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Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
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Extracranial Etiology of Acute Onset Ataxia and Weakness
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
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Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
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Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
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The Acquired Metabolic Disorders of the Nervous System, Hashimoto Encephalopathy (Steroid Responsive Encephalopathy Syndrome)
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Mitochondrial DNA Polymerase-y and Human Disease
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Clinical Manifestations of Sarin Nerve Gas Exposure
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Neurological Complications of Coeliac Disease
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A Six-Year-Old Girl with Tick paralysis
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Prader-Willi and Angelman Syndromes
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Mitochondrial DNA and Disease
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MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
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Angelman Syndrome: Clinical Profile
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Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
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Herpes Zoster-Associated Encephalitis:Clinicopathologic Report of 12 Cases and Review of the Literature
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Neuroimaging Features of Biotinidase Deficiency
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Wernekinck Commissure Syndrome
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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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A Triad of Tremor, Ataxia, and Cognitive Impairment
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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
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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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A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
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Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
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Complex Ataxia
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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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When MRI is a Clue in Episodic Ataxia
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Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
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A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
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