Precipitous Deterioration of Motor Function, Cognition, and Behavior
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
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Paraneoplastic Upbeat Nystagmus
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Progressive Supranuclear Palsy: A Current Review
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Tau Forms in CSF as a Reliable Biomarker for Progressive Supranuclear Palsy
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Niemann-Pick Disease Type C: Two Cases and an Update
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Posterior Cerebral Artery Syndromes
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The Clinical Features & Natural History of the Steele-Richardson-Olszewski Syndrome (Prog Supranuclear Palsy)
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Oculomasticatory Myorhythmia:A Unique Movement Disorder Occurring in Whipple's Disease
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The Syndrome of Bilateral Paramedian Thalamic Infarction
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Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
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Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
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Adult Dystonic Lipidosis, Clin Histo & Biochem Findings of a Neurovisceral Storage Dis
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Encephalopathy Complicating Whipple's Disease
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Whipple's Disease with Predominating Neuro-ophthalmic Manifestations
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Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
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Progressive Supranuclear Palsy:A Clinical, Pathological & Biochemical Study
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Whipple's Disease & Papilledema
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Creutzfeldt-Jakob Disease in a Young Woman
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Niemann-Pick Disease Type C from Bench to Bedside
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Diagnostic Guidelines in Central Nervous System Whipple's Disease
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
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Cortical-Basal Ganglionic Degeneration
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Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
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A 60-Year-Old Man with Weakness and Gait Dysfunction
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Adults with Cerebral Palsy Require Ongoing Neurologic Care
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Chronic Meningitis
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Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
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Ears of the Lynx Magnetic Resonance Imaging Sign
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Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A 54-year-old woman with Dementia, Myoclonus, and Ataxia
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Amyotrophic Lateral Sclerosis
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A Young Man with Progressive Language Difficulty and Early-Onset Dementia
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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
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Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
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Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
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