Zobrazeno 1 - 10
of 557
pro vyhledávání: '"Sabroe I"'
Autor:
Ammit Alaina, Sabroe I, Peck MJ, Van Keulen BJ, Jorritsma A, Simmons G, Clapham PR, Williams TJ, Pease JE
Publikováno v:
Respiratory Research, Vol 2, Pp 68565-25992 (2000)
Externí odkaz:
https://doaj.org/article/1593ccfc3563423b91ff25bc157f7138
Akademický článek
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Autor:
Wardle, M., Nair, A., Saunders, S., Armstrong, I., Charalampopoulos, A., Elliot, C., Hameed, A., Hamilton, N., Harrington, J., Keen, C., Lewis, R., Sabroe, I., Thompson, A.A.R., Kerry, R.M., Condliffe, R., Kiely, D.G.
Patients with pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension (PH) are at increased risk when undergoing anesthesia and major surgery. Data on outcomes for elective orthopedic surgery in patients with PH are limited.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::e8fe3108e6e17a21e475b7993da19a7d
Autor:
Kariotis, S, Jammeh, E, Swietlik, EM, Pickworth, JA, Rhodes, CJ, Otero, P, Wharton, J, Iremonger, J, Dunning, MJ, Pandya, D, Mascarenhas, TS, Errington, N, Thompson, AAR, Romanoski, CE, Rischard, F, Garcia, JGN, Yuan, JX-J, An, T-HS, Desai, AA, Coghlan, G, Lordan, J, Corris, PA, Howard, LS, Condliffe, R, Kiely, DG, Church, C, Pepke-Zaba, J, Toshner, M, Wort, S, Gräf, S, Morrell, NW, Wilkins, MR, Lawrie, A, Wang, D, Bleda, M, Hadinnapola, C, Haimel, M, Auckland, K, Tilly, T, Martin, JM, Yates, K, Treacy, CM, Day, M, Greenhalgh, A, Shipley, D, Peacock, AJ, Irvine, V, Kennedy, F, Moledina, S, MacDonald, L, Tamvaki, E, Barnes, A, Cookson, V, Chentouf, L, Ali, S, Othman, S, Ranganathan, L, Gibbs, JSR, DaCosta, R, Pinguel, J, Dormand, N, Parker, A, Stokes, D, Ghedia, D, Tan, Y, Ngcozana, T, Wanjiku, I, Polwarth, G, Mackenzie Ross, RV, Suntharalingam, J, Grover, M, Kirby, A, Grove, A, White, K, Seatter, A, Creaser-Myers, A, Walker, S, Roney, S, Elliot, CA, Charalampopoulos, A, Sabroe, I, Hameed, A, Armstrong, I, Hamilton, N, Rothman, AMK, Swift, AJ, Wild, JM, Soubrier, F, Eyries, M, Humbert, M, Montani, D, Girerd, B, Scelsi, L, Ghio, S, Gall, H, Ghofrani, A, Bogaard, HJ, Noordegraaf, AV, Houweling, AC, Veld, AHI, Schotte, G
Idiopathic pulmonary arterial hypertension (IPAH) is a rare but fatal disease diagnosed by right heart catheterisation and the exclusion of other forms of pulmonary arterial hypertension, producing a heterogeneous population with varied treatment res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::54d642bd341cee9decc1a0bef54e4884
https://eprints.gla.ac.uk/260156/1/260156.pdf
https://eprints.gla.ac.uk/260156/1/260156.pdf
Autor:
Mussell, G.T., Marshall, H., Smith, L.J., Biancardi, A.M., Hughes, P.J.C., Capener, D.J., Bray, J., Swift, A.J., Rajaram, S., Condliffe, A.M., Collier, G.J., Johns, C.S., Weatherley, N.D., Wild, J.M., Sabroe, I.
Background: Hyperpolarised gas MRI can be used to assess ventilation patterns. Previous studies have shown the image derived metric of ventilation defect percent (VDP) to correlate with FEV1/FVC and FEV1 in asthma.\ud \ud Objectives: To explore the u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::54ec7139732049a73af2bf37fdd91141
https://eprints.whiterose.ac.uk/176552/16/00785-2020.full.pdf
https://eprints.whiterose.ac.uk/176552/16/00785-2020.full.pdf
Autor:
Stewart, N.J., Smith, L.J., Chan, H.-F., Eaden, J.A., Rajaram, S., Swift, A.J., Weatherley, N.D., Biancardi, A., Collier, G.J., Hughes, D., Klafkowski, G., Johns, C.S., West, N., Ugonna, K., Bianchi, S.M., Lawson, R., Sabroe, I., Marshall, H., Wild, J.M.
The use of pulmonary MRI in a clinical setting has historically been limited. Whilst CT remains the gold-standard for structural lung imaging in many clinical indications, technical developments in ultrashort and zero echo time MRI techniques are beg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::37acac8624aa6e028966d94ef6b954db
https://eprints.whiterose.ac.uk/176562/3/bjr.20210207.pdf
https://eprints.whiterose.ac.uk/176562/3/bjr.20210207.pdf
Autor:
Burnap, S.A., Mayr, U., Shankar-Hari, M., Cuello, F., Thomas, M.R., Shah, A.M., Sabroe, I., Storey, R.F., Mayr, M.
We have previously shown that multimers of plasma pentraxin-3 (PTX3) were predictive of survival in patients with sepsis. To characterize the release kinetics and cellular source of plasma protein changes in sepsis, serial samples were obtained from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::c6c2bde3da217192dfb095b9600879ab
https://eprints.whiterose.ac.uk/172395/1/1-s2.0-S1535947620351355-main.pdf
https://eprints.whiterose.ac.uk/172395/1/1-s2.0-S1535947620351355-main.pdf
Autor:
Lewis, R.A., Billings, C.G., Hurdman, J.A., Smith, I.A., Austin, M., Armstrong, I.J., Middleton, J., Rothman, A.M.K., Harrington, J., Hamilton, N., Hameed, A.G., Thompson, A.A.R., Charalampopoulos, A., Elliot, C.A., Lawrie, A., Sabroe, I., Wild, J.M., Swift, A.J., Condliffe, R., Kiely, D.G.
Rationale: Exercise capacity predicts mortality in pulmonary arterial hypertension but limited data exist on the routine use of maximal exercise testing. Objectives: This study evaluates a simple to perform maximal test, the incremental shuttle walki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::e0afa9b583d01bd3f684f109a6506658
https://eprints.whiterose.ac.uk/166013/8/annalsats.202005-423oc.pdf
https://eprints.whiterose.ac.uk/166013/8/annalsats.202005-423oc.pdf
Autor:
Rawlings, G.H., Beail, N., Armstrong, I., Condliffe, R., Kiely, D.G., Sabroe, I., Thompson, A.R.
Objectives Pulmonary hypertension is a life-shortening disease that has a considerable impact on quality of life. Improving our understanding of how individuals are affected and cope with the disease will help to improve services and outcomes. This r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::99ba9e506bb2b5a8f223d564cce4fc7c
https://eprints.whiterose.ac.uk/169113/1/e041428.full.pdf
https://eprints.whiterose.ac.uk/169113/1/e041428.full.pdf
Autor:
Kariotis, S, Jammeh, E, Swietlik, EM, Pickworth, JA, Rhodes, CJ, Otero, P, Wharton, J, Iremonger, J, Dunning, MJ, Pandya, D, Mascarenhas, TS, Errington, N, Thompson, AAR, Romanoski, CE, Rischard, F, Garcia, JGN, Yuan, JX-J, An, T-HS, Desai, AA, Coghlan, G, Lordan, J, Corris, PA, Howard, LS, Condliffe, R, Kiely, DG, Church, C, Pepke-Zaba, J, Toshner, M, Wort, S, Graf, S, Morrell, NW, Wilkins, MR, Lawrie, A, Wang, D, Bleda, M, Hadinnapola, C, Haimel, M, Auckland, K, Tilly, T, Martin, JM, Yates, K, Treacy, CM, Day, M, Greenhalgh, A, Shipley, D, Peacock, AJ, Irvine, V, Kennedy, F, Moledina, S, MacDonald, L, Tamvaki, E, Barnes, A, Cookson, V, Chentouf, L, Ali, S, Othman, S, Ranganathan, L, Gibbs, JSR, DaCosta, R, Pinguel, J, Dormand, N, Parker, A, Stokes, D, Ghedia, D, Tan, Y, Ngcozana, T, Wanjiku, I, Polwarth, G, Mackenzie Ross, RV, Suntharalingam, J, Grover, M, Kirby, A, Grove, A, White, K, Seatter, A, Creaser-Myers, A, Walker, S, Roney, S, Elliot, CA, Charalampopoulos, A, Sabroe, I, Hameed, A, Armstrong, I, Hamilton, N, Rothman, AMK, Swift, AJ, Wild, JM, Soubrier, F, Eyries, M, Humbert, M, Montani, D, Girerd, B, Scelsi, L, Ghio, S, Gall, H, Ghofrani, A, Bogaard, HJ, Noordegraaf, AV, Houweling, AC, Veld, AHI, Schotte, G
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
UK National PAH Cohort Study Consortium 2021, ' Biological heterogeneity in idiopathic pulmonary arterial hypertension identified through unsupervised transcriptomic profiling of whole blood ', Nature Communications, vol. 12, no. 1, 7104 . https://doi.org/10.1038/s41467-021-27326-0
Nature Communications, 12(1):7104. Nature Publishing Group UK
Nature Communications
UK National PAH Cohort Study Consortium 2021, ' Biological heterogeneity in idiopathic pulmonary arterial hypertension identified through unsupervised transcriptomic profiling of whole blood ', Nature Communications, vol. 12, no. 1, 7104 . https://doi.org/10.1038/s41467-021-27326-0
Nature Communications, 12(1):7104. Nature Publishing Group UK
Nature Communications
Idiopathic pulmonary arterial hypertension (IPAH) is a rare but fatal disease diagnosed by right heart catheterisation and the exclusion of other forms of pulmonary arterial hypertension, producing a heterogeneous population with varied treatment res