Results 91 to 100 of about 5,863 (207)

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

open access: yes, 2011
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 ...
C. Vollmar   +29 more
core   +1 more source

Motor Unit Territories in Juvenile Myoclonic Epilepsy Patients

open access: yes, 2021
In this study, the scanning EMG technique was implemented to investigate electrophysiological cross-sections of the motor unit (MU) territories in healthy volunteers and in subjects with juvenile myoclonic epilepsy and spinal muscular atrophy ...
ERTAS, M.   +3 more
core   +1 more source

Juvenile Myoclonic Epilepsy Adventure: A Retrospective Study

open access: yesActa Neurologica Taiwanica
Background: Juvenile Myoclonic Epilepsy (JME) is one of the most common idiopathic generalized epilepsies, typically emerging during adolescence. Despite its characteristic clinical and EEG features, diagnosis may sometimes be delayed.
Arzu Eroğlu   +2 more
doaj   +1 more source

Risky Decision Making in Juvenile Myoclonic Epilepsy

open access: yesFrontiers in Neurology, 2018
It is not known whether patients with juvenile myoclonic epilepsy (JME) differ from healthy people in decision making under risk, i.e., when the decision-making context offers explicit information about options, probabilities, and consequences already ...
Iris Unterberger   +8 more
doaj   +1 more source

Cognitive performance in juvenile myoclonic epilepsy patients with specific endophenotypes

open access: yes, 2016
Purpose: Juvenile myoclonic epilepsy (JME) is a heterogeneous syndrome in which seizures can be precipitated not only by non-specific factors, such as sleep deprivation and stress, but also by specific stimuli, such as photic stimuli, eye-closure, praxis,
Pedroso Uchida, Carina Goncalves [UNIFESP]   +5 more
core   +1 more source

Unverricht-Lundborg disease in an adult female patient: a clinical case

open access: yesНеврология, нейропсихиатрия, психосоматика, 2018
We have considered it appropriate to publish this case due to the rarity of progressive myoclonus epilepsy; diagnostic difficulties, particularly in the early stages of the disease (the female patient has been long followed up for diagnosed juvenile ...
V. A. Karlov   +9 more
doaj   +1 more source

HYPERCONNECTIVITY IN JUVENILE MYOCLONIC EPILEPSY - A NETWORK ANALYSIS

open access: yes, 2022
HYPERCONNECTIVITY IN JUVENILE MYOCLONIC EPILEPSY - A NETWORK ...
K Hamandi (10456454)   +3 more
core  

Myoclonic seizures subside in the fourth decade in juvenile myoclonic epilepsy

open access: yes, 2008
Objective: Our aim was to assess the long-term follow-up of juvenile myoclonic epilepsy (JME), with an emphasis on the course of the myoclonic ...
Öztürk, Ali   +7 more
core   +1 more source

Efficacy of levetiracetam, lamotrigine and sodium valproate on seizure attacks and EEG disorders in patients with juvenile myoclonic epilepsy: A double blind randomized clinical trial

open access: yesCaspian Journal of Internal Medicine, 2022
Background: Juvenile myoclonic epilepsy (JME) is one of the most important types of generalized idiopathic epilepsy. Patients generally respond quickly and perfectly to standard antiepileptic drugs but lifelong medication is necessary.
Sajjad Daneshyar   +3 more
doaj  

Association mapping of genomic microdeletions and common susceptibility variants predisposing to genetic generalized epilepsies

open access: yes, 2013
Approximately 3% of the general population is affected by epilepsy during lifetime, making epilepsy one of the most common neurological diseases. Genetic generalized epilepsies (GGE) are the most common of genetic epilepsies and account for 20-30% of ...
Trucks, Holger Sebastian
core  

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