Epilepsy Complex Partial
Mostrando 1-12 de 37 artigos, teses e dissertações.
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1. Expressão e purificação de proteinas relacionadas a epilepsia / Expression and purification of epilepsy related proteins
Non-ion channel genes, as LGI1 and EFHC1, have been shown to indirectly affect ion channel currents in genetically determined epilepsy syndromes. LGI1 (Leucine-rich, glioma inactivated gene 1) is linked to a rare form of partial epilepsy (autosomal dominant partial epilepsy with auditory features, ADPEAF). Recently, LGI1 protein was associated with ADAM22 in
Publicado em: 2007
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2. Malformações fetais, defeitos de desenvolvimento e sinais dismorficos em filhos de mães com epilepsia / Fetal malformations, development defects and dysmorphic signs in outcomes of women with epilepsy
Rationale: The majority of women with epilepsy do not experience significant changes during pregnancy; however the persistence of seizures and the effect of antiepileptic drugs (AED) may affect the fetus. These effects include lower intrauterine growth, dysmorphisms, fetal malformation and neuropsicomotor developmental delay. Most studies report that the ris
Publicado em: 2007
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3. Importance of Heart Rate Analysis in the differentiation of epileptic and non epileptic events / ImportÃncia da anÃlise da frequÃncia cardiÃca na diferenciaÃÃo de eventos epilÃpticos e nÃo epilÃpticos
As convulsÃes dialÃpticas tÃm como principais alteraÃÃes ictais as alteraÃÃes de consciÃncia que sÃo independentes das manifestaÃÃes ictais no eletroencefalograma. Essa classificaÃÃo de convulsÃes epilÃpticas foi proposta por LÃders et al em 1998 e tem como base exclusivamente a semiologia ictal. O presente estudo avalia um total de 59 evento
Publicado em: 2006
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4. Crisis del lóbulo temporal registrada mediante magnetoencefalografía: caso clínico
Ictal onset localization is a important factor in presurgical evaluation of epilepsy. This paper describes the localization of a seizure onset recorded by magnetoencephalography (MEG) from a 12-year-old male patient who suffered from complex partial drug-resistant seizures. MRI revealed a 20mm diameter lesion located in left hippocampus. Scalp EEG showed lef
Arquivos de Neuro-Psiquiatria. Publicado em: 2004-09
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5. Disturbios cognitivos na epilepsia
The present research refers to the the relationship between epileptic syndrome - Complex Partial Seizures - and cognitive performance. In order to study this subject we defined the following aims: 1) Characterization of neuroclinic condition of epileptic patients; 2) We studied the correlations between Epilepsy and Neuropsychological disorders; and 3) Contri
Publicado em: 1998
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6. Estudo de 34 casos enviados a um grupo de trabalho de epilepsia resistente
The author analysed 34 cases of resistant epilepsy (20 males and 14 females, mean age 23 years), treated clinically between february/1984 and may/1986. The patients underwent neurological, neuropsychological, psychological, psychiatric, cerebrospinalfluid, electroencephalographic, tomographic and/or angiographic examination. Most of the patients had complex
Publicado em: 1988
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7. Heautoscopy, epilepsy, and suicide.
Heautoscopy (the doppelgänger experience), epilepsy, and suicide is a triad primarily known from literary accounts. This paper reports a patient with complex partial seizures who tried to commit suicide during the experience of heautoscopy.
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8. Interhemispheric and intrahemispheric language reorganization in complex partial epilepsy
American Academy of Neurology.
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9. Early detection of abnormalities in partial epilepsy using magnetic resonance.
The incidence of brain abnormalities determined by magnetic resonance in 30 consecutive children presenting with intractable complex partial seizures is reported. Images were optimised to visualise the hippocampus and cortical grey matter. Abnormalities of the hippocampus or temporal lobe were seen in all 19 children with clinical features of temporal lobe e
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10. Epilepsy in a mitochondrial disorder.
In a large family with maternally inherited mitochondrial disease, a mild defect in the NADH-ubiquinone oxidoreductase step (complex 1) in the respiratory chain was found. Epilepsy was seen in nine (22%) of the 37 family members. Five of them, belonging to one branch of the family, had myoclonus epilepsy and EEG abnormalities consistent with this. The remain
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11. Herpes simplex encephalitis in a patient with complex partial epilepsy: confirmation by the polymerase chain reaction with necropsy studies.
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12. Causes of late onset epilepsy in Saudi Arabia: the role of cerebral granuloma.
Cerebral granulomas, due to infections, have been rarely reported as a cause of late onset epilepsy. The incidence of cerebral granulomas was 7% in this prospective study of 56 consecutive patients with onset of seizures after the age of 20 years. Other main causes included cerebral tumours (20%), arteriovenous malformations (5%) and cerebrovascular disease