McColley SA - Search Results

1

Aminoglycoside resistance of Pseudomonas aeruginosa in cystic fibrosis results from convergent evolution in the mexZ gene.

Prickett MH, Hauser AR, McColley SA, Cullina J, Potter E, Powers C, Jain M. Prickett MH, et al. Among authors: mccolley sa. Thorax. 2017 Jan;72(1):40-47. doi: 10.1136/thoraxjnl-2015-208027. Epub 2016 Jun 20. Thorax. 2017. PMID: 27325751 Free PMC article.

2

Serum vascular endothelial growth factor is elevated in cystic fibrosis and decreases with treatment of acute pulmonary exacerbation.

McColley SA, Stellmach V, Boas SR, Jain M, Crawford SE. McColley SA, et al. Am J Respir Crit Care Med. 2000 Jun;161(6):1877-80. doi: 10.1164/ajrccm.161.6.9905022. Am J Respir Crit Care Med. 2000. PMID: 10852760

3

Type III secretion phenotypes of Pseudomonas aeruginosa strains change during infection of individuals with cystic fibrosis.

Jain M, Ramirez D, Seshadri R, Cullina JF, Powers CA, Schulert GS, Bar-Meir M, Sullivan CL, McColley SA, Hauser AR. Jain M, et al. Among authors: mccolley sa. J Clin Microbiol. 2004 Nov;42(11):5229-37. doi: 10.1128/JCM.42.11.5229-5237.2004. J Clin Microbiol. 2004. PMID: 15528719 Free PMC article.

4

Evolution of Pseudomonas aeruginosa type III secretion in cystic fibrosis: a paradigm of chronic infection.

Jain M, Bar-Meir M, McColley S, Cullina J, Potter E, Powers C, Prickett M, Seshadri R, Jovanovic B, Petrocheilou A, King JD, Hauser AR. Jain M, et al. Transl Res. 2008 Dec;152(6):257-64. doi: 10.1016/j.trsl.2008.10.003. Epub 2008 Oct 31. Transl Res. 2008. PMID: 19059160 Free PMC article.

5

Clinical significance of microbial infection and adaptation in cystic fibrosis.

Hauser AR, Jain M, Bar-Meir M, McColley SA. Hauser AR, et al. Among authors: mccolley sa. Clin Microbiol Rev. 2011 Jan;24(1):29-70. doi: 10.1128/CMR.00036-10. Clin Microbiol Rev. 2011. PMID: 21233507 Free PMC article. Review.

6

A CFTR potentiator in patients with cystic fibrosis and the G551D mutation.

Ramsey BW, Davies J, McElvaney NG, Tullis E, Bell SC, Dřevínek P, Griese M, McKone EF, Wainwright CE, Konstan MW, Moss R, Ratjen F, Sermet-Gaudelus I, Rowe SM, Dong Q, Rodriguez S, Yen K, Ordoñez C, Elborn JS; VX08-770-102 Study Group. Ramsey BW, et al. N Engl J Med. 2011 Nov 3;365(18):1663-72. doi: 10.1056/NEJMoa1105185. N Engl J Med. 2011. PMID: 22047557 Free PMC article. Clinical Trial.

7

Lung function decline from adolescence to young adulthood in cystic fibrosis.

Vandenbranden SL, McMullen A, Schechter MS, Pasta DJ, Michaelis RL, Konstan MW, Wagener JS, Morgan WJ, McColley SA; Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Vandenbranden SL, et al. Among authors: mccolley sa. Pediatr Pulmonol. 2012 Feb;47(2):135-43. doi: 10.1002/ppul.21526. Epub 2011 Aug 24. Pediatr Pulmonol. 2012. PMID: 22241571 Free PMC article.

8

Risk factors for onset of persistent respiratory symptoms in children with cystic fibrosis.

McColley SA, Ren CL, Schechter MS, Regelmann WE, Pasta DJ, Konstan MW; Epidemiologic Study of Cystic Fibrosis. McColley SA, et al. Pediatr Pulmonol. 2012 Oct;47(10):966-72. doi: 10.1002/ppul.22519. Epub 2012 Feb 22. Pediatr Pulmonol. 2012. PMID: 22359344 Free PMC article.

9

Standard care versus protocol based therapy for new onset Pseudomonas aeruginosa in cystic fibrosis.

Mayer-Hamblett N, Rosenfeld M, Treggiari MM, Konstan MW, Retsch-Bogart G, Morgan W, Wagener J, Gibson RL, Khan U, Emerson J, Thompson V, Elkin EP, Ramsey BW; EPIC; ESCF Investigators. Mayer-Hamblett N, et al. Pediatr Pulmonol. 2013 Oct;48(10):943-53. doi: 10.1002/ppul.22693. Epub 2013 Jul 2. Pediatr Pulmonol. 2013. PMID: 23818295 Free PMC article. Clinical Trial.

10

Improved patient safety through reduced airway infection rates in a paediatric cystic fibrosis programme after a quality improvement effort to enhance infection prevention and control measures.

Savant AP, O'Malley C, Bichl S, McColley SA. Savant AP, et al. Among authors: mccolley sa. BMJ Qual Saf. 2014 Apr;23 Suppl 1:i73-i80. doi: 10.1136/bmjqs-2013-002315. BMJ Qual Saf. 2014. PMID: 24608553

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