nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Adherence to Ivacaftor is suboptimal
|
Abbott, Janice |
|
2015 |
14 |
5 |
p. 547-548 2 p. |
artikel |
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. |
artikel |
3 |
Can biliary endoscopy play a role in liver disease associated to cystic fibrosis?
|
Cantù, P. |
|
2015 |
14 |
5 |
p. E21-E23 nvt p. |
artikel |
4 |
Cystic fibrosis microbiology: Advances in antimicrobial therapy
|
Waters, Valerie |
|
2015 |
14 |
5 |
p. 551-560 10 p. |
artikel |
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. |
artikel |
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. |
artikel |
7 |
Different approaches to evaluate patient experience and satisfaction in CF centres
|
Steinkamp, Gratiana |
|
2015 |
14 |
5 |
p. E19-E20 nvt p. |
artikel |
8 |
Editorial Board
|
|
|
2015 |
14 |
5 |
p. ii- 1 p. |
artikel |
9 |
Electronic monitoring reveals highly variable adherence patterns in patients prescribed ivacaftor
|
Siracusa, Christopher M. |
|
2015 |
14 |
5 |
p. 621-626 6 p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
14 |
News
|
|
|
2015 |
14 |
5 |
p. 549-550 2 p. |
artikel |
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. |
artikel |
16 |
Reduced risk of nontuberculous mycobacteria in cystic fibrosis adults receiving long-term azithromycin
|
Coolen, Nathalie |
|
2015 |
14 |
5 |
p. 594-599 6 p. |
artikel |
17 |
Risk of hemoptysis in cystic fibrosis clinical trials: A retrospective cohort study
|
Thompson, V. |
|
2015 |
14 |
5 |
p. 632-638 7 p. |
artikel |
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. |
artikel |
19 |
Should diffuse bronchiectasis still be considered a CFTR-related disorder?
|
Bergougnoux, Anne |
|
2015 |
14 |
5 |
p. 646-653 8 p. |
artikel |
20 |
Strain rate echocardiography uncovers subclinical left ventricular dysfunction in cystic fibrosis
|
Sellers, Zachary M. |
|
2015 |
14 |
5 |
p. 654-660 7 p. |
artikel |
21 |
Targeting ion channels in cystic fibrosis
|
Mall, Marcus A. |
|
2015 |
14 |
5 |
p. 561-570 10 p. |
artikel |
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. |
artikel |
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. |
artikel |
24 |
Vaccine coverage in CF children: A French multicenter study
|
Masson, A. |
|
2015 |
14 |
5 |
p. 615-620 6 p. |
artikel |