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Journal of Inherited Metabolic Disease|January 1, 1995
Elevated plasma chitotriosidase activity in various lysosomal storage disordersY Guo, W He, A M Boer, et al.Biochimica Et Biophysica Acta|March 17, 1988
Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylationJ M Aerts, A W Schram, A Strijland, et al.European Journal of Biochemistry|August 1, 1985
The occurrence of two immunologically distinguishable beta-glucocerebrosidases in human spleenJ M Aerts, W E Donker-Koopman, M K van der Vliet, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 16, 1991
The identification of type 1 Gaucher disease patients, asymptomatic cases and carriers in The Netherlands using urine samples: an evaluationJ M Aerts, M C Sa Miranda, L Wanzeller de Lacerda, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 17, 2017
Simultaneous quantitation of sphingoid bases by UPLC-ESI-MS/MS with identical 13C-encoded internal standardsM Mirzaian, P Wisse, M J Ferraz, et al.Annals of Neurology|October 24, 1997
Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's diseaseR Schiffmann, M P Heyes, J M Aerts, et al.Human Mutation|January 1, 1997
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic valueR G Boot, C E Hollak, M Verhoek, et al.Journal of Inherited Metabolic Disease|June 19, 2001
Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapyF M Platt, M Jeyakumar, U Andersson, et al.Pageof 8