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2019 Journal Article Indoor hospital air and the impact of ventilation on bioaerosols: a systematic reviewStockwell, Rebecca E., Ballard, Emma L., O’Rourke, Peter, Knibbs, Luke D., Morawska, Lidia and Bell, Scott C. (2019). Indoor hospital air and the impact of ventilation on bioaerosols: a systematic review. Journal of Hospital Infection, 103 (2), 175-184. doi: 10.1016/j.jhin.2019.06.016 |
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2019 Journal Article Non-invasive ventilation versus oxygen therapy in cystic fibrosis: a 12-month randomized trialMilross, Maree A., Piper, Amanda J., Dwyer, Tiffany J., Wong, Keith, Bell, Scott C., Bye, Peter T. P., Robbins, Lisel, Dobbin, Catherine, Moriarty, Carmel, Willson, G., Norman, M., Regnis, Jeff, Sullivan, Colin, Grunstein, Ron and Douglas, James (2019). Non-invasive ventilation versus oxygen therapy in cystic fibrosis: a 12-month randomized trial. Respirology, 24 (12) resp.13604, 1191-1197. doi: 10.1111/resp.13604 |
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2019 Journal Article A non-randomised single centre cohort study, comparing standard and modified bowel preparations, in adults with cystic fibrosis requiring colonoscopyMatson, A. G., Bunting, J. P., Kaul, A., Smith, D. J., Stonestreet, J., Herd, K., Hodgson, R. S. and Bell, S. C. (2019). A non-randomised single centre cohort study, comparing standard and modified bowel preparations, in adults with cystic fibrosis requiring colonoscopy. BMC Gastroenterology, 19 (1) 89. doi: 10.1186/s12876-019-0979-z |
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2019 Journal Article Multi-centre ethics and research governance review can impede non-interventional clinical researchDuplancic, Christine, Crough, Tania, Bell, Scott C., Australian NTM in CF Study Group and Thomson, Rachel (2019). Multi-centre ethics and research governance review can impede non-interventional clinical research. Internal Medicine Journal, 49 (6), 722-728. doi: 10.1111/imj.14158 |
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2019 Journal Article Reply: More on causal inference studiesLederer, David J., Bell, Scott C., Smyth, Alan R. and Chalmers, James D. (2019). Reply: More on causal inference studies. Annals of the American Thoracic Society, 16 (5), 646-646. doi: 10.1513/AnnalsATS.201901-070LE |
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2019 Journal Article Abolition of Pseudomonas aeruginosa AUST-01 from an Australian CF center: Do other strains remain?Kidd, Timothy J, Grimwood, Keith and Bell, Scott C (2019). Abolition of Pseudomonas aeruginosa AUST-01 from an Australian CF center: Do other strains remain?. Pediatric Pulmonology, 54 (5), 515-516. doi: 10.1002/ppul.24258 |
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2019 Journal Article Infection risks for patients from healthcare workers with cystic fibrosis - ReplyBell, Scott C. and Stuart, Rhonda L. (2019). Infection risks for patients from healthcare workers with cystic fibrosis - Reply. Respirology, 24 (4), 393-394. doi: 10.1111/resp.13489 |
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2019 Journal Article Transmission of bacteria in bronchiectasis and chronic obstructive pulmonary disease: Low burden of cough aerosolsStockwell, Rebecca E., Chin, Melanie, Johnson, Graham R., Wood, Michelle E., Sherrard, Laura J., Ballard, Emma, O'Rourke, Peter, Ramsay, Kay A., Kidd, Timothy J., Jabbour, Nassib, Thomson, Rachel M., Knibbs, Luke D., Morawska, Lidia and Bell, Scott C. (2019). Transmission of bacteria in bronchiectasis and chronic obstructive pulmonary disease: Low burden of cough aerosols. Respirology, 24 (10) resp.13544, 980-987. doi: 10.1111/resp.13544 |
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2019 Journal Article Antimicrobial susceptibility testing (AST) and associated clinical outcomes in individuals with cystic fibrosis: A systematic reviewSomayaji, Ranjani, Parkins, Michael D., Shah, Anand, Martiniano, Stacey L., Tunney, Michael M., Kahle, Jennifer S., Waters, Valerie J., Elborn, J. Stuart, Bell, Scott C., Flume, Patrick A. and VanDevanter, Donald R. (2019). Antimicrobial susceptibility testing (AST) and associated clinical outcomes in individuals with cystic fibrosis: A systematic review. Journal of Cystic Fibrosis, 18 (2), 236-243. doi: 10.1016/j.jcf.2019.01.008 |
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2019 Journal Article Mutations in the HFE gene can be associated with increased lung disease severity in cystic fibrosisSmith, Daniel J., Klein, Kerenaftali, Hartel, Gunter, Wainwright, Claire E., Bell, Scott C., Anderson, Gregory J. and Reid, David W. (2019). Mutations in the HFE gene can be associated with increased lung disease severity in cystic fibrosis. Gene, 683, 12-17. doi: 10.1016/j.gene.2018.10.002 |
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2019 Journal Article Correction: Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis (PLoS One (2017) 12:3 (e0172179) DOI: 10.1371/journal.pone.0172179)Sherrard, Laura J., Tai, Anna S., Wee, Bryan A., Ramsay, Kay A., Kidd, Timothy J., Ben Zakour, Nouri L., Whiley, David M., Beatson, Scott A. and Bell, Scott C. (2019). Correction: Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis (PLoS One (2017) 12:3 (e0172179) DOI: 10.1371/journal.pone.0172179). PLoS ONE, 14 (1) e0210929. doi: 10.1371/journal.pone.0210929 |
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2019 Journal Article Control of confounding and reporting of results in causal inference studiesLederer, David J., Bell, Scott C., Branson, Richard D., Chalmers, James D., Marshall, Rachel, Maslove, David M., Ost, David E., Punjabi, Naresh M., Schatz, Michael, Smyth, Alan R., Stewart, Paul W., Suissa, Samy, Adjei, Alex A., Akdis, Cezmi A., Azoulay, Élie, Bakker, Jan, Ballas, Zuhair K., Bardin, Philip G., Barreiro, Esther, Bellomo, Rinaldo, Bernstein, Jonathan A., Brusasco, Vito, Buchman, Timothy G., Chokroverty, Sudhansu, Collop, Nancy A., Crapo, James D., Fitzgerald, Dominic A., Hale, Lauren, Hart, Nicholas ... Vincent, Jean-Louis (2019). Control of confounding and reporting of results in causal inference studies. Annals of the American Thoracic Society, 16 (1), 22-28. doi: 10.1513/AnnalsATS.201808-564PS |
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2019 Journal Article JCF – progress in 2018Bell, Scott C., Castellani, Carlo and Flume, Patrick A. (2019). JCF – progress in 2018. Journal of Cystic Fibrosis, 18 (1), 1-5. doi: 10.1016/j.jcf.2018.12.008 |
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2018 Journal Article Reply to: Use of masks in cystic fibrosis patientsWood, Michelle E, Stockwell, Rebecca E and Bell, Scott C (2018). Reply to: Use of masks in cystic fibrosis patients. American Journal of Respiratory and Critical Care Medicine, 198 (12) rccm.201808-1476LE, 1589-1590. doi: 10.1164/rccm.201808-1476LE |
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2018 Journal Article Expression of Pseudomonas aeruginosa antibiotic resistance genes varies greatly during infections in cystic fibrosis patientsMartin, Lois W., Robson, Cynthia L., Watts, Annabelle M., Gray, Andrew R., Wainwright, Claire E., Bell, Scott C., Ramsay, Kay A., Kidd, Timothy J., Reid, David W., Brockway, Ben and Lamont, Iain L. (2018). Expression of Pseudomonas aeruginosa antibiotic resistance genes varies greatly during infections in cystic fibrosis patients. Antimicrobial Agents and Chemotherapy, 62 (11) e01789-18. doi: 10.1128/AAC.01789-18 |
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2018 Journal Article Bronchiectasis: treatment decisions for pulmonary exacerbations and their preventionBell, Scott C., Elborn, Joseph S. and Byrnes, Catherine A. (2018). Bronchiectasis: treatment decisions for pulmonary exacerbations and their prevention. Respirology, 23 (11), 1006-1022. doi: 10.1111/resp.13398 |
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2018 Journal Article Defining antimicrobial resistance in cystic fibrosisKidd, Timothy J., Canton, Rafael, Ekkelenkamp, Miquel, Johansen, Helle Krogh, Gilligan, Peter, LiPuma, John J., Bell, Scott C., Elborn, J. Stuart, Flume, Patrick A., VanDevanter, Donald R. and Waters, Valerie J. (2018). Defining antimicrobial resistance in cystic fibrosis. Journal of Cystic Fibrosis, 17 (6), 696-704. doi: 10.1016/j.jcf.2018.08.014 |
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2018 Journal Article Antimicrobial resistance in cystic fibrosis: Does it matter?Flume, Patrick A., Waters, Valerie J., Bell, Scott C., Van Devanter, Donald R. and Stuart Elborn, J. (2018). Antimicrobial resistance in cystic fibrosis: Does it matter?. Journal of Cystic Fibrosis, 17 (6), 687-689. doi: 10.1016/j.jcf.2018.08.015 |
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2018 Journal Article Human epididymis protein 4 (HE4) levels inversely correlate with lung function improvement (delta FEV1) in cystic fibrosis patients receiving ivacaftor treatmentNagy, Béla, Bene, Zsolt, Fejes, Zsolt, Heltshe, Sonya L, Reid, David, Ronan, Nicola J, McCarthy, Yvonne, Smith, Daniel, Nagy, Attila, Joseloff, Elizabeth, Balla, György, Kappelmayer, János, Macek, Milan, Bell, Scott C, Plant, Barry J, Amaral, Margarida D and Balogh, István (2018). Human epididymis protein 4 (HE4) levels inversely correlate with lung function improvement (delta FEV1) in cystic fibrosis patients receiving ivacaftor treatment. Journal of Cystic Fibrosis, 18 (2), 271-277. doi: 10.1016/j.jcf.2018.08.013 |
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2018 Journal Article Work environment risks for health care workers with cystic fibrosisBell, Scott C., Armstrong, David, Harrington, Glenys, Jardine, Luke, Divakaran, Rebekah, Loff, Bebe, Middleton, Peter G., McDonald, Tim, Rowland, Karen, Wishart, Michael, Wood, Michelle E. and Stuart, Rhonda L. (2018). Work environment risks for health care workers with cystic fibrosis. Respirology, 23 (12), 1190-1197. doi: 10.1111/resp.13404 |
