Short- and long-interval intracortical inhibition in EPM1 is related to genotype

Article

Abstract: Objective: Progressive myoclonic epilepsy type 1 (EPM1) is caused by biallelic alterations in the CS

Palabras claves:

LICI, progressive myoclonic epilepsy, SICI, transcranial magnetic stimulation, Unverricht-Lundborg disease

Autores:

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:

scopus