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Results 1-10 of 34 (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.
2002Ectopic posterior pituitary lobe and periventricular heterotopia: cerebral malformations with the same underlying mechanism?Mitchell, L.; Thomas, P.; Zacharin, M.; Scheffer, I.
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.
2005SCN1A mutations and epiliepsyMulley, J.; Scheffer, I.; Petrou, S.; Dibbens, L.; Berkovic, S.; Harkin, L.
2004Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathyBerkovic, S.; Heron, S.; Giordano, L.; Marini, C.; Guerrini, R.; Kaplan, R.; Gambardella, A.; Steinlein, O.; Grinton, B.; Dean, J.; Bordo, L.; Hodgson, B.; Yamamoto, T.; Mulley, J.; Zara, F.; Scheffer, I.
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.
2006Genetic dissection of the common epilepsiesTan, N.; Mulley, J.; Scheffer, I.

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