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A Man with Tingling Fingers
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Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
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Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
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Neuroimaging Features of Biotinidase Deficiency
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Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Progressive Ataxia and Doenbeat Nystagmus in an Adult
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Nonalcoholic Wernicke Encephalopathy
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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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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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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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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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Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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A 54-year-old woman with Dementia, Myoclonus, and Ataxia
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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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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Reversible Cognitive Decline Diagnosed on Ear Examination
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A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Extraintestinal Manifestations of Coeliac Disease
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Progressive Cerebellar Ataxia and New-Onset Diabetes
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Copper Deficiency
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Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
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Diseases of the Nervous System Caused by Nutritional Deficiency, Wernicke-Korsakoff Syndrome (Thiamine B1) Deficiency
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Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
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Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin E Deficiency
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
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Cognitive Delay in a 7-year-old Girl
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Miller Fisher Syndrome with Positivity of Anti-GAD Antibodies
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The Autosomal Recessive Cerebellar Ataxias
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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
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Heterogeneity of Coenzyme Q10 Deficiency
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Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
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