Significance of immune response to enzyme-replacement therapy for patients with a lysosomal storage disorder
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference19 articles.
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2. α-glucosidase deficiency in generalized glycogen-storage disease (Pompe's Disease);Hers;Biochem. J.,1963
3. From cytases to lysosomes;De Duve;Fed. Proc.,1964
4. Replacement therapy for inherited enzyme deficiency: use of purified glucocerebrosidase in Gaucher's disease;Brady;N. Engl. J. Med.,1974
5. Immunosurveillance of alglucerase enzyme therapy for Gaucher patients: induction of humoral tolerance in seroconverted patients after repeat administration;Rosenberg;Blood,1999
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