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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.
Surgical Neurology International|May 5, 2022
Lumbar spinal stenosis in a patient with complex spinal dysraphism caused by a supplementary midline muscle: A case reportSem M M Hermans, Jasper van Aalst, Jan Beckervordersandforth, et al.
Experimental Eye Research|April 1, 1990
Differential synthesis of crystallins in the developing rat eye lensC E Voorter, W A De Haard-Hoekman, M M Hermans, et al.
Molecular Biology of the Cell|December 1, 1995
Differential regulation of distinct types of gap junction channels by similar phosphorylating conditionsB R Kwak, M M Hermans, H R De Jonge, et al.
Biochemical and Biophysical Research Communications|September 16, 1991
Identification of a point mutation in the human lysosomal alpha-glucosidase gene causing infantile glycogenosis type IIM M Hermans, E de Graaff, M A Kroos, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|September 25, 2018
Unexpected prolapse of the anterior leaflet during saline testing in mitral valve repairJules R Olsthoorn, Samuel Heuts, Sebastian A F Streukens, et al.
Human Mutation|April 1, 1998
Glycogen Storage Disease type II: genetic and biochemical analysis of novel mutations in infantile patients from Turkish ancestryM M Hermans, M A Kroos, J A Smeitink, et al.
The Biochemical Journal|February 1, 1993
The conservative substitution Asp-645-->Glu in lysosomal alpha-glucosidase affects transport and phosphorylation of the enzyme in an adult patient with glycogen-storage disease type IIM M Hermans, E de Graaff, M A Kroos, et al.
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