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Comment
. 2013 Oct;144(4):1418.
doi: 10.1378/chest.13-1320.

Understanding the relationship between sweat chloride and lung function in cystic fibrosis

Sonya L Heltshe  1 , Nicole Mayer-Hamblett  2 , Steven M Rowe  3
Affiliations
Comment

Understanding the relationship between sweat chloride and lung function in cystic fibrosis

Sonya L Heltshe et al. Chest. 2013 Oct.
No abstract available

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Comment in

  • Response.
    Durmowicz AG, Witzmann KA, Rosebraugh CJ, Chowdhury BA. Durmowicz AG, et al. Chest. 2013 Oct;144(4):1418-1419. doi: 10.1378/chest.13-1517. Chest. 2013. PMID: 24081359 No abstract available.

Comment on

References

    1. Durmowicz AG, Witzmann KA, Rosebraugh CJ, Chowdhury BA. Change in sweat chloride as a clinical end point in cystic fibrosis clinical trials: the ivacaftor experience. Chest. 2013;143(1):14–18. - PubMed
    1. Farrell PM, Rosenstein BJ, White TB, et al. Cystic Fibrosis Foundation Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. J Pediatr. 2008;153(2):S4–S14. - PMC - PubMed
    1. Seliger VI, Rodman D, Van Goor F, Schmelz A, Mueller P. The predictive potential of the sweat chloride test in cystic fibrosis patients with the G551D mutation [published online ahead of print April 26, 2013]. J Cyst Fibros. . - DOI - PubMed

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