Imiglucerase and its use for the treatment of Gaucher's disease
Author:
Publisher
Informa Healthcare
Subject
Pharmacology (medical),Pharmacology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1517/14656566.9.11.1987
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1. Prevalence of Lysosomal Storage Disorders
2. Recent clinical progress in Gaucher disease
3. Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's disease
4. The occurrence of psychosine and other glycolipids in spleen and liver from the three major types of gaucher's disease
5. Type I Gaucher Disease, a Glycosphingolipid Storage Disorder, Is Associated with Insulin Resistance
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