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An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
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Mycoplasma Pneumoniae Encephalitis in Childhood
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HIV Encephalopathy and Dementia
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Cat Scratch Disease, Acute Encephalopathy & Other Neurologic Manifestations
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Progressive Rubella Panencephalitis
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Central Nervous System Manifestations of Lyme Disease
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Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or Macrocytosis
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Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
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Diffusely Enhancing Lesions on MRI in DPPX Antibody-Associated Encephalitis
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Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Neuroimaging Features of Biotinidase Deficiency
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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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Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
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An 8-Year-Old with Acute Onset Ataxia
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Progressive Ataxia and Doenbeat Nystagmus in an Adult
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Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
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Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
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Stridor in Multiple System Atrophy
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Neurosyphilis
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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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A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
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A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
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Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Cerebellar Ataxia and Hearing Impairment
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A Woman in Her 60s with Chronic Meningitis from Aspergillus
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Reversible Gait Ataxia
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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CNS Posttransplant Lymphoproliferative Disorder
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Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
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An 82-year-old man with Worsening Gait
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Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
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A 57-year-old Woman with Ataxia and Oscillopsia
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A 52-year-old Man with Diplopia and Ataxia
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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
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