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Results 11-20 of 30 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2011MLVA and phage typing as complementary tools in the epidemiological investigation of Salmonella enterica serovar typhimurium clustersRoss, I.; Davos, D.; Mwanri, L.; Raupach, J.; Heuzenroeder, M.
2003Analysis of CFTR mutation screening in cases of isolated fetal echogenic bowel in the South Australian populationNicholls, C.; Nelson, P.; Poplawski, N.; Chin, S.; Fong, B.; Solly, P.; Fietz, M.; Fletcher, J.
2011A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxiaCorbett, M.; Schwake, M.; Bahlo, M.; Dibbens, L.; Lin, M.; Gandolfo, L.; Vears, D.; O'Sullivan, J.; Robertson, T.; Bayly, M.; Gardner, A.; Vlaar, A.; Korenke, G.; Bloem, B.; de Coo, I.; Verhagen, J.; Lehesjoki, A.; Gecz, J.; Berkovic, S.
2003Dietry intakes and food sources of omega-6 and omega-3 polyunsaturated fatty acidsMeyer, B.; Mann, N.; Lewis, J.; Milligan, G.; Sinclair, A.; Howe, P.
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.
2013Mutations in DEPDC5 cause familial focal epilepsy with variable fociDibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; 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.
2011Deteriorating pneumococcal-specific B-cell memory in minimally symptomatic African children with HIV infectionIwajomo, O.; Finn, A.; Moons, P.; Nkhata, R.; Sepako, E.; Ogunniyi, A.; Williams, N.; Heyderman, R.
2001CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyPhillips, H.; Favre, I.; Kirkpatrick, M.; Zuberi, S.; Goudie, D.; Heron, S.; Scheffer, I.; Sutherland, G.; Berkovic, S.; Bertrand, D.; Mulley, J.
2008Treatment of scedosporiosis with Voriconazole: Clinical experience with 107 patientsTroke, P.; Aguirrebengoa, K.; Arteaga, C.; Ellis, D.; Heath, C.; Lutsar, I.; Rovira, M.; Nguyen, Q.; Slavin, M.; Chen, S.

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