Zobrazeno 1 - 10
of 175
pro vyhledávání: '"Bem, D"'
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
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
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
Publikováno v:
In Value in Health June 2023 26(6) Supplement:S287-S287
Publikováno v:
In Value in Health December 2022 25(12) Supplement:S117-S117
Publikováno v:
In Value in Health January 2022 25(1) Supplement:S20-S21
Publikováno v:
PLOS ONE
PLoS ONE, Vol 13, Iss 5, p e0196877 (2018)
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
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
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