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Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Epstein-Barr Virus Infections of the Nervous System
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Biochemical And Clinical Aspects of Methotrexate Neurotoxicity
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Neurological Complications of Coeliac Disease
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
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Neurologic Complications in Children with Enterovirus 71 Infection
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Cytomegalovirus Encephalitis
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Diagnostic Guidelines in Central Nervous System Whipple's Disease
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Mitochondrial DNA and Disease
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Sarcoidosis of the Nervous System, A Clinical Approach
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The Thyroid Gland:Its Relationship to Neurology
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
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A 67-YEar-Old Man with Multiple Intracranial Lesions
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
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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 57-Year-Old Woman with Progressive Ataxia and Falls
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Neurosyphilis
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
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Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
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