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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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Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
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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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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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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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Familial Paroxysmal Dystonic Choreoathetosis & Response to Alternate-Day Oxazepam Therapy
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Acetazolamide-Responsive Episodic Ataxia Syndrome
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Abnormal Computed Tomograms in Paroxysmal Kinesigenic Choreoathetosis
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Hereditary Paroxysmal Ataxia:Response to Acetazolamide
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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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