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CHD2 variants are a risk factor for photosensitivity in epilepsy
ArticleAbstract: Photosensitivity is a heritable abnormal cortical response to flickering light, manifesting as partiPalabras claves:Eyelid myoclonia with absences, Photosensitive, SeizureAutores:Afrikanova T., Berkovic S.F., Boustred C., Cantonetti L., Capovilla G., Chinthapalli V.K., Coppola A., Covanis A., Crawford A.D., De Kovel C.G.F., Del Gaudio L., Drury S., Esguerra C.V., Galizia E.C., Helbig I., Jacmin M., Jocic-Jakubi B., Koeleman B.P.C., Krause R., Lehesjoki A.E., Lench N., Lerche H., Leu C., María Lorena Cordero-Maldonado, Martins T.G., Mefford H.C., Moller R.S., Muhle H., Mullen S.A., Myers C.T., Nürnberg P., Palotie A., Parisi P., Pendziwiat M., Piccioli M., Ruppert A.K., Sadleir L.G., Sander T., Scheffer I.E., Schneider A.L., Schubert J., Sisodiya S.M., Stephani U., Striano S., Thiele H., Trenité D.G.A.K.N., Veggiotti P.Fuentes:scopusShort- and long-interval intracortical inhibition in EPM1 is related to genotype
ArticleAbstract: Objective: Progressive myoclonic epilepsy type 1 (EPM1) is caused by biallelic alterations in the CSPalabras claves:LICI, progressive myoclonic epilepsy, SICI, transcranial magnetic stimulation, Unverricht-Lundborg diseaseAutores:Balestrini S., D'Ambrosio S., Diego Jiménez-Jiménez, Hyppönen J., Julkunen P., Kälviäinen R., Karjalainen P.A., Mervaala E., Rissanen S.M., Rothwell J.C., Säisänen L., Silvennoinen K., Sisodiya S.M., Zagaglia S.Fuentes:scopusPhysiological symmetry of transcranial magnetic stimulation-evoked EEG spectral features
ArticleAbstract: Transcranial magnetic stimulation (TMS)-evoked EEG potentials (TEPs) have been used to study the excPalabras claves:Brain stimulation, cortical excitability, Neurophysiology, symmetry, TMS-EEGAutores:Balestrini S., Comolatti R., D'Ambrosio S., Diego Jiménez-Jiménez, Fecchio M., Perulli M., Poole J., Silvennoinen K., Sisodiya S.M., Zagaglia S.Fuentes:scopus