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Journal Abstract Search

225 related items for PubMed ID: 6413751

  • 1. [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]

  • 2. [Childhood acid maltase deficiency. A case report].
    Higashi Y, Shirabe T, Yasuda T, Inoue S, Sawayama T.
    Rinsho Shinkeigaku; 1988 Jan 01; 28(1):83-91. PubMed ID: 3133150
    [No Abstract] [Full Text] [Related]

  • 3. 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 Jan 01; 28(3):245-55. PubMed ID: 6440527
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  • 4. 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 01; 45(1):37-50. PubMed ID: 6199886
    [Abstract] [Full Text] [Related]

  • 5. [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 Jan 01; 44(1):49-62. PubMed ID: 6784694
    [No Abstract] [Full Text] [Related]

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  • 7. 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 01; 13(4):173-6. PubMed ID: 6818487
    [Abstract] [Full Text] [Related]

  • 8. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 36-1986. A 29-year-old woman with slowly progressive proximal-muscle weakness.
    N Engl J Med; 1986 Sep 11; 315(11):694-701. PubMed ID: 3092049
    [No Abstract] [Full Text] [Related]

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  • 11. 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 Sep 11; 45(1):51-61. PubMed ID: 6199887
    [Abstract] [Full Text] [Related]

  • 12. [Two autopsy cases of adult-type acid maltase deficiency with vacuolation of cerebral arterial walls].
    Matsuoka Y, Hirayama M, Senda Y, Matsui T.
    Rinsho Shinkeigaku; 1985 Jan 11; 25(1):39-45. PubMed ID: 3922655
    [No Abstract] [Full Text] [Related]

  • 13. [Muscle type acid maltase deficiency. An intermediate case between childhood type and adult type (author's transl)].
    Nakagawa M, Nakazato O, Osame M, Nakashima H, Igata A.
    Rinsho Shinkeigaku; 1982 Jan 11; 22(1):57-65. PubMed ID: 6807597
    [No Abstract] [Full Text] [Related]

  • 14. Acid maltase deficiency: a case study and review of the pathophysiological changes and proposed therapeutic measures.
    Isaacs H, Savage N, Badenhorst M, Whistler T.
    J Neurol Neurosurg Psychiatry; 1986 Sep 11; 49(9):1011-8. PubMed ID: 3093639
    [Abstract] [Full Text] [Related]

  • 15. 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 11; 70(9):536-42. PubMed ID: 2960768
    [No Abstract] [Full Text] [Related]

  • 16. Infantile acid maltase deficiency. I. Muscle fiber destruction after lysosomal rupture.
    Griffin JL.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984 Sep 11; 45(1):23-36. PubMed ID: 6199885
    [Abstract] [Full Text] [Related]

  • 17. Adult form acid maltase deficiency -- a case report.
    Akamatsu A, Nomoto R, Nagao H, Murakami H, Nonaka I, Tara M, Kato M.
    Jpn J Med; 1982 Jul 11; 21(3):203-9. PubMed ID: 6815356
    [Abstract] [Full Text] [Related]

  • 18. [Pompe's disease or glycogen storage disease].
    Vanto T, Salmi TT, Kalimo H, Lang H, Näntö V, Berlin M, Penttinen R.
    Duodecim; 1982 Jul 11; 98(9):709-16. PubMed ID: 7049663
    [No Abstract] [Full Text] [Related]

  • 19. 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 11; 181(5):627-32. PubMed ID: 2947052
    [Abstract] [Full Text] [Related]

  • 20. 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 11; 79(6):1689-99. PubMed ID: 3108320
    [Abstract] [Full Text] [Related]

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