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Niemann-Pick Disease Type C
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Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
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Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
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Rapidly Progressive Thalamic Dementia
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Cocaine and Levamisole Cerebral Toxicity
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Precipitous Deterioration of Motor Function, Cognition, and Behavior
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A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
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Assessment and Management of Behavioral and Psychological Symptoms of 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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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Molybdenum Cofactor Deficiency
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A 14-Year-Boy with Spells of Somnolence and Cognitive Changes
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Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Normal Pressure Hydrocephalus
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Sturge-Weber Syndrome
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Granulomatous Meningitis due to Rheumatoid Arthritis
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Clinicopathologic Conference, Susacs Syndrome (retinocochleocerebral vasculopathy)
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Clinicopath Conf., Progressive Multifocal Leukoencephalopathy
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Progressive Supranuclear Palsy: A Current Review
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Intracranial Haemorrhages in French Haemophilia Patients (1991-2001): Clinical Presentation, Management and Prognosis Factors for Death
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Mucolipidosis Type IV; Characteristic MRI Findings
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Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
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Methylphenidate in Early Poststroke Recovery:A Double-Blind, Placebo-Controlled Study
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Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
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Cerebromeningeal Haemophagocytic Lymphohistiocytosis
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Cockayne Syndrome: Review of 140 Cases
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Neurologic Manifestations of AIDS
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Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
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Alternating Hemiplegia in Infants:Report of Five Cases
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Diphenylhydantoin & Selected Congenital Malformations
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