Decreased mucosal oxygen tension in the maxillary sinuses in patients with cystic fibrosis
Research output: Contribution to journal › Journal article › Research › peer-review
Pseudomonas aeruginosa in the sinuses plays a role in the lungs in cystic fibrosis (CF) patients, but little is known about the sinus environment where the bacteria adapt. Anoxic areas are found in the lower respiratory airways but it is unknown if the same conditions exist in the sinuses.
|Journal||Journal of Cystic Fibrosis|
|Number of pages||7|
|Publication status||Published - 2011|