Results 31 to 40 of about 11,842 (158)

Emergency electroencephalogram: Usefulness in the diagnosis of nonconvulsive status epilepticus by the on-call neurologist

Neurología (English Edition), 2018
Introduction: We aim to describe the use of emergency electroencephalogram (EmEEG) by the on-call neurologist when nonconvulsive status epilepticus (NCSE) is suspected, and in other indications, in a tertiary hospital. Subjects and methods: Observational
J.U. Máñez Miró, F.J. Díaz de Terán, P. Alonso Singer, M.J. Aguilar-Amat Prior   +3 more
doaj   +1 more source

Estereoelectroencefalografía y ablación focal por radiofrecuencia para epilepsia farmacoresistente: primer caso en México

Anales Médicos, 2023
La SEEG fue desarrollada en Francia a partir de 1949. Con las nuevas tecnologías de imagen y STX se ha perfeccionado vertiginosamente. Este método permite registrar fuera del quirófano, la actividad eléctrica por medio de electrodos intracerebrales ...
Enrique de Font-Réaulx, Javier Terrazo-y Lluch, Miguel A. Collado-Corona, Paul Shkurovich-Bialik, Luis G. Díaz-López, Ernesto Ramírez-Navarrete, Israel Romero-Rangel, Adalberto González-Astiazarán   +7 more
doaj   +1 more source

Effectiveness and tolerability of fenfluramine in pediatric and adult patients with developmental and epileptic encephalopathies: A multicenter, retrospective, real‐world clinical‐practice study

Epilepsia, EarlyView.
Abstract Objective Developmental and epileptic encephalopathies (DEEs) are characterized by drug‐resistant seizures and developmental slowing/regression. We examined the efficacy and tolerability of fenfluramine (FFA) in pediatric and adult patients with Lennox–Gastaut syndrome (LGS), Dravet syndrome (DS), and other DEEs.
Vicente Villanueva, Elena González‐Alguacil, Patricia Smeyers, Sara Hernández, Victor Soto‐Insuga, Alejandro Fernández‐Cabrera, Laura Olivié, Teresa de Santos, Beatriz Parejo, Lucas Iacampo, Belén Ortuño, Javier Aparicio, Montserrat Fuentes, Juan Rodriguez‐Uranga, Paula Martínez‐Agredano, José Carlos Estévez, Angel Aledo‐Serrano, Rocio Martin‐Alvarez, David Conejo, Belen Baena, Blanca Mercedes‐Álvarez, Yolanda López, Alba Sierra‐Marcos, Rocio Trincado‐Lamuño, Mouna Ennazeh, Jesús González de la Aleja, Julia Renau, Maria Dolores Castro‐Vilanova, Fátima Romero‐Aguilera, José M. Serratosa   +29 more
wiley   +1 more source

Inherited metabolic epilepsies–established diseases, new approaches

Epilepsia Open, EarlyView.
Abstract Inherited metabolic epilepsies (IMEs) represent the inherited metabolic disorders (IMDs) in which epilepsy is a prevailing component, often determining other neurodevelopmental outcomes associated with the disorder. The different metabolic pathways affected by individual IMEs are the basis of their rarity and heterogeneity.
Itay Tokatly Latzer, Phillip L. Pearl
wiley   +1 more source

Long-term surgical outcomes in patients with drug-resistant temporal lobe epilepsy and no histological abnormalities

Neurología (English Edition), 2013
Introduction: Reports on surgical outcomes in patients with drug-resistant temporal lobe epilepsy without histological abnormalities are scarce. Methods: Retrospective review of data from patients with drug-resistant temporal lobe epilepsy and no ...
J.C. Benedetti-Isaac, M. Torres-Zambrano, J. Fandiño-Franky, J. Dussán-Ordóñez, A. Herrera-Trujillo, R. Guerra-Olivares, G. Alcalá-Cerra   +6 more
doaj   +1 more source

Epilepsy syndromes classification

Epilepsia Open, EarlyView.
Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell, Nicola Specchio, Rima Nabbout, Phillip L. Pearl, Kate Riney   +4 more
wiley   +1 more source

Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes

Epilepsia Open, EarlyView.
Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola, Marica Rubino, Antonella Riva, Pasquale Striano   +3 more
wiley   +1 more source

Epilepsias

Revista Neurociências, 1999
Este é um artigo de revisão no qual os autores fazem uma abordagem geral dos principais tratamentos alternativos atualmente utilizados para as epilepsias, dentre eles: acelazolamida, brometos, alopurinol, piracelam, leviracetam, imunoglobulina, dieta cetogénica e corticostertides.
Sueli Rizzutti, Alzira Nobuko Nishiyama, Mauro Muszkat, Carlos José Reis de Campos   +3 more
openaire   +2 more sources

Precision therapies for genetic epilepsies in 2025: Promises and pitfalls

Epilepsia Open, EarlyView.
Abstract By targeting the underlying etiology, precision therapies offer an exciting paradigm shift to improve the stagnant outcomes of drug‐resistant epilepsies, including developmental and epileptic encephalopathies. Unlike conventional antiseizure medications (ASMs) which only treat the symptoms (seizures) but have no effect on the underlying ...
Shuyu Wang, Emilio Perucca, Samuel F. Berkovic, Piero Perucca   +3 more
wiley   +1 more source

Epilepsia y mujer

Revista Médica Clínica Las Condes, 2013
Hay muchos aspectos por abordar en el manejo de las mujeres con epilepsia, relacionados con su rol en la reproducción. Algunos de éstos necesitan ser considerados en la adolescencia, otros están relacionados con el embarazo, afectando tanto a la madre ...
S. Andrea Contreras, Dra., O. Larisa Fabres, Dra.   +1 more
doaj   +1 more source