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2016

Journal Article

The changing prevalence of pulmonary infection in adults with cystic fibrosis: a longitudinal analysis

Ramsay, Kay A., Sandhu, Harpreet, Geake, James B., Ballard, Emma, O'Rourke, Peter, Wainwright, Claire E., Reid, David W., Kidd, Timothy J. and Bell, Scott C. (2016). The changing prevalence of pulmonary infection in adults with cystic fibrosis: a longitudinal analysis. Journal of Cystic Fibrosis, 16 (1), 70-77. doi: 10.1016/j.jcf.2016.07.010

The changing prevalence of pulmonary infection in adults with cystic fibrosis: a longitudinal analysis

2016

Journal Article

Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study

Wells, J. Michael, Farris, Roopan F., Gosdin, Taylor A., Dransfield, Mark T., Wood, Michelle E., Bell, Scott C. and Rowe, Steven M. (2016). Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study. Lancet Respiratory Medicine, 4 (8), 636-645. doi: 10.1016/S2213-2600(16)30105-9

Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort study

2016

Journal Article

The role of anaerobic bacteria in the cystic fibrosis airway

Sherrard, Laura J., Bell, Scott C. and Tunney, Michael M. (2016). The role of anaerobic bacteria in the cystic fibrosis airway. Current Opinion in Pulmonary Medicine, 22 (6), 637-643. doi: 10.1097/MCP.0000000000000299

The role of anaerobic bacteria in the cystic fibrosis airway

2016

Journal Article

A novel method and its application to measuring pathogen decay in bioaerosols from patients with respiratory disease

Johnson, Graham R., Knibbs, Luke D., Kidd, Timothy J., Wainwright, Claire E., Wood, Michelle E., Ramsay, Kay A., Bell, Scott C. and Morawska, Lidia (2016). A novel method and its application to measuring pathogen decay in bioaerosols from patients with respiratory disease. PLoS One, 11 (7) e0158763, e0158763. doi: 10.1371/journal.pone.0158763

A novel method and its application to measuring pathogen decay in bioaerosols from patients with respiratory disease

2016

Journal Article

The cystic fibrosis foundation patient registry: Design and methods of a national observational disease registry

Stephenson, Anne L. and Bell, Scott C. (2016). The cystic fibrosis foundation patient registry: Design and methods of a national observational disease registry. Annals of the American Thoracic Society, 13 (7), 1014-1015. doi: 10.1513/AnnalsATS.201604-250ED

The cystic fibrosis foundation patient registry: Design and methods of a national observational disease registry

2016

Journal Article

A phase 3, multi-center, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of levofloxacin inhalation solution (APT-1026) in stable cystic fibrosis patients

Flume, Patrick A., VanDevanter, Donald R., Morgan, Elizabeth E., Dudley, Michael N., Loutit, Jeffery S., Bell, Scott C., Kerem, Eitan, Fischer, Rainald, Smyth, Alan R., Aaron, Shawn D., Conrad, Douglas, Geller, David E. and Elborn, J. Stuart (2016). A phase 3, multi-center, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of levofloxacin inhalation solution (APT-1026) in stable cystic fibrosis patients. Journal of Cystic Fibrosis, 15 (4), 495-502. doi: 10.1016/j.jcf.2015.12.004

A phase 3, multi-center, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of levofloxacin inhalation solution (APT-1026) in stable cystic fibrosis patients

2016

Journal Article

Methicillin-resistant Staphylococcus aureus acquisition in healthcare workers with cystic fibrosis: a retrospective cross-sectional study

Wood, Michelle E., Sherrard, Laura J., Ramsay, Kay A., Yerkovich, Stephanie T., Reid, David W., Kidd, Timothy J. and Bell, Scott C. (2016). Methicillin-resistant Staphylococcus aureus acquisition in healthcare workers with cystic fibrosis: a retrospective cross-sectional study. BMC Pulmonary Medicine, 16 (78) 78, 1-7. doi: 10.1186/s12890-016-0243-z

Methicillin-resistant Staphylococcus aureus acquisition in healthcare workers with cystic fibrosis: a retrospective cross-sectional study

2016

Journal Article

A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review

Merner, Nancy, Forgeot d'Arc, Baudouin, Bell, Scott C., Maussion, Gilles, Peng, Huashan, Gauthier, Julie, Crapper, Liam, Hamdan, Fadi F., Michaud, Jacques L., Mottron, Laurent, Rouleau, Guy A. and Ernst, Carl (2016). A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review. American Journal of Medical Genetics Part A, 170 (5), 1225-1235. doi: 10.1002/ajmg.a.37566

A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review

2016

Journal Article

High ambient temperature and risk of intestinal obstruction in cystic fibrosis

Ooi, Chee Y., Jeyaruban, Christina, Lau, Jasmine, Katz, Tamarah, Matson, Angela, Bell, Scott C., Adams, Susan E. and Krishnan, Usha (2016). High ambient temperature and risk of intestinal obstruction in cystic fibrosis. Journal of Paediatrics and Child Health, 52 (4), 430-435. doi: 10.1111/jpc.13096

High ambient temperature and risk of intestinal obstruction in cystic fibrosis

2016

Journal Article

Infection in cystic fibrosis: impact of the environment and climate

Ramsay, K. A., Stockwell, R. E., Bell, S. C. and Kidd, T. J. (2016). Infection in cystic fibrosis: impact of the environment and climate. Expert Review of Respiratory Medicine, 10 (5), 505-519. doi: 10.1586/17476348.2016.1162715

Infection in cystic fibrosis: impact of the environment and climate

2016

Journal Article

The effect of CFTR modulation on the disease progression of cystic fibrosis in the era of precision medicine

Stuart Elborn, J., Davies, Jane, Bell, Scott and Derichs, Nico (2016). The effect of CFTR modulation on the disease progression of cystic fibrosis in the era of precision medicine. Journal of Cystic Fibrosis, 15 (2). doi: 10.1016/j.jcf.2015.12.012

The effect of CFTR modulation on the disease progression of cystic fibrosis in the era of precision medicine

2016

Journal Article

Report of the European respiratory society/European cystic fibrosis society task force on the care of adults with cystic fibrosis

Elborn, J. Stuart, Bell, Scott C., Madge, Susan L., Burgel, Pierre-Regis, Castellani, Carlo, Conway, Steven, De Rijcke, Karleen, Dembski, Birgit, Drevinek, Pavel, Heijerman, Harry G.M., Innes, J. Alistair, Lindblad, Anders, Marshall, Bruce, Olesen, Hanne V., Reimann, Andreas L., Solé, Ampara, Viviani, Laura, Wagner, Thomas O.F., Welte, Tobias and Blasi, Francesco (2016). Report of the European respiratory society/European cystic fibrosis society task force on the care of adults with cystic fibrosis. European Respiratory Journal, 47 (2), 420-428. doi: 10.1183/13993003.00592-2015

Report of the European respiratory society/European cystic fibrosis society task force on the care of adults with cystic fibrosis

2016

Journal Article

Pseudomonas aeruginosa antibiotic resistance in Australian cystic fibrosis centres

Smith, Daniel J., Ramsay, Kay A., Yerkovich, Stephanie T., Reid, David W., Wainwright, Claire E., Grimwood, Keith, Bell, Scott C. and Kidd, Timothy J. (2016). Pseudomonas aeruginosa antibiotic resistance in Australian cystic fibrosis centres. Respirology, 21 (2), 329-337. doi: 10.1111/resp.12714

Pseudomonas aeruginosa antibiotic resistance in Australian cystic fibrosis centres

2016

Conference Publication

Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis

Sherrard, L., Tai, A., Wee, B., Ramsay, K., Kidd, T., Ben Zakour, N., Whiley, D., Beatson, S. and Bell, S. C. (2016). Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis. Annual North American Cystic Fibrosis Conference, Orlando, FL, United States, 27-29 October 2016. Hoboken, NJ, United States: John Wiley & Sons.

Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis

2016

Journal Article

JCF-2015

Bell, Scott C., Hartl, Dominik and Flume, Patrick (2016). JCF-2015. Journal of Cystic Fibrosis, 15 (1). doi: 10.1016/S1569-1993(15)00319-7

JCF-2015

2016

Journal Article

Infection in cystic fibrosis: impact of the environment and climate (vol 10, pg 505, 2016)

Ramsay, K. A., Stockwell, R. E. and Bell, S. C. (2016). Infection in cystic fibrosis: impact of the environment and climate (vol 10, pg 505, 2016). Expert Review of Respiratory Medicine, 10 (6), 713-713. doi: 10.1080/17476348.2016.1184473

Infection in cystic fibrosis: impact of the environment and climate (vol 10, pg 505, 2016)

2015

Journal Article

Genotypic Diversity within a Single Pseudomonas aeruginosa Strain Commonly Shared by Australian Patients with Cystic Fibrosis

Tai, Anna Sze, Bell, Scott Cameron, Kidd, Timothy James, Trembizki, Ella, Buckley, Cameron, Ramsay, Kay Annette, David, Michael, Wainwright, Claire Elizabeth, Grimwood, Keith and Whiley, David Mark (2015). Genotypic Diversity within a Single Pseudomonas aeruginosa Strain Commonly Shared by Australian Patients with Cystic Fibrosis. Plos One, 10 (12) e0144022, e0144022. doi: 10.1371/journal.pone.0144022

Genotypic Diversity within a Single Pseudomonas aeruginosa Strain Commonly Shared by Australian Patients with Cystic Fibrosis

2015

Journal Article

An international, multicentre evaluation and description of Burkholderia pseudomallei infection in cystic fibrosis

Geake, James B., Reid, David W., Currie, Bart J., Bell, Scott C., Bright-Thomas, Rowland, Dewar, Jane, Holden, Steve, Simmonds, Nicholas, Gyi, Khin, Kenna, Dervla, Waters, Valerie, Jackson, Mary, O'Sullivan, Brian, Taccetti, Giovanni, Kolbe, John, O'Carroll ,Mark, Campbell, Dee, Jaksic, Mirjana, Radhakrishna, Naghmeh, Kidd, Timothy J. and Flight, William (2015). An international, multicentre evaluation and description of Burkholderia pseudomallei infection in cystic fibrosis. BMC Pulmonary Medicine, 15 (1) 116. doi: 10.1186/s12890-015-0109-9

An international, multicentre evaluation and description of Burkholderia pseudomallei infection in cystic fibrosis

2015

Journal Article

Clinical utilization of genomics data produced by the international Pseudomonas aeruginosa consortium

Freschi, Luca, Jeukens, Julie, Kukavica-Ibrulj, Irene, Boyle, Brian, Dupont, Marie-Josee, Laroche, Jerome, Larose, Stephane, Maaroufi, Halim, Fothergill, Joanne L., Moore, Matthew, Winsor, Geoffrey L., Aaron, Shawn D., Barbeau, Jean, Bell, Scott C., Burns, Jane L., Camara, Miguel, Cantin, Andre, Charette, Steve J., Dewar, Ken, Deziel, Eric, Grimwood, Keith, Hancock, Robert E. W., Harrison, Joe J., Heebs, Stephan, Jelsbak, Lars, Jia, Baofeng, Kenna, Dervla T., Kidd, Timothy J., Klockgether, Jens ... Levesque, Roger C. (2015). Clinical utilization of genomics data produced by the international Pseudomonas aeruginosa consortium. Frontiers in Microbiology, 6 (SEP) 01036, 1-8. doi: 10.3389/fmicb.2015.01036

Clinical utilization of genomics data produced by the international Pseudomonas aeruginosa consortium

2015

Journal Article

A new phase of CFTR treatment for cystic fibrosis?

Bell, Scott C. (2015). A new phase of CFTR treatment for cystic fibrosis?. The Lancet Respiratory Medicine, 3 (9) 203, 662-663. doi: 10.1016/S2213-2600(15)00282-9

A new phase of CFTR treatment for cystic fibrosis?