Rasmussen encephalitis (RE) is a unilateral hemispheric encephalitis whose main clinical
features include refractory focal epilepsy or epilepsia partialis continua, hemiparesis, and …

Introduction Infantile spasm (IS) is an epileptic syndrome with typical onset within the first 2
years of life. This condition might be caused by several etiologies. IS is associated with …

BACKGROUND: Rasmussen encephalitis (RE) is a rare inflammatory disease affecting one
hemisphere, causing progressive neurological deficits and intractable seizures …

Purpose Rasmussen's encephalitis (RE) is a hemispheric inflammatory disorder resulting in
progressive epilepsy, hemiparesis, and cognitive decline. Controversy surrounds the most …

Objective Our purpose was to characterize neuropsychological evaluation (NP) outcome
following functional hemispherectomy in a large, representative cohort of pediatric patients …

Introduction The surgical procedure for severe, drug-resistant, unilateral hemispheric
epilepsy is challenging. Over the last decades the surgical landscape for hemispheric …

OBJECTIVE Rasmussen encephalitis (RE) is a rare inflammatory neurological disorder
typically involving one hemisphere and resulting in drug-resistant epilepsy and progressive …

Background: Although previous studies have reported soft-tissue management in surgical
treatment of Sturge–Weber syndrome (SWS), there are few reports describing facial bone …

Rasmussen's encephalitis is a rare neurological pathology affecting one cerebral
hemisphere, therefore, posing unique challenges. Patients may undergo hemispherectomy …

Surgery for pediatric drug resistant epilepsy: a narrative review of its history, surgical
implications, and treatment strategies - PMC Back to Top Skip to main content NIH NLM Logo …