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Biochimica Et Biophysica Acta|May 12, 1977
Enzymological properties and immunological characterization of alpha-galactosidase isoenzymes from normal and Fabry human liverA W Schram, M N Hamers, B Brouwer-Kelder, et al.Biochimica Et Biophysica Acta|April 12, 1979
Use of immobilized antibodies in investigating acid alpha-glucosidase in urine in relation to Pompe's diseaseA W Schram, B Brouwer-Kelder, W E Donker-Koopman, et al.Biochimica Et Biophysica Acta|November 18, 1981
Monoclonal antibodies against human acid alpha-glucosidaseJ Hilkens, J M Tager, F Buijs, et al.Clinical Genetics|January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)M C Loonen, A W Schram, J F Koster, et al.Neurology|October 1, 1981
A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studiesM C Loonen, H F Busch, J F Koster, 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.Pageof 1