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Journal Abstract Search

156 related items for PubMed ID: 17490

  • 1. Urinary alpha-glucosidase analysis for the detection of the adult form of Pompe's disease.
    Soyama K, Ono E, Shimada N, Tanaka K, Kusunoki T.
    Clin Chim Acta; 1977 May 16; 77(1):61-7. PubMed ID: 17490
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  • 2. Properties of the alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease).
    Soyama K, Ono E, Shimada N, Tanaka K, Oya N.
    Clin Chim Acta; 1977 Aug 01; 78(3):473-8. PubMed ID: 267530
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  • 3. 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
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  • 5. 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
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  • 6. 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
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  • 7. 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
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  • 8. 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
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  • 9. [Tests for the detection of inborn errors of metabolism--urinary alpha-glucosidase analysis for the detection of glycogen storage disease type II (author's transl)].
    Soyama K, Ono E.
    Rinsho Byori; 1978 Dec 15; 26(12):1022-6. PubMed ID: 370427
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  • 10. Two alpha-glucosidases in cultured amniotic fluid cells and their differentiation in the prenatal diagnosis of Pompe's disease.
    Fujimoto A, Fluharty AL, Stevens RL, Kihara H, Wilson MG.
    Clin Chim Acta; 1976 Apr 15; 68(2):177-86. PubMed ID: 4249
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  • 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
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  • 12. 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
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  • 13. Enhanced enzyme activity after incubation with zinc can be used to distinguish heterozygotes of Pompe's disease.
    Lin CY.
    Pediatr Res; 1988 Mar 22; 23(3):283-7. PubMed ID: 3281122
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  • 14. Pompe's disease: diagnosis in kidney and leucocytes using 4-methylumbelliferyl-alpha-D-glucopyranoside.
    Broadhead DM, Butterworth J.
    Clin Genet; 1978 Jun 22; 13(6):504-10. PubMed ID: 352582
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  • 17. 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 22; 12(9):894-8. PubMed ID: 362358
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  • 18. [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 22; 7(6):475-7. PubMed ID: 2940012
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  • 19. alpha-glucosidase activity in human leucocytes: choice of lymphocytes for the diagnosis of Pompe's disease and the carrier state.
    Taniguchi N, Kato E, Yoshida H, Iwaki S, Ohki T, Koizumi S.
    Clin Chim Acta; 1978 Oct 16; 89(2):293-9. PubMed ID: 361294
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  • 20. 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]

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