The dopamine system in idiopathic generalized epilepsies: identification of syndrome-related changes
C Ciumas, TBR Wahlin, C Espino, I Savic - Neuroimage, 2010 - Elsevier
The present study tests the hypothesis that the dopamine system is altered in idiopathic
generalized epilepsy (IGE), and that the pattern of possible changes differs between juvenile …
generalized epilepsy (IGE), and that the pattern of possible changes differs between juvenile …
Energy landscape of resting magnetoencephalography reveals fronto-parietal network impairments in epilepsy
Juvenile myoclonic epilepsy (JME) is a form of idiopathic generalized epilepsy. It is yet
unclear to what extent JME leads to abnormal network activation patterns. Here, we …
unclear to what extent JME leads to abnormal network activation patterns. Here, we …
Social cognition in idiopathic generalized epilepsies and potential neuroanatomical correlates
M Guida, L Caciagli, M Cosottini, U Bonuccelli… - Epilepsy & Behavior, 2019 - Elsevier
Social cognition allows us to elaborate mental representations of social relationships and
use them appropriately in a social environment. One of its main attributes is the so-called …
use them appropriately in a social environment. One of its main attributes is the so-called …
[HTML][HTML] Subcortical structural abnormalities in juvenile myoclonic epilepsy (JME): MR volumetry and vertex based analysis
PURPOSE: Imaging studies in juvenile myoclonic epilepsy (JME) have shown abnormalities
of the thalamus and frontal cortex. The purpose of this study was to systematically …
of the thalamus and frontal cortex. The purpose of this study was to systematically …
Microstructural alterations of white matter in juvenile myoclonic epilepsy
Juvenile myoclonic epilepsy (JME) is a common type of idiopathic generalized epilepsy that
is characterized by myoclonic jerks of the upper limbs and generalized tonic-clonic seizures …
is characterized by myoclonic jerks of the upper limbs and generalized tonic-clonic seizures …
Hippocampal atrophy and memory dysfunction in patients with juvenile myoclonic epilepsy
Juvenile myoclonic epilepsy (JME) is a well-defined idiopathic generalized epilepsy (IGE)
syndrome, being the most common IGE in adults and accounting for 5–11% of patients with …
syndrome, being the most common IGE in adults and accounting for 5–11% of patients with …
Mutations of EFHC1, linked to juvenile myoclonic epilepsy, disrupt radial and tangential migrations during brain development
L de Nijs, N Wolkoff, B Coumans… - Human molecular …, 2012 - academic.oup.com
Heterozygous mutations in Myoclonin1/EFHC1 cause juvenile myoclonic epilepsy (JME),
the most common form of genetic generalized epilepsies, while homozygous F229L …
the most common form of genetic generalized epilepsies, while homozygous F229L …
[HTML][HTML] Fronto-insula network activity explains emotional dysfunctions in juvenile myoclonic epilepsy: combined evidence from pupillometry and fMRI
Emotional instability, difficulties in social adjustment, and disinhibited behavior are the most
common symptoms of the psychiatric comorbidities in juvenile myoclonic epilepsy (JME) …
common symptoms of the psychiatric comorbidities in juvenile myoclonic epilepsy (JME) …
[HTML][HTML] Extrafrontal structural changes in juvenile myoclonic epilepsy: a topographic analysis of combined structural and microstructural brain imaging
SH Kim, SC Lim, W Kim, O Kwon, S Jeon, JM Lee… - Seizure, 2015 - Elsevier
Purpose An increasing amount of evidence has demonstrated that juvenile myoclonic
epilepsy (JME) is associated with structural abnormalities in not only the thalamofrontal …
epilepsy (JME) is associated with structural abnormalities in not only the thalamofrontal …