Immunologic considerations for enzyme replacement therapy in the treatment of lysosomal storage disorders

Author:

Richards Susan M

Publisher

Elsevier BV

Subject

Infectious Diseases,Immunology,Immunology and Allergy,Microbiology

Reference44 articles.

1. An introduction to the basic science and biology of the lysosome and storage disease;Hopwood,1997

2. Prevalence of lysosomal storage disorders;Meikle;JAMA,1999

3. The uptake of native and desialylated glucocerebrosidase by rat hepatocytes and kupffer cells;Furbish;Biochem Biophys Res Commun,1978

4. Replacement therapy for inherited deficiency macrophage targeted glucocerebrosidase for Gaucher's disease;Barton;N Engl J Med,1991

5. Newborn screening for lysosomal storage disorders;Meikle;Southeast Asian J Trop Med Public Health,1999

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