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epilepsy refractary

E G Lopez-Meza, F Cerda-Tellez, I M Alanis-Guevara, M C Fernández González-Aragón, L A Ruano-Calderón
INTRODUCTION: Lafora s disease is a type of progressive myoclonic epilepsy with poor prognosis, is characterized by myoclonic crisis, tonic clonic seizures, absence or partial complex seizures and other neurological manifestations with a progressive course and a poor response to the treatment. It has not been considered as a cause of epileptic status. CASE REPORTS: Two women without important past medical history with normal psychomotor development before their suffering, with manifestations of 2 years of evolution the first one and 8 years on the second case characterized by myoclonic generalized, partial complex seizures and progressive deterioration of the mental functions that joined to our institution in a non convulsive epileptic status and they featured with a different evolution...
November 16, 2003: Revista de Neurologia
R Caraballo, J Trípoli, L Escobal, R Cersósimo, S Tenembaum, C Palacios, N Fejerman
INTRODUCTION: Prospective study to evaluate efficacy of ketogenic diet (KD) in the treatment of children with intractable epilepsies (IE). Tolerability of the KD was also considered. MATERIAL AND METHODS: Criteria for inclusion were: 1. Epilepsy refractary to treatments with antiepileptic drugs (AED) in monotherapy and combining two or three AED. 2. Acknowledgment of blood levels of these drugs in therapeutic range. 3. Absence of liver or kidney disease, metabolic abnormalities, inborn errors of metabolism or other progressive encephalopathies...
January 1998: Revista de Neurologia
E Palacios, J Court, J C Kase
No abstract text is available yet for this article.
September 1976: Revista Médica de Chile
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