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                             24 results found
no title author magazine year volume issue page(s) type
1 Adherence to Ivacaftor is suboptimal Abbott, Janice
2015
14 5 p. 547-548
2 p.
article
2 Association of sweat chloride concentration at time of diagnosis and CFTR genotype with mortality and cystic fibrosis phenotype McKone, Edward F.
2015
14 5 p. 580-586
7 p.
article
3 Can biliary endoscopy play a role in liver disease associated to cystic fibrosis? Cantù, P.
2015
14 5 p. E21-E23
nvt p.
article
4 Cystic fibrosis microbiology: Advances in antimicrobial therapy Waters, Valerie
2015
14 5 p. 551-560
10 p.
article
5 Cystic fibrosis-related bone disease in children: Examination of peripheral quantitative computed tomography (pQCT) data Brookes, Denise S.K.
2015
14 5 p. 668-677
10 p.
article
6 Cystic fibrosis transmembrane conductance regulator gene variants are associated with autoimmune pancreatitis and slow response to steroid treatment Chang, Ming-Chu
2015
14 5 p. 661-667
7 p.
article
7 Different approaches to evaluate patient experience and satisfaction in CF centres Steinkamp, Gratiana
2015
14 5 p. E19-E20
nvt p.
article
8 Editorial Board 2015
14 5 p. ii-
1 p.
article
9 Electronic monitoring reveals highly variable adherence patterns in patients prescribed ivacaftor Siracusa, Christopher M.
2015
14 5 p. 621-626
6 p.
article
10 Enhancement of Pulmozyme activity in purulent sputum by combination with poly-aspartic acid or gelsolin Bucki, Robert
2015
14 5 p. 587-593
7 p.
article
11 Identification of outer membrane Porin D as a vitronectin-binding factor in cystic fibrosis clinical isolates of Pseudomonas aeruginosa Paulsson, Magnus
2015
14 5 p. 600-607
8 p.
article
12 Inspiratory muscle strength relative to disease severity in adults with stable cystic fibrosis Dekerlegand, Robert L.
2015
14 5 p. 639-645
7 p.
article
13 Is the home environment an important factor in the occurrence of fungal events in cystic fibrosis? Sapet, A.
2015
14 5 p. E16-E18
nvt p.
article
14 News 2015
14 5 p. 549-550
2 p.
article
15 Persistent Bordetella bronchiseptica infection in a child with cystic fibrosis: Relationship to bacterial phenotype El Khatib, Nevine
2015
14 5 p. E13-E15
nvt p.
article
16 Reduced risk of nontuberculous mycobacteria in cystic fibrosis adults receiving long-term azithromycin Coolen, Nathalie
2015
14 5 p. 594-599
6 p.
article
17 Risk of hemoptysis in cystic fibrosis clinical trials: A retrospective cohort study Thompson, V.
2015
14 5 p. 632-638
7 p.
article
18 Short-term effects of physiotherapy on ventilation inhomogeneity in cystic fibrosis patients with a wide range of lung disease severity Pfleger, A.
2015
14 5 p. 627-631
5 p.
article
19 Should diffuse bronchiectasis still be considered a CFTR-related disorder? Bergougnoux, Anne
2015
14 5 p. 646-653
8 p.
article
20 Strain rate echocardiography uncovers subclinical left ventricular dysfunction in cystic fibrosis Sellers, Zachary M.
2015
14 5 p. 654-660
7 p.
article
21 Targeting ion channels in cystic fibrosis Mall, Marcus A.
2015
14 5 p. 561-570
10 p.
article
22 The hsa-miR-125a/hsa-let-7e/hsa-miR-99b cluster is potentially implicated in Cystic Fibrosis pathogenesis Endale Ahanda, Marie-Laure
2015
14 5 p. 571-579
9 p.
article
23 Tiotropium Respimat® in cystic fibrosis: Phase 3 and Pooled phase 2/3 randomized trials Ratjen, Felix
2015
14 5 p. 608-614
7 p.
article
24 Vaccine coverage in CF children: A French multicenter study Masson, A.
2015
14 5 p. 615-620
6 p.
article
                             24 results found
 
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