Childhood absence epilepsy evolving to juvenile myoclonic epilepsy: electroclinical and genetic features

Autor:	Medina, M. T., Durón, R. M., Alonso, M. E., Dravet, C., León, L., López-Ruiz, M., Ramos-Ramírez, R., Castroviejo, I. P., Weissbecker, K., Westling, B., Perez-Gosiengfiao, K. T., Khan, S., Pineda, G., Morita, R., Rasmussen, A., Peek, J. R., Cordova, S., Martínez-Juárez, I. E., Rubio-Donnadieu, F., Ochoa-Morales, A., Aurelio Jara-Prado, Bailey, J. N., Tanaka, M., Bai, D., Machado-Salas, J., Delgado-Escueta, A. V.
Předmět:	Adult Diagnostic Imaging Family Health Male Neurologic Examination Risk Adolescent Myoclonic Epilepsy Juvenile Infant Electroencephalography Epilepsy Absence Child Preschool Humans Female Age of Onset Lod Score Child
Zdroj:	Europe PubMed Central Scopus-Elsevier
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::30bf21f139180cb1cd842752f8c8df60 http://europepmc.org/abstract/med/15508924 Zobrazit plný text záznamu