| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
74 Adherence to rhDNase inhaled via an AKITA2® APIXNEB device during a clinical trial
|
Kroneberg, P.
|
|
2011
|
10 |
Supplement 1 |
p. S19-
1 p.
|
artikel
|
| 2 |
315* Cardiac autonomic neuropathy (CAN) is more likely to occur in cystic fibrosis (CF) patients with or without diabetes than in patients with type 1 diabetes (T1DM)
|
Rashid, R.
|
|
2011
|
10 |
Supplement 1 |
p. S80-
1 p.
|
artikel
|
| 3 |
Chronic pulmonary infection with Stenotrophomonas maltophilia and lung function in patients with cystic fibrosis
|
Dalbøge, C.S.
|
|
2011
|
10 |
Supplement 1 |
p. 318-325
8 p.
|
artikel
|
| 4 |
Colon cancer in lung transplant recipients with CF: Increased risk and results of screening
|
Meyer, Keith C.
|
|
2011
|
10 |
Supplement 1 |
p. 366-369
4 p.
|
artikel
|
| 5 |
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 1 |
p. S28-
1 p.
|
artikel
|
| 6 |
1* Comparison of bioinformatics, reporter minigene and mRNA study to analyse the effect of unclassified variants on CFTR mRNA splicing
|
Audrézet, M.-P.
|
|
2011
|
10 |
Supplement 1 |
p. S1-
1 p.
|
artikel
|
| 7 |
252* Correlation of physical performance and quality of life in adult patients with cystic fibrosis
|
Hofer, M.
|
|
2011
|
10 |
Supplement 1 |
p. S64-
1 p.
|
artikel
|
| 8 |
Cystic fibrosis in Chilean patients: Analysis of 36 common CFTR gene mutations
|
Lay-Son, Guillermo
|
|
2011
|
10 |
Supplement 1 |
p. 66-70
5 p.
|
artikel
|
| 9 |
388 Detection of a novel CFTR mutation c.122C>G (p.Pro41Arg) in a young cystic fibrosis (CF) patient with recurrent respiratory symptoms
|
De Wachter, E.
|
|
2011
|
10 |
Supplement 1 |
p. S100-
1 p.
|
artikel
|
| 10 |
Effect of an antioxidant-rich multivitamin supplement in cystic fibrosis
|
Sagel, Scott D.
|
|
2011
|
10 |
Supplement 1 |
p. 31-36
6 p.
|
artikel
|
| 11 |
116 Effect of nebulised antibiotics on Aspergillus colonisation and complications
|
Lumb, C.
|
|
2011
|
10 |
Supplement 1 |
p. S30-
1 p.
|
artikel
|
| 12 |
329* Effects of clinical variables and social status on clinic defaulting in adult CF (cystic fibrosis) patients
|
Ashish, A.
|
|
2011
|
10 |
Supplement 1 |
p. S84-
1 p.
|
artikel
|
| 13 |
206 Eosinopenia and severity of pulmonary exacerbations in adult cystic fibrosis patients
|
Williams, K.
|
|
2011
|
10 |
Supplement 1 |
p. S52-
1 p.
|
artikel
|
| 14 |
165 Evaluation of antibody against Pseudomonas aeruginosa in intermittently infected cystic fibrosis patients
|
Dolce, D.
|
|
2011
|
10 |
Supplement 1 |
p. S42-
1 p.
|
artikel
|
| 15 |
375 Expression of cystic fibrosis (CF) at diagnosis in a reference center in Rio de Janeiro
|
Schwan, P.J.
|
|
2011
|
10 |
Supplement 1 |
p. S96-
1 p.
|
artikel
|
| 16 |
294 High requirement of pancreatic enzyme dose
|
Araujo, M.
|
|
2011
|
10 |
Supplement 1 |
p. S75-
1 p.
|
artikel
|
| 17 |
162* Identical obligate anaerobic bacteria in periodontal pockets and sputum of cystic fibrosis patients
|
Huse, A.
|
|
2011
|
10 |
Supplement 1 |
p. S41-
1 p.
|
artikel
|
| 18 |
Impact of polymorphism of Multidrug Resistance-associated Protein 1 (ABCC1) gene on the severity of cystic fibrosis
|
Mafficini, Andrea
|
|
2011
|
10 |
Supplement 1 |
p. 228-233
6 p.
|
artikel
|
| 19 |
Impact of the A (H1N1) pandemic influenza (season 2009–2010) on patients with cystic fibrosis
|
Viviani, Laura
|
|
2011
|
10 |
Supplement 1 |
p. 370-376
7 p.
|
artikel
|
| 20 |
Impaired expression of hypoxia-inducible factor-1α in cystic fibrosis airway epithelial cells – A role for HIF-1 in the pathophysiology of CF?
|
Legendre, Claire
|
|
2011
|
10 |
Supplement 1 |
p. 286-290
5 p.
|
artikel
|
| 21 |
Measuring health-related quality of life in clinical trials in cystic fibrosis
|
Abbott, J.
|
|
2011
|
10 |
Supplement 1 |
p. S82-S85
4 p.
|
artikel
|
| 22 |
Multicentre trial of weekly risedronate on bone density in adults with cystic fibrosis
|
Haworth, Charles S.
|
|
2011
|
10 |
Supplement 1 |
p. 470-476
7 p.
|
artikel
|
| 23 |
270* Neuroendocrine characterization of the intestine of F508del CFTR mice
|
Hielte, L.
|
|
2011
|
10 |
Supplement 1 |
p. S69-
1 p.
|
artikel
|
| 24 |
312* New onset diabetes after lung transplantation in patients with cystic fibrosis compared with patients suffering from other lung diseases
|
van Meerkerk, G.
|
|
2011
|
10 |
Supplement 1 |
p. S79-
1 p.
|
artikel
|
| 25 |
238 Paediatric physiotherapy review following the introduction of newborn screening in cystic fibrosis
|
Byrne, N.M.
|
|
2011
|
10 |
Supplement 1 |
p. S60-
1 p.
|
artikel
|
| 26 |
344 Patient education: a pedagogic tool for cystic fibrosis transmission and fertility: GENOUTIL
|
David, V
|
|
2011
|
10 |
Supplement 1 |
p. S88-
1 p.
|
artikel
|
| 27 |
130 Prevalence of TSST-1-, PVL- and SEA-producing Staphylococcus aureus in cystic fibrosis patients
|
Filleron, A.
|
|
2011
|
10 |
Supplement 1 |
p. S33-
1 p.
|
artikel
|
| 28 |
220 Respiratory and nutritional effects of long-term treatment with azithromycin in patients with cystic fibrosis
|
Fustik, S.
|
|
2011
|
10 |
Supplement 1 |
p. S56-
1 p.
|
artikel
|
| 29 |
378 Saliva sodium and chloride levels: a useful tool for cystic fibrosis (CF) diagnosis?
|
Gonçalves, A.C.
|
|
2011
|
10 |
Supplement 1 |
p. S97-
1 p.
|
artikel
|
| 30 |
56 The calpain-calpastatin system in cystic fibrosis: physiopathological implications
|
Averna, M.
|
|
2011
|
10 |
Supplement 1 |
p. S14-
1 p.
|
artikel
|
| 31 |
71 The effect of N-acetylcysteine on the visco-elasticity of sputum of cystic fibrosis patients
|
van Daele, S.G.
|
|
2011
|
10 |
Supplement 1 |
p. S18-
1 p.
|
artikel
|
| 32 |
361 The influence of experiential avoidance on depression, anxiety and life quality in adult cystic fibrosis (CF) patients
|
Schusser, S.
|
|
2011
|
10 |
Supplement 1 |
p. S92-
1 p.
|
artikel
|
| 33 |
148 The influence of moulds as an independent risk factor for decreasing lung function in cystic fibrosis
|
Guy, C.E.
|
|
2011
|
10 |
Supplement 1 |
p. S37-
1 p.
|
artikel
|
| 34 |
298 Vitamin deficiency in children with cystic fibrosis
|
Olesen, A.M.
|
|
2011
|
10 |
Supplement 1 |
p. S75-
1 p.
|
artikel
|
| 35 |
41* Who should be analyzed in a cystic fibrosis registry?
|
Thomas, M.
|
|
2011
|
10 |
Supplement 1 |
p. S10-
1 p.
|
artikel
|
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