A Dizzy Architect
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The Autosomal Recessive Cerebellar Ataxias
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Neurotoxicity of Commonly Used Antineoplastic Agents
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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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The Phenotypic Continuum of ATP1A3-Related Disorders
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Progressive Ataxia and Doenbeat Nystagmus in an Adult
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
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Cerebellar Ataxia and Hearing Impairment
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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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Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
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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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Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
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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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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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Autoantibodies to Glutamic Acid Decarboxylase in Downbeat Nystagmus
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Reversible Metronidazole-Induced Lesions of the Cerebellar Dentate Nuclei
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Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
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Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
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Neurology of Ciguatera
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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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Acute Cerebellar Ataxia in a Child with Transient Pontine Lesions Demonstrated by MRI
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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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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988
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
Fusiform Basilar Artery Aneurysm in a Child
Neurol 29:1045-1049, Read,D.,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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