griffin JL.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984 Nov 01; 45(1):51-61. PubMed ID: 6199887
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 79(6):1689-99. PubMed ID: 3108320
    [Abstract] [Full Text] [Related]

  • 19. Adult glycogenosis type II (Pompe's disease): morphological abnormalities in muscle and skin biopsies compared with acid alpha-glucosidase activity.
    Wierzba-Bobrowicz T, Lewandowska E, Lugowska A, Rola R, Stepień T, Ryglewicz D, Pasennik E.
    Folia Neuropathol; 2007 Jun 01; 45(4):179-86. PubMed ID: 18176891
    [Abstract] [Full Text] [Related]

  • 20. Late form of Pompe disease with glycogen storage in peripheral nerves axons.
    Fidziańska A, Ługowska A, Tylki-Szymańska A.
    J Neurol Sci; 2011 Feb 15; 301(1-2):59-62. PubMed ID: 21109266
    [Abstract] [Full Text] [Related]

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