Research & Innovation
Publications
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.
PMU Authors
C. von Stülpnagel, Till Hartlieb, Thomas Herberhold, Gerhard Kluger
All Authors
C. von Stülpnagel, M. Ensslen, R S Møller, D K Pal, S. Masnada, P. Veggiotti, E. Piazza, M. Dreesmann, Till Hartlieb, Thomas Herberhold, E. Hughes, M. Koch, C. Kutzer, K. Hoertnagel, J. Nitanda, M. Pohl, K. Rostásy, T B Haack, K. Stöhr, Gerhard Kluger, I. Borggraefe
Journal association
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
Abstract
Keywords
MUTATIONS, CHILDREN, COGNITIVE FUNCTION, FOCAL EPILEPSY, BENIGN CHILDHOOD EPILEPSY, CENTROTEMPORAL SPIKES, ROLANDIC EPILEPSY, SULTHIAME, ENCEPHALOPATHIES, SPEECH