Bell, Scott C.
Prince Charles Hospital
7 papers on CoChatORCID 0000-0001-8651-7139
Most cited papers
- Verified
A CFTR Potentiator in Patients with Cystic Fibrosis and the G551D Mutation
Ramsey, B. W., Davies, J., McElvaney, N. G., Tullis, E., Bell, S. C., Dřevínek, P., Griese, M., McKone, E. F., Wainwright, C. E., Konstan, M. W., et al. (2011) · New England Journal of Medicine
Cystic Fibrosis Research AdvancesInhalation and Respiratory Drug Delivery
Cited by 2,195
- Verified
ECFS best practice guidelines: the 2018 revision
Castellani, C., Duff, A. J. A., Bell, S. C., Heijerman, H. G. M., Munck, A., Ratjen, F., Sermet-Gaudelus, I., Southern, K. W., Barben, J., Flume, P. A., et al. (2018) · Journal of Cystic Fibrosis
Cystic Fibrosis Research AdvancesNeonatal Respiratory Health Research
Cited by 765
- Verified
Control of confounding and reporting of results in causal inference studies. Guidance for authors from editors of respiratory, sleep, and critical care journals
Lederer, D. J., Bell, S. C., Branson, R. D., Chalmers, J. D., Marshall, R., Maslove, D. M., Ost, D. E., Punjabi, N. M., Schatz, M., Smyth, A. R., et al. (2019) · Annals of the American Thoracic Society
Advanced Causal Inference TechniquesStatistical Methods in Epidemiology
Cited by 715
- Verified
European cystic fibrosis society standards of care: best practice guidelines
Smyth, A. R., Bell, S. C., Bojcin, S., Bryon, M., Duff, A., Flume, P., Kashirskaya, N., Munck, A., Ratjen, F., Schwarzenberg, S. J., et al. (2014) · Journal of Cystic Fibrosis
Cystic Fibrosis Research AdvancesNeonatal Respiratory Health Research
Cited by 582
- Verified
Development and Reporting of Prediction Models: Guidance for Authors From Editors of Respiratory, Sleep, and Critical Care Journals
Leisman, D. E., Harhay, M. O., Lederer, D. J., Abramson, M., Adjei, A. A., Bakker, J., Ballas, Z. K., Barreiro, E., Bell, S. C., Bellomo, R., et al. (2020) · Critical Care Medicine
Statistical Methods in EpidemiologyMeta-analysis and systematic reviews
Cited by 271
- Verified
Cough-Generated Aerosols of Pseudomonas aeruginosa and Other Gram-Negative Bacteria from Patients with Cystic Fibrosis
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., et al. (2009) · Thorax
Cystic Fibrosis Research AdvancesInfection Control and Ventilation
Cited by 135
- Verified
Lumacaftor/Ivacaftor Treatment of Patients with Cystic Fibrosis Heterozygous for F508del-CFTR
Rowe, S. M., McColley, S. A., Rietschel, E., Li, X., Bell, S. C., Konstan, M. W., Marigowda, G., Waltz, D., & Boyle, M. P. (2017) · Annals of the American Thoracic Society
Cystic Fibrosis Research AdvancesInhalation and Respiratory Drug Delivery
Cited by 92
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