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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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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Complex Ataxia
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
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Degenerative Diseases of the Nervous System, Multiple System Atrophy
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Degenerative Diseases of the Nervous System, Cerebellar Degeneration
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The Autosomal Recessive Cerebellar Ataxias
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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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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Gluten Sensitivity in Sporadic and Hereditary Cerebellar Ataxia
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Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
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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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The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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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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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
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Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
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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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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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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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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
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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 Progressive Cerebellar Ataxia
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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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Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
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