Results 191 to 200 of about 26,347 (231)
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Oxcarbazepina en el tratamiento de la epilepsia focal refractaria.
Gaceta Medica De Bilbao, 2007Resumen Introduccion Los objetivos del estudio son analizar la eficacia y la tolerabilidad de la oxcarbazepina en pacientes afectos de epilepsia focal refractaria. Material y metodos Estudio prospectivo con treinta pacientes tratados con oxcarbazepina a dosis de 1.200–1.800 mg. Visita basal y visitas a los dos, cuatro y seis meses. Resultados
José Mª. Losada +5 more
exaly +2 more sources
Acta Neuropathologica, 1992
A limited cortical resection including the rolandic fissure and the pre- and postcentral cortical regions was carried out in a patient suffering from epilepsia partialis continua resistant to antiepileptic drugs. The histological examination revealed several foci of very large neurons distributed with no laminar organization in the depth of the ...
Soledad Alcántara
exaly +3 more sources
A limited cortical resection including the rolandic fissure and the pre- and postcentral cortical regions was carried out in a patient suffering from epilepsia partialis continua resistant to antiepileptic drugs. The histological examination revealed several foci of very large neurons distributed with no laminar organization in the depth of the ...
Soledad Alcántara
exaly +3 more sources
Focal Status Epilepticus and Epilepsia Partialis Continua in Adults and Children
Epilepsia, 1993Summary: Focal status epilepticus and epilepsia partialis continua (FSE‐EPC) are most frequently seen with chronic focal progressive encephalitis of Rasmussen and Russian spring‐summer encephalitis. FSE‐EPC may be the presenting feature of nonketotic hyperglycemic diabetes mellitus but is more often noted as a late complication especially if there is ...
exaly +3 more sources
Evaluación neuropsicológica prequirúrgica en epilepsias focales pediátricas
Revista de Neurología, 2010Introduccion. La evaluacion neuropsicologica esta incorporada a los protocolos de valoracion de un paciente candidato a cirugia de la epilepsia, proporciona informacion de las disfunciones cognitivas presentes en cada paciente, permite predecir los posibles riesgos cognitivos de la cirugia y proporciona medidas objetivas de cambio postquirurgico.
María Concepción Fournier del Castillo +4 more
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Lipoma de convexidad cerebral y epilepsia focal refractaria
Revista de Neurología, 2002INTRODUCTION Intracranial lipomas make up approximately 0.1% of all cerebral tumours. They are considered to be congenital malformations, caused by poor differentiation and abnormal persistence of the primitive meninges, which has become adipose tissue during the development of the subarachnoid space. They are usually found in the midline, often in the
Rosario Vela Yebra +5 more
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Displasia cortical focal y epilepsia farmacorresistente. Tratamiento con cirugía
Revista de Neurología, 2001INTRODUCTION Focal cortical dysplasia (FCD) is an unusual cause of refractory epilepsy, in which the morbid anatomy is characterized by cortical laminar dysplasia and the presence of balloon like cells. CLINICAL CASE A 36 year old woman who had had drug-resistant epilepsy since the age of 9 years old, with daily complex partial seizures and seizures in
Francisco Escamilla Sevilla +5 more
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Cirugía de la epilepsia en niños con displasias corticales focales
Revista de Neurología, 2013Introduccion. Las displasias corticales focales (DCF) son la primera etiologia de cirugia de la epilepsia pediatrica. La evaluacion prequirurgica en DCF a menudo es compleja, ya que son lesiones que pueden ser altamente epileptogenas y, a la vez, conservar funcion neurologica, y no visualizarse en la resonancia magnetica. El exito de la cirugia depende,
Francisco Javier Villarejo Ortega +2 more
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Epilepsias focales benignas en la infancia, niñez y adolescencia
Revista de Neurología, 2002The last proposal for a classification of epileptic seizures and syndromes of the International League Against Epilepsy (ILAE) includes recognition of several groups of epileptic syndromes and among them one of idiopathicfocal epilepsies of infancy and childhood, and another offamilial (autosomal dominant) focal epilepsies. The syndromes here described
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