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Showing articles 0 to 8 of 8 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 A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks Neurol 82:e194-e197, Duncan, M.,et al, 2014 Endozepine Stupor. Recurring Stupor Linked to Endozepine-4 Accumulation Brain 121:127-133, Lugaresi,E.,et al, 1998 Paroxysmal Choreoathetosis as a Presenting Symptom in Idiopathic Hypoparathyroidism JNNP 40:692, Soffer,D.,et al, 1977 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 Hereditary Paroxysmal Ataxia:Response to Acetazolamide Neurol 28:1259-1264, Griggs,R.C.,et al, 1978 Showing articles 0 to 8 of 8