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Results 1-10 of 13 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2007Fragile X Syndrome and other causes of X-Linked mental handicapSutherland, G.; Gecz, J.; Mulley, J.; Rimoin, D.; Connor, J.; Emery, A.; Pyeritz, R.; Korf, B.
2007Reduced cortical inhibition in a mouse model of familial childhood absence epilepsyTan, 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.
2007What is the role of genetics in epilepsy?Scheffer, I.; Dibbens, L.; Berkovic, S.; Mulley, J.; Sanjay Sisodiya,; Epilepsy Research Foundation workshop (6th : 2006 : Oxford, UK)
2007Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell linesMcRae, A.; Matigian, N.; Vadlamudi, L.; Mulley, J.; Mowry, B.; Martin, N.; Berkovic, S.; Hayward, N.; Visscher, P.
2007Temporal lobe epilepsy and GEFS(+) phenotypes associated with SCN1B mutationsScheffer, 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.
2007eneralized epilepsy with febrile seizures plus-associated sodium channel β1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel functionXu, R.; Thomas, E.; Gazina, E.; Richards, K.; Quick, M.; Wallace, R.; Harkin, L.; Heron, S.; Berkovic, S.; Scheffer, I.; Mulley, J.; Petrou, S.
2007A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channelXu, R.; Thomas, E.; Jenkins, M.; Gazina, E.; Chiu, C.; Heron, S.; Mulley, J.; Scheffer, I.; Berkovic, S.; Petrou, S.
2007Association studies and functional validation or functional validation alone?Heron, S.; Sanchez, L.; Scheffer, I.; Berkovic, S.; Mulley, J.
2007Channelopathies in idiopathic epilepsyHeron, S.; Scheffer, I.; Berkovic, S.; Dibbens, L.; Mulley, J.
2007Is 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.

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