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                             31 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 215 Adherence with TOBI® among cystic fibrosis patients with Pseudomonas aeruginosa infection Joish, V.N.
 2011
 10 Supplement 2 p. S55-
1 p.
 artikel
2 Ambulatory quantitative waking and sleeping cough assessment in patients with cystic fibrosis Kerem, Eitan
 2011
 10 Supplement 2 p. 193-200
8 p.
 artikel
3 122 A one-year experience of routine identification by MALDI-TOF MS of non-fermenting Gram-negative rods recovered from respiratory samples from cystic fibrosis patients Olmos, A. Fernandez
 2011
 10 Supplement 2 p. S31-
1 p.
 artikel
4 80* A randomised, double-blind, placebo-controlled parallel group study to investigate the safety and efficacy of two doses of tiotropium bromide (2.5 μg and 5 μg) administered once daily via the Respimat® device for 12 weeks in patients with cystic fibrosis Elborn, J.S.
 2011
 10 Supplement 2 p. S21-
1 p.
 artikel
5 353 Are elastomeric diffusers delivering what they claim? Vigier, J.-P
 2011
 10 Supplement 2 p. S90-
1 p.
 artikel
6 184* Basophil CD203c as a potential clinically relevant biomarker in cystic fibrosis and allergic bronchopulmonary aspergillosis Gernez, Y.
 2011
 10 Supplement 2 p. S46-
1 p.
 artikel
7 47 CFTR gene mutations and the risk for developing a pancreatic cancer: is it only a consequence of chronic inflammation? Alghisi, F.
 2011
 10 Supplement 2 p. S12-
1 p.
 artikel
8 Chronic pulmonary infection with Stenotrophomonas maltophilia and lung function in patients with cystic fibrosis Dalbøge, C.S.
 2011
 10 Supplement 2 p. 318-325
8 p.
 artikel
9 108 Comparative in vitro characterisation of colistimethate sodium 1 MIU/3 ml versus 2 MIU/4 ml in an eFlow® rapid Nebuliser Bucholski, A.
 2011
 10 Supplement 2 p. S28-
1 p.
 artikel
10 125* Comparison of real time diagnostic chemistries to detect early and chronic Pseudomonas aeruginosa colonisation in cystic fibrosis patients Fothergill, J.L.
 2011
 10 Supplement 2 p. S32-
1 p.
 artikel
11 394 Cystic fibrosis liver disease: an emerging clinical issue showing a multifactorial pathogenesis Alghisi, F.
 2011
 10 Supplement 2 p. S101-
1 p.
 artikel
12 Diversified harmony: Supranational and domestic regulation of pediatric clinical trials in the European Union Pinxten, Wim
 2011
 10 Supplement 2 p. S183-S198
16 p.
 artikel
13 280 Do children with cystic fibrosis really need more energy? Jones, K.
 2011
 10 Supplement 2 p. S73-
1 p.
 artikel
14 14 Genotype-phenotype correlations of the recurrent mRNA intron 6b splicing defect, 1002-1113_1110delGAAT Costa, C.
 2011
 10 Supplement 2 p. S4-
1 p.
 artikel
15 Impact of the A (H1N1) pandemic influenza (season 2009–2010) on patients with cystic fibrosis Viviani, Laura
 2011
 10 Supplement 2 p. 370-376
7 p.
 artikel
16 370* Increasing incidence of cystic fibrosis being diagnosed in adulthood over time: an analysis of two decades of care Weir, M.
 2011
 10 Supplement 2 p. S95-
1 p.
 artikel
17 244* Influence of inhaled hypertonic saline (NaCI 6%) before or during autogenic drainage on sputum weight, oxygen saturation, heart frequency and dyspnoea in cystic fibrosis patients Van Ginderdeuren, F.
 2011
 10 Supplement 2 p. S62-
1 p.
 artikel
18 KPC-2 Carbapenemase-producing Klebsiella pneumoniae isolates from patients with Cystic Fibrosis Leão, Robson S.
 2011
 10 Supplement 2 p. 140-142
3 p.
 artikel
19 50* Low temperature and chemical rescue affect the molecular proximity of DF508-CFTR and ENaC Rennolds, J.
 2011
 10 Supplement 2 p. S13-
1 p.
 artikel
20 Marked increase in incidence of Achromobacter xylosoxidans infections caused by sporadic acquisition from the environment Ridderberg, Winnie
 2011
 10 Supplement 2 p. 466-469
4 p.
 artikel
21 367 Motivational interviewing (Ml); evaluating the learning outcomes of UK CF team training Duff, A.
 2011
 10 Supplement 2 p. S93-
1 p.
 artikel
22 262* Non-invasive (NI) rehabilitation program in cystic fibrosis patients with urinary incontinence Donà, M.
 2011
 10 Supplement 2 p. S66-
1 p.
 artikel
23 65 Phase 3 study of ataluren (PTC124®) in nonsense mutation cystic fibrosis (nmCF): baseline data Kerem, E.
 2011
 10 Supplement 2 p. S17-
1 p.
 artikel
24 384 Pregnancy and motherhood in women with cystic fibrosis: experience and outcomes in a regional adult UK centre Etherington, C.
 2011
 10 Supplement 2 p. S98-
1 p.
 artikel
25 140 Retrospective analysis of isolation of non-tuberculous mycobacteria from cystic fibrosis sputum samples Burnett, K.
 2011
 10 Supplement 2 p. S35-
1 p.
 artikel
26 171* The chitinase-like protein YKL-40 modulates cystic fibrosis lung disease Hector, A.
 2011
 10 Supplement 2 p. S43-
1 p.
 artikel
27 247 The tolerability of nebulised meropenem within an adult cystic fibrosis centre Parker-Stafford, J.
 2011
 10 Supplement 2 p. S62-
1 p.
 artikel
28 321 Timing of inhaled tobramycin affects intravenous tobramycin trough levels Stenbit, A.E.
 2011
 10 Supplement 2 p. S82-
1 p.
 artikel
29 338 Variability of clinical outcomes and impact of risk factors in cystic fibrosis (CF) patients in a regional CF center in a developing country Dracea, L.-L.
 2011
 10 Supplement 2 p. S86-
1 p.
 artikel
30 157 Variation in canide production between different strains of Pseudomonas aeruginosa Gilchrist, F.J.
 2011
 10 Supplement 2 p. S40-
1 p.
 artikel
31 304 Vitamin K status in young children with cystic fibrosis Krzyzanowska, P.
 2011
 10 Supplement 2 p. S77-
1 p.
 artikel
                             31 gevonden resultaten
 
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