Results 161 to 170 of about 73,639 (264)
Abstract Intracranial electroencephalographic (iEEG) connectivity analysis is a promising method to localize epileptic networks and guide surgical planning in focal drug‐resistant epilepsy. Despite numerous studies exploring its utility, the added value of iEEG connectivity over standard clinical presurgical evaluation remains unclear.
Nishant Sinha +15 more
wiley +1 more source
Pediatric Epilepsy Surgery: The Noninvasive Presurgical Evaluation.
Mohanty D, Quach M.
europepmc +1 more source
Longitudinal changes in hippocampal morphology before and after temporal lobe epilepsy surgery. [PDF]
Velicky Buecheler M +11 more
europepmc +1 more source
Defining the end point of status epilepticus: A scoping review and framework for standardization
Abstract Status epilepticus (SE) is a life‐threatening neurological emergency with consensus‐driven definitions for onset but no standardized criteria for its end point. This gap creates uncertainty in research and clinical practice. We conducted a scoping review to evaluate how end points have been defined in SE research and to identify key areas of ...
Fawad A. Khan +6 more
wiley +1 more source
Epilepsy Surgery in Drug-Resistant Epilepsy Facilitated by Artificial Intelligence: A Case of Left Temporal Encephalocele. [PDF]
Crossman MH +5 more
europepmc +1 more source
Abstract Objective Systematic reviews and meta‐analyses (SRMAs) are critical for synthesizing evidence and guiding clinical and public health decision‐making. This study aims to evaluate the reliability, validity and reproducibility of the International League Against Epilepsy (ILAE) Commission on Epidemiology Risk of Bias Tool by comparing it against ...
Churl‐Su Kwon +3 more
wiley +1 more source
Utility of Interictal Data in Guiding Pediatric Epilepsy Surgery.
Hartman EK +6 more
europepmc +1 more source
Multimodal integration of magnetic resonance imaging and intracranial electroencephalographic abnormalities in temporal lobe epilepsy surgery. [PDF]
Kozma C +12 more
europepmc +1 more source
Long‐lasting remodeling of astrocytes in an Scna1+/− mouse model of Dravet syndrome
Abstract Objective Dravet syndrome (DS) is a prototypical developmental and epileptic encephalopathy caused by mutations in the SCN1A gene, leading to loss of function of the voltage‐gated sodium channel Naᵥ1.1. The latter causes early onset drug‐resistant seizures and enduring cognitive and behavioral deficits.
Athénaïs Genin +10 more
wiley +1 more source

