| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Advanced glycation end products are elevated in cystic fibrosis-related diabetes and correlate with worse lung function
|
Hunt, William R.
|
|
2016
|
15 |
5 |
p. 681-688
8 p.
|
artikel
|
| 2 |
Are CF carriers predisposed to asthma?
|
Corvol, H.
|
|
2016
|
15 |
5 |
p. 555-556
2 p.
|
artikel
|
| 3 |
Challenge for a new era—importance of ensuring accuracy of genotype in cystic fibrosis registries
|
Hartley, Claire L.
|
|
2016
|
15 |
5 |
p. e50-e51
nvt p.
|
artikel
|
| 4 |
Clinical outcomes in cystic fibrosis patients with Trichosporon respiratory infection
|
Esther Jr., Charles R.
|
|
2016
|
15 |
5 |
p. e45-e49
nvt p.
|
artikel
|
| 5 |
Comparison of two pancreatic enzyme products for exocrine insufficiency in patients with cystic fibrosis
|
Taylor, C.J.
|
|
2016
|
15 |
5 |
p. 675-680
6 p.
|
artikel
|
| 6 |
Controversies with Kalydeco: Newspaper coverage in Canada and the United States of the cystic fibrosis “wonder drug”
|
Rachul, Christen
|
|
2016
|
15 |
5 |
p. 624-629
6 p.
|
artikel
|
| 7 |
Corrigendum to “Risk of hemoptysis in cystic fibrosis clinical trials: A retrospective cohort study” [J Cyst Fibros (2015) 632–638]
|
Thompson, V.
|
|
2016
|
15 |
5 |
p. e54-e55
nvt p.
|
artikel
|
| 8 |
Daily Observations of Nebuliser Use and Technique (DONUT) in children with cystic fibrosis
|
Bos, Aukje C.
|
|
2016
|
15 |
5 |
p. 645-651
7 p.
|
artikel
|
| 9 |
Disease disclosure in individuals with cystic fibrosis: Association with psychosocial and health outcomes
|
Borschuk, Adrienne P.
|
|
2016
|
15 |
5 |
p. 696-702
7 p.
|
artikel
|
| 10 |
Editorial Board
|
|
|
2016
|
15 |
5 |
p. ii-
1 p.
|
artikel
|
| 11 |
Epidemiology of nontuberculous mycobacteria (NTM) amongst individuals with cystic fibrosis (CF)
|
Viviani, Laura
|
|
2016
|
15 |
5 |
p. 619-623
5 p.
|
artikel
|
| 12 |
Episodic oral antibiotic use in CF: Discordance between the electronic medical record and self-report
|
Caverly, Lindsay J.
|
|
2016
|
15 |
5 |
p. 630-633
4 p.
|
artikel
|
| 13 |
Host response to Staphylococcus aureus cytotoxins in children with cystic fibrosis
|
Chadha, Ashley D.
|
|
2016
|
15 |
5 |
p. 597-604
8 p.
|
artikel
|
| 14 |
Insulin secretion abnormalities in patients with cystic fibrosis
|
Schnyder, Marie-Angela
|
|
2016
|
15 |
5 |
p. e52-e53
nvt p.
|
artikel
|
| 15 |
Killing effect of nanoencapsulated colistin sulfate on Pseudomonas aeruginosa from cystic fibrosis patients
|
Sans-Serramitjana, E.
|
|
2016
|
15 |
5 |
p. 611-618
8 p.
|
artikel
|
| 16 |
Microbiological yield from induced sputum compared to oropharyngeal swab in young children with cystic fibrosis
|
Zampoli, Marco
|
|
2016
|
15 |
5 |
p. 605-610
6 p.
|
artikel
|
| 17 |
Nasal potential difference outcomes support diagnostic decisions in cystic fibrosis
|
Tridello, Gloria
|
|
2016
|
15 |
5 |
p. 579-582
4 p.
|
artikel
|
| 18 |
News
|
|
|
2016
|
15 |
5 |
p. 561-562
2 p.
|
artikel
|
| 19 |
Non-allergic asthma as a CFTR-related disorder
|
Schulz, Angela
|
|
2016
|
15 |
5 |
p. 641-644
4 p.
|
artikel
|
| 20 |
Ode to the exocrine pancreas
|
Coffey, Michael J.
|
|
2016
|
15 |
5 |
p. 557-558
2 p.
|
artikel
|
| 21 |
Optimizing beta-lactam pharmacodynamics against Pseudomonas aeruginosa in adult cystic fibrosis patients
|
Thompson, R. Zachary
|
|
2016
|
15 |
5 |
p. 660-663
4 p.
|
artikel
|
| 22 |
Pancreatic Elastase-1 Quick Test for rapid assessment of pancreatic status in cystic fibrosis patients
|
Walkowiak, Jarosław
|
|
2016
|
15 |
5 |
p. 664-668
5 p.
|
artikel
|
| 23 |
Potentiator synergy in rectal organoids carrying S1251N, G551D, or F508del CFTR mutations
|
Dekkers, Johanna F.
|
|
2016
|
15 |
5 |
p. 568-578
11 p.
|
artikel
|
| 24 |
Preliminary report of the 13C-mixed triglyceride breath test to assess timing of pancreatic enzyme replacement therapy in children with cystic fibrosis
|
van der Haak, Natalie
|
|
2016
|
15 |
5 |
p. 669-674
6 p.
|
artikel
|
| 25 |
Psychological resilience and intolerance of uncertainty in coping with cystic fibrosis
|
Mitmansgruber, Horst
|
|
2016
|
15 |
5 |
p. 689-695
7 p.
|
artikel
|
| 26 |
Reversible airway obstruction in cystic fibrosis: Common, but not associated with characteristics of asthma
|
Levine, Hagit
|
|
2016
|
15 |
5 |
p. 652-659
8 p.
|
artikel
|
| 27 |
Risk of asthma in heterozygous carriers for cystic fibrosis: A meta-analysis
|
Nielsen, Anne Orholm
|
|
2016
|
15 |
5 |
p. 563-567
5 p.
|
artikel
|
| 28 |
Safety and efficacy of prolonged levofloxacin inhalation solution (APT-1026) treatment for cystic fibrosis and chronic Pseudomonas aeruginosa airway infection
|
Elborn, J. Stuart
|
|
2016
|
15 |
5 |
p. 634-640
7 p.
|
artikel
|
| 29 |
The power of mental adaptation to genetic abnormality
|
Goldbeck, Lutz
|
|
2016
|
15 |
5 |
p. 559-560
2 p.
|
artikel
|
| 30 |
The role of basophil activation test in allergic bronchopulmonary aspergillosis and Aspergillus fumigatus sensitization in cystic fibrosis patients
|
Katelari, Anna
|
|
2016
|
15 |
5 |
p. 587-596
10 p.
|
artikel
|
| 31 |
YKL-40 as marker of severe lung disease in cystic fibrosis patients
|
Leonardi, Salvatore
|
|
2016
|
15 |
5 |
p. 583-586
4 p.
|
artikel
|
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