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Low rates of Pseudomonas aeruginosa misidentification in isolates from cystic fibrosis patients.
Kidd TJ, Ramsay KA, Hu H, Bye PT, Elkins MR, Grimwood K, Harbour C, Marks GB, Nissen MD, Robinson PJ, Rose BR, Sloots TP, Wainwright CE, Bell SC; ACPinCF Investigators. Kidd TJ, et al. Among authors: harbour c. J Clin Microbiol. 2009 May;47(5):1503-9. doi: 10.1128/JCM.00014-09. Epub 2009 Mar 4. J Clin Microbiol. 2009. PMID: 19261796 Free PMC article.
Type 3 secretion system effector genotype and secretion phenotype of longitudinally collected Pseudomonas aeruginosa isolates from young children diagnosed with cystic fibrosis following newborn screening.
Hu H, Harmer C, Anuj S, Wainwright CE, Manos J, Cheney J, Harbour C, Zablotska I, Turnbull L, Whitchurch CB, Grimwood K, Rose B; FBAL study investigators. Hu H, et al. Among authors: harbour c. Clin Microbiol Infect. 2013 Mar;19(3):266-72. doi: 10.1111/j.1469-0691.2012.03770.x. Epub 2012 Feb 13. Clin Microbiol Infect. 2013. PMID: 22329595 Free article.
Virulence factor expression patterns in Pseudomonas aeruginosa strains from infants with cystic fibrosis.
Manos J, Hu H, Rose BR, Wainwright CE, Zablotska IB, Cheney J, Turnbull L, Whitchurch CB, Grimwood K, Harmer C, Anuj SN, Harbour C; ACFBAL study group. Manos J, et al. Among authors: harbour c. Eur J Clin Microbiol Infect Dis. 2013 Dec;32(12):1583-92. doi: 10.1007/s10096-013-1916-7. Epub 2013 Jul 7. Eur J Clin Microbiol Infect Dis. 2013. PMID: 23832143
A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis.
Elkins MR, Robinson M, Rose BR, Harbour C, Moriarty CP, Marks GB, Belousova EG, Xuan W, Bye PT; National Hypertonic Saline in Cystic Fibrosis (NHSCF) Study Group. Elkins MR, et al. Among authors: harbour c. N Engl J Med. 2006 Jan 19;354(3):229-40. doi: 10.1056/NEJMoa043900. N Engl J Med. 2006. PMID: 16421364 Free article. Clinical Trial.
84 results