| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Activity of liposomal formulations on sputum isolated from CF Patients
|
Halwani, M.
|
|
2009
|
8 |
Supplement 1 |
p. S29-
1 p.
|
artikel
|
| 2 |
Airways surface liquid depletion causes MMP-12 dependent emphysema in βENaC-overexpressing mice
|
Schubert, S.C.
|
|
2009
|
8 |
Supplement 1 |
p. S53-
1 p.
|
artikel
|
| 3 |
An appropriate diagnostic approach can improve detection of CFTR mutations: the experience in Patients with Classical Form of Cystic Fibrosis coming from an Italian Region with high genetic heterogeneity
|
Ravani, A.
|
|
2009
|
8 |
Supplement 1 |
p. S6-
1 p.
|
artikel
|
| 4 |
An overview of international literature from cystic fibrosis registries: 1. Mortality and survival studies in cystic fibrosis
|
Buzzetti, R.
|
|
2009
|
8 |
Supplement 1 |
p. 229-237
9 p.
|
artikel
|
| 5 |
Assessment of bone mass density by quantitative ultrasonography in children with cystic fibrosis
|
Turcu, O.
|
|
2009
|
8 |
Supplement 1 |
p. S85-
1 p.
|
artikel
|
| 6 |
Assessment of bone mineralisation in cystic fibrosis
|
Rolin, S.A.
|
|
2009
|
8 |
Supplement 1 |
p. S83-
1 p.
|
artikel
|
| 7 |
Assessment of specific exercise for correction of postural disorders in CF patients
|
Almajan-Guta, B.
|
|
2009
|
8 |
Supplement 1 |
p. S72-
1 p.
|
artikel
|
| 8 |
Audit of deaths in a single adult CF centre
|
Saffy, A.
|
|
2009
|
8 |
Supplement 1 |
p. S103-
1 p.
|
artikel
|
| 9 |
Author Index
|
|
|
2009
|
8 |
Supplement 1 |
p. S113-S121
9 p.
|
artikel
|
| 10 |
Bacterial contamination of cystic fibrosis clinics
|
Zuckerman, Jonathan B.
|
|
2009
|
8 |
Supplement 1 |
p. 186-192
7 p.
|
artikel
|
| 11 |
Bronchiectasis (BE) on CT is a strong predictor of respiratory tract exacerbations in children with CF
|
Loeve, M.
|
|
2009
|
8 |
Supplement 1 |
p. S68-
1 p.
|
artikel
|
| 12 |
Common mutations in cuban cystic fibrosis patients
|
Collazo, Teresa
|
|
2009
|
8 |
Supplement 1 |
p. 47-49
3 p.
|
artikel
|
| 13 |
Comparison of biofilm formation between Burkholderia multivorans Burkholderia cenocepacia Pseudomonas aeruginosa in the presence or absence of mucin
|
Einarsson, G.G.
|
|
2009
|
8 |
Supplement 1 |
p. S34-
1 p.
|
artikel
|
| 14 |
Connexin 26 is implied in the regulation of airway epithelium repair
|
Crespin, S.
|
|
2009
|
8 |
Supplement 1 |
p. S19-
1 p.
|
artikel
|
| 15 |
Cytotoxic activity evidence of Achromobacter xylosoxidans for pulmonar tissue
|
Levy, C.E.
|
|
2009
|
8 |
Supplement 1 |
p. S46-
1 p.
|
artikel
|
| 16 |
Development of a secure, on-line clinical health record to improve care in cystic fibrosis (CF)
|
Finlayson, F.A.
|
|
2009
|
8 |
Supplement 1 |
p. S108-
1 p.
|
artikel
|
| 17 |
Early colonization by Staphylococcus aureus and Pseudomonas aeruginosa in newborn screening children
|
Champs, N.S.
|
|
2009
|
8 |
Supplement 1 |
p. S64-
1 p.
|
artikel
|
| 18 |
Early referral to cystic fibrosis specialist centre impacts on respiratory outcome
|
Lebecque, P.
|
|
2009
|
8 |
Supplement 1 |
p. 26-30
5 p.
|
artikel
|
| 19 |
Editorial Board
|
|
|
2009
|
8 |
Supplement 1 |
p. CO2-
1 p.
|
artikel
|
| 20 |
Editorial Board
|
|
|
2009
|
8 |
Supplement 1 |
p. IFC-
1 p.
|
artikel
|
| 21 |
Effects of denufosol on sinusitis-related complaints in a phase 3 trial in cystic fibrosis patients
|
Mospan, A.R.
|
|
2009
|
8 |
Supplement 1 |
p. S26-
1 p.
|
artikel
|
| 22 |
Estrogen and phytoestrogens increase the CFTR and F508del CFTR expression and function
|
Hamdaoui, N.
|
|
2009
|
8 |
Supplement 1 |
p. S18-
1 p.
|
artikel
|
| 23 |
Evaluation of salt supplementation in CF infants
|
Coates, Alison J.
|
|
2009
|
8 |
Supplement 1 |
p. 382-385
4 p.
|
artikel
|
| 24 |
Experience of a 1 year therapeutic education program
|
Clairicia, M.
|
|
2009
|
8 |
Supplement 1 |
p. S98-
1 p.
|
artikel
|
| 25 |
Genotyping of Pseudomonas aeruginosa isolates from aquatic environment at a Swedish hospital and relation to infection of lung transplanted patients with Pseudomonas
|
Johansson, E.
|
|
2009
|
8 |
Supplement 1 |
p. S38-
1 p.
|
artikel
|
| 26 |
Histidinylated linear PEIs as new DNA carriers for in vitro and in vivo gene transfer with low toxicity
|
Guégan, P.
|
|
2009
|
8 |
Supplement 1 |
p. S30-
1 p.
|
artikel
|
| 27 |
Human Neutrophil Peptide-1 (HNP-1) and a truncated analogue display antimicrobial activity against respiratory pathogens
|
Lundy, F.T.
|
|
2009
|
8 |
Supplement 1 |
p. S47-
1 p.
|
artikel
|
| 28 |
Identification of a novel frameshift mutation in CFTR gene: description, and clinical data
|
Gaillyová, R.
|
|
2009
|
8 |
Supplement 1 |
p. S6-
1 p.
|
artikel
|
| 29 |
Identification of CFTR rearrangements by a CGH locus specific array
|
Quéméner, S.
|
|
2009
|
8 |
Supplement 1 |
p. S15-
1 p.
|
artikel
|
| 30 |
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 1 |
p. S4-
1 p.
|
artikel
|
| 31 |
Implementation of the UK Newborn Screening Programme
|
Southern, K.W.
|
|
2009
|
8 |
Supplement 1 |
p. S11-
1 p.
|
artikel
|
| 32 |
Improvement in aerobic fitness and quality of life does not depend on severity of pulmonary disease in CF patients
|
Jung, A.
|
|
2009
|
8 |
Supplement 1 |
p. S60-
1 p.
|
artikel
|
| 33 |
Infection by Nocardia farcinica in CF
|
Beucher, J.
|
|
2009
|
8 |
Supplement 1 |
p. S69-
1 p.
|
artikel
|
| 34 |
Intestinal inflammation is present in young infants with cystic fibrosis
|
Lisowska, A.
|
|
2009
|
8 |
Supplement 1 |
p. S79-
1 p.
|
artikel
|
| 35 |
Intravenous peripherally-inserted central catheters for antibiotic therapy in children with cystic fibrosis
|
Bui, S.
|
|
2009
|
8 |
Supplement 1 |
p. 326-331
6 p.
|
artikel
|
| 36 |
Is dietetics the cinderella of the CF multidisciplinary team?
|
Lake, E.
|
|
2009
|
8 |
Supplement 1 |
p. S88-
1 p.
|
artikel
|
| 37 |
Long acting β2-agonist and corticosteroid restore airway glandular cell functionality altered by Staphylococcus aureus virulence factors
|
Zahm, J.M.
|
|
2009
|
8 |
Supplement 1 |
p. S23-
1 p.
|
artikel
|
| 38 |
Long-term, low-dose azithromycin treatment reduces the incidence but increases macrolide resistance in Staphylococcus aureus in Danish CF patients
|
Hansen, C.R.
|
|
2009
|
8 |
Supplement 1 |
p. 58-62
5 p.
|
artikel
|
| 39 |
Lung defense against Pseudomonas aeruginosa: the recognition by host cells of either LPS or flagellin is necessary and sufficient
|
Raoust, E.
|
|
2009
|
8 |
Supplement 1 |
p. S52-
1 p.
|
artikel
|
| 40 |
Lung function variability in cystic fibrosis
|
Jifon, G.
|
|
2009
|
8 |
Supplement 1 |
p. S61-
1 p.
|
artikel
|
| 41 |
Mentoring people with cystic fibrosis: evaluation of the preparation and process
|
Jessup, M.
|
|
2009
|
8 |
Supplement 1 |
p. S97-
1 p.
|
artikel
|
| 42 |
Molecular mechanisms of the pro-inflammatory role of membrane-associated PR3 during neutrophil apoptosis in cystic fibrosis
|
Gabillet, J.
|
|
2009
|
8 |
Supplement 1 |
p. S56-
1 p.
|
artikel
|
| 43 |
Monitoring of the Initial Pseudomonas aeruginosa Colonization in Cystic Fibrosis Patients Demonstrated High Clonal Diversity
|
Fernández-Olmos, A.
|
|
2009
|
8 |
Supplement 1 |
p. S37-
1 p.
|
artikel
|
| 44 |
MRSA and macrolide resistant Staphylococcus aureus colonization rates in a Turkish CF center
|
Dogan, O.
|
|
2009
|
8 |
Supplement 1 |
p. S41-
1 p.
|
artikel
|
| 45 |
Open monitoring of adherence; is it better in those patients who bring their device for download?
|
McCormack, P.
|
|
2009
|
8 |
Supplement 1 |
p. S92-
1 p.
|
artikel
|
| 46 |
Pharmacokinetics and safety of tobramycin administered by the PARI eFlow® rapid nebulizer in cystic fibrosis
|
Hubert, Dominique
|
|
2009
|
8 |
Supplement 1 |
p. 332-337
6 p.
|
artikel
|
| 47 |
Pharmacological inhibition of CFTR modifies cyclooxygenase-1 and -2 expression and PGD2 production in Calu-3 cells
|
Baudouin-Legros, M.
|
|
2009
|
8 |
Supplement 1 |
p. S21-
1 p.
|
artikel
|
| 48 |
Pilot newborn screening project for cystic fibrosis in the Czech Republic: Defining role of the delay in its symptomatic diagnosis and influence of ultrasound-based prenatal diagnosis on the incidence of the disease
|
Balaščaková, Miroslava
|
|
2009
|
8 |
Supplement 1 |
p. 224-227
4 p.
|
artikel
|
| 49 |
Prevalence and clinical significance of autoantibodies in 144 adult patients with cystic fibrosis
|
Lachenal, F.
|
|
2009
|
8 |
Supplement 1 |
p. S50-
1 p.
|
artikel
|
| 50 |
Safety/Efficacy of Inhaled Human Alpha-1 Antitrypsin (AAT) in CF: A Phase II Clinical Study
|
Kerem, E.
|
|
2009
|
8 |
Supplement 1 |
p. S25-
1 p.
|
artikel
|
| 51 |
Serum matrix metalloproteinases in adult CF patients: Relation to pulmonary exacerbation
|
Roderfeld, Martin
|
|
2009
|
8 |
Supplement 1 |
p. 338-347
10 p.
|
artikel
|
| 52 |
Telephone calls by CF nurses
|
Panzo, R.
|
|
2009
|
8 |
Supplement 1 |
p. S101-
1 p.
|
artikel
|
| 53 |
The French CF Laboratory Network: seven years' experience
|
Girodon, E.
|
|
2009
|
8 |
Supplement 1 |
p. S2-
1 p.
|
artikel
|
| 54 |
The perceived quality of the cystic fibrosis service and the subjective dimension of the illness experience for patient's parents and caregivers: a survey method to improve the care relationship
|
Grossi, R.
|
|
2009
|
8 |
Supplement 1 |
p. S100-
1 p.
|
artikel
|
| 55 |
The Use of Patient Held Drug Information Cards to improve adherence: a questionnaire survey
|
Brady, G.
|
|
2009
|
8 |
Supplement 1 |
p. S93-
1 p.
|
artikel
|
| 56 |
Trends in pathogens colonising the respiratory tract of adult patients with cystic fibrosis, 1985–2005
|
Millar, F.A.
|
|
2009
|
8 |
Supplement 1 |
p. 386-391
6 p.
|
artikel
|
| 57 |
Use of the insulin pump in treat cystic fibrosis related diabetes
|
Hardin, Dana S.
|
|
2009
|
8 |
Supplement 1 |
p. 174-178
5 p.
|
artikel
|
| 58 |
Wilson disease as a cause of liver injury in cystic fibrosis
|
Kotalová, Radana
|
|
2009
|
8 |
Supplement 1 |
p. 63-65
3 p.
|
artikel
|
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