Results 91 to 100 of about 18,296 (263)
Abstract Objective To assess informed acceptance and perceptions of the 2025 update of the International League Against Epilepsy (ILAE) seizure classification—after participants had received a focused educational introduction to the updated classification. Methods We analyzed anonymized live poll responses from two educational webinars dedicated to the
Sándor Beniczky +6 more
wiley +1 more source
Abstract Objective To identify clinically meaningful patterns in ictal electroclinical features of focal epilepsy using a data‐driven, unsupervised learning approach, and to assess whether such patterns can localize and lateralize the epileptogenic zone (EZ) more accurately than conventional electroclinical interpretation.
Maria Vlachou +8 more
wiley +1 more source
Catatonia in Subacute Sclerosing Panencephalitis: A Rare and Overlooked Presentation
Background: Subacute sclerosing panencephalitis (SSPE) is a rare progressive neurodegenerative disease caused by measles virus. The clinical course is usually characterized by progressive cognitive decline and behavior changes followed by focal or ...
Khushboo Taparia +2 more
doaj +1 more source
On the Nature of the Knee-Jerk [PDF]
openaire +2 more sources
Exploring the efficacy and safety of perampanel in epilepsia partialis continua: A case series
Abstract Background Epilepsia partialis continua (EPC) is a form of focal motor status epilepticus (SE), which is commonly drug‐resistant requiring treatment with multiple antiseizure medications (ASM). There are no established guidelines for pharmacological management.
Setareh Lahsaee +3 more
wiley +1 more source
A DEBILITATING COMPLICATION OF MEASLES VIRUS: SSPE
Subacute sclerosing panencephalitis (SSPE) is a rare and chronic neurodegenerative disease caused by an unceasing infection of the brain by an altered form of the measles virus acquired earlier in life.
Neha Kamran, Fatima Jehangir
doaj
Occipital lobe epilepsy presenting as content‐specific reading‐induced seizures
Epileptic Disorders, EarlyView.
Christopher M. Kyper +2 more
wiley +1 more source
Abstract Objective To develop and evaluate a simple‐to‐use checklist to support physicians with the timely diagnosis of Lennox–Gastaut syndrome (LGS). Methods A panel of 10 pediatric and adult epileptologists used the International League Against Epilepsy (ILAE) criteria for LGS classification and definition to develop seven questions for the checklist,
Nicola Specchio +9 more
wiley +1 more source
NMDAR‐antibody encephalitis: Seizure semiology and EEG findings
Abstract Background N‐methyl‐D‐aspartate receptor antibody encephalitis (NMDAR‐Ab‐E) is an autoantibody‐mediated disorder, characterized by acute development of neuropsychiatric symptoms, seizures, movement disorders, and autonomic instability. Objectives To describe acute seizure semiology and electroencephalogram (EEG) findings in patients with a ...
Maria Emilia C. Andraus +6 more
wiley +1 more source

