Enter your terms above and click the 'Search' button.

Showing articles 0 to 10 of 10 Filter Applied: enzyme,defect (Click to remove) Clinicopath Conf, Infantile Krabbe Disease NEJM 362:346-356, Case 3-2010, 2010 Neurologic Crises in Hereditary Tyrosinemia NEJM 322:432-437, Mitchell,G.,et al, 1990 Late Adult-onset Metachromatic Leukodystrophy Arch Neurol 35:475, Bosch,E.P., 1978 Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis) NEJM 370:1830-1841, Case 14-2014, 2014 Inherited Metabolic Diseases of the Nervous System, Fabry Disease Adams & Victors Principles of Neurology, Chp 37, pg 991, Ropper, A.H.,et al, 2014 Clumsiness, Confusion, Coma, and Valproate Lancet 353:1408, Ellaway,C.J.,et al, 1999 Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic J Pediatr 118:744-746, Dionisi,C.,et al, 1991 Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I) Ann Neurol 7:450-456, Steinman,L.,et al, 1980 Neuropathology of Sanfilippo Syndrome Ann Neurol 2:161, Ghatak,N.R.,et al, 1977 Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem Neurol 23:1030, Sipe,J.C., 1973 Showing articles 0 to 10 of 10