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Pediatric Pulmonology|October 16, 2009
Transforming growth factor-beta(1) in bronchoalveolar lavage fluid from children with cystic fibrosisWilliam T Harris, Marianne S Muhlebach, Robert A Oster, et al.
American Journal of Respiratory and Critical Care Medicine|June 26, 2013
Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical diseaseMichael R Knowles, Leigh Anne Daniels, Stephanie D Davis, et al.
The Journal of Pediatrics|August 17, 2002
Serum pancreatic enzymes define the pancreatic phenotype in patients with Shwachman-Diamond syndromeWan F Ip, Annie Dupuis, Lynda Ellis, et al.
American Journal of Respiratory and Critical Care Medicine|August 31, 2017
Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease SeverityDeepika Polineni, Hong Dang, Paul J Gallins, et al.
Thorax|April 17, 2012
Comparing the American and European diagnostic guidelines for cystic fibrosis: same disease, different language?Chee Y Ooi, Annie Dupuis, Lynda Ellis, et al.
Proteomics|December 13, 2005
Detection of gender differences in rat lens proteins using 2-D-DIGEPaul C Guest, Heather A Skynner, Kamran Salim, et al.
American Journal of Respiratory and Critical Care Medicine|November 2, 2002
Increasing concentration of inhaled saline with or without amiloride: effect on mucociliary clearance in normal subjectsNamita Sood, William D Bennett, Kirby Zeman, et al.
The New England Journal of Medicine|January 20, 2006
Mucus clearance and lung function in cystic fibrosis with hypertonic salineScott H Donaldson, William D Bennett, Kirby L Zeman, et al.
American Journal of Respiratory Cell and Molecular Biology|November 25, 2003
Investigation of the possible role of a novel gene, DPCD, in primary ciliary dyskinesiaMaimoona Zariwala, Wanda K O'Neal, Peadar G Noone, et al.
The Journal of General Physiology|January 5, 2002
In vivo airway surface liquid Cl- analysis with solid-state electrodesRay A Caldwell, Barbara R Grubb, Robert Tarran, et al.
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