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Results 1-10 of 35 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2007A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyCavalleri, G.; Walley, N.; Soranzo, N.; Mulley, J.; Doherty, C.; Kapoor, A.; Depondt, C.; Lynch, J.; Scheffer, I.; Heils, A.; Gehrmann, A.; Kinirons, P.; Gandhi, S.; Satishchandra, P.; Wood, N.; Anand, A.; Sander, T.; Berkovic, S.; Delanty, N.; Goldstein, D.; et al.
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.
2011Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patientsConlin, L.; Kramer, W.; Hutchinson, A.; Li, X.; Riethman, H.; Hakonarson, H.; Mulley, J.; Scheffer, I.; Berkovic, S.; Hosain, S.; Spinner, N.
2007What is the role of genetics in epilepsy?Scheffer, I.; Dibbens, L.; Berkovic, S.; Mulley, J.; Epilepsy Research Foundation workshop (6th : 2006 : Oxford, UK)
2006A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1AMulley, J.; Nelson, P.; Guerrero, S.; Dibbens, L.; Iona, X.; McMahon, J.; Harkin, L.; Schouten, J.; Yu, S.; Berkovic, S.; Scheffer, I.
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.
2006Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adultsJansen, F.; Sadleir, L.; Harkin, L.; Vadlamudi, L.; McMahon, J.; Mulley, J.; Scheffer, I.; Berkovic, 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.