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Showing articles 0 to 6 of 6 Filter Applied: paroxysmal neurologic deficits (Click to remove) 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 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 Paroxysmal Dyskinesias:Clinical Features and Classification Ann Neurol 38:571-579, Demirkiran,M.&Jankovic,J., 1995 Hereditary Paroxysmal Ataxia:Response to Acetazolamide Neurol 28:1259-1264, Griggs,R.C.,et al, 1978 Paroxysmal Choreoathetosis Following Head Injury Ann Neurol 2:447, Robin,J.J., 1977 Showing articles 0 to 6 of 6