Showing 1 - 3 results of 3 for search 'Vrielynck, P', query time: 0.02s
Refine Results
-
1
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction by Lesca, G, Rudolf, G, Bruneau, N, Lozovaya, N, Labalme, A, Boutry-Kryza, N, Salmi, M, Tsintsadze, T, Addis, L, Motte, J, Wright, S, Tsintsadze, V, Michel, A, Doummar, D, Lascelles, K, Strug, L, Waters, P, De Bellescize, J, Vrielynck, P, De Saint Martin, A, Ville, D, Ryvlin, P, Arzimanoglou, A, Hirsch, E, Vincent, A
Published 2013Journal article -
2
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction. by Lesca, G, Rudolf, G, Bruneau, N, Lozovaya, N, Labalme, A, Boutry-Kryza, N, Salmi, M, Tsintsadze, T, Addis, L, Motte, J, Wright, S, Tsintsadze, V, Michel, A, Doummar, D, Lascelles, K, Strug, L, Waters, P, de Bellescize, J, Vrielynck, P, de Saint Martin, A, Ville, D, Ryvlin, P, Arzimanoglou, A, Hirsch, E, Vincent, A
Published 2013Journal article -
3
IDENTIFICATION OF A FIRST AND MAJOR GENE FOR ACQUIRED EPILEPTIC APHASIA (LANDAU-KLEFFNER SYNDROME) AND RELATED CHILDHOOD FOCAL EPILEPSIES AND ENCEPHALOPATHIES WITH SPEECH AND LANGU... by Lesca, G, Rudolf, G, Bruneau, N, Lozovaya, N, Labalme, A, Boutry-Kryza, N, Salmi, M, Tsintsadze, T, Addis, L, Motte, J, Wright, S, Tsintsadze, V, Michel, A, Doummar, D, Lascelles, K, Strug, L, Waters, P, de Bellescize, J, Vrielynck, P, de Saint Martin, A, Ville, D, Ryvlin, P, Arzimanoglou, A, Hirsch, E, Vincent, A
Published 2013Conference item