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)

341 - 360 of 411 works

2003

Journal Article

Genomovar diversity amongst Burkholderia cepacia complex isolates from an Australian adult cystic fibrosis unit

Kidd, T. J., Bell, S. C. and Coulter, C. (2003). Genomovar diversity amongst Burkholderia cepacia complex isolates from an Australian adult cystic fibrosis unit. European Journal of Clinical Microbiology & Infectious Diseases, 22 (7), 434-437. doi: 10.1007/s10096-003-0949-8

Genomovar diversity amongst Burkholderia cepacia complex isolates from an Australian adult cystic fibrosis unit

2003

Conference Publication

Pseudomonas aeruginosa exposed to sub-inhibitory ceftazidime or tobramycin has reduced homoserine lactones

Garske, L., Bell, S. C., Beatson, S., Walsh, S., Mattick, J., Leach, A. and Whitchurch, C. (2003). Pseudomonas aeruginosa exposed to sub-inhibitory ceftazidime or tobramycin has reduced homoserine lactones. The Thoracic Society of Australia and New Zealand 2003 Annual Scientific Meeting, Adelaide, Australia, 4 - 9 April 2003. Carlton, VIC: Blackwell Science. doi: 10.1111/j.1440-1843.2003.supp_1.x

Pseudomonas aeruginosa exposed to sub-inhibitory ceftazidime or tobramycin has reduced homoserine lactones

2003

Conference Publication

Total energy expenditure in cystic fibrosis: Comparison of measurement by double labelled water vs heart rate technique

Greer, R., Bell, S. C., Richards, M. L. and Davies, P.S.W. (2003). Total energy expenditure in cystic fibrosis: Comparison of measurement by double labelled water vs heart rate technique. 26th European Cystic Fibrosis Conference, Belfast, Ireland, 5–7 June 2003. Amsterdam, Netherlands: Elsevier BV. doi: 10.1016/S1569-1993(03)00027-4

Total energy expenditure in cystic fibrosis: Comparison of measurement by double labelled water vs heart rate technique

2003

Journal Article

Antibiotic desensitization in adults with cystic fibrosis

Burrows, J. A., Toon, M. and Bell, S. C. (2003). Antibiotic desensitization in adults with cystic fibrosis. Respirology, 8 (3), 359-364. doi: 10.1046/j.1440-1843.2003.00461.x

Antibiotic desensitization in adults with cystic fibrosis

2003

Conference Publication

Presence of epidemic Pseudomonas aeruginosa shared between paediatric and adult cystic fibrosis

O'Carroll, M. R., Coulter, C., Bell, S. C., Syrmis, M., Wainwright, C. E., Nissen, M. and Sloots, T. (2003). Presence of epidemic Pseudomonas aeruginosa shared between paediatric and adult cystic fibrosis. 26th European CF Conference, Belfast, Ireland, 5–7 June , 2003. Netherlands: Elsevier Science. doi: 10.1016/S1569-1993(03)00027-4

Presence of epidemic Pseudomonas aeruginosa shared between paediatric and adult cystic fibrosis

2003

Journal Article

Assessment of bioelectrical impedance analysis for the prediction of total body water in cystic fibrosis

Richards, M.L., Bell, S.C., Edmiston, K.A. and Davies, P.S.W. (2003). Assessment of bioelectrical impedance analysis for the prediction of total body water in cystic fibrosis. Asia Pacific Journal of Clinical Nutrition, 12 (2), 161-165.

Assessment of bioelectrical impedance analysis for the prediction of total body water in cystic fibrosis

2003

Conference Publication

Gender differences in CF phenotype associated with low bone mineral density

Greer, R., O'Rourke, P. K., Buntain, H. M., Batch, J. A., Francis, P. W. and Bell, S. C. (2003). Gender differences in CF phenotype associated with low bone mineral density. 26th Congress of the European Cystic Fibrosis Society, Belfast, 5 Jun, 2003. Amsterdam: Elsevier BV.

Gender differences in CF phenotype associated with low bone mineral density

2003

Conference Publication

Achromobacter xylosoxidans and stenotrophomonas maltophilia in an adult cystic fibrosis population: prevalence and clinical characteristics

Masel, P. J., Bunting, J. P., Franks, C., Kim, S., Kidd, T. J. and Bell, S. C. (2003). Achromobacter xylosoxidans and stenotrophomonas maltophilia in an adult cystic fibrosis population: prevalence and clinical characteristics. 5th Australian & New Zealand Cystic Fibrosis Conference 2003, Melbourne, 21-23 Aug, 2003.

Achromobacter xylosoxidans and stenotrophomonas maltophilia in an adult cystic fibrosis population: prevalence and clinical characteristics

2003

Conference Publication

Rapid genotyping of Pseudomonas aeruginosa using repetitive element based PCr assays

O'Carroll, M. R., Bell, S. C., Coulter, C., Wainwright, C. E., Nissen, M., Sloots, T. and Syrmis, M. (2003). Rapid genotyping of Pseudomonas aeruginosa using repetitive element based PCr assays. TSANZ 2003 Annual Scientific Meeting, Adelaide, Australia, 4-9 April, 2003. Carlton South, Australia: doi: 10.1111/j.1440-1843.2003.supp_1.x

Rapid genotyping of Pseudomonas aeruginosa using repetitive element based PCr assays

2003

Conference Publication

Differences in lung function, growth parameters and frequency of hospital admissions between adolescents with cystic fibrosis-related diabetes and controls

Matson, A., McMahon, S., Bell, S. C., Batch, J. and Francis, P. (2003). Differences in lung function, growth parameters and frequency of hospital admissions between adolescents with cystic fibrosis-related diabetes and controls. 26th European CF Conference, Belfast, Ireland, 5–7 June 2003. Amsterdam, Netherlands: Elsevier. doi: 10.1016/S1569-1993(03)00027-4

Differences in lung function, growth parameters and frequency of hospital admissions between adolescents with cystic fibrosis-related diabetes and controls

2003

Journal Article

Abnormalities of the PTH-vitamin D axis and bone turnover markers in children, adolescents and adults with cystic fibrosis: comparison with healthy controls

Greer, Ristan M., Buntain, Helen M., Potter, Julia M., Wainwright, Claire E., Wong, Joseph C., O'Rourke, Peter K., Francis, Paul W., Bell, Scott C. and Batch, Jennifer A. (2003). Abnormalities of the PTH-vitamin D axis and bone turnover markers in children, adolescents and adults with cystic fibrosis: comparison with healthy controls. Osteoporosis International, 14 (5), 404-411. doi: 10.1007/s00198-003-1388-1

Abnormalities of the PTH-vitamin D axis and bone turnover markers in children, adolescents and adults with cystic fibrosis: comparison with healthy controls

2002

Journal Article

Novel application of biological glue in the management of a complicated pneumothorax in cystic fibrosis

Garske, Luke A., Tam, Robert K.W., Windsor, Morgan F. and Bell, Scott C. (2002). Novel application of biological glue in the management of a complicated pneumothorax in cystic fibrosis. Pediatric Pulmonology, 34 (2), 138-140. doi: 10.1002/ppul.10112

Novel application of biological glue in the management of a complicated pneumothorax in cystic fibrosis

2002

Journal Article

Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: A randomised trial

Wolter, J., Seeney, S., Bell, S., Bowler, S., Masel, P. and McCormack, J. (2002). Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: A randomised trial. Thorax, 57 (3), 212-216. doi: 10.1136/thorax.57.3.212

Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: A randomised trial

2002

Journal Article

Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: a randomised trial

Wolter, J., Seeney, S., Bell, S., Bowler, S., Masel, P. and McCormack, J. (2002). Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: a randomised trial. Thorax, 57 (3), 212-216. doi: 10.1136/thorax.57.3.212

Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: a randomised trial

2002

Conference Publication

Prevalence of cystic fibrosis-related diabetes (CFRD) in an adult cystic fibrosis (CF) unit

Matson, A., Walker, F., Matson, K. and Bell, S. C. (2002). Prevalence of cystic fibrosis-related diabetes (CFRD) in an adult cystic fibrosis (CF) unit. TSANZ Annual Scientific Meeting, Cairns, 22-27 Mar, 2002. Carlton: Blackwell Asia.

Prevalence of cystic fibrosis-related diabetes (CFRD) in an adult cystic fibrosis (CF) unit

2002

Journal Article

Nebulised dornase alpha: adherence in adults with cystic fibrosis

Burrows, J. A., Bunting, J. P., Masel, P. J. and Bell, S. C. (2002). Nebulised dornase alpha: adherence in adults with cystic fibrosis. Journal of Cystic Fibrosis, 1 (4), 255-259. doi: 10.1016/S1569-1993(02)00095-4

Nebulised dornase alpha: adherence in adults with cystic fibrosis

2002

Conference Publication

Uncoupled bone turnover in cystic fibrosis: bone markers and the PTH-vitamin D axis

Greer, R. M., Buntain, H., Wainwright, C. E., Potter, J. M., Munns, C., O'Rourke, P., Francis, P., Batch, J. and Bell, S. C. (2002). Uncoupled bone turnover in cystic fibrosis: bone markers and the PTH-vitamin D axis. 16th Annual North American Cystic Fibrosis Conference, Louisiana, 3-6 October, 2002. New York: Wiley-Liss. doi: 10.1002/ppul.70012

Uncoupled bone turnover in cystic fibrosis: bone markers and the PTH-vitamin D axis

2002

Conference Publication

Puberty and bone mineral accrual in cystic fibrosis

Buntain, H. M., Greer, R. M., Batch, J., Wong, J., Lewindon, P., Schluter, P., Bell, S. C., Potter, J. and Wainwright, C. E. (2002). Puberty and bone mineral accrual in cystic fibrosis. TSANZ 2002 Annual Scientific Meeting. Respirology, Cairns, QLD, Australia, 22-27 March 2002. Carlton, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1843.2004.supp_2.x

Puberty and bone mineral accrual in cystic fibrosis

2002

Conference Publication

Age appropriate pubertal development in cystic fibrosis

Buntain, H., Greer, R. M., Schluter, P., Batch, J., Bell, S. C. and Wainwright, C. E. (2002). Age appropriate pubertal development in cystic fibrosis. The 16th Annual North American Cystic Fibrosis Conference, Louisiana, 3-6 October, 2002. New York: Wiley-Liss. doi: 10.1002/ppul.70012

Age appropriate pubertal development in cystic fibrosis

2002

Conference Publication

Rifampicin and fusidic acid reduces the frequency of MRSA isolation and need for intravenous antibiotics in adult patients with cystic fibrosis and chronic MRSA infection

Garske, L., Bunting, J., Franks, C., Masel, P. and Bell, S. (2002). Rifampicin and fusidic acid reduces the frequency of MRSA isolation and need for intravenous antibiotics in adult patients with cystic fibrosis and chronic MRSA infection. TSANZ Annual Scientific Meeting, Cairns, 22-27 Mar, 2002. Carlton: Blackwell Asia.

Rifampicin and fusidic acid reduces the frequency of MRSA isolation and need for intravenous antibiotics in adult patients with cystic fibrosis and chronic MRSA infection

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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