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Preview	Issue Date	Title	Author(s)
	2003	Channelopathies as a genetic cause of epilepsy	Mulley, J.; Scheffer, I.; Petrou, S.; Berkovic, S.
	2007	Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy	Tan, H.; Reid, C.; Single, F.; Davies, P.; Chiu, C.; Murphy, S.; Clarke, A.; Dibbens, L.; Krestel, H.; Mulley, J.; Jones, M.; Seeburg, P.; Sakmann, B.; Berkovic, S.; Sprengel, R.; Petrou, S.
	2005	SCN1A mutations and epiliepsy	Mulley, J.; Scheffer, I.; Petrou, S.; Dibbens, L.; Berkovic, S.; Harkin, L.
	2002	Altered kinetics and benzodiazepine sensitivity of a GABAA receptor subunit mutation [g2(R43Q)] found in human epilepsy	Bowser, D.; Wagner, D.; Czajkowski, C.; Cromer, B.; Parker, M.; Wallace, R.; Harkin, L.; Mulley, J.; Marini, C.; Berkovic, S.; Williams, D.; Jones, M.; Petrou, S.
	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.
	2006	Human epilepsies: interaction of genetic and acquired factors	Berkovic, S.; Mulley, J.; Scheffer, I.; Petrou, S.
	2007	eneralized epilepsy with febrile seizures plus-associated sodium channel β1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function	Xu, R.; Thomas, E.; Gazina, E.; Richards, K.; Quick, M.; Wallace, R.; Harkin, L.; Heron, S.; Berkovic, S.; Scheffer, I.; Mulley, J.; Petrou, S.
	2001	Mutant GABAA receptor g2-subunit in childhood absence epilepsy and febrile seizures	Wallace, R.; Marini, C.; Petrou, S.; Harkin, L.; Bowser, D.; Panchal, R.; Williams, D.; Sutherland, G.; Mulley, J.; Scheffer, I.; Berkovic, S.
	2007	A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel	Xu, R.; Thomas, E.; Jenkins, M.; Gazina, E.; Chiu, C.; Heron, S.; Mulley, J.; Scheffer, I.; Berkovic, S.; Petrou, S.