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Results 1-10 of 97 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2011Allergic contact dermatitis: a case series and review for the ophthalmologistMorris, S.; Barlow, R.; Selva-Nayagam, D.; Malhotra, R.
2015Location and severity of root resorption related to impacted maxillary canines: a cone beam computed tomography (CBCT) evaluationDogramaci, E.; Sherriff, M.; Rossi-Fedele, G.; McDonald, F.
2009ASPREN surveillance system for influenza-like illness: a comparison with FluTracking and the National Notifiable Diseases Surveillance SystemParrella, A.; Dalton, C.B.; Pearce, R.; Litt, J.C.B.; Stocks, N.
2007Comparing cancer profiles and survival of Aboriginal and non-Aboriginal patients in South Australia: Where are the opportunities for improving Aboriginal healthCottrell, J.; Street, J.; Chong, A.; Roder, D.
2010The second national oral health survey of Vietnam - 1999: variation in the prevalence of dental diseasesRoberts-Thomson, K.; Do, L.; Spencer, A.; Hai, T.
2010The Second National Oral Health Survey of Vietnam, 1999: background and methodologyRoberts-Thomson, K.; Spencer, A.; Do, L.; Szuster, F.; Hai, T.; Nguyen, T.
2019Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2Corbett, M.A.; Kroes, T.; Veneziano, L.; Bennett, M.F.; Florian, R.; Schneider, A.L.; Coppola, A.; Licchetta, L.; Franceschetti, S.; Suppa, A.; Wenger, A.; Mei, D.; Pendziwiat, M.; Kaya, S.; Delledonne, M.; Straussberg, R.; Xumerle, L.; Regan, B.; Crompton, D.; van Rootselaar, A.-F.; et al.
2019Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmissionGuo, H.; Li, Y.; Shen, L.; Wang, T.; Jia, X.; Liu, L.; Xu, T.; Ou, M.; Hoekzema, K.; Wu, H.; Gillentine, M.A.; Liu, C.; Ni, H.; Peng, P.; Zhao, R.; Zhang, Y.; Phornphutkul, C.; Stegmann, A.P.A.; Prada, C.E.; Hopkin, R.J.; et al.
2019The performance of practitioners conducting facial comparisons on images of children across ageMichalski, D.; Heyer, R.; Semmler, C.; Schwenker, F.
2020Heterozygous rare genetic variants in non-syndromic early-onset obesitySerra-Juhé, C.; Martos-Moreno, G.; Bou de Pieri, F.; Flores, R.; Chowen, J.A.; Pérez-Jurado, L.A.; Argente, J.