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A systematic review and meta-analysis of factors related to first line drugs refractoriness in patients with juvenile myoclonic epilepsy (JME). [PDF]
PLoS OneFayad C +6 more
europepmc +1 more source
Altered effective connectivity of the default mode network in juvenile myoclonic epilepsy. [PDF]
Cogn NeurodynKe M, Wang F, Liu G.
europepmc +1 more source
Correction to: Resting-state electroencephalography microstates as a marker of photosensitivity in juvenile myoclonic epilepsy. [PDF]
Brain Communeuropepmc +1 more source
Lacosamide treatment of juvenile myoclonic epilepsy
Seizure: the Journal of the British Epilepsy Association, 2012 Juvenile myoclonic epilepsy is the most common form of idiopathic generalized epilepsy with onset at puberty or late teenage years. About 80–90% of patients with juvenile myoclonic epilepsy respond to appropriate antiepileptic treatment and achieve ...
Pegah Afra
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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
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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
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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
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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
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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
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