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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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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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Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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Cerebromeningeal Haemophagocytic Lymphohistiocytosis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
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Neurotoxicity of Commonly Used Antineoplastic Agents
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Neuroimaging Features of Biotinidase Deficiency
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
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More Than a Little Unsteady
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Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
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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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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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A Middle-Aged Man with Progressive Gait Abnormalities
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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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Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Complex Ataxia
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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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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Stridor in Multiple System Atrophy
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Neurosyphilis
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When MRI is a Clue in Episodic Ataxia
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GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Recurrent Dysarthria and Ataxia in a Young Girl
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An Unusual Fundus Finding in a Teenage Girl
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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Progressive Cerebellar Ataxia and New-Onset Diabetes
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Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
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