|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
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 |
|
2018 Journal Article Whole genome sequencing reveals the emergence of a Pseudomonas aeruginosa shared strain sub-lineage among patients treated within a single cystic fibrosis centreWee, Bryan A., Tai, Anna S., Sherrard, Laura J., Ben Zakour, Nouri L., Hanks, Kirt R., Kidd, Timothy J., Ramsay, Kay A., Lamont, Iain, Whiley, David M., Bell, Scott C. and Beatson, Scott A. (2018). Whole genome sequencing reveals the emergence of a Pseudomonas aeruginosa shared strain sub-lineage among patients treated within a single cystic fibrosis centre. BMC Genomics, 19 (1) 644, 644. doi: 10.1186/s12864-018-5018-x |
|
2018 Journal Article Face Masks Reduce the Release of Pseudomonas aeruginosa Cough Aerosols when Worn for Clinically-Relevant Time PeriodsStockwell, Rebecca E., Wood, Michelle E., He, Congrong, Sherrard, Laura J., Ballard, Emma L., Kidd, Timothy J., Johnson, Graham R., Knibbs, Luke D., Morawska, Lidia, Bell, Scott C., CF Cough Aerosol Group and Duplancic, Christine (2018). Face Masks Reduce the Release of Pseudomonas aeruginosa Cough Aerosols when Worn for Clinically-Relevant Time Periods. American Journal of Respiratory and Critical Care Medicine, 198 (10) rccm.201805-0823LE, 1339-1342. doi: 10.1164/rccm.201805-0823LE |
|
2018 Journal Article Transcriptomic analysis of longitudinal Burkholderia pseudomallei infecting the cystic fibrosis lungPrice, Erin P., Viberg, Linda T., Kidd, Timothy J., Bell, Scott C., Currie, Bart J. and Sarovich, Derek S. (2018). Transcriptomic analysis of longitudinal Burkholderia pseudomallei infecting the cystic fibrosis lung. Microbial Genomics, 4 (8) 000194. doi: 10.1099/mgen.0.000194 |
|
2018 Journal Article Anomalies in T cell function are associated with individuals at risk of Mycobacterium abscessus complex infectionLutzky, Viviana P., Ratnatunga, Champa N., Smith, Daniel J., Kupz, Andreas, Doolan, Denise L., Reid, David W., Thomson, Rachel M., Bell, Scott C. and Miles, John J. (2018). Anomalies in T cell function are associated with individuals at risk of Mycobacterium abscessus complex infection. Frontiers in Immunology, 9 (June) 1319, 1319. doi: 10.3389/fimmu.2018.01319 |
|
2018 Journal Article Biomarkers: their role in CFTR modulator therapies from early development to the clinicBell, Scott C. and Wood, Michelle E. (2018). Biomarkers: their role in CFTR modulator therapies from early development to the clinic. American Journal of Respiratory and Critical Care Medicine, 197 (11), 1375-1376. doi: 10.1164/rccm.201801-0177ED |
|
2018 Journal Article Optimism, opportunities, outcomes: the Australian Cystic Fibrosis Data RegistryAhern, Susannah, Sims, Geoff, Earnest, Arul and Bell, Scott C. (2018). Optimism, opportunities, outcomes: the Australian Cystic Fibrosis Data Registry. Internal Medicine Journal, 48 (6), 721-723. doi: 10.1111/imj.13807 |
|
2018 Journal Article Inhaled corticosteroids for bronchiectasis (review)Kapur, Nitin, Petsky, Helen L., Bell, Scott, Kolbe, John and Chang, Anne B. (2018). Inhaled corticosteroids for bronchiectasis (review). Cochrane Database of Systematic Reviews, 2018 (5) CD000996. doi: 10.1002/14651858.CD000996.pub3 |
|
2018 Journal Article Bronchiectasis: yet another systemic disease?Geake, James and Bell, Scott C. (2018). Bronchiectasis: yet another systemic disease?. Respirology, 23 (9), 797-798. doi: 10.1111/resp.13322 |
