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Journal Abstract Search

347 related items for PubMed ID: 13954110

  • 1. alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).
    HERS HG.
    Biochem J; 1963 Jan; 86(1):11-6. PubMed ID: 13954110
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  • 2. 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
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  • 4. Prenatal diagnosis of glycogenosis type II (Pompe's disease) using chorionic villi biopsy.
    Besançon AM, Castelnau L, Nicolesco H, Dumez Y, Poenaru L.
    Clin Genet; 1985 May 13; 27(5):479-82. PubMed ID: 3891160
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  • 5. 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
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  • 6. Use of immobilized antibodies in investigating acid alpha-glucosidase in urine in relation to Pompe's disease.
    Schram AW, Brouwer-Kelder B, Donker-Koopman WE, Loonen C, Hamers MN, Tager JM.
    Biochim Biophys Acta; 1979 Apr 12; 567(2):370-83. PubMed ID: 36157
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  • 8. Physico-chemical and immunological properties of acid alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease).
    Koster JF, Slee RG, Van der Klei-Van Moorsel JM, Rietra PJ, Lucas CJ.
    Clin Chim Acta; 1976 Apr 01; 68(1):49-58. PubMed ID: 4245
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  • 9. alpha-Glucosidase in Pompe's disease.
    Broadhead DM, Butterworth J.
    J Inherit Metab Dis; 1978 Apr 01; 1(4):153-4. PubMed ID: 41974
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  • 10. Lysosomal glycogen storage mimicking the cytological picture of Pompe's disease as induced in rats by injection of an alpha-glucosidase inhibitor. I. Alterations in liver.
    Lüllmann-Rauch R.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1981 Apr 01; 38(1):89-100. PubMed ID: 6119839
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  • 11. Amniotic cell 4-methylumbelliferyl-alpha-glucosidase activity for prenatal diagnosis of Pompe's disease.
    Fensom AH, Benson PF, Blunt S, Brown SP, Coltart TM.
    J Med Genet; 1976 Apr 01; 13(2):148-9. PubMed ID: 1064728
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  • 12. alpha-Glucosidase deficiency (Pompe's disease).
    Tager JM, Oude Elferink RP, Reuser A, Kroos M, Ginsel LA, Fransen JA, Klumperman J.
    Enzyme; 1987 Apr 01; 38(1-4):280-5. PubMed ID: 3126044
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  • 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
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  • 14. A sensitive semi-automated kinetic assay of alpha-D-glucosidase for the prenatal diagnosis of type 2 glycogenosis (Pompe's disease).
    Blau K.
    J Inherit Metab Dis; 1978 Sep 01; 1(3):85-8. PubMed ID: 116083
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  • 18. A micro-radiochemical assay for alpha-1,4-glucosidase and its use in the assessment of type II glycogenosis (Pompe's disease).
    Nelson PV, Carey WF, Pollard AC.
    Clin Chim Acta; 1977 Jun 15; 77(3):337-42. PubMed ID: 17494
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  • 19. Diagnosis of Pompe's disease using pyridylamino-maltooligosaccharides as substrates of alpha-1,4-glucosidase.
    Midorikawa M, Okada S, Kato T, Yutaka T, Yabuuchi H.
    Clin Chim Acta; 1985 Apr 15; 147(2):97-102. PubMed ID: 3886206
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