nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A cocktail drug therapy for patients with cystic fibrosis?
|
Chen, Jeng-Haur |
|
2014 |
13 |
5 |
p. 489-490 2 p. |
artikel |
2 |
Agreement of bioelectric impedance analysis and dual-energy X-ray absorptiometry for body composition evaluation in adults with cystic fibrosis
|
Ziai, S. |
|
2014 |
13 |
5 |
p. 585-588 4 p. |
artikel |
3 |
A new method of sweat testing: the CF Quantum®sweat test
|
Rock, Michael J. |
|
2014 |
13 |
5 |
p. 520-527 8 p. |
artikel |
4 |
An observational study of matrix metalloproteinase (MMP)-9 in cystic fibrosis
|
Devereux, Graham |
|
2014 |
13 |
5 |
p. 557-563 7 p. |
artikel |
5 |
Antibacterial properties of the CFTR potentiator ivacaftor
|
Reznikov, Leah R. |
|
2014 |
13 |
5 |
p. 515-519 5 p. |
artikel |
6 |
Bronchiectases at early chest computed tomography in children with cystic fibrosis are associated with increased risk of subsequent pulmonary exacerbations and chronic pseudomonas infection
|
Bortoluzzi, Carla-Federica |
|
2014 |
13 |
5 |
p. 564-571 8 p. |
artikel |
7 |
Combined effects of VX-770 and VX-809 on several functional abnormalities of F508del-CFTR channels
|
Kopeikin, Z. |
|
2014 |
13 |
5 |
p. 508-514 7 p. |
artikel |
8 |
Contamination of hypertonic saline solutions in use by cystic fibrosis patients in Israel
|
Peled, Orit |
|
2014 |
13 |
5 |
p. 550-556 7 p. |
artikel |
9 |
Early detection of infection with Pseudomonas aeruginosa in cystic fibrosis: The Holy Grail or an achievable goal?
|
Taccetti, Giovanni |
|
2014 |
13 |
5 |
p. 491-493 3 p. |
artikel |
10 |
Editorial Board
|
|
|
2014 |
13 |
5 |
p. ii- 1 p. |
artikel |
11 |
Effect of a dietary intervention on growth and energy expenditure in children with cystic fibrosis
|
Groleau, Veronique |
|
2014 |
13 |
5 |
p. 572-578 7 p. |
artikel |
12 |
Medical consensus, guidelines, and position papers: A policy for the ECFS
|
De Boeck, K. |
|
2014 |
13 |
5 |
p. 495-498 4 p. |
artikel |
13 |
Nasal saline as a placebo in chronic rhinosinusitis
|
Karadag, Ahmet |
|
2014 |
13 |
5 |
p. 601- 1 p. |
artikel |
14 |
News
|
|
|
2014 |
13 |
5 |
p. 494- 1 p. |
artikel |
15 |
Prediction of acute pancreatitis risk based on PIP score in children with cystic fibrosis
|
Terlizzi, V. |
|
2014 |
13 |
5 |
p. 579-584 6 p. |
artikel |
16 |
Predictive values of antibodies against Pseudomonas aeruginosa in patients with cystic fibrosis one year after early eradication treatment
|
Kappler, Matthias |
|
2014 |
13 |
5 |
p. 534-541 8 p. |
artikel |
17 |
Response to Karadag
|
Mainz, Jochen G. |
|
2014 |
13 |
5 |
p. 602-603 2 p. |
artikel |
18 |
Serology as a diagnostic tool for predicting initialPseudomonas aeruginosa acquisition in childrenwith cystic fibrosis
|
Daines, Cori |
|
2014 |
13 |
5 |
p. 542-549 8 p. |
artikel |
19 |
Serum antibodies to Pseudomonas aeruginosa in cystic fibrosis as a diagnostic tool: A systematic review
|
Mauch, Renan Marrichi |
|
2014 |
13 |
5 |
p. 499-507 9 p. |
artikel |
20 |
Spiritual coping predicts 5-year health outcomes in adolescents with cystic fibrosis
|
Reynolds, Nina |
|
2014 |
13 |
5 |
p. 593-600 8 p. |
artikel |
21 |
Sweat conductivity: An accurate diagnostic test for cystic fibrosis?
|
Mattar, Ana Claudia Veras |
|
2014 |
13 |
5 |
p. 528-533 6 p. |
artikel |
22 |
The screening and diagnosis of cystic fibrosis-related diabetes in the United Kingdom
|
Wickens-Mitchell, Kate L. |
|
2014 |
13 |
5 |
p. 589-592 4 p. |
artikel |