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PreviewIssue DateTitleAuthor(s)
2015Five-year survival of children with chronic critical illness in Australia and New ZealandNamachivayam, S.; Alexander, J.; Slater, A.; Millar, J.; Erickson, S.; Tibballs, J.; Festa, M.; Ganu, S.; Segedin, L.; Schlapbach, L.; Williams, G.; Shann, F.; Butt, W.
2015A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotypeTerhal, P.; Nievelstein, R.; Verver, E.; Topsakal, V.; van Dommelen, P.; Hoornaert, K.; Le Merrer, M.; Zankl, A.; Simon, M.; Smithson, S.; Marcelis, C.; Kerr, B.; Clayton-Smith, J.; Kinning, E.; Mansour, S.; Elmslie, F.; Goodwin, L.; van der Hout, A.; Veenstra-Knol, H.; Herkert, J.; et al.
2018The multifaceted presentation of chronic recurrent multifocal osteomyelitis: a series of 486 cases from the Eurofever international registryGirschick, H.; Finetti, M.; Orlando, F.; Schalm, S.; Insalaco, A.; Ganser, G.; Nielsen, S.; Herlin, T.; Koné-Paut, I.; Martino, S.; Cattalini, M.; Anton, J.; Al-Mayouf, S.; Hofer, M.; Quartier, P.; Boros, C.; Kuemmerle-Deschner, J.; Pires Marafon, D.; Alessio, M.; Schwarz, T.; et al.
2014Outcomes of repair of complete atrioventricular septal defect in the current eraXie, O.; Brizard, C.; D'udekem, Y.; Galati, J.; Kelly, A.; Yong, M.; Weintraub, R.; Konstantinov, I.
2014Development of paediatric biochemistry centile charts as a complement to laboratory reference intervalsLoh, T.; Antoniou, G.; Baghurst, P.; Metz, M.
2014Oxygen saturation targeting in preterm infants receiving continuous positive airway pressureLim, K.; Wheeler, K.; Gale, T.; Jackson, H.; Kihlstrand, J.; Sand, C.; Dawson, J.; Dargaville, P.
2013PRRT2 mutation in Japanese children with benign infantile epilepsyOkumura, A.; Shimojima, K.; Kubota, T.; Abe, S.; Yamashita, S.; Imai, K.; Okanishi, T.; Enoki, H.; Fukasawa, T.; Tanabe, T.; Dibbens, L.; Shimizu, T.; Yamamoto, T.
2014Genetics of hereditary neurological disorders in childrenHuang, Y.; Yu, S.; Wu, Z.; Tang, B.
2011An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutationsRatnayake, P.; Wakefield, C.; Meiser, B.; Suthers, G.; Price, M.; Duffy, J.; Tucker, K.
2010The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletionMacKinnon, R.; Selan, C.; Wall, M.; Baker, E.; Nandurkar, H.; Campbell, L.