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Journal Abstract Search

213 related items for PubMed ID: 6418415

  • 1. 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]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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 15; 12(9):894-8. PubMed ID: 362358
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 49(9):1011-8. PubMed ID: 3093639
    [Abstract] [Full Text] [Related]

  • 5. [Mitigated adult forms of acid maltase deficiency (Pompe's disease). Morphologic and pathobiochemical studies].
    Pongratz D, Hübner G, Deufel T, Wieland OH.
    Klin Wochenschr; 1983 Aug 01; 61(15):743-50. PubMed ID: 6413751
    [No Abstract] [Full Text] [Related]

  • 6. Glycogenosis type II (acid maltase deficiency).
    Reuser AJ, Kroos MA, Hermans MM, Bijvoet AG, Verbeet MP, Van Diggelen OP, Kleijer WJ, Van der Ploeg AT.
    Muscle Nerve Suppl; 1995 Aug 01; 3():S61-9. PubMed ID: 7603530
    [Abstract] [Full Text] [Related]

  • 7. alpha-Glucosidase in Pompe's disease.
    Broadhead DM, Butterworth J.
    J Inherit Metab Dis; 1978 Aug 01; 1(4):153-4. PubMed ID: 41974
    [Abstract] [Full Text] [Related]

  • 8. Angiocardiographic and enzyme studies in a patient with type II glycogenosis (Pompe's disease). A case report.
    Bonnici F, Shapiro R, Joffe HS, Petersen EM.
    S Afr Med J; 1980 Nov 22; 58(21):860-2. PubMed ID: 6777881
    [Abstract] [Full Text] [Related]

  • 9. 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 Nov 22; 45(1):37-50. PubMed ID: 6199886
    [Abstract] [Full Text] [Related]

  • 10. [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 22; 15(12):705-8. PubMed ID: 342670
    [No Abstract] [Full Text] [Related]

  • 11. A micro-radiochemical assay for alpha-1,4-glucosidase and its use in the assessment of type II glycogenosis (Pompe's disease).
    Nelson PV, Carey WF, Pollard AC.
    Clin Chim Acta; 1977 Jun 15; 77(3):337-42. PubMed ID: 17494
    [Abstract] [Full Text] [Related]

  • 12. Laboratory diagnosis of the neuromuscular glycogen storage diseases.
    Farmer PM.
    Ann Clin Lab Sci; 1982 Jun 15; 12(6):431-8. PubMed ID: 6817693
    [Abstract] [Full Text] [Related]

  • 13. [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 15; 7(6):475-7. PubMed ID: 2940012
    [No Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of glycogenosis type II (Pompe's disease) using chorionic villi biopsy.
    Besançon AM, Castelnau L, Nicolesco H, Dumez Y, Poenaru L.
    Clin Genet; 1985 May 15; 27(5):479-82. PubMed ID: 3891160
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. The change in the pH 4 and pH 6 forms of alpha-glucosidase in cultured amniotic fluid cells and its implication in prenatal diagnosis of Pompe's disease.
    Fujimoto A, Fluharty AL.
    Clin Chim Acta; 1978 Dec 01; 90(2):157-61. PubMed ID: 31251
    [Abstract] [Full Text] [Related]

  • 17. Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle cultures.
    Meola G, Scarpini E, Manfredi L, Velicogna M, Pellegrini G, Redi CA, Scarlato G.
    Basic Appl Histochem; 1984 Dec 01; 28(3):245-55. PubMed ID: 6440527
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 98(4):1041-7. PubMed ID: 3935646
    [Abstract] [Full Text] [Related]

  • 19. Pompe's disease: diagnosis in kidney and leucocytes using 4-methylumbelliferyl-alpha-D-glucopyranoside.
    Broadhead DM, Butterworth J.
    Clin Genet; 1978 Jun 01; 13(6):504-10. PubMed ID: 352582
    [Abstract] [Full Text] [Related]

  • 20. Acid maltase deficiency in adolescence: report of an unusual case.
    Olguntürk R, Bilgiç A, Cağlar M, Sinangil F.
    Turk J Pediatr; 1982 Jun 01; 24(2):115-9. PubMed ID: 6214067
    [No Abstract] [Full Text] [Related]

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