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Journal Abstract Search

206 related items for PubMed ID: 3891151

  • 21. Pompe's disease in Chinese and prenatal diagnosis by determination of alpha-glucosidase activity.
    Lin CY, Hwang B, Hsiao KJ, Jin YR.
    J Inherit Metab Dis; 1987; 10(1):11-7. PubMed ID: 3106710
    [Abstract] [Full Text] [Related]

  • 22. Enzyme inhibitory assay using monoclonal antibody against acid alpha-D-glucosidase in prenatal diagnosis to identify homozygotes of Pompe's disease.
    Wei CY, Yeh GP, Chen HF, Wang LY, Lin CY.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1992; 33(2):104-11. PubMed ID: 1514400
    [Abstract] [Full Text] [Related]

  • 23. Prenatal detection of Pompe's disease by induction of alkaline phosphatase in cultured amniotic fluid cells.
    Hähnel R, Stratton CJ, Wysocki SJ, Hockey A.
    Aust N Z J Obstet Gynaecol; 1981 Feb; 21(1):43-6. PubMed ID: 7020685
    [No Abstract] [Full Text] [Related]

  • 24. Properties of the alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease).
    Soyama K, Ono E, Shimada N, Tanaka K, Oya N.
    Clin Chim Acta; 1977 Aug 01; 78(3):473-8. PubMed ID: 267530
    [Abstract] [Full Text] [Related]

  • 25. A fluorometric assay of alpha-glucosidase and its application in the study of Pompe's disease.
    Salafsky IS, Nadler HL.
    J Lab Clin Med; 1973 Mar 01; 81(3):450-4. PubMed ID: 4265648
    [No Abstract] [Full Text] [Related]

  • 26. Human amniotic fluid alpha-glucosidase.
    Poenaru L, Vinet MC, Dreyfus JC.
    Clin Chim Acta; 1981 Nov 25; 117(1):53-62. PubMed ID: 7037230
    [Abstract] [Full Text] [Related]

  • 27. The characteristics of acid 1,4-alpha-glucosidase in various human adult and fetal tissues.
    Shin-Bühring YS, Unterreithmeier J, Wilsmann T, Schaub J.
    J Inherit Metab Dis; 1978 Nov 25; 1(4):159-60. PubMed ID: 41975
    [No Abstract] [Full Text] [Related]

  • 28. Uptake and stability of human and bovine acid alpha-glucosidase in cultured fibroblasts and skeletal muscle cells from glycogenosis type II patients.
    Reuser AJ, Kroos MA, Ponne NJ, Wolterman RA, Loonen MC, Busch HF, Visser WJ, Bolhuis PA.
    Exp Cell Res; 1984 Nov 25; 155(1):178-89. PubMed ID: 6237928
    [Abstract] [Full Text] [Related]

  • 29. 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 25; 19(1):55-63. PubMed ID: 7006871
    [Abstract] [Full Text] [Related]

  • 30. Subcellular distribution of acid alpha-glucosidase in fibroblasts and of antigenically cross-reactive material in Pompe's disease fibroblasts.
    Iwamasa T, Nashiro K, Ohshita T, Matsuda I.
    Histochem J; 1986 Jan 25; 18(11-12):613-24. PubMed ID: 3549635
    [Abstract] [Full Text] [Related]

  • 31. Biochemical, immunological, and cell genetic studies in glycogenosis type II.
    Reuser AJ, Koster JF, Hoogeveen A, Galjaard H.
    Am J Hum Genet; 1978 Mar 25; 30(2):132-43. PubMed ID: 350041
    [Abstract] [Full Text] [Related]

  • 32. alpha-Glucosidase deficiency (Pompe's disease).
    Tager JM, Oude Elferink RP, Reuser A, Kroos M, Ginsel LA, Fransen JA, Klumperman J.
    Enzyme; 1987 Mar 25; 38(1-4):280-5. PubMed ID: 3126044
    [Abstract] [Full Text] [Related]

  • 33. Angiocardiographic and enzyme studies in a patient with type II glycogenosis (Pompe's disease). A case report.
    Bonnici F, Shapiro R, Joffe HS, Petersen EM.
    S Afr Med J; 1980 Nov 22; 58(21):860-2. PubMed ID: 6777881
    [Abstract] [Full Text] [Related]

  • 34. Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease).
    Steckel F, Gieselmann V, Waheed A, Hasilik A, von Figura K, Oude Elferink R, Kalsbeek R, Tager JM.
    FEBS Lett; 1982 Dec 13; 150(1):69-76. PubMed ID: 6761145
    [Abstract] [Full Text] [Related]

  • 35. A simple differential immunoprecipitation assay of urinary acid and neutral alpha-glucosidases for glycogenosis II.
    Tsuji A, Yang RC, Omura K, Imabayashi T, Suzuki Y.
    Clin Chim Acta; 1987 Aug 31; 167(3):313-20. PubMed ID: 3304722
    [Abstract] [Full Text] [Related]

  • 36. 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 31; 26(13):1914-5. PubMed ID: 7002367
    [Abstract] [Full Text] [Related]

  • 37. Searching for molecular abnormalities in genetic diseases by the use of a double labeling technique. II. Deficiency of a basic protein in fibroblasts of patients with Pompe's disease.
    Pena SD, Quilliam NM, Hamerton JL, Wrogemann K.
    Pediatr Res; 1978 Sep 31; 12(9):894-8. PubMed ID: 362358
    [Abstract] [Full Text] [Related]

  • 38.
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    [No Abstract] [Full Text] [Related]

  • 39. Zonal differences of alpha-glucosidases in human kidney: studies in controls and in patients with glycogenosis type II.
    Pfister K, Gitzelmann R, Steinmann B.
    Clin Chim Acta; 1983 Nov 15; 134(3):307-15. PubMed ID: 6357553
    [Abstract] [Full Text] [Related]

  • 40. Enhanced enzyme activity after incubation with zinc can be used to distinguish heterozygotes of Pompe's disease.
    Lin CY.
    Pediatr Res; 1988 Mar 15; 23(3):283-7. PubMed ID: 3281122
    [Abstract] [Full Text] [Related]

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