Results 31 to 40 of about 568 (146)

Chromatic Sensitive Epilepsy

Pediatric Neurology Briefs, 1999
A study of 4 boys with cartoon-evoked epileptic seizures, conducted at Kyushu University, Fukuoka, Japan, was prompted by a report of 685 Japanese children and some adults who suffered generalized convulsions while watching an animated TV program called “
J Gordon Millichap
doaj   +1 more source

Sex-specific disease modifiers in juvenile myoclonic epilepsy

Scientific Reports, 2022
Juvenile myoclonic epilepsy (JME) is a common idiopathic generalised epilepsy with variable seizure prognosis and sex differences in disease presentation.
Amy Shakeshaft, Naim Panjwani, Amber Collingwood, Holly Crudgington, Anna Hall, Danielle M. Andrade, Christoph P. Beier, Choong Yi Fong, Elena Gardella, Joanna Gesche, David A. Greenberg, Khalid Hamandi, Jeanette Koht, Kheng Seang Lim, Rikke S. Møller, Ching Ching Ng, Alessandro Orsini, Mark I. Rees, Guido Rubboli, Kaja K. Selmer, Pasquale Striano, Marte Syvertsen, Rhys H. Thomas, Jana Zarubova, Mark P. Richardson, Lisa J. Strug, Deb K. Pal   +26 more
doaj   +1 more source

The value of repeating intermittent photic stimulation in patients with juvenile myoclonic epilepsy [PDF]

Romanian Journal of Neurology
Background. Intermittent photic stimulation (IPS) entails systematic variation of stroboscopic light frequency and may provoke a photoparoxysmal response (PPR) in susceptible individuals. Objectives.
Sarah Ismail Almubarak, Salam Fuad Mohammed Rabeea, Farqad Bader Hamdan   +2 more
doaj   +1 more source

Symmetry and interhemispheric propagation of paediatric photoparoxysmal response

Neurologia i Neurochirurgia Polska, 2020
To investigate the speculated interhemispheric symmetry and the pattern of propagation of paediatric photoparoxysmal response.Quantitative analysis of the photoparoxysmal response (PPR) to intermittent photic stimulation is a promising method of assessing photosensitivity (PS).
Tymon, Skadorwa, Jolanta, Strzelecka
openaire   +3 more sources

Electroencephalography in the Diagnosis of Genetic Generalized Epilepsy Syndromes

Frontiers in Neurology, 2017
Genetic generalized epilepsy (GGE) consists of several syndromes diagnosed and classified on the basis of clinical features and electroencephalographic (EEG) abnormalities. The main EEG feature of GGE is bilateral, synchronous, symmetric, and generalized
Udaya Seneviratne, Udaya Seneviratne, Mark J. Cook, Wendyl Jude D’Souza   +3 more
doaj   +1 more source

EEG in genetic generalized epilepsies

Эпилепсия и пароксизмальные состояния, 2020
Genetic, or idiopathic, generalized epilepsies (GGEs or IGEs) includes childhood absence epilepsy (CAE), juvenile absence epilepsy (JAE), juvenile myoclonic epilepsy (JME), and epilepsy with generalized tonic-clonic seizures alone (GTCS-a).Aim.
V. Yu. Nogovitsyn, A. A. Sharkov
doaj   +1 more source

A translational multimodal machine‐learning prototype predicting valproate response in epilepsy treatment

Epilepsia, EarlyView.
Abstract Objective Epilepsy affects ~1% of the global population and often requires lifelong antiseizure medication (ASM) therapy. Valproic acid (VPA) is a commonly prescribed first‐line ASM, yet only approximately half of patients achieve sustained seizure freedom. Treatment selection remains largely empirical.
Simeon Platte, Afsheen Kumar, Giorgia Guerini, Massimo Pandolfo, Denise Haslinger, Colin B. Josephson, Guillermo Delgado‐García, Navprabhjot Kaur, Michaela‐Pauline Lux, Heiko Stempfle, Chantal Depondt, Reetta Kälviäinen, Felix Rosenow, Sophie von Brauchitsch, Karl Martin Klein, Andreas G. Chiocchetti   +15 more
wiley   +1 more source

Association of the carriage of BRD2 rs206787 and rs516535 and GJD2 rs3743123 polymorphisms with juvenile myoclonic epilepsy in Caucasian patients of Siberia

Неврология, нейропсихиатрия, психосоматика, 2019
In recent years, the genetics of juvenile myoclonic epilepsy (JME) has been actively studied; the association of JME with the carriage of polymorphic allelic variants of the BRD2 (EJM3 locus) and GJD2 (EJM2 locus) genes has been established.
O. S. Shilkina, N. A. Shnayder, S. N. Zobova, D. V. Dmitrenko, P. V. Moskaleva   +4 more
doaj   +1 more source

Progress report on new epilepsy treatments: A summary of the Eighteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XVIII). II. Treatments in more advanced clinical development

Epilepsia, EarlyView.
Abstract This article summarizes data for 13 investigational treatments for which at least preliminary seizure outcome data in patients with epilepsy were reported at the Eighteenth Eilat Conference on New Antiepileptic Drugs and Devices held in Madrid, Spain, on May 3–6, 2026.
Meir Bialer, Cecilie Johannessen Landmark, Matthias J. Koepp, Emilio Perucca, Piero Perucca, Torbjörn Tomson, H. Steve White, Elaine Wirrell   +7 more
wiley   +1 more source

Semiology of functional/dissociative seizures in idiopathic generalized epilepsy: An inpatient video‐electroencephalographic study

Epilepsia, EarlyView.
Abstract Objective This study was undertaken to estimate the prevalence and characterize the semiology of co‐occurring functional/dissociative seizures (FDSs) and identify clinical features potentially associated with the development of video‐electroencephalography (video‐EEG)‐diagnosed FDSs in patients with idiopathic generalized epilepsy (IGE ...
Javier Peña‐Ceballos, Kishen Radhakrishna, Tenzin Choekyi, Clodagh O'Keeffe, Mohamed Ali, Alma O'Donnell, Tudor Munteanu, Patrick B. Moloney, Hany El Naggar, Gerard Mullins, Peter Widdess‐Walsh, Ronan D. Kilbride, Norman Delanty, Nuala McNicholas   +13 more
wiley   +1 more source