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2014 Journal Article Challenges of providing care to adults with cystic fibrosisBell, Scott C. and Reid, David W. (2014). Challenges of providing care to adults with cystic fibrosis. European Respiratory Monograph, 64 (64), 286-303. doi: 10.1183/1025448x.10010513 |
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2014 Journal Article A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: A phase 2 randomised controlled trialBoyle, Michael P., Bell, Scott C., Konstan, Michael W., McColley, Susanna A., Rowe, Steven M., Rietschel, Ernst, Huang, Xiaohong, Waltz, David, Patel, Naimish R. and Rodman, David (2014). A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: A phase 2 randomised controlled trial. The Lancet Respiratory Medicine, 2 (7), 527-538. doi: 10.1016/S2213-2600(14)70132-8 |
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2014 Journal Article Pregnancy and cystic fibrosis: approach to contemporary managementGeake, James, Tay, George, Callaway, Leonie and Bell, Scott C. (2014). Pregnancy and cystic fibrosis: approach to contemporary management. Obstetric Medicine, 7 (4), 147-155. doi: 10.1177/1753495X14554022 |
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2013 Journal Article Factors influencing acquisition of Burkholderia cepacia complex organisms in patients with cystic fibrosisRamsay, Kay A., Butler, Claire A., Paynter, Stuart, Ware, Robert S., Kidd, Timothy J., Wainwright, Claire E. and Bell, Scott C. (2013). Factors influencing acquisition of Burkholderia cepacia complex organisms in patients with cystic fibrosis. Journal of Clinical Microbiology, 51 (12), 3975-3980. doi: 10.1128/JCM.01360-13 |
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2013 Journal Article Ivacaftor in severe cystic fibrosis lung disease and a G551D mutationWood, Michelle E., Smith, Daniel J., Reid, David W., Masel, Philip J., France, Megan W. and Bell, Scott C. (2013). Ivacaftor in severe cystic fibrosis lung disease and a G551D mutation. Respirology Case Reports, 1 (2), 52-54. doi: 10.1002/rcr2.27 |
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2013 Journal Article Change in the executive editorial team at JCFBell, Scott, Hartl, Dominik and Heijerman, Harry (2013). Change in the executive editorial team at JCF. Journal of Cystic Fibrosis, 12 (6), 545-546. doi: 10.1016/j.jcf.2013.10.006 |
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2013 Journal Article Within-host evolution of Burkholderia pseudomallei over a twelve-year chronic carriage infectionPrice E.P., Sarovich D.S., Mayo M., Tuanyok A., Drees K.P., Kaestli M., Beckstrom-Sternberg S.M., Babic-Sternberg J.S., Kidd T.J., Bell S.C., Keim P., Pearson T. and Currie B.J. (2013). Within-host evolution of Burkholderia pseudomallei over a twelve-year chronic carriage infection. mBio, 4 (4) e00388-13, e00388-13.1-e00388-13.11. doi: 10.1128/mBio.00388-13 |
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2013 Journal Article High-throughput single-nucleotide polymorphism-based typing of shared Pseudomonas aeruginosa strains in cystic fibrosis patients using the Sequenom iPLEX platformSyrmis, Melanie W., Moser, Ralf J., Kidd, Timothy J., Hunt, Priscilla, Ramsay, Kay A., Bell, Scott C., Wainwright, Claire E., Grimwood, Keith, Nissen, Michael D., Sloots, Theo P. and Whiley, David M. (2013). High-throughput single-nucleotide polymorphism-based typing of shared Pseudomonas aeruginosa strains in cystic fibrosis patients using the Sequenom iPLEX platform. Journal of Medical Microbiology, 62 (5), 734-740. doi: 10.1099/jmm.0.055905-0 |
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2013 Journal Article ICU outcomes in cystic fibrosis following invasive ventilationReid, David W. and Bell, Scott C. (2013). ICU outcomes in cystic fibrosis following invasive ventilation. Respirology, 18 (4), 585-586. doi: 10.1111/resp.12077 |
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2013 Journal Article Management of comorbidities in older patients with cystic fibrosisPlant, Barry J, Goss, Christopher H, Plant, William D and Bell, Scott C (2013). Management of comorbidities in older patients with cystic fibrosis. The Lancet Respiratory Medicine, 1 (2), 164-174. doi: 10.1016/S2213-2600(13)70025-0 |
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2013 Journal Article Screening bacterial metabolites for inhibitory effects against Batrachochytrium dendrobatidis using a spectrophotometric assayBell, Sara C., Alford, Ross A., Garland, Stephen, Padilla, Gabriel and Thomas, Annette D. (2013). Screening bacterial metabolites for inhibitory effects against Batrachochytrium dendrobatidis using a spectrophotometric assay. Diseases of Aquatic Organisms, 103 (1), 77-+. doi: 10.3354/dao02560 |
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2013 Journal Article Aztreonam for inhalation solution, challenges to drug approval and integration into CF careGoss, Christopher H. and Bell, Scott C. (2013). Aztreonam for inhalation solution, challenges to drug approval and integration into CF care. Journal of Cystic Fibrosis, 12 (2), 99-101. doi: 10.1016/j.jcf.2012.08.006 |
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2013 Journal Article Geographical differences in first acquisition of Pseudomonas aeruginosa in cystic fibrosisRanganathan, Sarath C., Skoric, Billy, Ramsay, Kay A., Carzino, Rosemary, Gibson, Anne-Marie, Hart, Emily, Harrison, Jo, Bell, Scott C. and Kidd, Timothy J. (2013). Geographical differences in first acquisition of Pseudomonas aeruginosa in cystic fibrosis. Annals of the American Thoracic Society, 10 (2), 108-114. doi: 10.1513/AnnalsATS.201209-077OC |
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2013 Journal Article Sputum neutrophils in cystic fibrosis patients display a reduced respiratory burstHouston, Neralee, Stewart, Niall, Smith, Daniel S., Bell, Scott C., Champion, Alan C. and Reid, David W. (2013). Sputum neutrophils in cystic fibrosis patients display a reduced respiratory burst. Journal of Cystic Fibrosis, 12 (4), 352-362. doi: 10.1016/j.jcf.2012.11.004 |
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2012 Journal Article New insights into gene-specific management in cystic fibrosis from the 2012 European Cystic Fibrosis ConferenceButler, Claire Ann and Bell, Scott Cameron (2012). New insights into gene-specific management in cystic fibrosis from the 2012 European Cystic Fibrosis Conference. Expert Review of Respiratory Medicine, 6 (5), 499-501. doi: 10.1586/ERS.12.52 |
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2012 Journal Article Accurate assessment of systemic iron status in cystic fibrosis will avoid the hazards of inappropriate iron supplementationSmith, D.J., Anderson, G.J., Lamont, I.L., Masel, P., Bell, S.C. and Reid, D.W. (2012). Accurate assessment of systemic iron status in cystic fibrosis will avoid the hazards of inappropriate iron supplementation. Journal of Cystic Fibrosis, 12 (3), 303-304. doi: 10.1016/j.jcf.2012.10.001 |
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2012 Journal Article Pseudomonas aeruginosa exhibits frequent recombination, but only a limited association between genotype and ecological settingKidd, Timothy J., Richie, Stephen R., Ramsay, Kay A., Grimwood, Keith, Bell, Scott C. and Rainey, Paul B. (2012). Pseudomonas aeruginosa exhibits frequent recombination, but only a limited association between genotype and ecological setting. PLoS One, 7 (9) e44199, e44199.1-e44199.14. doi: 10.1371/journal.pone.0044199 |
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2012 Journal Article Shared pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centresKidd, Timothy J., Ramsay, Kay A., Hu, Honghua, Marks, Guy B., Wainwright, Claire E., Bye, Peter T., Elkins, Mark R., Robinson, Philip J., Rose, Barbara R., Wilson, John W., Grimwood, Keith, Bell, Scott C., ACPinCF Investigator Group, Serisier, David J. and Smith, Daniel J. (2012). Shared pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centres. European Respiratory Journal, 41 (5), 1091-1100. doi: 10.1183/09031936.00060512 |
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2012 Journal Article The risk of airborne influenza transmission in passenger carsKnibbs, L. D., Morawska, L. and Bell, S. C. (2012). The risk of airborne influenza transmission in passenger cars. Epidemiology and Infection, 140 (3), 474-478. doi: 10.1017/S0950268811000835 |
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2012 Journal Article Comparison of the US and Australian Cystic Fibrosis Registries: The impact of newborn screeningMartin, Bradley, Schechter, Michael S., Jaffe, Adam, Cooper, Peter, Bell, Scott C. and Ranganathan, Sarath (2012). Comparison of the US and Australian Cystic Fibrosis Registries: The impact of newborn screening. Pediatrics, 129 (2), E348-E355. doi: 10.1542/peds.2011-0567 |
