Results 91 to 100 of about 26,347 (231)

The multiple hit model of infantile and epileptic spasms: The 2025 update

Epilepsia Open, EarlyView.
Abstract Objective Infantile and epileptic spasms syndrome (IESS) is a developmental and epileptic encephalopathy manifesting with epileptic spasms and poor neurodevelopmental outcomes. There is an urgent need for the development of more effective and tolerated therapies.
Aristea S. Galanopoulou, Wenzhu B. Mowrey, Wei Liu, Anna Maria Katsarou, Qianyun Li, Oleksii Shandra, Solomon L. Moshé   +6 more
wiley   +1 more source

Efficacy and safety of levetiracetam as adjunctive therapy for refractory focal epilepsy. [PDF]

Arq Neuropsiquiatr, 2021
Manreza MLG, Pan TA, Carbone EQ, Vattimo ACA, Herrera R, Morais DC, Cardoso RA, Lacerda GCB, Lin K, Nakano FN, Kowacs PA, Palmini ALF, Souza AMMH, Zung S, Yacubian EMT.   +14 more
europepmc   +1 more source

Natural language processing‐based emotion and usage analysis of an AI‐powered chatbot for epilepsy support

Epilepsia Open, EarlyView.
Abstract Objective Artificial intelligence (AI)‐powered chatbots are increasingly used for patient education and mental health support, yet their effectiveness in epilepsy care remains underexplored. This study examines text‐based interactions between users and EpiloBot, an epilepsy‐focused chatbot, to understand conversational patterns and emotional ...
Keiichi Watanuki, Ryoya Oba, Naoki Nozawa, Tomoki Ishihara, Koko Oga, Takayuki Iwayama, Takafumi Shiganami, Sayaka Kobayashi, Hironori Kuga, Haruo Yoshimasu, Izumi Kuramochi   +10 more
wiley   +1 more source

Emergent responsive neurostimulation in pediatric super‐refractory epilepsia partialis continua

Annals of Clinical and Translational Neurology
Focal status epilepticus, particularly the motor variant of epilepsia partialis continua (EPC), is a rare condition characterized by near‐continuous, chronic focal motor seizures, and associated with poor outcomes. Medications, including anesthetics, are
Peter N. Hadar, Pranav Nanda, Katherine G. Walsh, John McLaren, Alexandra Geffrey, Mirela Simon, Kristopher Kahle, R. Mark Richardson, Catherine J. Chu   +8 more
doaj   +1 more source

Lateralização da área epileptogênica através de ressonância magnética na epilepsia do lobo temporal

Arquivos de Neuro-Psiquiatria, 1994
Métodos especiais de MRI foram utilizados em 5 pacientes com epilepsia do lobo temporal refratários ao tratamento clínico, com a finalidade de localizar a área epileptogênica.
M.C. Sandmann, E. Rogacheski, S. Mazer, P.R.M. de Bittencourt   +3 more
doaj   +1 more source

EEG–fMRI of idiopathic and secondarily generalized epilepsies [PDF]

, 2006
We used simultaneous EEG and functional MRI (EEG–fMRI) to study generalized spike wave activity (GSW) in idiopathic and secondary generalized epilepsy (SGE).
Duncan, J.S., Fish, D.R., Friston, K., Hamandi, K., Laufs, H., Lemieux, L., Liston, A., Salek-Haddadi, A.   +7 more
core   +1 more source

Epilepsias focales benignas atípicas

Acta Neurológica Colombiana, 2008
Inicialmente se creía que las epilepsias focales benignas de la niñez no dejaban secuelas cognitivas ni comportamentales y que su manejo era fácil, pero con el transcurso del tiempo se encontraron otros tipos de crisis que se acompañan de cambios cognitivos y de comportamiento, que fueron denominadas epilepsias atípicas.
openaire   +2 more sources

How to report neurotechnology and artificial intelligence studies in epilepsy: Peer‐review‐inspired recommendations

Epilepsia Open, EarlyView.
Abstract Objective The integration of neurotechnology and artificial intelligence (AI) in epilepsy research has led to significant advancements in diagnosis, monitoring, and treatment. However, the impact of these innovations is often diminished by inadequate and inaccurate reporting, limiting their reproducibility and implementation.
Pedro F. Viana, Matthew McWilliam, Andrea Biondi, Jesus Servando Medel‐Matus, Naoto Kuroda, Giulia Sofia Cereda, Aristea S. Galanopoulou   +6 more
wiley   +1 more source

Provável síndrome de Rasmussen: relato de caso

Arquivos de Neuro-Psiquiatria, 1999
A síndrome de encefalite crônica com epilepsia (síndrome de Rasmussen) ocorre tipicamente em crianças e é caracterizada pelo desenvolvimento de epilepsia focal intratável, hemiparesia progressiva e deterioração intelectual.
CORAL LUÍZ CARLOS, HAAS LEANDRO JOSÉ
doaj  

Caracterização da epilepsia com início após os 60 anos de idade

Revista Brasileira de Geriatria e Gerontologia
Resumo Introdução: Apesar da elevada incidência, a epilepsia no idoso ainda exibe peculiaridades pouco estudadas. A apresentação clínica na maioria das vezes é atípica e os achados nos exames complementares pouco ajudam no diagnóstico.
Igor Silvestre Bruscky, Ricardo André Amorim Leite, Carolina da Cunha Correia, Maria Lúcia Brito Ferreira   +3 more
doaj   +1 more source