Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Stuart J, Elborn"'
Publikováno v:
PLoS ONE, Vol 15, Iss 10, p e0235803 (2020)
Cystic Fibrosis (CF), caused by mutations affecting the CFTR gene, is characterised by viscid secretions in multiple organ systems. CF airways contain thick mucus, creating a gradient of hypoxia, which promotes the establishment of polymicrobial infe
Externí odkaz:
https://doaj.org/article/5541b51bad5747ea873af6503b09070a
Autor:
Ravishankar Chandrasekaran, Micheál Mac Aogáin, James D. Chalmers, Stuart J. Elborn, Sanjay H. Chotirmall
Publikováno v:
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-14 (2018)
Abstract Bronchiectasis is a disease associated with chronic progressive and irreversible dilatation of the bronchi and is characterised by chronic infection and associated inflammation. The prevalence of bronchiectasis is age-related and there is so
Externí odkaz:
https://doaj.org/article/5faf6142a2794db58b34514b9b9f799d
Background: In Cystic Fibrosis (CF) airways, mutations in the Cystic Fibrosis Transmembrane Regulator (CFTR) lead to dehydrated, thick mucus which promotes the establishment of persistent polymicrobial infections and drives chronic airways inflammati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::799a4240584b7b906c35fda1f9d5ed47
https://doi.org/10.21203/rs.3.rs-40957/v1
https://doi.org/10.21203/rs.3.rs-40957/v1
Autor:
Michael R, Loebinger, Eva, Polverino, James D, Chalmers, Harm A W M, Tiddens, Herman, Goossens, Michael, Tunney, Felix C, Ringshausen, Adam T, Hill, Rashidkhan, Pathan, Gerhild, Angyalosi, Francesco, Blasi, Stuart J, Elborn, Charles S, Haworth
Publikováno v:
The European respiratory journal. 57(1)
The study aimed to determine the efficacy of a safe and well-tolerated dose and regimen of tobramycin inhalation powder (TIP) on