| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Apolipoprotein E polymorphism determines vitamin K supplementation effectiveness in cystic fibrosis patients
|
Krzyżanowska-Jankowska, Patrycja
|
|
2018
|
17 |
4 |
p. e39-e40
|
artikel
|
| 2 |
Back to the source – Modern insights into pulmonary exacerbations and lung function decline from CF registry data
|
Rayment, Jonathan H.
|
|
2018
|
17 |
4 |
p. 425-427
|
artikel
|
| 3 |
Chronic infection sustained by a Pseudomonas aeruginosa High-Risk clone producing the VIM-1 metallo-β-lactamase in a cystic fibrosis patient after lung transplantation
|
Pollini, Simona
|
|
2018
|
17 |
4 |
p. 470-474
|
artikel
|
| 4 |
Comparison of facemask and mouthpiece interfaces for multiple breath washout measurements
|
Robinson, Paul D.
|
|
2018
|
17 |
4 |
p. 511-517
|
artikel
|
| 5 |
Cystic fibrosis: Beyond the airways. Report on the meeting of the basic science working group in Loutraki, Greece
|
Amaral, Margarida D.
|
|
2018
|
17 |
4 |
p. 441-443
|
artikel
|
| 6 |
Cystic fibrosis patient registries: A valuable source for clinical research
|
Dasenbrook, Elliott C.
|
|
2018
|
17 |
4 |
p. 433-440
|
artikel
|
| 7 |
Early life growth patterns persist for 12 years and impact pulmonary outcomes in cystic fibrosis
|
Sanders, Don B.
|
|
2018
|
17 |
4 |
p. 528-535
|
artikel
|
| 8 |
Editorial Board
|
|
|
2018
|
17 |
4 |
p. ii
|
artikel
|
| 9 |
End-of-life practice patterns at U.S. adult cystic fibrosis care centers: A national retrospective chart review
|
Chen, Elaine
|
|
2018
|
17 |
4 |
p. 548-554
|
artikel
|
| 10 |
Hypoglycaemia in cystic fibrosis: An analysis of a single centre adult cystic fibrosis clinic
|
Armaghanian, Natasha
|
|
2018
|
17 |
4 |
p. 542-547
|
artikel
|
| 11 |
Hypoglycaemia in patients with cystic fibrosis- harbinger of poor outcomes or innocent bystander?
|
Moheet, Amir
|
|
2018
|
17 |
4 |
p. 428-429
|
artikel
|
| 12 |
Insights into the cystic fibrosis care in Eastern Europe: Results of survey
|
Walicka-Serzysko, Katarzyna
|
|
2018
|
17 |
4 |
p. 475-477
|
artikel
|
| 13 |
KB001-A, a novel anti-inflammatory, found to be safe and well-tolerated in cystic fibrosis patients infected with Pseudomonas aeruginosa
|
Jain, Raksha
|
|
2018
|
17 |
4 |
p. 484-491
|
artikel
|
| 14 |
Lung function decline is delayed but not decreased in patients with cystic fibrosis and the R117H gene mutation
|
Wagener, Jeffrey S.
|
|
2018
|
17 |
4 |
p. 503-510
|
artikel
|
| 15 |
Molecular characterization of gene regulatory networks in primary human tracheal and bronchial epithelial cells
|
Gillen, Austin E.
|
|
2018
|
17 |
4 |
p. 444-453
|
artikel
|
| 16 |
Multicentre standardisation of chest MRI as radiation-free outcome measure of lung disease in young children with cystic fibrosis
|
Wielpütz, Mark O.
|
|
2018
|
17 |
4 |
p. 518-527
|
artikel
|
| 17 |
News
|
|
|
2018
|
17 |
4 |
p. 430-432
|
artikel
|
| 18 |
No easy road to better cystic fibrosis care in Eastern Europe?
|
De Boeck, Kris
|
|
2018
|
17 |
4 |
p. 423-424
|
artikel
|
| 19 |
Poor recovery from a pulmonary exacerbation does not lead to accelerated FEV1 decline
|
Sanders, Don B.
|
|
2018
|
17 |
4 |
p. 492-495
|
artikel
|
| 20 |
Prevalence and characteristics of chronic kidney disease among Danish adults with cystic fibrosis
|
Berg, Kristina H.
|
|
2018
|
17 |
4 |
p. 478-483
|
artikel
|
| 21 |
Prevalence of hypoglycemia during oral glucose tolerance testing in adults with cystic fibrosis and risk of developing cystic fibrosis-related diabetes
|
Mannik, Lisa A.
|
|
2018
|
17 |
4 |
p. 536-541
|
artikel
|
| 22 |
Pulmonary exacerbations and acute declines in lung function in patients with cystic fibrosis
|
Wagener, Jeffrey S.
|
|
2018
|
17 |
4 |
p. 496-502
|
artikel
|
| 23 |
Sweat test for cystic fibrosis: Wearable sweat sensor vs. standard laboratory test
|
Choi, Dong-Hoon
|
|
2018
|
17 |
4 |
p. e35-e38
|
artikel
|
| 24 |
The association between Staphylococcus aureus and subsequent bronchiectasis in children with cystic fibrosis
|
Caudri, Daan
|
|
2018
|
17 |
4 |
p. 462-469
|
artikel
|
| 25 |
The expression of Mirc1/Mir17–92 cluster in sputum samples correlates with pulmonary exacerbations in cystic fibrosis patients
|
Krause, Kathrin
|
|
2018
|
17 |
4 |
p. 454-461
|
artikel
|
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