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Clinica Chimica Acta; International Journal of Clinical Chemistry|July 30, 1986
Deficient activity of glucocerebrosidase in urine from patients with type 1 Gaucher diseaseJ M Aerts, W E Donker-Koopman, M Koot, et al.The Journal of Biological Chemistry|February 5, 1990
Interaction of saposins, acidic lipids, and glucosylceramidaseS Morimoto, Y Kishimoto, J Tomich, et al.Biochimica Et Biophysica Acta|January 28, 1985
Soluble sphingomyelinase from human urine as antigen for obtaining anti-sphingomyelinase antibodiesG Weitz, M Driessen, E M Brouwer-Kelder, et al.The Journal of Biological Chemistry|February 25, 1991
Characterization of human glucocerebrosidase from different mutant allelesT Ohashi, C M Hong, S Weiler, et al.Analytical Biochemistry|May 1, 1986
A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodiesJ M Aerts, W E Donker-Koopman, G J Murray, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1985
Gene mapping and leader polypeptide sequence of human glucocerebrosidase: implications for Gaucher diseaseE I Ginns, P V Choudary, S Tsuji, et al.Journal of Clinical Ultrasound : JCU|July 1, 1981
B-scan echo-amplitude measurement in patients with diffuse infiltrative liver diseaseT H Shawker, B Moran, M Linzer, et al.Cancer Genetics and Cytogenetics|March 1, 1992
Cytogenetic analysis of 39 pediatric central nervous system tumorsP S Karnes, T N Tran, M Y Cui, et al.Biochimica Et Biophysica Acta|October 18, 1990
Conditions affecting the activity of glucocerebrosidase purified from spleens of control subjects and patients with type 1 Gaucher diseaseJ M Aerts, M C Sa Miranda, E M Brouwer-Kelder, et al.The New England Journal of Medicine|March 5, 1987
A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's diseaseS Tsuji, P V Choudary, B M Martin, et al.Pageof 11