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Results 51-56 of 56 (Search time: 0.001 seconds).
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PreviewIssue DateTitleAuthor(s)
2016Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsyCorbett, M.A.; Bellows, S.T.; Li, M.; Carroll, R.; Micallef, S.; Carvill, G.L.; Myers, C.T.; Howell, K.B.; Maljevic, S.; Lerche, H.; Gazina, E.V.; Mefford, H.C.; Bahlo, M.; Berkovic, S.F.; Petrou, S.; Scheffer, I.E.; Gecz, J.
2017Modelling predictors of molecular response to frontline imatinib for patients with chronic myeloid leukaemiaBanjar, H.; Ranasinghe, D.; Brown, F.; Adelson, D.; Kroger, T.; Leclercq, T.; White, D.; Hughes, T.; Chaudhri, N.; Speletas, M.
2014Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, global BPgen, and ICBP consortiaSimino, J.; Shi, G.; Bis, J.; Chasman, D.; Ehret, G.; Gu, X.; Guo, X.; Hwang, S.; Sijbrands, E.; Smith, A.; Verwoert, G.; Bragg-Gresham, J.; Cadby, G.; Chen, P.; Cheng, C.; Corre, T.; De Boer, R.; Goel, A.; Johnson, T.; Khor, C.; et al.
2018Long-term trends in singleton preterm birth in South Australia from 1986 to 2014Verburg, P.E.; Dekker, G.A.; Venugopal, K.; Scheil, W.; Erwich, J.J.H.; Mol, B.W.; Roberts, C.T.
2014Endogenous amylin and glucagon-like peptide-1 concentrations are not associated with gastric emptying in critical illnessSummers, M.; Di Bartolomeo, A.; Zaknic, A.; Chapman, M.; Nguyen, Q.; Zacharakis, B.; Rayner, C.; Horowitz, M.; Deane, A.
2019A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayMucha, B.E.; Banka, S.; Ajeawung, N.F.; Molidperee, S.; Chen, G.G.; Koenig, M.K.; Adejumo, R.B.; Till, M.; Harbord, M.; Perrier, R.; Lemyre, E.; Boucher, R.M.; Skotko, B.G.; Waxler, J.L.; Thomas, M.A.; Hodge, J.C.; Gecz, J.; Nicholl, J.; McGregor, L.; Linden, T.; et al.