Mostrando 3 resultados de: 3
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:scopusThe impact of Transcranial Magnetic Stimulation (TMS) on seizure course in people with and without epilepsy
ArticleAbstract: Objective: To elucidate the effects of single and paired-pulse TMS on seizure activity at electrograPalabras claves:Alternating hemiplegia of childhood, Paired pulse, safety, Single pulse, TMSAutores:Balestrini S., Battaglia G., D'Ambrosio S., Diego Jiménez-Jiménez, Pang S., Perulli M., Silvennoinen K., Sisodiya S.M., Zagaglia S.Fuentes:scopus