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Motor system hyperconnectivity in juvenile myoclonic epilepsy: a cognitive functional magnetic resonance imaging study

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

Focal structural changes and cognitive dysfunction in juvenile myoclonic epilepsy

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

Benign myoclonic epilepsy in infancy followed by childhood absence epilepsy

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 ...

Chronic high‐frequency deep‐brain stimulation in progressive myoclonic epilepsy in adulthood—Report of five cases

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

Benign myoclonic epilepsy of infancy as the initial clinical presentation of a SLC2A1 mutation

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 ...
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