1. R. O. Brady, J. N. Kanfer and D. Shapiro, Metabolism of glucocerebrosides. II. Evidence of an enzymatic deficiency in Gaucher’s disease., Biochem. Biophys. Res. Commun 18: 221 (1965)
2. A. D. Patrick, A deficiency of glucocerebrosidase in Gaucher’s disease., Biochem. J. 97: 17c (1965)
3. R. O. Brady and J.A. Barranger, Glucosylceramide lipidosis: Gaucher’s disease., in: The Metabolic Basis of Inherited Disease (J. B. Stanbury, J. B. Wijngaarden, D. S. Frederickson, J. L. Goldstein and M. S. Brown, eds.) p. 842 McGraw-Hill, New York (1983)
4. E. I. Ginns, R. O. Brady, S. Pirrucello, C. Moore, S. Sorrell, F. S. Furbish, G. J. Murray, J. M. Tager and J. A. Barranger, Mutations of glucocerebrosidase. Discrimination of neurologic and non-neurologic phenotypes of Gaucher disease., Proc. Natl. Acad. Sci. USA 79: 5067 (1983)
5. E. I. Ginns, F. P. W. Tegelaers, R. Barneveld, H. Galjaard, A. J. J. Reuser, R. O. Brady, J. M. Tager and J. A. Barranger, Determination of Gaucher’s disease phenoptypes with monoclonal antibodies. Clin. Chim. Acta 131: 283 (1983)