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Showing articles 0 to 8 of 8 Filter Applied: paroxysmal neurologic deficits (Click to remove) The Phenotypic Continuum of ATP1A3-Related Disorders Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022 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 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 Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome) Neurol 69:586-595, Fertleman,C.R.,et al, 2007 An Open-Label Trial of Gabapentin Treatment of Paroxysmal Symptoms in Multiple Sclerosis Patients Neurol 51:609-611, Solaro,C.,et al, 1998 Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis JNNP 43:296-304, Twomey,J.A.,et al, 1980 Hereditary Paroxysmal Ataxia:Response to Acetazolamide Neurol 28:1259-1264, Griggs,R.C.,et al, 1978 Showing articles 0 to 8 of 8