Professor

Scott Bell

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Availability

Professor Scott Bell is:
Available for supervision

Fields of research

Clinical sciences Medical microbiology

Search Professor Scott Bell’s works on UQ eSpace

411 works between 1991 and 2025
All (411) Journal Article (292) Book Chapter (6) Conference Publication (109) Other Outputs (4)

141 - 160 of 411 works

2016

Journal Article

Lesch-Nyhan syndrome: Models, theories, and therapies

Bell, Scott, Kolobova, Ilaria, Crapper, Liam and Ernst, Carl (2016). Lesch-Nyhan syndrome: Models, theories, and therapies. Molecular Syndromology, 7 (6), 302-311. doi: 10.1159/000449296

Lesch-Nyhan syndrome: Models, theories, and therapies

2016

Journal Article

Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki

Smyth, Alan R., Bell, Scott C., Bojcin, Snezana, Bryon, Mandy, Duff, Alistair, Flume, Patrick, Kashirskaya, Nataliya, Munck, Anne, Ratjen, Felix, Schwarzenberg, Sarah Jane, Sermet-Gaudelus, Isabelle, Southern, Kevin W., Taccetti, Giovanni, Ullrich, Gerald and Wolfe, Sue (2016). Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki. Pediatria Polska, 91 (Supp.1), S30-S53. doi: 10.1016/j.pepo.2016.08.014

Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki

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

Current funding

  • 2019 - 2025
    Finding the Optimal Regimen for Mycobacterium Abscessus Treatment (FORMAT)
    Cystic Fibrosis Foundation USA
    Open grant
  • 2019 - 2025
    Queensland cystic fibrosis research program
    The Children's Hospital Foundation
    Open grant
  • 2018 - 2025
    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

Availability

Professor Scott Bell is:
Available for supervision

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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

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

    Principal Advisor

    Other advisors: Professor Rachel Thomson

  • Doctor Philosophy

    Pharmacokinetics of anti-mycobacterial drugs in patients with cystic fibrosis

    Associate Advisor

    Other advisors: Professor Rachel Thomson, Professor Jason Roberts

Completed supervision

Enquiries

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