421 related articles for article (PubMed ID: 26585432)
1. Changes in airway inflammation during pulmonary exacerbations in patients with cystic fibrosis and primary ciliary dyskinesia.
Ratjen F; Waters V; Klingel M; McDonald N; Dell S; Leahy TR; Yau Y; Grasemann H
Eur Respir J; 2016 Mar; 47(3):829-36. PubMed ID: 26585432
[TBL] [Abstract][Full Text] [Related]
2. Mucus properties in children with primary ciliary dyskinesia: comparison with cystic fibrosis.
Bush A; Payne D; Pike S; Jenkins G; Henke MO; Rubin BK
Chest; 2006 Jan; 129(1):118-23. PubMed ID: 16424421
[TBL] [Abstract][Full Text] [Related]
3. Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study.
Maglione M; Montella S; Mollica C; Carnovale V; Iacotucci P; De Gregorio F; Tosco A; Cervasio M; Raia V; Santamaria F
Ital J Pediatr; 2017 Apr; 43(1):34. PubMed ID: 28403885
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Bacterial infections in patients with primary ciliary dyskinesia: Comparison with cystic fibrosis.
Wijers CD; Chmiel JF; Gaston BM
Chron Respir Dis; 2017 Nov; 14(4):392-406. PubMed ID: 29081265
[TBL] [Abstract][Full Text] [Related]
6. Recovery of baseline lung function after pulmonary exacerbation in children with primary ciliary dyskinesia.
Sunther M; Bush A; Hogg C; McCann L; Carr SB
Pediatr Pulmonol; 2016 Dec; 51(12):1362-1366. PubMed ID: 27273679
[TBL] [Abstract][Full Text] [Related]
7. Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations.
Zemanick ET; Harris JK; Wagner BD; Robertson CE; Sagel SD; Stevens MJ; Accurso FJ; Laguna TA
PLoS One; 2013; 8(4):e62917. PubMed ID: 23646159
[TBL] [Abstract][Full Text] [Related]
8. Digitoxin for Airway Inflammation in Cystic Fibrosis: Preliminary Assessment of Safety, Pharmacokinetics, and Dose Finding.
Zeitlin PL; Diener-West M; Callahan KA; Lee S; Talbot CC; Pollard B; Boyle MP; Lechtzin N
Ann Am Thorac Soc; 2017 Feb; 14(2):220-229. PubMed ID: 28006108
[TBL] [Abstract][Full Text] [Related]
9. Fitness and lung function in children with primary ciliary dyskinesia and cystic fibrosis.
Ring AM; Buchvald FF; Holgersen MG; Green K; Nielsen KG
Respir Med; 2018 Jun; 139():79-85. PubMed ID: 29858006
[TBL] [Abstract][Full Text] [Related]
10. Sputum club cell protein concentration is associated with pulmonary exacerbation in cystic fibrosis.
Laguna TA; Williams CB; Brandy KR; Welchlin-Bradford C; Moen CE; Reilly CS; Wendt CH
J Cyst Fibros; 2015 May; 14(3):334-40. PubMed ID: 25456770
[TBL] [Abstract][Full Text] [Related]
11. Do pulmonary and extrapulmonary features differ among cystic fibrosis, primary ciliary dyskinesia, and healthy children?
Denizoglu Kulli H; Gurses HN; Zeren M; Ucgun H; Cakir E
Pediatr Pulmonol; 2020 Nov; 55(11):3067-3073. PubMed ID: 32877003
[TBL] [Abstract][Full Text] [Related]
12. Gas exchanges in children with cystic fibrosis or primary ciliary dyskinesia: A retrospective study.
Fuger M; Aupiais C; Thouvenin G; Taytard J; Tamalet A; Escudier E; Boizeau P; Corvol H; Beydon N
Respir Physiol Neurobiol; 2018 May; 251():1-7. PubMed ID: 29366817
[TBL] [Abstract][Full Text] [Related]
13. Bacteriology and treatment of infections in the upper and lower airways in patients with primary ciliary dyskinesia: adressing the paranasal sinuses.
Alanin MC
Dan Med J; 2017 May; 64(5):. PubMed ID: 28552099
[TBL] [Abstract][Full Text] [Related]
14. Induced sputum matrix metalloproteinase-9 correlates with lung function and airway inflammation in children with cystic fibrosis.
Sagel SD; Kapsner RK; Osberg I
Pediatr Pulmonol; 2005 Mar; 39(3):224-32. PubMed ID: 15635615
[TBL] [Abstract][Full Text] [Related]
15. Molecular analysis of changes in Pseudomonas aeruginosa load during treatment of a pulmonary exacerbation in cystic fibrosis.
Reid DW; Latham R; Lamont IL; Camara M; Roddam LF
J Cyst Fibros; 2013 Dec; 12(6):688-99. PubMed ID: 23706827
[TBL] [Abstract][Full Text] [Related]
16. Structural and functional lung disease in primary ciliary dyskinesia.
Santamaria F; Montella S; Tiddens HAWM; Guidi G; Casotti V; Maglione M; de Jong PA
Chest; 2008 Aug; 134(2):351-357. PubMed ID: 18403663
[TBL] [Abstract][Full Text] [Related]
17. Differences in disease expression between primary ciliary dyskinesia and cystic fibrosis with and without pancreatic insufficiency.
Cohen-Cymberknoh M; Simanovsky N; Hiller N; Hillel AG; Shoseyov D; Kerem E
Chest; 2014 Apr; 145(4):738-744. PubMed ID: 24091606
[TBL] [Abstract][Full Text] [Related]
18. Factors associated with response to treatment of pulmonary exacerbations in cystic fibrosis patients.
Waters VJ; Stanojevic S; Sonneveld N; Klingel M; Grasemann H; Yau YC; Tullis E; Wilcox P; Freitag A; Chilvers M; Ratjen FA
J Cyst Fibros; 2015 Nov; 14(6):755-62. PubMed ID: 25690407
[TBL] [Abstract][Full Text] [Related]
19. Matrix metalloproteinases and airway remodeling and function in primary ciliary dyskinesia.
Pifferi M; Bush A; Caramella D; Metelli MR; Di Cicco M; Piras M; Gherarducci G; Capristo C; Maggi F; Peroni D; Boner AL
Respir Med; 2017 Mar; 124():49-56. PubMed ID: 28284321
[TBL] [Abstract][Full Text] [Related]
20. Bacterial evolution in PCD and CF patients follows the same mutational steps.
Sommer LM; Alanin MC; Marvig RL; Nielsen KG; Høiby N; von Buchwald C; Molin S; Johansen HK
Sci Rep; 2016 Jun; 6():28732. PubMed ID: 27349973
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
