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Results 51-57 of 57 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosisHerold, T.; Schneider, S.; Metzeler, K.; Neumann, M.; Hartmann, L.; Roberts, K.; Konstandin, N.; Greif, P.; Braeundl, K.; Ksienzyk, B.; Huk, N.; Schneider, I.; Zellmeier, E.; Jurinovic, V.; Mansmann, U.; Hiddemann, W.; Mullighan, C.; Bohlander, S.; Spiekermann, K.; Hoelzer, D.; et al.
2015Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013Global Burden of Disease Study 2013 Collaborators,; Vos, T.; Barber, R.; Bell, B.; Bertozzi-Villa, A.; Biryukov, S.; Bolliger, I.; Charlson, F.; Davis, A.; Degenhardt, L.; Dicker, D.; Duan, L.; Erskine, H.; Feigin, V.; Ferrari, A.; Fitzmaurice, C.; Fleming, T.; Graetz, N.; Guinovart, C.; Haagsma, J.; et al.
2022Microsatellite instability in young patients with rectal cancer: molecular findings and treatment responseZaborowski, A.M.; Abdile, A.; Adamina, M.; Aigner, F.; d'Allens, L.; Allmer, C.; Álvarez, A.; Anula, R.; Andric, M.; Atallah, S.; Bach, S.; Bala, M.; Barussaud, M.; Bausys, A.; Beggs, A.; Bellolio, F.; Bennett, M.-R.; Berdinskikh, A.; Bevan, V.; Biondo, S.; et al.
2020Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespanHollis, B.; Day, F.R.; Busch, A.S.; Thompson, D.J.; Soares, A.L.G.; Timmers, P.R.H.J.; Kwong, A.; Easton, D.F.; Joshi, P.K.; Timpson, N.J.; The PRACTICAL Consortium,; 23andMe Research Team,; Ong, K.K.; Perry, J.R.B.; Eeles, R.A.; Henderson, B.E.; Haiman, C.A.; Kote-Jarai, Z.; Schumacher, F.R.; Olama, A.A.A.; et al.
2020LekCheck: A Prospective Study to Identify Perioperative Modifiable Risk Factors for Anastomotic Leakage in Colorectal SurgeryHuisman, D.E.; Reudink, M.; van Rooijen, S.J.; Bootsma, B.T.; van de Brug, T.; Stens, J.; Bleeker, W.; Stassen, L.P.S.; Jongen, A.; Feo, C.V.; Targa, S.; Komen, N.; Kroon, H.M.; Sammour, T.; Lagae, E.; Talsma, A.K.; Wegdam, J.A.; de Vries Reilingh, T.S.; van Wely, B.; van Hoogstraten, M.J.; et al.
2011Progesterone receptor gene variants and risk of endometrial cancerO'Mara, T.; Fahey, P.; Ferguson, K.; Marquart, L.; Lambrechts, D.; Despierre, E.; Vergote, I.; Amant, F.; Hall, P.; Liu, J.; Czene, K.; SASBAC,; Rebbeck, T.; WISE Study Group,; AOCS Management Group,; SEARCH,; Ahmed, S.; Dunning, A.; Gregory, C.; Shah, M.; et al.
2019A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayMucha, B.E.; Banka, S.; Ajeawung, N.F.; Molidperee, S.; Chen, G.G.; Koenig, M.K.; Adejumo, R.B.; Till, M.; Harbord, M.; Perrier, R.; Lemyre, E.; Boucher, R.M.; Skotko, B.G.; Waxler, J.L.; Thomas, M.A.; Hodge, J.C.; Gecz, J.; Nicholl, J.; McGregor, L.; Linden, T.; et al.