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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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Ictal Cardiorespiratory Arrest in Panayiotopoulos Syndrome
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MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
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Clinicopathologic Conference, Infant Botulism, Case 3-2024
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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CASPR2 Autoimmunity in Children Expanding to Mild Encephalopathy with Hypertension
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An Infant with Episodic Facial Flushing
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Paraneoplastic and Autoimmune Encephalitis
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Progressive Development of Cardiomyopathy Following Altered Autonomic Activity in Status Epilepticus
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Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease
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Serotonin Syndrome
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Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
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Morvan Syndrome: Clinical and Serological Observations in 29 Cases
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Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
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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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Clinicopath Conf., Anti-MNDAR Antibody Mediated Paraneoplastic Limbic Encephalitis Associated With Ovarian Teratoma
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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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Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
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Insular Involvement in Brain Infarction Increases Risk for Cardiac Arrhythmia and Death
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The Serotonin Syndrome
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Prognositc Implications of Right-Sided Insular Damage, Cardiac Autonomic Derangement, and Arrhythmias After Acute Ischemic Stroke
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Intrathecal Baclofen Withdrawal Mimicking Sepsis
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Fever, Convulsions and Coma in Scleromyxedema:A"Dermato-Neuro Syndrome"
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Reflex Sympathetic Dystrophy
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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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Cardiovascular Effects of Human Insular Cortex Stimulation
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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A Prospective Study on Sudden Unexpected Death in Epilepsy
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Autonomic Nervous Function in Huntington's Disease
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Delirium Tremens, Update on an Old Disorder
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Alternating Hemiplegia of Childhood
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Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
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