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Autor:
Leo, V.C. *, Morgan, N.V., Bem, D., Jones, M.L., Lowe, G.C., Lordkipanidzé, M., Drake, S., Simpson, M.A., Gissen, P., Mumford, A., Watson, S.P., Daly, M.E.
Publikováno v:
In Journal of Thrombosis and Haemostasis April 2015 13(4):643-650
Publikováno v:
In Value in Health June 2024 27(6) Supplement:S67-S67
Akademický článek
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Autor:
Rozenbaum MH; Pfizer Inc., Capelle a/d IJssel, The Netherlands., Begier E; Pfizer Vaccines, Dublin, Ireland. Elizabeth.Begier@pfizer.com., Kurosky SK; Pfizer Inc., New York, NY, USA., Whelan J; HEOR Ltd, Cardiff, UK., Bem D; HEOR Ltd, Cardiff, UK., Pouwels KB; University of Oxford, Oxford, UK., Postma M; University of Groningen, Groningen, The Netherlands., Bont L; University Medical Center Utrecht, Utrecht, The Netherlands.
Publikováno v:
Infectious diseases and therapy [Infect Dis Ther] 2023 Jun; Vol. 12 (6), pp. 1487-1504. Date of Electronic Publication: 2023 May 23.
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
https://www.repository.cam.ac.uk/handle/1810/317770
Autor:
Makumi SW; Materials Science and Engineering Department, University of Utah, Salt Lake City, UT, United States of America.; Department of Physics, Kenyatta University, Nairobi, Kenya., Bem D; Department of Physics, Kenyatta University, Nairobi, Kenya., Musila N; Department of Physics, Kenyatta University, Nairobi, Kenya., Foss C; Electrical and Computer Engineering, University of Massachusetts Amherst, Amherst, MA, United States of America., Aksamija Z; Materials Science and Engineering Department, University of Utah, Salt Lake City, UT, United States of America.; Electrical and Computer Engineering, University of Massachusetts Amherst, Amherst, MA, United States of America.
Publikováno v:
Journal of physics. Condensed matter : an Institute of Physics journal [J Phys Condens Matter] 2023 Feb 17; Vol. 35 (15). Date of Electronic Publication: 2023 Feb 17.
Publikováno v:
In Value in Health June 2023 26(6) Supplement:S287-S287
Autor:
Smith, Isaac H.1 (AUTHOR), DeTienne, Kristen Bell1 (AUTHOR), Ingerson, Marc-Charles2 (AUTHOR), Cherrington, David J.1 (AUTHOR)
Publikováno v:
Academy of Management Review. Nov2024, p1-27. 27p.
Publikováno v:
In Value in Health December 2022 25(12) Supplement:S117-S117
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
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