Zobrazeno 1 - 10
of 171
pro vyhledávání: '"Renzoni EA"'
Autor:
Molyneaux, PL, Fahy, WA, Byrne, AJ, Braybrooke, R, Saunders, P, Toshner, R, Albers, G, Chua, F, Renzoni, EA, Wells, AU, Karkera, Y, Oballa, E, Saini, G, Nicholson, AG, Jenkins, G, Maher, TM
OBJECTIVES: Idiopathic pulmonary fibrosis (IPF) is a progressive and inevitably fatal condition for which there are a lack of effective biomarkers to guide therapeutic decision making. RATIONALE: To determine the relationship between serum levels of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::cb09d049c6a81360d9f5438da54ea8bd
http://hdl.handle.net/10044/1/96287
http://hdl.handle.net/10044/1/96287
Autor:
Kouranos, V, Ward, S, Kokosi, MA, Castillo, D, Chua, F, Judge, EP, Thomas, S, Van Tonder, F, Devaraj, A, Nicholson, AG, Maher, TM, Renzoni, EA, Wells, AU
Publikováno v:
CHEST
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
BACKGROUND: In cohort studies of pulmonary sarcoidosis, abnormal ventilatory patterns have generally been subdivided into restrictive and obstructive defects. Mixed ventilatory defects have largely been overlooked in pulmonary sarcoidosis, as total l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::82f97cb77d21e6cb7b153b89a7d87e4b
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=13532
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=13532
Autor:
George, PM, Spagnolo, P, Kreuter, M, Altinisik, G, Bonifazi, M, Martinez, FJ, Molyneaux, PL, Renzoni, EA, Richeldi, L, Tomassetti, S, Valenzuela, C, Vancheri, C, Varone, F, Cottin, V, Costabel, U
Within the spectrum of fibrosing interstitial lung diseases (ILDs) is a subset of patients who have inexorable progression of pulmonary fibrosis despite treatment, which is known as the progressive fibrotic phenotype. Although the concept of progress
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::03a51a933e915808d25aced2f19d3158
Autor:
George, PM, Spagnolo, P, Kreuter, M, Altinisik, G, Bonifazi, M, Martinez, FJ, Molyneaux, PL, Renzoni, EA, Richeldi, L, Tomassetti, S, Valenzuela, C, Vancheri, C, Varone, F, Cottin, V, Costabel, U, Erice ILD working group
Within the spectrum of fibrosing interstitial lung diseases (ILDs) is a subset of patients who have inexorable progression of pulmonary fibrosis despite treatment, which is known as the progressive fibrotic phenotype. Although the concept of progress
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::231267c2bd1b03beaac436abbb2d893e
http://hdl.handle.net/11577/3365628
http://hdl.handle.net/11577/3365628
Autor:
Barber, CM, Burge, PS, Feary, JR, Parfrey, H, Renzoni, EA, Spencer, LG, Walters, GI, Wiggans, RE, Adamali, H, Babu, S, Barrat, S, Basran, A, Beirne, P, Bianchi, S, Chalmers, G, Chaudhuri, N, Davies, S, Dempsey, O, Eccles, S, Fiddler, C, Foley, N, Forrest, I, Fletcher, S, George, P, Ghani, S, Gibbons, M, Greenstone, M, Hart, S, Hirani, N, Hoyle, J, Hoyles, R, Hutchinson, J, Jenkins, G, Judge, E, Kamath, A, Kokosi, M, Lee, C, Maher, T, Marshall, B, McAndrew, N, Molyneux, P, Morrison, D, O'Hickey, S, Porter, J, Renshaw, S, Sharp, C, Simler, N, Spears, M, Spiers, A, Spinks, K, Spiteri, M, Stenton, C, Sturney, S, Warburton, C, Wiscombe, S, Woodhead, F
Publikováno v:
Barber, CM, Burge, PS, Feary, JR, Parfrey, H, Renzoni, EA, Spencer, LG, Walters, GI, Wiggans, RE & Participants, GB HP S 2019, ' Identifying causation in hypersensitivity pneumonitis: a British perspective. ', BMJ Open Respiratory Research . https://doi.org/10.1136/bmjresp-2019-000469
BMJ Open Respiratory Research
BMJ Open Respiratory Research
BackgroundEstablishing whether patients are exposed to a ‘known cause’ is a key element in both the diagnostic assessment and the subsequent management of hypersensitivity pneumonitis (HP).ObjectiveThis study surveyed British interstitial lung di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57cb1c200344ccd337d54c63a6c0142b
http://hdl.handle.net/10044/1/75869
http://hdl.handle.net/10044/1/75869
Autor:
Evans, IC, Barnes, JL, Garner, IM, Pearce, DR, Maher, TM, Shiwen, X, Renzoni, EA, Wells, AU, Denton, CP, Laurent, GJ, Abraham, DJ, McAnulty, RJ
Publikováno v:
Clinical Science (London, England : 1979)
The present study demonstrates that hypermethylation and silencing of chromosome 8 open reading frame 4 (thyroid cancer protein 1, TC-1) (c8orf4), a transcriptional regulator of cyclooxygenase-2 (COX-2), is a major contributor to failure of fibroblas
Autor:
Keir, GJ, John Wort, S, Kokosi, M, George, PM, Walsh, SLF, Jacob, J, Price, L, Bax, S, Renzoni, EA, Maher, TM, MacDonald, P, Hansell, DM, Wells, AU
BACKGROUND AND OBJECTIVE: In interstitial lung disease (ILD), pulmonary hypertension (PH) is a major adverse prognostic determinant. Transthoracic echocardiography (TTE) is the most widely used tool when screening for PH, although discordance between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4e500770d76e1b3728a33b9fa45232fe
https://hdl.handle.net/10453/133660
https://hdl.handle.net/10453/133660
Autor:
Goh, NS, Hoyles, RK, Denton, CP, Hansell, DM, Renzoni, EA, Maher, TM, Nicholson, AG, Wells, AU
OBJECTIVE: To determine the prognostic value of pulmonary function test (PFT) trends at one and two years in interstitial lung disease associated with systemic sclerosis (SSc-ILD). METHODS: The prognostic significance of PFT trends at one year (n=162
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::08985691d913c3ed2434370e61498943
http://hdl.handle.net/10044/1/48422
http://hdl.handle.net/10044/1/48422