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Journal Abstract Search

176 related items for PubMed ID: 16185859

  • 1. Exploring the mechanisms of macrolides in cystic fibrosis.
    Equi AC, Davies JC, Painter H, Hyde S, Bush A, Geddes DM, Alton EW.
    Respir Med; 2006 Apr; 100(4):687-97. PubMed ID: 16185859
    [Abstract] [Full Text] [Related]

  • 2. Azithromycin increases chloride efflux from cystic fibrosis airway epithelial cells.
    Oliynyk I, Varelogianni G, Schalling M, Asplund MS, Roomans GM, Johannesson M.
    Exp Lung Res; 2009 Apr; 35(3):210-21. PubMed ID: 19337904
    [Abstract] [Full Text] [Related]

  • 3. Effect of macrolides on in vivo ion transport across cystic fibrosis nasal epithelium.
    Barker PM, Gillie DJ, Schechter MS, Rubin BK.
    Am J Respir Crit Care Med; 2005 Apr 15; 171(8):868-71. PubMed ID: 15657462
    [Abstract] [Full Text] [Related]

  • 4. Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations.
    Wilschanski M, Yahav Y, Yaacov Y, Blau H, Bentur L, Rivlin J, Aviram M, Bdolah-Abram T, Bebok Z, Shushi L, Kerem B, Kerem E.
    N Engl J Med; 2003 Oct 09; 349(15):1433-41. PubMed ID: 14534336
    [Abstract] [Full Text] [Related]

  • 5. Clinical response to azithromycin in cystic fibrosis correlates with in vitro effects on Pseudomonas aeruginosa phenotypes.
    Nguyen D, Emond MJ, Mayer-Hamblett N, Saiman L, Marshall BC, Burns JL.
    Pediatr Pulmonol; 2007 Jun 09; 42(6):533-41. PubMed ID: 17469154
    [Abstract] [Full Text] [Related]

  • 6. Maintenance azithromycin treatment in pediatric patients with cystic fibrosis: long-term outcomes related to macrolide resistance and pulmonary function.
    Tramper-Stranders GA, Wolfs TF, Fleer A, Kimpen JL, van der Ent CK.
    Pediatr Infect Dis J; 2007 Jan 09; 26(1):8-12. PubMed ID: 17195698
    [Abstract] [Full Text] [Related]

  • 7. The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.
    Sermet-Gaudelus I, Roussel D, Bui S, Deneuville E, Huet F, Reix P, Bellon G, Lenoir G, Edelman A.
    BMC Pediatr; 2006 Oct 03; 6():25. PubMed ID: 17018149
    [Abstract] [Full Text] [Related]

  • 8. Improved lung function and body mass index associated with long-term use of Macrolide antibiotics.
    Pirzada OM, McGaw J, Taylor CJ, Everard ML.
    J Cyst Fibros; 2003 Jun 03; 2(2):69-71. PubMed ID: 15463852
    [Abstract] [Full Text] [Related]

  • 9. Repeat administration of DNA/liposomes to the nasal epithelium of patients with cystic fibrosis.
    Hyde SC, Southern KW, Gileadi U, Fitzjohn EM, Mofford KA, Waddell BE, Gooi HC, Goddard CA, Hannavy K, Smyth SE, Egan JJ, Sorgi FL, Huang L, Cuthbert AW, Evans MJ, Colledge WH, Higgins CF, Webb AK, Gill DR.
    Gene Ther; 2000 Jul 03; 7(13):1156-65. PubMed ID: 10918483
    [Abstract] [Full Text] [Related]

  • 10. Long-term azitromycin treatment of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection; an observational cohort study.
    Hansen CR, Pressler T, Koch C, Høiby N.
    J Cyst Fibros; 2005 Mar 03; 4(1):35-40. PubMed ID: 15752679
    [Abstract] [Full Text] [Related]

  • 11. Nasal airway ion transport is linked to the cystic fibrosis phenotype in adult patients.
    Fajac I, Hubert D, Guillemot D, Honoré I, Bienvenu T, Volter F, Dall'Ava-Santucci J, Dusser DJ.
    Thorax; 2004 Nov 03; 59(11):971-6. PubMed ID: 15516474
    [Abstract] [Full Text] [Related]

  • 12. Long-term azithromycin in cystic fibrosis: another possible mechanism of action?
    Pradal U, Delmarco A, Morganti M, Cipolli M, Mini E, Cazzola G.
    J Chemother; 2005 Aug 03; 17(4):393-400. PubMed ID: 16167518
    [Abstract] [Full Text] [Related]

  • 13. The effect of varying tonicity on nasal epithelial ion transport in cystic fibrosis.
    Davies MG, Geddes DM, Alton EW.
    Am J Respir Crit Care Med; 2005 Apr 01; 171(7):760-3. PubMed ID: 15618459
    [Abstract] [Full Text] [Related]

  • 14. Basic protocol for transepithelial nasal potential difference measurements.
    Schüler D, Sermet-Gaudelus I, Wilschanski M, Ballmann M, Dechaux M, Edelman A, Hug M, Leal T, Lebacq J, Lebecque P, Lenoir G, Stanke F, Wallemacq P, Tümmler B, Knowles MR.
    J Cyst Fibros; 2004 Aug 01; 3 Suppl 2():151-5. PubMed ID: 15463949
    [Abstract] [Full Text] [Related]

  • 15. Azithromycin for improving pulmonary function in cystic fibrosis.
    Carr RR, Nahata MC.
    Ann Pharmacother; 2004 Sep 01; 38(9):1520-4. PubMed ID: 15213312
    [Abstract] [Full Text] [Related]

  • 16. ENaCbeta and gamma genes as modifier genes in cystic fibrosis.
    Viel M, Leroy C, Hubert D, Fajac I, Bienvenu T.
    J Cyst Fibros; 2008 Jan 01; 7(1):23-9. PubMed ID: 17560176
    [Abstract] [Full Text] [Related]

  • 17. Role of the cystic fibrosis transmembrane conductance regulator in internalization of Pseudomonas aeruginosa by polarized respiratory epithelial cells.
    Darling KE, Dewar A, Evans TJ.
    Cell Microbiol; 2004 Jun 01; 6(6):521-33. PubMed ID: 15104594
    [Abstract] [Full Text] [Related]

  • 18. Long-term daily high and low doses of azithromycin in children with cystic fibrosis: a randomized controlled trial.
    Kabra SK, Pawaiya R, Lodha R, Kapil A, Kabra M, Vani AS, Agarwal G, Shastri SS.
    J Cyst Fibros; 2010 Jan 01; 9(1):17-23. PubMed ID: 19818694
    [Abstract] [Full Text] [Related]

  • 19. Macrolide resistance of Staphylococcus aureus and Haemophilus species associated with long-term azithromycin use in cystic fibrosis.
    Phaff SJ, Tiddens HA, Verbrugh HA, Ott A.
    J Antimicrob Chemother; 2006 Apr 01; 57(4):741-6. PubMed ID: 16469851
    [Abstract] [Full Text] [Related]

  • 20. Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF mice.
    Ostrowski LE, Yin W, Diggs PS, Rogers TD, O'Neal WK, Grubb BR.
    Gene Ther; 2007 Oct 01; 14(20):1492-501. PubMed ID: 17637798
    [Abstract] [Full Text] [Related]

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