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Respiration; International Review of Thoracic Diseases|August 10, 2002
Moving from CFC aerosol to HFA aerosol or dry powder inhalers: what do patients think?Thomas K Hartung, Helen Allbutt, Maria Dewar, et al.The Journal of Rheumatology|July 6, 2007
Hypersensitivity pneumonitis associated with leflunomide therapyNeil Martin, J Alastair Innes, C Michael Lambert, et al.Respiratory Medicine|September 18, 2007
Intravenous magnesium sulphate provides no additive benefit to standard management in acute asthmaTracey A Bradshaw, Simon P Matusiewicz, Graham K Crompton, et al.American Journal of Respiratory and Critical Care Medicine|June 21, 2008
Sputum proteomics in inflammatory and suppurative respiratory diseasesRobert D Gray, Gordon MacGregor, Donald Noble, et al.Plos One|June 1, 2013
Forced expiratory volume in one second predicts length of stay and in-hospital mortality in patients undergoing cardiac surgery: a retrospective cohort studyDavid A McAllister, Sarah H Wild, John D MacLay, et al.Respiratory Physiology & Neurobiology|July 16, 2008
Effects of cystic fibrosis lung disease on gas mixing indices derived from alveolar slope analysisAlex R Horsley, Kenneth A Macleod, Andrew G Robson, et al.Chest|October 6, 2009
Sputum trace metals are biomarkers of inflammatory and suppurative lung diseaseRobert D Gray, Andrew Duncan, Donald Noble, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 5, 2008
Biomarkers for cystic fibrosis lung disease: application of SELDI-TOF mass spectrometry to BAL fluidGordon MacGregor, Robert D Gray, Thomas N Hilliard, et al.Pediatric Pulmonology|September 24, 2016
Genetic medicines for CF: Hype versus realityEric W F W Alton, A Christopher Boyd, Jane C Davies, et al.Thorax|March 26, 2013
A randomised, double-blind, placebo-controlled phase IIB clinical trial of repeated application of gene therapy in patients with cystic fibrosisEric W F W Alton, A Christopher Boyd, Seng H Cheng, et al.Pageof 2