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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1991 2
1992 1
1993 5
1994 5
1996 5
1997 4
1998 1
1999 9
2000 4
2002 2
2003 2
2004 1
2005 2
2006 3
2007 2
2008 3
2009 1
2010 4
2011 3
2012 4
2013 4
2015 4
2016 2
2017 5
2018 6
2019 9
2020 6
2021 5
2022 4
2023 5
2024 1

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102 results

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Page 1
Pseudomonas aeruginosa infection in cystic fibrosis: pathophysiological mechanisms and therapeutic approaches.
Lund-Palau H, Turnbull AR, Bush A, Bardin E, Cameron L, Soren O, Wierre-Gore N, Alton EW, Bundy JG, Connett G, Faust SN, Filloux A, Freemont P, Jones A, Khoo V, Morales S, Murphy R, Pabary R, Simbo A, Schelenz S, Takats Z, Webb J, Williams HD, Davies JC. Lund-Palau H, et al. Among authors: connett g. Expert Rev Respir Med. 2016 Jun;10(6):685-97. doi: 10.1080/17476348.2016.1177460. Epub 2016 May 13. Expert Rev Respir Med. 2016. PMID: 27175979 Free article. Review.
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 HGM, McKone EF, Downey DG, Van Braeckel E, Rowe SM, Tullis E, Mall MA, Welter JJ, Ramsey BW, McKee CM, Marigowda G, Moskowitz SM, Waltz D, Sosnay PR, Simard C, Ahluwalia N, Xuan F, Zhang Y, Taylor-Cousar JL, McCoy KS; VX17-445-103 Trial Group. Heijerman HGM, et al. Lancet. 2019 Nov 23;394(10212):1940-1948. doi: 10.1016/S0140-6736(19)32597-8. Epub 2019 Oct 31. Lancet. 2019. PMID: 31679946 Free PMC article. Clinical Trial.
Triple Therapy for Cystic Fibrosis Phe508del-Gating and -Residual Function Genotypes.
Barry PJ, Mall MA, Álvarez A, Colombo C, de Winter-de Groot KM, Fajac I, McBennett KA, McKone EF, Ramsey BW, Sutharsan S, Taylor-Cousar JL, Tullis E, Ahluwalia N, Jun LS, Moskowitz SM, Prieto-Centurion V, Tian S, Waltz D, Xuan F, Zhang Y, Rowe SM, Polineni D; VX18-445-104 Study Group. Barry PJ, et al. N Engl J Med. 2021 Aug 26;385(9):815-825. doi: 10.1056/NEJMoa2100665. N Engl J Med. 2021. PMID: 34437784 Free PMC article. Clinical Trial.
Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis.
Southern KW, Castellani C, Lammertyn E, Smyth A, VanDevanter D, van Koningsbruggen-Rietschel S, Barben J, Bevan A, Brokaar E, Collins S, Connett GJ, Daniels TWV, Davies J, Declercq D, Gartner S, Gramegna A, Hamilton N, Hauser J, Kashirskaya N, Kessler L, Lowdon J, Makukh H, Martin C, Morrison L, Nazareth D, Noordhoek J, O'Neill C, Owen E, Oxley H, Raraigh KS, Raynal C, Robinson K, Roehmel J, Schwarz C, Sermet I, Shteinberg M, Sinha I, Takawira C, van Mourik P, Verkleij M, Waller MD, Duff A. Southern KW, et al. Among authors: connett gj. J Cyst Fibros. 2023 Jan;22(1):17-30. doi: 10.1016/j.jcf.2022.10.002. Epub 2022 Oct 28. J Cyst Fibros. 2023. PMID: 36916675 Free article.
Bronchoalveolar lavage.
Connett GJ. Connett GJ. Paediatr Respir Rev. 2000 Mar;1(1):52-6. doi: 10.1053/prrv.2000.0007. Paediatr Respir Rev. 2000. PMID: 16263445 Review.
Reply to Cooper.
Causer AJ, Shute JK, Cummings MH, Shepherd AI, Bright V, Connett G, Allenby MI, Carroll MP, Daniels T, Saynor ZL. Causer AJ, et al. Among authors: connett g. J Appl Physiol (1985). 2019 Jan 1;126(1):265. doi: 10.1152/japplphysiol.00839.2018. J Appl Physiol (1985). 2019. PMID: 30694712 Free article. No abstract available.
Reply to Askew and Green.
Causer AJ, Shute JK, Cummings MH, Shepherd AI, Bright V, Connett G, Allenby MI, Carroll MP, Daniels T, Saynor ZL. Causer AJ, et al. Among authors: connett g. J Appl Physiol (1985). 2019 Feb 1;126(2):512. doi: 10.1152/japplphysiol.00939.2018. J Appl Physiol (1985). 2019. PMID: 30799675 Free article. No abstract available.
Juvenile laryngeal papillomatosis.
Coope G, Connett G. Coope G, et al. Among authors: connett g. Prim Care Respir J. 2006 Apr;15(2):125-7. doi: 10.1016/j.pcrj.2006.02.004. Epub 2006 Mar 9. Prim Care Respir J. 2006. PMID: 16701772 Free PMC article.
102 results