Anaphylactoid Reaction to Imiglucerase, but Not to Alglucerase, in a Type I Gaucher Patient
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference10 articles.
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3. Replacement therapy for inherited enzyme deficiency - macrophage-targeted glucocerebrosidase for Gaucher disease;Barton;N Engl J Med,1991
4. A less costly regimen of alglucerase to treat Gaucher's disease;Figuerosa;N Engl J Med,1992
5. Enzyme therapy in Gaucher disease type I: dosage, efficacy, and adverse events in 33 patients treated for 6 to 24 months;Pastores;Blood,1993
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1. Successful switch from enzyme replacement therapy to miglustat in an adult patient with type 1 Gaucher disease: a case report;Journal of Medical Case Reports;2016-11-08
2. Successful rapid desensitization to imiglucerase in an adult patient with Gaucher disease and documented IgE-mediated hypersensitivity;The Journal of Allergy and Clinical Immunology: In Practice;2015-07
3. Successful Desensitization to Imiglucerase of an Adult Patient Diagnosed with Type I Gaucher Disease;International Archives of Allergy and Immunology;2013
4. Idursulfase: enzyme replacement therapy for mucopolysaccharidosis Type II (Hunter syndrome);Expert Review of Endocrinology & Metabolism;2007-01
5. An open-label, noncomparative study of miglustat in type I Gaucher disease: Efficacy and tolerability over 24 months of treatment;Clinical Therapeutics;2005-08
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