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European Journal of Biochemistry|December 15, 1995
Isolation and characterisation of a recombinant, precursor form of lysosomal acid alpha-glucosidaseM Fuller, A Van der Ploeg, A J Reuser, et al.
American Journal of Medical Genetics|November 1, 1984
Biochemical genetics of the Lapland dog model of glycogen storage disease type II (acid alpha-glucosidase deficiency)H C Walvoort, R G Slee, K J Sluis, et al.
Biological Chemistry Hoppe-Seyler|March 1, 1989
Isolation and structural characterization of twenty-one sialyloligosaccharides from galactosialidosis urine. An intact N,N'-diacetylchitobiose unit at the reducing end of a diantennary structureJ van Pelt, K Hård, J P Kamerling, et al.
The Histochemical Journal|September 1, 1985
Monoclonal antibody to human lysosomal alpha-glucosidase in immunocytochemistry: unexpected reactivity with cytoskeletal structuresH J Sips, N De Jonge, H M Van Dongen, et al.
Human Genetics|January 19, 1979
A two-year-old patient with an atypical expression of GM1-beta-galactosidase deficiency: biochemical, immunological, and cell genetic studiesA J Reuser, G Andria, E de Wit-Verbeek, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
A novel acid alpha-glucosidase mutation identified in a Pakistani family with glycogen storage disease type IIM A Kroos, A E Waitfield, M Joosse, et al.
The Journal of Clinical Investigation|February 1, 1991
Intravenous administration of phosphorylated acid alpha-glucosidase leads to uptake of enzyme in heart and skeletal muscle of miceA T Van der Ploeg, M A Kroos, R Willemsen, et al.
The Histochemical Journal|August 1, 1995
A biochemical and immunocytochemical study on the targeting of alglucerase in murine liverR Willemsen, J J Tibbe, M A Kroos, et al.
American Journal of Human Genetics|June 1, 1989
Glycogenosis type II: protein and DNA analysis in five South African families from various ethnic originsA T Van der Ploeg, L H Hoefsloot, M Hoogeveen-Westerveld, et al.
European Journal of Biochemistry|November 15, 1985
Biosynthesis and intracellular transport of alpha-glucosidase and cathepsin D in normal and mutant human fibroblastsR P Oude Elferink, J Van Doorn-Van Wakeren, A Strijland, et al.
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