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Results 11-20 of 42 (Search time: 0.006 seconds).
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PreviewIssue DateTitleAuthor(s)
2003Channelopathies as a genetic cause of epilepsyMulley, J.; Scheffer, I.; Petrou, S.; Berkovic, 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.
2005Susceptibility genes for complex epilepsyMulley, J.; Scheffer, I.; Harkin, L.; Berkovic, S.; Dibbens, L.
2002Altered kinetics and benzodiazepine sensitivity of a GABAA receptor subunit mutation [g2(R43Q)] found in human epilepsyBowser, 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.
2002Truncation of the GABAA-receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plusHarkin, L.; Bowser, D.; Dibbens, L.; Singh, R.; Phillips, F.; Wallace, R.; Richards, M.; Williams, D.; Mulley, J.; Berkovic, S.; Scheffer, I.; Petrou, S.
2001Mutant GABAA receptor g2-subunit in childhood absence epilepsy and febrile seizuresWallace, R.; Marini, C.; Petrou, S.; Harkin, L.; Bowser, D.; Panchal, R.; Williams, D.; Sutherland, G.; Mulley, J.; Scheffer, I.; Berkovic, S.
2006Human epilepsies: interaction of genetic and acquired factorsBerkovic, S.; Mulley, J.; Scheffer, I.; Petrou, S.
2006De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective studyBerkovic, S.; Harkin, L.; McMahon, J.; Pelekanos, J.; Zuberi, S.; Wirrell, E.; Gill, D.; Iona, X.; Mulley, J.; Scheffer, I.
2001Neuronal sodium-channel a1-subunit mutations in generalized epilepsy with febrile seizures plusWallace, 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.
2000A de novo mutation in sporadic nocturnal frontal lobe epilepsyPhillips, H.; Marini, C.; Scheffer, I.; Sutherland, G.; Mulley, J.; Berkovic, S.