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22. Metachromasia in cultured fibroblasts of subjects with glycogenosis type II. Tenconi R; Baccichetti C; Zacchello F; Sartori E Experientia; 1970 Nov; 26(11):1238-9. PubMed ID: 4098624 [No Abstract] [Full Text] [Related]
23. 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; 77(3):337-42. PubMed ID: 17494 [TBL] [Abstract][Full Text] [Related]
24. Qualitative characteristics of the beta-glucosidase isozymes. Choy FY; Davidson RG Prog Clin Biol Res; 1982; 95():415-41. PubMed ID: 6812079 [No Abstract] [Full Text] [Related]
25. Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methods. Ninomiya N; Iwamasa T; Matsuda I; Nonaka I J Inherit Metab Dis; 1983; 6(3):131-2. PubMed ID: 6422147 [No Abstract] [Full Text] [Related]
26. Deficiency of acid alpha glucosidase in the urine of patients with Pompe's disease. Salafsky IS; Nadler HL J Pediatr; 1973 Feb; 82(2):294-7. PubMed ID: 4265199 [No Abstract] [Full Text] [Related]
27. Amylo-1,6-glucosidase in human fibroblasts: studies 3 glycogen storage disease. Justice P; Ryan C; Hsia DY; Krmpotik E Biochem Biophys Res Commun; 1970 May; 39(3):301-6. PubMed ID: 5270292 [No Abstract] [Full Text] [Related]
28. Zonal differences of alpha-glucosidases in human kidney: studies in controls and in patients with glycogenosis type II. Pfister K; Gitzelmann R; Steinmann B Clin Chim Acta; 1983 Nov; 134(3):307-15. PubMed ID: 6357553 [TBL] [Abstract][Full Text] [Related]
29. Deficiency of glucosylsphingosine: beta-glucosidase in Gaucher disease. Raghavan SS; Mumford RA; Kanfer JN Biochem Biophys Res Commun; 1973 Sep; 54(1):256-63. PubMed ID: 4741565 [No Abstract] [Full Text] [Related]
30. Immunological studies on glycogen storage diseases type 3 and V. Demonstration of the presence of an immunoreactive protein in one case of muscle phosphorylase deficiency. Dreyfus JC; Alexandre Y Biochem Biophys Res Commun; 1971 Sep; 44(6):1364-70. PubMed ID: 5003690 [No Abstract] [Full Text] [Related]
31. A method for rapid prenatal diagnosis of glycogenosis II (Pompe's disease). Galjaard H; Mekes M; Josselin de Jong JE DE; Niermeijer MF Clin Chim Acta; 1973 Dec; 49(3):361-75. PubMed ID: 4272965 [No Abstract] [Full Text] [Related]
32. Enzymes of glycogen metabolism in human skin with particular reference to differential diagnosis of the glycogen storage diseases. Leathwood PD; Ryman BE Clin Sci; 1971 Mar; 40(3):261-9. PubMed ID: 4323870 [No Abstract] [Full Text] [Related]
33. The molecular heterogeneity of purified human liver lysosomal alpha-glucosidase (acid alpha-glucosidase). Murray AK; Brown BI; Brown DH Arch Biochem Biophys; 1978 Jan; 185(2):511-24. PubMed ID: 24417 [No Abstract] [Full Text] [Related]
34. Multiple neutral maltase activities in normal and acid maltase-deficient human muscle. Shanske S; Bresolin N; DiMauro S Exp Neurol; 1984 Jun; 84(3):565-78. PubMed ID: 6426997 [TBL] [Abstract][Full Text] [Related]
35. The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease). Koster JF; Slee RG; Hülsmann WC Clin Chim Acta; 1974 Mar; 51(3):319-25. PubMed ID: 4524047 [No Abstract] [Full Text] [Related]