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Showing articles 0 to 10 of 10 Filter Applied: lysosomal storage disease (Click to remove) 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 Pes Cavus and Neuropathy Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019 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 "Im fine; Im just waiting for my disease" The New and Growing Class of Presymptomatic Patients Neurol 77:522-523, Kwon, J.M.et al, 2011 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 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 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 10 of 10