A neurological symptom survey of patients with type I Gaucher disease
Author:
Affiliation:
1. ; Neurogenetics Unit, Department of Neurology and Pediatrics; New York University School of Medicine; New York USA
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/B:BOLI.0000005623.60471.51/fullpdf
Reference12 articles.
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2. The health-related quality of life of adults with Gaucher disease receiving enzyme replacement: results from a retrospective study;Damiano;Qual Life Res,1998
3. Neurological complications of non-neuronopathic Gauchers' disease;Grewel;Arch Neurol,1991
4. Low-dose N-butyldeoxynojirimycin (OGT 918) for type I Gaucher disease;Heitner;Blood Cells Mol Dis,2002
5. Spinal cord compression secondary to Gaucher's disease;Markin;Surg Neurol,1984
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