Results 81 to 90 of about 344,528 (212)

Epilepsia sem mistérios

open access: yes, 2016
Áudio produzido a partir do acervo radiofônico da Rádio Educativa - Programa Na Onda da Vida. Discute sobre as possíveis causas da epilepsia, tipos, tratamento e preconceito em relação aos portadores da doençaEnsino Médio ...
Vilas Boas, Adlane
core   +2 more sources

Tegretol no tratamento da epilepsia Tegretol in the treatment of epilepsy

open access: yesArquivos de Neuro-Psiquiatria, 1968
O Tegretol (5-carbamil-5H-dibenzo-b,L-azepina) foi usado no tratamento de 68 pacientes com epilepsia; 54 apresentavam epilepsia temporal (42 com crises psicomotoras e 12 com crises complexas), 11 epilepsia focal de projeção não temporal e 3 epilepsia ...
Jorge Armbrust-Figueiredo
doaj  

Reply to: Does the generalized paroxysmal fast activity‐underrepresented cluster represent Lennox–Gastaut syndrome or other severe developmental and epileptic encephalopathies?

open access: yes
Epilepsia, EarlyView.
Emanuele Cerulli Irelli   +5 more
wiley   +1 more source

Expanding the electroclinical spectrum of TANC2‐related disorders: Lennox–Gastaut syndrome and related developmental epileptic phenotypes

open access: yesEpilepsia Open, EarlyView.
Abstract Objective Neurodevelopmental disorders (NDDs) and epilepsy are often associated. Increasing evidence highlights a pivotal role for pathogenic variants in genes encoding synaptic scaffolding proteins. Within this group, TANC2 has recently been implicated in intellectual developmental disorder with autistic features and language delay, with or ...
Lorenzo Perilli   +12 more
wiley   +1 more source

Heterotopía Subependimaria Pediátrica: correlación clínico-radiológica por resonancia magnética

open access: yesRevista Ciencias Biomédicas
Introducción: la heterotopía subependimaria es una malformación congénita del desarrollo neuronal caracterizada por la presencia de nódulos de sustancia gris en la pared de los ventrículos laterales.
Jose David Saenz Lopez   +5 more
doaj   +1 more source

Epilepsias focales benignas atípicas

open access: yesActa 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

The spatial learning task of Lhermitte and Signoret: Marker of bilateral hippocampal dysfunction in temporal lobe epilepsy

open access: yesEpilepsia Open, EarlyView.
Abstract Objective Bilateral hippocampal compromise in temporal lobe epilepsy (TLE) substantially increases the risk of significant adverse memory outcomes following unilateral anterior temporal lobectomy and may contraindicate surgery. The Spatial Learning Task (SLT) of Lhermitte and Signoret (1972) is a simple object–location arbitrary associative ...
Andy Sitoh   +6 more
wiley   +1 more source

Afasia Paroxismal: Epilepsia focal por cisticercosis cerebral, reporte de un caso

open access: yesRevista de Neuro-Psiquiatría, 2015
Se reporta el caso de un paciente varón de 63 años; natural y procedente de Juliaca, que ingresó por un cuadro de episodios paroxismales de afasia transitoria, de 2 minutos de duración asociado acefalea, sin trastorno de conciencia. No antecedentes de epilepsia, ni otros antecedentes patológicos.
Saquisela, Víctor V., Barreto, Elliot
openaire   +4 more sources

Provável síndrome de Rasmussen: relato de caso

open access: yesArquivos 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  

Emergent responsive neurostimulation in pediatric super‐refractory epilepsia partialis continua

open access: yesAnnals 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   +8 more
doaj   +1 more source

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