nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Adherence to clinical care guidelines for cystic fibrosis-related diabetes in 659 German/Austrian patients
|
Scheuing, Nicole |
|
2014 |
13 |
6 |
p. 730-736 7 p. |
artikel |
2 |
An exploratory study of microbial diversity in sinus infections of cystic fibrosis patients by molecular methods
|
Rudkjøbing, Vibeke Børsholt |
|
2014 |
13 |
6 |
p. 645-652 8 p. |
artikel |
3 |
Chronic ivacaftor treatment: Getting F508del-CFTR into more trouble?
|
Mall, Marcus A. |
|
2014 |
13 |
6 |
p. 605-607 3 p. |
artikel |
4 |
Comparison of two tobramycin nebuliser solutions: Pharmacokinetic, efficacy and safety profiles of T100 and TNS
|
Sands, Dorota |
|
2014 |
13 |
6 |
p. 653-660 8 p. |
artikel |
5 |
Cytokine gene polymorphisms and severity of CF lung disease
|
de Vries, Leonieke |
|
2014 |
13 |
6 |
p. 699-705 7 p. |
artikel |
6 |
Depression and anxiety in adolescents and adults with cystic fibrosis in the UK: A cross-sectional study
|
Duff, Alistair J.A. |
|
2014 |
13 |
6 |
p. 745-753 9 p. |
artikel |
7 |
Early attained weight and length predict growth faltering better than velocity measures in infants with CF
|
Heltshe, Sonya L. |
|
2014 |
13 |
6 |
p. 723-729 7 p. |
artikel |
8 |
Editorial Board
|
|
|
2014 |
13 |
6 |
p. ii- 1 p. |
artikel |
9 |
Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation
|
De Boeck, Kris |
|
2014 |
13 |
6 |
p. 674-680 7 p. |
artikel |
10 |
Electronic care records — Can they fulfil their promise?
|
Wainwright, Claire E. |
|
2014 |
13 |
6 |
p. 608-609 2 p. |
artikel |
11 |
Feasibility of parental collected nasal swabs for virus detection in young children with cystic fibrosis
|
Gangell, C.L. |
|
2014 |
13 |
6 |
p. 661-666 6 p. |
artikel |
12 |
How does heart rate recovery after sub-maximal exercise correlate with maximal exercise testing in children with CF?
|
Cohen, Sarah P. |
|
2014 |
13 |
6 |
p. 712-715 4 p. |
artikel |
13 |
Impact of Scedosporium apiospermum complex seroprevalence in patients with cystic fibrosis
|
Parize, Perrine |
|
2014 |
13 |
6 |
p. 667-673 7 p. |
artikel |
14 |
Improvement of digestive health and reduction in proteobacterial populations in the gut microbiota of cystic fibrosis patients using a Lactobacillus reuteri probiotic preparation: A double blind prospective study
|
del Campo, Rosa |
|
2014 |
13 |
6 |
p. 716-722 7 p. |
artikel |
15 |
Inhaled versus nebulised tobramycin: A real world comparison in adult cystic fibrosis (CF)
|
Harrison, M.J. |
|
2014 |
13 |
6 |
p. 692-698 7 p. |
artikel |
16 |
JCF — 2014 and beyond
|
Bell, Scott C. |
|
2014 |
13 |
6 |
p. 610-611 2 p. |
artikel |
17 |
Lung clearance index during hospital admission in school-age children with cystic fibrosis
|
Welsh, Liam |
|
2014 |
13 |
6 |
p. 687-691 5 p. |
artikel |
18 |
Meconium ileus in cystic fibrosis is not linked to central repetitive region length variation in MUC1, MUC2, and MUC5AC
|
Guo, XueLiang |
|
2014 |
13 |
6 |
p. 613-616 4 p. |
artikel |
19 |
Neutrophil elastase-mediated increase in airway temperature during inflammation
|
Schmidt, Annika |
|
2014 |
13 |
6 |
p. 623-631 9 p. |
artikel |
20 |
News
|
|
|
2014 |
13 |
6 |
p. 612- 1 p. |
artikel |
21 |
Physiological response during activity programs using Wii-based video games in patients with cystic fibrosis (CF)
|
del Corral, Tamara |
|
2014 |
13 |
6 |
p. 706-711 6 p. |
artikel |
22 |
Pneumococcal polysaccharide vaccine responses are impaired in a subgroup of children with cystic fibrosis
|
Browning, Michael J. |
|
2014 |
13 |
6 |
p. 632-638 7 p. |
artikel |
23 |
Prenatal diagnosis for CF using High Resolution Melting Analysis and simultaneous haplotype analysis through QF-PCR
|
Poulou, Myrto |
|
2014 |
13 |
6 |
p. 617-622 6 p. |
artikel |
24 |
Skin contamination leading to falsely elevated fingerprick tobramycin levels in a patient taking dry powder inhaled tobramycin
|
Barry, Peter J. |
|
2014 |
13 |
6 |
p. 754- 1 p. |
artikel |
25 |
Stigma and optimism in adolescents and young adults with cystic fibrosis
|
Oliver, Kendea N. |
|
2014 |
13 |
6 |
p. 737-744 8 p. |
artikel |
26 |
The development and deployment of integrated electronic care records in a regional adult and paediatric cystic fibrosis unit
|
Peckham, D. |
|
2014 |
13 |
6 |
p. 681-686 6 p. |
artikel |
27 |
The value of soluble transferrin receptor and hepcidin in the assessment of iron status in children with cystic fibrosis
|
Uijterschout, Lieke |
|
2014 |
13 |
6 |
p. 639-644 6 p. |
artikel |