<--- Back to Details
| First Page | Document Content | |
|---|---|---|
 Date: 2010-08-10 22:40:31Inborn errors of carbohydrate metabolism Enzymes Rare diseases Glycogen storage disease type II Alpha-glucosidase Maltase Erasmus MC Medical genetics Glycogen storage disease Medicine Health Hepatology |
Add to Reading List |
Register or Login: Password: Search This Periodical | How one patient with a rare disease coped with his genetic disorderDocID: 1r9mW - View Document |
| LUMIZYME (alglucosidase alfa) for InjectionDocID: 1qeuI - View Document |
| United States Court of Appeals for the Federal Circuit ______________________ GENZYME THERAPEUTIC PRODUCTS LIMITED PARTNERSHIP,DocID: 1oYEH - View Document |
| Pompe disease (Glycogen storage disease type II) Glycogen storage disease type II is also known as acid maltase deficiency or generalized glDocID: 1lJGD - View Document |
| Association for Glycogen Storage Disease 2015 Membership Registration Sheet --------------------------------------------------------------------------------------------------------------------------------------------- PrDocID: 1laBq - View Document |