Enter your terms above and click the 'Search' button.

Showing articles 0 to 8 of 8 Filter Applied: lysosomal storage disease (Click to remove) Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation JNNP 69: 5-12, Gray,R.G.F. et al, 2000 Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 MR Brain Imaging of Fucosidosis Type I AJNR 22:777-780, Galluzzi,P.,et al, 2001 Mucolipidosis Type IV; Characteristic MRI Findings Neurol 51:565-569, Frei,K.P.,et al, 1998 Nervous System Involvement in Fabry's Disease:Clinicopath & Biochemical Correlation Ann Neurol 23:505-509, Kaye,E.M.,et al, 1988 Anderson-Fabray Disease, A Commonly Missed Diagnosis BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988 Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis NEJM 392:1461-1464, Gahl,W.A.,et al, 1988 Showing articles 0 to 8 of 8