A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Recessive Ataxia With Ocular Apraxia
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Neurological Manifestations in Xeroderma Pigmentosum
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Dominant Spinopontine Atrophy
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Nerve-Growth Factor in Familial Dysautonomia
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Complex Ataxia
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An Unusual Fundus Finding in a Teenage Girl
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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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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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Mitochondrial DNA Polymerase-y and Human Disease
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
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Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
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MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Refsum Disease
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Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
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Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
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Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
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Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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Juvenile Metachromatic Leukodystrophy
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A Family with Hereditary Ataxia:HLA Typing
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Abetalipoproteinemia, Report of Two Cases & Review of Therapy
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Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
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Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
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