Davies JC - Search Results

1

Targeted exhaled breath analysis for detection of Pseudomonas aeruginosa in cystic fibrosis patients.

Kos R, Brinkman P, Neerincx AH, Paff T, Gerritsen MG, Lammers A, Kraneveld AD, Heijerman HGM, Janssens HM, Davies JC, Majoor CJ, Weersink EJ, Sterk PJ, Haarman EG, Bos LD, Maitland-van der Zee AH; Amsterdam Mucociliary Clearance Disease (AMCD) Research Group and the Amsterdam UMC Breath Research Group. Kos R, et al. Among authors: davies jc. J Cyst Fibros. 2022 Jan;21(1):e28-e34. doi: 10.1016/j.jcf.2021.04.015. Epub 2021 May 18. J Cyst Fibros. 2022. PMID: 34016557 Free article. Review.

2

CFTR gene transfer reduces the binding of Pseudomonas aeruginosa to cystic fibrosis respiratory epithelium.

Davies JC, Stern M, Dewar A, Caplen NJ, Munkonge FM, Pitt T, Sorgi F, Huang L, Bush A, Geddes DM, Alton EW. Davies JC, et al. Am J Respir Cell Mol Biol. 1997 Jun;16(6):657-63. doi: 10.1165/ajrcmb.16.6.9191467. Am J Respir Cell Mol Biol. 1997. PMID: 9191467

3

Reduction in the adherence of Pseudomonas aeruginosa to native cystic fibrosis epithelium with anti-asialoGM1 antibody and neuraminidase inhibition.

Davies J, Dewar A, Bush A, Pitt T, Gruenert D, Geddes DM, Alton EW. Davies J, et al. Eur Respir J. 1999 Mar;13(3):565-70. doi: 10.1183/09031936.99.13356599. Eur Respir J. 1999. PMID: 10232427 Free article.

4

Pseudomonas aeruginosa in cystic fibrosis: pathogenesis and persistence.

Davies JC. Davies JC. Paediatr Respir Rev. 2002 Jun;3(2):128-34. doi: 10.1016/s1526-0550(02)00003-3. Paediatr Respir Rev. 2002. PMID: 12297059 Review.

5

Airway surface pH in subjects with cystic fibrosis.

McShane D, Davies JC, Davies MG, Bush A, Geddes DM, Alton EW. McShane D, et al. Among authors: davies mg, davies jc. Eur Respir J. 2003 Jan;21(1):37-42. doi: 10.1183/09031936.03.00027603. Eur Respir J. 2003. PMID: 12570106 Free article.

6

Multiresistant Pseudomonas aeruginosa in a pediatric cystic fibrosis center: natural history and implications for segregation.

Davies G, McShane D, Davies JC, Bush A. Davies G, et al. Among authors: davies jc. Pediatr Pulmonol. 2003 Apr;35(4):253-6. doi: 10.1002/ppul.10262. Pediatr Pulmonol. 2003. PMID: 12629620

7

Bronchoscopy following diagnosis with cystic fibrosis.

Hilliard TN, Sukhani S, Francis J, Madden N, Rosenthal M, Balfour-Lynn I, Bush A, Davies JC. Hilliard TN, et al. Among authors: davies jc. Arch Dis Child. 2007 Oct;92(10):898-9. doi: 10.1136/adc.2006.105825. Epub 2006 Nov 6. Arch Dis Child. 2007. PMID: 17088336 Free PMC article.

8

Detection of antibodies to Pseudomonas aeruginosa in serum and oral fluid from patients with cystic fibrosis.

Weisner AM, Chart H, Bush A, Davies JC, Pitt TL. Weisner AM, et al. Among authors: davies jc. J Med Microbiol. 2007 May;56(Pt 5):670-674. doi: 10.1099/jmm.0.46833-0. J Med Microbiol. 2007. PMID: 17446292

9

Biomarkers for cystic fibrosis lung disease: application of SELDI-TOF mass spectrometry to BAL fluid.

MacGregor G, Gray RD, Hilliard TN, Imrie M, Boyd AC, Alton EW, Bush A, Davies JC, Innes JA, Porteous DJ, Greening AP. MacGregor G, et al. Among authors: davies jc. J Cyst Fibros. 2008 Sep;7(5):352-8. doi: 10.1016/j.jcf.2007.12.005. Epub 2008 Feb 1. J Cyst Fibros. 2008. PMID: 18243068 Free article.

10

Pseudomonas aeruginosa, cyanide accumulation and lung function in CF and non-CF bronchiectasis patients.

Ryall B, Davies JC, Wilson R, Shoemark A, Williams HD. Ryall B, et al. Among authors: davies jc. Eur Respir J. 2008 Sep;32(3):740-7. doi: 10.1183/09031936.00159607. Epub 2008 May 14. Eur Respir J. 2008. PMID: 18480102 Free article.

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