Results 91 to 100 of about 412,527 (171)

Juvenile Myoclonic Epilepsy Adventure: A Retrospective Study

Acta 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, Ahmet Sami Güven, Huseyin Caksen   +2 more
doaj   +1 more source

Lamotrigine induced seizures in juvenile myoclonic epilepsy

, 2013
Juvenile myoclonic epilepsy (JME) is a common epileptic syndrome. Before the development of the new antiepileptic drugs (AEDs) after the 1990s, Valproate (VPA) was the first-line treatment in juvenile myoclonic epilepsy.
Acar, Betül, Türkel, Yakup, Dağ, Ersel   +2 more
core  

Juvenile myoclonic epilepsy: Psychiatric comorbidity and impact on outcome

, 2013
Juvenile myoclonic epilepsy (JME) is a well-defined age-related idiopathic epilepsy syndrome. Past studies have emphasized the difficulties in the treatment of patients with JME, which have been attributed to some specific psychiatric, psychological, and
Targas Yacubian, Elza Marcia [UNIFESP], Araujo Filho, Gerardo Maria de [UNIFESP]   +1 more
core   +1 more source

Movement Disorders in Developmental and Epileptic Encephalopathies

Movement Disorders Clinical Practice, Volume 13, Issue 10, Page 2328-2340, October 2026.
Abstract Background Monogenic developmental and epileptic encephalopathies (DEE) frequently feature co‐occurring movement disorders. Gene discovery has expanded epilepsy‐dyskinesia syndromes (EDS) from classic associations such as stereotypies in Rett syndrome to PRRT2‐related infantile seizures with paroxysmal dyskinesia and crouched gait in SCN1A ...
Shekeeb Mohammad, Darius Ebrahimi‐Fakhari, Hugo Morales‐Briceno   +2 more
wiley   +1 more source

The treatment of juvenile myoclonic epilepsy

, 2006
Juvenile myoclonic epilepsy is a common type of epilepsy with onset occuring during adolescence. This review provides a collection of evidence relating to the treatment of this type of epilepsy. Historically, the large majority of patients become seizure-
Verrotti, Alberto, Franzoni, Emilio, Manco, Rossella, Di Marco, Giovanna, Chiarelli, Francesco   +4 more
core   +3 more sources

Risky Decision Making in Juvenile Myoclonic Epilepsy

Frontiers 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, Laura Zamarian, Manuela Prieschl, Melanie Bergmann, Gerald Walser, Gerhard Luef, Andrija Javor, Gerhard Ransmayr, Margarete Delazer   +8 more
doaj   +1 more source

Genetic analysis of human absence epilepsy [PDF]

, 2010
Idiopathic Mendelian epilepsies have been typically identified as channelopathies. Evidence suggests that mutations in genes encoding GABAA receptors, GABAB receptors or voltage-dependent calcium channels (VDCCs) may underlie childhood absence epilepsy ...
Robinson, R.A.
core  

Clinical and Electroencephalographic Characteristics of Juvenile Myoclonic Epilepsy in   a Tertiary Care Hospital

Pakistan Armed Forces Medical Journal
Objective: To determine the clinical and electroencephalographic features in juvenile myoclonic epilepsy (JME) patients Study Design: Prospective longitudinal study.
Fawad Ahmad, Imran Ahmad, Saima Shafat, Jahanzeb Liaqat, Naveed Ahmed, Jalil Khan   +5 more
doaj   +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

Caspian 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, Masoud Ghiasian, Sahar Moradi, Elham Khanlarzadeh   +3 more
doaj  

Commentary on the usefulness of a morning routine EEG recording in patients with juvenile myoclonic epilepsy

, 2008
Lack of differences of motorcortical excitability in the morning as compared to the evening in juvenile myoclonic epilepsy--a study using transcranial magnetic ...
PARISI, Pasquale, Nolst Trenate Dga Kasteleijn, Marta Piccioli, Edouard Hirsch, Piccioli, Marta, Hirsch, Edouard, Trenite, Dorothe Kasteleijn-Nolst   +6 more
core   +1 more source