Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Alan Smyth"'
Autor:
Barry J Plant, Daniel Peckham, Pierre-Régis Burgel, Alan Smyth, Andreas Jung, Manfred Ballmann, Giovanni Taccetti, Harry Heijerman, Pavel Drevinek, Jochen G Mainz, Carsten Schwarz
Publikováno v:
BMJ Open Respiratory Research, Vol 11, Iss 1 (2024)
The major cause of mortality in people with cystic fibrosis (pwCF) is progressive lung disease characterised by acute and chronic infections, the accumulation of mucus, airway inflammation, structural damage and pulmonary exacerbations. The prevalenc
Externí odkaz:
https://doaj.org/article/ce777e645bdb4ad08771fda0a6783f30
Autor:
Sophie Herbert, Sherie Smith, Katie Gathercole, Christabella Ng, Nicola Rowbotham, Gwyneth Davies, Sarah J Collins, Zoe Elliott, Lorna Allen, Alan Smyth
Publikováno v:
BMJ Open Respiratory Research, Vol 7, Iss 1 (2020)
Introduction Relieving gastrointestinal (GI) symptoms was identified as a ‘top ten’ priority by our James Lind Alliance Priority Setting Partnership in cystic fibrosis (CF). We conducted an online survey to find out more about the effect of GI sy
Externí odkaz:
https://doaj.org/article/bfa05a56b9fa4e60beb38b3347b63029
Autor:
Helen L. Barr, Miguel Cámara, David Barrett, Paul Williams, Doug Forrester, Alan Smyth, David Honeybourne, Joanna Whitehouse, Edward Nash, Jane Dewar, Alan Knox, Andrew W. Fogarty
Publikováno v:
ERJ Open Research, Vol 3, Iss 3 (2017)
Externí odkaz:
https://doaj.org/article/942cee38757d4164861c97342c292943
Autor:
Matthew Hurley, Alan Smyth
Publikováno v:
Therapeutic Advances in Respiratory Disease, Vol 6 (2012)
Fluoroquinolones are commonly used to treat lung infections in patients with cystic fibrosis. These patients are susceptible to lung infection with common bacteria such as Staphylococcus aureus and Haemophilus influenza e, but are also prone to infec
Externí odkaz:
https://doaj.org/article/e6dac825171f4a87a62dacd03a6599d7
Autor:
David E. Ost, David J. Feller-Kopman, Anne V. Gonzalez, Horiana B. Grosu, Felix Herth, Peter Mazzone, John E.S. Park, José M. Porcel, Samira Shojaee, Ioana Tsiligianni, Anil Vachani, Jonathan Bernstein, Richard Branson, Patrick A. Flume, Cezmi A. Akdis, Martin Kolb, Esther Barreiro Portela, Alan Smyth
Publikováno v:
Journal of Bronchology & Interventional Pulmonology.
Autor:
Kevin W. Southern, Carlo Castellani, Elise Lammertyn, Alan Smyth, Donald VanDevanter, Silke van Koningsbruggen-Rietschel, Jürg Barben, Amanda Bevan, Edwin Brokaar, Sarah Collins, Gary J. Connett, Thomas W.V. Daniels, Jane Davies, Dimitri Declercq, Silvia Gartner, Andrea Gramegna, Naomi Hamilton, Jenny Hauser, Nataliya Kashirskaya, Laurence Kessler, Jacqueline Lowdon, Halyna Makukh, Clémence Martin, Lisa Morrison, Dilip Nazareth, Jacquelien Noordhoek, Ciaran O'Neill, Elizabeth Owen, Helen Oxley, Karen S. Raraigh, Caroline Raynal, Karen Robinson, Jobst Roehmel, Carsten Schwarz, Isabelle Sermet, Michal Shteinberg, Ian Sinha, Constance Takawira, Peter van Mourik, Marieke Verkleij, Michael D. Waller, Alistair Duff
Publikováno v:
Journal of Cystic Fibrosis. Elsevier
Southern, K W, Castellani, C, Lammertyn, E, Smyth, A, VanDevanter, D, van Koningsbruggen-Rietschel, S, Barben, J, Bevan, A, Brokaar, E, Collins, S, Connett, G J, Daniels, T W V, Davies, J, Declercq, D, Gartner, S, Gramegna, A, Hamilton, N, Hauser, J, Kashirskaya, N, Kessler, L, Lowdon, J, Makukh, H, Martin, C, Morrison, L, Nazareth, D, Noordhoek, J, O'Neill, C, Owen, E, Oxley, H, Raraigh, K S, Raynal, C, Robinson, K, Roehmel, J, Schwarz, C, Sermet, I, Shteinberg, M, Sinha, I, Takawira, C, van Mourik, P, Verkleij, M, Waller, M D & Duff, A 2023, ' Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis ', Journal of Cystic Fibrosis, vol. 22, no. 1, pp. 17-30 . https://doi.org/10.1016/j.jcf.2022.10.002
Scientia
Southern, K W, Castellani, C, Lammertyn, E, Smyth, A, VanDevanter, D, van Koningsbruggen-Rietschel, S, Barben, J R, Bevan, A, Brokaar, E, Collins, S, Connett, G J, Daniels, T W V, Davies, J, Declercq, D, Gartner, S, Gramegna, A, Hamilton, N, Hauser, J, Kashirskaya, N, Kessler, L, Lowdon, J, Makukh, H, Martin, C, Morrison, L, Nazareth, D, Noordhoek, J, O'Neill, C, Owen, E, Oxley, H, Raraigh, K S, Raynal, C, Robinson, K, Roehmel, J, Schwarz, C, Sermet, I, Shteinberg, M, Sinha, I, Takawira, C, van Mourik, P, Verkleij, M, Waller, M D & Duff, A 2023, ' Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis ', Journal of Cystic Fibrosis, vol. 22, no. 1, pp. 17-30 . https://doi.org/10.1016/j.jcf.2022.10.002
JOURNAL OF CYSTIC FIBROSIS
Southern, K W, Castellani, C, Lammertyn, E, Smyth, A, VanDevanter, D, van Koningsbruggen-Rietschel, S, Barben, J, Bevan, A, Brokaar, E, Collins, S, Connett, G J, Daniels, T W V, Davies, J, Declercq, D, Gartner, S, Gramegna, A, Hamilton, N, Hauser, J, Kashirskaya, N, Kessler, L, Lowdon, J, Makukh, H, Martin, C, Morrison, L, Nazareth, D, Noordhoek, J, O'Neill, C, Owen, E, Oxley, H, Raraigh, K S, Raynal, C, Robinson, K, Roehmel, J, Schwarz, C, Sermet, I, Shteinberg, M, Sinha, I, Takawira, C, van Mourik, P, Verkleij, M, Waller, M D & Duff, A 2023, ' Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis ', Journal of Cystic Fibrosis, vol. 22, no. 1, pp. 17-30 . https://doi.org/10.1016/j.jcf.2022.10.002
Scientia
Southern, K W, Castellani, C, Lammertyn, E, Smyth, A, VanDevanter, D, van Koningsbruggen-Rietschel, S, Barben, J R, Bevan, A, Brokaar, E, Collins, S, Connett, G J, Daniels, T W V, Davies, J, Declercq, D, Gartner, S, Gramegna, A, Hamilton, N, Hauser, J, Kashirskaya, N, Kessler, L, Lowdon, J, Makukh, H, Martin, C, Morrison, L, Nazareth, D, Noordhoek, J, O'Neill, C, Owen, E, Oxley, H, Raraigh, K S, Raynal, C, Robinson, K, Roehmel, J, Schwarz, C, Sermet, I, Shteinberg, M, Sinha, I, Takawira, C, van Mourik, P, Verkleij, M, Waller, M D & Duff, A 2023, ' Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis ', Journal of Cystic Fibrosis, vol. 22, no. 1, pp. 17-30 . https://doi.org/10.1016/j.jcf.2022.10.002
JOURNAL OF CYSTIC FIBROSIS
Cystic fibrosis; Guidelines; Variant-specific therapy Fibrosis quística; Pautas; Terapia variante específica Fibrosi quística; Pautes; Teràpia variant específica Cystic fibrosis (CF) has entered the era of variant-specific therapy, tailored to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c6ded04c482379180be18ea1ab6cf12
https://research.vumc.nl/en/publications/6fa8f077-49b9-4675-b900-f20dc3826455
https://research.vumc.nl/en/publications/6fa8f077-49b9-4675-b900-f20dc3826455
Autor:
Alan Smyth
Publikováno v:
Chiricú Journal: Latina/o Literatures, Arts, and Cultures. 4:195-197
Autor:
Diana Bilton, Tacjana Pressler, Isabelle Fajac, John Paul Clancy, Dorota Sands, Predrag Minic, Marco Cipolli, Ivanka Galeva, Amparo Solé, Alexandra L. Quittner, Keith Liu, John P. McGinnis, Gina Eagle, Renu Gupta, Michael W. Konstan, Sabine Renner, Christiane Knoop, Anne Malfroot, Lieven Dupont, Kristine Desager, Frans De Baets, Miroslava Bosheva, Vania Nedkova, Ivan Galabov, Andreas Freitag, Nancy Morrison, Pearce Wilcox, Tanja Pressler, Yves Martinet, Raphael Chiron, Stephan Dominique, Philippe Reix, Anne Prevotat, Isabelle Sermet, Isabelle Durieu, Rainald Fischer, Rudolf Huber, Doris Staab, Uwe Mellies, Wolfgang Sextro, Tobias Welte, Heinrike Wilkens, Urte Sommerwerk, Burkhard Bewig, Ilias Inglezos, Stavros-Eleftherios Doudounakis, Olga Bede, Ferenc Gönczi, Rita Újhelyi, Edward McKone, Paul McNally, Vincenzina Lucidi, Mario La Rosa, Laura Minicucci, Rita Padoan, Giovanna Pisi, Rolando Gagliardini, Carla Colombo, Inez Bronsveld, Ewa Sapiejka, Henryk Mazurek, Grażyna Górnicka, Iwona Stelmach, Halina Batura-Gabryel, Marta Rachel, Jaroslava Orosova, Branko Takac, Anna Feketova, Carmen Martinez, Gloria Garcia Hernandez, Jose Ramon Villa-Asensi, Silvia Gartner, Amparo Sole, Anders Lindblad, Martin Ledson, Joanna Whitehouse, Alan Smyth, Ian Ketchell, Timothy Lee, Gordon MacGregor
Publikováno v:
J Cyst Fibros
Background Shortcomings of inhaled antibiotic treatments for Pseudomonas aeruginosa infection in patients with cystic fibrosis (CF) include poor drug penetration, inactivation by sputum, poor efficiency due to protective biofilm, and short residence
Autor:
Matthew Hurley, Alan Smyth
Publikováno v:
Paediatrics and Child Health. 25:165-171
Publikováno v:
Thorax. 70(12)