Results 1 to 10 of about 1,335,280 (195)

Language after Hemispherotomy in Rasmussen Syndrome [PDF]

open access: yesPediatric Neurology Briefs, 2016
Investigators from Rothschild Foundation Hospital in Paris report language outcome in children after (left) dominant-hemisphere hemispherotomy for Rasmussen Syndrome.
Sophia Varadkar, Martin Tisdall
doaj   +9 more sources

Functional hemispherotomy in Rasmussen syndrome in the absence of classic MRI findings [PDF]

open access: yesEpilepsy and Behavior Case Reports, 2017
A 7-year-old previously healthy girl presented with a left-sided focal seizure without impaired consciousness and subsequently developed epilepsia partialis continua.
Yasunori Nagahama   +6 more
doaj   +3 more sources

Efficacy and tolerability of mycophenolate mofetil in a pediatric Rasmussen syndrome [PDF]

open access: yesEpilepsy & Behavior Reports, 2020
Rasmussen syndrome (RS) is a chronic encephalopathy with uncertain etiology and immune-mediated pathogenesis. The only definitive treatment is represented by functional hemispherectomy.
A. Orsini   +8 more
doaj   +2 more sources

Clinical spectrum, diagnosis, cognitive outcomes and therapeutic strategies in pediatric Rasmussen syndrome: a 10-year cohort from a tertiary pediatric center [PDF]

open access: yesOrphanet Journal of Rare Diseases
Background Rasmussen syndrome (RS) is a rare, immune-mediated, progressive epileptic encephalopathy. A comprehensive understanding of its heterogeneous clinical course, along with the identification of prognostic and early determinants, is crucial for ...
Verónica Cantarín-Extremera   +9 more
doaj   +2 more sources

Immunomodulatory Therapy for Rasmussen Syndrome

open access: yesPediatric Neurology Briefs, 2013
Investigators from the National Epilepsy Center, Shizuoka, Gifu University, Tokyo Women’s Medical University, National Center of Neurology and Psychiatry, and Okayama University School of Medicine, Japan, examined seizure, cognitive, and motor outcomes ...
J Gordon Millichap
doaj   +4 more sources

A rare complication of pulmonary tuberculosis in childhood: Rasmussen`s aneurysm in a 9-year-old child with Down syndrome

open access: yesThe Turkish Journal of Pediatrics, 2022
Background. As an extremely rare entity reported in children, Rasmussen`s aneurysm is an inflammatory pseudo-aneurysmal dilatation of a branch of the pulmonary artery adjacent to or within a tuberculous cavity. Case.
Elif Böncüoğlu   +6 more
doaj   +1 more source

Rasmussen syndrome in a tropical environment: a study of six (6) observations

open access: yesThe Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2021
Background In sub-Saharan Africa, encephalitis of various etiologies is a major public health problem and Rasmussen syndrome is rarely diagnosed due to under-medicalization.
Carlos Othon Guelngar   +25 more
doaj   +1 more source

Cerebral hemiatrophy: Case series of three cases

open access: yesCHRISMED Journal of Health and Research, 2021
Pediatric cerebral hemiatrophy is a rare entity with widespread etiology. Imaging in form of computed tomography and magnetic resonance imaging is helpful in differentiating between the etiologies of hemiatrophy.
Suhail Rafiq   +3 more
doaj   +1 more source

Posterior-onset Rasmussen's encephalitis with ipsilateral cerebellar atrophy and uveitis resistant to rituximab

open access: yesEpilepsy & Behavior Reports, 2020
Rasmussen encephalitis (RE) is a disorder characterized by drug-resistant seizures and progressive unihemispheric atrophy, hemiparesis, and varying degrees of cognitive decline.
Arnold J. Sansevere   +9 more
doaj   +1 more source

Late exacerbation of Rasmussen encephalitis with childhood onset [PDF]

open access: yesRomanian Journal of Neurology, 2011
We describe the case of a 21 year old woman that presented for epilepsia partialis continua syndrome that she had been having in the last 8 months. Slight diminished speech fluency, cortical discriminative sensibility impairment and neuroradiological ...
Alexandra Comanescu, Monica Sabau
doaj   +1 more source

Home - About - Disclaimer - Privacy