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Results 1-10 of 43 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2004Familial partial epilepsy with variable foci: Clinical features and linkage to chromosome 22q12Berkovic, S.; Serratosa, J.; Phillips, H.; Xiong, L.; Andermann, E.; Diaz-Otero, F.; Gomez-Garre, P.; Martin, M.; Fernandez-Bullido, Y.; Andermann, F.; Lopes-Cendes, I.; Dubeau, F.; Desbiens, R.; Scheffer, I.; Wallace, R.; Mulley, J.; Pandolfo, M.
2003Channelopathies as a genetic cause of epilepsyMulley, J.; Scheffer, I.; Petrou, S.; Berkovic, S.
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.
2002Sodium-channel defects in benign familial neonatal-infantile seizuresHeron, S.; Crossland, K.; Andermann, E.; Phillips, H.; Hall, A.; Bleasel, A.; Shevell, M.; Mercho, S.; Seni, M.; Guiot, M.; Mulley, J.; Berkovic, S.; Scheffer, I.
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)
2000A de novo mutation in sporadic nocturnal frontal lobe epilepsyPhillips, H.; Marini, C.; Scheffer, I.; Sutherland, G.; Mulley, J.; Berkovic, S.
2013Do mutations in SCN1B cause Dravet syndrome?Kim, Y.; Dibbens, L.; Marini, C.; Suls, A.; Chemaly, N.; Mei, D.; McMahon, J.; Iona, X.; Berkovic, S.; De Jonghe, P.; Guerrini, R.; Nabbout, R.; Scheffer, I.
2014Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive declineKim, Y.; Bellows, S.; Mcmahon, J.; Iona, X.; Damiano, J.; Dibbens, L.; Kelley, K.; Gill, D.; Cross, J.; Berkovic, S.; Scheffer, I.
2005SCN1A mutations and epiliepsyMulley, J.; Scheffer, I.; Petrou, S.; Dibbens, L.; Berkovic, S.; Harkin, L.
2016Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsyBagnall, R.; Crompton, D.; Petrovski, S.; Lam, L.; Cutmore, C.; Garry, S.; Sadleir, L.; Dibbens, L.; Cairns, A.; Kivity, S.; Afawi, Z.; Regan, B.; Duflou, J.; Berkovic, S.; Scheffer, I.; Semsarian, C.

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