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Preview	Issue Date	Title	Author(s)
	2005	SCN1A mutations and epiliepsy	Mulley, J.; Scheffer, I.; Petrou, S.; Dibbens, L.; Berkovic, S.; Harkin, L.
	2007	Temporal lobe epilepsy and GEFS(+) phenotypes associated with SCN1B mutations	Scheffer, I.; Harkin, L.; Grinton, B.; Dibbens, L.; Turner, S.; Zielinski, M.; Xu, R.; Jackson, G.; Adams, J.; Connellan, M.; Petrou, S.; Wellard, R.; Briellmann, R.; Wallace, R.; Mulley, J.; Berkovic, S.
	2002	Truncation of the GABAA-receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plus	Harkin, L.; Bowser, D.; Dibbens, L.; Singh, R.; Phillips, F.; Wallace, R.; Richards, M.; Williams, D.; Mulley, J.; Berkovic, S.; Scheffer, I.; Petrou, S.
	2005	Susceptibility genes for complex epilepsy	Mulley, J.; Scheffer, I.; Harkin, L.; Berkovic, S.; Dibbens, L.
	2001	Neuronal sodium-channel a1-subunit mutations in generalized epilepsy with febrile seizures plus	Wallace, R.; Scheffer, I.; Barnett, S.; Richards, M.; Dibbens, L.; Desai, R.; Lerman-Sagie, T.; Lev, D.; Mazarib, A.; Brand, N.; Ben-Zeev, B.; Goikhman, I.; Singh, R.; Kremmidiotis, G.; Gardner, A.; Sutherland, G.; George Jr., A.; Mulley, J.; Berkovic, S.
	2007	Channelopathies in idiopathic epilepsy	Heron, S.; Scheffer, I.; Berkovic, S.; Dibbens, L.; Mulley, J.
	2007	Is photosensitive epilepsy less common in males due to variation in X chromosome photopigment genes?	Taylor, I.; Hodgson, B.; Scheffer, I.; Mulley, J.; Berkovic, S.; Dibbens, L.
	2003	Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms	Wallace, R.; Hodgson, B.; Grinton, B.; Gardiner, R.; Robinson, R.; Rodriguez-Casero, V.; Sadleir, L.; Morgan, J.; Harkin, L.; Dibbens, L.; Yamamoto, T.; Andermann, E.; Mulley, J.; Berkovic, S.; Scheffer, I.
	2006	A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A	Mulley, J.; Nelson, P.; Guerrero, S.; Dibbens, L.; Iona, X.; McMahon, J.; Harkin, L.; Schouten, J.; Yu, S.; Berkovic, S.; Scheffer, I.