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Showing articles 0 to 8 of 8 Filter Applied: lysosomal storage disease (Click to remove) Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006 Neurological Presentation of Fabry's Disease in a 52 Year Old Man JNNP 73:340-342, Mohanraj,R.,et al, 2002 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 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 Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype NEJM 347:672-680, Case 27-2002, 2002 Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998 Neurologic Complications in Long-Standing Nephropathic Cystinosis Arch Neurol 46:543-548, Fink,J.K.,et al, 1989 Showing articles 0 to 8 of 8