Skip to menu Skip to content Skip to footer
Professor

Scott Bell

Email: 

Overview

Availability

Professor Scott Bell is:
Available for supervision

Works

Search Professor Scott Bell’s works on UQ eSpace

424 works between 1991 and 2025

181 - 200 of 424 works

2015

Journal Article

Molecular surveillance for carbapenemase genes in carbapenem-resistant Pseudomonas aeruginosa in Australian patients with cystic fibrosis

Tai, Anna S., Kidd, Timothy J., Whiley, David M., Ramsay, Kay A., Buckley, Cameron, Bell, Scott C., The ACPinCF Investigator Group and David, Michael (2015). Molecular surveillance for carbapenemase genes in carbapenem-resistant Pseudomonas aeruginosa in Australian patients with cystic fibrosis. Pathology, 47 (2), 156-160. doi: 10.1097/PAT.0000000000000216

Molecular surveillance for carbapenemase genes in carbapenem-resistant Pseudomonas aeruginosa in Australian patients with cystic fibrosis

2015

Journal Article

Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand

Chang, Anne B., Bell, Scott C., Torzillo, Paul J., King, Paul T., Maguire, Graeme P., Byrnes, Catherine A., Holland, Anne E., O’Mara, Peter, Grimwood, Keith, Alison, Jenny, Cull, Chris, Currie, Bart, Gardner, Inge, Holmes, Peter, Hunter, Cameron, Kolbe, John, Maclennan, Carolyn, McDonald, Malcolm, Morris, Peter, Nicolson, Caroline, Petsky, Helen, Pillarisetti, Naveen, Reynolds, Emma, Serisier, David, Thein, Frank, van Asperen, Peter, Voss, Lesley and Wong, Conroy (2015). Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand. Medical Journal of Australia, 202 (1), 21-24. doi: 10.5694/mja14.00287

Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand

2015

Journal Article

Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years

Kidd, Timothy J., Ramsay, Kay A., Vidmar, Suzanna, Carlin, John B., Bell, Scott C., Wainwright, Claire E. and Grimwood, Keith (2015). Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years. Journal of Cystic Fibrosis, 14 (3), 361-369. doi: 10.1016/j.jcf.2014.12.007

Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years

2015

Journal Article

A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT-1026) versus tobramycin inhalation solution in stable cystic fibrosis patients

Stuart Elborn, J., Geller, David E., Conrad, Douglas, Aaron, Shawn D., Smyth, Alan R., Fischer, Rainald, Kerem, Eitan, Bell, Scott C., Loutit, Jeffery S., Dudley, Michael N., Morgan, Elizabeth E., VanDevanter, Donald R. and Flume, Patrick A. (2015). A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT-1026) versus tobramycin inhalation solution in stable cystic fibrosis patients. Journal of Cystic Fibrosis, 14 (4), 507-514. doi: 10.1016/j.jcf.2014.12.013

A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT-1026) versus tobramycin inhalation solution in stable cystic fibrosis patients

2015

Journal Article

Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: A randomised trial

Dwyer, Tiffany J., Robbins, Lisel, Kelly, Patrick, Piper, Amanda J., Bell, Scott C. and Bye, Peter T.P. (2015). Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: A randomised trial. Journal of Physiotherapy, 61 (3), 142-147. doi: 10.1016/j.jphys.2015.05.019

Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: A randomised trial

2015

Journal Article

Future trends in cystic fibrosis demography in 34 European countries

Burgel, Pierre-Régis, Bellis, Gil, Olesen, Hanne V., Viviani, Laura, Zolin, Anna, Blasi, Francesco, Elborn, J. Stuart, Bell, Scott, Castellani, Carlo, Dembski, Birgit, Drevinek, Pavel, Heijerman, Harry, Innes, Alastair, Lindblad, Anders, Madge, Susan, De Rijcke, Karleen and Solé, Amparo (2015). Future trends in cystic fibrosis demography in 34 European countries. European Respiratory Journal, 46 (1), 133-141. doi: 10.1183/09031936.00196314

Future trends in cystic fibrosis demography in 34 European countries

2015

Journal Article

New pharmacological approaches for cystic fibrosis: Promises, progress, pitfalls

Bell, S.C., De Boeck, K. and Amaral, M.D. (2015). New pharmacological approaches for cystic fibrosis: Promises, progress, pitfalls. Pharmacology and Therapeutics, 145, 19-34. doi: 10.1016/j.pharmthera.2014.06.005

New pharmacological approaches for cystic fibrosis: Promises, progress, pitfalls

2014

Journal Article

JCF - 2014 and beyond

Bell, Scott C., Heijerman, Harry and Hartl, Dominik (2014). JCF - 2014 and beyond. Journal of Cystic Fibrosis, 13 (6), 610-611. doi: 10.1016/j.jcf.2014.09.009

JCF - 2014 and beyond

2014

Journal Article

Reduced mucosal associated invariant T-cells are associated with increased disease severity and Pseudomonas aeruginosa infection in cystic fibrosis

Smith, Daniel J., Hill, Geoffrey R., Bell, Scott C. and Reid, David W. (2014). Reduced mucosal associated invariant T-cells are associated with increased disease severity and Pseudomonas aeruginosa infection in cystic fibrosis. PLoS ONE, 9 (10) e109891, 1-8. doi: 10.1371/journal.pone.0109891

Reduced mucosal associated invariant T-cells are associated with increased disease severity and Pseudomonas aeruginosa infection in cystic fibrosis

2014

Journal Article

Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics

Smith, Daniel J., Badrick, Alison C., Zakrzewski, Martha, Krause, Lutz, Bell, Scott C., Anderson, Gregory J. and Reid, David W. (2014). Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics. European Respiratory Journal, 44 (4), 922-930. doi: 10.1183/09031936.00203013

Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics

2014

Journal Article

Antimicrobial treatment of non-cystic fibrosis bronchiectasis

Grimwood, K., Bell, S.C. and Chang, A.B. (2014). Antimicrobial treatment of non-cystic fibrosis bronchiectasis. Expert Review of Anti-Infective Therapy, 12 (10), 1277-1296. doi: 10.1586/14787210.2014.952282

Antimicrobial treatment of non-cystic fibrosis bronchiectasis

2014

Journal Article

Viability of Pseudomonas aeruginosa in cough aerosols generated by persons with cystic fibrosis

Knibbs, Luke D., Johnson, Graham R., Kidd, Timothy J., Cheney, Joyce, Grimwood, Keith, Kattenbelt, Jacqueline A., O'Rourke, Peter K., Ramsay, Kay A., Sly, Peter D., Wainwright, Claire E., Wood, Michelle E., Morawska, Lidia and Bell, Scott C. (2014). Viability of Pseudomonas aeruginosa in cough aerosols generated by persons with cystic fibrosis. Thorax, 69 (8), 740-745. doi: 10.1136/thoraxjnl-2014-205213

Viability of Pseudomonas aeruginosa in cough aerosols generated by persons with cystic fibrosis

2014

Journal Article

A comparison of two informative SNP-based strategies for typing Pseudomonas aeruginosa isolates from patients with cystic fibrosis

Syrmis, Melanie W., Kidd, Timothy J., Moser, Ralf J., Ramsay, Kay A., Gibson, Kristen M., Anuj, Snehal, Bell, Scott C., Wainwright, Claire E., Grimwood, Keith, Nissen, Michael, Sloots, Theo P. and Whiley, David M. (2014). A comparison of two informative SNP-based strategies for typing Pseudomonas aeruginosa isolates from patients with cystic fibrosis. BMC Infectious Diseases, 14 (1) 307, 307.1-307.8. doi: 10.1186/1471-2334-14-307

A comparison of two informative SNP-based strategies for typing Pseudomonas aeruginosa isolates from patients with cystic fibrosis

2014

Journal Article

Elevated metal concentrations in the CF airway correlate with cellular injury and disease severity

Smith, Daniel J., Anderson, Gregory J., Bell, Scott C. and Reid, David W. (2014). Elevated metal concentrations in the CF airway correlate with cellular injury and disease severity. Journal of Cystic Fibrosis, 13 (3), 289-295. doi: 10.1016/j.jcf.2013.12.001

Elevated metal concentrations in the CF airway correlate with cellular injury and disease severity

2014

Journal Article

European Cystic Fibrosis Society standards of care: best practice guidelines

Smyth, A.R., Bell, S.C., Bojcin, S., Bryon, M., Duff, A., Flume, P., Kashirskaya, N., Munck, A., Ratjen, F., Schwarzenberg, S.J., Sermet-Gaudelus, I., Southern, K.W., Taccetti, G., Ullrich, G. and Wolfe, S. (2014). European Cystic Fibrosis Society standards of care: best practice guidelines. Journal of Cystic Fibrosis, 13 (S1), S23-S42. doi: 10.1016/j.jcf.2014.03.010

European Cystic Fibrosis Society standards of care: best practice guidelines

2014

Journal Article

Molecular imprint of exposure to naturally occurring genetic variants of human cytomegalovirus on the T cell repertoire

Smith, Corey, Gras, Stephanie, Brennan, Rebekah M., Bird, Nicola L., Valkenburg, Sophie A., Twist, Kelly-Anne, Burrows, Jacqueline M., Miles, John J., Chambers, Daniel, Bell, Scott, Campbell, Scott, Kedzierska, Katherine, Burrows, Scott R., Rossjohn, Jamie and Khanna, Rajiv (2014). Molecular imprint of exposure to naturally occurring genetic variants of human cytomegalovirus on the T cell repertoire. Scientific Reports, 4 (1) 3993, 3993.1-3993.10. doi: 10.1038/srep03993

Molecular imprint of exposure to naturally occurring genetic variants of human cytomegalovirus on the T cell repertoire

2014

Conference Publication

Spreading the Word: Introducing Pre-Service Teachers to Programming in the K-12 Classroom

Bell, Scott, Frey, Tim and Vasserman, Eugene (2014). Spreading the Word: Introducing Pre-Service Teachers to Programming in the K-12 Classroom. 45th ACM SIGCSE Technical Symposium on Computer Science Education (SIGCSE), Atlanta Ga, Mar 05-08, 2014. NEW YORK: ASSOC COMPUTING MACHINERY. doi: 10.1145/2538862.2538963

Spreading the Word: Introducing Pre-Service Teachers to Programming in the K-12 Classroom

2014

Journal Article

Challenges of providing care to adults with cystic fibrosis

Bell, 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

Challenges of providing care to adults with cystic fibrosis

2014

Conference Publication

The Effect of Ivacaftor in Individuals with Cystic Fibrosis and Severe Lung Disease: Analysis of Data From the Australian Named Patient Programme

Wainwright, C., Bell, S., Morton, J., Ryan, G., Serisier, D., Bye, P., Mulrennan, S., Daley, C. and Greville, H. (2014). The Effect of Ivacaftor in Individuals with Cystic Fibrosis and Severe Lung Disease: Analysis of Data From the Australian Named Patient Programme. Annual Scientific Meeting of the Thoracic Society of Australia and New Zealand and the Australian and New Zealand Society of Respiratory Science 2014, Adelaide, SA Australia, 4-9 April 2014. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/resp.12263_10

The Effect of Ivacaftor in Individuals with Cystic Fibrosis and Severe Lung Disease: Analysis of Data From the Australian Named Patient Programme

2014

Conference Publication

Evidence of Cross-Transmission of a Multidrug Resistant (Mdr) Pseudomonas Aeruginosa Strain in Patient with Cystic Fibrosis (Cf)

Tai, A., Kidd, T., Ramsay, K., Bell, S. and Whiley, D. (2014). Evidence of Cross-Transmission of a Multidrug Resistant (Mdr) Pseudomonas Aeruginosa Strain in Patient with Cystic Fibrosis (Cf). Annual Scientific Meeting of the Thoracic Society of Australia and New Zealand and the Australian and New Zealand Society of Respiratory Science 2014, Adelaide, SA Australia, 4-9 April 2014. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/resp.12263_10

Evidence of Cross-Transmission of a Multidrug Resistant (Mdr) Pseudomonas Aeruginosa Strain in Patient with Cystic Fibrosis (Cf)

Funding

Current funding

  • 2025 - 2028
    Combating pathogens from biofilms in premise plumbing systems
    ARC Linkage Projects
    Open grant
  • 2023 - 2026
    Making Australia resilient to airborne infection transmission (ARC Linkage Project administered by Queensland University of Technology)
    Queensland University of Technology
    Open grant
  • 2019 - 2026
    Finding the Optimal Regimen for Mycobacterium Abscessus Treatment (FORMAT)
    Cystic Fibrosis Foundation USA
    Open grant
  • 2019 - 2026
    Queensland cystic fibrosis research program
    The Children's Hospital Foundation
    Open grant
  • 2018 - 2026
    Multi-drug resistant non-tuberculous mycobacteria infection research
    Research Donation Generic
    Open grant

Past funding

  • 2021 - 2023
    Prevention of SARS-CoV-2 transmission in aged care (PETRA formerly PreSTAC): Effective evidence-based measures for rapid translation - External led SAHMRI
    South Australian Health and Medical Research Institute Limited
    Open grant
  • 2020
    BD Bactec MGIT 320 System
    Prince Charles Hospital Foundation
    Open grant
  • 2020 - 2023
    The emerging problem of non-tuberculous mycobacteria infection: Understanding aetiology, geospatial epidemiology and developing interventions
    NHMRC Project Grant
    Open grant
  • 2019 - 2024
    Early life origins of cystic fibrosis lung disease
    Cystic Fibrosis Foundation USA
    Open grant
  • 2019
    Establishing UQ Centre for Clinical Research as the centre for Aerosol therapy in critical care by optimising particle size of aerosols for effective drug delivery.
    UQ Major Equipment and Infrastructure
    Open grant
  • 2018 - 2021
    Enhancing detection and management of Mycobacterium abscessus complex (MABSC) infection in children with cystic fibrosis
    The Children's Hospital Foundation
    Open grant
  • 2016 - 2019
    Macrophages: the forgotten cells in CF lung disease
    Cystic Fibrosis Foundation Therapeutics Inc
    Open grant
  • 2016 - 2020
    The acquired resistome of Pseudomonas aeruginosa strains in people with cystic fibrosis (Joint UQ/QIMR AID seed grant awarded to QIMRB)
    Queensland Institute of Medical Research
    Open grant
  • 2016 - 2019
    The emerging problem of non-tuberculous mycobacteria infection: understanding aetiology, geospatial epidemiology and developing interventions (NHMRC Project led by QIMR Berghofer)
    Queensland Institute of Medical Research
    Open grant
  • 2015 - 2017
    Abnormal lung iron homeostasis in cystic fibrosis (NHMRC Project Grant administered by QIMR)
    Queensland Institute of Medical Research
    Open grant
  • 2014 - 2016
    Intra-strain diversity of Pseudomonas aeruginosa in the lungs of patients with CF and their role in exacerbation
    Prince Charles Hospital Foundation
    Open grant
  • 2013 - 2014
    Purchase of -80C Freezer - XYCYST
    Prince Charles Hospital Foundation
    Open grant
  • 2012 - 2014
    Airborne Infection Transport in Hospitals
    Prince Charles Hospital Foundation
    Open grant
  • 2010 - 2016
    Inflammatory airways disease in children with a focus on cystic fibrosis
    Royal Children's Hospital Foundation
    Open grant
  • 2010 - 2011
    Longitudinal study of clonal Pseudomonas aeruginosa in cystic fibrosis
    Queensland Health
    Open grant
  • 2010 - 2011
    Development of a novel assay for the detection of clonal P.aeruginosa in persons with CF
    Australian Cystic Fibrosis Research Trust
    Open grant
  • 2010 - 2011
    Longitudinal study of clonal Pseudomonas aeruginosa in cystic fibrosis
    Royal Children's Hospital Foundation
    Open grant
  • 2009 - 2015
    A statewide, electronic, disease specific, clinical record/database for children and adults with cystic fibrosis (electronic medical record for cystic fibrosis)
    Royal Children's Hospital Foundation
    Open grant
  • 2007 - 2010
    Clinical impact of clonal Pseudomonas aeruginosa in cystic fibrosis
    NHMRC Project Grant
    Open grant
  • 2005 - 2010
    How Children and adults with cystic fibrosis get lung infections with Pseudomonas aeruginosa
    Royal Children's Hospital Foundation
    Open grant

Supervision

Availability

Professor Scott Bell is:
Available for supervision

Looking for a supervisor? Read our advice on how to choose a supervisor.

Supervision history

Current supervision

  • Doctor Philosophy

    Risk and mitigation of cough aerosols for people with cystic fibrosis.

    Principal Advisor

    Other advisors: Professor Rachel Thomson

  • Doctor Philosophy

    The Pharmacokinetics & Pharmacodynamics of Antimycobacterial Drugs in People with Cystic Fibrosis and Drug-Resistant Tuberculosis Infection

    Associate Advisor

    Other advisors: Professor Rachel Thomson, Professor Jason Roberts

Completed supervision

Media

Enquiries

For media enquiries about Professor Scott Bell's areas of expertise, story ideas and help finding experts, contact our Media team:

communications@uq.edu.au