Results 131 to 140 of about 4,695 (177)
Successful seizure control with cenobamate in juvenile myoclonic epilepsy. [PDF]
Epileptic DisordTényi D, Horváth R, Janszky J.
europepmc +1 more source
Glymphatic system dysfunction in epilepsy: a review of mechanisms and clinical evidence. [PDF]
EncephalitisByun JI.
europepmc +1 more source
Enhanced response inhibition in patients with drug-resistant juvenile myoclonic epilepsy: Event-related potentials evidence of excitatory-inhibitory imbalance. [PDF]
Epilepsia OpenSarah L +5 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Archives of Neurology, 2001
A one of the most common types of idiopathic epilepsies, juvenile myoclonic epilepsy (JME) has been the subject of intensive research, which culminated in a comprehensive monograph,' published in honor of Prof Dieter Janz, after whom the condition is often named.
P, Genton, P, Gelisse
openaire +2 more sources
A one of the most common types of idiopathic epilepsies, juvenile myoclonic epilepsy (JME) has been the subject of intensive research, which culminated in a comprehensive monograph,' published in honor of Prof Dieter Janz, after whom the condition is often named.
P, Genton, P, Gelisse
openaire +2 more sources
Juvenile myoclonic epilepsy and sleep
Epilepsy & Behavior, 2018Juvenile myoclonic epilepsy (JME) is a sleep-related epilepsy syndrome, and only a few studies have addressed the relationship between JME and sleep disorders. In this review, the sleep characteristics of patients with JME were summarized based on the features of circadian rhythm, the possible cause of the early morning seizures, the common subjective ...
Lin, Xu +5 more
openaire +2 more sources
Juvenile myoclonic epilepsy of Janz
Neurology, 1984We studied 43 patients, aged 15 to 69 years, whose convulsive seizures were uncontrolled because the syndrome of juvenile myoclonic epilepsy was not recognized. Awakening myoclonic jerks appeared with tonic-clonic (18 patients), clonic-tonic-clonic (24 patients), and absence seizures (17 patients), with a mean age at onset of 13.6 years.
A V, Delgado-Escueta, F, Enrile-Bacsal
openaire +2 more sources
Epidemiology of juvenile myoclonic epilepsy
Epilepsy & Behavior, 2013Juvenile myoclonic epilepsy (JME) is a widely recognized presumed genetic, electroclinical idiopathic generalized epilepsy syndrome. The prevalence of JME in large cohorts has been estimated to be 5% to 10% of all epilepsies and around 18% of idiopathic generalized epilepsies but may be lower in some settings.
Camfield CS +2 more
openaire +2 more sources
Neurophysiology of juvenile myoclonic epilepsy
Epilepsy & Behavior, 2013Juvenile myclonic epilepsy (JME) can be firmly diagnosed by a careful interview of the patient focusing on the seizures and by the EEG with the help, if necessary, of long-term video-EEG monitoring using sleep and/or sleep deprivation. Background activity is normal. The interictal EEG shows diffuse or generalized spike-wave (SW) and polyspike-wave (PSW)
Rubboli, Guido +4 more
openaire +2 more sources
The history of juvenile myoclonic epilepsy
Epilepsy & Behavior, 2013Juvenile myoclonic epilepsy (JME) has been the subject of intensive research over the past 25years. It was discovered stepwise in Switzerland and France in the 19th century, adequately described in Germany and Uruguay in the 1950s, and rediscovered in North America in the early 1980s.
Pierre, Genton, Philippe, Gelisse
openaire +2 more sources