EpiNet as a way of involving more physicians and patients in epilepsy research: Validation study and accreditation process

Por Bergin, Peter S., Beghi, Ettore, Sadleir, Lynette G., Brockington, Alice, Tripathi, Manjari, Richardson, Mark P., Bianchi, Elisa, Srivastava, Kavita, Jayabal, Jayaganth, Legros, Benjamin, Ossemann, Michel, McGrath, Nicole, Verrotti, Alberto, Tan, Hui Jan, Beretta, Simone, Frith, Richard, Iniesta, Ivan, Whitham, Emma, Wanigasinghe, Jithangi, Ezeala‐Adikaibe, Birinus, Striano, Pasquale, Rosemergy, Ian, Walker, Elizabeth B., Alkhidze, Maia, Rodriguez‐Leyva, Ildefonso, Ramírez González, Jose Alfredo, D'Souza, Wendyl J.
Publicado no Epilepsia Open (2017)

Defects of mutant DNMT1 are linked to a spectrum of neurological disorders

Por Baets, Jonathan, Duan, Xiaohui, Wu, Yanhong, Smith, Gordon, Seeley, William W., Mademan, Inès, McGrath, Nicole M., Beadell, Noah C., Khoury, Julie, Botuyan, Maria-Victoria, Mer, Georges, Worrell, Gregory A., Hojo, Kaori, DeLeon, Jessica, Laura, Matilde, Liu, Yo-Tsen, Senderek, Jan, Weis, Joachim, Van den Bergh, Peter, Merrill, Shana L., Reilly, Mary M., Houlden, Henry, Grossman, Murray, Scherer, Steven S., De Jonghe, Peter, Dyck, Peter J., Klein, Christopher J.
Publicado no Brain (2015)