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Journal Abstract Search
146 related items for PubMed ID: 2688540
21. Genetic heterogeneity in acid alpha-glucosidase deficiency. Beratis NG, LaBadie GU, Hirschhorn K. Am J Hum Genet; 1983 Jan; 35(1):21-33. PubMed ID: 6401921 [Abstract] [Full Text] [Related]
27. 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 15; 134(3):307-15. PubMed ID: 6357553 [Abstract] [Full Text] [Related]
28. Adenovirus-mediated transfer of the acid alpha-glucosidase gene into fibroblasts, myoblasts and myotubes from patients with glycogen storage disease type II leads to high level expression of enzyme and corrects glycogen accumulation. Nicolino MP, Puech JP, Kremer EJ, Reuser AJ, Mbebi C, Verdière-Sahuqué M, Kahn A, Poenaru L. Hum Mol Genet; 1998 Oct 15; 7(11):1695-702. PubMed ID: 9736771 [Abstract] [Full Text] [Related]
31. Partial characterization of leucocyte alpha-glucosidase in late onset glycogenosis type II. Kohriyama T, Kuriyama M, Hiwatari R, Osame M, Igata A. Tohoku J Exp Med; 1989 Apr 15; 157(4):355-63. PubMed ID: 2662474 [Abstract] [Full Text] [Related]
32. A simple differential immunoprecipitation assay of urinary acid and neutral alpha-glucosidases for glycogenosis II. Tsuji A, Yang RC, Omura K, Imabayashi T, Suzuki Y. Clin Chim Acta; 1987 Aug 31; 167(3):313-20. PubMed ID: 3304722 [Abstract] [Full Text] [Related]
33. Chemical chaperones improve transport and enhance stability of mutant alpha-glucosidases in glycogen storage disease type II. Okumiya T, Kroos MA, Vliet LV, Takeuchi H, Van der Ploeg AT, Reuser AJ. Mol Genet Metab; 2007 Jan 31; 90(1):49-57. PubMed ID: 17095274 [Abstract] [Full Text] [Related]