Davies JC - Search Results

1

Does mass spectrometric breath analysis detect Pseudomonas aeruginosa in cystic fibrosis?

Pabary R, Huang J, Kumar S, Alton EW, Bush A, Hanna GB, Davies JC. Pabary R, et al. Among authors: davies jc. Eur Respir J. 2016 Mar;47(3):994-7. doi: 10.1183/13993003.00944-2015. Epub 2016 Feb 4. Eur Respir J. 2016. PMID: 26846826 Free article. No abstract available.

2

Severe small airways disease resistant to medical treatment in a child with cystic fibrosis.

Davies J, Rosenthal M, Bush A. Davies J, et al. J R Soc Med. 1996 Mar;89(3):172P-3P. J R Soc Med. 1996. PMID: 8683527 Free PMC article.

3

Retrospective review of the effects of rhDNase in children with cystic fibrosis.

Davies J, Trindade MT, Wallis C, Rosenthal M, Crawford O, Bush A. Davies J, et al. Pediatr Pulmonol. 1997 Apr;23(4):243-8. doi: 10.1002/(sici)1099-0496(199704)23:4<243::aid-ppul1>3.0.co;2-n. Pediatr Pulmonol. 1997. PMID: 9141109

4

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

5

The clinical use of rhDNAse.

Davies J, Trindale M, Wallis C, Rosenthal M, Bush A. Davies J, et al. Pediatr Pulmonol Suppl. 1997;16:273-4. doi: 10.1002/ppul.19502308141. Pediatr Pulmonol Suppl. 1997. PMID: 9443309 Review. No abstract available.

6

Distal 10q trisomy syndrome with unusual cardiac and pulmonary abnormalities.

Davies J, Jaffé A, Bush A. Davies J, et al. J Med Genet. 1998 Jan;35(1):72-4. doi: 10.1136/jmg.35.1.72. J Med Genet. 1998. PMID: 9475101 Free PMC article.

7

Prospects for gene therapy for cystic fibrosis.

Davies JC, Geddes DM, Alton EW. Davies JC, et al. Mol Med Today. 1998 Jul;4(7):292-9. doi: 10.1016/s1357-4310(98)01265-9. Mol Med Today. 1998. PMID: 9743990 Review.

8

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.

9

Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis: a double-blind placebo-controlled trial.

Alton EW, Stern M, Farley R, Jaffe A, Chadwick SL, Phillips J, Davies J, Smith SN, Browning J, Davies MG, Hodson ME, Durham SR, Li D, Jeffery PK, Scallan M, Balfour R, Eastman SJ, Cheng SH, Smith AE, Meeker D, Geddes DM. Alton EW, et al. Lancet. 1999 Mar 20;353(9157):947-54. doi: 10.1016/s0140-6736(98)06532-5. Lancet. 1999. PMID: 10459902 Clinical Trial.

10

Differential binding of mannose-binding lectin to respiratory pathogens in cystic fibrosis.

Davies J, Neth O, Alton E, Klein N, Turner M. Davies J, et al. Lancet. 2000 May 27;355(9218):1885-6. doi: 10.1016/S0140-6736(00)02297-2. Lancet. 2000. PMID: 10866448

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