Nash, Edward F

Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial

Heijerman, H. G. M., McKone, E. F., Downey, D. G., Van Braeckel, E., Rowe, S. M., Tullis, E., Mall, M. A., Welter, J. J., Ramsey, B. W., McKee, C. M., et al. (2019) · The Lancet

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The top 10 research priorities in cystic fibrosis developed by a partnership between people with CF and healthcare providers

Rowbotham, N. J., Smith, S., Leighton, P. A., Rayner, O. C., Gathercole, K., Elliott, Z. C., Nash, E. F., Daniels, T., Duff, A. J. A., Collins, S., et al. (2018) · Thorax

Cystic Fibrosis Research AdvancesDelphi Technique in Research

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Characterising burden of treatment in cystic fibrosis to identify priority areas for clinical trials

Davies, G., Rowbotham, N. J., Smith, S., Elliot, Z. C., Gathercole, K., Rayner, O., Leighton, P. A., Herbert, S., Duff, A. J., Chandran, S., et al. (2020) · Journal of Cystic Fibrosis

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Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study

Flume, P. A., Biner, R. F., Downey, D. G., Brown, C., Jain, M., Fischer, R., De Boeck, K., Sawicki, G. S., Chang, P., Paz-Diaz, H., et al. (2021) · The Lancet Respiratory Medicine

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Outcomes of patients with cystic fibrosis undergoing lung transplantation with and without cystic fibrosis-associated liver cirrhosis

Nash, E. F., Volling, C., Gutierrez, C. A., Tullis, E., Coonar, A., McRae, K., Keshavjee, S., Singer, L. G., Durie, P. R., & Chaparro, C. (2012) · Clinical Transplantation

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