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Neurologic Aspects of Boxing
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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More Than a Little Unsteady
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Complex Ataxia
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Stridor in Multiple System Atrophy
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Antibiotic-Associated Encephalopathy
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Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
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Central Nervous System Involvement in Whipple Disease
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Mycoplasma Pneumoniae Infection: Neurologic Complications
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The Autosomal Recessive Cerebellar Ataxias
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Recessive Ataxia With Ocular Apraxia
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Brainstem Gliomas in Adults: Prognostic Factors and Classification
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Neuroradiologic Findings in Marinesco-Sjogren Syndrome
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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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Course and Outcome of Acute Cerebellar Ataxia
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