Digital Library
Close Browse articles from a journal
 
Search for with title:
ABCDEFGHIJKLMNOPQRSTUVWXYZ

     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
                                       All articles of the corresponding issues
 
                             58 results found
no title author magazine year volume issue page(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.
 article
2 Are serum vitamin D levels >75nmol/L achievable in children with cystic fibrosis? Creedon, M.
 2010
 9 Supplement 2 p. S91-
1 p.
 article
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.
 article
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.
 article
5 Characteristics of gastroesophageal reflux in adults with cystic fibrosis Sabati, Arash A.
 2010
 9 Supplement 2 p. 365-370
6 p.
 article
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.
 article
7 Clinical utility of the oxygen uptake efficiency slope in cystic fibrosis patients Gruet, M.
 2010
 9 Supplement 2 p. 307-313
7 p.
 article
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.
 article
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.
 article
10 Cystic fibrosis – Pregnancy after IVF, CFTR Genotype: p.[F508del]+[Q685PfsX4] Gaillyová, R.
 2010
 9 Supplement 2 p. S120-
1 p.
 article
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.
 article
12 Depression and anxiety in patients with cystic fibrosis in Spain Olveira, G.
 2010
 9 Supplement 2 p. S96-
1 p.
 article
13 Does a joint CF–diabetes team outpatient clinic improve HbA1c? Lee, J.
 2010
 9 Supplement 2 p. S83-
1 p.
 article
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.
 article
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.
 article
16 Establishment of the CF Registry in Hungary Krisztina, K.
 2010
 9 Supplement 2 p. S115-
1 p.
 article
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.
 article
18 ΔF508-CFTR and ENaC association Khristoforov, R.R.
 2010
 9 Supplement 2 p. S15-
1 p.
 article
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.
 article
20 Growth of Inquilinus limosus after visiting in Zimbabwe, Africa Hollsing, A.
 2010
 9 Supplement 2 p. S120-
1 p.
 article
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.
 article
22 Hepatic corticosteroid-binding globulin expression in CF patients Rebeyrol, C.
 2010
 9 Supplement 2 p. S19-
1 p.
 article
23 Histone deacetylases (HDACs) and IFRD1 in CF airway epithelial cell models Blanchard, E.
 2010
 9 Supplement 2 p. S46-
1 p.
 article
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.
 article
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.
 article
26 Inhaled hypertonic saline effect on nutritional status Fogazzi, A.
 2010
 9 Supplement 2 p. S64-
1 p.
 article
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.
 article
28 Is rhinovirus associated with exacerbations in adults with CF? Helm, J.
 2010
 9 Supplement 2 p. S37-
1 p.
 article
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.
 article
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.
 article
31 Lung clearance index: wash-in data compared to wash-out data Ophoff, J.
 2010
 9 Supplement 2 p. S57-
1 p.
 article
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.
 article
33 Multilocus sequence typing (MLST) of Pseudomonas aeruginosa collected from different ecological niches Kidd, T.J.
 2010
 9 Supplement 2 p. S30-
1 p.
 article
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.
 article
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.
 article
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.
 article
37 Overweight/obese CF patients, cause for concern? Rezaie, M.
 2010
 9 Supplement 2 p. S87-
1 p.
 article
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.
 article
39 Pneumothorax in cystic fibrosis: Prevalence and outcomes in Scotland MacDuff, A.
 2010
 9 Supplement 2 p. 246-249
4 p.
 article
40 Prevalence and mechanism of adverse reactions to colistin in patients with cystic fibrosis Whitaker, P.
 2010
 9 Supplement 2 p. S50-
1 p.
 article
41 Prevalence of erectile dysfunction in cystic fibrosis Henman, S.
 2010
 9 Supplement 2 p. S103-
1 p.
 article
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.
 article
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.
 article
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.
 article
45 R117H homozygosity and the genotype–phenotype relationship Bronsveld, I.
 2010
 9 Supplement 2 p. S11-
1 p.
 article
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.
 article
47 Spectrum of CFTR mutations in the Czech Republic Krenkova, P.
 2010
 9 Supplement 2 p. S2-
1 p.
 article
48 The analysis of phenotype of CF patients HFE mutations carriers Bober, L.
 2010
 9 Supplement 2 p. S79-
1 p.
 article
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.
 article
50 The International Depression and Anxiety Epidemiological Study (TIDES): results from Italy Catastini, P.
 2010
 9 Supplement 2 p. S95-
1 p.
 article
51 The mechanism of PAR-2 mediated mucus secretion in airway submucosal gland Lee, H.-J.
 2010
 9 Supplement 2 p. S18-
1 p.
 article
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.
 article
53 Transient effectiveness of vitamin D2 therapy in pediatric cystic fibrosis patients Green, Deanna M.
 2010
 9 Supplement 2 p. 143-149
7 p.
 article
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.
 article
55 Use of different preparations of tobramycin solution for inhalation (TSI) in the UK Collins, A.
 2010
 9 Supplement 2 p. S42-
1 p.
 article
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.
 article
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.
 article
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.
 article
                             58 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands