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Journal Abstract Search


247 related items for PubMed ID: 15213312

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

  • 2. 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; 26(1):8-12. PubMed ID: 17195698
    [Abstract] [Full Text] [Related]

  • 3. 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; 2(2):69-71. PubMed ID: 15463852
    [Abstract] [Full Text] [Related]

  • 4. Once-weekly azithromycin in cystic fibrosis with chronic Pseudomonas aeruginosa infection.
    Steinkamp G, Schmitt-Grohe S, Döring G, Staab D, Pfründer D, Beck G, Schubert R, Zielen S.
    Respir Med; 2008 Nov; 102(11):1643-53. PubMed ID: 18701270
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  • 5. Pharmacokinetics of azithromycin in plasma, blood, polymorphonuclear neutrophils and sputum during long-term therapy in patients with cystic fibrosis.
    Wilms EB, Touw DJ, Heijerman HG.
    Ther Drug Monit; 2006 Apr; 28(2):219-25. PubMed ID: 16628134
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  • 8. 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; 4(1):35-40. PubMed ID: 15752679
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  • 10. 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; 42(6):533-41. PubMed ID: 17469154
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  • 12. 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
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  • 13. [Macrolides, Pseudomonas aeruginosa and cystic fibrosis].
    Guillot M, Amiour M, El Hachem C, Harchaoui S, Ribault V, Paris C.
    Arch Pediatr; 2006 Oct; 13 Suppl 1():S48-50. PubMed ID: 17370396
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  • 14. Long-term, low-dose azithromycin treatment reduces the incidence but increases macrolide resistance in Staphylococcus aureus in Danish CF patients.
    Hansen CR, Pressler T, Hoiby N, Johansen HK.
    J Cyst Fibros; 2009 Jan; 8(1):58-62. PubMed ID: 18849202
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  • 16. Open-label, follow-on study of azithromycin in pediatric patients with CF uninfected with Pseudomonas aeruginosa.
    Saiman L, Mayer-Hamblett N, Anstead M, Lands LC, Kloster M, Goss CH, Rose LM, Burns JL, Marshall BC, Ratjen F, AZ0004 Macrolide Study Team.
    Pediatr Pulmonol; 2012 Jul; 47(7):641-8. PubMed ID: 22684984
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  • 17. [Effects of azithromycin on the virulence of Pseudomonas aeruginosa].
    Reinert P.
    Pathol Biol (Paris); 1995 Jun; 43(6):551-3. PubMed ID: 8539081
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  • 18. Aztreonam inhalation solution for suppressive treatment of chronic Pseudomonas aeruginosa lung infection in cystic fibrosis.
    Assael BM.
    Expert Rev Anti Infect Ther; 2011 Nov; 9(11):967-73. PubMed ID: 22029514
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  • 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; 57(4):741-6. PubMed ID: 16469851
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  • 20. The use of macrolide antibiotics in patients with cystic fibrosis.
    Saiman L.
    Curr Opin Pulm Med; 2004 Nov; 10(6):515-23. PubMed ID: 15510060
    [Abstract] [Full Text] [Related]


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