| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Achromobacter species in cystic fibrosis: Cross-infection caused by indirect patient-to-patient contact
|
Hansen, C.R.
|
|
2013
|
12 |
6 |
p. 609-615
7 p.
|
artikel
|
| 2 |
Amoxicillin–clavulanic acid resistance in fecal Enterobacteriaceae from patients with cystic fibrosis and healthy siblings
|
Duytschaever, Gwen
|
|
2013
|
12 |
6 |
p. 780-783
4 p.
|
artikel
|
| 3 |
A pilot outreach physiotherapy and dietetic quality improvement initiative reduces IV antibiotic requirements in children with moderate–severe cystic fibrosis
|
Ledger, Sean J.
|
|
2013
|
12 |
6 |
p. 766-772
7 p.
|
artikel
|
| 4 |
ARFI and transient elastography for characterization of cystic fibrosis related liver disease: First longitudinal follow-up data in adult patients
|
Karlas, Thomas
|
|
2013
|
12 |
6 |
p. 826-827
2 p.
|
artikel
|
| 5 |
CFTR: Effect of ICL2 and ICL4 amino acids in close spatial proximity on the current properties of the channel
|
Billet, Arnaud
|
|
2013
|
12 |
6 |
p. 737-745
9 p.
|
artikel
|
| 6 |
Change in the Executive Editorial Team at JCF
|
Bell, Scott
|
|
2013
|
12 |
6 |
p. 545-546
2 p.
|
artikel
|
| 7 |
Comparison of real time diagnostic chemistries to detect Pseudomonas aeruginosa in respiratory samples from cystic fibrosis patients
|
Fothergill, J.L.
|
|
2013
|
12 |
6 |
p. 675-681
7 p.
|
artikel
|
| 8 |
Cystic fibrosis CFBE41o‐ cells contain TLR1 SNP I602S and fail to respond to Mycobacterium abscessus
|
Kempaiah, Prakasha
|
|
2013
|
12 |
6 |
p. 773-779
7 p.
|
artikel
|
| 9 |
Cytokines in nasal lavages and plasma and their correlation with clinical parameters in cystic fibrosis
|
Paats, Marthe S.
|
|
2013
|
12 |
6 |
p. 623-629
7 p.
|
artikel
|
| 10 |
Development of a quantitative immunofluorescence assay for detection of Stenotrophomonas maltophilia antibodies in patients with cystic fibrosis
|
Vidigal, P. Gonçalves
|
|
2013
|
12 |
6 |
p. 651-654
4 p.
|
artikel
|
| 11 |
Drug induced complications; can we do more?
|
Peckham, Daniel
|
|
2013
|
12 |
6 |
p. 547-558
12 p.
|
artikel
|
| 12 |
Early treatment with inhaled antibiotics postpones next occurrence of Achromobacter in cystic fibrosis
|
Wang, M.
|
|
2013
|
12 |
6 |
p. 638-643
6 p.
|
artikel
|
| 13 |
Editorial Board
|
|
|
2013
|
12 |
6 |
p. ii-
1 p.
|
artikel
|
| 14 |
Effect of supervised training on FEV1 in cystic fibrosis: A randomised controlled trial
|
Kriemler, Susi
|
|
2013
|
12 |
6 |
p. 714-720
7 p.
|
artikel
|
| 15 |
Effect of VX-770 (Ivacaftor) and OAG on Ca2+ influx and CFTR activity in G551D and F508del-CFTR expressing cells
|
Vachel, Laura
|
|
2013
|
12 |
6 |
p. 584-591
8 p.
|
artikel
|
| 16 |
Effects of ivacaftor on severely ill patients with cystic fibrosis carrying a G551D mutation
|
Hebestreit, Helge
|
|
2013
|
12 |
6 |
p. 599-603
5 p.
|
artikel
|
| 17 |
Elevated levels of miR-145 correlate with SMAD3 down-regulation in Cystic Fibrosis patients
|
Megiorni, Francesca
|
|
2013
|
12 |
6 |
p. 797-802
6 p.
|
artikel
|
| 18 |
Enteral tube feeding in adults with cystic fibrosis; patient choice and impact on long term outcomes
|
White, H.
|
|
2013
|
12 |
6 |
p. 616-622
7 p.
|
artikel
|
| 19 |
Eradication of chronic methicillin-resistant Staphylococcus aureus infection in cystic fibrosis patients. An observational prospective cohort study of 11 patients
|
Vanderhelst, Eef
|
|
2013
|
12 |
6 |
p. 662-666
5 p.
|
artikel
|
| 20 |
Erratum to “Secretory IgA as a diagnostic tool for Pseudomonas aeruginosa respiratory colonization” [J Cyst Fibros 12 (1) (2013) 81–7]
|
Aanaes, Kasper
|
|
2013
|
12 |
6 |
p. 830-
1 p.
|
artikel
|
| 21 |
Evidence of diminished FEV1 and FVC in 6-year-olds followed in the European cystic fibrosis patient registry, 2007–2009
|
VanDevanter, Donald R.
|
|
2013
|
12 |
6 |
p. 786-789
4 p.
|
artikel
|
| 22 |
Extensive diversification is a common feature of Pseudomonas aeruginosa populations during respiratory infections in cystic fibrosis
|
Ashish, Abdul
|
|
2013
|
12 |
6 |
p. 790-793
4 p.
|
artikel
|
| 23 |
Factors influencing the acquisition of Stenotrophomonas maltophilia infection in cystic fibrosis patients
|
Stanojevic, Sanja
|
|
2013
|
12 |
6 |
p. 575-583
9 p.
|
artikel
|
| 24 |
Impaired CFTR function in mild cystic fibrosis associated with the S977F/T5TG12complex allele in trans with F508del mutation
|
Sorio, Claudio
|
|
2013
|
12 |
6 |
p. 821-825
5 p.
|
artikel
|
| 25 |
Improved air trapping evaluation in chest computed tomography in children with cystic fibrosis using real-time spirometric monitoring and biofeedback
|
Kongstad, Thomas
|
|
2013
|
12 |
6 |
p. 559-566
8 p.
|
artikel
|
| 26 |
Inhaled nitric oxide decreases the bacterial load in a rat model of Pseudomonas aeruginosa pneumonia
|
Miller, Christopher C.
|
|
2013
|
12 |
6 |
p. 817-820
4 p.
|
artikel
|
| 27 |
Maximal daily dose of pancreatic enzyme replacement therapy in infants with cystic fibrosis: A reconsideration
|
Borowitz, Drucy
|
|
2013
|
12 |
6 |
p. 784-785
2 p.
|
artikel
|
| 28 |
Mitochondrial OXPHOS function is unaffected by chronic azithromycin treatment
|
Negari, Shelly Ben-Harush
|
|
2013
|
12 |
6 |
p. 682-687
6 p.
|
artikel
|
| 29 |
Modification of the salivary secretion assay in F508del mice — The murine equivalent of the human sweat test
|
Droebner, Karoline
|
|
2013
|
12 |
6 |
p. 630-637
8 p.
|
artikel
|
| 30 |
Molecular analysis of changes in Pseudomonas aeruginosa load during treatment of a pulmonary exacerbation in cystic fibrosis
|
Reid, D.W.
|
|
2013
|
12 |
6 |
p. 688-699
12 p.
|
artikel
|
| 31 |
Multilocus sequence typing of Scedosporium apiospermum and Pseudallescheria boydii isolates from cystic fibrosis patients
|
Bernhardt, A.
|
|
2013
|
12 |
6 |
p. 592-598
7 p.
|
artikel
|
| 32 |
Newborn screening for cystic fibrosis in Switzerland — Consequences after analysis of a 4 months pilot study
|
Torresani, Toni
|
|
2013
|
12 |
6 |
p. 667-674
8 p.
|
artikel
|
| 33 |
Nutritional status is associated with health-related quality of life in children with cystic fibrosis aged 9–19years
|
Shoff, Suzanne M.
|
|
2013
|
12 |
6 |
p. 746-753
8 p.
|
artikel
|
| 34 |
P. aeruginosa in the paranasal sinuses and transplanted lungs have similar adaptive mutations as isolates from chronically infected CF lungs
|
Ciofu, Oana
|
|
2013
|
12 |
6 |
p. 729-736
8 p.
|
artikel
|
| 35 |
Peripheral neuropathy in cystic fibrosis: A prevalence study
|
Chakrabarty, Biswaroop
|
|
2013
|
12 |
6 |
p. 754-760
7 p.
|
artikel
|
| 36 |
Prevalence of Helicobacter pylori infection in patients with cystic fibrosis
|
Drzymała-Czyż, Sławomira
|
|
2013
|
12 |
6 |
p. 761-765
5 p.
|
artikel
|
| 37 |
Prognostic relevance of dynamic hyperinflation during cardiopulmonary exercise testing in adult patients with cystic fibrosis
|
Stevens, D.
|
|
2013
|
12 |
6 |
p. 655-661
7 p.
|
artikel
|
| 38 |
Pro-inflammatory effect of cystic fibrosis sputum microparticles in the murine lung
|
Porro, Chiara
|
|
2013
|
12 |
6 |
p. 721-728
8 p.
|
artikel
|
| 39 |
Rapid emergence of a ceftazidime-resistant Burkholderia multivorans strain in a Cystic Fibrosis patient
|
Stokell, Joshua R.
|
|
2013
|
12 |
6 |
p. 812-816
5 p.
|
artikel
|
| 40 |
Reproducibility of maximal cardiopulmonary exercise testing for young cystic fibrosis patients
|
Saynor, Zoe L.
|
|
2013
|
12 |
6 |
p. 644-650
7 p.
|
artikel
|
| 41 |
Screening for depression in a single CF centre
|
Latchford, Gary
|
|
2013
|
12 |
6 |
p. 794-796
3 p.
|
artikel
|
| 42 |
The effect of gastric juice on interleukin-8 production by cystic fibrosis primary bronchial epithelial cells
|
Pauwels, Ans
|
|
2013
|
12 |
6 |
p. 700-705
6 p.
|
artikel
|
| 43 |
The effect of intravenous antibiotics on anaemia in cystic fibrosis
|
Kathiresan, Bhuvaneswari
|
|
2013
|
12 |
6 |
p. 828-829
2 p.
|
artikel
|
| 44 |
The predictive potential of the sweat chloride test in cystic fibrosis patients with the G551D mutation
|
Seliger, Verena I.
|
|
2013
|
12 |
6 |
p. 706-713
8 p.
|
artikel
|
| 45 |
Tobramycin is a suppressor of premature termination codons
|
Altamura, Nicola
|
|
2013
|
12 |
6 |
p. 806-811
6 p.
|
artikel
|
| 46 |
Treatment response of airway clearance assessed by single-breath washout in children with cystic fibrosis
|
Abbas, Chiara
|
|
2013
|
12 |
6 |
p. 567-574
8 p.
|
artikel
|
| 47 |
Xbox Kinect™ represents high intensity exercise for adults with cystic fibrosis
|
Holmes, Hayley
|
|
2013
|
12 |
6 |
p. 604-608
5 p.
|
artikel
|
| 48 |
ZnT8 antibodies in patients with cystic fibrosis: An expression of secondary beta-cell damage?
|
Bizzarri, Carla
|
|
2013
|
12 |
6 |
p. 803-805
3 p.
|
artikel
|
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