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Journal Abstract Search

131 related items for PubMed ID: 11596653

  • 1.
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  • 2. Lysosomal glycogen storage disease with normal acid maltase with early fatal outcome.
    Morisawa Y, Fujieda M, Murakami N, Naruse K, Okada T, Morita H, Sawada K, Miyazaki J, Kurashige T, Nonaka I.
    J Neurol Sci; 1998 Oct 08; 160(2):175-9. PubMed ID: 9849802
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  • 3. Lysosomal glycogen storage with normal acid maltase: a familial study with successful heart transplant.
    Dworzak F, Casazza F, Mora M, De Maria R, Gronda E, Baroldi G, Rimoldi M, Morandi L, Cornelio F.
    Neuromuscul Disord; 1994 May 08; 4(3):243-7. PubMed ID: 7919972
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  • 7. [Lysosomal glycogen storage disease with normal acid maltase (Danon) without apparent cardiomyopathy and mental retardation].
    Kawamura H, Shimojo S, Nonaka I, Abe M, Tadokoro M.
    Rinsho Shinkeigaku; 2000 Mar 08; 40(3):259-62. PubMed ID: 10885338
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  • 8. Incorporation of [14C]glucose into alpha-1,4 bonds of glycogen by leukocytes and fibroblasts of patients with type III glycogen storage disease.
    Gutman A, Barash V, Schramm H, Deckelbaum RJ, Granot E, Aker M, Kohn G.
    Pediatr Res; 1985 Jan 08; 19(1):28-32. PubMed ID: 3918291
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  • 9. Glycogen storage disease with normal acid maltase: skeletal and cardiac muscles.
    Tachi N, Tachi M, Sasaki K, Tomita H, Wakai S, Annaka S, Minami R, Tsurui S, Sugie H.
    Pediatr Neurol; 1989 Jan 08; 5(1):60-3. PubMed ID: 2496694
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  • 10. Determination of acid alpha-glucosidase protein: evaluation as a screening marker for Pompe disease and other lysosomal storage disorders.
    Umapathysivam K, Whittle AM, Ranieri E, Bindloss C, Ravenscroft EM, van Diggelen OP, Hopwood JJ, Meikle PJ.
    Clin Chem; 2000 Sep 08; 46(9):1318-25. PubMed ID: 10973860
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  • 11. [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 08; 15(12):705-8. PubMed ID: 342670
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  • 12. Immunocytochemical analysis of normal and acid maltase-deficient muscle cultures.
    Miranda AF, Shanske S, Hays AP, DiMauro S.
    Arch Neurol; 1985 Apr 08; 42(4):371-3. PubMed ID: 3921010
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  • 13. Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscle.
    Van der Ploeg AT, Loonen MC, Bolhuis PA, Busch HM, Reuser AJ, Galjaard H.
    Pediatr Res; 1988 Jul 08; 24(1):90-4. PubMed ID: 2970619
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  • 14. Apparent normal leukocyte acid maltase activity in glycogen storage disease type II (Pompe's disease).
    Potter JL, Robinson HB, Kramer JD, Schafter IA.
    Clin Chem; 1980 Dec 08; 26(13):1914-5. PubMed ID: 7002367
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  • 15. 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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  • 16. Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels.
    Byrne E, Dennett X, Crotty B, Trounce I, Sands JM, Hawkins R, Hammond J, Anderson S, Haan EA, Pollard A.
    Brain; 1986 Jun 31; 109 ( Pt 3)():523-36. PubMed ID: 3087571
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  • 17. Prenatal diagnosis in glycogen storage diseases.
    Chen YT, Bali D, Sullivan J.
    Prenat Diagn; 2002 May 31; 22(5):357-9. PubMed ID: 12001186
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  • 18. Comparative investigation of alpha-glucosidase activity in leucocytes and skeletal muscle of patients with Morbus Pompe.
    Didt L, Winkler M, Bührdel P, Bormann M, Böhme HJ, Hofmann E.
    Z Med Lab Diagn; 1988 May 31; 29(1):7-11. PubMed ID: 3129881
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  • 20. A new variant form of hepatic glycogenosis with acid maltase deficiency.
    Ninomiya N, Terashima T, Iwamasa T, Matsuda I.
    Jinrui Idengaku Zasshi; 1984 Jun 31; 29(2):113-9. PubMed ID: 6439921
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