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Journal Abstract Search

206 related items for PubMed ID: 3891151

  • 41. 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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  • 42. Preparation of monoclonal antibodies against acid alpha-D-glucosidase for study of Chinese glycogenosis type II patients.
    Lin CY, Lee SY, Chang ZN, Su SN, Hwang B, Han SH.
    Hybridoma; 1992 Aug 20; 11(4):493-505. PubMed ID: 1398685
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  • 43. Late-onset Pompe's disease.
    Teener JW.
    Semin Neurol; 2012 Nov 20; 32(5):506-11. PubMed ID: 23677658
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  • 44. The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease).
    Koster JF, Slee RG, Hülsmann WC.
    Clin Chim Acta; 1974 Mar 26; 51(3):319-25. PubMed ID: 4524047
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  • 46. 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 26; 64(9):274-6. PubMed ID: 3122715
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  • 47. 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 26; 70(9):536-42. PubMed ID: 2960768
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  • 48. Glycogen storage disease type II in Israel.
    Bashan N, Potashnik R, Barash V, Gutman A, Moses SW.
    Isr J Med Sci; 1988 Sep 26; 24(4-5):224-7. PubMed ID: 3132435
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  • 49. The natural course of non-classic Pompe's disease; a review of 225 published cases.
    Winkel LP, Hagemans ML, van Doorn PA, Loonen MC, Hop WJ, Reuser AJ, van der Ploeg AT.
    J Neurol; 2005 Aug 26; 252(8):875-84. PubMed ID: 16133732
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  • 52. [Characterization of alpha-glucosidase in skin fibroblasts in the diagnosis of glycogenosis type 2 (Pompe disease)].
    Braulke T, Sandig KR.
    Kinderarztl Prax; 1984 Aug 26; 52(8):377-82. PubMed ID: 6384623
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  • 56. [Laboratory diagnosis of lysosomal storage disease (glycoproteinosis Pompe's disease and Gaucher disease)].
    Shi HP, Zhang GX, Guo YF, Fang BL, Zhang WM, Chen F, Luo HY.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1985 Dec 26; 7(6):475-7. PubMed ID: 2940012
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  • 57. Thin-layer chromatography of oligosaccharides in urine as a rapid indication for the diagnosis of lysosomal acid maltase deficiency (Pompe's disease).
    Blom W, Luteyn JC, Kelholt-Dijkman HH, Huijmans JG, Loonen MC.
    Clin Chim Acta; 1983 Oct 31; 134(1-2):221-7. PubMed ID: 6418415
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