Gaucher disease and bone: laboratory and skeletal mineral density variations during a long period of enzyme replacement therapy
Ciana G., et al. Gaucher disease and bone: laboratory and skeletal mineral density variations during a long period of enzyme replacement therapy. J. Inherit. Metab. Dis. 2005, 28(5):723-732. 10.1007/s10545-005-0032-y.
Osseous manifestations of adult Gaucher disease in the era of enzyme replacement therapy
Deegan P.B., et al. Osseous manifestations of adult Gaucher disease in the era of enzyme replacement therapy. Medicine 2011, 90(1):52-60. 10.1097/MD.0b013e3182057be4.
Lipoproteins, not lipopolysaccharide, are the key mediators of the proinflammatory response elicited by heat-killed Brucella abortus
Retrieved from
Giambartolomei G.H., Zwerdling A., Cassataro J., Bruno L., Fossati C.A., Philipp M.T. Lipoproteins, not lipopolysaccharide, are the key mediators of the proinflammatory response elicited by heat-killed Brucella abortus. J. Immunol. 2004, 173(7):4635-4642. (Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/15383598).
(2004)J. Immunol., vol.173, Issue.7, pp. 4635-4642
Bone marrow microenvironment in an in vitro model of Gaucher disease: consequences of glucocerebrosidase deficiency
Lecourt S., et al. Bone marrow microenvironment in an in vitro model of Gaucher disease: consequences of glucocerebrosidase deficiency. Stem Cells Dev. 2011, 1-33. 10.1089/scd.2011.0365.
Glucocerebrosidase gene-deficient mouse recapitulates Gaucher disease displaying cellular and molecular dysregulation beyond the macrophage
Mistry P.K., et al. Glucocerebrosidase gene-deficient mouse recapitulates Gaucher disease displaying cellular and molecular dysregulation beyond the macrophage. Proc. Natl. Acad. Sci. U. S. A. 2010, 107(45):19473-19478. 10.1073/pnas.1003308107.
Induction of osteoclastogenesis in an in vitro model of Gaucher disease is mediated by T cells via TNF-α
Mucci J.M., et al. Induction of osteoclastogenesis in an in vitro model of Gaucher disease is mediated by T cells via TNF-α. Gene 2012, 509(1):51-59. 10.1016/j.gene.2012.07.071.
Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48-month longitudinal cohort study
Sims K.B., et al. Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48-month longitudinal cohort study. Clin. Genet. 2008, 73(5):430-440. 10.1111/j.1399-0004.2008.00978.x.
Bone events and evolution of biologic markers in Gaucher disease before and during treatment
Stirnemann J., Belmatoug N., Vincent C., Fain O., Fantin B., Mentré F. Bone events and evolution of biologic markers in Gaucher disease before and during treatment. Arthritis Res. Ther. 2010, 12(4):R156. 10.1186/ar3111.
Wenstrup R.J., Roca-Espiau M., Weinreb N.J., Bembi B. Skeletal aspects of Gaucher disease: a review. Br. J. Radiol. 2002, 75(Suppl. 1):A2-A12. (Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/12036828).