These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. Colonization of CF patients' upper airways with S. aureus contributes more decisively to upper airway inflammation than P. aeruginosa. Janhsen WK; Arnold C; Hentschel J; Lehmann T; Pfister W; Baier M; Böer K; Hünniger K; Kurzai O; Hipler UC; Mainz JG Med Microbiol Immunol; 2016 Oct; 205(5):485-500. PubMed ID: 27377929 [TBL] [Abstract][Full Text] [Related]
9. Sinus bacteriology in patients with cystic fibrosis or primary ciliary dyskinesia: A systematic review. Møller ME; Alanin MC; Grønhøj C; Aanæs K; Høiby N; von Buchwald C Am J Rhinol Allergy; 2017 Sep; 31(5):293-298. PubMed ID: 28859703 [TBL] [Abstract][Full Text] [Related]
10. [Chinese experts consensus statement: diagnosis and treatment of cystic fibrosis (2023)]. ; ; Zhonghua Jie He He Hu Xi Za Zhi; 2023 Apr; 46(4):352-372. PubMed ID: 36990700 [TBL] [Abstract][Full Text] [Related]
11. Bacterial sinusitis can be a focus for initial lung colonisation and chronic lung infection in patients with cystic fibrosis. Aanæs K J Cyst Fibros; 2013 Sep; 12 Suppl 2():S1-20. PubMed ID: 24064077 [TBL] [Abstract][Full Text] [Related]
12. Ivacaftor Reduces Inflammatory Mediators in Upper Airway Lining Fluid From Cystic Fibrosis Patients With a G551D Mutation: Serial Non-Invasive Home-Based Collection of Upper Airway Lining Fluid. Mainz JG; Arnold C; Wittstock K; Hipler UC; Lehmann T; Zagoya C; Duckstein F; Ellemunter H; Hentschel J Front Immunol; 2021; 12():642180. PubMed ID: 34025651 [TBL] [Abstract][Full Text] [Related]
13. The burden of sinus disease in cystic fibrosis lung transplant recipients. Morlacchi LC; Greer M; Tudorache I; Blasi F; Welte T; Haverich A; Mainz JG; Gottlieb J Transpl Infect Dis; 2018 Oct; 20(5):e12924. PubMed ID: 29797646 [TBL] [Abstract][Full Text] [Related]
14. Upper and lower airway cultures in children with cystic fibrosis: do not neglect the upper airways. Bonestroo HJ; de Winter-de Groot KM; van der Ent CK; Arets HG J Cyst Fibros; 2010 Mar; 9(2):130-4. PubMed ID: 20110197 [TBL] [Abstract][Full Text] [Related]
15. The CF-Sputum Induction Trial (CF-SpIT) to assess lower airway bacterial sampling in young children with cystic fibrosis: a prospective internally controlled interventional trial. Ronchetti K; Tame JD; Paisey C; Thia LP; Doull I; Howe R; Mahenthiralingam E; Forton JT Lancet Respir Med; 2018 Jun; 6(6):461-471. PubMed ID: 29778403 [TBL] [Abstract][Full Text] [Related]
16. Non-invasive assessment of upper and lower airway infection and inflammation in CF patients. Fischer N; Hentschel J; Markert UR; Keller PM; Pletz MW; Mainz JG Pediatr Pulmonol; 2014 Nov; 49(11):1065-75. PubMed ID: 24464968 [TBL] [Abstract][Full Text] [Related]
17. Increased cytokines in cystic fibrosis patients' upper airways during a new P. aeruginosa colonization. Jaudszus A; Arnold C; Hentschel J; Hünniger K; Baier M; Mainz JG Pediatr Pulmonol; 2018 Jul; 53(7):881-887. PubMed ID: 29624919 [TBL] [Abstract][Full Text] [Related]
18. The microbial community of the cystic fibrosis airway is disrupted in early life. Renwick J; McNally P; John B; DeSantis T; Linnane B; Murphy P; PLoS One; 2014; 9(12):e109798. PubMed ID: 25526264 [TBL] [Abstract][Full Text] [Related]
19. Directly sampling the lung of a young child with cystic fibrosis reveals diverse microbiota. Brown PS; Pope CE; Marsh RL; Qin X; McNamara S; Gibson R; Burns JL; Deutsch G; Hoffman LR Ann Am Thorac Soc; 2014 Sep; 11(7):1049-55. PubMed ID: 25072206 [TBL] [Abstract][Full Text] [Related]
20. Sequential genotyping of Pseudomonas aeruginosa from upper and lower airways of cystic fibrosis patients. Jung A; Kleinau I; Schönian G; Bauernfeind A; Chen C; Griese M; Döring G; Göbel U; Wahn U; Paul K Eur Respir J; 2002 Dec; 20(6):1457-63. PubMed ID: 12503704 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]