Juvenile 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 …

Juvenile myoclonic epilepsy (JME) is characterized by myoclonic jerks on awakening,
generalized tonic–clonic seizures (GTCS) and is associated with absence seizures in more …

Although diagnosis of juvenile myoclonic epilepsy (JME), a common form of idiopathic
generalized epilepsy, is based on clinical and electroencephalogram (EEG) criteria, at times …

Juvenile myoclonic epilepsy (JME) is a recognizable, frequent epileptic syndrome. The most
typical ictal phenomenon is bilateral myoclonia without loss of consciousness (M), with most …

We aimed to characterize the clinical profile and EEG features of 43 patients with juvenile
myoclonic epilepsy. In a retrospective design we studied the records of, and re‐interviewed …

In juvenile myoclonic epilepsy (JME), occurrence of seizures and epileptiform EEG
discharges is influenced by internal and external factors. The most important internal factor …

Juvenile myoclonic epilepsy (JME), a common form of idiopathic generalized epilepsy, has a
distinct clinical and electroencephalographic profile. Often JME is not recognized, with …

Atypical clinical and/or EEG presentation may complicate the diagnosis of juvenile
myoclonic epilepsy (JME). To assess the sensitivity of a standard EEG recording, we …

Juvenile myoclonic epilepsy (JME) is a common idiopathic generalized epileptic syndrome
distinctively characterized by myoclonic jerks often associated to generalized tonic-clonic …

Objective Juvenile myoclonic epilepsy (JME) is a young‐onset electroclinical syndrome,
characterized by myoclonic, generalized tonic–clonic, and possibly typical absence …