Complex Ataxia
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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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The Motor Disorder of Multiple System Atrophy
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Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
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A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021
Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020
Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017
A 27-year-old man with Acute-Onset Ataxia
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017
A 54-year-old woman with Dementia, Myoclonus, and Ataxia
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An 82-year-old man with Worsening Gait
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Deep Brain Stimulation of the Dentate Nucleus Improves Cerebellar Ataxia After Cerebellar Stroke
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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, Cerebellar Degeneration
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The Autosomal Recessive Cerebellar Ataxias
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Heterogeneity of Coenzyme Q10 Deficiency
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A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
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Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
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Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005
Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
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Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
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Neurology of Ciguatera
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Brainstem Gliomas in Adults: Prognostic Factors and Classification
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Paraneoplastic Cerebellar Degeneration
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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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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Movement Disorders in Alcoholism:A Review
Neurol 40:741-746, Neiman,J.,et al, 1990
Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
Ann Neurol 25:419-420, Iwasaki,Y.,et al, 1989
Neurologic Sequelae of Chronic Solvent Vapor Abuse
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Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
NEJM 311:1649-1652, Berginer,V.M.,et al, 1984
Persisting Neurologic Sequelae of Lithium Carbonate Therapy
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Neurologic Complications of Primary Sjogren's Syndrome
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Adult Celiac Disease Presenting as Cerebellar Syndrome
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Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
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Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
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Nervous System Toxicity of Chemo Agents
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Acute & Chronic Progressive Encephalopathy Due to Gasoline Sniffing
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Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977
Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976
Neurotoxicity of Commonly Used Antineoplastic Agents
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Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
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