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                             51 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Adherence over multiple courses of Aztreonam Lysine for Inhalation (AZLI): effect on disease-related endpoints in patients with cystic fibrosis (CF) and Pseudomonas aeruginosa (PA) Oermann, C.M.
 2009
 8 Supplement 2 p. S28-
1 p.
 artikel
2 A rheological investigation of cystic fibrosis sputum Britland, S.
 2009
 8 Supplement 2 p. S74-
1 p.
 artikel
3 Azithromycin fails to reduce increased expression of neutrophil-related cytokines in primary-cultured epithelial cells from cystic fibrosis mice Gavilanes, Ximena
 2009
 8 Supplement 2 p. 203-210
8 p.
 artikel
4 Bronchodilator responsiveness and IgE in pediatric cystic fibrosis patients Castanhinha, S.
 2009
 8 Supplement 2 p. S67-
1 p.
 artikel
5 CF Diagnosis Announcement Practices following a neonatal screening in France Guéganton, L.J.
 2009
 8 Supplement 2 p. S13-
1 p.
 artikel
6 Clinical and genetic profile of patients from Moldova diagnosed with cystic fibrosis Sciuca, S.
 2009
 8 Supplement 2 p. S106-
1 p.
 artikel
7 Comparison of the sensitivity of six PCR formats for the detection of P. aeruginosa Deschaght, P.
 2009
 8 Supplement 2 p. S36-
1 p.
 artikel
8 Desaturation on 3-minute step test is associated with impaired outcomes at 12 months in adults with cystic fibrosis Holland, A.E.
 2009
 8 Supplement 2 p. S70-
1 p.
 artikel
9 Early referral to cystic fibrosis specialist centre impacts on respiratory outcome Lebecque, P.
 2009
 8 Supplement 2 p. 26-30
5 p.
 artikel
10 Editorial Board 2009
 8 Supplement 2 p. iii-
1 p.
 artikel
11 Efficacy of slow release insulin in patients with Cystic Fibrosis and Glucide Intolerance Minicucci, L.
 2009
 8 Supplement 2 p. S82-
1 p.
 artikel
12 Emotional condition of adult with cystic fibrosis (CF): implication of illness or structure of personality? Catastini, P.
 2009
 8 Supplement 2 p. S91-
1 p.
 artikel
13 Eradication of Pseudomonas aeruginosa in adults with CF Kenny, S.
 2009
 8 Supplement 2 p. S39-
1 p.
 artikel
14 Evaluation and management of fungal risk in Cystic Fibrosis: first results of a national French study Leroy, S.
 2009
 8 Supplement 2 p. S44-
1 p.
 artikel
15 Evidence of aminoglycoside cochleotoxicity measured by standard & high frequency audiometry and Distortion-Product otoacoustic emissions in paediatric Cystic Fibrosis patients Al-Malky, G.
 2009
 8 Supplement 2 p. S48-
1 p.
 artikel
16 Exercise-induced hypoxemia and cardiac arrhythmia in cystic fibrosis Ruf, Katharina
 2009
 8 Supplement 2 p. 83-90
8 p.
 artikel
17 Exonic sequence variations affecting splicing within exons 3, 4 and 5 Hinzpeter, A.
 2009
 8 Supplement 2 p. S1-
1 p.
 artikel
18 High treatment burden in adults with cystic fibrosis: Challenges to disease self-management Sawicki, Gregory S.
 2009
 8 Supplement 2 p. 91-96
6 p.
 artikel
19 Human Neutrophil Peptide-1 (HNP-1) and a truncated analogue display antimicrobial activity against respiratory pathogens Lundy, F.T.
 2009
 8 Supplement 2 p. S47-
1 p.
 artikel
20 Immunity in CF associated liver disease Ciuca, I.M.
 2009
 8 Supplement 2 p. S77-
1 p.
 artikel
21 Impact of the polymorphic variant 5 FR/G-260C in the Multidrug Resistance-associate Protein-1 gene on severity of cystic fibrosis Mafficini, A.
 2009
 8 Supplement 2 p. S4-
1 p.
 artikel
22 Intestinal Current Measurement (ICM) in Europe: towards a harmonised protocol for clinical trials in cystic fibrosis Derichs, N.
 2009
 8 Supplement 2 p. S32-
1 p.
 artikel
23 Intravenous peripherally-inserted central catheters for antibiotic therapy in children with cystic fibrosis Bui, S.
 2009
 8 Supplement 2 p. 326-331
6 p.
 artikel
24 In-vitro inhibition of neutrophil elastase activity by inhaled antibiotics used in cystic fibrosis patients Hector, A.
 2009
 8 Supplement 2 p. S63-
1 p.
 artikel
25 8-isoprostaglandinF-2-alfa in urine as a marker of oxidative stress in cystic fibrosis patients. A longitudinal study Schiøtz, P.O.
 2009
 8 Supplement 2 p. S51-
1 p.
 artikel
26 Lack of Differences in Mutant Prevention Concentration Rates Between Cystic Fibrosis Pseudomonas aeruginosa Isolates in Planktonic and Biofilm Type of Growth Garcia-Castillo, M.
 2009
 8 Supplement 2 p. S40-
1 p.
 artikel
27 Lactate as a non-invasive marker of CF lung inflammation Bensel, T.
 2009
 8 Supplement 2 p. S62-
1 p.
 artikel
28 Life satisfaction of adolescents and adults with cystic fibrosis: Impact of partnership and gender Besier, Tanja
 2009
 8 Supplement 2 p. 104-109
6 p.
 artikel
29 Listing patients to lung transplantation (LTx). Experience of 110 cases in the CF Center of Verona Assael, B.M.
 2009
 8 Supplement 2 p. S59-
1 p.
 artikel
30 Long acting β2-agonist and corticosteroid restore airway glandular cell functionality altered by Staphylococcus aureus virulence factors Zahm, J.M.
 2009
 8 Supplement 2 p. S23-
1 p.
 artikel
31 Optimizing aerosol administration in Cystic Fibrosis and Asthma treatment with improved Smart Card technology Kroneberg, P.
 2009
 8 Supplement 2 p. S32-
1 p.
 artikel
32 Patient satisfaction in a District General Hospital cystic fibrosis service Johnstone, A.
 2009
 8 Supplement 2 p. S110-
1 p.
 artikel
33 Patient satisfaction survey of the annual review service at a regional adult cystic fibrosis (CF) centre Evans, C.
 2009
 8 Supplement 2 p. S99-
1 p.
 artikel
34 Perks and pitfalls of interstitial glucose monitoring – early experience from an ongoing pilot study Helm, J.M.
 2009
 8 Supplement 2 p. S81-
1 p.
 artikel
35 Pharmacological inhibition of CFTR modifies cyclooxygenase-1 and -2 expression and PGD2 production in Calu-3 cells Baudouin-Legros, M.
 2009
 8 Supplement 2 p. S21-
1 p.
 artikel
36 Quality improvement in newborn screening for cystic fibrosis by process failure mode effects analysis (PFMEA) Farrell, P.M.
 2009
 8 Supplement 2 p. S9-
1 p.
 artikel
37 Requirement of endosomal SNARE protein complex in CFTR activity/trafficking regulation Clément, R.
 2009
 8 Supplement 2 p. S21-
1 p.
 artikel
38 Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770 Van Goor, F.
 2009
 8 Supplement 2 p. S17-
1 p.
 artikel
39 Revealing potential plasma lipid biomarkers of cystic fibrosis by mass spectrometry Guerrera, C.
 2009
 8 Supplement 2 p. S9-
1 p.
 artikel
40 Serum matrix metalloproteinases in adult CF patients: Relation to pulmonary exacerbation Roderfeld, Martin
 2009
 8 Supplement 2 p. 338-347
10 p.
 artikel
41 The experience of using megestrol acetate (MA) in a large UK adult CF centre Barrett, J.
 2009
 8 Supplement 2 p. S86-
1 p.
 artikel
42 The “1km challenge” – a novel method to measure changes in exercise tolerance in children with cystic fibrosis during hospital admissions Lester, L.
 2009
 8 Supplement 2 p. S71-
1 p.
 artikel
43 Totally Implantable Venous Access devices (TIVADs) in Cystic Fibrosis with particular reference to associated complications Mills, H.L.
 2009
 8 Supplement 2 p. S95-
1 p.
 artikel
44 Transition from paediatric to adult: experience of a cystic fibrosis care center Wagner, A.C.
 2009
 8 Supplement 2 p. S102-
1 p.
 artikel
45 Trisomy 21 – possible cause for false positive sweat test? Pop, L.
 2009
 8 Supplement 2 p. S16-
1 p.
 artikel
46 UMD-CFTR: a database dedicated to CF and CFTR-related diseases Bareil, C.
 2009
 8 Supplement 2 p. S105-
1 p.
 artikel
47 Use of the insulin pump in treat cystic fibrosis related diabetes Hardin, Dana S.
 2009
 8 Supplement 2 p. 174-178
5 p.
 artikel
48 Validation of insulin secretion indices in cystic fibrosis patients Hammana, I.
 2009
 8 Supplement 2 p. 378-381
4 p.
 artikel
49 Vascular stenosis in CF patients with totally implantable vascular access devices Greenwood, J.
 2009
 8 Supplement 2 p. S95-
1 p.
 artikel
50 Very high-dose ergocalciferol is effective for correcting vitamin D deficiency in children and young adults with cystic fibrosis Boas, Steven R.
 2009
 8 Supplement 2 p. 270-272
3 p.
 artikel
51 Weak anti-inflammatory effects of glucocorticoids on CF bronchial epithelial cells Rebeyrol, C.
 2009
 8 Supplement 2 p. S54-
1 p.
 artikel
                             51 gevonden resultaten
 
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