A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018
Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017
Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023
Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
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Neurosyphilis
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A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Epilepsy Syndromes in Infancy
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998
The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
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Mitochondrial DNA and Disease
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Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
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HIV Encephalopathy and Dementia
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
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Relapsing Ophthalmoparesis-Sensory Neuropathy Syndrome
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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Mitral Valve Prolapse & Ophthalmoplegia:A Progressive, Cardioneurologic Syndrome
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Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
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Neurotoxicity of Commonly Used Antineoplastic Agents
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Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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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 Dizzy Architect
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A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021
Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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An Adolescent Girl Presenting with Worsening Vertigo, Headache, and 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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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018
Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018
Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018
Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
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