nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('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. |
artikel |
2 |
Amplification of the challenges facing families with multiple siblings newly diagnosed with CF
|
Armoni, S. |
|
2008 |
7 |
Supplement 3 |
p. S104- 1 p. |
artikel |
3 |
Anxiety and depression in adult patients with cystic fibrosis
|
Heslop Sr, K. |
|
2008 |
7 |
Supplement 3 |
p. S106- 1 p. |
artikel |
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. |
artikel |
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. |
artikel |
6 |
ATYPICAL CYSTIC FIBROSIS ASSOCIATED WITH COMPLEX ALLELE: DIAGNOSTIC AND MANAGEMENT DILEMMAS
|
Polizzi, A.M. |
|
2008 |
7 |
Supplement 3 |
p. S11- 1 p. |
artikel |
7 |
Author Index
|
|
|
2008 |
7 |
Supplement 3 |
p. S125-S134 10 p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
11 |
Clinical and polysomnographic profile in miscigenated patients with cystic fibrosis
|
Ramos, R.T. |
|
2008 |
7 |
Supplement 3 |
p. S60- 1 p. |
artikel |
12 |
Clinical outcome and CF care costs justify the need of newborn screening
|
Skalicka, V. |
|
2008 |
7 |
Supplement 3 |
p. S14- 1 p. |
artikel |
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. |
artikel |
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. |
artikel |
15 |
Comparison of cystic fibrosis inpatient blood glucose monitoring with the unit policy
|
Robb, L. |
|
2008 |
7 |
Supplement 3 |
p. S96- 1 p. |
artikel |
16 |
Comparison of nutritional status and lung function in CF patients in R.Macedonia
|
Spirevska, L. |
|
2008 |
7 |
Supplement 3 |
p. S91- 1 p. |
artikel |
17 |
Consideration on relation between pulmonary status and MBL deficiency in CF patients
|
Popa, I. |
|
2008 |
7 |
Supplement 3 |
p. S61- 1 p. |
artikel |
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. |
artikel |
19 |
Cystic fibrosis and gender: a complex relationship
|
Trouvé, P. |
|
2008 |
7 |
Supplement 3 |
p. S68- 1 p. |
artikel |
20 |
Cystic fibrosis and tobacco smoke exposure
|
Cloquet, D. |
|
2008 |
7 |
Supplement 3 |
p. S100- 1 p. |
artikel |
21 |
Cystic fibrosis-related diabetes (CFRD) in the Czech Republic
|
Kolouskova, S. |
|
2008 |
7 |
Supplement 3 |
p. S84- 1 p. |
artikel |
22 |
Developing a musculoskeletal service for adults with cystic fibrosis
|
Ruane, M. |
|
2008 |
7 |
Supplement 3 |
p. S72- 1 p. |
artikel |
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. |
artikel |
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. |
artikel |
25 |
Do prophylactic antibiotics reduce isolation of Staphylococcus aureus in adult CF patients?
|
Brennan, A.L. |
|
2008 |
7 |
Supplement 3 |
p. S45- 1 p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
29 |
Emergence and spread of a phylogenetic cluster of Corynebacteria in cystic fibrosis patients
|
Cassagne, C. |
|
2008 |
7 |
Supplement 3 |
p. S49- 1 p. |
artikel |
30 |
ENaCβ and γ genes as modifier genes in cystic fibrosis
|
Viel, Marion |
|
2008 |
7 |
Supplement 3 |
p. 23-29 7 p. |
artikel |
31 |
Enteropathy – a new finding in cystic fibrosis
|
Werlin, S. |
|
2008 |
7 |
Supplement 3 |
p. S79- 1 p. |
artikel |
32 |
Establishing sweat salt levels in normal healthy adults
|
Senthamilarasu, P. |
|
2008 |
7 |
Supplement 3 |
p. S10- 1 p. |
artikel |
33 |
Evaluation of CF database in Republic of Macedonia
|
Jakovska-Maretti, T. |
|
2008 |
7 |
Supplement 3 |
p. S116- 1 p. |
artikel |
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. |
artikel |
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. |
artikel |
36 |
First European CF microbiology quality assurance trial
|
Hogardt, M. |
|
2008 |
7 |
Supplement 3 |
p. S30- 1 p. |
artikel |
37 |
HOME INTRAVENOUS ANTIBIOTIC THERAPY IN CYSTIC FIBROSIS PATIENTS
|
Zappa, C. |
|
2008 |
7 |
Supplement 3 |
p. S8- 1 p. |
artikel |
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. |
artikel |
39 |
Immunomodulatory properties of vitamin D in Scandinavian cystic fibrosis patients
|
Pincikova, T. |
|
2008 |
7 |
Supplement 3 |
p. S52- 1 p. |
artikel |
40 |
Impaired glucose metabolism in patients with CF during acute exacerbations
|
Nezer, N. |
|
2008 |
7 |
Supplement 3 |
p. S83- 1 p. |
artikel |
41 |
IMPROVEMENT OF MOLECULAR TECHNOLOGIES AND PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS
|
Pelo, E. |
|
2008 |
7 |
Supplement 3 |
p. S11-S12 2 p. |
artikel |
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. |
artikel |
43 |
Is there a role for influenza vaccination in cystic fibrosis?
|
Wat, Dennis |
|
2008 |
7 |
Supplement 3 |
p. 85-88 4 p. |
artikel |
44 |
LONG TERM FOLLOW-UP OF A CYSTIC FIBROSIS (CF) PATIENT WITH PREVIOUS NEUROBLASTOMA
|
Casciaro, R. |
|
2008 |
7 |
Supplement 3 |
p. S24- 1 p. |
artikel |
45 |
Management of adults with CF: what assessments and interventions do physiotherapists value?
|
Stiller, K. |
|
2008 |
7 |
Supplement 3 |
p. S76- 1 p. |
artikel |
46 |
Method validation in cystic fibrosis DNA diagnostics: a basic tool for quality assurance
|
Stambergova, A. |
|
2008 |
7 |
Supplement 3 |
p. S5- 1 p. |
artikel |
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. |
artikel |
48 |
Optimal delivery of end of life care for CF patients families and staff
|
Braithwaite, M. |
|
2008 |
7 |
Supplement 3 |
p. S100- 1 p. |
artikel |
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. |
artikel |
50 |
Plasma ghrelin and leptin in adult cystic fibrosis patients
|
Cohen, Rubin I |
|
2008 |
7 |
Supplement 3 |
p. 398-402 5 p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
54 |
QUALITY OF LIFE IN ITALIAN PATIENTS WITH CYSTIC FIBROSIS (CF)
|
Bella, S. |
|
2008 |
7 |
Supplement 3 |
p. S15- 1 p. |
artikel |
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. |
artikel |
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. |
artikel |
57 |
Testosterone deficiency in adult males with cystic fibrosis
|
Katz, M.F. |
|
2008 |
7 |
Supplement 3 |
p. S87- 1 p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
61 |
THE COMMUNICATION IN THE TEAM: ASSERTIVENESS AND CONFLICT MANAGEMENT
|
Ferens, S. |
|
2008 |
7 |
Supplement 3 |
p. S1- 1 p. |
artikel |
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. |
artikel |
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. |
artikel |
64 |
THE EUROPEAN CYSTIC FIBROSIS REGISTRY
|
Mehta, A. |
|
2008 |
7 |
Supplement 3 |
p. S4-S5 2 p. |
artikel |
65 |
The variable phenotype of (TGJ^Ts or L997F compound heterozygotes
|
Narzi, L. |
|
2008 |
7 |
Supplement 3 |
p. S5- 1 p. |
artikel |
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. |
artikel |