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PreviewIssue DateTitleAuthor(s)
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.
2003X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3Gedeon, A.; Nelson, J.; Gecz, J.; Mulley, J.
2010A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.
2004Genetic association studies in epilepsy: The truth is out thereTan, N.; Mulley, J.; Berkovic, S.
2000Genes for cognitive function: Developments on the XGecz, J.; Mulley, J.
2001Cloning and characterization of the human activity-dependent neuroprotective proteinZamostiano, R.; Pinhasov, A.; Gelber, E.; Steingart, R.; Seroussi, E.; Giladi, E.; Bassan, M.; Wollman, Y.; Eyre, H.; Mulley, J.; Brenneman, D.; Gozes, I.
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.
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.
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.
2006Genetic dissection of the common epilepsiesTan, N.; Mulley, J.; Scheffer, I.

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