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Preview	Issue Date	Title	Author(s)
	2009	Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?	Scheffer, I.; Zhang, Y.; Jansen, F.; Dibbens, L.
	2009	Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance	Dibbens, L.; Mullen, S.; Helbig, I.; Mefford, H.; Bayly, M.; Bellows, S.; Leu, C.; Trucks, H.; Obermeier, T.; Wittig, M.; Franke, A.; Caglayan, H.; Yapici, Z.; Sander, T.; Eichler, E.; Scheffer, I.; Mulley, J.; Berkovic, S.
	2009	The role of neuronal GABAA receptor subunit mutations in idiopathic generalized epilepsies	Dibbens, L.; Harkin, L.; Richards, M.; Hodgson, B.; Clarke, A.; Petrou, S.; Scheffer, I.; Berkovic, S.; Mulley, J.
	2009	Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?	Sijben, A.; Sithinamsuwan, P.; Radhakrishnan, A.; Badawy, R.; Dibbens, L.; Mazarib, A.; Lev, D.; Lerman-Sagie, T.; Straussberg, R.; Berkovic, S.; Scheffer, I.
	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.
	2009	Chipping away at the common epilepsies with complex genetics: the 15q13.3 microdeletion shows the way	Mulley, J.; Dibbens, L.
	2009	SCARB2 Mutations in Progressive Myoclonus Epilepsy (PME) Without Renal Failure	Dibbens, L.; Michelucci, R.; Gambardella, A.; Andermann, F.; Rubboli, G.; Bayly, M.; Joensuu, T.; Vears, D.; Franceschetti, S.; Canafoglia, L.; Wallace, R.; Bassuk, A.; Power, D.; Tassinari, C.; Andermann, E.; Lehesjoki, A.; Berkovic, S.