The Phenotypic Continuum of ATP1A3-Related Disorders
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Hereditary Paroxysmal Ataxia:Response to Acetazolamide
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Paroxysmal Choreoathetosis Following Head Injury
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Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
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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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The Accuracy of the Diagnosis of Paroxysmal Events in Children
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000
Paroxysmal Tonic Upgaze:a Reappraisal of Outcome
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Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
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Paroxysmal Dyskinesias:Clinical Features and Classification
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Visual Symptoms in the Migraine Syndrome
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