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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
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Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
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Paroxysmal Tonic Upgaze:a Reappraisal of Outcome
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A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Internal Capsule Plaque and Tonic Spasms in Multiple Sclerosis
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Idiopathic Hypoparathyroidism and Paroxysmal Dystonic Choreoathetosis
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Sporadic Paroxysmal Dystonic Choreoathetosis Associated with Basal Ganglia Calcifications
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Abnormal Computed Tomograms in Paroxysmal Kinesigenic Choreoathetosis
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Paroxysmal Choreoathetosis Following Head Injury
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