Elkins MR - Search Results

1

Inhaled hypertonic saline as a therapy for cystic fibrosis.

Elkins MR, Bye PT. Elkins MR, et al. Curr Opin Pulm Med. 2006 Nov;12(6):445-52. doi: 10.1097/01.mcp.0000245714.89632.b2. Curr Opin Pulm Med. 2006. PMID: 17053496 Review.

2

Evaluation of the SenseWear activity monitor during exercise in cystic fibrosis and in health.

Dwyer TJ, Alison JA, McKeough ZJ, Elkins MR, Bye PT. Dwyer TJ, et al. Among authors: elkins mr. Respir Med. 2009 Oct;103(10):1511-7. doi: 10.1016/j.rmed.2009.04.013. Epub 2009 May 23. Respir Med. 2009. PMID: 19464863

3

Positive expiratory pressure physiotherapy for airway clearance in people with cystic fibrosis.

Elkins MR, Jones A, van der Schans C. Elkins MR, et al. Cochrane Database Syst Rev. 2006 Apr 19;(2):CD003147. doi: 10.1002/14651858.CD003147.pub3. Cochrane Database Syst Rev. 2006. PMID: 16625571 Updated. Review.

4

Positive expiratory pressure physiotherapy for airway clearance in people with cystic fibrosis.

Elkins MR, Jones A, Schans C. Elkins MR, et al. Cochrane Database Syst Rev. 2004;(1):CD003147. doi: 10.1002/14651858.CD003147.pub2. Cochrane Database Syst Rev. 2004. PMID: 14974007 Updated. Review.

5

Method for detection of respiratory viruses in the sputa of patients with cystic fibrosis.

Punch G, Syrmis MW, Rose BR, Harbour C, Bye PT, Nissen MD, Elkins MR, Sloots TP. Punch G, et al. Among authors: elkins mr. Eur J Clin Microbiol Infect Dis. 2005 Jan;24(1):54-7. doi: 10.1007/s10096-004-1273-7. Eur J Clin Microbiol Infect Dis. 2005. PMID: 15616837 Free PMC article.

6

Timing of dornase alfa inhalation for cystic fibrosis.

Dentice R, Elkins M. Dentice R, et al. Cochrane Database Syst Rev. 2013 Jun 5;(6):CD007923. doi: 10.1002/14651858.CD007923.pub3. Cochrane Database Syst Rev. 2013. PMID: 23737088 Updated. Review.

7

Timing of hypertonic saline inhalation for cystic fibrosis.

Elkins M, Dentice R. Elkins M, et al. Cochrane Database Syst Rev. 2012 Feb 15;(2):CD008816. doi: 10.1002/14651858.CD008816.pub2. Cochrane Database Syst Rev. 2012. PMID: 22336853 Review.

8

Timing of dornase alfa inhalation for cystic fibrosis.

Dentice R, Elkins M. Dentice R, et al. Cochrane Database Syst Rev. 2011 May 11;(5):CD007923. doi: 10.1002/14651858.CD007923.pub2. Cochrane Database Syst Rev. 2011. PMID: 21563162 Updated. Review.

9

Clinical profile of adult cystic fibrosis patients with frequent epidemic clones of Pseudomonas aeruginosa.

Tingpej P, Elkins M, Rose B, Hu H, Moriarty C, Manos J, Barras B, Bye P, Harbour C. Tingpej P, et al. Respirology. 2010 Aug;15(6):923-9. doi: 10.1111/j.1440-1843.2010.01792.x. Epub 2010 Jun 21. Respirology. 2010. PMID: 20573059

10

Phenotypic characterization of clonal and nonclonal Pseudomonas aeruginosa strains isolated from lungs of adults with cystic fibrosis.

Tingpej P, Smith L, Rose B, Zhu H, Conibear T, Al Nassafi K, Manos J, Elkins M, Bye P, Willcox M, Bell S, Wainwright C, Harbour C. Tingpej P, et al. J Clin Microbiol. 2007 Jun;45(6):1697-704. doi: 10.1128/JCM.02364-06. Epub 2007 Mar 28. J Clin Microbiol. 2007. PMID: 17392437 Free PMC article.

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