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

Showing articles 0 to 9 of 9 Filter Applied: paroxysmal neurologic deficits (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 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 Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 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 Paroxysmal Dyskinesias:Clinical Features and Classification Ann Neurol 38:571-579, Demirkiran,M.&Jankovic,J., 1995 Internal Capsule Plaque and Tonic Spasms in Multiple Sclerosis Arch Neurol 48:427-429, Maimone,D.,et al, 1991 Transient Paroxysmal Dystonia in Infancy Neuropediatr 19:171-174, Angelini,L.,et al, 1988 Showing articles 0 to 9 of 9