Results 81 to 90 of about 22,438 (261)
Journal of Contemporary Pharmacy, 2018 Objective: This study was under taken for the evaluation of pediatric epileptic patients and to determine the antiepileptic drugs used in treatment of different epilepsy types and its comparison with other studies.
Mujeeb Ur Rehman +5 more
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Localizing value of verbal automatisms, vocal automatisms, singing, and humming: A systematic review
Epileptic Disorders, EarlyView.Abstract Objective We performed a systematic review of the localizing and lateralizing value of verbal automatisms, vocal automatisms, ictal singing, and humming in focal epilepsy with the view to summarize the state‐of‐the‐art clinico‐anatomical correlations in the field and help guide interpretation of ictal semiology within the framework of ...
Vit Vsiansky, Martin Pail, Milan Brazdil
wiley +1 more source
Drug-resistant epilepsy cases in chromosomal pathology
Эпилепсия и пароксизмальные состоянияTwo cases of epilepsy in patients with a rare hereditary pathology associated with a chromosomal mutation caused deletion of chromosome 14 are presented.
L. B. Novikova +3 more
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Sudden Unexpected Death in Epilepsy: A Case Report
Archives of Epilepsy, 2018 Sudden unexpected death in epilepsy (SUDEP) is a serious problem, and its importance has increased in recent years. It is responsible for the death of 17% of epilepsy patients. As the age of onset rises, the risk increases.
Gülser KARADABAN EMİR +3 more
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Dynamic control of modeled tonic-clonic seizure states with closed-loop stimulation
Frontiers in Neural Circuits, 2013 Seizure control using deep brain stimulation (DBS) provides an alternative therapy to patients with intractable and drug resistant epilepsy. This paper presents novel DBS stimulus protocols to disrupt seizures.
Bryce eBeverlin II, Theoden I Netoff
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KBG syndrome: A scoping review of electroclinical features of patients with epilepsy
Epileptic Disorders, EarlyView.Abstract Background and Objectives KBG syndrome is a rare autosomal developmental disorder caused by pathogenic variants of the ANKRD11 gene. This scoping review aimed to explore all current literature data regarding clinical and electroencephalographic features of patients with KBG syndrome and epilepsy. Materials and Methods We conducted a literature
Stefania Kalampokini +6 more
wiley +1 more source
Epileptic Disorders, EarlyView.Abstract Objective Epilepsy with eyelid myoclonia is a childhood‐onset generalized epilepsy syndrome with variable recognition of eyelid myoclonia, eye‐closure sensitivity, and photosensitivity during follow‐up. We aimed to characterize longitudinal clinical and electroencephalographic features in pediatric epilepsy with eyelid myoclonia, focusing on ...
Hande Aygün +3 more
wiley +1 more source
Analysis of ictal electrical-clinical characteristics of focal seizures in children with epilepsy
Chinese Journal of Contemporary Neurology and Neurosurgery, 2019 Objective To explore the ictal electrical-clinical features of focal seizures in childhood with epilepsy. Methods The video electroencephalography (VEEG) results of 409 focal seizures of 257 patients with epilepsy during January 2017 to June 2018 in EEG ...
Li-ming YANG +4 more
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