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Results 21-30 of 47 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2012Comparison of intraabdominal abscess formation after laparoscopic and open appendicectomies in childrenNataraja, R.; Teague, W.; Galea, J.; Moore, L.; Haddad, M.; Tsang, T.; Khurana, S.; Clarke, S.
2013Parental perspectives of vaccine safety and experience of adverse events following immunisationParrella, A.; Gold, M.; Marshall, H.; Braunack-Mayer, A.; Baghurst, P.
2010CP or not CP? A review of diagnoses in a cerebral palsy registerZarrinkalam, R.; Russo, R.; Gibson, C.; van Essen, P.; Peek, A.; Haan, E.
2010Preemptive alloimmune intervention in high-risk pediatric acute lymphoblastic leukemia patients guided by minimal residual disease level before stem cell transplantationLankester, A.; Bierings, M.; van Wering, E.; Wijkhuijs, A.; de Weger, R.; Wijnen, J.; Vossen, J.; Versluys, B.; Egeler, R.; van Tol, M.; Putter, H.; Revesz, T.; van Dongen, J.; van der Velden, V.; Schilham, M.
2010A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delayHaan, E.; Gecz, J.
2010Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective studyMcIntosh, A.; McMahon, J.; Dibbens, L.; Iona, X.; Mulley, J.; Scheffer, I.; Berkovic, S.
2011Functional performance in young Australian children with achondroplasiaIreland, P.; McGill, J.; Zankl, A.; Ware, R.; Pacey, V.; Ault, J.; Savarirayan, R.; Sillence, D.; Thompson, E.; Townshend, S.; Johnston, L.
2012Development in children with achondroplasia: a prospective clinical cohort studyIreland, P.; Donaghey, S.; McGill, J.; Zankl, A.; Ware, R.; Pacey, V.; Ault, J.; Savarirayan, R.; Sillence, D.; Thompson, E.; Townshend, S.; Johnston, L.
2012Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencingCalvo, S.; Compton, A.; Hershman, S.; Lim, S.; Lieber, D.; Tucker, E.; Laskowski, A.; Garone, C.; Liu, S.; Jaffe, D.; Christodoulou, J.; Fletcher, J.; Bruno, D.; Goldblatt, J.; DiMauro, S.; Thorburn, D.; Mootha, V.
2011De novo SCN1A mutations in migrating partial seizures of infancyCarranza Rojo, D.; Hamiwka, L.; McMahon, J.; Dibbens, L.; Arsov, T.; Suls, A.; Stodberg, T.; Kelley, K.; Wirrell, E.; Appleton, B.; Mackay, M.; Freeman, J.; Yendle, S.; Berkovic, S.; Bienvenu, T.; De Jonghe, P.; Thorburn, D.; Mulley, J.; Mefford, H.; Scheffer, I.