| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Audiometric assessment of pediatric patients with cystic fibrosis
|
Kreicher, Kathryn L.
|
|
2018
|
17 |
3 |
p. 383-390
|
artikel
|
| 2 |
Ceftaroline pharmacokinetics and pharmacodynamics in patients with cystic fibrosis
|
Barsky, Emily E.
|
|
2018
|
17 |
3 |
p. e25-e31
|
artikel
|
| 3 |
Comparison of ex vivo and in vitro intestinal cystic fibrosis models to measure CFTR-dependent ion channel activity
|
Zomer-van Ommen, Domenique D.
|
|
2018
|
17 |
3 |
p. 316-324
|
artikel
|
| 4 |
Defining chronic Pseudomonas aeruginosa infection in cystic fibrosis
|
Waters, Valerie
|
|
2018
|
17 |
3 |
p. 292-293
|
artikel
|
| 5 |
Defining palliative care in cystic fibrosis: A Delphi study
|
Dellon, E.P.
|
|
2018
|
17 |
3 |
p. 416-421
|
artikel
|
| 6 |
Developments in cystic fibrosis personalised epithelial assays: Science and patient perspectives
|
Kaiko, Gerard E.
|
|
2018
|
17 |
3 |
p. 289-291
|
artikel
|
| 7 |
Do cystic fibrosis centres with the lowest FEV1 still use the least amount of intravenous antibiotics? A registry-based comparison of intravenous antibiotic use among adult CF centres in the UK
|
Hoo, Zhe Hui
|
|
2018
|
17 |
3 |
p. 360-367
|
artikel
|
| 8 |
Editorial Board
|
|
|
2018
|
17 |
3 |
p. ii
|
artikel
|
| 9 |
Epidemiology of CF: How registries can be used to advance our understanding of the CF population
|
Jackson, Abaigeal D.
|
|
2018
|
17 |
3 |
p. 297-305
|
artikel
|
| 10 |
Glucose trajectories in cystic fibrosis and their association with pulmonary function
|
Reynaud, Quitterie
|
|
2018
|
17 |
3 |
p. 400-406
|
artikel
|
| 11 |
IgG avidity to Pseudomonas aeruginosa over the course of chronic lung biofilm infection in cystic fibrosis
|
Mauch, Renan Marrichi
|
|
2018
|
17 |
3 |
p. 356-359
|
artikel
|
| 12 |
Improvement in Exophiala dermatitidis airway persistence and respiratory decline in response to interferon-gamma therapy in a patient with cystic fibrosis
|
Eades, Christopher P.
|
|
2018
|
17 |
3 |
p. e32-e34
|
artikel
|
| 13 |
Lack of efficacy of Lactobacillus GG in reducing pulmonary exacerbations and hospital admissions in children with cystic fibrosis: A randomised placebo controlled trial
|
Bruzzese, Eugenia
|
|
2018
|
17 |
3 |
p. 375-382
|
artikel
|
| 14 |
Longitudinal development of initial, chronic and mucoid Pseudomonas aeruginosa infection in young children with cystic fibrosis
|
Heltshe, S.L.
|
|
2018
|
17 |
3 |
p. 341-347
|
artikel
|
| 15 |
Mini-guts in a dish: Perspectives of adult Cystic Fibrosis (CF) patients and parents of young CF patients on organoid technology
|
Boers, Sarah N.
|
|
2018
|
17 |
3 |
p. 407-415
|
artikel
|
| 16 |
Multiple reaction monitoring mass spectrometry to identify novel plasma protein biomarkers of treatment response in cystic fibrosis pulmonary exacerbations
|
Roberts, James M.
|
|
2018
|
17 |
3 |
p. 333-340
|
artikel
|
| 17 |
News
|
|
|
2018
|
17 |
3 |
p. 294-296
|
artikel
|
| 18 |
One time quantitative PCR detection of Pseudomonas aeruginosa to discriminate intermittent from chronic infection in cystic fibrosis
|
Boutin, Sébastien
|
|
2018
|
17 |
3 |
p. 348-355
|
artikel
|
| 19 |
Pooling of bronchoalveolar lavage in children with cystic fibrosis does not adversely affect the microbiological yield or sensitivity in detecting pulmonary inflammation
|
McNally, Paul
|
|
2018
|
17 |
3 |
p. 391-399
|
artikel
|
| 20 |
Prevalence of severe fatigue among adults with cystic fibrosis: A single center study
|
Nap-van der Vlist, Merel M.
|
|
2018
|
17 |
3 |
p. 368-374
|
artikel
|
| 21 |
Real life practice of sweat testing in Europe
|
Cirilli, N.
|
|
2018
|
17 |
3 |
p. 325-332
|
artikel
|
| 22 |
Strategies for newborn screening for cystic fibrosis: A systematic review of health economic evaluations
|
Schmidt, Masja
|
|
2018
|
17 |
3 |
p. 306-315
|
artikel
|
| 23 |
The impact of National Cystic Fibrosis Registries: A review series
|
Stephenson, Anne L.
|
|
2018
|
17 |
3 |
p. 287-288
|
artikel
|
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