Gaucher's disease management protocol

1. Краснопольская К.Д. Наследственные болезни обмена веществ. М., 2005. с. 20—2.

2. Руководство по гематологии. Под ред. А.И. Воробьева. Т. 2. М.: Ньюдиамед, 2003. с. 202—5.

3. Brady R.O., Kanfer J.N., Shapiro D. Metabolism of glucocerebrosides: evidence of an enzymatic deficiency in Gaucher disease. Biochem Biophys Res Commun 1965;18:221—5.

4. Di Rocco M., Giona F., Carubbi F. et al. A new severity score index for phenotypic classification and evaluation of responses to treatment in type I Gaucher disease. Haematologica 2008;93: 1211—8.

5. Gaucher disease. Ed. A.H. Futerman and A. Zimran, 2007. Taylor & Francis Group, LLC.

6. Lee R.E. The pathology of Gaucher disease. Prog Clin Biol Res 1982;95: 177—217.

7. Mistry P.K. Gaucher disease: a model for modern maqnagement of a genetic disease. J Hepatol 1999;30:1—5.

8. Poll L.W, Terk M.R. Skeletal aspects of Gaucher disease. Br J Radiol 2002;75(Suppl 1):1—42.

9. Zimran A., Kay A., Beutler E. et al. Gaucher disease: clinical, laboratory, radiologic and genetic features of 53 patients. Medicine 1992;71:337—53.

10. Weinreb N.J. Type I Gaucher disease in elderly patients. Gaucher Clin Perspect 1999;7(2):1—8.