| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A bioassay using intestinal organoids to measure CFTR modulators in human plasma
|
Dekkers, R.
|
|
2015
|
14 |
2 |
p. 178-181
4 p.
|
artikel
|
| 2 |
Acknowledgement to Reviewers 2014
|
|
|
2015
|
14 |
2 |
p. 161-163
3 p.
|
artikel
|
| 3 |
Aggregates of mutant CFTR fragments in airway epithelial cells of CF lungs: New pathologic observations
|
Du, Kai
|
|
2015
|
14 |
2 |
p. 182-193
12 p.
|
artikel
|
| 4 |
Authors' response
|
Welsh, Liam
|
|
2015
|
14 |
2 |
p. 287-
1 p.
|
artikel
|
| 5 |
Cost-effectiveness of newborn screening for cystic fibrosis determined with real-life data
|
van der Ploeg, C.P.B.
|
|
2015
|
14 |
2 |
p. 194-202
9 p.
|
artikel
|
| 6 |
Cystic fibrosis and the role of gastrointestinal outcome measures in the new era of therapeutic CFTR modulation
|
Bodewes, Frank A.J.A.
|
|
2015
|
14 |
2 |
p. 169-177
9 p.
|
artikel
|
| 7 |
Cystic fibrosis mortality trend in Italy from 1970 to 2011
|
Alicandro, Gianfranco
|
|
2015
|
14 |
2 |
p. 267-274
8 p.
|
artikel
|
| 8 |
Editorial Board
|
|
|
2015
|
14 |
2 |
p. ii-
1 p.
|
artikel
|
| 9 |
Evaluation of mold exposure in cystic fibrosis patients' dwellings and allergic bronchopulmonary risk
|
Rocchi, Steffi
|
|
2015
|
14 |
2 |
p. 242-247
6 p.
|
artikel
|
| 10 |
High-frequency audiometry reveals high prevalence of aminoglycoside ototoxicity in children with cystic fibrosis
|
Al-Malky, Ghada
|
|
2015
|
14 |
2 |
p. 248-254
7 p.
|
artikel
|
| 11 |
Long-term treatment with oral N-acetylcysteine: Affects lung function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trial
|
Conrad, C.
|
|
2015
|
14 |
2 |
p. 219-227
9 p.
|
artikel
|
| 12 |
Managing central venous obstruction in cystic fibrosis recipients—lung transplant considerations
|
Otani, Shinji
|
|
2015
|
14 |
2 |
p. 255-261
7 p.
|
artikel
|
| 13 |
News
|
|
|
2015
|
14 |
2 |
p. 167-168
2 p.
|
artikel
|
| 14 |
Pharmacokinetics and tolerability of oral sildenafil in adults with cystic fibrosis lung disease
|
Taylor-Cousar, J.L.
|
|
2015
|
14 |
2 |
p. 228-236
9 p.
|
artikel
|
| 15 |
Prevalence of Scedosporium species and Lomentospora prolificans in patients with cystic fibrosis in a multicenter trial by use of a selective medium
|
Sedlacek, L.
|
|
2015
|
14 |
2 |
p. 237-241
5 p.
|
artikel
|
| 16 |
Randomized controlled trial of biofilm antimicrobial susceptibility testing in cystic fibrosis patients
|
Yau, Yvonne C.W.
|
|
2015
|
14 |
2 |
p. 262-266
5 p.
|
artikel
|
| 17 |
Randomized, single blind, controlled trial of inhaled glutathione vs placebo in patients with cystic fibrosis
|
Calabrese, C.
|
|
2015
|
14 |
2 |
p. 203-210
8 p.
|
artikel
|
| 18 |
Retinal screening of patients with cystic fibrosis-related diabetes in Wales — A real eye opener
|
Roberts, R.
|
|
2015
|
14 |
2 |
p. 282-284
3 p.
|
artikel
|
| 19 |
Safety and efficacy of Creon® Micro in children with exocrine pancreatic insufficiency due to cystic fibrosis
|
Kashirskaya, Nataliya Y.
|
|
2015
|
14 |
2 |
p. 275-281
7 p.
|
artikel
|
| 20 |
The challenges of developing effective anti-inflammatory agents in cystic fibrosis
|
Sagel, Scott D.
|
|
2015
|
14 |
2 |
p. 164-166
3 p.
|
artikel
|
| 21 |
The effect of short-term, high-dose oral N-acetylcysteine treatment on oxidative stress markers in cystic fibrosis patients with chronic P. aeruginosa infection — A pilot study
|
Skov, Marianne
|
|
2015
|
14 |
2 |
p. 211-218
8 p.
|
artikel
|
| 22 |
The Lung Clearance Index as a probe for the effectiveness of short-term therapies in cystic fibrosis lung disease
|
Vanderhelst, Eef
|
|
2015
|
14 |
2 |
p. 285-286
2 p.
|
artikel
|
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