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The Journal of Clinical Investigation|March 1, 1993
Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher diseaseS van Weely, M van den Berg, J A Barranger, et al.
Ultrastructural Pathology|September 1, 1988
An immunoelectron microscopic study of glucocerebrosidase in type 1 Gaucher's disease spleenR Willemsen, J M van Dongen, J M Aerts, et al.
Methods of Information in Medicine|June 29, 2010
Assessment of pain expression in infant cry signals using empirical mode decompositionB Mijović, M Silva, B R H Van den Bergh, et al.
Biochimica Et Biophysica Acta|December 16, 1996
Plasma tumor necrosis factor-a (TNF-a) levels in Gaucher diseaseH Michelakakis, C Spanou, A Kondyli, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 2007
Short-term manipulation of plasma free fatty acids does not change skeletal muscle concentrations of ceramide and glucosylceramide in lean and overweight subjectsM J Serlie, A J Meijer, J E Groener, et al.
Experimental Cell Research|August 1, 1988
Characterization of glucocerebrosidase in peripheral blood cells and cultured blastoid cellsJ M Aerts, J Heikoop, S van Weely, et al.
The American Journal of Medicine|October 8, 1997
Differential effects of enzyme supplementation therapy on manifestations of type 1 Gaucher diseaseC E Hollak, E P Corssmit, J M Aerts, et al.
Biochimica Et Biophysica Acta|December 1, 1986
Comparison of the properties of a soluble form of glucocerebrosidase from human urine with those of the membrane-associated tissue enzymeJ M Aerts, W E Donker-Koopman, M Koot, et al.
Biochimica Et Biophysica Acta|May 12, 1988
Heterogeneity in human acid beta-glucosidase revealed by cellulose-acetate electrophoresisM C Sa Miranda, J M Aerts, R A Pinto, et al.
The Journal of Biological Chemistry|September 25, 1998
The human chitotriosidase gene. Nature of inherited enzyme deficiencyR G Boot, G H Renkema, M Verhoek, et al.
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