Adelaide Research & Scholarship
Browsing "Paediatrics publications" by Author Sadleir, L.
Showing results 1 to 3 of 3
Preview | Issue Date | Title | Author(s) |
| 2012 | PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome | Heron, S.; Grinton, B.; Kivity, S.; Afawi, Z.; Zuberi, S.; Hughes, J.; Pridmore, C.; Hodgson, B.; Iona, X.; Sadleir, L.; Pelekanos, J.; Herlenius, E.; Goldberg-Stern, H.; Bassan, H.; Haan, E.; Korczyn, A.; Gardner, A.; Corbett, M.; Gecz, J.; Thomas, P.; et al. |
| 2013 | Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome | Mulley, J.; Hodgson, B.; McMahon, J.; Iona, X.; Bellows, S.; Mullen, S.; Farrell, K.; Mackay, M.; Sadleir, L.; Bleasel, A.; Gill, D.; Webster, R.; Wirrell, E.; Harbord, M.; Sisodiya, S.; Andermann, E.; Kivity, S.; Berkovic, S.; Scheffer, I.; Dibbens, L. |
| 2007 | The spectrum of SCNIA-related infantile epileptic encephalopathies | Harkin, L.; McMahon, J.; Iona, X.; Dibbens, L.; Pelekanos, J.; Zuberi, S.; Sadleir, L.; Andermann, E.; Gill, D.; Farrell, K.; Connolly, M.; Stanley, T.; Harbord, M.; Andermann, F.; Wang, J.; Batish, S.; Jones, J.; Seltzer, W.; Gardner, A.; Sutherland, G.; et al. |