Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
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Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
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Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
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An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
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Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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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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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Progressive Cerebellar Ataxia and New-Onset Diabetes
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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A Man with Tingling Fingers
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Miller Fisher Syndrome with Positivity of Anti-GAD Antibodies
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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
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Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
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Opsoclonus-Myoclonus-Ataxia Syndrome with Autoantibodies to Glutamic Acid Decarboxylase
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
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Retinocochleocerebral Vasculopathy
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Susac Syndrome
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Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
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Neurotoxicity Related to the Use of Topical Tretinoin (Retin-A)
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Diagnostic Guidelines in Central Nervous System Whipple's Disease
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MR Findings in Seven Patients with Organic Mercury Poisoning (Minamata Disease)
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Angelman Syndrome: Clinical Profile
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Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or Macrocytosis
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Clinicopathological Conference
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
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Changes in the Basal Ganglia Following Cyanide Poisoning
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Heredopathia Atactica Polyneuritiformis
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Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
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Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
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