A 35-Year-Old Woman with Personality Change and Gait Impairment
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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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Shrimp Sign in Ataxic Cerebellar Progressive Multifocal Leukoencephalopathy
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Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
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The Autosomal Recessive Cerebellar Ataxias
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Legionella Infection
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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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Sarcoidosis of the Nervous System, A Clinical Approach
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The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
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Primary Cerebellopontine Progressive Multifocal Leukoencephalopathy Diagnosed Premortem by Cerebellar Biopsy
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Wernekinck Commissure Syndrome
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Complex Ataxia
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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Antibiotic-Associated Encephalopathy
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Deep Brain Stimulation of the Dentate Nucleus Improves Cerebellar Ataxia After Cerebellar Stroke
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
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Mycoplasma Pneumoniae Infection: Neurologic Complications
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Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Reversible Metronidazole-Induced Lesions of the Cerebellar Dentate Nuclei
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Brainstem Gliomas in Adults: Prognostic Factors and Classification
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
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The Motor Disorder of Multiple System Atrophy
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Acute Cerebellar Ataxia in a Child with Transient Pontine Lesions Demonstrated by MRI
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Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Neurologic Sequelae of Chronic Solvent Vapor Abuse
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Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
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Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
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Cerebellar Involvement in Multifocal Eosinophilic Granuloma:Demonstration by CT Scan
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Legionnaires'Disease With Profound Cerebellar Involvement
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Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
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Chronic Meningitis
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