Results 11 to 20 of about 2,345,783 (392)
Criticism of “epileptic personality” syndrome
“Epileptic personality” syndrome, sometimes known as Waxman-Geschwind syndrome, is a constellation of interictal changes of emotions, thinking and behaviour, long associated with epilepsy.
A. Jasionis
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We report on the case of an adolescent with juvenile myoclonic epilepsy exhibiting compulsory sporadic voluntary movement. These movements entailed the deliberate act of touching her forehead with her hand and were triggered by a short and indefinable ...
Edgar Matringe+3 more
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Epilepsy and epileptic syndrome. [PDF]
Epilepsy is one of the most common neurological disorders. In most patients with epilepsy, seizures respond to available medications. However, a significant number of patients, especially in the setting of medically-intractable epilepsies, may experience different degrees of memory or cognitive impairment, behavioral abnormalities or psychiatric ...
Tomonori Ono, A. Galanopoulou
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Perisylvian Polymicrogyria Epileptic Syndrome
The epileptic spectrum and EEG findings in 31 patients with a congenital bilateral perisylvian syndrome are reported from the University of Alabama at Birmingham and the CBPS Multicenter Collaborative Study Group.
J Gordon Millichap
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Insights in classification of seizures and epilepsies – review of key concepts throughout history [PDF]
Since the Babylonian era up to nowadays, the large complexity of epileptic disorders made the attempt of classifying and organizing concepts one of the most challenging.
Ioana Mindruta+2 more
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Background. Neuronal and mixed neuronal-glial tumors are rare brain tumors that are most commonly observed in pediatric patients. The main clinical manifestations are presented by epilepsy substantially affecting child’s physical and neurocognitive ...
L. A. Gorlova+6 more
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Epilepsy syndromes: the 2022 ILAE definition and classification
Until recently, no classification of epileptic syndromes officially approved by the International League Against Epilepsy (ILAE) was available. In 2022, owing to many year-persistent efforts made by experts and the public community, the studies providing
D. V. Blinov
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Lennox–Gastaut syndrome is an epileptic encephalopathy with onset in childhood. The classical triad of diagnostic criteria is well known: 1) presence of various types of refractory epileptic seizures (tonic, atypical absences, myoclonic, tonic/atonic ...
E. D. Belousova+3 more
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Transient epileptic opercular syndrome [PDF]
Ictal transient opercular syndrome is rarely observed in benign epilepsy with centro-temporal spikes in children, and even more rarely in epilepsia partialis continua and symptomatic focal status epilepticus in adults. Here we report the ictal and interictal neuroimaging and electrophysiological findings in an adult female suffering from discontinuous ...
Susanne G. Mueller+5 more
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We aimed to assess the roles of the cortex and thalamus (centromedian nucleus [CM]) during epileptic activity in Lennox‐Gastaut syndrome (LGS) patients undergoing deep brain stimulation (DBS) surgery as part of the ESTEL (Electrical Stimulation of the ...
Linda J. Dalic+6 more
semanticscholar +1 more source