A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Antibody-Mediated Encephalitis
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Aicardi-Gouti�res Syndrome
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Acute and Progressive Cognitive Decline in a 38-Year-Old Man
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HIV-Associated CD8 Encephalitis: A UK Case Series and Review of Histopathologically Confirmed Cases
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Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
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Sarcoidosis Limbic Encephalitis
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Reversible Cognitive Decline Diagnosed on Ear Examination
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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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IgG4-Related Leptomeningitis: A Reversible Cause of Rapidly Progressive Cognitive Decline
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Immunotherapy-Responsive Chorea as the Presenting Feature of LGI1-Antibody Encephalitis
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West Nile Virus Neuroinvasive Disease
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Donepezil for Cognitive Impairment in Parkinson's Disease: A Randomised Controlled Study
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Out of Africa, Trypanosomiasis
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Niemann-Pick Disease Type C from Bench to Bedside
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Effects of HIV on Cognitive & Motor Devel in Children Born to HIV-Seropositive Women with no Reported Drug Use:Birth-24 mo
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Treatment of Convulsive Status Epilepticus
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Coma Assoc with Bursts of Abnor Movements & Cognitive Disturb:Acute Encephalopathy of Obscure Origin
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CNS Side Effects of Nonsteroidal Anti-Inflammatory Drugs, Aseptic Meningitis, Psychosis & Cognitive Dysf
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AIDS and the Nervous System
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Congenital AIDS:Review of Neurological Problems
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Release Of Adenylate Kinase Into CSF During Open-Heart Surgery & Its Relation To Postop. Intellectual Function
Lancet 1:1139-1142, Aberg,T.,et al, 1982
Two Cases of Van Buchem's Disease
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The Intelligence of Hydrocephalic Children
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Niemann-Pick Type C Disease
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The Spectrum of Fragile X Disorders
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Tuberous Sclerosis Complex:Clinical Features
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Congenital Cytomegalovirus Infection
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Diagnosis and Management of the Antiphospholipid Syndrome
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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Primary Angiitis of the Central Nervous System
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An 11-year-old Boy with Language Disorder and Epilepsy
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Mystery Case: A Young Boy with Myoclonic Jerks
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Cognitive Delay in a 7-year-old Girl
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Sturge-Weber Syndrome
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Effects of Fetal Antiepileptic Drug Exposure
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Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
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A 23-Year-Old Man With Seizures and Visual Deficit
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Infant Developmental Milestones and Subsequent Cognitive Function
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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