Results 71 to 80 of about 2,375 (202)

Longitudinal PET and MRI Evaluation in Late Onset Rasmussen Encephalitis: A Series of Three Cases

open access: yesEuropean Journal of Neurology, Volume 32, Issue 7, July 2025.
ABSTRACT Background Rasmussen's encephalitis (RE) is a rare, chronic, neurological disorder characterized by progressive focal epilepsy and hemispheric atrophy. Late‐onset RE poses diagnostic challenges due to atypical clinical features and nonspecific early MRI findings.
Laura Rozenblum   +6 more
wiley   +1 more source

New-Onset Refractory Status Epilepticus with Claustrum Damage: Definition of the Clinical and Neuroimaging Features [PDF]

open access: yes, 2017
New-onset refractory status epilepticus (NORSE) is a rare but challenging condition occurring in a previously healthy patient, often with no identifiable cause.
Alexopoulos, Haris   +11 more
core   +1 more source

Intracranial stimulation for pediatric refractory epilepsy: A single institutional experience using evolving therapies

open access: yesEpilepsia Open, Volume 10, Issue 3, Page 694-704, June 2025.
Abstract Objective Neuromodulation for pediatric refractory epilepsy (PRE) is preferred when the seizure onset zone is not amenable to surgical resection, due to multifocal onset or involvement of eloquent cortex. Given its rapidly evolving landscape, we describe our institutional experience with neurostimulation therapies including deep brain ...
Rohin Singh   +9 more
wiley   +1 more source

Epilepsia partialis continua responsive to intravenous levetiracetam [PDF]

open access: yesSeizure, 2009
We report on a case of epilepsia partialis continua with rapid response to intravenous bolus administration of levetiracetam. A 60-year-old woman presented with continuous jerking of the right foot and hallux persisting for more than two days. She had a 9-year history of epilepsy due to a left temporoparietal oligodendroglioma with occasional focal ...
Eggers, Carsten   +3 more
openaire   +2 more sources

Three cases of atypical Rasmussen's encephalitis with delayed‐onset seizures

open access: yesEpilepsia Open, Volume 10, Issue 2, Page 411-426, April 2025.
Abstract We retrospectively analyzed the clinical characteristics of three ARE cases with delayed‐onset seizures treated at Peking University First Hospital and Sanbo Brain Hospital from May 2021 to January 2023. We also reviewed previously reported atypical cases of Rasmussen's encephalitis (RE) in the literature, summarizing onset symptoms, seizure ...
Hongru Guo   +7 more
wiley   +1 more source

Paresia poscrítica durante estudios de monitorización de vídeo-EEG [PDF]

open access: yes, 2002
To know the frequency of Todd s paralysis during the video EEG monitoring studies, to investigate in its pathophysiology, and to confirm its value to localise the epileptic focus.
Alegre-Esteban, M. (Manuel)   +6 more
core  

How Reliable Is the G41 Discharge Code for Status Epilepticus?

open access: yesBrain and Behavior, Volume 15, Issue 3, March 2025.
Sorbonne University Hospitals (5 hospitals, 1.1% of hospitalizations in France Extraction of all hospitalizations with a G41 discharge code (n = 797). Review of medical reports and labeling of hospitalizations using a sensitive and a specific approach. True positive (TP): hospitalization with a G41 code that corresponds to a hospitalization for Status ...
Quentin Calonge   +2 more
wiley   +1 more source

Prognostic significance of acute epilepsia partialis continua [PDF]

open access: yesPediatric Neurology, 1991
We present 3 patients in whom epilepsia partialis continua was the presenting sign of an acute, rapidly evolving and catastrophic neurologic illness. Initial seizures were partial simple (i.e., eye deviation in one, finger twitching in one) which progressed to multifocal partial seizures.
Baram, Tallie Z   +2 more
openaire   +4 more sources

Ovarioleukodystrophy due to EIF2B5 mutations [PDF]

open access: yes, 2016
Ovarioleukodystrophy – the co-occurrence of leukodystrophy and premature ovarian failure – is a rare presentation which is now recognised to be part of the clinical spectrum of vanishing white matter disease.
Faulkner, Howard   +4 more
core   +2 more sources

Probable sporadic Creutzfeldt–Jakob disease mimicking focal epilepsy

open access: yesEpilepsy and Behavior Case Reports, 2019
Creutzfeldt–Jakob disease (CJD) presents with seizures as an early symptom in only approximately 3% of cases. These seizures often present as nonconvulsive status epilepticus (NCSE) or epilepsia partialis continua (EPC).
Pei-Shan Hsiao   +5 more
doaj   +1 more source

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