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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 Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment JIEMS 4:1-5, Politeri,J.M.,et al, 2016 Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis) NEJM 370:1830-1841, Case 14-2014, 2014 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype NEJM 347:672-680, Case 27-2002, 2002 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 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