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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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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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An Unusual Fundus Finding in a Teenage Girl
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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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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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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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The Autosomal Recessive Cerebellar Ataxias
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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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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SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
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Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
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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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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
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Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
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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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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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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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Angelman Syndrome: Clinical Profile
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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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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Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
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Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
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Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
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Ataxia with Aniridia of Gillespie:A Case Report
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
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Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
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