| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Airway hyperresponsiveness in FVB/N delta F508 cystic fibrosis transmembrane conductance regulator mice
|
Bazett, Mark
|
|
2014
|
13 |
4 |
p. 378-383
6 p.
|
artikel
|
| 2 |
CFTR functional measurements in human models for diagnosis, prognosis and personalized therapy
|
Beekman, Jeffrey M.
|
|
2014
|
13 |
4 |
p. 363-372
10 p.
|
artikel
|
| 3 |
Commentary for JCF review “Drug induced complications; can we do more?” J Cyst Fibros 2013 Dec;12(6):547–58
|
Taylor, C.J.
|
|
2014
|
13 |
4 |
p. 485-
1 p.
|
artikel
|
| 4 |
Daily serum creatinine monitoring promotes earlier detection of acute kidney injury in children and adolescents with cystic fibrosis
|
Downes, Kevin J.
|
|
2014
|
13 |
4 |
p. 435-441
7 p.
|
artikel
|
| 5 |
Development of IgG antibodies to Exophiala dermatitidis is associated with inflammatory responses in patients with cystic fibrosis
|
Kondori, Nahid
|
|
2014
|
13 |
4 |
p. 391-399
9 p.
|
artikel
|
| 6 |
Early assessment of glucose abnormalities during continuous glucose monitoring associated with lung function impairment in cystic fibrosis patients
|
Leclercq, A.
|
|
2014
|
13 |
4 |
p. 478-484
7 p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
2014
|
13 |
4 |
p. ii-
1 p.
|
artikel
|
| 8 |
Efficacy and tolerability of a new nasal spray formulation containing hyaluronate and tobramycin in cystic fibrosis patients with bacterial rhinosinusitis
|
Di Cicco, Maurizio
|
|
2014
|
13 |
4 |
p. 455-460
6 p.
|
artikel
|
| 9 |
ESCF Care Guidelines beyond Europe
|
Gutierrez M.D., Hector H.
|
|
2014
|
13 |
4 |
p. 359-360
2 p.
|
artikel
|
| 10 |
European cystic fibrosis society standards of care: A road map to improve CF outcome
|
Kerem, Eitan
|
|
2014
|
13 |
4 |
p. 357-358
2 p.
|
artikel
|
| 11 |
Impact of pulmonary hypertension on survival in patients with cystic fibrosis undergoing lung transplantation: An analysis of the UNOS registry
|
Hayes Jr., Don
|
|
2014
|
13 |
4 |
p. 416-423
8 p.
|
artikel
|
| 12 |
Nebulized voriconazole in infections with Scedosporium apiospermum — Case report and review of the literature
|
Holle, J.
|
|
2014
|
13 |
4 |
p. 400-402
3 p.
|
artikel
|
| 13 |
Neonatal screening for cystic fibrosis: Comparing the performances of IRT/DNA and IRT/PAP
|
Sarles, Jacques
|
|
2014
|
13 |
4 |
p. 384-390
7 p.
|
artikel
|
| 14 |
Neonates with cystic fibrosis have a reduced nasal liquid pH; A small pilot study
|
Abou Alaiwa, Mahmoud H.
|
|
2014
|
13 |
4 |
p. 373-377
5 p.
|
artikel
|
| 15 |
Paranasal sinus pathogens in children with cystic fibrosis: Do they relate to lower respiratory tract pathogens and is eradication successful?
|
Wilson, P.
|
|
2014
|
13 |
4 |
p. 449-454
6 p.
|
artikel
|
| 16 |
Prescribing practices for intravenous aminoglycosides in UK Cystic Fibrosis clinics: A questionnaire survey
|
Smyth, Alan R.
|
|
2014
|
13 |
4 |
p. 424-427
4 p.
|
artikel
|
| 17 |
Rate of improvement of CF life expectancy exceeds that of general population—Observational death registration study
|
Hurley, Matthew N.
|
|
2014
|
13 |
4 |
p. 410-415
6 p.
|
artikel
|
| 18 |
Reply to Professor Taylor
|
Peckham, Daniel
|
|
2014
|
13 |
4 |
p. 486-487
2 p.
|
artikel
|
| 19 |
Safety of inhaled (Tobi®) and intravenous tobramycin in young children with cystic fibrosis
|
Hennig, Stefanie
|
|
2014
|
13 |
4 |
p. 428-434
7 p.
|
artikel
|
| 20 |
Simultaneous liver–pancreas transplantation for cystic fibrosis-related liver disease: A multicenter experience
|
Bandsma, R.H.J.
|
|
2014
|
13 |
4 |
p. 471-477
7 p.
|
artikel
|
| 21 |
Sinonasal inhalation of dornase alfa administered by vibrating aerosol to cystic fibrosis patients: A double-blind placebo-controlled cross-over trial
|
Mainz, Jochen G.
|
|
2014
|
13 |
4 |
p. 461-470
10 p.
|
artikel
|
| 22 |
Sinonasal manifestations of cystic fibrosis: A correlation between genotype and phenotype?
|
Berkhout, M.C.
|
|
2014
|
13 |
4 |
p. 442-448
7 p.
|
artikel
|
| 23 |
The challenge of improving outcomes for patients with CF sinonasal disease
|
VanDevanter, Donald R.
|
|
2014
|
13 |
4 |
p. 361-362
2 p.
|
artikel
|
| 24 |
The relative frequency of CFTR mutation classes in European patients with cystic fibrosis
|
De Boeck, K.
|
|
2014
|
13 |
4 |
p. 403-409
7 p.
|
artikel
|
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