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Showing articles 0 to 8 of 8 Filter Applied: paroxysmal neurologic deficits (Click to remove) GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks Neurol 82:e194-e197, Duncan, M.,et al, 2014 Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome) Neurol 69:586-595, Fertleman,C.R.,et al, 2007 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 Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998 Paroxysmal Tonic Upgaze:a Reappraisal of Outcome Ann Neurol 43:514-520, Hayman,M.,et al, 1998 A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995 Internal Capsule Plaque and Tonic Spasms in Multiple Sclerosis Arch Neurol 48:427-429, Maimone,D.,et al, 1991 Showing articles 0 to 8 of 8