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Journal Abstract Search

202 related items for PubMed ID: 3290163

  • 1. [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]

  • 2. 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]

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

  • 4. 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]

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

  • 6. 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; 70(9):536-42. PubMed ID: 2960768
    [No Abstract] [Full Text] [Related]

  • 7. [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
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 109(10):921-5. PubMed ID: 3899054
    [Abstract] [Full Text] [Related]

  • 9. [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
    [Abstract] [Full Text] [Related]

  • 10. [Acid maltase deficiency myopathy infantile and adult forms (author's transl)].
    Saenz Lope E, Cocero Oviedo E, Ricoy Campo JR, Benlloch T.
    Arch Neurobiol (Madr); 1981 Apr 15; 44(1):49-62. PubMed ID: 6784694
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. [Acid maltase deficiency in 2 adolescent siblings].
    Gracia P, Benlloch T, de la Fuente G, Durántez A, Espanña P, Cánovas A, Illera ER.
    Med Clin (Barc); 1982 Sep 16; 79(5):227-31. PubMed ID: 6755088
    [No Abstract] [Full Text] [Related]

  • 13. 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 16; 176(2-4):236-52. PubMed ID: 6304667
    [Abstract] [Full Text] [Related]

  • 14. The pattern of involvement of adult-onset acid maltase deficiency at autopsy.
    van der Walt JD, Swash M, Leake J, Cox EL.
    Muscle Nerve; 1987 Mar 16; 10(3):272-81. PubMed ID: 2951596
    [Abstract] [Full Text] [Related]

  • 15. [Acid alpha-glucosidase deficiency: Pompe's disease].
    Iwamasa T.
    Tanpakushitsu Kakusan Koso; 1988 Apr 16; 33(5):686-92. PubMed ID: 3152090
    [No Abstract] [Full Text] [Related]

  • 16. 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 16; 28(3):245-55. PubMed ID: 6440527
    [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 Apr 16; 45(1):51-61. PubMed ID: 6199887
    [Abstract] [Full Text] [Related]

  • 18. 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 16; 361(1-2):191-8. PubMed ID: 15993875
    [Abstract] [Full Text] [Related]

  • 19. Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.
    Beratis NG, LaBadie GU, Hirschhorn K.
    J Clin Invest; 1978 Dec 16; 62(6):1264-74. PubMed ID: 34626
    [Abstract] [Full Text] [Related]

  • 20. [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]

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