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Journal Abstract Search

194 related items for PubMed ID: 6761145

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  • 3. 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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  • 4. Immunochemical studies of human acid alpha-1,4-glucosidase in type II glycogenosis.
    Bienvenu J, Mathieu M.
    Enzyme; 1981 Apr 12; 26(4):182-90. PubMed ID: 7018896
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  • 5. Biosynthesis and intracellular transport of alpha-glucosidase and cathepsin D in normal and mutant human fibroblasts.
    Oude Elferink RP, Van Doorn-Van Wakeren J, Strijland A, Reuser AJ, Tager JM.
    Eur J Biochem; 1985 Nov 15; 153(1):55-63. PubMed ID: 3905406
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  • 6. 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 Nov 15; 10(1):11-7. PubMed ID: 3106710
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  • 8. Defects in synthesis, phosphorylation, and maturation of acid alpha-glucosidase in glycogenosis type II.
    Reuser AJ, Kroos M, Oude Elferink RP, Tager JM.
    J Biol Chem; 1985 Jul 15; 260(14):8336-41. PubMed ID: 3159730
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  • 9. 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 15; 155(1):178-89. PubMed ID: 6237928
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  • 10. 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 15; 79(6):1689-99. PubMed ID: 3108320
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  • 11. Adult forms of glycogenosis type II. A defect in an early stage of acid alpha-glucosidase realization.
    Reuser AJ, Kroos M.
    FEBS Lett; 1982 Sep 20; 146(2):361-4. PubMed ID: 6754447
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  • 12. 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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  • 14. 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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  • 15. 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 01; 19(1):55-63. PubMed ID: 7006871
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  • 18. 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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  • 19. 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 01; 12(9):894-8. PubMed ID: 362358
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  • 20. 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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