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Results 31-40 of 78 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2010PHF6 mutations in T-cell acute lymphoblastic leukemiaVan Vlierberghe, P.; Palomero, T.; Khiabanian, H.; Van der Meulen, J.; Castillo, M.; Van Roy, N.; De Moerloose, B.; Philippe, J.; Gonzalez-Garcia, M.; Toribio, M.; Taghon, T.; Zuurbier, L.; Cauwelier, B.; Harrison, C.; Schwab, C.; Pisecker, M.; Strehl, S.; Langerak, A.; Gecz, J.; Sonneveld, E.; et al.
2011Calculating the mean amplitude of glycemic excursion from continuous glucose monitoring data: An automated algorithmBaghurst, P.
2010Discrepancy in factor VIII 1-stage/2-stage activity in a child with Arg(531) -> His mutationNath, S.; Williams, V.; Griffiths, A.; Revesz, T.
2011Clinical effects and treatment of envenoming by Hoplocephalus spp. snakes in Australia: Australian Snakebite Project (ASP-12)Isbister, G.; White, J.; Currie, B.; O'Leary, M.; Brown, S.
2013Gastroesophageal reflux, esophageal function, gastric emptying, and the relationship to dysphagia before and after antireflux surgery in childrenLoots, C.; Van Herwaarden, M.; Benninga, M.; VanderZee, D.; van Wijk, M.; Omari, T.
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.