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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
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The Inherited Ataxias and the New Genetics
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Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
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Spinocerebellar Ataxias and Ataxins
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Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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Paroxysmal Cerebellar Ataxia
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Primary Position Vertical Nystagmus & Cerebellar Ataxia
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Double-blind, Triple-crossover Trial of Low Doses of Oral Physostigmine in Inherited Ataxias
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Familial Periodic Ataxia
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Hereditary Paroxysmal Ataxia:Response to Acetazolamide
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Physostigmine in Familial Ataxias
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Azorean Disease of the Nervous System
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Ocular Motor Abnormalities in Hereditary Cerebellar Ataxia
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Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
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