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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
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Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
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Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
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The Phenotypic Continuum of ATP1A3-Related Disorders
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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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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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Recurrent Dysarthria and Ataxia in a Young Girl
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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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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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Progressive Cerebellar Ataxia and New-Onset Diabetes
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A Man with Tingling Fingers
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Subacute Sclerosing Panencephalitis
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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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Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
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Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
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Epstein-Barr Virus Infections of the Nervous System
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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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Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Clinical Spectrum of Episodic Ataxia Type 2
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Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
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Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
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Rotational Vertebral Artery Occlusion Syndrome with Vertigo Due to "Labyrinthine Excitation"
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Retinocochleocerebral Vasculopathy
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Susac Syndrome
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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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