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Journal Abstract Search

122 related items for PubMed ID: 4531383

  • 1. 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
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  • 2. Deficiency of acid alpha glucosidase in the urine of patients with Pompe's disease.
    Salafsky IS, Nadler HL.
    J Pediatr; 1973 Feb 05; 82(2):294-7. PubMed ID: 4265199
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  • 6. [Myopathy due to acid maltase deficiency. Pompe's disease in adolescence and adult (author's transl)].
    Kölmel HW, Assmus H, Seiler D.
    Arch Psychiatr Nervenkr (1970); 1974 Feb 05; 218(2):93-106. PubMed ID: 4522354
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  • 7. [Glycogenosis 3 - Pompe's disease - in a 1 1/2-month-old child].
    Papilova EI, Revenkova LA.
    Pediatriia; 1975 May 05; (5):84-6. PubMed ID: 1056587
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  • 8. 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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  • 15. [Oligosaccharides of human milk].
    Wiegandt H, Egge H.
    Fortschr Chem Org Naturst; 1970 Oct 31; 28():404-28. PubMed ID: 4950983
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  • 18. Glycogen storage disease of the heart (Pompe's disease): report of a case and review of diagnostic features.
    Pilapil VR, Lynch JI.
    Mil Med; 1971 Aug 31; 136(8):699-702. PubMed ID: 5005332
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  • 20. Hepatic glycogenosis with defects in the glycogen breakdown pathway: urinary oligosaccharide profile.
    Giros ML, Alvarez L.
    J Inherit Metab Dis; 1991 Aug 31; 14(3):311-3. PubMed ID: 1770780
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