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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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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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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Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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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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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, Friedreich Ataxia
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Degenerative Diseases of the Nervous System, Cerebellar Degeneration
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Extensive Striatal, Cortical, and White Matter Brain MRI Abnormalities in Wilson Disease
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The Autosomal Recessive Cerebellar Ataxias
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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A 23-Year-Old Man With Seizures and Visual Deficit
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Spinocerebellar Ataxia Type 8
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Niemann-Pick Disease Type C: Two Cases and an Update
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N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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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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Niemann-Pick Disease Type C from Bench to Bedside
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Isolated Vitamin E Deficiency
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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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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The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
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Wilson Disease
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Wilson's Disease:The Problem of Delayed Diagnosis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Wilson Disease:Clinical Presentation, Treatment, and Survival
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
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Paroxysmal Cerebellar Ataxia
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MR Imaging of a Group I Case of Hallervorden-Spatz Disease
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Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
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Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
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Familial Periodic Ataxia
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Dominant Spinopontine Atrophy
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Hereditary Paroxysmal Ataxia:Response to Acetazolamide
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Azorean Disease of the Nervous System
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