| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
65 Acute respiratory infections in young CF children
|
van Ewijk, B.
|
|
2006
|
5 |
Supplement 1 |
p. S15-
1 p.
|
artikel
|
| 2 |
Altered steady state pharmacokinetics of levofloxacin in adult cystic fibrosis patients receiving calcium carbonate
|
Pai, Manjunath P.
|
|
2006
|
5 |
Supplement 1 |
p. 153-157
5 p.
|
artikel
|
| 3 |
290 Aquagenic wrinkling of the palms in patients with Cystic Fibrosis: a pilot study
|
Tolland, J.P.
|
|
2006
|
5 |
Supplement 1 |
p. S68-
1 p.
|
artikel
|
| 4 |
311 A randomised controlled trial of a behavioural nutrition education programme “Eat Well with CF” for adults with CF
|
Watson, H.
|
|
2006
|
5 |
Supplement 1 |
p. S73-
1 p.
|
artikel
|
| 5 |
431 Audit of End-of-Life care in Cystic Fibrosis in Australia
|
Finlayson, E.
|
|
2006
|
5 |
Supplement 1 |
p. S96-
1 p.
|
artikel
|
| 6 |
115 Azithromycin affects the processing of tight junction proteins and ENaC in human airway epithelia in vitro
|
Asgrimsson, V.
|
|
2006
|
5 |
Supplement 1 |
p. S26-
1 p.
|
artikel
|
| 7 |
276 Bone age in English children with CF using the RUS (TW2) method
|
Hattingh, L.
|
|
2006
|
5 |
Supplement 1 |
p. S64-
1 p.
|
artikel
|
| 8 |
130 Characteristics of a new transmissible multiresistant Pseudomonas aeruginosa strain with a unique genotype
|
Meyer, P.
|
|
2006
|
5 |
Supplement 1 |
p. S29-
1 p.
|
artikel
|
| 9 |
349 Chest physiotherapy in Cystic Fibrosis: short-term effects of Autogenic Drainage combined with wet inhalation of saline (saline-AD) versus Autogenic Drainage combined with Intrapulmonary Percussive Ventilation with saline (IPV-AD)
|
Van Cauwelaert, K.
|
|
2006
|
5 |
Supplement 1 |
p. S77-
1 p.
|
artikel
|
| 10 |
28 Curcumin rescues deltaF508-CFTR via the keratin 18 network
|
Lipecka, J.
|
|
2006
|
5 |
Supplement 1 |
p. S6-
1 p.
|
artikel
|
| 11 |
10 cystic fibrosis: genetic-clinical correlation
|
González, C.
|
|
2006
|
5 |
Supplement 1 |
p. S3-
1 p.
|
artikel
|
| 12 |
Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Asians with chronic pulmonary disease: A pilot study
|
Ngiam, Nicola S.P.
|
|
2006
|
5 |
Supplement 1 |
p. 159-164
6 p.
|
artikel
|
| 13 |
177 Delivery of tobramycin via the I-nebTM adaptive aerosol delivery (AADO) system and the Pari LC Plus® nebulizer
|
Hardaker, L.E.
|
|
2006
|
5 |
Supplement 1 |
p. S41-
1 p.
|
artikel
|
| 14 |
485 Detection of CFTR mutations using a 4-MATTM microarray technology
|
Van Loon, C.
|
|
2006
|
5 |
Supplement 1 |
p. S106-
1 p.
|
artikel
|
| 15 |
211 Determinants of dyspnoea in Cystic Fibrosis: impact of inspiratory muscles endurance
|
Leroy, S.
|
|
2006
|
5 |
Supplement 1 |
p. S49-
1 p.
|
artikel
|
| 16 |
257 Different evolution in CF patients with hepatobiliary disease and identical genotype
|
Popa, I.M.
|
|
2006
|
5 |
Supplement 1 |
p. S60-
1 p.
|
artikel
|
| 17 |
273 Does insulin treatment influence growth and lung function in children with abnormal oral glucose tolerance test (OGTT) but normal fasting glucose?
|
Hardy, J.
|
|
2006
|
5 |
Supplement 1 |
p. S64-
1 p.
|
artikel
|
| 18 |
Dysregulated interleukin-8 secretion and NF-κB activity in human cystic fibrosis nasal epithelial cells
|
Carrabino, Salvatore
|
|
2006
|
5 |
Supplement 1 |
p. 113-119
7 p.
|
artikel
|
| 19 |
400 Effecting change with creative thinking: outpatient intravenous antibiotic utilisation
|
Player, R.
|
|
2006
|
5 |
Supplement 1 |
p. S88-
1 p.
|
artikel
|
| 20 |
144 Effect of nebuliser suspension solutions on survival of Pseudomonas aeruginosa (PA) within artificially generated aerosols
|
Clifton, I.J.
|
|
2006
|
5 |
Supplement 1 |
p. S33-
1 p.
|
artikel
|
| 21 |
243 Enhanced coefficient of fat absorption using a novel pancreatic enzyme preparation, ALTU-135, with concomitant use of a proton pump inhibitor
|
Borowitz, D.
|
|
2006
|
5 |
Supplement 1 |
p. S56-
1 p.
|
artikel
|
| 22 |
240 Exocrine pancreatic function and resting energy expenditure in Cystic Fibrosis
|
Moudiou, T.
|
|
2006
|
5 |
Supplement 1 |
p. S56-
1 p.
|
artikel
|
| 23 |
83 Exopolysaccharide production in the Burkholderia cepacia in response to growth on onion agar
|
Bartholdson, J.
|
|
2006
|
5 |
Supplement 1 |
p. S19-
1 p.
|
artikel
|
| 24 |
397 Exploring adolescents' adherence to CF treatment regimes
|
Cowlard, J.
|
|
2006
|
5 |
Supplement 1 |
p. S88-
1 p.
|
artikel
|
| 25 |
428 Extramural care of the specialist CF social worker
|
Tijtgat, A.
|
|
2006
|
5 |
Supplement 1 |
p. S95-
1 p.
|
artikel
|
| 26 |
Fecal elastase-1: Utility in pancreatic function in cystic fibrosis
|
Daftary, Ameet
|
|
2006
|
5 |
Supplement 1 |
p. 71-76
6 p.
|
artikel
|
| 27 |
376 Functional health status in Cystic Fibrosis
|
Saveci, S.
|
|
2006
|
5 |
Supplement 1 |
p. S83-
1 p.
|
artikel
|
| 28 |
7 Identification of DNA variants in non-coding regions of the CFTR gene
|
Markiewicz, D.
|
|
2006
|
5 |
Supplement 1 |
p. S2-
1 p.
|
artikel
|
| 29 |
147 Identification of genomovar status, virulence genes and genotyping of Burkholderia cepacia complex strains isolated from Brazilian CF patients
|
Martins, K.M.
|
|
2006
|
5 |
Supplement 1 |
p. S33-
1 p.
|
artikel
|
| 30 |
Influence of digital clubbing on oxygen saturation measurements by pulse-oximetry in cystic fibrosis patients
|
Van Ginderdeuren, Filip
|
|
2006
|
5 |
Supplement 1 |
p. 125-128
4 p.
|
artikel
|
| 31 |
445 Inhalation therapy compliance in teen patients with Cystic Fibrosis
|
González Peralta, N.
|
|
2006
|
5 |
Supplement 1 |
p. S100-
1 p.
|
artikel
|
| 32 |
46 Inhaled dry powder mannitol (Bronchitol) improves FEV1 in Cystic Fibrosis
|
Charlton, B.
|
|
2006
|
5 |
Supplement 1 |
p. S11-
1 p.
|
artikel
|
| 33 |
42 Nasal epithelial brushing: a valuable method to study airway epithelial cells in CF and non-CF infants
|
Mosler, K.
|
|
2006
|
5 |
Supplement 1 |
p. S10-
1 p.
|
artikel
|
| 34 |
475 Newborn cystic fibrosis (CF) screening in Canada: Our first experience
|
Montgomery, M.D.
|
|
2006
|
5 |
Supplement 1 |
p. S104-
1 p.
|
artikel
|
| 35 |
308 Nutritional therapy for catch-up growth in malnourished infants with Cystic Fibrosis — the role of semi-elemental formula with medium chain triglycerides
|
Mosescu, S.
|
|
2006
|
5 |
Supplement 1 |
p. S72-
1 p.
|
artikel
|
| 36 |
Phenotypic discordance in three siblings affected by atypical cystic fibrosis with the F508del/D614G genotype
|
Castaldo, Giuseppe
|
|
2006
|
5 |
Supplement 1 |
p. 193-195
3 p.
|
artikel
|
| 37 |
414 Pregnancy in Cystic Fibrosis — a multidisciplinary approach
|
Lyons, A.M.
|
|
2006
|
5 |
Supplement 1 |
p. S92-
1 p.
|
artikel
|
| 38 |
359 Prevalence and importance of muscle weakness in adults with CF
|
Vrijsen, B.
|
|
2006
|
5 |
Supplement 1 |
p. S79-
1 p.
|
artikel
|
| 39 |
180 Pulmonary deposition of inhaled tobramycin (TOBI), before and after physiotherapy and inhaled salbutamol and correlation with Shwachman Score (SS) in Cystic Fibrosis (CF) patients
|
Grotta, M.B.
|
|
2006
|
5 |
Supplement 1 |
p. S41-
1 p.
|
artikel
|
| 40 |
Relationship between glycosylated haemoglobin and mean plasma glucose concentration in cystic fibrosis
|
Brennan, Amanda L.
|
|
2006
|
5 |
Supplement 1 |
p. 27-31
5 p.
|
artikel
|
| 41 |
221 Relationship between growth, nutritional status and pulmonary function in children and adolescents with Cystic Fibrosis
|
Hatziagorou, E.
|
|
2006
|
5 |
Supplement 1 |
p. S52-
1 p.
|
artikel
|
| 42 |
194 Remote monitoring in the early detection of pulmonary exacerbation in Cystic Fibrosis
|
Sarfaraz, S.
|
|
2006
|
5 |
Supplement 1 |
p. S45-
1 p.
|
artikel
|
| 43 |
488 Severe and mild CFTR genotypes: age and presenting symptoms in patients diagnosed through newborn screening versus clinical symptoms
|
Munck, A.
|
|
2006
|
5 |
Supplement 1 |
p. S107-
1 p.
|
artikel
|
| 44 |
Stem cells and cystic fibrosis
|
Conese, Massimo
|
|
2006
|
5 |
Supplement 1 |
p. 141-143
3 p.
|
artikel
|
| 45 |
105 The determination of the synergistic antibiotic combinations for the treatment of multiresistant Pseudomonas aeruginosa isolates from CF patients
|
Sener, B.
|
|
2006
|
5 |
Supplement 1 |
p. S23-
1 p.
|
artikel
|
| 46 |
The genetic background of osteoporosis in cystic fibrosis: Association analysis with polymorphic markers in four candidate genes
|
Castellani, Carlo
|
|
2006
|
5 |
Supplement 1 |
p. 229-235
7 p.
|
artikel
|
| 47 |
161 The impact of Scedosporium and Exophiala in sputum samples on the clinical progress of patients with CF
|
Barker, L.
|
|
2006
|
5 |
Supplement 1 |
p. S37-
1 p.
|
artikel
|
| 48 |
504 Three methods of monitoring adherence in a long-term trial in Cystic Fibrosis
|
Elkins, M.
|
|
2006
|
5 |
Supplement 1 |
p. S111-
1 p.
|
artikel
|
| 49 |
102 Treatment of intermittent Pseudomonas aeruginosa colonization with colistin and ciprofloxacin result in very low antibiotic resistance — 15 years follow up
|
Hansen, C.R.
|
|
2006
|
5 |
Supplement 1 |
p. S22-
1 p.
|
artikel
|
| 50 |
Unresponsive or non-compliant steatorrhea in cystic fibrosis?
|
Lisowska, Aleksandra
|
|
2006
|
5 |
Supplement 1 |
p. 253-255
3 p.
|
artikel
|
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