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Results 11-20 of 1391 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2012Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculatureKazenwadel, J.; Secker, G.; Liu, Y.; Rosenfeld, J.; Wildin, R.; Cuellar-Rodriguez, J.; Hsu, A.; Dyack, S.; Fernandez, C.; Chong, C.; Babic, M.; Bardy, P.; Shimamura, A.; Zhang, M.; Walsh, T.; Holland, S.; Hickstein, D.; Horwitz, M.; Hahn, C.; Scott, H.; et al.
2013Studies of nucleon resonance structure in exclusive meson electroproductionAznauryan, I.; Bashir, A.; Braun, V.; Brodsky, S.; Burkert, V.; Chang, L.; Chen, C.; El-Bennich, B.; Cloet, I.; Cole, P.; Edwards, R.; Fedotov, G.; Giannini, M.; Gothe, R.; Gross, F.; Lin, H.W.; Kroll, P.; Lee, T.S.; Melnitchouk, W.; Mokeev, V.; et al.
2010LPIN1 gene mutations: A major cause of severe rhabdomyolysis in early childhoodMichot, C.; Hubert, L.; Brivet, M.; De Meirleir, L.; Valayannopoulos, V.; Muller-Felber, W.; Venkateswaran, R.; Ogier, H.; Desguerre, I.; Altuzarra, C.; Thompson, E.; Smitka, M.; Huebner, A.; Husson, M.; Horvath, R.; Chinnery, P.; Vaz, F.; Munnich, A.; Elpeleg, O.; Delahodde, A.; et al.
2010Derepression of an endogenous long terminal repeat activates the CSF1R proto-oncogene in human lymphomaLamprecht, B.; Walter, K.; Kreher, S.; Kumar, R.; Hummel, M.; Lenze, D.; Kochert, K.; Bouhlel, M.; Richter, J.; Soler, E.; Stadhouders, R.; Johrens, K.; Wurster, K.; Callen, D.; Harte, M.; Giefing, M.; Barlow, R.; Stein, H.; Anagnostopoulos, I.; Janz, M.; et al.
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.
2013A genome-wide association study for malignant mesothelioma riskCadby, G.; Mukherjee, S.; Musk, A.; Reid, A.; Garlepp, M.; Dick, I.; Robinson, C.; Hui, J.; Fiorito, G.; Guarrera, S.; Beilby, J.; Melton, P.; Moses, E.; Ugolini, D.; Mirabelli, D.; Bonassi, S.; Magnani, C.; Dianzani, I.; Matullo, G.; Robinson, B.; et al.
2011Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)Roberts, A.; Nancarrow, D.; Clendenning, M.; Buchanan, D.; Jenkins, M.; Duggan, D.; Taverna, D.; McKeone, D.; Walters, R.; Walsh, M.; Young, B.; Jass, J.; Rosty, C.; Gattas, M.; Pelzer, E.; Hopper, J.; Goldblatt, J.; George, J.; Suthers, G.; Phillips, K.; et al.
2010Gastroparesis and functional dyspepsia: excerpts from the AGA/ANMS meetingParkman, H.; Camilleri, M.; Farrugia, G.; McCallum, R.; Bharucha, A.; Mayer, E.; Tack, J.; Spiller, R.; Horowitz, M.; Vinik, A.; Galligan, J.; Pasricha, P.; Kuo, B.; Szarka, L.; Marciani, L.; Jones, K.; Parrish, C.; Sandroni, P.; Abell, T.; Ordog, T.; et al.
2013Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin AReinstein, E.; Frentz, S.; Morgan, T.; Garcia-Minaur, S.; Leventer, R.; McGillivray, G.; Pariani, M.; van der Steen, A.; Pope, M.; Holder-Espinasse, M.; Scott, R.; Thompson, E.; Robertson, T.; Coppin, B.; Siegel, R.; Zurita, M.; Rodriguez, J.; Morales, C.; Rodrigues, Y.; Arcas, J.; et al.
2012Risk factors to predict the incidence of surgical adverse events following open or laparoscopic surgery for apparent early stage endometrial cancer: results from a randomised controlled trialKondalsamy-Chennakesavan, S.; Janda, M.; Gebski, V.; Baker, J.; Brand, A.; Hogg, R.; Jobling, T.W.; Land, R.; Manolitsas, T.; Nascimento, M.; Neesham, D.; Nicklin, J.L.; Oehler, M.K.; Otton, G.; Perrin, L.; Salfinger, S.; Hammond, I.; Leung, Y.; Sykes, P.; Ngan, H.; et al.