GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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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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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Paroxysmal Tonic Upgaze:a Reappraisal of Outcome
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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
Neurol 82:e194-e197, Duncan, M.,et al, 2014
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
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999
Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999
Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998
A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Paroxysmal Cerebellar Ataxia
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Transient Paroxysmal Dystonia in Infancy
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Familial Paroxysmal Dystonic Choreoathetosis & Response to Alternate-Day Oxazepam Therapy
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Hereditary Paroxysmal Ataxia:Response to Acetazolamide
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