M Trivisano, N Specchio, S Cappelletti… - Epilepsy Research, 2011 - Elsevier The objective of the study was to explore clinical, electroencephalography (EEG), neuropsychological features and prognosis of myoclonic-astatic epilepsy (MAE). Of 327 children aged between 1 and 9 years with a diagnosis of generalized epilepsy followed between 2000 and 2008, ...
S Mangano, A Fontana, C Spitaleri, GR Mangano… - Seizure, 2011 - Elsevier Benign myoclonic epilepsy in infancy (BMEI) is a rare syndrome included among idiopathic generalized epilepsies (IGE) and syndromes with age-related onset. Recently, it has been shown that a few patients with BMEI later had other epilepsy types mainly IGE but never childhood ...
R Dhamija, BD Moseley… - Neurology, 2011 - AAN Enterprises ... He was product of a healthy term pregnancy, born to nonconsanguineous parents, and was developmentally normal until the onset of myoclonicseizures at 8 months. Following this, developmental regression was noted. ... What is a myoclonicseizure? ... Related articles - All 2 versions
S Auvin, S Chhun, P Berquin, E Ponchel… - European Journal of …, 2011 - Elsevier ... It has been notably reported with carbamazepine in absence seizures and lamotrigine that aggravates myoclonicseizure in juvenile myoclonic epilepsy. ... For example, it is now established that lamotrigine (LTG) can worsen myoclonicseizures in juvenile myoclonic epilepsy. ... Related articles - All 2 versions
N Gaspard, A Suls, C Vilain, P De Jonghe… - 9th EPNS …, 2011 - epns2011.com ... been reported. Benign myoclonic epilepsy of infancy (BMEI) is a rare form of age-dependent GGE, characterized by myoclonicseizures in an otherwise healthy infant. Its etiology remains unknown. Aim of the work. To report ... Cached