Abstract The ILAE's Task Force on Nosology and Definitions revised in 2022 its definition of
juvenile myoclonic epilepsy (JME), the most common idiopathic generalized epilepsy …

Introduction Juvenile Myoclonic Epilepsy (JME) is a prevalent form of epileptic disorder,
specifically categorized within the realm of Genetic Generalized Epilepsy (GGE). Its hallmark …

Juvenile myoclonic epilepsy (JME) is a clinically and genetically heterogenous, generalized
epilepsy syndrome usually starting in adolescence. An age-related, predominantly …

Juvenile myoclonic epilepsy (JME) is a common epilepsy syndrome characterized by
bilateral myoclonic and tonic-clonic seizures typically starting in adolescence and …

Juvenile myoclonic epilepsy (JME) is a common genetic epilepsy syndrome usually
presenting in adolescence and characterized by myoclonic jerks, predominately in the arms …

Objective To determine treatment responses to various antiseizure medicines (ASMs) in
patients with drug resistant juvenile myoclonic epilepsy (DRJME) Methods We reviewed …

Reliable definitions, classifications and prognostic models are the cornerstones of stratified
medicine, but none of the current classifications systems in epilepsy address prognostic or …

Background and purpose Juvenile myoclonic epilepsy (JME) is a common epilepsy
syndrome for which treatment response is generally assumed to be good. We aimed to …

Juvenile myoclonic epilepsy (JME) is among the most common types of genetic epilepsies,
displaying a good prognosis when treated with appropriate drugs, but with a well-known …

Purpose Since its initial 1957 description, juvenile myoclonic epilepsy (JME) has been
recognized as a common epileptic syndrome worldwide. Methods We reviewed a series of …