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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 Endozepine Stupor. Recurring Stupor Linked to Endozepine-4 Accumulation Brain 121:127-133, Lugaresi,E.,et al, 1998 Paroxysmal Limb Hemiataxia with Crossed Facial Paresthesias in Multiple Sclerosis JAMA 250:2843-2844, Skillrud,D.M.,et al, 1983 Phenytoin Plasma Concentrations in Paroxysmal Kinesigenic Choreoathetosis Neurol 30:673-676, Homan,R.W.,et al, 1980 Paroxysmal Choreoathetosis as a Presenting Symptom in Idiopathic Hypoparathyroidism JNNP 40:692, Soffer,D.,et al, 1977 Showing articles 0 to 6 of 6