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Clinicopath Conf., Progressive Multifocal Leukoencephalopathy
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Multiple Sclerosis Associated with Defects in Neuromuscular Transmission
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Clinopathologic Conference, Celiac Disease
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Human Neurexin-3a Antibodies Associate with Encephalitis and Alter Synapse Development
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Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
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Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
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Potentially Reversible Autoimmune Limbic ncephalitis with Neuronal Potassium Channel Antibody
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Neurologic Manifestations of SLE 1972
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Central Nervous System Manifestations of Periarteritis Nodosa
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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
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Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
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Neuromyelitis Optica Spectrum Disorder
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Sequential Bilateral Vision Loss in a Woman with Scalp Tenderness and Jaw Claudication
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Thymoma and Autoimmune Encephalitis
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Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
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Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
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Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
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An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
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A 23-Year-Old Man with Headaches, Confusion, and Lower Extremity Weakness
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Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
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A Case of Muscle Twitching with Psoriasis
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Diagnosis and Management of the Antiphospholipid Syndrome
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Autoimmune Pancerebellitis Associated with Pembrolizumab Therapy
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Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
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Clinicopathologic Conference, Susacs Syndrome
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Overview of IgG4-related Disease
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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 Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Seizing the Clinical Presentation in Adult Onset Stills Disease
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