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Paraneoplastic and Autoimmune Encephalitis
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Morvan Syndrome: Clinical and Serological Observations in 29 Cases
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Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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Clinicopath Conf., Anti-MNDAR Antibody Mediated Paraneoplastic Limbic Encephalitis Associated With Ovarian Teratoma
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Glucose Hypermetabolism in the Basal Ganglia
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A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
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A 75-year-old man with parkinsonism, mood depression, and weight loss
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The Writing on the Wall
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Sympathetic Cardioneuropathy in Dysautonomias
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Computed Tomography in Prognostic Stroke Evaluation
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Spinal Cord Compression from Epidural Metastases
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Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
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Unilateral Hyperhidrosis after Cerebral Infarction
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease
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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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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Sjogren Syndrome: Neurologic Complications
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Anti-NMDA-Receptor Encephalitis: Case Series and Analysis of the Effects of Antibodies
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Anti-NMDA-Receptor Encephalitis: Case Series and Analysis of the Effects of Antibodies
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Acute Intermittent Porphyria Presenting as Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome
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Paraneoplastic Anti-N-methyl-D-aspartate Receptor Encephalitis Associated With Ovarian Teratoma
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Insular Involvement in Brain Infarction Increases Risk for Cardiac Arrhythmia and Death
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Intrathecal Baclofen Withdrawal Mimicking Sepsis
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Reflex Sympathetic Dystrophy in Children
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Alternating Hemiplegia of Childhood
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Supraventricular Tachycardia in Patients with Right Hemisphere Strokes
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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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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
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Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
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Sudden Unexpected Death Associated with Seizures:Analysis of 66 Cases
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Clinicopathologic Conference, Infant Botulism, Case 3-2024
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Recent Advances in the Diagnosis and Management of Cluster Headache
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