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Out of Africa, Trypanosomiasis
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Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
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Neurologic Disorders in Renal Failure (1st of Two Parts)
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Neurologic Manifest. of Infective Endocarditis:A Review
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Encephalitis with mGluR5 antibodies
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Paediatric Autoimmune Encephalopathies: Clinical Features, Laboratory Investigations and Outcomes in Patients with or without Antibodies to known Central Nervous System Autoantigens
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A 35-Year-Old Woman with Acute Seizures and Behavior Change
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Frequency and Characteristics of Isolated Psychiatric Episodes in Anti-N-Methyl-D-Aspartate Receptor Encephalitis
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The Frequency of Autoimmune N-Methyl-D-Aspartate Receptor Encephalitis Surpasses That of Individual Viral Etiologies in Young Individuals Enrolled in the California Encephalitis Project
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Reversible Paraneoplpastic Limbic Encephalitis Associated with Antibodies to the AMPA Receptor
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Clinicopath Conf, Intravascular Large-B-Cell Lympoma
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Pediatric Encephalitis: What Is the Role of Mycoplasma Pneumoniae
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An Unusual Cause of Psychosis
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Mycoplasma Pneumoniae Encephalitis in Childhood
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CNS Side Effects of Nonsteroidal Anti-Inflammatory Drugs, Aseptic Meningitis, Psychosis & Cognitive Dysf
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Clinical Pathological Conference
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Neuropsychiatric Manifest. of SLE:Diagnosis, Clinical Spectrum, & Relationship to Other Features of the Disease
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Neurotoxicity of Commonly Used Antineoplastic Agents
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Choroid Plexus in SLE
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Neurologic Manifestations of Bacterial Endocarditis
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Confused About Confusion
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A 48-Year-Old Woman with 6 Months of Vivid Visual Hallucinations
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Morvan Syndrome and Diffuse Large B-Cell Lymphoma in the Central Nervous System
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Morvan Syndrome as a Paraneoplastic Disorder of Thymoma with Anti-CASPR2 antibodies
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Anti-DPPX Encephalitis,Pathogenic Effects of Antibodies on Gut and Brain Neurons
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Morvan Syndrome: Clinical and Serological Observations in 29 Cases
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Clinicopathologic Conference, Limbic Encephaitis with Antibodies to Leucine - Rich Glioma - inactivated 1 (LGI 1).
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Creutzfeldt-Jakob Disease in a Young Woman
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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