Cited by

• Type 2 Gaucher disease: phenotypic variation and genotypic heterogeneity.

  Gupta N, Oppenheim IM, Kauvar EF, Tayebi N, Sidransky E. Gupta N, et al. Blood Cells Mol Dis. 2011 Jan 15;46(1):75-84. doi: 10.1016/j.bcmd.2010.08.012. Epub 2010 Sep 28. Blood Cells Mol Dis. 2011. PMID: 20880730 Free PMC article. Review.
• Electrophoresis of glucocerebrosidase from normal and Gaucher disease fibroblasts.

  Dale GL, Gudas J, Woloszyn W, Beutler E. Dale GL, et al. Am J Hum Genet. 1979 Jul;31(4):518-21. Am J Hum Genet. 1979. PMID: 484554 Free PMC article.
• Gaucher's disease, type I (adult type), with massive involvement of the kidneys and lungs.

  Morimura Y, Hojo H, Abe M, Wakasa H. Morimura Y, et al. Virchows Arch. 1994;425(5):537-40. doi: 10.1007/BF00197558. Virchows Arch. 1994. PMID: 7850079
• Histoenzymological activities of Gaucher cells.

  Lageron A. Lageron A. J Inherit Metab Dis. 1981;4(2):75-6. doi: 10.1007/BF02263598. J Inherit Metab Dis. 1981. PMID: 6790855
• Studies in vivo of the tissue uptake, cellular distribution and catabolic turnover of exogenous glucocerebrosidase in rat.

  Morrone S, Pentchev PG, Baynes J, Thorpe S. Morrone S, et al. Biochem J. 1981 Mar 15;194(3):733-42. doi: 10.1042/bj1940733. Biochem J. 1981. PMID: 7306020 Free PMC article.