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                             65 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 ACHROMOBACTER XYLOSOXIDANS: FOLLOW-UP OF 20 PATIENTS WITH CHRONIC INFECTION Costantini, D.
 2008
 7 Supplement 2 p. S22-
1 p.
 artikel
2 A German external quality survey of diagnostic microbiology of respiratory tract infections in patients with cystic fibrosis Balke, Beate
 2008
 7 Supplement 2 p. 7-14
8 p.
 artikel
3 Age specific guidelines developed for scheduled monitoring and investigations in a pediatric CF clinic Houlden, D.K.
 2008
 7 Supplement 2 p. S117-
1 p.
 artikel
4 An audit of the importance of nose clips for spirometry in CF Boyle, L.
 2008
 7 Supplement 2 p. S77-
1 p.
 artikel
5 An experiential approach to understanding adherence in CF Ashby, B.
 2008
 7 Supplement 2 p. S98-
1 p.
 artikel
6 ANTIBIOTIC RESISTANCE AND VIRULENCE DETERMINANTS IN STAPHYLOCOCCUS AUREUS ISOLATED IN CYSTIC FIBROSIS PATIENTS Stefani, S.
 2008
 7 Supplement 2 p. S2-
1 p.
 artikel
7 A pilot study on the safety and efficacy of a novel antioxidant rich formulation in patients with cystic fibrosis Papas, Konstantinos A.
 2008
 7 Supplement 2 p. 60-67
8 p.
 artikel
8 Bacteriology of sputum in cystic fibrosis – 2 years of systematic monitoring Sad, I.
 2008
 7 Supplement 2 p. S48-
1 p.
 artikel
9 Biofilm formation and antimicrobial susceptibility of P. aeruginosa isolates cultured before and after antibiotic treatment of an acute exacerbation of pulmonary infection Gilpin, D.F.
 2008
 7 Supplement 2 p. S39-
1 p.
 artikel
10 CALPROTECTIN: AN INFLAMMATORY INTESTINAL MARKER IN CYSTIC FIBROSIS? Farina, S.
 2008
 7 Supplement 2 p. S17-
1 p.
 artikel
11 Cascade carrier testing for cystic fibrosis: an Australian experience McClaren, B.J.
 2008
 7 Supplement 2 p. S12-
1 p.
 artikel
12 Challenge of Living with Cystic Fibrosis (CLCF): psychometric validation Glasscoe, C.
 2008
 7 Supplement 2 p. S108-
1 p.
 artikel
13 Chronic sinusitis in CF child carrying two missense mutations S519G and G576A in the NBF1 domain of CFTR Feuillet-Fieux, M.N.
 2008
 7 Supplement 2 p. S7-
1 p.
 artikel
14 Clear illustration of improved survival in CF: the experience of Brittany (France) Scotet, V.
 2008
 7 Supplement 2 p. S113-
1 p.
 artikel
15 Clinical difference between cystic fibrosis patients colonized with different bacteria Reis, P.
 2008
 7 Supplement 2 p. S58-
1 p.
 artikel
16 Clinical effect of long term oral DHA supplementation in cystic fibrosis patients Van Biervliet, S.
 2008
 7 Supplement 2 p. S93-
1 p.
 artikel
17 Communication processes and outcome following an impaired glucose tolerance test: findings from a clinical audit McKenna, D.
 2008
 7 Supplement 2 p. S88-
1 p.
 artikel
18 Development and characterization of IgY as oral treatment in CF care Nilsson, E.
 2008
 7 Supplement 2 p. S51-
1 p.
 artikel
19 Disadvantage for patients over 24 months at diagnosis of cystic fibrosis de Monestrol, I.
 2008
 7 Supplement 2 p. S113-
1 p.
 artikel
20 Do Danish children with and without CF share nutritional habits? Sundstrup, J.
 2008
 7 Supplement 2 p. S90-
1 p.
 artikel
21 Duration of decreasing the nasal potential difference by amiloride-mannitol dry powder Schüler, P.
 2008
 7 Supplement 2 p. S23-
1 p.
 artikel
22 Editorial Board 2008
 7 Supplement 2 p. IFC-
1 p.
 artikel
23 Effects of inhaled salmeterol-fluticasone propionate on lung and epithelial cell functions in cystic fibrosis children: a double blind crossover study Bessaci, K.
 2008
 7 Supplement 2 p. S66-
1 p.
 artikel
24 EFFICACY OF HIGH FREQUENCY CHEST COMPRESSION (HFCC) IN THE CLEARANCE OF MUCUS IN PATIENTS WITH CYSTIC FIBROSIS (CF) Ambroni, M.
 2008
 7 Supplement 2 p. S9-
1 p.
 artikel
25 Efficiency of West Airway Clearance System in combination with autogenic drainage physiotherapy technique in adult CF patients during lung exacerbation Scherbakova, A.
 2008
 7 Supplement 2 p. S74-
1 p.
 artikel
26 EMERGENCE OF COLISTIN-RESISTANT PSEUDOMONAS AERUGINOSA FROM ITALIAN CYSTIC FIBROSIS PATIENTS Manno, G.
 2008
 7 Supplement 2 p. S13-S14
2 p.
 artikel
27 Epidemiological profile of bacteria isolated from the respiratory tract of cystic fibrosis patients Reis, P.
 2008
 7 Supplement 2 p. S47-
1 p.
 artikel
28 Experience using centralized spirometry in the phase 2 randomized, placebo-controlled, double-blind trial of denufosol in patients with mild to moderate cystic fibrosis Goss, C.H.
 2008
 7 Supplement 2 p. 147-153
7 p.
 artikel
29 Extensive genetic analysis in non-classic CF patients Fichou, Y.
 2008
 7 Supplement 2 p. S7-
1 p.
 artikel
30 Feasibility of nasal epithelial brushing for the study of airway epithelial functions in CF infants Mosler, Katharina
 2008
 7 Supplement 2 p. 44-53
10 p.
 artikel
31 Fifteen years of lung transplantation (LTx) in patients with cystic fibrosis (CF): the Zurich experience Hofer, M.
 2008
 7 Supplement 2 p. S70-
1 p.
 artikel
32 Getting children to wash their hands. What will work? Sharpe, C.
 2008
 7 Supplement 2 p. S105-
1 p.
 artikel
33 High prevalence of inducible clindamycin resistance among Staphylococcus aureus isolates from patients with cystic fibrosis Moore, Zack S.
 2008
 7 Supplement 2 p. 206-209
4 p.
 artikel
34 How long can TIVADS be left unflushed? Govin, B.
 2008
 7 Supplement 2 p. S121-
1 p.
 artikel
35 Hypoglycosylation and disease modifying polymorphism in cystic fibrosis Marklova, E.
 2008
 7 Supplement 2 p. S3-
1 p.
 artikel
36 Immunoglobulin levels in cystic fibrosis patients: influence of age, gender and disease severity Hatziagorou, E.
 2008
 7 Supplement 2 p. S54-
1 p.
 artikel
37 Inhaled high-dose ceftazidime in CF patients with multi-resistant, Gram-negative infections Hansen, C.R.
 2008
 7 Supplement 2 p. S46-
1 p.
 artikel
38 Insights into the structural features of the full length CFTR protein Mornon, J.P.
 2008
 7 Supplement 2 p. S16-
1 p.
 artikel
39 Intravenous methylprednisolone pulse therapy vs. oral prednisone for allergic bronchopulmonary aspergillosis (ABPA) in CF Cohen-Cymberknoh, M.
 2008
 7 Supplement 2 p. S58-
1 p.
 artikel
40 Invasion of Burkholderia cepacia complex isolates into lung epithelial cells involves glycolipid receptors Mullen, T.
 2008
 7 Supplement 2 p. S43-
1 p.
 artikel
41 INVESTIGATION OF CFTR ESONIC REARRANGEMENTS IN INFERTILE COUPLES De Toffol, S.
 2008
 7 Supplement 2 p. S13-
1 p.
 artikel
42 Is intestinal inflammation present in CF patients? Tomasova, H.
 2008
 7 Supplement 2 p. S80-
1 p.
 artikel
43 Is it possible to obtain high adherence to positive expiratory pressure (PEP) in infants with cystic fibrosis (CF) between 0 and 2 years? Jakobsen, U.
 2008
 7 Supplement 2 p. S75-
1 p.
 artikel
44 Is presence of cystic fibrosis-related diabetes really associated with a faster decline in pulmonary functions? van den Berg, J.M.
 2008
 7 Supplement 2 p. S85-
1 p.
 artikel
45 Is there a role for influenza vaccination in cystic fibrosis? Wat, Dennis
 2008
 7 Supplement 2 p. 85-88
4 p.
 artikel
46 Lung clearance index vs. FEV1 in healthy adults and patients with cystic fibrosis Pantalitschka, T.
 2008
 7 Supplement 2 p. S62-
1 p.
 artikel
47 NEW DIAGNOSTIC AND THERAPEUTIC APPROACHES IN CYSTIC FIBROSIS RELATED DIABETES (CFRD) Minicucci, L.
 2008
 7 Supplement 2 p. S6-
1 p.
 artikel
48 New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma Bustamante-Aragones, Ana
 2008
 7 Supplement 2 p. 505-510
6 p.
 artikel
49 Omalizumab – a treatment option against incipient allergic bronchopulmonary aspergillosis when combined with severe allergic asthma and diabetes mellitus Meyer, P.
 2008
 7 Supplement 2 p. S27-
1 p.
 artikel
50 Origin of lactate in CF sputum Worlitzsch, D.
 2008
 7 Supplement 2 p. S39-
1 p.
 artikel
51 Oxidative stress and cystic fibrosis-related diabetes: A pilot study in children Ntimbane, Thierry
 2008
 7 Supplement 2 p. 373-384
12 p.
 artikel
52 Patient held drug information cards MacDougall, L.
 2008
 7 Supplement 2 p. S102-
1 p.
 artikel
53 PULMONARY MALFORMATION AND CYSTIC FIBROSIS (CF): WHICH DIAGNOSIS, HOW TO TREAT AND TIMING OF PROCEDURE (CASE REPORT) Padoan, R.
 2008
 7 Supplement 2 p. S25-
1 p.
 artikel
54 Regulation of the KCa3.1 channel by AMP-activated protein kinase in Cl− secreting cells Klein, H.
 2008
 7 Supplement 2 p. S20-
1 p.
 artikel
55 ROLE OF INFECTIOUS PULMONARY COMPLICATIONS IN LUNG TRANSPLANTATION FOR CYSTIC FIBROSIS: 10 YEARS FOLLOW-UP Locorriere, L.
 2008
 7 Supplement 2 p. S21-
1 p.
 artikel
56 Sleep problems in patients of an Adult Cystic Fibrosis Centre Sharma, I.
 2008
 7 Supplement 2 p. S102-
1 p.
 artikel
57 Stimulation of salivary secretion in vivo by CFTR potentiators in Cftr +/+ and Cftr −/− mice Noël, Sabrina
 2008
 7 Supplement 2 p. 128-133
6 p.
 artikel
58 The changing prevalence of clonal strains of Pseudomonas aeruginosa (Psa) at two Australian CF centres France, M.W.
 2008
 7 Supplement 2 p. S31-
1 p.
 artikel
59 The effect of N-acetylcysteine on chloride efflux from airway epithelial cells Varelogianni, G.
 2008
 7 Supplement 2 p. S24-
1 p.
 artikel
60 The increasing range and complexity of surgery in patients with cystic fibrosis Moisey, E.
 2008
 7 Supplement 2 p. S121-
1 p.
 artikel
61 The pancreas is not visible as an entity by magnetic resonance imaging in the majority of cystic fibrosis patients Sequeiros, I.
 2008
 7 Supplement 2 p. S81-
1 p.
 artikel
62 The revertant mutants G550E and 4RK alter the processing efficiency and gating behaviour of the CF mutant G551D Pissarra, L.S.
 2008
 7 Supplement 2 p. S16-
1 p.
 artikel
63 The sensibility of Ps. aeruginosa isolates in children with cystic fibrosis Chioroglo, E.
 2008
 7 Supplement 2 p. S35-
1 p.
 artikel
64 Transmission of Pseudomonas aeruginosa in children with cystic fibrosis attending summer camps in The Netherlands Brimicombe, R.W.
 2008
 7 Supplement 2 p. 30-36
7 p.
 artikel
65 Treatment requirements and associated costs with lung transplantation in adults with cystic fibrosis Tse, T.
 2008
 7 Supplement 2 p. S70-
1 p.
 artikel
                             65 gevonden resultaten
 
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