A Dizzy Architect
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Neurological Problems in Endocrine Diseases
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An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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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 54-year-old woman with Dementia, Myoclonus, and Ataxia
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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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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Antibiotic-Associated Encephalopathy
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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The Autosomal Recessive Cerebellar Ataxias
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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
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Heterogeneity of Coenzyme Q10 Deficiency
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Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
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A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
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Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
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Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
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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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Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
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Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
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Neurology of Ciguatera
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Paraneoplastic Syndromes
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Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Sarcoidosis of the Nervous System, A Clinical Approach
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Progressive Rubella Panencephalitis
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Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
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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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Persisting Neurologic Sequelae of Lithium Carbonate Therapy
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981
Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980
Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980
Self-Limited Granulomatous Angiitis of the Cerebellum
Ann Neurol 5:490-492, Beresford,H.R.,et al, 1979
Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
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Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
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The Thyroid Gland:Its Relationship to Neurology
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Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
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