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Results 31-40 of 41 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2015
HPV.edu study protocol: a cluster randomised controlled evaluation of education, decisional support and logistical strategies in school-based human papillomavirus (HPV) vaccination of adolescents
Skinner, S.R.
;
Davies, C.
;
Cooper, S.
;
Stoney, T.
;
Marshall, H.
;
Jones, J.
;
Collins, J.
;
Hutton, H.
;
Parrella, A.
;
Zimet, G.
;
Regan, D.G.
;
Whyte, P.
;
Brotherton, J.M.L.
;
Richmond, P.
;
McCaffrey, K.
;
Garland, S.M.
;
Leask, J.
;
Kang, M.
;
Braunack-Mayer, A.
;
Kaldor, J.
;
et al.
2012
Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010
Murray, C.
;
Vos, T.
;
Lozano, R.
;
Naghavi, M.
;
Flaxman, A.
;
Michaud, C.
;
Ezzati, M.
;
Shibuya, K.
;
Salomon, J.
;
Abdalla, S.
;
Aboyans, V.
;
Abraham, J.
;
Ackerman, I.
;
Aggarwal, R.
;
Ahn, S.
;
Ali, M.
;
Alvarado, M.
;
Anderson, H.
;
Anderson, L.
;
Andrews, K.
;
et al.
2012
Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010
Vos, T.
;
Flaxman, A.
;
Naghavi, M.
;
Lozano, R.
;
Michaud, C.
;
Ezzati, M.
;
Shibuya, K.
;
Salomon, J.
;
Abdalla, S.
;
Aboyans, V.
;
Abraham, J.
;
Ackerman, I.
;
Aggarwal, R.
;
Ahn, S.
;
Ali, M.
;
Alvarado, M.
;
Anderson, H.
;
Anderson, L.
;
Andrews, K.
;
Atkinson, C.
;
et al.
2017
Long-term efficacy and safety of α1 proteinase inhibitor treatment for emphysema caused by severe α1 antitrypsin deficiency: an open-label extension trial (RAPID-OLE)
McElvaney, N.
;
Burdon, J.
;
Holmes, M.
;
Glanville, A.
;
Wark, P.
;
Thompson, P.
;
Hernandez, P.
;
Chlumsky, J.
;
Teschler, H.
;
Ficker, J.
;
Seersholm, N.
;
Altraja, A.
;
Mäkitaro, R.
;
Chorostowska-Wynimko, J.
;
Sanak, M.
;
Stoicescu, P.
;
Piitulainen, E.
;
Vit, O.
;
Wencker, M.
;
Tortorici, M.
;
et al.
2018
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease
Branford, S.
;
Wang, P.
;
Yeung, D.T.
;
Thomson, D.
;
Purins, A.
;
Wadham, C.
;
Shahrin, N.H.
;
Marum, J.E.
;
Nataren, N.
;
Parker, W.T.
;
Geoghegan, J.
;
Feng, J.
;
Shanmuganathan, N.
;
Mueller, M.C.
;
Dietz, C.
;
Stangl, D.
;
Donaldson, Z.
;
Altamura, H.
;
Georgievski, J.
;
Braley, J.
;
et al.
2018
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
Frints, S.G.M.
;
Ozanturk, A.
;
Rodríguez Criado, G.
;
Grasshoff, U.
;
de Hoon, B.
;
Field, M.
;
Manouvrier-Hanu, S.
;
E Hickey, S.
;
Kammoun, M.
;
Gripp, K.W.
;
Bauer, C.
;
Schroeder, C.
;
Toutain, A.
;
Mihalic Mosher, T.
;
Kelly, B.J.
;
White, P.
;
Dufke, A.
;
Rentmeester, E.
;
Moon, S.
;
Koboldt, D.C.
;
et al.
2018
A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency
Jansen, S.
;
Hoischen, A.
;
Coe, B.
;
Carvill, G.
;
van Esch, H.
;
Bosch, D.
;
Andersen, U.
;
Baker, C.
;
Bauters, M.
;
Bernier, R.
;
van Bon, B.
;
Claahsen-van der Grinten, H.
;
Gecz, J.
;
Gilissen, C.
;
Grillo, L.
;
Hackett, A.
;
Kleefstra, T.
;
Koolen, D.
;
Kvarnung, M.
;
Larsen, M.
;
et al.
2016
Characterization of leukemias with ETV6-ABL1 fusion
Zaliova, M.
;
Moorman, A.V.
;
Cazzaniga, G.
;
Stanulla, M.
;
Harvey, R.C.
;
Roberts, K.G.
;
Heatley, S.L.
;
Loh, M.L.
;
Konopleva, M.
;
Chen, I.M.
;
Zimmermannova, O.
;
Schwab, C.
;
Smith, O.
;
Mozziconacci, M.J.
;
Chabannon, C.
;
Kim, M.
;
Frederik Falkenburg, J.H.
;
Norton, A.
;
Marshall, K.
;
Haas, O.A.
;
et al.
;
Annual Meeting of the American-Society-of-Hematology (5 Dec 2015 - 8 Dec 2015 : Orlando, FL)
2012
Common values in assessing health outcomes from disease and injury: Disability weights measurement study for the Global Burden of Disease Study 2010
Salomon, J.A.
;
Vos, T.
;
Hogan, D.R.
;
Gagnon, M.
;
Naghavi, M.
;
Mokdad, A.
;
Begum, N.
;
Shah, R.
;
Karyana, M.
;
Kosen, S.
;
Farje, M.R.
;
Moncada, G.
;
Dutta, A.
;
Sazawal, S.
;
Dyer, A.
;
Seiler, J.
;
Aboyans, V.
;
Baker, L.
;
Baxter, A.
;
Benjamin, E.J.
;
et al.
2017
Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosis
Herold, 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.
Discover
Author
5
Vos, T.
3
Aboyans, V.
3
Anderson, H.
3
Andrews, K.
3
Flaxman, A.
3
Naghavi, M.
3
Shibuya, K.
2
Abdalla, S.
2
Abraham, J.
2
Ackerman, I.
.
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Subject
41
Humans
38
Female
33
Adult
29
Young Adult
24
Child
24
Middle Aged
18
Child, Preschool
12
Aged
12
Infant
10
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2015
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2012
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