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Journal Abstract Search

135 related items for PubMed ID: 3122715

  • 1. Inhibition of bovine alpha-glucosidase by Castanospermum australe and its effect on the biochemical identification of heterozygotes for generalised glycogenosis type II (Pompe's disease) in cattle.
    Reichmann KG, Twist JO, McKenzie RA, Rowan KJ.
    Aust Vet J; 1987 Sep; 64(9):274-6. PubMed ID: 3122715
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  • 2. Inhibition of alpha-glucosidase in cattle by Castanospermum australe: an attempted phenocopy of Pompe's disease.
    Reichmann KG, Twist JO, McKenzie RA.
    Aust Vet J; 1989 Mar; 66(3):86-9. PubMed ID: 2653294
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  • 3. Skeletal-muscle alpha-glucosidases in bovine generalized glycogenosis type II.
    Dorling PR, Howell JM, Gawthorne JM.
    Biochem J; 1981 Aug 15; 198(2):409-12. PubMed ID: 7034730
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  • 5. E7 (1057ΔTA) mutation of the acidic α-glucosidase gene causes Pompe's disease in Droughtmaster cattle.
    Lyons RE, Johnston DJ, McGowan MR, Laing A, Robinson B, Owen H, Hill BD, Burns BM.
    Aust Vet J; 2017 May 15; 95(5):138-142. PubMed ID: 28444756
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  • 6. First trimester diagnosis of Pompe's disease (glycogenosis type II) with normal outcome: assay of acid alpha-glucosidase in chorionic villous biopsy using antibodies.
    Grubisic A, Shin YS, Meyer W, Endres W, Becker U, Wischerath H.
    Clin Genet; 1986 Oct 15; 30(4):298-301. PubMed ID: 3098466
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  • 7. alpha-glucosidase activity in human leucocytes: choice of lymphocytes for the diagnosis of Pompe's disease and the carrier state.
    Taniguchi N, Kato E, Yoshida H, Iwaki S, Ohki T, Koizumi S.
    Clin Chim Acta; 1978 Oct 16; 89(2):293-9. PubMed ID: 361294
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  • 8. Generalised glycogenosis in Brahman cattle.
    O'Sullivan BM, Healy PJ, Fraser IR, Nieper RE, Whittle RJ, Sewell CA.
    Aust Vet J; 1981 May 16; 57(5):227-9. PubMed ID: 6945845
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  • 10. Heterozygote detection in a family of Lapland dogs with a recessively inherited metabolic disease: canine glycogen storage disease type II.
    Walvoort HC, Koster JF, Reuser AJ.
    Res Vet Sci; 1985 Mar 16; 38(2):174-8. PubMed ID: 3923581
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  • 12. 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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  • 16. 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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  • 17. 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 12; 155(1):178-89. PubMed ID: 6237928
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  • 18. 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 12; 19(1):55-63. PubMed ID: 7006871
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  • 19. 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 Jan 12; 1(3):85-8. PubMed ID: 116083
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