| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adherence to nebulised therapies for Pseudomonas eradication in a paediatric CF population
|
McCormack, P.
|
|
2008
|
7 |
Supplement 1 |
p. S64-
1 p.
|
artikel
|
| 2 |
Aerosol characteristics of eFlow® using different control units
|
Tservistas, M.
|
|
2008
|
7 |
Supplement 1 |
p. S28-
1 p.
|
artikel
|
| 3 |
A German external quality survey of diagnostic microbiology of respiratory tract infections in patients with cystic fibrosis
|
Balke, Beate
|
|
2008
|
7 |
Supplement 1 |
p. 7-14
8 p.
|
artikel
|
| 4 |
Analysis of the CFTR gene in Iranian cystic fibrosis patients: Identification of eight novel mutations
|
Alibakhshi, Reza
|
|
2008
|
7 |
Supplement 1 |
p. 102-109
8 p.
|
artikel
|
| 5 |
An RCT of macerated garlic oil in patients with CF & chronic Pseudomonas aeruginosa
|
Cifelli, P.
|
|
2008
|
7 |
Supplement 1 |
p. S68-
1 p.
|
artikel
|
| 6 |
Anti-inflammatory effect of miglustat in bronchial epithelial cells
|
Dechecchi, Maria Cristina
|
|
2008
|
7 |
Supplement 1 |
p. 555-565
11 p.
|
artikel
|
| 7 |
Anxiety and depression in CF patients after lung transplantation
|
Matossian, A.
|
|
2008
|
7 |
Supplement 1 |
p. S106-
1 p.
|
artikel
|
| 8 |
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 1 |
p. 60-67
8 p.
|
artikel
|
| 9 |
A QUALITATIVE CHARACTERIZATION OF THE CFTR GENE BY mRNA ANALYSIS
|
Costantino, L.
|
|
2008
|
7 |
Supplement 1 |
p. S11-
1 p.
|
artikel
|
| 10 |
A rare presenting symptom of cystic fibrosis: acrodermatitis enteropathica-like skin eruptions
|
Pekcan, S.
|
|
2008
|
7 |
Supplement 1 |
p. S123-
1 p.
|
artikel
|
| 11 |
A single centre experience of liver disease in adults with cystic fibrosis 1995–2006
|
Nash, K.L.
|
|
2008
|
7 |
Supplement 1 |
p. 252-257
6 p.
|
artikel
|
| 12 |
A solution for severe urinary incontinence in women with cystic fibrosis: a case series
|
Helm, J.
|
|
2008
|
7 |
Supplement 1 |
p. S119-
1 p.
|
artikel
|
| 13 |
CFTR gene mutations in IRT/DNA cystic fibrosis newborn screening in Poland
|
Sobczynska-Tomaszewska, A.
|
|
2008
|
7 |
Supplement 1 |
p. S9-
1 p.
|
artikel
|
| 14 |
Chocolate – thats no way to treat a hypoglycaemic attack!
|
Williams, S.
|
|
2008
|
7 |
Supplement 1 |
p. S95-
1 p.
|
artikel
|
| 15 |
COMMUNICATION OF DIAGNOSIS TO CHILDREN: MEDICAL ROLE
|
Risso, C.
|
|
2008
|
7 |
Supplement 1 |
p. S15-
1 p.
|
artikel
|
| 16 |
COMPARISON AMONG AUXOLOGIC INDEXES TO EVALUATE NUTRITIONAL STATUS OF PEDIATRIC CF PATIENTS AND CREATION OF CF GROWTH CHARTS: A MULTI-CENTRIC ITALIAN STUDY
|
Lucidi, V.
|
|
2008
|
7 |
Supplement 1 |
p. S19-
1 p.
|
artikel
|
| 17 |
Coping with cystic fibrosis – CF adults and parents of a child with CF in Czech Republic
|
Hodkova, P.
|
|
2008
|
7 |
Supplement 1 |
p. S110-
1 p.
|
artikel
|
| 18 |
Cystic fibrosis: A new mutation in the Lebanese population
|
Farra, Chantal
|
|
2008
|
7 |
Supplement 1 |
p. 429-432
4 p.
|
artikel
|
| 19 |
β-DEFENSIN-1 GENE POLYMORPHISMS IN CYSTIC FIBROSIS LUNG DISEASE
|
Santostasi, T.
|
|
2008
|
7 |
Supplement 1 |
p. S12-
1 p.
|
artikel
|
| 20 |
Detection of large intra-CFTR rearrangements by MLPA: utilization of a new web-based software “eMLPA” for the analysis of raw data
|
Camajova, J.
|
|
2008
|
7 |
Supplement 1 |
p. S4-
1 p.
|
artikel
|
| 21 |
Detection of two Alu insertions in the CFTR gene
|
Chen, Jian-Min
|
|
2008
|
7 |
Supplement 1 |
p. 37-43
7 p.
|
artikel
|
| 22 |
DIAGNOSIS IN ATYPICAL CF: A CASE-REPORT TO LEARN
|
Lucidi, V.
|
|
2008
|
7 |
Supplement 1 |
p. S10-S11
2 p.
|
artikel
|
| 23 |
Diagnostic multiplex PCR assay for the identification of the Liverpool, Midlands 1 and Manchester CF epidemic strains of Pseudomonas aeruginosa
|
Fothergill, Joanne L.
|
|
2008
|
7 |
Supplement 1 |
p. 258-261
4 p.
|
artikel
|
| 24 |
Does cough severity influence pelvic fascia displacement in adolescent females with cystic fibrosis?
|
Depiazzi, J.
|
|
2008
|
7 |
Supplement 1 |
p. S76-
1 p.
|
artikel
|
| 25 |
Does the R117H mutation cause cystic fibrosis or not?
|
Norek, A.
|
|
2008
|
7 |
Supplement 1 |
p. S5-
1 p.
|
artikel
|
| 26 |
Effect of multiple aztreonam lysine for inhalation (AZLI) cycles on disease-related endpoints and safety in patients with cystic fibrosis (CF) and Pseudomonas aeruginosa (PA): Interim analysis of 12 month data
|
Oermann, C.
|
|
2008
|
7 |
Supplement 1 |
p. S25-
1 p.
|
artikel
|
| 27 |
Effect on quality of life and treatment adherence of nebulizations duration in cystic fibrosis (CF)
|
Thuilliez, C.
|
|
2008
|
7 |
Supplement 1 |
p. S67-
1 p.
|
artikel
|
| 28 |
Elevated IL-17 and IL-23 mRNA levels in sputum of stable CF patients
|
Decraene, A.
|
|
2008
|
7 |
Supplement 1 |
p. S56-
1 p.
|
artikel
|
| 29 |
Eradication of first sputum isolates of MRSA in adults with cystic fibrosis (CF)
|
Palamarthy, A.B.
|
|
2008
|
7 |
Supplement 1 |
p. S44-
1 p.
|
artikel
|
| 30 |
Evaluation of “patient readiness” to graduate from pediatric to adult health care
|
Gravelle, A.M.
|
|
2008
|
7 |
Supplement 1 |
p. S99-
1 p.
|
artikel
|
| 31 |
EXCEPTIONALLY EARLY OCCURRENCE OF EBV RELATED LYMPHOMA AFTER LUNG TRANSPLANTATION
|
D'Alù, V.
|
|
2008
|
7 |
Supplement 1 |
p. S23-
1 p.
|
artikel
|
| 32 |
EZRIN PHOSPHORYLATION AND ACTIVATION OF RHOA PLAY A ROLE IN THE RESCUE OF ΔF508CFTR IN CFBE41O– CELLS BY NHERF1
|
Favia, M.
|
|
2008
|
7 |
Supplement 1 |
p. S18-S19
2 p.
|
artikel
|
| 33 |
Feasibility of nasal epithelial brushing for the study of airway epithelial functions in CF infants
|
Mosler, Katharina
|
|
2008
|
7 |
Supplement 1 |
p. 44-53
10 p.
|
artikel
|
| 34 |
First year of Polish National CF Newborn Screening
|
Sands, D.A.
|
|
2008
|
7 |
Supplement 1 |
p. S13-
1 p.
|
artikel
|
| 35 |
Gastroesophageal reflux and aspiration in CF patients
|
Blondeau, K.
|
|
2008
|
7 |
Supplement 1 |
p. S79-
1 p.
|
artikel
|
| 36 |
Identification of Burkholderia cepacia complex species by SNuPE and LAMP analysis of histidine biosynthetic genes
|
Papaleo, M.C.
|
|
2008
|
7 |
Supplement 1 |
p. S41-
1 p.
|
artikel
|
| 37 |
Impact on physiotherapy workload at the Leeds Regional Paediatric CF Unit following the first full year of the UK National CF Screening Programme
|
Ball, R.
|
|
2008
|
7 |
Supplement 1 |
p. S14-
1 p.
|
artikel
|
| 38 |
Improvement in clinical markers in CF patients using a reduced glutathione regimen: An uncontrolled, observational study
|
Visca, Alfredo
|
|
2008
|
7 |
Supplement 1 |
p. 433-436
4 p.
|
artikel
|
| 39 |
Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients
|
Raskin, Salmo
|
|
2008
|
7 |
Supplement 1 |
p. 15-22
8 p.
|
artikel
|
| 40 |
Integrating therapeutic education into healthcare: taking up all the opportunities to educate
|
Joachim, H.
|
|
2008
|
7 |
Supplement 1 |
p. S104-
1 p.
|
artikel
|
| 41 |
Is the 1-meter distance enough to prevent cross-infection in cystic fibrosis? Preliminary results of a prospective study
|
Festini, F.
|
|
2008
|
7 |
Supplement 1 |
p. S32-
1 p.
|
artikel
|
| 42 |
Is there a role for influenza vaccination in cystic fibrosis?
|
Wat, Dennis
|
|
2008
|
7 |
Supplement 1 |
p. 85-88
4 p.
|
artikel
|
| 43 |
Methicillin-resistant Staphylococcus aureus infection – what impact in cystic fibrosis patients morbidity?
|
Fermeiro, J.
|
|
2008
|
7 |
Supplement 1 |
p. S45-
1 p.
|
artikel
|
| 44 |
Microbiologic resistance and clinical efficacy of aztreonam lysine for inhalation (AZLI) in cystic fibrosis (CF)
|
McCoy, K.
|
|
2008
|
7 |
Supplement 1 |
p. S36-
1 p.
|
artikel
|
| 45 |
Microvascular complications in patients with cystic fibrosis-related diabetes (CFRD)
|
van den Berg, Johanna M.W.
|
|
2008
|
7 |
Supplement 1 |
p. 515-519
5 p.
|
artikel
|
| 46 |
NATIONAL CONSENSUS STANDARDS FOR THE NURSING MANAGEMENT OF CYSTIC FIBROSIS BY UK CF NURSE SPECIALIST GROUP (MAY 2001): REMARKS AND COMPARISON WITH THE ITALIAN EXPERIENCE
|
Milella, I.
|
|
2008
|
7 |
Supplement 1 |
p. S1-
1 p.
|
artikel
|
| 47 |
NEW DRUGS TO CORRECT THE BASIC CF DEFECT
|
Sheppard, D.N.
|
|
2008
|
7 |
Supplement 1 |
p. S4-
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 1 |
p. 505-510
6 p.
|
artikel
|
| 49 |
Nutritional status in Turkish cystic fibrosis patients
|
Kelebek, O.
|
|
2008
|
7 |
Supplement 1 |
p. S91-
1 p.
|
artikel
|
| 50 |
Occurrence of fungi in the respiratory tract of adults with cystic fibrosis
|
Sauteur, E.
|
|
2008
|
7 |
Supplement 1 |
p. S48-
1 p.
|
artikel
|
| 51 |
Ototoxicity following once daily aminoglycoside administration in adults with CF
|
Elston, C.
|
|
2008
|
7 |
Supplement 1 |
p. S37-
1 p.
|
artikel
|
| 52 |
Pelvic floor muscle training in adolescent females with cystic fibrosis
|
Depiazzi, J.
|
|
2008
|
7 |
Supplement 1 |
p. S72-
1 p.
|
artikel
|
| 53 |
Phase II study in young CF adults with the recombinant acid lipase MERISPASE®
|
Lenoir, G.
|
|
2008
|
7 |
Supplement 1 |
p. S29-
1 p.
|
artikel
|
| 54 |
Plasma ghrelin and leptin in adult cystic fibrosis patients
|
Cohen, Rubin I
|
|
2008
|
7 |
Supplement 1 |
p. 398-402
5 p.
|
artikel
|
| 55 |
Prevalence of cystic fibrosis-related diabetes (CFRD) and its microvascular complications in an adult CF population
|
Choudhury, M.
|
|
2008
|
7 |
Supplement 1 |
p. S83-
1 p.
|
artikel
|
| 56 |
PROLONGING THE DURATION OF PERIPHERAL VENOUS CATHETERS IN CYSTIC FIBROSIS PATIENTS. RANDOMIZED CONTROLLED STUDY ON THE EFFECT OF DIFFERENT CONCENTRATIONS OF ANTIBIOTICS IN NORMAL SALINE
|
Festini, F.
|
|
2008
|
7 |
Supplement 1 |
p. S8-
1 p.
|
artikel
|
| 57 |
Quality of life in women with cystic fibrosis and urinary incontinence
|
Madge, S.
|
|
2008
|
7 |
Supplement 1 |
p. S100-
1 p.
|
artikel
|
| 58 |
Recurrence of PSA after early treatment: a long-term follow-up study
|
Rebmann, K.
|
|
2008
|
7 |
Supplement 1 |
p. S33-
1 p.
|
artikel
|
| 59 |
Renal cyst formation as tool for CFTR research
|
Li, H.
|
|
2008
|
7 |
Supplement 1 |
p. S18-
1 p.
|
artikel
|
| 60 |
Renal impairment in the adult cystic fibrosis population
|
King, S.J.
|
|
2008
|
7 |
Supplement 1 |
p. S87-
1 p.
|
artikel
|
| 61 |
The β-defensin region affects CF lung disease severity
|
Nuytten, H.
|
|
2008
|
7 |
Supplement 1 |
p. S1-
1 p.
|
artikel
|
| 62 |
The effect of vitamin D supplementation on vitamin D level in children with cystic fibrosis (CF)
|
Roddy, M.F.
|
|
2008
|
7 |
Supplement 1 |
p. S92-
1 p.
|
artikel
|
| 63 |
The expert CF patient; an untapped resource
|
MacDonald, K.
|
|
2008
|
7 |
Supplement 1 |
p. S110-
1 p.
|
artikel
|
| 64 |
The prognosis of cystic fibrosis in the Western Cape province of South Africa: a 33 year study
|
Westwood, A.T.
|
|
2008
|
7 |
Supplement 1 |
p. S115-
1 p.
|
artikel
|
| 65 |
The study of cystic fibrosis transmembrane conductance regulator gene mutations in a group of patients from Romania
|
Frenţescu, Lucian
|
|
2008
|
7 |
Supplement 1 |
p. 423-428
6 p.
|
artikel
|
| 66 |
Transient in utero expression of CFTR does not improve survival of CF knockout mice
|
Gill, D.R.
|
|
2008
|
7 |
Supplement 1 |
p. S22-
1 p.
|
artikel
|
| 67 |
Transmission of Pseudomonas aeruginosa in children with cystic fibrosis attending summer camps in The Netherlands
|
Brimicombe, R.W.
|
|
2008
|
7 |
Supplement 1 |
p. 30-36
7 p.
|
artikel
|
| 68 |
Undercarboxylated osteocalcin and bone mass in 8–12 year old children with cystic fibrosis
|
Fewtrell, M.S.
|
|
2008
|
7 |
Supplement 1 |
p. 307-312
6 p.
|
artikel
|
| 69 |
Walking distance as an outcome of antibiotic course in patients with cystic fibrosis
|
Grzincich, G.L.
|
|
2008
|
7 |
Supplement 1 |
p. S60-
1 p.
|
artikel
|
| 70 |
When is a lung function test to be performed evaluating the effects of an airway clearance therapy session in CF?
|
Rodriguez, C.
|
|
2008
|
7 |
Supplement 1 |
p. S75-
1 p.
|
artikel
|
| 71 |
Working capacity and oxygen uptake in CF
|
Gilljam, M.
|
|
2008
|
7 |
Supplement 1 |
p. S60-
1 p.
|
artikel
|
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