Professor Scott Bell

Butler, Claire A. and Bell, Scott C. (2011). Integrative Therapies for People with Cystic Fibrosis. Integrative Therapies in Lung Health and Sleep. (pp. 113-126) Totowa, NJ: Humana Press. doi: 10.1007/978-1-61779-579-4_6

Kidd, Timothy J., Whiley, David M., Bell, Scott C. and Grimwood, Keith (2011). Pseudomonas. Molecular detection of human bacterial pathogens. (pp. 1009-1021) edited by Dongyou Liu. Boca Raton, FL, USA: Taylor & Francis.

Smith, D. J., Chang, A. B. and Bell, S. C. (2011). Anti-inflammatory therapies in bronchiectasis. Bronchiectasis. (pp. 233-238) edited by R.A. Floto and C.S. Haworth. Lausanne, Switzerland: European Respiratory Society. doi: 10.1183/1025448x.100004510

Jones, A. M. and Bell, S. C. (2006). Cystic Fibrosis Infection with Clonal Strains of Pseudomonas Aeruginosa: Current Knowledge and Future Management. Cystic Fibrosis. (pp. 105-126) edited by K. Webb and F. Ratjen. London: Maney Publishing.

Yang, I. A., Kim, S. T. and Bell, S. C. (2005). Antiobiotics in chronic obstructive pulmonary disease, bronchiectasis and cystic fibrosis. Evidence-based Respiratory Medicine. (pp. 389-414) edited by P. Gibson. Carlton South, Australia: Blackwell Publishing Asia. doi: 10.1002/9780470987377.ch30

Davidson, Sarah J, France, Megan, Callaway, Leonie K, Lust, Karin, Chambers, Daniel, Hopkins, Peter, Bell, Scott C, Burr, Lucy, Keating, Rebecca and Barrett, Helen L (2022). Pregnancy in women with cystic fibrosis and diabetes: An audit of outcomes at two tertiary obstetric hospitals in Australia in the pre-cystic fibrosis transmembrane conductance regulator modulator era. Obstetric Medicine, 1753495X2211463. doi: 10.1177/1753495x221146342

Ruseckaite, Rasa, Salimi, Farhad, Earnest, Arul, Bell, Scott C., Douglas, Tonia, Frayman, Katherine, Keatley, Lucy, King, Susannah, Kotsimbos, Tom, Middleton, Peter G., Morey, Sue, Mulrennan, Siobhain, Schultz, Andre, Wainwright, Claire, Ward, Nathan, Wark, Peter and Ahern, Susannah (2022). Survival of people with cystic fibrosis in Australia. Scientific Reports, 12 (1) 19748, 1-9. doi: 10.1038/s41598-022-24374-4

Ratnatunga, Champa N., Tungatt, Katie, Proietti, Carla, Halstrom, Sam, Holt, Michael R., Lutzky, Viviana P., Price, Patricia, Doolan, Denise L., Bell, Scott C., Field, Matt A., Kupz, Andreas, Thomson, Rachel M. and Miles, John J. (2022). Characterizing and correcting immune dysfunction in non-tuberculous mycobacterial disease. Frontiers in Immunology, 13 1047781, 1-20. doi: 10.3389/fimmu.2022.1047781

Madden, Danielle E., McCarthy, Kate L., Bell, Scott C., Olagoke, Olusola, Baird, Timothy, Neill, Jane, Ramsay, Kay A., Kidd, Timothy J., Stewart, Adam G., Subedi, Shradha, Choong, Keat, Fraser, Tamieka A., Sarovich, Derek S. and Price, Erin P. (2022). Rapid fluoroquinolone resistance detection in Pseudomonas aeruginosa using mismatch amplification mutation assay-based real-time PCR. Journal of Medical Microbiology, 71 (10), 1-10. doi: 10.1099/jmm.0.001593

Nguyen, Thi Tham, He, Congrong, Carter, Robyn, Ballard, Emma L., Smith, Kim, Groth, Robert, Jaatinen, Esa, Kidd, Timothy J., Nguyen, Thuy-Khanh, Stockwell, Rebecca E., Tay, George, Johnson, Graham R., Bell, Scott C. and Knibbs, Luke D. (2022). The effectiveness of ultraviolet-C (UV-C) irradiation on the viability of airborne Pseudomonas aeruginosa. International Journal of Environmental Research and Public Health, 19 (20) 13706, 1-15. doi: 10.3390/ijerph192013706

Nguyen, Thi Tham, He, Congrong, Carter, Robyn, Ballard, Emma L., Smith, Kim, Groth, Robert, Jaatinen, Esa, Kidd, Timothy J., Thomson, Rachel, Tay, George, Johnson, Graham R., Bell, Scott C. and Knibbs, Luke D. (2022). Quantifying the effectiveness of ultraviolet-C (UV-C) light at inactivating airborne Mycobacterium abscessus. Journal of Hospital Infection. doi: 10.1016/j.jhin.2022.10.008

Coriati, Adèle, Ma, Xiayi, Sykes, Jenna, Stanojevic, Sanja, Ruseckaite, Rasa, Lemonnier, Lydie, Dehillotte, Clémence, Tate, Jan, Byrnes, Catherine Ann, Bell, Scott C, Burgel, Pierre Regis and Stephenson, Anne L (2022). Beyond borders: cystic fibrosis survival between Australia, Canada, France and New Zealand. Thorax 219086, thoraxjnl-2022. doi: 10.1136/thorax-2022-219086

Lloyd, Elizabeth C., Cogen, Jonathan D., Maples, Holly, Bell, Scott C. and Saiman, Lisa (2022). Antimicrobial Stewardship in Cystic Fibrosis. Journal of the Pediatric Infectious Diseases Society, 11 (2), S53-S61. doi: 10.1093/jpids/piac071

Smith, Daniel J and Bell, Scott C (2022). Next steps on managing pulmonary exacerbations: Is the future less, shorter and or more targeted treatments?. Journal of Cystic Fibrosis, 21 (5), 739-740. doi: 10.1016/j.jcf.2022.08.015

Madden, Danielle E., Olagoke, Olusola, Baird, Timothy, Neill, Jane, Ramsay, Kay A., Fraser, Tamieka A., Bell, Scott C., Sarovich, Derek S. and Price, Erin P. (2022). Express yourself: quantitative real-time PCR assays for rapid chromosomal antimicrobial resistance detection in Pseudomonas aeruginosa. Antimicrobial Agents and Chemotherapy, 66 (5) e0020422, e0020422. doi: 10.1128/aac.00204-22

Karunathilaka, Amali, Halstrom, Samuel, Price, Patricia, Holt, Michael, Lutzky, Viviana P., Doolan, Denise L., Kupz, Andreas, Bell, Scott C., Thomson, Rachel M., Miles, John J. and Ratnatunga, Champa N. (2022). CD161 expression defines new human γδ T cell subsets. Immunity and Ageing, 19 (1) 11, 1-8. doi: 10.1186/s12979-022-00269-w

Webb, Kasey A., Olagoke, Olusola, Baird, Timothy, Neill, Jane, Pham, Amy, Wells, Timothy J., Ramsay, Kay A., Bell, Scott C., Sarovich, Derek S. and Price, Erin P. (2022). Genomic diversity and antimicrobial resistance of Prevotella species isolated from chronic lung disease airways. Microbial Genomics, 8 (2) 000754. doi: 10.1099/mgen.0.000754

Ramsey, Bonnie W and Bell, Scott C. (2022). Cystic fibrosis: a disease in transformation, yet more work to be done!. American Journal of Respiratory and Critical Care Medicine, 205 (5), 487-489. doi: 10.1164/rccm.202112-2782ed

Nguyen, Thi Tham, Johnson, Graham R., Bell, Scott C. and Knibbs, Luke D. (2022). A systematic literature review of indoor air disinfection techniques for airborne bacterial respiratory pathogens. International Journal of Environmental Research and Public Health, 19 (3) 1197. doi: 10.3390/ijerph19031197

Kelk, Dean, Logan, Jayden, Andersen, Isabella, Gutierrez Cardenas, Diana, Bell, Scott C., Wainwright, Claire E., Sly, Peter D. and Fantino, Emmanuelle (2022). Neutrophil respiratory burst activity is not exaggerated in cystic fibrosis. Journal of Cystic Fibrosis, 21 (4), 707-712. doi: 10.1016/j.jcf.2021.12.015

Chin, Melanie, Brennan, Amanda L. and Bell, Scott C. (2022). Emerging Nonpulmonary Complications for Adults With Cystic Fibrosis. Chest, 161 (5), 1211-1224. doi: 10.1016/j.chest.2021.11.001

Martin, Elizabeth, Campbell, Megan, Parsonage, William, Rosengren, David, Bell, Scott C. and Graves, Nick (2021). What it takes to build a health services innovation training program. International Journal of Medical Education, 12, 259-263. doi: 10.5116/ijme.61af.30bd

Ruis, Christopher, Bryant, Josephine M., Bell, Scott C., Thomson, Rachel, Davidson, Rebecca M., Hasan, Nabeeh A., van Ingen, Jakko, Strong, Michael, Floto, R. Andres and Parkhill, Julian (2021). Dissemination of Mycobacterium abscessus via global transmission networks. Nature Microbiology, 6 (10), 1279-1288. doi: 10.1038/s41564-021-00963-3

Brass, Amanda, Shoubridge, Andrew P., Crotty, Maria, Morawska, Lidia, Bell, Scott C., Qiao, Ming, Woodman, Richard J., Whitehead, Craig, Inacio, Maria C., Miller, Caroline, Corlis, Megan, Larby, Nicolas, Elms, Levi, Sims, Sarah K., Taylor, Steven L., Flynn, Erin, Papanicolas, Lito E. and Rogers, Geraint B. (2021). Prevention of SARS-CoV-2 (COVID-19) transmission in residential aged care using ultraviolet light (PETRA): a two-arm crossover randomised controlled trial protocol. BMC Infectious Diseases, 21 (1) 967. doi: 10.1186/s12879-021-06659-7

Semasinghe Bandaralage, Sahan P., Tay, George, Hay, Karen, Megram, Emma, Smith, Daniel, Gadowski, Tahlia, Wright, Eimear, France, Megan, Bell, Scott and Reid, David (2021). Outcomes of artery embolisation for cystic fibrosis patients with haemoptysis: a 20-year experience at a major Australian tertiary centre. Internal Medicine Journal, 51 (9), 1526-1529. doi: 10.1111/imj.15483

Pham, Amy, Ledger, Emma L., Coggon, Carrie F., Henderson, Ian R., Reid, David W., Bell, Scott C., Smith, Daniel J. and Wells, Timothy J. (2021). Anti-LPS IgA and IgG can inhibit serum killing of Pseudomonas aeruginosa in patients with cystic fibrosis. Infection and Immunity, 89 (12) e00412-21, e0041221. doi: 10.1128/iai.00412-21

Wark, Peter AB, MacIntyre, C Raina, Bell, Scott, Oliver, Brian and Marks, Guy B (2021). We are not doing enough to prevent the spread of COVID-19 and other respiratory viruses in Australian hospitals. Medical Journal of Australia, 215 (4), 152-153.e1. doi: 10.5694/mja2.51183

Burke, Andrew, Smith, Daniel, Coulter, Chris, Bell, Scott C., Thomson, Rachel and Roberts, Jason A. (2021). Clinical pharmacokinetic and pharmacodynamic considerations in the drug treatment of non-tuberculous mycobacteria in cystic fibrosis. Clinical Pharmacokinetics, 60 (9), 1081-1102. doi: 10.1007/s40262-021-01010-4

Bullington, Wendy, Hempstead, Sarah, Smyth, Alan R., Drevinek, Pavel, Saiman, Lisa, Waters, Valerie J., Bell, Scott C., VanDevanter, Donald R., Flume, Patrick A., Elborn, Stuart and Muhlebach, Marianne S (2021). Antimicrobial resistance: concerns of healthcare providers and people with CF. Journal of Cystic Fibrosis, 20 (3), 407-412. doi: 10.1016/j.jcf.2020.05.009

Bordin, Amanda, Pandey, Sushil, Coulter, Christopher, Syrmis, Melanie, Pardo, Carolyn, Hackett, Hazel, Bell, Scott C., Wainwright, Claire E., Nimmo, Graeme R., Jennison, Amy V., Clark, Julia E. and Whiley, David M. (2021). Rapid macrolide and amikacin resistance testing for Mycobacterium abscessus in people with cystic fibrosis. Journal of Medical Microbiology, 70 (4) 001349, 1-11. doi: 10.1099/jmm.0.001349

Ahern, Susannah, Dean, Joanne, Liman, John, Ruseckaite, Rasa, Burke, Nettie, Gollan, Morgan, Keatley, Lucy, King, Susannah, Kotsimbos, Tom, Middleton, Peter G., Schultz, Andre, Wainwright, Claire, Wark, Peter and Bell, Scott (2021). Redesign of the Australian Cystic Fibrosis Data Registry: a multidisciplinary collaboration. Paediatric Respiratory Reviews, 37, 37-43. doi: 10.1016/j.prrv.2020.03.001

Hall, Kathleen, Maxwell, Lyndal, Cobb, Robyn, Steele, Michael, Chambers, Rebecca, Roll, Mark, Bell, Scott Cameron and Kuys, Suzanne (2021). Physiotherapy service provision in a specialist adult cystic fibrosis service: a pre-post design study with the inclusion of an allied health assistant. Chronic Respiratory Disease, 18, 14799731211017895. doi: 10.1177/14799731211017895

Sherrard, Laura J., Wee, Bryan A., Duplancic, Christine, Ramsay, Kay A., Dave, Keyur A., Ballard, Emma, Wainwright, Claire E., Grimwood, Keith, Sidjabat, Hanna E., Whiley, David M., Beatson, Scott A., Kidd, Timothy J. and Bell, Scott C. (2021). Emergence and impact of oprD mutations in Pseudomonas aeruginosa strains in cystic fibrosis. Journal of Cystic Fibrosis, 21 (1), e35-e43. doi: 10.1016/j.jcf.2021.03.007

Thomson, Rachel M., Furuya-Kanamori, Luis, Coffey, Cushla, Bell, Scott C., Knibbs, Luke D. and Lau, Colleen L. (2020). Influence of climate variables on the rising incidence of nontuberculous mycobacterial (NTM) infections in Queensland, Australia 2001–2016. Science of the Total Environment, 740 139796, 139796. doi: 10.1016/j.scitotenv.2020.139796

Earnest, Arul, Salimi, Farhad, Wainwright, Claire E., Bell, Scott C., Ruseckaite, Rasa, Ranger, Tom, Kotsimbos, Tom and Ahern, Susannah (2020). Lung function over the life course of paediatric and adult patients with cystic fibrosis from a large multi-centre registry. Scientific Reports, 10 (1) 17421, 17421. doi: 10.1038/s41598-020-74502-1

Somayaji, Ranjani, Nichols, Dave P. and Bell, Scott C. (2020). Cystic fibrosis–Ten promising therapeutic approaches in the current era of care. Expert Opinion on Investigational Drugs, 29 (10), 1107-1124. doi: 10.1080/13543784.2020.1805733

Price, Erin P., Soler Arango, Valentina, Kidd, Timothy J., Fraser, Tamieka A., Nguyen, Thuy-Khanh, Bell, Scott C. and Sarovich, Derek S. (2020). Duplex real-time PCR assay for the simultaneous detection of Achromobacter xylosoxidans and Achromobacter spp. Microbial Genomics, 6 (7) 000406, 1-11. doi: 10.1099/mgen.0.000406

Hall, Kathleen, Maxwell, Lyndal, Cobb, Robyn, Chambers, Rebecca, Roll, Mark, Bell, Scott C. and Kuys, Suzanne (2020). Benchmarking service provision, scope of practice, and skill mix for physiotherapists in adult cystic fibrosis care delivery. Physiotherapy Theory and Practice, 38 (4), 1-7. doi: 10.1080/09593985.2020.1777606

Cosgriff, Rebecca, Ahern, Susannah, Bell, Scott C., Brownlee, Keith, Burgel, Pierre-Régis, Byrnes, Cass, Corvol, Harriet, Cheng, Stephanie Y., Elbert, Alexander, Faro, Albert, Goss, Christopher H., Gulmans, Vincent, Marshall, Bruce C., McKone, Edward, Middleton, Peter G., Ruseckaite, Rasa, Stephenson, Anne L. and Carr, Siobhán B (2020). A multinational report to characterise SARS-CoV-2 infection in people with cystic fibrosis. Journal of Cystic Fibrosis, 19 (3), 355-358. doi: 10.1016/j.jcf.2020.04.012

Zemanick, Edith, Burgel, Pierre-Régis, Taccetti, Giovanni, Holmes, Alison, Ratjen, Felix, Byrnes, Catherine A., Waters, Valerie J., Bell, Scott C., VanDevanter, Donald R., Stuart Elborn, J. and Flume, Patrick A. (2020). Antimicrobial resistance in cystic fibrosis: A Delphi approach to defining best practices. Journal of Cystic Fibrosis, 19 (3), 370-375. doi: 10.1016/j.jcf.2019.10.006

Bell, Scott C., Flume, Patrick A. and Castellani, Carlo (2020). Seven P's of publication practices. Journal of Cystic Fibrosis, 19 (3), 333-335. doi: 10.1016/j.jcf.2020.02.007

Pearson, Talima, Sahl, Jason W., Hepp, Crystal M., Handady, Karthik, Hornstra, Heidie, Vazquez, Adam J., Settles, Erik, Mayo, Mark, Kaestli, Mirjam, Williamson, Charles H. D., Price, Erin P., Sarovich, Derek S., Cook, James M., Wolken, Spenser R., Bowen, Richard A., Tuanyok, Apichai, Foster, Jeffrey T., Drees, Kevin P., Kidd, Timothy J., Bell, Scott C., Currie, Bart J. and Keim, Paul (2020). Pathogen to commensal? Longitudinal within-host population dynamics, evolution, and adaptation during a chronic >16-year Burkholderia pseudomallei infection. PLoS Pathogens, 16 (3) e1008298, e1008298. doi: 10.1371/journal.ppat.1008298

Flume, Patrick, Bell, Scott C. and Castellani, Carlo (2020). Pursuit of Equity. Journal of Cystic Fibrosis, 19 (2), 171. doi: 10.1016/j.jcf.2020.02.019

Cogen, Jonathan D., Kahl, Barbara C., Maples, Holly, McColley, Susanna A., Roberts, Jason A., Winthrop, Kevin L., Morris, Andrew M., Holmes, Alison, Flume, Patrick A., VanDevanter, Donald R., Waters, Valerie, Muhlebach, Marianne S., Elborn, J. Stuart, Saiman, Lisa and Bell, Scott C. (2020). Finding the relevance of antimicrobial stewardship for cystic fibrosis. Journal of Cystic Fibrosis, 19 (4), 511-520. doi: 10.1016/j.jcf.2020.02.012

Geake, James, Ballard, Emma, O'Rourke, Peter, Wainwright, Claire E., Reid, David W. and Bell, Scott C. (2020). Centralised versus outreach models of cystic fibrosis care should be tailored to the needs of the individual patient. Internal Medicine Journal, 50 (2), 232-235. doi: 10.1111/imj.14724

Stockwell, Rebecca Elizabeth, Wood, Michelle ELizabeth, Ballard, Emma, Moore, Vanessa, Wainwright, Claire Elizabeth and Bell, Scott Cameron (2020). Current infection control practices used in Australian and New Zealand cystic fibrosis centers. BMC Pulmonary Medicine, 20 (1) 16, 16. doi: 10.1186/s12890-020-1052-y

Mayer-Hamblett, N., van Koningsbruggen-Rietschel, S., Nichols, D. P., VanDevanter, D. R., Davies, J. C., Lee, T., Durmowicz, A. G., Ratjen, F., Konstan, M. W., Pearson, K., Bell, S. C., Clancy, J. P., Taylor-Cousar, J. L., De Boeck, K., Donaldson, S. H., Downey, D. G., Flume, P. A., Drevinek, P., Goss, C. H., Fajac, I., Magaret, A. S., Quon, B. S., Singleton, S. M., VanDalfsen, J. M. and Retsch-Bogart, G. Z. (2020). Building global development strategies for cf therapeutics during a transitional cftr modulator era. Journal of Cystic Fibrosis, 19 (5), 677-687. doi: 10.1016/j.jcf.2020.05.011

Ratnatunga, Champa N., Lutzky, Viviana P., Kupz, Andreas, Doolan, Denise L., Reid, David W., Field, Matthew, Bell, Scott C., Thomson, Rachel M. and Miles, John J. (2020). The rise of non-tuberculosis mycobacterial lung disease. Frontiers in Immunology, 11 303, 303. doi: 10.3389/fimmu.2020.00303

Bell, Scott C, Mall, Marcus A, Gutierrez, Hector, Macek, Milan, Madge, Susan, Davies, Jane C, Burgel, Pierre-Régis, Tullis, Elizabeth, Castaños, Claudio, Castellani, Carlo, Byrnes, Catherine A, Cathcart, Fiona, Chotirmall, Sanjay H, Cosgriff, Rebecca, Eichler, Irmgard, Fajac, Isabelle, Goss, Christopher H, Drevinek, Pavel, Farrell, Philip M, Gravelle, Anna M, Havermans, Trudy, Mayer-Hamblett, Nicole, Kashirskaya, Nataliya, Kerem, Eitan, Mathew, Joseph L, McKone, Edward F, Naehrlich, Lutz, Nasr, Samya Z, Oates, Gabriela R ... Ratjen, Felix (2020). The future of cystic fibrosis care: a global perspective. The Lancet Respiratory Medicine, 8 (1), 65-124. doi: 10.1016/S2213-2600(19)30337-6

Bell, Scott C., Castellani, Carlo and Flume, Patrick A. (2019). Disruption in research publishing – the open access revolution. Journal of Cystic Fibrosis, 18 (6), 747-749. doi: 10.1016/j.jcf.2019.10.024

Zemanick, Edith T. and Bell, Scott C. (2019). Prevention of chronic infection with Pseudomonas aeruginosa infection in cystic fibrosis. Current Opinion in Pulmonary Medicine, 25 (6), 636-645. doi: 10.1097/MCP.0000000000000616

Ramsay, Kay A., Wardell, Samuel J. T., Patrick, Wayne M., Brockway, Ben, Reid, David W., Winstanley, Craig, Bell, Scott C. and Lamont, Iain L. (2019). Genomic and phenotypic comparison of environmental and patient-derived isolates of Pseudomonas aeruginosa suggest that antimicrobial resistance is rare within the environment. Journal of Medical Microbiology, 68 (11), 1591-1595. doi: 10.1099/jmm.0.001085

Fraser, Tamieka A., Bell, Mikaela G., Harris, Patrick N. A., Bell, Scott C., Bergh, Haakon, Thuy-Khanh Nguyen,, Kidd, Timothy J., Nimmo, Graeme R., Sarovich, Derek S. and Price, Erin P. (2019). Quantitative real-time PCR assay for the rapid identification of the intrinsically multidrug-resistant bacterial pathogen Stenotrophomonas maltophilia. Microbial Genomics, 5 (10) 000307. doi: 10.1099/mgen.0.000307

Bell, Scott C., Barry, Peter J., De Boeck, Kris, Drevinek, Pavel, Elborn, J. Stuart, Plant, Barry J., Minić, Predag, Van Braeckel, Eva, Verhulst, Stijn, Muller, Karine, Kanters, Desirée, Bellaire, Susan, de Kock, Herman, Geller, David E., Conrath, Katja, Van de Steen, Olivier and van der Ent, Kors (2019). CFTR activity is enhanced by the novel corrector GLPG2222, given with and without ivacaftor in two randomized trials. Journal of Cystic Fibrosis, 18 (5), 700-707. doi: 10.1016/j.jcf.2019.04.014

Bell, Scott C., Mainz, Jochen G., MacGregor, Gordon, Madge, Susan, MacEy, Julie, Fridman, Moshe, Suthoff, Ellison D., Narayanan, Siva and Kinnman, Nils (2019). Patient-reported outcomes in patients with cystic fibrosis with a G551D mutation on ivacaftor treatment: Results from a cross-sectional study. BMC Pulmonary Medicine, 19 (1) 146, 1-9. doi: 10.1186/s12890-019-0887-6

Stockwell, Rebecca E., Ballard, Emma L., O’Rourke, Peter, Knibbs, Luke D., Morawska, Lidia and Bell, Scott C. (2019). Indoor hospital air and the impact of ventilation on bioaerosols: a systematic review. Journal of Hospital Infection, 103 (2), 175-184. doi: 10.1016/j.jhin.2019.06.016

Milross, Maree A., Piper, Amanda J., Dwyer, Tiffany J., Wong, Keith, Bell, Scott C., Bye, Peter T. P., Robbins, Lisel, Dobbin, Catherine, Moriarty, Carmel, Willson, G., Norman, M., Regnis, Jeff, Sullivan, Colin, Grunstein, Ron and Douglas, James (2019). Non-invasive ventilation versus oxygen therapy in cystic fibrosis: a 12-month randomized trial. Respirology, 24 (12) resp.13604, 1191-1197. doi: 10.1111/resp.13604

Matson, A. G., Bunting, J. P., Kaul, A., Smith, D. J., Stonestreet, J., Herd, K., Hodgson, R. S. and Bell, S. C. (2019). A non-randomised single centre cohort study, comparing standard and modified bowel preparations, in adults with cystic fibrosis requiring colonoscopy. BMC Gastroenterology, 19 (1) 89. doi: 10.1186/s12876-019-0979-z

Duplancic, Christine, Crough, Tania, Bell, Scott C., Australian NTM in CF Study Group and Thomson, Rachel (2019). Multi-centre ethics and research governance review can impede non-interventional clinical research. Internal Medicine Journal, 49 (6), 722-728. doi: 10.1111/imj.14158

Lederer, David J., Bell, Scott C., Smyth, Alan R. and Chalmers, James D. (2019). Reply: More on causal inference studies. Annals of the American Thoracic Society, 16 (5), 646-646. doi: 10.1513/AnnalsATS.201901-070LE

Kidd, Timothy J, Grimwood, Keith and Bell, Scott C (2019). Abolition of Pseudomonas aeruginosa AUST-01 from an Australian CF center: Do other strains remain?. Pediatric Pulmonology, 54 (5), 515-516. doi: 10.1002/ppul.24258

Bell, Scott C. and Stuart, Rhonda L. (2019). Infection risks for patients from healthcare workers with cystic fibrosis - Reply. Respirology, 24 (4), 393-394. doi: 10.1111/resp.13489

Stockwell, Rebecca E., Chin, Melanie, Johnson, Graham R., Wood, Michelle E., Sherrard, Laura J., Ballard, Emma, O'Rourke, Peter, Ramsay, Kay A., Kidd, Timothy J., Jabbour, Nassib, Thomson, Rachel M., Knibbs, Luke D., Morawska, Lidia and Bell, Scott C. (2019). Transmission of bacteria in bronchiectasis and chronic obstructive pulmonary disease: Low burden of cough aerosols. Respirology, 24 (10) resp.13544, 980-987. doi: 10.1111/resp.13544

Somayaji, 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

Smith, 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

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

Bell, 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

Lederer, 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

Wood, 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

Kidd, 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

Martin, 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

Bell, 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

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

Nagy, 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

Bell, 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

Wee, 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

Stockwell, 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

Price, 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). doi: 10.1099/mgen.0.000194

Lutzky, 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

Bell, 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

Ahern, 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

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

Geake, James and Bell, Scott C. (2018). Bronchiectasis: yet another systemic disease?. Respirology, 23 (9), 797-798. doi: 10.1111/resp.13322

Wood, Michelle E., Stockwell, Rebecca E., Johnson, Graham R., Ramsay, Kay A., Sherrard, Laura J., Kidd, Timothy J., Cheney, Joyce, Ballard, Emma L., O'Rourke, Peter, Jabbour, Nassib, Wainwright, Claire E., Knibbs, Luke D., Sly, Peter D., Morawska, Lidia and Bell, Scott C. (2018). Cystic fibrosis pathogens survive for extended periods within cough-generated droplet nuclei. Thorax, 74 (1), thoraxjnl-2018. doi: 10.1136/thoraxjnl-2018-211567

Jessup, Melanie, Li, Anne, Fulbrook, Paul and Bell, Scott (2018). The experience of men and women with cystic fibrosis who have become a parent: a qualitative study. Journal of Clinical Nursing, 27 (7-8), 1702-1712. doi: 10.1111/jocn.14229

Castellani, Carlo, Duff, Alistair J. A., Bell, Scott C., Heijerman, Harry G. M., Munck, Anne, Ratjen, Felix, Sermet-Gaudelus, Isabelle, Southern, Kevin W., Barben, Jurg, Flume, Patrick A., Hodková, Pavla, Kashirskaya, Nataliya, Kirszenbaum, Maya N., Madge, Sue, Oxley, Helen, Plant, Barry, Schwarzenberg, Sarah Jane, Smyth, Alan R., Taccetti, Giovanni, Wagner, Thomas O. F., Wolfe, Susan P. and Drevinek, Pavel (2018). ECFS best practice guidelines: the 2018 revision. Journal of Cystic Fibrosis, 17 (2), 153-178. doi: 10.1016/j.jcf.2018.02.006

Wood, Michelle E., Stockwell, Rebecca E., Johnson, Graham R., Ramsay, Kay A., Sherrard, Laura J., Jabbour, Nassib, Ballard, Emma, O'Rourke, Peter, Kidd, Timothy J., Wainwright, Claire E., Knibbs, Luke D., Sly, Peter D., Morawska, Lidia and Bell, Scott C. (2018). Face masks and cough etiquette reduce the cough aerosol concentration of Pseudomonas aeruginosa in people with cystic fibrosis. American Journal of Respiratory and Critical Care Medicine, 197 (3), 338-355. doi: 10.1164/rccm.201707-1457OC

Tarique, Abdullah A., Sly, Peter D., Cardenas, Diana G., Luo, Lin, Stow, Jennifer L., Bell, Scott C., Wainwright, Claire E. and Fantino, Emmanuelle (2018). Differential expression of genes and receptors in monocytes from patients with cystic fibrosis. Journal of Cystic Fibrosis, 18 (3), 342-348. doi: 10.1016/j.jcf.2018.07.012

Sherrard, Laura J. and Bell, Scott C. (2018). Lower airway microbiota for biomarker measurements of cystic fibrosis disease progression?. Thorax, 73 (11), 1001-1003. doi: 10.1136/thoraxjnl-2018-212165

Tai, Anna S., Sherrard, Laura J., Kidd, Timothy J., Ramsay, Kay A., Buckley, Cameron, Syrmis, Melanie, Grimwood, Keith, Bell, Scott C. and Whiley, David M. (2017). Antibiotic perturbation of mixed-strain Pseudomonas aeruginosa infection in patients with cystic fibrosis. BMC pulmonary medicine, 17 (1) 138, 1-10. doi: 10.1186/s12890-017-0482-7

Bell, Scott C., Castellani, Carlo and Flume, Patrick A. (2017). Learning's from the Editors Desk – 2017. Journal of Cystic Fibrosis, 16 (6), 645-646. doi: 10.1016/j.jcf.2017.10.001

Bell, Scott C. (2017). Early intervention of cystic fibrosis pulmonary exacerbations based on home monitoring eICE through the looking glass. American Journal of Respiratory and Critical Care Medicine, 196 (9), 1090-1092. doi: 10.1164/rccm.201706-1207ED

Chin, Melanie, Aaron, Shawn D. and Bell, Scott C. (2017). The treatment of the pulmonary and extrapulmonary manifestations of cystic fibrosis. Presse Medicale, 46 (6), E139-E164. doi: 10.1016/j.lpm.2016.11.030

Sherrard, Laura J., Tay, George T., Butler, Claire A., Wood, Michelle E., Yerkovich, Stephanie, Ramsay, Kay A., Reid, David W., Moore, Vanessa L., Kidd, Timothy J. and Bell, Scott C. (2017). Tropical Australia is a potential reservoir of non-tuberculous mycobacteria in cystic fibrosis. European Respiratory Journal, 49 (5) 1700046, 1700046. doi: 10.1183/13993003.00046-2017

Pereira, M. L., Knibbs, L. D., He, C., Grzybowski, P., Johnson, G. R., Huffman, J. A., Bell, S. C., Wainwright, C. E., Matte, D. L., Dominski, F. H., Andrade, A. and Morawska, L. (2017). Sources and dynamics of fluorescent particles in hospitals. Indoor Air, 27 (5), 988-1000. doi: 10.1111/ina.12380

Tarique, Abdullah A., Sly, Peter D., Holt, Patrick G., Bosco, Anthony, Ware, Robert S., Logan, Jayden, Bell, Scott C., Wainwright, Claire E. and Fantino, Emmanuelle (2017). CFTR-dependent defect in alternatively-activated macrophages in cystic fibrosis. Journal of Cystic Fibrosis, 16 (4), 475-482. doi: 10.1016/j.jcf.2017.03.011

Viberg, Linda T., Sarovich, Derek S., Kidd, Timothy J., Geake, James B., Bell, Scott C., Currie, Bart J. and Price, Erin P. (2017). Within-host evolution of Burkholderia pseudomallei during chronic infection of seven Australasian cystic fibrosis patients. mBio, 8 (2) e00356-17, 1-17. doi: 10.1128/mBio.00356-17

Bell, Scott C. and Flume, Patrick A. (2017). Treatment decisions for MRSA in patients with cystic fibrosis (CF): When is enough, enough?. Thorax, 72 (4), 297-299. doi: 10.1136/thoraxjnl-2016-209605

Bell, Scott, Peng, Huashan, Crapper, Liam, Kolobova, Ilaria, Maussion, Gilles, Vasuta, Cristina, Yerko, Volodymyr, Pan Wong, Tak and Ernst, Carl (2017). A rapid pipeline to model rare neurodevelopmental disorders with simultaneous CRISPR/Cas9 gene editing. Stem Cells Translational Medicine, 6 (3), 886-896. doi: 10.1002/sctm.16-0158

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. (2017). Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis. PLoS One, 12 (3) e0172179, e0172179.1-e0172179.15. doi: 10.1371/journal.pone.0172179

Rowe, Steven M., McColley, Susanna A., Rietschel, Ernst, Li, Xiaolei, Bell, Scott C., Konstan, Michael W., Marigowda, Gautham, Waltz, David and Boyle, Michael P. (2017). Lumacaftor/ivacaftor treatment of patients with cystic fibrosis heterozygous for F508del-CFTR. Annals of the American Thoracic Society, 14 (2), 213-219. doi: 10.1513/AnnalsATS.201609-689OC

Maussion, Gilles, Cruceanu, Cristiana, Rosenfeld, Jill A., Bell, Scott C., Jollant, Fabrice, Szatkiewicz, Jin, Collins, Ryan L., Hanscom, Carrie, Kolobova, Ilaria, de Champfleur, Nicolas Menjot, Blumenthal, Ian, Chiang, Colby, Ota, Vanessa, Hultman, Christina, O'Dushlaine, Colm, McCarroll, Steve, Alda, Martin, Jacquemont, Sebastien, Ordulu, Zehra, Marshall, Christian R., Carter, Melissa T., Shaffer, Lisa G., Sklar, Pamela, Girirajan, Santhosh, Morton, Cynthia C., Gusella, James F., Turecki, Gustavo, Stavropoulos, Dimitri J., Sullivan, Patrick F. ... Ernst, Carl (2017). Implication of LRRC4C and DPP6 in neurodevelopmental disorders. American Journal of Medical Genetics, Part A, 173 (2), 395-406. doi: 10.1002/ajmg.a.38021

Madge, Susan, Bell, Scott C., Burgel, Pierre- Régis, De Rijcke, Karleen, Blasi, Francesco and Elborn, J. Stuart (2017). Limitations to providing adult cystic fibrosis care in Europe: results of a care centre survey. Journal of Cystic Fibrosis, 16 (1), 85-88. doi: 10.1016/j.jcf.2016.07.001

Montgomery, Shaylyn H., Shamji, Colleen M., Yi, Grace S., Yarnold, Cynthia H., Head, Stephen J., Bell, Scott C. and Schwarz, Stephan K. W. (2017). Effect of Nerve Stimulation Use on the Success Rate of Ultrasound-Guided Subsartorial Saphenous Nerve Block A Randomized Controlled Trial. Regional Anesthesia and Pain Medicine, 42 (1), 25-31. doi: 10.1097/AAP.0000000000000522

Bell, Scott C., Castellani, Carlo and Flume, Patrick A. (2017). JCF - 2016. Journal of Cystic Fibrosis, 16 (1), 6-6. doi: 10.1016/j.jcf.2016.12.014

Piccolo, Francesco, Tai, Anna Sze, Ee, Hooi, Mulrennan, Siobhain, Bell, Scott and Ryan, Gerard (2017). Clostridium difficile infection in cystic fibrosis: an uncommon but life-threatening complication. Respirology Case Reports, 5 (1) e00204, e00204. doi: 10.1002/rcr2.204

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Kidd, Timothy J., Magalhaes, Ricardo J. Soares, Paynter, Stuart and Bell, Scott C. (2015). The social network of cystic fibrosis centre care and shared Pseudomonas aeruginosa strain infection: a cross-sectional analysis. The Lancet Respiratory Medicine, 3 (8), 640-650. doi: 10.1016/S2213-2600(15)00228-3

De Smet, Birgit., Mayo, Mark., Peeters, Charlotte., Zlosnik, James E.A., Spilker, Theodore., Hird, Trevor J., Li Puma, John J., Kidd, Timothy J., Kaestli, Mirjam., Ginther, Jennifer L., Wagner, David M., Keim, Paul., Bell, Scott C., Jacobs, Jan A., Currie, Bart J. and Vandamme, Peter. (2015). Burkholderia stagnalis sp. nov. and Burkholderia territorii sp. nov., two novel Burkholderia cepacia complex species from environmental and human sources. International Journal of Systematic and Evolutionary Microbiology, 65 (7), 2265-2271. doi: 10.1099/ijs.0.000251

Ratjen, Felix, Bell, Scott C., Rowe, Steven M., Goss, Christopher H., Quittner, Alexandra L. and Bush, Andrew (2015). Cystic fibrosis. Nature Reviews. Disease Primers, 1 (1) 15010 . doi: 10.1038/nrdp.2015.10

Jong, T., Geake, J., Yerkovich, S. and Bell, S. C. (2015). Idiosyncratic reactions are the most common cause of abnormal liver function tests in patients with cystic fibrosis. Internal Medicine Journal, 45 (4), 395-401. doi: 10.1111/imj.12707

Tai, Anna S., Sidjabat, Hanna E., Kidd, Timothy J., Whiley, David M., Paterson, David L. and Bell, Scott C. (2015). Evaluation of phenotypic screening tests for carbapenemase production in Pseudomonas aeruginosa from patients with cystic fibrosis. Journal of Microbiological Methods, 111, 105-107. doi: 10.1016/j.mimet.2015.02.006

Viberg, Linda T., Price, Erin P., Kidd, Timothy J., Bell, Scott C., Currie, Bart J. and Sarovich, Derek S. (2015). Whole-genome sequences of five Burkholderia pseudomallei isolates from australian cystic fibrosis patients. Genome Announcements, 3 (2) e00254-15. doi: 10.1128/genomeA.00254-15

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Boyle, Michael P., Bell, Scott C., Konstan, Michael W., McColley, Susanna A., Rowe, Steven M., Rietschel, Ernst, Huang, Xiaohong, Waltz, David, Patel, Naimish R. and Rodman, David (2014). A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: A phase 2 randomised controlled trial. The Lancet Respiratory Medicine, 2 (7), 527-538. doi: 10.1016/S2213-2600(14)70132-8

Geake, James, Tay, George, Callaway, Leonie and Bell, Scott C. (2014). Pregnancy and cystic fibrosis: approach to contemporary management. Obstetric Medicine, 7 (4), 147-155. doi: 10.1177/1753495X14554022

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

Bell, Scott, Hartl, Dominik and Heijerman, Harry (2013). Change in the executive editorial team at JCF. Journal of Cystic Fibrosis, 12 (6), 545-546. doi: 10.1016/j.jcf.2013.10.006

Wood, Michelle E., Smith, Daniel J., Reid, David W., Masel, Philip J., France, Megan W. and Bell, Scott C. (2013). Ivacaftor in severe cystic fibrosis lung disease and a G551D mutation. Respirology Case Reports, 1 (2), 52-54. doi: 10.1002/rcr2.27

Ramsay, Kay A., Butler, Claire A., Paynter, Stuart, Ware, Robert S., Kidd, Timothy J., Wainwright, Claire E. and Bell, Scott C. (2013). Factors influencing acquisition of Burkholderia cepacia complex organisms in patients with cystic fibrosis. Journal of Clinical Microbiology, 51 (12), 3975-3980. doi: 10.1128/JCM.01360-13

Price E.P., Sarovich D.S., Mayo M., Tuanyok A., Drees K.P., Kaestli M., Beckstrom-Sternberg S.M., Babic-Sternberg J.S., Kidd T.J., Bell S.C., Keim P., Pearson T. and Currie B.J. (2013). Within-host evolution of Burkholderia pseudomallei over a twelve-year chronic carriage infection. mBio, 4 (4) e00388-13, e00388-13.1-e00388-13.11. doi: 10.1128/mBio.00388-13

Syrmis, Melanie W., Moser, Ralf J., Kidd, Timothy J., Hunt, Priscilla, Ramsay, Kay A., Bell, Scott C., Wainwright, Claire E., Grimwood, Keith, Nissen, Michael D., Sloots, Theo P. and Whiley, David M. (2013). High-throughput single-nucleotide polymorphism-based typing of shared Pseudomonas aeruginosa strains in cystic fibrosis patients using the Sequenom iPLEX platform. Journal of Medical Microbiology, 62 (5), 734-740. doi: 10.1099/jmm.0.055905-0

Plant, Barry J, Goss, Christopher H, Plant, William D and Bell, Scott C (2013). Management of comorbidities in older patients with cystic fibrosis. The Lancet Respiratory Medicine, 1 (2), 164-174. doi: 10.1016/S2213-2600(13)70025-0

Goss, Christopher H. and Bell, Scott C. (2013). Aztreonam for inhalation solution, challenges to drug approval and integration into CF care. Journal of Cystic Fibrosis, 12 (2), 99-101. doi: 10.1016/j.jcf.2012.08.006

Houston, Neralee, Stewart, Niall, Smith, Daniel S., Bell, Scott C., Champion, Alan C. and Reid, David W. (2013). Sputum neutrophils in cystic fibrosis patients display a reduced respiratory burst. Journal of Cystic Fibrosis, 12 (4), 352-362. doi: 10.1016/j.jcf.2012.11.004

Ranganathan, Sarath C., Skoric, Billy, Ramsay, Kay A., Carzino, Rosemary, Gibson, Anne-Marie, Hart, Emily, Harrison, Jo, Bell, Scott C. and Kidd, Timothy J. (2013). Geographical differences in first acquisition of Pseudomonas aeruginosa in cystic fibrosis. Annals of the American Thoracic Society, 10 (2), 108-114. doi: 10.1513/AnnalsATS.201209-077OC

Butler, Claire Ann and Bell, Scott Cameron (2012). New insights into gene-specific management in cystic fibrosis from the 2012 European Cystic Fibrosis Conference. Expert Review of Respiratory Medicine, 6 (5), 499-501. doi: 10.1586/ERS.12.52

Smith, D.J., Anderson, G.J., Lamont, I.L., Masel, P., Bell, S.C. and Reid, D.W. (2012). Accurate assessment of systemic iron status in cystic fibrosis will avoid the hazards of inappropriate iron supplementation. Journal of Cystic Fibrosis, 12 (3), 303-304. doi: 10.1016/j.jcf.2012.10.001

Kidd, Timothy J., Richie, Stephen R., Ramsay, Kay A., Grimwood, Keith, Bell, Scott C. and Rainey, Paul B. (2012). Pseudomonas aeruginosa exhibits frequent recombination, but only a limited association between genotype and ecological setting. PLoS One, 7 (9) e44199, e44199.1-e44199.14. doi: 10.1371/journal.pone.0044199

Kidd, Timothy J., Ramsay, Kay A., Hu, Honghua, Marks, Guy B., Wainwright, Claire E., Bye, Peter T., Elkins, Mark R., Robinson, Philip J., Rose, Barbara R., Wilson, John W., Grimwood, Keith, Bell, Scott C., ACPinCF Investigator Group, Serisier, David J. and Smith, Daniel J. (2012). Shared pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centres. European Respiratory Journal, 41 (5), 1091-1100. doi: 10.1183/09031936.00060512

Knibbs, L. D., Morawska, L. and Bell, S. C. (2012). The risk of airborne influenza transmission in passenger cars. Epidemiology and Infection, 140 (3), 474-478. doi: 10.1017/S0950268811000835

Martin, Bradley, Schechter, Michael S., Jaffe, Adam, Cooper, Peter, Bell, Scott C. and Ranganathan, Sarath (2012). Comparison of the US and Australian Cystic Fibrosis Registries: The impact of newborn screening. Pediatrics, 129 (2), E348-E355. doi: 10.1542/peds.2011-0567

Knibbs, Luke D., Morawska, Lidia, Bell, Scott C. and Grzybowski, Piotr (2011). Room ventilation and the risk of airborne infection transmission in 3 health care settings within a large teaching hospital. American Journal of Infection Control, 39 (10), 866-872. doi: 10.1016/j.ajic.2011.02.014

Collaco, Joseph M., McGready, John, Green, Deanna M., Naughton, Kathleen M., Watson, Christopher P., Shields, Timothy, Bell, Scott C., Wainwright, Claire E. and Cutting, Garry R. (2011). Effect of temperature on cystic fibrosis lung disease and infections: A replicated cohort study. PLoS One, 6 (11) e27784, 1-7. doi: 10.1371/journal.pone.0027784

Smith, Daniel J., Reid, David W. and Bell, Scott C. (2011). Treatment of pulmonary exacerbations in cystic fibrosis. Therapy, 8 (6), 623-643. doi: 10.2217/thy.11.77

Ramsey, Bonnie W., Davies, Jane, McElvaney, N. Gerard, Tullis, Elizabeth, Bell, Scott C., Drevinek, Pavel, Griese, Matthias, McKone, Edward F., Wainwright, Claire E., Konstan, Michael W., Moss, Richard, Ratjen, Felix, Sermet-Gaudelus, Isabelle, Rowe, Steven M., Dong, Qunming, Rodriguez, Sally, Yen, Karl, Ordonez, Claudia and Elborn, J. Stuart (2011). A CFTR potentiator in patients with Cystic Fibrosis and the G551D Mutation. New England Journal of Medicine, 365 (18), 1663-1672. doi: 10.1056/NEJMoa1105185

Bell, Scott C., Bye, Peter T.P., Cooper, Peter J., Martin, A. James, McKay, Karen O., Robinson, Phillip J., Ryan, Gerard F. and Sims, Geoff C. (2011). Cystic fibrosis in Australia, 2009: Results from a data registry. Medical Journal of Australia, 195 (7), 396-400. doi: 10.5694/mja11.10719

Anuj, S. N., Whiley, D. M., Kidd, T. J., Ramsay, K. A., Bell, S. C., Syrmis, M. W., Grimwood, K., Wainwright, C. E., Nissen, M. D. and Sloots, T. P. (2011). Rapid single-nucleotide polymorphism-based identification of clonal Pseudomonas aeruginosa isolates from patients with cystic fibrosis by the use of real-time PCR and high-resolution melting curve analysis. Clinical Microbiology and Infection, 17 (9), 1403-1408. doi: 10.1111/j.1469-0691.2010.03439.x

Kidd, Timothy J., Gibson, Justine S., Moss, Susan, Greer, Ristan M., Cobbold, Rowland N., Wright, John D., Ramsay, Kay A., Grimwood, Keith and Bell, Scott C. (2011). Clonal complex Pseudomonas aeruginosa in horses. Veterinary Microbiology, 149 (3-4), 508-512. doi: 10.1016/j.vetmic.2010.11.030

Towns, Susan Joy and Bell, Scott Cameron (2011). Transition of adolescents with cystic fibrosis from paediatric to adult care. Clinical Respiratory Journal, 5 (2), 64-75. doi: 10.1111/j.1752-699X.2010.00226.x

Kuys, Suzanne S., Hall, Kathleen, Peasey, Maureen, Wood, Michelle, Cobb, Robyn and Bell, Scott C. (2011). Gaming console exercise and cycle or treadmill exercise provide similar cardiovascular demand in adults with cystic fibrosis: A randomised cross-over trial. Journal of Physiotherapy, 57 (1), 35-40. doi: 10.1016/S1836-9553(11)70005-4

Lewindon, Peter J., Shepherd, Ross W., Walsh, Meagan J., Greer, Ristan M., Williamson, Richard, Pereria, Tamara N., Frawley, Kieran, Bell, Scott C., Smith, Jeffery L. and Ramm, Grant A. (2011). Importance of hepatic fibrosis in cystic fibrosis and the predictive value of liver biopsy. Hepatology, 53 (1), 193-201. doi: 10.1002/hep.24014

Smith, Daniel, Reid, David, Slaughter, Richard, Masel, Philip, Tai, Anna and Bell, Scott (2011). Superior vena cava obstruction due to total implantable venous access devices in cystic fibrosis: Case series and review. Respiratory Medicine CME, 4 (3), 99-104. doi: 10.1016/j.rmedc.2010.12.005

Kidd, Timothy J., Grimwood, Keith, Ramsay, Kay A., Rainey, Paul B. and Bell, Scott C. (2011). Comparison of three molecular techniques for typing pseudomonas aeruginosa isolates in sputum samples from patients with cystic fibrosis. Journal of Clinical Microbiology, 49 (1), 263-268. doi: 10.1128/JCM.01421-10

Bell, Scott C. and Morris, Norman R. (2010). Exercise testing in patients with cystic fibrosis: Why and which?. Journal of Cystic Fibrosis, 9 (5), 299-301. doi: 10.1016/j.jcf.2010.05.005

Chang, AB, Bell, SC, Byrnes, CA, Grimwood, K, Holmes, PW, King, PT, Kolbe, J, Landau, LI, Maguire, GP, McDonald, MI, Reid, DW, Thien, FC and Torzillo, PJ (2010). Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand. Medical Journal of Australia, 193 (6), 356-365. doi: 10.5694/j.1326-5377.2010.tb03949.x

France, Megan W., Tai, Szeanna, Masel, Phillip J., Moore, Vanessa L., McMahon, Tracy L., Ritchie, Alexander J. and Bell, Scott C. (2010). The month of July: an early experience with pandemic influenza A (H1N1) in adults with cystic fibrosis. BMC Pulmonary Medicine, 10 (1) 8. doi: 10.1186/1471-2466-10-8

Tiller, Rebekah V, Gee, Jay E., Lonsway, David R., Gribble, Sonali, Bell, Scott C., Jennison, Amy V., Bates, John, Coulter, Chris, Hoffmaster, Alex R. and De, Barun K. (2010). Identification of an unusual Brucella strain (BO2) from a lung biopsy in a 52 year-old patient with chronic destructive pneumonia. BMC Microbiology, 10 (Article number 23) 23, 1-11. doi: 10.1186/1471-2180-10-23

Wainwright, C. E., France, M. W., O'Rourke, P., Anuj, S., Kidd, T. J., Nissen, M. D., Sloots, T. P., Coulter, C., Ristovski, Z., Hargreaves, M., Rose, B. R., Harbour, C., Bell, SC and Fennelly, KP (2009). Cough-generated aerosols of Pseudomonas aeruginosa and other Gram-negative bacteria from patients with cystic fibrosis.. Thorax, 64 (11), 926-931. doi: 10.1136/thx.2008.112466

Barraclough, Katherine A., O'Connor, Annette, Bell, Scott C., Freitag, Andreas, Bye, Peter, Jeanneret, Alphonse, Berthiaume, Yves, Brown, Neil, Wilcox, Pearce, Ryan, Gerard, Brager, Nancy, Rabin, Harvey, Morrison, Nancy, Gibson, Peter, Jackson, Mary, Paterson, Nigel, Middleton, Peter and Aaron, Shawn D. (2009). Randomized trial of a decision aid for patients with cystic fibrosis considering lung transplantation. American Journal of Respiratory and Critical Care Medicine, 180 (8), 761-768. doi: 10.1164/rccm.200903-0421OC

Wynn, Katherine K., Crough, Tania, Campbell, Scott, McNeil, Keith, Galbraith, Andrew, Moss, Denis J., Silins, Sharon L., Bell, Scott and Khanna, Rajiv (2009). Narrowing of T-cell receptor beta variable repertoire during symptomatic herpesvirus infection in transplant patients. Immunology and Cell Biology, 88 (2), 125-135. doi: 10.1038/icb.2009.74

Kidd, TJ, Marks, GB, Bye, PTP, Wainwright, CE, Robinson, PJ, Rose, BR, Harbour, C and Bell, SC (2009). Multi-centre research in Australia: Analysis of a recent National Health and Medical Research Council-funded project. RESPIROLOGY, 14 (7), 1051-1055. doi: 10.1111/j.1440-1843.2009.01595.x

Soulsby, N., Bell, S., Greville, H. and Doecke, C. (2009). Intravenous aminoglycoside usage and monitoring of patients with cystic fibrosis in Australia. What's new?. Internal Medicine Journal, 39 (8), 527-531. doi: 10.1111/j.1445-5994.2008.01787.x

Kidd, Timothy J., Ramsay, Kay A., Hu, Honghua Hu, Bye, Peter T. P., Elkins, Mark R., Grimwood, Keith, Harbour, Colin, Marks, Guy B., Nissen, Michael D., Robinson, Phillip J., Rose, Barbara R., Sloots, Theo P., Wainwright, Claire E., Bell, Scott C. and ACPinCF Investigators (2009). Low rates of Pseudomonas aeruginosa misidentification in isolates from Cystic Fibrosis patients.. Journal of Clinical Microbiology, 47 (5), 1503-1509. doi: 10.1128/JCM.00014-09

Reid, D. W. and Bell, S. C. (2009). Sugar sweet and deadly?. Microbiology, 155 (3), 665-666. doi: 10.1099/mic.0.024752-0

Manos, Jim, Arthur, Jonathan, Rose, Barbara, Bell, Scott, Tingpej, Pholawat, Hu, Honghua, Webb, Jeremy, Kjelleberg, Staffan, Gorrell, Mark Douglas, Bye, Peter and Harbour, Colin (2009). Gene expression characteristics of a cystic fibrosis epidemic strain of Pseydomonas aeruginosa during biofilm and planktonic growth. FEMS Microbiology Letters, 292 (1), 107-114. doi: 10.1111/j.1574-6968.2008.01472.x

Hopkins, P. M., Kidd, T. J., Coulter, C., Feather, I. H., Derrington, P. and Bell, S. C. (2009). Death after lung transplantation in cystic fibrosis patients infected with Burkholderia cepacia. American Journal of Respiratory and Critical Care Medicine, 179 (3), 257-258. doi: 10.1164/ajrccm.179.3.257

Anuj, Snehal N., Whiley, David M., Kidd, Timothy J., Bell, Scott C., Wainwright, Claire E., Nissen, Michael D. and Sloots, Theo P. (2009). Identification of Pseudomonas aeruginosa by a duplex real-time polymerase chain reaction assay targeting the ecfX and the gyrB genes. Diagnostic Microbiology And Infectious Disease, 63 (2), 127-131. doi: 10.1016/j.diagmicrobio.2008.09.018

Downey, D. G., Bell, S. C. and Elborn, J. S. (2009). Neutrophils in cystic fibrosis. Thorax, 64 (1), 81-88. doi: 10.1136/thx.2007.082388

Kapur, Nitin, Bell, Scott, Kolbe, John and Chang, Anne B. (2009). Inhaled steroids for bronchiectasis. Cochrane Database of Systematic Reviews (1) CD000996, CD000996.1-CD000996.29. doi: 10.1002/14651858.CD000996.pub2

Syrmis, Melanie, Bell, Scott, Bye, Peter, Coulter, Chris, Harbour, Colin, Iredell, Jon, Kidd, Tim, O'Carroll, Mark, Rose, Barbara, Wainwright, Claire, Sloots, Theo and Nissen, Michael (2008). High prevalence of a class 1 integron-associated aadB gene cassette in Pseudomonas aeruginosa isolates from an Australian cystic fibrosis patient population. Pathology, 40 (5), 524-525. doi: 10.1080/00313020802197921

Kidd, Timothy J., Douglas, Joel M., Bergh, Haakon A., Coulter, Chris and Bell, Scott C. (2008). Burkholderia cepacia complex epidemiology in persons with cystic fibrosis from Australia and New Zealand. Research in Microbiology, 159 (3), 194-199. doi: 10.1016/j.resmic.2008.01.001

Crough, Tania, Fazou, Chrysa, Weiss, Julissa, Campbell, Scott, Davenport, Miles P., Bell, Scott C., Galbraith, Andrew, McNeil, Keith and Khanna, Rajiv (2007). Symptomatic and asymptomatic viral recrudescence in solid-organ transplant recipients and its relationship with the antigen-specific CD8+ T-cell response. Journal of Virology, 81 (20), 11538-11542. doi: 10.1128/JVI.00581-07

McCormack, J. G., Bell, S. C., Senini, S., Walmsley, K., Patel, K., Wainwright, C., Serisier, D., Harris, M. and Bowler, S. (2007). Daily versus weekly azithromycin in cystic fibrosis patients.. European Respiratory Journal, 30 (3), 487-495. doi: 10.1183/09031936.00163306

Bell, S. C. and Robinson, P. J. (2007). Exacerbations in cystic fibrosis: 2. Prevention. Thorax, 62 (8), 723-732. doi: 10.1136/thx.2006.060897

Burrows, Judith A., Nissen, Lisa M., Kirkpatrick, Carl M. J. and Bell, Scott. C. (2007). Beta-lactam allergy in adults with cystic fibrosis. Journal of Cystic Fibrosis, 6 (4), 297-303. doi: 10.1016/j.jcf.2006.11.001

Walker, S., Fazou, C., Crough, T., Holdsworth, R., Kiely, P., Veale, M., Bell, S. C., Gailbraith, A. J., McNeil, K., Jones, S. and Khanna, R. (2007). Ex vivo monitoring of human cytomegalovirus-specific CD8+ T-cell responses using QuantiFERON®-CMV. Transplant Infectious Disease, 9 (2), 165-170. doi: 10.1111/j.1399-3062.2006.00199.x

Tingpej, Pholawat, Smith, Lucas, Rose, Barbara, Zhu, Hua, Conibear, Tim, Al Nassafi, Khaled, Manos, Jim, Elkins, Mark, Bye, Peter, Willcox, Mark, Bell, Scott, Wainwright, Claire and Harbour, Colin (2007). Phenotypic characterization of clonal and nonclonal Psuedomonas aeruginosa strains isolated from lungs of adults with cystic fibrosis. Journal of Clinical Microbiology, 45 (6), 1697-1704. doi: 10.1128/JCM.02364-06

Elborn, J. S. and Bell, S. C. (2007). Pulmonary exacerbations in cystic fibrosis and bronchiectasis. Thorax, 62 (4), 288-290. doi: 10.1136/thx.2006.065664

Hennig, Stefanie, Waterhouse, Timothy H., Bell, Scott C., France, Megan, Wainwright, Claire E., Miller, Hugh, Charles, Bruce G. and Duffull, Stephen B. (2007). A D-optimal designed population pharmacokinetic study of oral itraconazole in adult cystic fibrosis patients. British Journal of Clinical Pharmacology, 63 (4), 438-450. doi: 10.1111/j.1365-2125.2006.02778.x

Yang, Ian A., Savarimuthu, Santiyagu, Kim, Samuel T., Holloway, John W., Bell, Scott C. and Fong, Kwun M. (2007). Gene-environmental interaction in asthma. Current Opinion in Allergy & Clinical Immunology, 7 (1), 75-82. doi: 10.1097/ACI.0b013e328012ce39

Smith, Lucas, Rose, Barbara, Tingpej, Pholawat, Zhu, Hua, Conibear, Tim, Manos, Jim, Bye, Peter, Elkins, Mark, Willcox, Mark, Bell, Scoot, Wainwright, Claire and Harbour, Colin (2006). Protease IV production in Pseudomonas aeruginosa from the lungs of adults with cystic fibrosis. Journal of Medical Microbiology, 55 (12), 1641-1644. doi: 10.1099/jmm.0.46845-0

Kidd, T. J., Coulter, C. and Bell, S. C. (2006). Epidemiological analysis of methicillin-resistant Staphylococcus aureus isolates from adult patients with cystic fibrosis. Infection Control and Hospital Epidemiology, 27 (2), 201-203. doi: 10.1086/501173

Buntain, H. M., Schluter, P. J., Bell, S. C., Greer, R. M., Wong, J. C. H., Batch, J., Lewindon, P. and Wainwright, C. E. (2006). Controlled longitudinal study of bone mass accrual in children and adolescents with cystic fibrosis. Thorax, 61 (2), 146-154. doi: 10.1136/thx.2005.046516

Hennig, S., Wainwright, C. E., Bell, S. C., Miller, H., Friberg, L. E. and Charles, B. G. (2006). Population pharmacokinetics of itraconazole and its active metabolite hydroxy-itraconazole in paediatric cystic fibrosis and bone marrow transplant patients. Clinical Pharmacokinetics, 45 (11), 1099-1114. doi: 10.2165/00003088-200645110-00004

Block, J. K., Vandemheen, K. L., Tullis, E., Fergusson, D., Doucette, S., Haase, D., Berthiaume, Y., Brown, N., Wilcox, P., Bye, P., Bell, S., Noseworthy, M., Pedder, L., Freitag, A. and Paterson, N. (2006). Predictors of pulmonary exacerbations in patients with cystic fibrosis infected with multi-resistant bacteria. Thorax, 61 (11), 969-974. doi: 10.1136/thx.2006.061366

Hill, Dominic, Rose, Barbara, Pajkos, Aniko, Robinson, Michael, Bye, Peter, Bell, Scott C., Elkins, Mark, Thompson, Barbara, MacLeod, Colin, Aaron, Shawn D. and Harbour, Colin (2005). Antibiotic susceptibilities of Pseudomonas aeruginosa isolates derived from patients with cystic fibrosis under aerobic, anaerobic, and biofilm conditions. Journal of Clinical Microbiology, 43 (10), 5085-5090. doi: 10.1128/JCM.43.10.5085-5090.2005

Downey, D. G., Kidd, T. J., Coulter, C. and Bell, S. C. (2005). MRSA eradication in a health care worker with cystic fibrosis; re-emergence or re-infection?. Journal of Cystic Fibrosis, 4 (3), 205-207. doi: 10.1016/j.jcf.2005.05.014

Buntain, Helen M., Greer, Ristan M., Wong, Joseph C.H., Schluter, Philip J., Batch, Jennifer, Lewindon, Peter, Bell, Scott C. and Wainwright, Claire E. (2005). Pubertal development and its influences on bone mineral density in Australian children and adolescents with cystic fibrosis. Journal of Paediatrics And Child Health, 41 (7), 317-322. doi: 10.1111/j.1440-1754.2005.00635.x

McCormack, J. G. and Bell, S. C. (2005). Has the time come to prescribe azithromycin in cystic fibrosis patients?. Internal Medicine Journal, 35 (2), 73-74. doi: 10.1111/j.1445-5994.2004.00762.x

Sweetser, Lisel J., Douglas, James A., Riha, Renata L. and Bell, Scott C. (2005). Clinical presentation of metabolic alkalosis in an adult patient with cystic fibrosis. Respirology, 10 (2), 254-256. doi: 10.1111/j.1440-1843.2005.00650.x

Bell, S. C., Senini, S. L. and McCormack, J. G. (2005). Macrolides in cystic fibrosis. Chronic Respiratory Disease, 2 (2), 85-98. doi: 10.1191/1479972305cd066rs

Garske, L. A., Beatson, S. A., Leech, A. J., Walsh, S. L. and Bell, S. C. (2004). Sub-inhibitory concentrations of ceftazidime and tobramycin reduce the quorum sensing signals of Pseudomonas aeruginosa. Pathology, 36 (6), 571-575. doi: 10.1080/00313020400011300

Syrmis, Melanie W., O'Carroll, Mark R., Sloots, Theo P., Coulter, Chris, Wainwright, Claire E., Bell, Scott C. and Nissen, Michael D. (2004). Rapid genotyping of Pseudomonas aeruginosa isolates harboured by adult and paediatric patients with cystic fibrosis using repetitive-element-based PCR assays. Journal of Medical Microbiology, 53 (11), 1089-1096. doi: 10.1099/jmm.0.45611-0

Greer, Ristan M., Buntain, Helen M., Lewindon, Peter J., Wainwright, Claire E., Potter, Julia M., Wong, Joseph C., Francis, Paul W., Batch, Jennifer A. and Bell, Scott C. (2004). Vitamin A levels in patients with CF are influenced by the inflammatory response. Journal of Cystic Fibrosis, 3 (3), 143-149. doi: 10.1016/j.jcf.2004.04.003

O'Carroll, M. R., Syrmis, M. W., Wainwright, C. E., Greer, R. M., Mitchell, P., Coulter, C., Sloots, T. P., Nissen, M. D. and Bell, S. C. (2004). Clonal strains of Pseudomonas aeruginosa in paediatric and adult cystic fibrosis units. European Respiratory Journal, 24 (1), 101-106. doi: 10.1183/09031936.04.00122903

Garske, L. A., Kidd, T. J., Gan, R., Bunting, J. P., Franks, C. A., Coulter, C., Masel, P. J. and Bell, S. C. (2004). Rifampicin and sodium fusidate reduces the frequency of methicillin-resistant Staphylococcus aureus (MRSA) isolation in adults with cystic fibrosis and chronic MRSA infection. Journal of Hospital Infection, 56 (3), 208-214. doi: 10.1016/j.jhin.2003.12.003

Buntain, HM, Greer, RM, Schluter, PJ, Wong, JCH, Batch, JA, Potter, JM, Lewindon, PJ, Powell, E, Wainwright, CE and Bell, SC (2004). Bone mineral density in Australian children, adolescents and adults with cystic fibrosis: a controlled cross sectional study. Thorax, 59 (2), 149-155. doi: 10.1136/thorax.2003.006726

Kim, Samuel T., Kaisar, Omar M., Clarke, Belinda E., Vandenburg, Russell A., Allen, David H., Bell, Scott C. and Fong, Kwun M. (2003). 'Iron lung': Distinctive bronchoscopic features of acute iron tablet aspiration. Respirology, 8 (4), 541-543. doi: 10.1046/j.1440-1843.2003.00506.x

O'Carroll, M. R., Kidd, T. J., Coulter, C., Smith, H. V., Rose, B. R., Harbour, C. and Bell, S. C. (2003). Burkholderia pseudomallei: Another emerging pathogen in cystic fibrosis. Thorax, 58 (12), 1087-1091. doi: 10.1136/thorax.58.12.1087

Armstrong, David, Bell, Scott, Robinson, Michael, Bye, Peter, Rose, Barbara, Harbour, Colin, Lee, Crystal, Service, Helen, Nissen, Michael, Syrmis, Melanie and Wainwright, Claire (2003). Evidence for spread of a clonal strain of Pseudomonas aeruginosa among cystic fibrosis clinics. Journal of Clinical Microbiology, 41 (5), 2266-2267. doi: 10.1128/JCM.41.5.2266-2267.2003

Sherritt, M. A., Bharadwaj, M., Burrows, J. M., Morrison, L. E., Elliott, S. L., Davis, J. E., Kear, L. M., Slaughter, R. E., Bell, S. C., Galbraith, A. J., Khanna, R. and Moss, D. J. (2003). Reconstitution of the latent T-lymphocyte response to Epstein-Barr virus is coincident with long-term recovery from post-transplant lymphoma after adoptive immunotherapy. Transplantation, 75 (9), 1556-1560. doi: 10.1097/01.TP.0000058745.02123.6F

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

Kidd, T. J., Bell, S. C. and Coulter, C. (2003). The genomovar distribution of Burkholderia cepacia complex isolates collected from Australian cystic fibrosis units. Journal of Cystic Fibrosis, 2 (1 Suppl), S33-S33.

O'Carroll, M. R., Kidd, T. J., Coulter, C. and Bell, S. C. (2003). Multi-resistant Pseudomonas aeruginosa (MRPA) in a large adult cystic fibrosis (CF) unit. Respirology, 8 (Suppl), A47-A47.

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

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

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.

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

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

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

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

Bell, S. C. and Shepherd, R. W. (2002). Optimising nutrition in cystic fibrosis. Journal of Cystic Fibrosis, 1 (2), 47-50. doi: 10.1016/S1569-1993(02)00031-0

Burrows, J. A., Bajramovic, J. and Bell, S. C. (2002). Prevalence of complementary and alternative medicine use by adults with cystic fibrosis. Journal of Pharmacy Practice and Research, 32 (4), 320-323. doi: 10.1002/jppr2002324320

Garske, L. A. and Bell, S. C. (2002). Pamidronate results in symptom control of hypertrophic pulmonary osteoarthropathy in cystic fibrosis. Chest, 121 (4), 1363-1364. doi: 10.1378/chest.121.4.1363

Bell, S. C. and Phillips, J. A. (2001). Pulmozyme adherence in an adult cf unit. Respirology, 6 (SUPPL. 1).

Welter, J. M., Seeney, S. L., Bowler, S. D., Masel, P. J., Bell, S. C. and McCormack, J. G. (2001). Azithromycin (azm) in adults with cystic fibrosis (cf). Respirology, 6 (SUPPL. 1).

Bell, S. C. and Stallard, K. (2001). Manpower and costings of physiotherapy: an adult cystic fibrosis service. Respirology, 6 (SUPPL. 1).

Stallard, K., Seale, H. and Bell, S.C. (2001). Cost of physiotherapy in CF. Thorax, 56 (12), 980-980. doi: 10.1136/thorax.56.12.980

Riha, R. L., Tubby, J., Duhig, E. E., Clarke, B. E., Haug, G. and Bell, S. C. (2001). Life-threatening haemoptysis presenting as a late complication of an ovarian tumour. International Journal of Clinical Practice, 55 (10), 729-730.

Richards, M.L., Davies, P.S.W. and Bell, S.C. (2001). Energy cost of physical activity in cystic fibrosis. European Journal of Clinical Nutrition, 55 (8), 690-697. doi: 10.1038/sj.ejcn.1601201

Phillips, J.A. and Bell, S.C. (2001). Aminoglycosides in cystic fibrosis: a descriptive study of current practice in Australia. Internal Medicine Journal, 31 (1), 23-26. doi: 10.1046/j.1445-5994.2001.00010.x

Scott, Andrew I.R., Clarke, Belinda E., Healy, Helen, D'Emden, Michael and Bell, Scott C. (2000). Microvascular complications in cystic fibrosis-related diabetes mellitus: A case report. Journal of the Pancreas, 1 (4), 208-210.

Bell, S.C., Bowerman, A.M., Nixon, L.E., Macdonald, I.A., Elborn, J.S. and Shale, D.J. (2000). Metabolic and inflammatory responses to pulmonary exacerbation in adults with cystic fibrosis. European Journal of Clinical Investigation, 30 (6), 553-559. doi: 10.1046/j.1365-2362.2000.00667.x

Bunting, J, Slaughter, RE, Masel, PJ, Kroll, WJ and Bell, SC (2000). Ultrasound placement of peripherally inserted central catheters (PICCs) in adults with cystic fibrosis.. Thorax, 55 (6), 535-535. doi: 10.1136/thorax.55.6.535

Rafter, Lee, Scott, Andrew, Tarn, Robert, Matar, Kevin, Windsor, Morgan, Seale, Helen, Galbraith, Andrew and Bell, Scott (1999). Lung volume reduction surgery (LVRS) - The prince charles hospital. Respirology, 4 (SUPPL. 1).

Khanna, R., Bell, S., Sherritt, M., Galbraith, A., Burrows, S. R., Rafter, L., Clarke, B., Slaughter, R., Falk, M. C., Douglass, J., Williams, T., Elliott, S. L. and Moss, D. J. (1999). Activation and adoptive transfer of Epstein-Barr virus-specific cytotoxic T cells in solid organ transplant patients with posttransplant lymphoproliferative disease. Proceedings of the National Academy of Sciences of the United States of America, 96 (18), 10391-10396. doi: 10.1073/pnas.96.18.10391

Bell, Scott C., Elborn, J. Stuart, Nixon, Lisette E., Macdonald, Ian A. and Shale, Dennis J. (1999). Repeatability and methodology of resting energy expenditure in patients with cystic fibrosis. Respiration Physiology, 115 (3), 301-307. doi: 10.1016/S0034-5687(99)00008-0

Yang, I.A., Bell, S.C., Fong, K.M. and Aldons, P.M. (1999). Trepopnoea due to positional narrowing of the left main bronchus. Australian and New Zealand Journal of Medicine, 29 (6), 838-839. doi: 10.1111/j.1445-5994.1999.tb00800.x

Bell, S.C., Bowerman, A.R., Davies, C.A., Campbell, I.A., Shale, D.J. and Elborn, J.S. (1998). Nutrition in adults with cystic fibrosis. Clinical Nutrition, 17 (5), 211-215. doi: 10.1016/S0261-5614(98)80061-7

Bell, S.C. and Anderson, E.G. (1998). Pulmonary eosinophilia associated with aminoglutethimide. Australian and New Zealand Journal of Medicine, 28 (5), 670-671. doi: 10.1111/j.1445-5994.1998.tb00672.x

Nixon, Lisette S., Yung, Bernard, Bell, Scott C., Elborn, J.Stuart and Shale, Dennis J. (1998). Circulating immunoreactive interleukin-6 in cystic fibrosis. American Journal of Respiratory and Critical Care Medicine, 157 (6), 1764-1769.

Watkin, S., Bell, S.C., Wynn, S., Hiller, J., Shale, D.J. and Elborn, J.S. (1998). Vitamin A and E and pulmonary function in cystic fibrosis. Medical Science Research, 26 (2), 97-99.

Nixon, L. S., Yung, B., Bell, S. C., Elborn, J. S. and Shale, D. J. (1996). Neutrophil responsiveness in cystic fibrosis patients is affected by clinical state. Thorax, 51 (SUPPL. 3).

Nixon, L. S., Yung, B., Bell, S. C., Elborn, J. S. and Shale, D. J. (1996). Blood and sputum sol inflammatory markers. Thorax, 51 (SUPPL. 3).

Nixon, L. S., Yung, B., Bell, S. C., Elborn, J. S. and Shale, D. J. (1996). Circulating immunoreactive Interleukin-6 (IL-6) in cystic fibrosis. Thorax, 51 (SUPPL. 3).

Elborn, J.S. and Bell, S.C. (1996). Nutrition and survival in cystic fibrosis. Thorax, 51 (10), 971-972. doi: 10.1136/thx.51.10.971

Bell, S.C., Saunders, M.J., Elborn, J.S. and Shale, D.J. (1996). Resting energy expenditure and oxygen cost of breathing in patients with cystic fibrosis. Thorax, 51 (2), 126-131. doi: 10.1136/thx.51.2.126

Field, Penelope I., Simmul, Rein, Bell, Scott C., Allen, David H. and Berend, Norbert (1996). Evidence for opioid modulation and generation of prostaglandins in sulphur dioxide (SO)(2)-induced bronchoconstriction. Thorax, 51 (2), 159-163. doi: 10.1136/thx.51.2.159

Elborn, J. Stuart, Delamare, Finola, Bell, Scott C. and Shale, Dennis J. (1995). Can tumor necrosis factor-alpha (TNF-alpha) be reliably measured in blood?. Pediatric Pulmonology, 19 (4), 226-230. doi: 10.1002/ppul.1950190407

Bell, S.C., Elborn, J.S., Campbell, I.A. and Shale, D.J. (1995). Candida albicans infection complicating percutaneous gastrostomy in cystic fibrosis. British Journal of Clinical Practice, 49 (2), 109-110.

Elborn, J. Stuart, Nixon, Lisette, Bell, Scott C. and Shale, Dennis J. (1994). On tumor necrosis factor alpha in CF. Pediatric Pulmonology, 17 (6), 411-411. doi: 10.1002/ppul.1950170615

Bell, S.C., Rynell, A.-C., Matheson, M.J., Finnimore, A.J. and Berend, N. (1993). Inhaled FMLP increases microvascular permeability in the rabbit trachea. Journal of Applied Physiology, 74 (3), 1337-1341. doi: 10.1152/jappl.1993.74.3.1337

Bell, S.C., Allen, D.H. and Vandenburg, R.A. (1991). An unusual intrabronchial foreight body in an asthmatic patient. Medical Journal of Australia, 154 (4), 291-291.

Stockwell, R., Wood, M., Moore, V and Bell, S. (2018). Infection control in Australian and New Zealand cystic fibrosis centres. ANZSRS/TSANZ Annual Scientific Meeting, Adelaide, Australia, 23-27 March 2018. Richmond, VIC, Australia: Wiley-Blackwell.

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.

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

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

Kidd, T. J., Magalhaes, R. J. Soares, Paynter, S. and Bell, S. C. (2013). The Social Network in Cystic Fibrosis (Cf) Centre Care and the Risk of Shared Pseudomonas Aeruginosa (Pa) Strain Infection. HOBOKEN: WILEY-BLACKWELL.

Tai, A., Kidd, T. J., Whiley, D. M., Sidjabat, H. E. and Bell, S. C. (2013). Molecular Surveillance and Prevalence of Acquired Carbapenem Resistance in Pseudomonas Aeruginosa (Pa) Amongst Australian Cystic Fibrosis (Cf) Patients. Thoracic Society of Australia & New Zealand and the Australian & New Zealand Society of Respiratory Science 2013 Annual Scientific Meetings, Darwin Convention Centre, Darwin, NT, 22-27 March 2013. Richmond Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/resp.12046

Wood, M. E., Smith, D. J., Reid, D. W. E. C. and Bell, S. C. (2013). Observational Study of the Clinical Effects of Ivacaftor in Patients with Severe Cystic Fibrosis (Cf) Lung Disease. 2013 Annual Scientific Meetings of The Thoracic Society of Australia and New Zealand and the Australian and New Zealand Society of Respiratory Science, Darwin, NT Australia, 22 - 27 March 2013. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/resp.12046

Wood, M. E., Ramsay, K. A., Kidd, T. J. and Bell, S. C. (2013). Methicillin-Resistant Staphyloccus Aureus (Mrsa) Infection in Health Care Workers with Cystic Fibrosis (Hcwcf). 2013 Annual Scientific Meetings of The Thoracic Society of Australia and New Zealand and the Australian and New Zealand Society of Respiratory Science, Darwin, NT Australia, 22 - 27 March 2013. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/resp.12045

Smith, D. J., Badrick, A. C., Krause, L., Bell, S. C., Anderson, G. J. and Reid, D. W. (2013). Perturbation of Sputum Microbiota by Intravenous Antibiotics in Cystic Fibrosis Is Short-Lived. 2013 Annual Scientific Meetings of The Thoracic Society of Australia and New Zealand and the Australian and New Zealand Society of Respiratory Science, Darwin, NT Australia, 22 - 27 March 2013. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/resp.12046

Kidd, T. J., Knibbs, L. D., Johnson, G., Kattenbelt, J. A., Ramsay, K. A., Wood, M., Beevers, A., O'Rourke, P. K., Wainwright, C. E., Grimwood, K., Sly, P., Morawska, L. and Bell, S. C. (2013). Viability of pseudomonas aeruginosa (Pa) in cough aerosols from adult cystic fibrosis (CF) patients. Thoracic Society of Australia & New Zealand and the Australian & New Zealand Society of Respiratory Science 2013 Annual Scientific Meetings, Darwin, NT Australia, 22-27 March 2013. Richmond, VIC Australia: Wiley-Blackwell. doi: 10.1111/resp.12045

Hanks-Thomson, Kirstin R., Kidd, Timothy J., Wainwright, Claire E., Ramsey, Kay A., Steen, Jason A., Bell, Scott C., Zakour, Nouri L. Ben and Beatson, Scott A. (2012). Acquired aminoglycoside resistance in pseudomonas aeruginosa from a cystic fibrosis patient. Australian Society for Microbiology Annual Scientific Meeting (ASM2012), Brisbane, Australia, 1-4 July 2012.

Ramsay, K. A., Butler, C., Kidd, T. J., Wainwright, C. E. and Bell, S. C. (2012). Burkholderia cepacia complex infection (bcc) in cystic fibrosis (cf): 2001-2010. Thoracic Society of Australia & New Zealand and the Australian & New Zealand Society of Respiratory Science 2012 Annual Scientific Meetings, Canberra ACT, Australia, 30 March-4 April 2012. Richmond Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1843.2012.02143.x

Smith, D. J., Badrick, A., Anderson, G. J., Bell, S. C. and Reid, D. W. (2012). Iron supplementation and defective iron homeostasis are associated with worse lung function in cystic fibrosis (CF). Thoracic Society of Australia & New Zealand and the Australian & New Zealand Society of Respiratory Science 2012 Annual Scientific Meetings, Canberra, ACT, 30 March - 4 April 2012. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1843.2012.02142.x

Smith, D., Kidd, T. J., Ramsay, K. A., Wainwright, C. E., Grimwood, K. and Bell, S. C. (2012). Pseudomonas aeruginosa resistance: Comparison between Australian cystic fibrosis (cf) centres. unknown, unknown, unknown. Richmond, VIC, Australia: John Wiley and Sons.

Timothy Kidd, Ritchie S, Keith Grimwood, Bell, Scott C. and Rainey PB (2011). Comparison of clinical and environmental Pseudomonas aeruginosa: evidence for recombination. 34th European Cystic Fibrosis Conference, Annual Scientific Meeting, Hamburg, Germany, 8-11 June 2011.

Timothy Kidd, Kay Ramsay, Bell, Scott C., Claire Wainwright and Keith Grimwood (2011). Australasian CF bronchoalveolar lavage (ACFBAL) Study: Pseudomonas aeruginosa (Pa) genotypes in pre-school CF children. 9th Australasian Cystic Fibrosis Conference, Melbourme, Australia, 20 - 23rd August 2011.

Smith DJ, Timothy Kidd, Kay Ramsay, Keith Grimwood, Claire Wainwright and Bell, Scott C. (2011). Pseudomonas aeruginosa antibiotic resistance: comparison between Australian paediatric and adult cystic fibrosis centres. 9th Australasian Cystic Fibrosis Conference, Melbourme, Australia, 20-23rd August 2011.

Kidd, Timothy, Gibson, J. S., Moss, S., Greer, R. M., Cobbold, R. N., Wright, J. D., Ramsay, Kay, Grimwood, Keith and Bell, Scott C. (2011). Clonal complex pseudomonas aeruginosa in horses: A model of CF infection. Thoracic Society of Australia and New Zealand Annual Scientific Meeting, Perth, Australia, 2-6 April 2012.

Timothy Kidd, Kay Ramsay, He Hu, Bye P, Elkins M, Marks G, Claire Wainwright, robinson P, Rose B, Harbour C, Keith Grimwood, Bell, Scott C. and ACPinCF Investigator Study Group (2011). Widespread prevalence of related Pseudomonas aeruginosa strains within Australian cystic fibrosis centres. 9th Australasian Cystic Fibrosis Conference, Melbourne , Australia, 20-23 August 2011.

Kidd, T. J., Rainey, P. B., Ramsay, K. A., Grimwood, K., Wainwright, C. E. and Bell, S. C. (2010). Multilocus sequence typing (MLST) of Pseudomonas aeruginosa collected from different ecological niches. 33rd European Cystic Fibrosis Conference, Valencia, Spain, 16-19 June 2010. Amsterdam: Elsevier Science. doi: 10.1016/S1569-1993(10)60114-2

Tse, T., Hopkins, P. M. A., France, M. W., Masel, P. J., Bell, S. C., Kermeen, F. D. and Chambers, D. C. (2010). Antibiotic desensitisation in cystic fibrosis patients with a history of hypersensitivity undergoing lung transplantation is not mandatory. 30th Annual Meeting and Scientific Sessions of the International-Society-for-Heart-and-Lung-Transplantation, Chicago Il, Apr 21-24, 2010. ELSEVIER SCIENCE INC.

Kidd, T. J., Rainey, P. B., Ramsay, K. A., Grimwood, K., Wainwright, C. E. and Bell, S. C. (2010). Multilocus sequence typing (MLST) of Pseudomonas aeruginosa collected from different ecological niches. Australian Society for Microbiology 51st Scientific Meeting, Sydney, NSW, Australia, 4-8 July 2010.

Kidd, T. J., Rainey, P. B., Ramsay, K. A., Grimwood, K., Wainwright, C. E. and Bell, S. C. (2010). Multilocus sequence typing (MLST) of Pseudomonas aeruginosa. Thoracic Society of Australia and New Zealand Annual Scientific Meeting, Brisbane, Qld Australia, 20-24 March 2010.

Kidd, T. J., Ramsay, K. A., Hu, H., Bye, P. T. P., Marks, G. B., Wainwright, C. E., Robinson, P. J., Rose, B. R., Harbour, C., Grimwood, K., Bell, S. C. and ACPinCF Investigator Study Group (2010). Clonal pseudomonas aeruginosa (PA) in Australians with cystic fibrosis (CF). Thoracic Society of Australia and New Zealand Annual Scientific Meeting, Brisbane, QLD Australia, 20-24 March 2010.

Walsh, M. J., Lewindon, P. J., Shepherd, R. W., Greer, R. M., Williamson, R., Pereira, T. N., Frawley, K, Bell, S., Smith, J. L. and Ramm, G. A. (2009). Detection and follow-up of hepatic fibrosis in cystic fibrosis: A role for diagnostic liver biopsy and serum markers in evaluating outcomes of cystic fibrosis liver disease. Australia & New Zealand Medical & Surgical Gastrointestinal Week 2009, Sydney, NSW, Australia, 21 - 24 October 2009. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1746.2009.06050.x

Bell, Scott C. (2009). Antibiotic allergy: Diagnosis and management. 23rd Annual North American Cystic Fibrosis Conference, Minneapolis, Minnesota, 15 - 17 October 2009. New York , U. S. A.: Wiley. doi: 10.1002/ppul.21130

Sawyer, S.M., Farrant, B., Wilson, J., Ryan, G., O'Carroll, M., Bye, P. and Bell, S. (2009). Sexual and reproductive health in men with cystic fibrosis: Consistent preferences, inconsistent practices. North American CF Foundation Conference, Orlando, Florida, USA, 24 October 2008. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.jcf.2009.05.005

Smith, H., Bell, S. and Nissen, L. (2007). Does antibiotic sensitivity testing for Pseudomonas aeruginosa exacerbations in cystic fibrosis patients influence clinical choice?. SHPA 28th Federal Conference 2007, Convention Centre, Sydney Australia, 8-11 November 2007.

Masel, P. J., Tse, T., Herd, K., Wood, P. and Bell, S. (2007). Audit of iron infusions in the cystic fibrosis (CF) and bronchiectasis populations. 7th Australasian Cystic Fibrosis Conference, Sydney, Australia, 11th - 14th August 2007.

Hennig, S, Wainwright, C E, Bell, S, Miller, H, Charles, B G and Duffull, S B (2006). A D-optimal designed population pharmacokinetic study of itraconazole. APSA Annual Meeting 2006, Adelaide, Australia, 2-5 December 2006. Adelaide:

Hennig, S, Wainwright, C E, Bell, S, Miller, H, Friberg, L. E. and Charles, B G (2006). Paediatric population pharmacokinetcis (popPK) of itraconazole (ITRA) and its active metabolite hydroxy-itraconazole in cystic fibrosis (CF) and bone marrow transplant patients (BMT). PAGANZ 06 9th Annual Scientific Meeting, Auckland New Zealand / School of Medicine, 7-9 February 2006. Brisbane, Australia: Poppulation Approach Group in Australia and New Zealand.

Hennig, S, Wainwright, C E, Bell, S, Miller, H, Friberg, L. E. and Charles, B G (2006). Pharmacokinetic study of itraconazole leads to new improved dosing regimens for paediatric cystic fibrosis and bone marrow transplant patients. The 6th Annual Health and Medical Research Conference of Queensland, Brisbane, Australia, 23-24 November 2006. Brisbane, Australia: Queensland Health.

Hennig, S., Wainwright, C. E., Bell, S. C., Miller, H., Friberg, L. E. and Charles, B. G. (2006). Paediatric population pharmacokinetics of itraconazole and its active metabolite hydroxy-itraconazole in cystic fibrosis and bone marrow transplant patients. Population Approach Group Europe: 15th Meeting, Bruges, Belgium, 14-16 June 2006. PAGE.

Hennig, S., Wainwright, C. E., Bell, S., Miller, H., Charles, B. G. and Duffull, S. B. (2006). A D-optimal designed population pharmacokinetic study of itraconazole capsules and solution in adults with cystic fibrosis. 15th Annual Meeting of the Population Approach Group in Europe, Bruges, Belgium, 14-16 June 2006. PAGE.

Burrows, J., Nissen, L. M., Kirkpatrick, C. M. J. and Bell, S. C. (2005). A study of desensitisation procedures to beta-lactam antibiotics in adult patients with cystic fibrosis: An update. Sixth Australian & New Zealand Cystic Fibrosis Conference, Adelaide, 20-23 Aug. 2005. Australia:

Burrows, J., Nissen, L. M., Kirkpatrick, C. M. J. and Bell, S. C. (2005). A study of allergic reactions to beta-lactam antibiotics in an adult cystic fibrosis unit. Sixth Australian & New Zealand Cystic Fibrosis Conference, Adelaide, 20-23 Aug. 2005. Australia:

Burrows, J., Nissen, L. M., Kirkpatrick, C. M. J. and Bell, S. C. (2005). A study of allergic reactions to beta-lactam antibiotics in adults with cystic fibrosis: What is new?. The Society of Hospital Pharmacists of Australia 27th Federal Conference, Brisbane, 10-13 Nov. 2005. Brisbane: Event Planners Australia.

Kim, S. T., Yang, I. A. and Bell, S. C. (2005). Antibiotics in cystic fibrosis (CF): A systematic review. 2005 Annual Scientific Meeting The Thoracic Society of Australia and New Zealand, Perth, Australia, 18-23 March, 2005.

Professor Scott Bell

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