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Results 1-10 of 27
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Issue DateTitleAuthor(s)
28-Apr-2019An activated-platelet-sensitive nanocarrier enables targeted delivery of tissue plasminogen activator for effective thrombolytic therapyHuang, Y; Yu, L; Ren, J; Gu, B; Longstaff, C, et al
5-Mar-2019Derivation and validation of a cardiovascular risk score for prediction of major acute cardiovascular events in non-alcoholic fatty liver disease; the importance of an elevated mean platelet volumeAbeles, RD; Mullish, BH; Forlano, R; Kimhofer, T; Adler, M, et al
7-Jan-2019Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic lociErzurumluoglu, AM; Chambers, JC; Elliott, P; Evangelou, E; Kooner, JS, et al
29-Jan-2019Multi-ancestry genome-wide association study of lipid levels incorporating gene-alcohol interactionsDe Vries, PS; Brown, MR; Bentley, AR; Sung, YJ; Winkler, TW, et al
7-Mar-2019Mathematical modelling of intravenous thrombolysis in acute ischaemic stroke: Effects of dose regimens on levels of fibrinolytic proteins and clot lysis timeGu, B; Piebalgs, A; Huang, Y; Longstaff, C; Hughes, A, et al
1-Apr-2019THU-331. Derivation and validation of a cardiovascular risk score for prediction of major acute cardiovascular events in non-alcoholic fatty liver disease: The importance of an elevated mean platelet volumeAbeles, RD; Mullish, BH; Forlano, R; Adler, M; Giannakeas, N, et al
16-Apr-2019Genetic variants associated with cancer therapy-induced cardiomyopathyGarcia-Pavia, P; Kim, Y; Restrepo-Cordoba, A; Ware, J; Barton, PJR, et al
25-Mar-2019Cutaneous polyarteritis nodosa presenting atypically with severe pharyngeal ulcerationMason, J; Olabi, B; Farah, Z; Imperial College Healthcare NHS Trust- BRC Funding
1-Jan-2019Fetal growth, stillbirth, infant mortality and other birth outcomes near UK municipal waste incinerators; retrospective population based cohort and case-control studyGhosh, R; Freni Sterrantino, A; Douglas, P; Parkes, B; Fecht, D, et al
29-Jan-2019Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: The case of hypertrophic cardiomyopathyWalsh, R; Mazzarotto, F; Whiffin, N; Buchan, R; Midwinter, W, et al