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                             66 results found
no title author magazine year volume issue page(s) type
1 Activation of chloride secretion in human airway epithelial cells by a new pyrrolo[2,3-b]pyrazine Dannhoffer, L.
 2008
 7 Supplement 3 p. S18-
1 p.
 article
2 Amplification of the challenges facing families with multiple siblings newly diagnosed with CF Armoni, S.
 2008
 7 Supplement 3 p. S104-
1 p.
 article
3 Anxiety and depression in adult patients with cystic fibrosis Heslop Sr, K.
 2008
 7 Supplement 3 p. S106-
1 p.
 article
4 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 3 p. 60-67
8 p.
 article
5 Aspergillus fumigatus-induced IL-8 synthesis by bronchial epithelial cells: lack of involvement of the TLR-MyD88 pathway Balloy, V.
 2008
 7 Supplement 3 p. S56-
1 p.
 article
6 ATYPICAL CYSTIC FIBROSIS ASSOCIATED WITH COMPLEX ALLELE: DIAGNOSTIC AND MANAGEMENT DILEMMAS Polizzi, A.M.
 2008
 7 Supplement 3 p. S11-
1 p.
 article
7 Author Index 2008
 7 Supplement 3 p. S125-S134
10 p.
 article
8 Bone mineral density and serum vitamin D levels in children with cystic fibrosis (CF) Jones, K.
 2008
 7 Supplement 3 p. S92-
1 p.
 article
9 Bone mineral density in cystic fibrosis patients – a 3-years follow-up and intervention Ocenaskova, E.
 2008
 7 Supplement 3 p. S90-
1 p.
 article
10 Changing features of patients with cystic fibrosis (CF) referred for lung transplantation assessment Doe, S.J.
 2008
 7 Supplement 3 p. S28-
1 p.
 article
11 Clinical and polysomnographic profile in miscigenated patients with cystic fibrosis Ramos, R.T.
 2008
 7 Supplement 3 p. S60-
1 p.
 article
12 Clinical outcome and CF care costs justify the need of newborn screening Skalicka, V.
 2008
 7 Supplement 3 p. S14-
1 p.
 article
13 Clinical value of Aspergillus detection in sputum obtained from 84 patients with cystic fibrosis Roussey, M.
 2008
 7 Supplement 3 p. S49-
1 p.
 article
14 Comparison of culture and molecular methods for detection and quantitation of aerobic and anaerobic bacteria in sputum from cystic fibrosis patients Tunney, M.M.
 2008
 7 Supplement 3 p. S41-
1 p.
 article
15 Comparison of cystic fibrosis inpatient blood glucose monitoring with the unit policy Robb, L.
 2008
 7 Supplement 3 p. S96-
1 p.
 article
16 Comparison of nutritional status and lung function in CF patients in R.Macedonia Spirevska, L.
 2008
 7 Supplement 3 p. S91-
1 p.
 article
17 Consideration on relation between pulmonary status and MBL deficiency in CF patients Popa, I.
 2008
 7 Supplement 3 p. S61-
1 p.
 article
18 Copying letters to patients with cystic fibrosis (CF): Letter content and patient perceptions of benefit Treacy, Katherine
 2008
 7 Supplement 3 p. 511-514
4 p.
 article
19 Cystic fibrosis and gender: a complex relationship Trouvé, P.
 2008
 7 Supplement 3 p. S68-
1 p.
 article
20 Cystic fibrosis and tobacco smoke exposure Cloquet, D.
 2008
 7 Supplement 3 p. S100-
1 p.
 article
21 Cystic fibrosis-related diabetes (CFRD) in the Czech Republic Kolouskova, S.
 2008
 7 Supplement 3 p. S84-
1 p.
 article
22 Developing a musculoskeletal service for adults with cystic fibrosis Ruane, M.
 2008
 7 Supplement 3 p. S72-
1 p.
 article
23 Development of a novel PCR assay for the identification of the black yeast, Exophiala (Wangiella) dermatitidis from adult patients with cystic fibrosis (CF) Nagano, Yuriko
 2008
 7 Supplement 3 p. 576-580
5 p.
 article
24 Disease severity in cystic fibrosis is modified by variants of the syntaxin 1A gene von Kanel, T.
 2008
 7 Supplement 3 p. S1-
1 p.
 article
25 Do prophylactic antibiotics reduce isolation of Staphylococcus aureus in adult CF patients? Brennan, A.L.
 2008
 7 Supplement 3 p. S45-
1 p.
 article
26 Early aggressive eradication therapy for intermittent Pseudomonas aeruginosa airway colonization in cystic fibrosis patients: 15 years experience Hansen, C.R.
 2008
 7 Supplement 3 p. 523-530
8 p.
 article
27 Early eradication therapy for Pseudomonas aeruginosa: impact of prior clinical status pseudomonas antibody level and antibiotic regimen on success rates Etherington, C.
 2008
 7 Supplement 3 p. S33-
1 p.
 article
28 Efficiency and compliance of physiotherapy combined techniques in children with age between 3 and 6 years Almăjan-Gută, B.
 2008
 7 Supplement 3 p. S75-
1 p.
 article
29 Emergence and spread of a phylogenetic cluster of Corynebacteria in cystic fibrosis patients Cassagne, C.
 2008
 7 Supplement 3 p. S49-
1 p.
 article
30 ENaCβ and γ genes as modifier genes in cystic fibrosis Viel, Marion
 2008
 7 Supplement 3 p. 23-29
7 p.
 article
31 Enteropathy – a new finding in cystic fibrosis Werlin, S.
 2008
 7 Supplement 3 p. S79-
1 p.
 article
32 Establishing sweat salt levels in normal healthy adults Senthamilarasu, P.
 2008
 7 Supplement 3 p. S10-
1 p.
 article
33 Evaluation of CF database in Republic of Macedonia Jakovska-Maretti, T.
 2008
 7 Supplement 3 p. S116-
1 p.
 article
34 Experience of inhaled tobramycin: impact in microbiological and clinical parameters in patients with cystic fibrosis Castanhinha, S.
 2008
 7 Supplement 3 p. S37-
1 p.
 article
35 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 3 p. 147-153
7 p.
 article
36 First European CF microbiology quality assurance trial Hogardt, M.
 2008
 7 Supplement 3 p. S30-
1 p.
 article
37 HOME INTRAVENOUS ANTIBIOTIC THERAPY IN CYSTIC FIBROSIS PATIENTS Zappa, C.
 2008
 7 Supplement 3 p. S8-
1 p.
 article
38 ‘I am normal’: young peoples perspectives of CF and the influence this has on treatment adherence Hogan, J.
 2008
 7 Supplement 3 p. S111-
1 p.
 article
39 Immunomodulatory properties of vitamin D in Scandinavian cystic fibrosis patients Pincikova, T.
 2008
 7 Supplement 3 p. S52-
1 p.
 article
40 Impaired glucose metabolism in patients with CF during acute exacerbations Nezer, N.
 2008
 7 Supplement 3 p. S83-
1 p.
 article
41 IMPROVEMENT OF MOLECULAR TECHNOLOGIES AND PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS Pelo, E.
 2008
 7 Supplement 3 p. S11-S12
2 p.
 article
42 Inhaled tobramycin nebulizer solution for treatment of early Pseudomonas aeruginosa infection: the ELITE study Ratjen, F.
 2008
 7 Supplement 3 p. S26-
1 p.
 article
43 Is there a role for influenza vaccination in cystic fibrosis? Wat, Dennis
 2008
 7 Supplement 3 p. 85-88
4 p.
 article
44 LONG TERM FOLLOW-UP OF A CYSTIC FIBROSIS (CF) PATIENT WITH PREVIOUS NEUROBLASTOMA Casciaro, R.
 2008
 7 Supplement 3 p. S24-
1 p.
 article
45 Management of adults with CF: what assessments and interventions do physiotherapists value? Stiller, K.
 2008
 7 Supplement 3 p. S76-
1 p.
 article
46 Method validation in cystic fibrosis DNA diagnostics: a basic tool for quality assurance Stambergova, A.
 2008
 7 Supplement 3 p. S5-
1 p.
 article
47 New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma Bustamante-Aragones, Ana
 2008
 7 Supplement 3 p. 505-510
6 p.
 article
48 Optimal delivery of end of life care for CF patients families and staff Braithwaite, M.
 2008
 7 Supplement 3 p. S100-
1 p.
 article
49 Perceived adherence of adults with cystic fibrosis and the views of the multidisciplinary team Plummer, A.
 2008
 7 Supplement 3 p. S119-
1 p.
 article
50 Plasma ghrelin and leptin in adult cystic fibrosis patients Cohen, Rubin I
 2008
 7 Supplement 3 p. 398-402
5 p.
 article
51 Prevalence and antimicrobial susceptibility of microorganisms isolated from sputa of patients with cystic fibrosis Valenza, Giuseppe
 2008
 7 Supplement 3 p. 123-127
5 p.
 article
52 PTC124 induces CFTR full-length production and activity in children with nonsense-mutation-mediated CF Sermet-Gaudelus, I.
 2008
 7 Supplement 3 p. S22-
1 p.
 article
53 PTC124 treatment over 3 months improves pharmacodynamic and clinical parameters in patients with nonsense-mutation-mediated CF Wilschanski, M.
 2008
 7 Supplement 3 p. S22-
1 p.
 article
54 QUALITY OF LIFE IN ITALIAN PATIENTS WITH CYSTIC FIBROSIS (CF) Bella, S.
 2008
 7 Supplement 3 p. S15-
1 p.
 article
55 RECURRENT PANCREATITIS AS THE FIRST MANIFESTATION OF CYSTIC FIBROSIS: A SINGLE CENTRE EXPERIENCE Lucidi, V.
 2008
 7 Supplement 3 p. S19-S20
2 p.
 article
56 Reported and objective adherence to nebulised therapy in adult patients with cystic fibrosis Hughes, T.E.
 2008
 7 Supplement 3 p. S64-
1 p.
 article
57 Testosterone deficiency in adult males with cystic fibrosis Katz, M.F.
 2008
 7 Supplement 3 p. S87-
1 p.
 article
58 The CD73/adenosine pathway regulates gap junctional intercellular communication in the CFTR-expressing Calu-3 airway cell line Scheckenbach, L.K.
 2008
 7 Supplement 3 p. S19-
1 p.
 article
59 The changing epidemiology of Burkholderia species infection at an adult cystic fibrosis centre France, Megan W.
 2008
 7 Supplement 3 p. 368-372
5 p.
 article
60 The characteristic of children with cystic fibrosis from Moldova according to European Registry criteria Sciuca, S.
 2008
 7 Supplement 3 p. S115-
1 p.
 article
61 THE COMMUNICATION IN THE TEAM: ASSERTIVENESS AND CONFLICT MANAGEMENT Ferens, S.
 2008
 7 Supplement 3 p. S1-
1 p.
 article
62 The effect of inhaled steroids on bronchial hyperreactivity, oxidative status clinical and inflammatory parameters in patients with cystic fibrosis Uyan, Z.S.
 2008
 7 Supplement 3 p. S68-
1 p.
 article
63 The effect of long term use of rhDNAse on pulmonary colonisation in children with cystic fibrosis Bonestroo, H.
 2008
 7 Supplement 3 p. S37-
1 p.
 article
64 THE EUROPEAN CYSTIC FIBROSIS REGISTRY Mehta, A.
 2008
 7 Supplement 3 p. S4-S5
2 p.
 article
65 The variable phenotype of (TGJ^Ts or L997F compound heterozygotes Narzi, L.
 2008
 7 Supplement 3 p. S5-
1 p.
 article
66 TOTIRESISTENT BURKHOLDERIA CEPACIA COMPLEX SEPSIS IN A 62-YEAR-OLD WOMAN WITH CYSTIC FIBROSIS Antonelli, A.
 2008
 7 Supplement 3 p. S23-
1 p.
 article
                             66 results found
 
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