C Vollmar, J O'Muircheartaigh, GJ Barker… - Brain, 2011 - Oxford Univ Press Juvenile myoclonic epilepsy is the most frequent idiopathic generalized epilepsy syndrome. It is characterized by predominant myoclonic jerks of upper limbs, often provoked by cognitive activities, and typically responsive to treatment with sodium valproate. ... Related articles - All 4 versions
J O'Muircheartaigh, C Vollmar, GJ Barker… - Neurology, 2011 - AAN Enterprises Results: Neuropsychological testing indicated subtle dysfunctions in verbal fluency, comprehension, and expression, as well as nonverbal memory and mental flexibility. Utilizing whole-brain voxel-based morphometry for gray matter MRI data and tract-based spatial ... Cited by 2 - Related articles - All 4 versions
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 ...
C Wille, BJ Steinhoff, DM Altenmüller… - Epilepsia, 2011 - Wiley Online Library Purpose: To assess the efficacy and tolerability of chronic high-frequency deep brain stimulation (DBS) in adult patients with progressive myoclonic epilepsy (PME) syndromes. Methods: Five adult patients (four male, 28–39 years) with PME underwent chronic high-frequency DBS ... Related articles - All 3 versions
N Gaspard, A Suls, C Vilain, P De Jonghe… - 9th EPNS …, 2011 - epns2011.com Mutations in the SLC2A1 gene are associated with a spectrum of neurological disorders, including De Vivo syndrome and genetic generalized epilepsy (GGE) syndromes. Within the GGEs, early-onset, juvenile or adult-onset absence epilepsy and febrile seizures have been ... Cached
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