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Showing articles 0 to 11 of 11 Filter Applied: lysosomal storage disease (Click to remove) Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment JIEMS 4:1-5, Politeri,J.M.,et al, 2016 Inherited Metabolic Diseases of the Nervous System, Metachromatic Leukodystrophy Adams & Victors Principles of Neurology, Chp 37, pg 971, Ropper, A.H.,et al, 2014 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Recurrent Acroparaesthesia During Febrile Infections Lancet 363:1698, Bodamer,O.A.,et al, 2004 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 Mucolipidosis Type IV; Characteristic MRI Findings Neurol 51:565-569, Frei,K.P.,et al, 1998 Late Onset Globoid Cell Leukodystrophy JNNP 54:1011-1012, Grewal,R.P.,et al, 1991 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Anderson-Fabry Disease Editorial, Lancet 336:24-251990., , 1990 Anderson-Fabray Disease, A Commonly Missed Diagnosis BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988 Showing articles 0 to 11 of 11