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Journal Abstract Search

121 related items for PubMed ID: 3935646

  • 1. Neutral oligosaccharides in the urine of a patient with glycogen storage disease type II.
    Kuriyama M, Hiwatari R, Ariga T, Sakano Y, Abe J, Osame M, Igata A.
    J Biochem; 1985 Oct; 98(4):1041-7. PubMed ID: 3935646
    [Abstract] [Full Text] [Related]

  • 2. 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
    [No Abstract] [Full Text] [Related]

  • 3. Structural and immunochemical analysis of three alpha-limit dextrin oligosaccharides.
    Kumlien J, Grönberg G, Nilsson B, Månsson O, Zopf D, Lundblad A.
    Arch Biochem Biophys; 1989 Mar 31; 269(2):678-89. PubMed ID: 2919890
    [Abstract] [Full Text] [Related]

  • 4. Leucocyte alpha-1,4- and alpha-1,6-glucosidase activities towards oligosaccharides in late onset glycogenosis type II.
    Kuriyama M, Hiwatari R, Osame M, Igata A.
    Tohoku J Exp Med; 1990 Aug 31; 161(4):343-51. PubMed ID: 2256108
    [Abstract] [Full Text] [Related]

  • 5. Acid maltase deficiency: a case study and review of the pathophysiological changes and proposed therapeutic measures.
    Isaacs H, Savage N, Badenhorst M, Whistler T.
    J Neurol Neurosurg Psychiatry; 1986 Sep 31; 49(9):1011-8. PubMed ID: 3093639
    [Abstract] [Full Text] [Related]

  • 6. Rapid ultraperformance liquid chromatography-tandem mass spectrometry assay for a characteristic glycogen-derived tetrasaccharide in Pompe disease and other glycogen storage diseases.
    Sluiter W, van den Bosch JC, Goudriaan DA, van Gelder CM, de Vries JM, Huijmans JG, Reuser AJ, van der Ploeg AT, Ruijter GJ.
    Clin Chem; 2012 Jul 31; 58(7):1139-47. PubMed ID: 22623745
    [Abstract] [Full Text] [Related]

  • 7. [Childhood acid maltase deficiency. A case report].
    Higashi Y, Shirabe T, Yasuda T, Inoue S, Sawayama T.
    Rinsho Shinkeigaku; 1988 Jan 31; 28(1):83-91. PubMed ID: 3133150
    [No Abstract] [Full Text] [Related]

  • 8. Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease).
    Hallgren P, Hansson G, Henriksson KG, Häger A, Lundblad A, Svensson S.
    Eur J Clin Invest; 1974 Dec 05; 4(6):429-33. PubMed ID: 4531383
    [No Abstract] [Full Text] [Related]

  • 9. Vacuolar myopathy with type 2 A fiber atrophy and type 2 B fiber deficiency. A case of childhood form acid alpha-1,4-glucosidase deficiency.
    Matsuishi T, Terasawa K, Yoshida I, Yano E, Yamashita F, Hidaka T, Ishihara O, Yoshino M, Nonaka I, Kurokawa T, Nakamura Y.
    Neuropediatrics; 1982 Nov 05; 13(4):173-6. PubMed ID: 6818487
    [Abstract] [Full Text] [Related]

  • 10. [Two autopsy cases of adult-type acid maltase deficiency with vacuolation of cerebral arterial walls].
    Matsuoka Y, Hirayama M, Senda Y, Matsui T.
    Rinsho Shinkeigaku; 1985 Jan 05; 25(1):39-45. PubMed ID: 3922655
    [No Abstract] [Full Text] [Related]

  • 11. 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 Jan 05; 29(1):7-11. PubMed ID: 3129881
    [No Abstract] [Full Text] [Related]

  • 12. Acid maltase deficiency in adults. Clinical, morphological and biochemical study of three patients.
    Bertagnolio B, Di Donato S, Peluchetti D, Rimoldi M, Storchi G, Cornelio F.
    Eur Neurol; 1978 Jan 05; 17(4):193-204. PubMed ID: 357152
    [Abstract] [Full Text] [Related]

  • 13. Glucose-containing oligosaccharides in the urine of patients with glycogen storage disease type II and type III.
    Lennartson G, Lundblad A, Lundsten J, Svensson S, Häger A.
    Eur J Biochem; 1978 Feb 05; 83(2):325-34. PubMed ID: 272984
    [Abstract] [Full Text] [Related]

  • 14. Lysosomal glycogen storage disease without acid maltase deficiency.
    Riggs JE, Schochet SS, Gutmann L, Shanske S, Neal WA, DiMauro S.
    Neurology; 1983 Jul 05; 33(7):873-7. PubMed ID: 6408499
    [Abstract] [Full Text] [Related]

  • 15. [Muscle type acid maltase deficiency. An intermediate case between childhood type and adult type (author's transl)].
    Nakagawa M, Nakazato O, Osame M, Nakashima H, Igata A.
    Rinsho Shinkeigaku; 1982 Jan 05; 22(1):57-65. PubMed ID: 6807597
    [No Abstract] [Full Text] [Related]

  • 16. Infantile acid maltase deficiency. II. Muscle fiber hypertrophy and the ultrastructure of end-stage fibers.
    Griffin JL.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984 Jan 05; 45(1):37-50. PubMed ID: 6199886
    [Abstract] [Full Text] [Related]

  • 17. Studies on the metabolic origin of a glucose-containing tetrasaccharide in human urine.
    Ugorski M, Seder A, Lundblad A, Zopf D.
    J Exp Pathol; 1983 Jan 05; 1(1):27-38. PubMed ID: 6400638
    [Abstract] [Full Text] [Related]

  • 18. Protein turnover in acid maltase deficiency before and after treatment with a high protein diet.
    Umpleby AM, Wiles CM, Trend PS, Scobie IN, Macleod AF, Spencer GT, Sonksen PH.
    J Neurol Neurosurg Psychiatry; 1987 May 05; 50(5):587-92. PubMed ID: 3108456
    [Abstract] [Full Text] [Related]

  • 19. Developmental study of alpha-glucosidases in Japanese quails with acid maltase deficiency.
    Usuki F, Ishiura S, Sugita H.
    Muscle Nerve; 1986 May 05; 9(6):537-43. PubMed ID: 3090432
    [Abstract] [Full Text] [Related]

  • 20. Reappearance of embryonic neutral alpha-glucosidase isoenzyme in acid maltase-deficient muscle of Japanese quail.
    Usuki F, Ishiura S, Higuchi I, Sugita H.
    Exp Neurol; 1988 May 05; 100(2):394-402. PubMed ID: 3129300
    [Abstract] [Full Text] [Related]

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