More articles from Original Articles: Cystic fibrosis

Cystic fibrosis neutrophils have normal intrinsic reactive oxygen species generation
D. J. McKeon, K. A. Cadwallader, S. Idris, A. S. Cowburn, M. C. Pasteur, H. Barker, C. S. Haworth, D. Bilton, E. R. Chilvers, A. M. Condliffe

European Respiratory Journal Jun 2010, 35 (6) 1264-1272; DOI: 10.1183/09031936.00089709
Absorptive clearance of DTPA as an aerosol-based biomarker in the cystic fibrosis airway
T. E. Corcoran, K. M. Thomas, M. M. Myerburg, A. Muthukrishnan, L. Weber, R. Frizzell, J. M. Pilewski

European Respiratory Journal Apr 2010, 35 (4) 781-786; DOI: 10.1183/09031936.00059009
Long-term effects of a partially supervised conditioning programme in cystic fibrosis
H. Hebestreit, S. Kieser, S. Junge, M. Ballmann, A. Hebestreit, C. Schindler, T. Schenk, H-G. Posselt, S. Kriemler

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Increased augmentation index in patients with cystic fibrosis
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Alveolar macrophages and CC chemokines are increased in children with cystic fibrosis
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Skeletal muscle weakness, exercise tolerance and physical activity in adults with cystic fibrosis
T. Troosters, D. Langer, B. Vrijsen, J. Segers, K. Wouters, W. Janssens, R. Gosselink, M. Decramer, L. Dupont

European Respiratory Journal Jan 2009, 33 (1) 99-106; DOI: 10.1183/09031936.00091607
Pseudomonas aeruginosa transmission is infrequent in New Zealand cystic fibrosis clinics
J. Schmid, L. J. Ling, J. L. S. Leung, N. Zhang, J. Kolbe, A. W. Wesley, G. D. Mills, P. J. Brown, D. T. Jones, R. T. R. Laing, P. K. Pattemore, D. R. Taylor, K. Grimwood

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Pseudomonas aeruginosa, cyanide accumulation and lung function in CF and non-CF bronchiectasis patients
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Bacterial cyanogenesis occurs in the cystic fibrosis lung
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Nonsteroidal anti-inflammatory drugs upregulate function of wild-type and mutant CFTR
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