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Journal Abstract Search

247 related items for PubMed ID: 6755088

  • 21. [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; 22(1):57-65. PubMed ID: 6807597
    [No Abstract] [Full Text] [Related]

  • 22. Demonstration of acid alpha-glucosidase in different types of Pompe disease by use of an immunochemical method.
    Ninomiya N, Matsuda I, Matsuoka T, Iwamasa T, Nonaka I.
    J Neurol Sci; 1984 Jan; 66(2-3):129-39. PubMed ID: 6442343
    [Abstract] [Full Text] [Related]

  • 23. Apparent normal leukocyte acid maltase activity in glycogen storage disease type II (Pompe's disease).
    Potter JL, Robinson HB, Kramer JD, Schafter IA.
    Clin Chem; 1980 Dec; 26(13):1914-5. PubMed ID: 7002367
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  • 26. Adult-onset acid maltase deficiency in siblings.
    Miyamoto Y, Etoh Y, Joh R, Noda K, Ohya I, Morimatsu M.
    Acta Pathol Jpn; 1985 Nov; 35(6):1533-42. PubMed ID: 3937437
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  • 27. Acid maltase deficiency in adolescence: report of an unusual case.
    Olguntürk R, Bilgiç A, Cağlar M, Sinangil F.
    Turk J Pediatr; 1982 Nov; 24(2):115-9. PubMed ID: 6214067
    [No Abstract] [Full Text] [Related]

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  • 29. Bone marrow transplantation in type IIa glycogen storage disease.
    Harris RE, Hannon D, Vogler C, Hug G.
    Birth Defects Orig Artic Ser; 1986 Nov; 22(1):119-32. PubMed ID: 3516240
    [No Abstract] [Full Text] [Related]

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  • 31. The constellation of adult acid maltase deficiency: clinical, electrophysiologic, and morphologic features.
    McComas CF, Schochet SS, Morris HH, Romansky SG, Gutmann L.
    Clin Neuropathol; 1983 Nov; 2(4):182-7. PubMed ID: 6418427
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  • 33. A new variant form of hepatic glycogenosis with acid maltase deficiency.
    Ninomiya N, Terashima T, Iwamasa T, Matsuda I.
    Jinrui Idengaku Zasshi; 1984 Jun; 29(2):113-9. PubMed ID: 6439921
    [No Abstract] [Full Text] [Related]

  • 34. 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]

  • 35. Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methods.
    Ninomiya N, Iwamasa T, Matsuda I, Nonaka I.
    J Inherit Metab Dis; 1983 Sep 11; 6(3):131-2. PubMed ID: 6422147
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  • 37. [Heterogeneity of glycogenosis with alpha-1,4-glucosidase deficiency: enzymatic studies in three families (author's transl)].
    Bienvenu J, Carrier H, Freycon F, Mathieu M.
    Clin Chim Acta; 1978 Mar 15; 84(3):277-92. PubMed ID: 346265
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  • 38. The "muscular variant" of Pompe disease: clinical, biochemical and histologic characteristics.
    Temple JK, Dunn DW, Blitzer MG, Shapira E.
    Am J Med Genet; 1985 Jul 15; 21(3):597-604. PubMed ID: 3895931
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  • 39. Morphologic characteristics of the placenta in glycogen storage disease type II (alpha-1,4-glucosidase deficiency).
    Bendon RW, Hug G.
    Am J Obstet Gynecol; 1985 Aug 15; 152(8):1021-6. PubMed ID: 2411138
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  • 40. Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency).
    Loonen MC, Schram AW, Koster JF, Niermeijer MF, Busch HF, Martin JJ, Brouwer-Kelder B, Mekes W, Slee RG, Tager JM.
    Clin Genet; 1981 Jan 15; 19(1):55-63. PubMed ID: 7006871
    [Abstract] [Full Text] [Related]

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