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Journal Abstract Search

146 related items for PubMed ID: 362358

  • 1. 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; 12(9):894-8. PubMed ID: 362358
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  • 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
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  • 3. Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease).
    Steckel F, Gieselmann V, Waheed A, Hasilik A, von Figura K, Oude Elferink R, Kalsbeek R, Tager JM.
    FEBS Lett; 1982 Dec 13; 150(1):69-76. PubMed ID: 6761145
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  • 6. alpha-Glucosidase in Pompe's disease.
    Broadhead DM, Butterworth J.
    J Inherit Metab Dis; 1978 Dec 13; 1(4):153-4. PubMed ID: 41974
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  • 7. 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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  • 10. Pompe's disease: diagnosis in kidney and leucocytes using 4-methylumbelliferyl-alpha-D-glucopyranoside.
    Broadhead DM, Butterworth J.
    Clin Genet; 1978 Jun 15; 13(6):504-10. PubMed ID: 352582
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  • 11. [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
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  • 12. 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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  • 15. 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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  • 16. 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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  • 17. Late-onset Pompe's disease.
    Teener JW.
    Semin Neurol; 2012 Nov 12; 32(5):506-11. PubMed ID: 23677658
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  • 18. Mitochondrial activity in Pompe's disease.
    Selak MA, de Chadarevian JP, Melvin JJ, Grover WD, Salganicoff L, Kaye EM.
    Pediatr Neurol; 2000 Jul 12; 23(1):54-7. PubMed ID: 10963971
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  • 19. 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 Jul 12; 3():S61-9. PubMed ID: 7603530
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  • 20. [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 12; 7(6):475-7. PubMed ID: 2940012
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