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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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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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Complex Ataxia
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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A 58-year-old man with Progressive Ptosis and Walking Difficulty
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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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Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
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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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Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
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Recessive Ataxia With Ocular Apraxia
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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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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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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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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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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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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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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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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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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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Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
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Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
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Genetic Counseling in Retinitis Pigmentosa
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