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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 31, 2015
Altered intestinal bile salt biotransformation in a cystic fibrosis (Cftr-/-) mouse model with hepato-biliary pathologyFrank A J A Bodewes, Mariëtte Y M van der Wulp, Satti Beharry, et al.Bone|October 9, 2007
Shwachman-Diamond syndrome is associated with low-turnover osteoporosisSanna Toiviainen-Salo, Mervi K Mäyränpää, Peter R Durie, et al.Chest|March 17, 2012
Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary diseaseTanja Gonska, Perry Choi, Anne Stephenson, et al.American Journal of Respiratory and Critical Care Medicine|November 16, 2002
Nontuberculous mycobacteria. II: nested-cohort study of impact on cystic fibrosis lung diseaseKenneth N Olivier, David J Weber, Ji-Hyun Lee, et al.Nucleic Acids Research|November 22, 2014
Ets homologous factor regulates pathways controlling response to injury in airway epithelial cellsSara L Fossum, Michael J Mutolo, Rui Yang, et al.Journal of Medical Case Reports|April 28, 2010
Lack of correlation between pulmonary disease and cystic fibrosis transmembrane conductance regulator dysfunction in cystic fibrosis: a case reportHara Levy, Carolynn L Cannon, Daniel Asher, et al.Gastroenterology|October 7, 2010
Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosisChee Y Ooi, Ruslan Dorfman, Marco Cipolli, et al.American Journal of Physiology. Gastrointestinal and Liver Physiology|November 11, 2006
Long-term docosahexaenoic acid therapy in a congenic murine model of cystic fibrosisSatti Beharry, Cameron Ackerley, Mary Corey, et al.AJR. American Journal of Roentgenology|April 24, 2007
High-resolution CT of patients with primary ciliary dyskinesiaMarcus P Kennedy, Peadar G Noone, Margaret W Leigh, et al.Annals of the American Thoracic Society|February 7, 2014
The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesiaRaymond H Kim, David A Hall, Ernest Cutz, et al.Pageof 23