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Journal Abstract Search

630 related items for PubMed ID: 24726420

  • 1. Bronchiectases at early chest computed tomography in children with cystic fibrosis are associated with increased risk of subsequent pulmonary exacerbations and chronic pseudomonas infection.
    Bortoluzzi CF, Volpi S, D'Orazio C, Tiddens HA, Loeve M, Tridello G, Assael BM.
    J Cyst Fibros; 2014 Sep; 13(5):564-71. PubMed ID: 24726420
    [Abstract] [Full Text] [Related]

  • 2. Chest computed tomography predicts the frequency of pulmonary exacerbations in children with cystic fibrosis.
    Sanders DB, Li Z, Brody AS.
    Ann Am Thorac Soc; 2015 Jan; 12(1):64-9. PubMed ID: 25474182
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  • 3. Validating chest MRI to detect and monitor cystic fibrosis lung disease in a pediatric cohort.
    Tepper LA, Ciet P, Caudri D, Quittner AL, Utens EM, Tiddens HA.
    Pediatr Pulmonol; 2016 Jan; 51(1):34-41. PubMed ID: 26436668
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  • 4. Bronchiectasis and pulmonary exacerbations in children and young adults with cystic fibrosis.
    Loeve M, Gerbrands K, Hop WC, Rosenfeld M, Hartmann IC, Tiddens HA.
    Chest; 2011 Jul; 140(1):178-185. PubMed ID: 21148242
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  • 5. Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: a randomized trial.
    Wainwright CE, Vidmar S, Armstrong DS, Byrnes CA, Carlin JB, Cheney J, Cooper PJ, Grimwood K, Moodie M, Robertson CF, Tiddens HA, ACFBAL Study Investigators.
    JAMA; 2011 Jul 13; 306(2):163-71. PubMed ID: 21750293
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  • 6. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis.
    Gustafsson PM, De Jong PA, Tiddens HA, Lindblad A.
    Thorax; 2008 Feb 13; 63(2):129-34. PubMed ID: 17675316
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  • 7. Pulmonary abnormalities on high-resolution CT demonstrate more rapid decline than FEV1 in adults with cystic fibrosis.
    Judge EP, Dodd JD, Masterson JB, Gallagher CG.
    Chest; 2006 Nov 13; 130(5):1424-32. PubMed ID: 17099020
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  • 11. Comparison of radiographic and clinical characteristics of low-risk and high-risk cystic fibrosis genotypes.
    Ferril GR, Nick JA, Getz AE, Barham HP, Saavedra MT, Taylor-Cousar JL, Nichols DP, Curran-Everett D, Kingdom TT, Ramakrishnan VR.
    Int Forum Allergy Rhinol; 2014 Nov 13; 4(11):915-20. PubMed ID: 25224556
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  • 12. Chronic Pseudomonas aeruginosa infection and respiratory muscle impairment in cystic fibrosis.
    Dassios TG, Katelari A, Doudounakis S, Dimitriou G.
    Respir Care; 2014 Mar 13; 59(3):363-70. PubMed ID: 23983273
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  • 13. Improved air trapping evaluation in chest computed tomography in children with cystic fibrosis using real-time spirometric monitoring and biofeedback.
    Kongstad T, Buchvald FF, Green K, Lindblad A, Robinson TE, Nielsen KG.
    J Cyst Fibros; 2013 Dec 13; 12(6):559-66. PubMed ID: 23810566
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  • 14. [New method of scoring lung changes using computed tomography in patients with cystic fibrosis].
    Iwanowska B.
    Med Wieku Rozwoj; 2012 Dec 13; 16(4):290-302. PubMed ID: 23378408
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  • 15. Early cystic fibrosis lung disease detected by bronchoalveolar lavage and lung clearance index.
    Belessis Y, Dixon B, Hawkins G, Pereira J, Peat J, MacDonald R, Field P, Numa A, Morton J, Lui K, Jaffe A.
    Am J Respir Crit Care Med; 2012 Apr 15; 185(8):862-73. PubMed ID: 22323305
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  • 17. Cystic fibrosis HRCT scores correlate strongly with Pseudomonas infection.
    Robinson TE, Leung AN, Chen X, Moss RB, Emond MJ.
    Pediatr Pulmonol; 2009 Nov 15; 44(11):1107-17. PubMed ID: 19824046
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