Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Fiona C. Ringholz"'
Autor:
Gerard Higgins, Isabelle Sermet-Gaudelus, Paul McNally, Monika Hollenhorst, Ahmad Moukachar, Aurélie Hatton, Coral Fustero-Torre, Valerie Urbach, Fiona C. Ringholz, Brian J. Harvey, Ali Sassi
Publikováno v:
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis, Elsevier, 2018, 17 (5), pp.607-615. ⟨10.1016/j.jcf.2017.11.017⟩
Journal of Cystic Fibrosis, Elsevier, 2018, 17 (5), pp.607-615. ⟨10.1016/j.jcf.2017.11.017⟩
Background Cystic Fibrosis (CF) lung disease is characterised by dysregulated ion transport that promotes chronic bacterial infection and inflammation. The impact of the specialised pro-resolution mediator resolvin D1 (RvD1) on airway surface liquid
Autor:
Fiona C. Ringholz (7959560)
CF is caused by a mutation in the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) and results in airway surface liquid (ASL) dehydration, impaired muco-ciliary clearance, chronic pulmonary infection and inflammation leading to progressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5078bae12469d61bc9cf439dfb560080
Autor:
Donna Clarke, P Mc Nally, Peter Greally, Fiona C. Ringholz, Des W. Cox, Michael P. McDermott, I Gorman, Barry Linnane
Publikováno v:
Respiratory Research
Respiratory Research, Vol 19, Iss 1, Pp 1-3 (2018)
Respiratory Research, Vol 19, Iss 1, Pp 1-3 (2018)
Pulmonary aspiration of gastric refluxate (PAGR) has been demonstrated in association with pulmonary inflammation in school aged children with Cystic Fibrosis (CF). We sought to determine if similar findings were present in preschool children. Pepsin
Autor:
Fiona C. Ringholz, Paul Buchanan, Brian J. Harvey, Michael P. McDermott, Paul McNally, Donna Clarke, Valerie Urbach, Barry Linnane, Roisin G Millar
Publikováno v:
European Respiratory Journal
European Respiratory Journal, European Respiratory Society, 2014, 44 (2), pp.394-404. ⟨10.1183/09031936.00106013⟩
European Respiratory Journal, European Respiratory Society, 2014, 44 (2), pp.394-404. ⟨10.1183/09031936.00106013⟩
Airway disease in cystic fibrosis (CF) is characterised by impaired mucociliary clearance, persistent bacterial infection and neutrophilic inflammation. Lipoxin A4 (LXA4) initiates the active resolution of inflammation and promotes airway surface hyd
Publikováno v:
Paediatric respiratory reviews. 15(1)
Over the course of a career most physicians will manage only a handful of children through End Stage Lung Disease. Nonetheless, the approach of the physician to this challenge will have a profound impact on the children and families they encounter. M
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 6, Iss 7 (2013)
Computational and Structural Biotechnology Journal
Computational and Structural Biotechnology Journal, Elsevier, 2013, 6 (7), pp.e201303018. ⟨10.5936/csbj.201303018⟩
Computational and Structural Biotechnology Journal
Computational and Structural Biotechnology Journal, Elsevier, 2013, 6 (7), pp.e201303018. ⟨10.5936/csbj.201303018⟩
In Cystic Fibrosis (CF), mutations of the CFTR gene result in defective Cl− secretion and Na+ hyperabsorption by epithelia which leads to airway lumen dehydration and mucus plugging and favours chronic bacterial colonization, persistent inflammatio