nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A high frequency of the Cystic Fibrosis 2184insA mutation in Western Ukraine: Genotype–phenotype correlations, relevance for newborn screening and genetic testing
|
Makukh, Halyna |
|
2010 |
9 |
Supplement 2 |
p. 371-375 5 p. |
artikel |
2 |
Are serum vitamin D levels >75nmol/L achievable in children with cystic fibrosis?
|
Creedon, M. |
|
2010 |
9 |
Supplement 2 |
p. S91- 1 p. |
artikel |
3 |
Assessment of the proposed training for community nurses in different French CF centres, to carry out home based antibiotic treatment
|
Kerbrat, M. |
|
2010 |
9 |
Supplement 2 |
p. S106- 1 p. |
artikel |
4 |
CFTR missing the last four transmembrane segments and nucleotide binding domain 2 resides in the ER but escapes the cell's quality control mechanism
|
Cebotaru, L. |
|
2010 |
9 |
Supplement 2 |
p. S14- 1 p. |
artikel |
5 |
Characteristics of gastroesophageal reflux in adults with cystic fibrosis
|
Sabati, Arash A. |
|
2010 |
9 |
Supplement 2 |
p. 365-370 6 p. |
artikel |
6 |
Clinical features and outcomes of cystic fibrosis pulmonary exacerbations presenting with normal inflammatory markers
|
Ibrahim, M. |
|
2010 |
9 |
Supplement 2 |
p. S56- 1 p. |
artikel |
7 |
Clinical utility of the oxygen uptake efficiency slope in cystic fibrosis patients
|
Gruet, M. |
|
2010 |
9 |
Supplement 2 |
p. 307-313 7 p. |
artikel |
8 |
Conceptual approach of an educational evaluation system for patients: perception of utility by patients and caregivers
|
David, V. |
|
2010 |
9 |
Supplement 2 |
p. S99- 1 p. |
artikel |
9 |
Contribution of mobile genetic elements to the competitiveness of a cystic fibrosis epidemic strain
|
Fothergill, J.L. |
|
2010 |
9 |
Supplement 2 |
p. S26- 1 p. |
artikel |
10 |
Cystic fibrosis – Pregnancy after IVF, CFTR Genotype: p.[F508del]+[Q685PfsX4]
|
Gaillyová, R. |
|
2010 |
9 |
Supplement 2 |
p. S120- 1 p. |
artikel |
11 |
Decline in pulmonary function after introduction of macrolide maintenance therapy
|
van den Berg, J.M.W. |
|
2010 |
9 |
Supplement 2 |
p. S60- 1 p. |
artikel |
12 |
Depression and anxiety in patients with cystic fibrosis in Spain
|
Olveira, G. |
|
2010 |
9 |
Supplement 2 |
p. S96- 1 p. |
artikel |
13 |
Does a joint CF–diabetes team outpatient clinic improve HbA1c?
|
Lee, J. |
|
2010 |
9 |
Supplement 2 |
p. S83- 1 p. |
artikel |
14 |
Drug delivery to the sinuses – deposition pattern and clearance of pulsating aerosols in healthy volunteers
|
Schuschnig, U. |
|
2010 |
9 |
Supplement 2 |
p. S24- 1 p. |
artikel |
15 |
Effects of inhaled MP-376 (aeroquin, levofloxacin inhalation solution) on lung function in stable cystic fibrosis (CF) patients with chronic Pseudomonas aeruginosa (PA) lung infection
|
Flume, P. |
|
2010 |
9 |
Supplement 2 |
p. S23- 1 p. |
artikel |
16 |
Establishment of the CF Registry in Hungary
|
Krisztina, K. |
|
2010 |
9 |
Supplement 2 |
p. S115- 1 p. |
artikel |
17 |
Experience with harmonizing the neonatal CF screening (NSCF) management via model IRT/PAP/DNA in the Czech Republic
|
Balascakova, M. |
|
2010 |
9 |
Supplement 2 |
p. S7- 1 p. |
artikel |
18 |
ΔF508-CFTR and ENaC association
|
Khristoforov, R.R. |
|
2010 |
9 |
Supplement 2 |
p. S15- 1 p. |
artikel |
19 |
Flagellin/TLR5-dependent modulation of alveolar macrophage and epithelial cell activity by the antimicrobial molecule trappin-2
|
Descamps, D. |
|
2010 |
9 |
Supplement 2 |
p. S45- 1 p. |
artikel |
20 |
Growth of Inquilinus limosus after visiting in Zimbabwe, Africa
|
Hollsing, A. |
|
2010 |
9 |
Supplement 2 |
p. S120- 1 p. |
artikel |
21 |
Haplotype analysis of the CFTR gene from the CDC Newborn Screening Quality Assurance Program's proficiency testing collection
|
Cordovado, S.K. |
|
2010 |
9 |
Supplement 2 |
p. S3- 1 p. |
artikel |
22 |
Hepatic corticosteroid-binding globulin expression in CF patients
|
Rebeyrol, C. |
|
2010 |
9 |
Supplement 2 |
p. S19- 1 p. |
artikel |
23 |
Histone deacetylases (HDACs) and IFRD1 in CF airway epithelial cell models
|
Blanchard, E. |
|
2010 |
9 |
Supplement 2 |
p. S46- 1 p. |
artikel |
24 |
Impact of influenza A/H1N1v infection in CF compared to other risk groups
|
De Schutter, I. |
|
2010 |
9 |
Supplement 2 |
p. S52- 1 p. |
artikel |
25 |
Increasing antibiotic resistance with the Liverpool Epidemic Pseudomonas aeruginosa Strain (LES) – a 5-year study
|
Ashish, A. |
|
2010 |
9 |
Supplement 2 |
p. S41- 1 p. |
artikel |
26 |
Inhaled hypertonic saline effect on nutritional status
|
Fogazzi, A. |
|
2010 |
9 |
Supplement 2 |
p. S64- 1 p. |
artikel |
27 |
Investigation of Colifin® (1 and 2 million international units colistimethate sodium, CMS) for aerosolisation in the eFlow® rapid and PARI LC SPRINT® nebuliser
|
Brendel, E. |
|
2010 |
9 |
Supplement 2 |
p. S42- 1 p. |
artikel |
28 |
Is rhinovirus associated with exacerbations in adults with CF?
|
Helm, J. |
|
2010 |
9 |
Supplement 2 |
p. S37- 1 p. |
artikel |
29 |
Longitudinal changes in bone mass in children with cystic fibrosis: effect of size adjustment using bone mineral apparent density
|
Williams, J.E. |
|
2010 |
9 |
Supplement 2 |
p. S88- 1 p. |
artikel |
30 |
Long-term daily high and low doses of azithromycin in children with cystic fibrosis: A randomized controlled trial
|
Kabra, S.K. |
|
2010 |
9 |
Supplement 2 |
p. 17-23 7 p. |
artikel |
31 |
Lung clearance index: wash-in data compared to wash-out data
|
Ophoff, J. |
|
2010 |
9 |
Supplement 2 |
p. S57- 1 p. |
artikel |
32 |
MRSA infection in cystic fibrosis patients leads to a more rapid decline in lung function
|
Cox, D.W. |
|
2010 |
9 |
Supplement 2 |
p. S33- 1 p. |
artikel |
33 |
Multilocus sequence typing (MLST) of Pseudomonas aeruginosa collected from different ecological niches
|
Kidd, T.J. |
|
2010 |
9 |
Supplement 2 |
p. S30- 1 p. |
artikel |
34 |
Myeloperoxidase-dependent oxidative metabolism of nitric oxide in the cystic fibrosis airway
|
Chapman, Anna L.P. |
|
2010 |
9 |
Supplement 2 |
p. 84-92 9 p. |
artikel |
35 |
Non-visualization of the gallbladder: a major risk of cystic fibrosis when associated with echogenic bowel
|
Duguépéroux, I. |
|
2010 |
9 |
Supplement 2 |
p. S11- 1 p. |
artikel |
36 |
Nursing practice with intravenous antibiotic home treatment for patients with cystic fibrosis – a Scandinavian Nurses Specialist Group – CF study
|
Hunstad, E.J. |
|
2010 |
9 |
Supplement 2 |
p. S105- 1 p. |
artikel |
37 |
Overweight/obese CF patients, cause for concern?
|
Rezaie, M. |
|
2010 |
9 |
Supplement 2 |
p. S87- 1 p. |
artikel |
38 |
Patient segregation and aggressive antibiotic eradication therapy can control methicillin-resistant Staphylococcus aureus at large cystic fibrosis centres
|
Doe, S.J. |
|
2010 |
9 |
Supplement 2 |
p. 104-109 6 p. |
artikel |
39 |
Pneumothorax in cystic fibrosis: Prevalence and outcomes in Scotland
|
MacDuff, A. |
|
2010 |
9 |
Supplement 2 |
p. 246-249 4 p. |
artikel |
40 |
Prevalence and mechanism of adverse reactions to colistin in patients with cystic fibrosis
|
Whitaker, P. |
|
2010 |
9 |
Supplement 2 |
p. S50- 1 p. |
artikel |
41 |
Prevalence of erectile dysfunction in cystic fibrosis
|
Henman, S. |
|
2010 |
9 |
Supplement 2 |
p. S103- 1 p. |
artikel |
42 |
Randomised controlled two-centre trial of non-invasive ventilation (NIV)-assisted chest physiotherapy (CPT) during an acute exacerbation of cystic fibrosis
|
Dwyer, T.J. |
|
2010 |
9 |
Supplement 2 |
p. S73- 1 p. |
artikel |
43 |
Relationship between the chest excursion and lung function, functional capacity and peripheral muscle strength in patients with cystic fibrosis
|
Ozaydin, Z. |
|
2010 |
9 |
Supplement 2 |
p. S69- 1 p. |
artikel |
44 |
Report of two patients with associated conditions in addition to cystic fibrosis
|
Jambhekar, Supriya K. |
|
2010 |
9 |
Supplement 2 |
p. 269-271 3 p. |
artikel |
45 |
R117H homozygosity and the genotype–phenotype relationship
|
Bronsveld, I. |
|
2010 |
9 |
Supplement 2 |
p. S11- 1 p. |
artikel |
46 |
Serum tobramycin levels following delivery of tobramycin (Tobi®) via eFlow® advanced nebuliser in children with cystic fibrosis
|
Guy, E.L. |
|
2010 |
9 |
Supplement 2 |
p. 292-295 4 p. |
artikel |
47 |
Spectrum of CFTR mutations in the Czech Republic
|
Krenkova, P. |
|
2010 |
9 |
Supplement 2 |
p. S2- 1 p. |
artikel |
48 |
The analysis of phenotype of CF patients HFE mutations carriers
|
Bober, L. |
|
2010 |
9 |
Supplement 2 |
p. S79- 1 p. |
artikel |
49 |
The experience of managing Mycobacterium abscessus in adults with cystic fibrosis in a large regional adult CF centre
|
Whitmill, R. |
|
2010 |
9 |
Supplement 2 |
p. S34- 1 p. |
artikel |
50 |
The International Depression and Anxiety Epidemiological Study (TIDES): results from Italy
|
Catastini, P. |
|
2010 |
9 |
Supplement 2 |
p. S95- 1 p. |
artikel |
51 |
The mechanism of PAR-2 mediated mucus secretion in airway submucosal gland
|
Lee, H.-J. |
|
2010 |
9 |
Supplement 2 |
p. S18- 1 p. |
artikel |
52 |
The sensitivity of lung disease surrogates in children with CF: limited value of FEV1
|
Sanders, D. |
|
2010 |
9 |
Supplement 2 |
p. S110- 1 p. |
artikel |
53 |
Transient effectiveness of vitamin D2 therapy in pediatric cystic fibrosis patients
|
Green, Deanna M. |
|
2010 |
9 |
Supplement 2 |
p. 143-149 7 p. |
artikel |
54 |
Transient low fecal elastase levels in two CF infants with G551D following newborn screening
|
Keelty, G. |
|
2010 |
9 |
Supplement 2 |
p. S77- 1 p. |
artikel |
55 |
Use of different preparations of tobramycin solution for inhalation (TSI) in the UK
|
Collins, A. |
|
2010 |
9 |
Supplement 2 |
p. S42- 1 p. |
artikel |
56 |
Use of Positive Expiratory Pressure physiotherapy in Australian children with cystic fibrosis under five years of age
|
Wilson, C.J. |
|
2010 |
9 |
Supplement 2 |
p. S72- 1 p. |
artikel |
57 |
12 years of spirometry in CF patients with lung transplantation: the experience of an Italian regional center
|
Ferrazza, A.M. |
|
2010 |
9 |
Supplement 2 |
p. S64- 1 p. |
artikel |
58 |
Year-to-year changes in lung function in individuals with cystic fibrosis
|
Liou, Theodore G. |
|
2010 |
9 |
Supplement 2 |
p. 250-256 7 p. |
artikel |