Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Katie J Bayfield"'
Autor:
Eric WFW Alton, David K Armstrong, Deborah Ashby, Katie J Bayfield, Diana Bilton, Emily V Bloomfield, A Christopher Boyd, June Brand, Ruaridh Buchan, Roberto Calcedo, Paula Carvelli, Mario Chan, Seng H Cheng, David S Collie, Steve Cunningham, Heather E Davidson, Gwyneth Davies, Jane C Davies, Lee A Davies, Maria H Dewar, Ann Doherty, Jackie Donovan, Natalie S Dwyer, Hala I Elgmati, Rosanna F Featherstone, Jemyr Gavino, Sabrina Gea-Sorli, Duncan M Geddes, James SR Gibson, Deborah R Gill, Andrew P Greening, Uta Griesenbach, David M Hansell, Katharine Harman, Tracy E Higgins, Samantha L Hodges, Stephen C Hyde, Laura Hyndman, J Alastair Innes, Joseph Jacob, Nancy Jones, Brian F Keogh, Maria P Limberis, Paul Lloyd-Evans, Alan W Maclean, Michelle C Manvell, Dominique McCormick, Michael McGovern, Gerry McLachlan, Cuixiang Meng, M Angeles Montero, Hazel Milligan, Laura J Moyce, Gordon D Murray, Andrew G Nicholson, Tina Osadolor, Javier Parra-Leiton, David J Porteous, Ian A Pringle, Emma K Punch, Kamila M Pytel, Alexandra L Quittner, Gina Rivellini, Clare J Saunders, Ronald K Scheule, Sarah Sheard, Nicholas J Simmonds, Keith Smith, Stephen N Smith, Najwa Soussi, Samia Soussi, Emma J Spearing, Barbara J Stevenson, Stephanie G Sumner-Jones, Minna Turkkila, Rosa P Ureta, Michael D Waller, Marguerite Y Wasowicz, James M Wilson, Paul Wolstenholme-Hogg, on behalf of the UK Cystic Fibrosis Gene Therapy Consortium
Publikováno v:
Efficacy and Mechanism Evaluation, Vol 3, Iss 5 (2016)
Background: Cystic fibrosis (CF) is a chronic, life-limiting disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene leading to abnormal airway surface ion transport, chronic lung infections, inflammation and eventual re
Externí odkaz:
https://doaj.org/article/09b29fe1b155492fba24a177fe4be24c
Publikováno v:
ERJ Open Research, Vol 6, Iss 1 (2020)
Externí odkaz:
https://doaj.org/article/1946be440e4f4341934b8b748ed94a98
Publikováno v:
ERJ Open Research, Vol 5, Iss 4 (2019)
Multiple-breath washout (MBW) can be performed with different gases (sulfur hexafluoride (SF6) and nitrogen (N2)) and different devices, all of which give discrepant results. This study aimed to confirm previously reported differences and explore f
Externí odkaz:
https://doaj.org/article/2444ddc754d84cdb9a2ef0190105ba50
Autor:
Ediane De Queiroz Andrade, Katie J. Bayfield, Anneliese Blaxland, Alexander Wong, Patricia De Gouveia Belinelo, Peter D. Sly, Adam Collison, Vanessa E. Murphy, Peter Gibson, Joerg Mattes, Paul D. Robinson
Publikováno v:
Pediatric Pulmonology. 57:1089-1091
Autor:
Ediane, De Queiroz Andrade, Katie J, Bayfield, Anneliese, Blaxland, Alexander, Wong, Patricia, De Gouveia Belinelo, Peter D, Sly, Adam, Collison, Vanessa E, Murphy, Peter, Gibson, Joerg, Mattes, Paul D, Robinson
Publikováno v:
Pediatric pulmonologyREFERENCES. 57(4)
Autor:
Alex Horsley, Katie J Bayfield, Jacky Smith, Anna Shawcross, Francis J Gilchrist, Andrew M. Jones, B. Bianco, Steve Cunningham, Catherine Fullwood, John Belcher, Anirban Maitra
Publikováno v:
Horsley, A, Belcher, J, Bayfield, K J, Bianco, B G, Cunningham, S, Fullwood, C, Jones, A M, Shawcross, A, Smith, J, Maitra, A & Gilchrist, F J 2022, ' Longitudinal assessment of lung clearance index to monitor disease progression in children and adults with cystic fibrosis ', Thorax, vol. 77, no. 4, pp. 357-363 . https://doi.org/10.1136/thoraxjnl-2021-216928
Horsley, A, Belcher, J, Bayfield, K J, Bianco, B, Cunningham, S, Fullwood, C, Jones, A M, Shawcross, A, Smith, J A, Maitra, A & Gilchrist, F J 2021, ' Longitudinal assessment of lung clearance index to monitor disease progression in children and adults with cystic fibrosis ', Thorax . https://doi.org/10.1136/thoraxjnl-2021-216928
Horsley, A, Belcher, J, Bayfield, K J, Bianco, B, Cunningham, S, Fullwood, C, Jones, A M, Shawcross, A, Smith, J A, Maitra, A & Gilchrist, F J 2021, ' Longitudinal assessment of lung clearance index to monitor disease progression in children and adults with cystic fibrosis ', Thorax . https://doi.org/10.1136/thoraxjnl-2021-216928
BackgroundLung clearance index (LCI) is a valuable research tool in cystic fibrosis (CF) but clinical application has been limited by technical challenges and uncertainty about how to interpret longitudinal change. In order to help inform clinical pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f55cc67a83fb742e6356532e2ffc57a
Autor:
Eric W.F.W. Alton, Andrew Bush, Katie J Bayfield, Alex Horsley, Samantha Irving, Jane C. Davies
Publikováno v:
ERJ Open Research, Vol 5, Iss 4 (2019)
Bayfield, K J, Horsley, A, Alton, E, Irving, S, Bush, A & Davies, J C 2019, ' Simultaneous sulfur hexafluoride and nitrogen multiple-breath washout (MBW) to examine inherent differences in MBW outcomes ', ERJ Open Research, vol. 5, no. 4, pp. 00234-2018 . https://doi.org/10.1183/23120541.00234-2018
ERJ Open Research
Bayfield, K J, Horsley, A, Alton, E, Irving, S, Bush, A & Davies, J C 2019, ' Simultaneous sulfur hexafluoride and nitrogen multiple-breath washout (MBW) to examine inherent differences in MBW outcomes ', ERJ Open Research, vol. 5, no. 4, pp. 00234-2018 . https://doi.org/10.1183/23120541.00234-2018
ERJ Open Research
Multiple-breath washout (MBW) can be performed with different gases (sulfur hexafluoride (SF6) and nitrogen (N2)) and different devices, all of which give discrepant results. This study aimed to confirm previously reported differences and explore f
Autor:
Christie Boyton, Geshani Jayasuriya, Lifeng Yu, Brendan Kennedy, Neil Caplain, Katie J Bayfield, Dominic A. Fitzgerald, Oliver Weinheimer, Terry E. Robinson, Hiran Selvadurai, Rachel Fitzpatrick, Brian J. Bartholmai, Paul Robinson, Per A. Gustafsson, Anneliese Blaxland, Anna Middleton, Craig J. Galbán, Mark Wielpuetz
Publikováno v:
Cystic fibrosis.
Introduction: Impact of ultra-low-dose (ULD) computed tomography (CT) on quantification of structural disease and structure-function relationships in early Cystic Fibrosis (CF) lung disease have not been studied to date. Aim: To quantify structural l
Autor:
Katie J Bayfield, Paul Robinson, Tonya A Douglas, Anthony Paproki, Tim Rosenow, Claire E. Wainwright, Peter D. Sly, Felix Ratjen, Stephen M. Stick, Stuart Elborn, Jane C. Davies, Alan R. Smyth, Marcus A. Mall
Publikováno v:
Thorax. 76(12)
Structural and functional defects within the lungs of children with cystic fibrosis (CF) are detectable soon after birth and progress throughout preschool years often without overt clinical signs or symptoms. By school age, most children have structu
Publikováno v:
ERJ Open Research, Vol 6, Iss 1 (2020)
ERJ Open Research
ERJ Open Research
Thank you for the opportunity to respond to the correspondence by J.G. Nielsen from Innovision about our recent paper [1]. We would like to respond with a few points to address any concerns that may have arisen from his comments amongst colleagues at