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Journal Abstract Search

194 related items for PubMed ID: 3899727

  • 21. Genetic relationship between lysosomal and lamellar body-specific alpha-glucosidases in human lung.
    de Vries AC, Schram AW, Tager JM, Batenburg JJ, van Golde LM.
    Biochim Biophys Acta; 1986 Sep 12; 878(2):288-91. PubMed ID: 3530334
    [Abstract] [Full Text] [Related]

  • 22. [Biochemical diagnosis of glycogenosis type II (acid maltase deficiency) (author's transl)].
    Pilz H, Goebel HH, Stefan H, Seidel D, Kohlschütter A.
    J Clin Chem Clin Biochem; 1977 Dec 12; 15(12):705-8. PubMed ID: 342670
    [No Abstract] [Full Text] [Related]

  • 23. Biochemical, immunological, and cell genetic studies in glycogenosis type II.
    Reuser AJ, Koster JF, Hoogeveen A, Galjaard H.
    Am J Hum Genet; 1978 Mar 12; 30(2):132-43. PubMed ID: 350041
    [Abstract] [Full Text] [Related]

  • 24. Multiple implantation of normal amnion into cattle with generalized glycogenosis type II.
    Howell JM, Dorling PR, Dimarco PN, Taylor EG.
    J Inherit Metab Dis; 1987 Mar 12; 10(1):3-10. PubMed ID: 3106714
    [Abstract] [Full Text] [Related]

  • 25. [Immunochemical study of acid alpha-1,4-glucosidase in 7 patients with type II glycogenosis].
    Bienvenu J, Mathieu M, Collombel C, Baltassat P, Divry P, Dorche C, Cotte J.
    Pediatrie; 1979 Sep 12; 34(6):659-76. PubMed ID: 388338
    [No Abstract] [Full Text] [Related]

  • 26. Recombinant human acid alpha-glucosidase corrects acid alpha-glucosidase-deficient human fibroblasts, quail fibroblasts, and quail myoblasts.
    Yang HW, Kikuchi T, Hagiwara Y, Mizutani M, Chen YT, Van Hove JL.
    Pediatr Res; 1998 Mar 12; 43(3):374-80. PubMed ID: 9505277
    [Abstract] [Full Text] [Related]

  • 27. Enzyme replacement in Pompe disease with an alpha-glucosidase-low density lipoprotein complex.
    Williams JC, Murray AK.
    Birth Defects Orig Artic Ser; 1980 Mar 12; 16(1):415-23. PubMed ID: 7004520
    [No Abstract] [Full Text] [Related]

  • 28. The effect of age on biochemical and morphological changes in the semitendinosus muscle of cattle with generalized glycogenosis type II.
    Howell JM, Dorling PR, Cook RD.
    Neuropathol Appl Neurobiol; 1984 Mar 12; 10(4):255-66. PubMed ID: 6435005
    [Abstract] [Full Text] [Related]

  • 29. Diagnosis of Pompe's disease using leukocyte preparations. Kinetic and immunological studies of 1,4-alpha-glucosidase in human fetal and adult tissues and cultured cells.
    Shin YS, Endres W, Unterreithmeier J, Rieth M, Schaub J.
    Clin Chim Acta; 1985 May 15; 148(1):9-19. PubMed ID: 3891151
    [Abstract] [Full Text] [Related]

  • 30. 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]

  • 31. Generalised glycogenosis in Brahman cattle.
    O'Sullivan BM, Healy PJ, Fraser IR, Nieper RE, Whittle RJ, Sewell CA.
    Aust Vet J; 1981 May 15; 57(5):227-9. PubMed ID: 6945845
    [Abstract] [Full Text] [Related]

  • 32. Isolation and characterisation of a recombinant, precursor form of lysosomal acid alpha-glucosidase.
    Fuller M, Van der Ploeg A, Reuser AJ, Anson DS, Hopwood JJ.
    Eur J Biochem; 1995 Dec 15; 234(3):903-9. PubMed ID: 8575451
    [Abstract] [Full Text] [Related]

  • 33. Variations of glycogen level and alpha-glucosidase activity in human malignant epithelial cell lines in culture.
    Paris H, Rousset M, Terrain B, Chevalier G, Zweibaum A, Murat JC.
    Int J Biochem; 1982 Dec 15; 14(2):141-5. PubMed ID: 6802687
    [Abstract] [Full Text] [Related]

  • 34. Glycogenosis type II.
    Hug G, Schubert WK.
    Arch Pathol; 1967 Aug 15; 84(2):141-52. PubMed ID: 21936116
    [No Abstract] [Full Text] [Related]

  • 35. Lysosomal glycogen storage disease with normal acid maltase.
    Danon MJ, Oh SJ, DiMauro S, Manaligod JR, Eastwood A, Naidu S, Schliselfeld LH.
    Neurology; 1981 Jan 15; 31(1):51-7. PubMed ID: 6450334
    [Abstract] [Full Text] [Related]

  • 36. 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 15; 66(3):86-9. PubMed ID: 2653294
    [Abstract] [Full Text] [Related]

  • 37. 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
    [Abstract] [Full Text] [Related]

  • 38. Diagnosis of genotypes for generalized glycogenosis in cattle.
    Healy PJ.
    Biochem Med; 1982 Oct 15; 28(2):224-8. PubMed ID: 6758769
    [No Abstract] [Full Text] [Related]

  • 39. 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
    [Abstract] [Full Text] [Related]

  • 40. Severe course of glycogen storage disease type II (Pompe's disease) without development of cardiomegalia.
    Ullrich K, Gröbe H, Korinthenberg R, von Bassewitz DB.
    Pathol Res Pract; 1986 Oct 01; 181(5):627-32. PubMed ID: 2947052
    [Abstract] [Full Text] [Related]

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