Low-dose high-frequency enzyme replacement therapy for very young children with severe Gaucher disease
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1993.tb03224.x/fullpdf
Reference11 articles.
1. Abnormal neutrophil chemotaxis in Gaucher disease
2. Replacement Therapy for Inherited Enzyme Deficiency — Macrophage-Targeted Glucocerebrosidase for Gaucher's Disease
3. Enzyme replacement therapy for Gaucher disease
4. Enzyme Augmentation in Moderate to Life-Threatening Gaucher Disease
5. A Less Costly Regimen of Alglucerase to Treat Gaucher's Disease
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3. Long-term hematological, visceral, and growth outcomes in children with Gaucher disease type 3 treated with imiglucerase in the International Collaborative Gaucher Group Gaucher Registry;Molecular Genetics and Metabolism;2017-01
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5. Individualized long-term enzyme therapy for Gaucher disease type 1 in Slovenia;Pediatrics International;2011-10-30
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