Adelaide Research & Scholarship
Browsing "University Library" by Author Nabbout, R.
Showing results 1 to 4 of 4
Preview | Issue Date | Title | Author(s) |
| 2013 | Do mutations in SCN1B cause Dravet syndrome? | Kim, Y.; Dibbens, L.; Marini, C.; Suls, A.; Chemaly, N.; Mei, D.; McMahon, J.; Iona, X.; Berkovic, S.; De Jonghe, P.; Guerrini, R.; Nabbout, R.; Scheffer, I. |
| 2006 | Exploration of the genetic architecture of idiopathic generalized epilepsies | Hempelmann, A.; Taylor, K.; Heils, A.; Lorenz, S.; Prud'Homme, J.; Nabbout, R.; Dulac, O.; Rudolf, G.; Zara, F.; Bianchi, A.; Robinson, R.; Gardiner, R.; Covanis, A.; Lindhout, D.; Stephani, U.; Elger, C.; Weber, Y.; Lerche, H.; Nurnberg, P.; Kron, K.; et al. |
| 2015 | Mutations in KCNT1 cause a spectrum of focal epilepsies | Møller, R.; Heron, S.; Larsen, L.; Lim, C.; Ricos, M.; Bayly, M.; Van Kempen, M.; Klinkenberg, S.; Andrews, I.; Kelley, K.; Ronen, G.; Callen, D.; McMahon, J.; Yendle, S.; Carvill, G.; Mefford, H.; Nabbout, R.; Poduri, A.; Striano, P.; Baglietto, M.; et al. |
| 2009 | SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis | Marini, C.; Scheffer, I.; Nabbout, R.; Mei, D.; Cox, K.; Dibbens, L.; McMahon, J.; Iona, X.; Carpintero, R.; Elia, M.; Cilio, M.; Specchio, N.; Giordano, L.; Striano, P.; Genarro, E.; Cross, J.; Kivity, S.; Neufeld, M.; Afawi, Z.; Andermann, E.; et al. |