1. Achord, D. T., Brot, F. E., Bell, C. E., and Sly, W. S.,1978, Human ß-glucuronidasP:In vivoclearance andin vitrouptake by a glycoprotein recognition system on reticuloendothelial cells,Cell 15:269–278.
2. Adachi, M., Wallace, B. J., Schneck, L., and Volk, B. W, 1967, Fine structure of central nervous system in early infantile Gaucher’s diseaseArch. Pathol. (Chicago) 83:513.
3. Aerts, J. M., Donker-Koopman, W. E., van Laar, C., Brul, S., Murray, G. J., Wenger, D. A., Barranger, J. A., Tager, J. M., and Schram, A. W, 1987, Relationship between the two immunologically distinguishable forms of glucocerebrosidase in tissue extractsEur. J. Biochem. 163:583–589.
4. Agmon, V, Cherbu, S., Degan, A., Grace, M. E., Grabowski, G. A., and Gatt, S., 1993, Synthesis of novel fluorescent glycosphingolipids: Use in determining acid ß-glucosidase activity insituand correlation with genotype in Gaucher disease, in review.
5. Amstutz, H. C., 1973, The hip in Gaucher’s diseaseClin. Orthop. 90:83–89.