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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 Pes Cavus and Neuropathy Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019 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 Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998 Mucolipidosis Type IV; Characteristic MRI Findings Neurol 51:565-569, Frei,K.P.,et al, 1998 NEurologic Complications of Nonneuronopathic Gaucher's Disease Arch Neurol 48:1271-1272, Grewal,R.P.,et al, 1991 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