EE57 Missed Opportunities? Gaps in Capturing the Full Value of Vaccination Across Health Economic Studies of COVID-19 Vaccination

Autor: Bem, D, Nassim, M, Wang, X, Van, de Velde N, Beck, E, Pritchard, C, Joshi, K

Publikováno v: In Value in Health June 2024 27(6) Supplement:S67-S67

Stroke risk following traumatic brain injury: Systematic review and meta-analysis

Autor: Turner, GM, McMullan, C, Aiyegbusi, OL, Bem, D, Marshall, T, Calvert, M, Mant, J, Belli, A

Background Traumatic brain injury (TBI) is a global health problem; worldwide, >60 million people experience a TBI each year and incidence is rising. TBI has been proposed as an independent risk factor for stroke. Aims To investigate the association

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f33a3448465668227b0bce9d47c0db7d
https://www.repository.cam.ac.uk/handle/1810/317770

EE320 Humanistic and Economic Burden of Advanced Hepatocellular Carcinoma: A Systematic Review

Autor: Bem, D, Shephard, C, Gaughan, A, Zile, I, Qin, L

Publikováno v: In Value in Health December 2022 25(12) Supplement:S117-S117

Transcatheter aortic valve implantation for aortic stenosis in high surgical risk patients: A systematic review and meta-analysis

Autor: Liu, Z, Kidney, E, Bem, D, Bramley, G, Bayliss, S, de Belder, MA, Cummins, C, Duarte, R

Publikováno v: PLOS ONE
PLoS ONE, Vol 13, Iss 5, p e0196877 (2018)
PLoS ONE

Background Symptomatic aortic stenosis has a poor prognosis. Many patients are considered inoperable or at high surgical risk for surgical aortic valve replacement (SAVR), reflecting their age, comorbidities and frailty. The clinical effectiveness an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d9e510db18d146cdca36081692637d68

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

Autor: Johnson, B., Lowe, G.C., Futterer, J., Lordkipanidze', M., MacDonald, D., Simpson, M.A., Sanchez Guiu', I., Drake, S., Bem, D., Leo, V., Fletcher, S.J., Dawood, B., Rivera, J., Allsup, D., Biss, T., Bolton-Maggs, P.H.B., Collins, P., Curry, N., Grimley, C., James, B., Makris, M., Motwani, J., Pavord, S., Talks, K., Thachil, J., Wilde, J., Williams, M., Harrison, P., Gissen, P., Mundell, S., Mumford, A., Daly, M.E., Watson, S.P., Morgan, N.V.

Publikováno v: Johnson, B, Lowe, G C, Futterer, J, Lordkipanidze', M, MacDonald, D, Simpson, M A, Sanchez Guiu', I, Drake, S, Bem, D, Leo, V, Fletcher, S J, Dawood, B, Rivera, J, Allsup, D, Biss, T, Bolton-Maggs, P H B, Collins, P, Curry, N, Grimley, C, James, B, Makris, M, Motwani, J, Pavord, S, Talks, K, Thachil, J, Wilde, J, Williams, M, Harrison, P, Gissen, P, Mundell, S J, Mumford, A, Daly, M E, Watson, S P, Morgan, N V 2016, ' Whole Exome Sequencing Identifies Genetic Variants In Inherited Thrombocytopenia With Secondary Qualitative Function Defects ', Haematologica, vol. 101, no. 10, pp. 1170-1179 . https://doi.org/10.3324/haematol.2016.146316
Johnson, B, Lowe, G C, Futterer, J, Lordkipanidzé, M, Macdonald, D, Simpson, M A, Sanchez-Guiú, I, Drake, S, Bem, D, Leo, V, Fletcher, S J, Dawood, B, Rivera, J, Allsup, D, Biss, T, Bolton-Maggs, P H, Collins, P, Curry, N, Grimley, C, James, B, Makris, M, Motwani, J, Pavord, S, Talks, K, Thachil, J, Wilde, J, Williams, M, Harrison, P, Gissen, P, Mundell, S, Mumford, A, Daly, M E, Watson, S P & Morgan, N V 2016, ' Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects ', Haematologica, vol. 101, no. 10, pp. 1170-1179 . https://doi.org/10.3324/haematol.2016.146316

Inherited thrombocytopenias are a heterogeneous group of disorders characterised\ud by abnormally low platelet counts which can be associated with abnormal bleeding.\ud Next generation sequencing has previously been employed in these disorders for th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4b64ab9faae29a46020c07215abdb67a