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Annals of Human Genetics|May 1, 1989
An investigation of the possible influence of neutral alpha-glucosidases on the clinical heterogeneity of glycogenosis type IIA T Van der Ploeg, M A Kroos, D M Swallow, et al.
The Journal of Clinical Investigation|June 1, 1987
Clinical diversity in glycogenosis type II. Biosynthesis and in situ localization of acid alpha-glucosidase in mutant fibroblastsA J Reuser, M Kroos, R Willemsen, et al.
Clinical Genetics|July 11, 1998
Glycogen storage disease type II: identification of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase geneM A Kroos, D van Leenen, J Verbiest, et al.
American Journal of Human Genetics|January 1, 1977
Characterization of beta-D-N-acetylhexosaminidase isoenzymes in man-Chinese hamster somatic cell hybridsH L Hoeksema, A J Reuser, A Hoogeveen, et al.
Biochimica Et Biophysica Acta|November 20, 1987
Cell-free translation of human lysosomal alpha-glucosidase: evidence for reduced precursor synthesis in an adult patient with glycogenosis type IIG T van der Horst, E H Hoefsloot, M A Kroos, et al.
Human Mutation|January 1, 1993
Two mutations affecting the transport and maturation of lysosomal alpha-glucosidase in an adult case of glycogen storage disease type IIM M Hermans, M A Kroos, E de Graaff, et al.
The Journal of Biological Chemistry|January 25, 1993
Structural and functional changes of lysosomal acid alpha-glucosidase during intracellular transport and maturationH A Wisselaar, M A Kroos, M M Hermans, et al.
The Journal of Biological Chemistry|July 25, 1991
Human lysosomal alpha-glucosidase. Characterization of the catalytic siteM M Hermans, M A Kroos, J van Beeumen, et al.
The Biochemical Journal|February 1, 1993
Human lysosomal alpha-glucosidase: functional characterization of the glycosylation sitesM M Hermans, H A Wisselaar, M A Kroos, et al.
Clinical Genetics|May 1, 1988
Km mutant of acid alpha-glucosidase in a case of cardiomyopathy without signs of skeletal muscle involvementY Suzuki, A Tsuji, K Omura, et al.
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