Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
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A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
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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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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
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A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Paroxysmal Cerebellar Ataxia
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Acetazolamide-Responsive Episodic Ataxia Syndrome
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Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
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Hereditary Paroxysmal Ataxia:Response to Acetazolamide
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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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The Accuracy of the Diagnosis of Paroxysmal Events in Children
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Paroxysmal Dyskinesias in Patients with HIV Infection
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Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
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Ion Channel Diseases:Episodic Disorders of the Nervous System
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An Open-Label Trial of Gabapentin Treatment of Paroxysmal Symptoms in Multiple Sclerosis Patients
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Endozepine Stupor. Recurring Stupor Linked to Endozepine-4 Accumulation
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Paroxysmal Tonic Upgaze:a Reappraisal of Outcome
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Exquisite Sensitivity of Paroxysmal Kinesigenic Choreoathetosis to Carbamazepine
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Paroxysmal Dyskinesias:Clinical Features and Classification
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Treatment of Paroxysmal Symptoms in Multiple Sclerosis with Ibuprofen
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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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Transient Paroxysmal Dystonia in Infancy
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Monosymptomatic Sensory Symptoms & Cerebrospinal Fluid Immunoglobulin Levels in Relation to Multiple Sclerosis
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Sporadic Paroxysmal Dystonic Choreoathetosis Associated with Basal Ganglia Calcifications
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Paroxysmal Dystonia as the Initial Manifestation of Multiple Sclerosis
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Familial Paroxysmal Dystonic Choreoathetosis & Response to Alternate-Day Oxazepam Therapy
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Paroxysmal Limb Hemiataxia with Crossed Facial Paresthesias in Multiple Sclerosis
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Abnormal Computed Tomograms in Paroxysmal Kinesigenic Choreoathetosis
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Clusters of Tonic Spasms as an Initial Manifestation of Multiple Sclerosis
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Phenytoin Plasma Concentrations in Paroxysmal Kinesigenic Choreoathetosis
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Paroxysmal Choreoathetosis Associated with Thyrotoxicosis
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Familial Paroxysmal Dystonic Choreoathetosis & its Differentiation From Related Syndromes
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Paroxysmal Choreoathetosis Following Head Injury
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Paroxysmal Choreoathetosis as a Presenting Symptom in Idiopathic Hypoparathyroidism
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Visual Symptoms in the Migraine Syndrome
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