| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A cross-sectional analysis of daytime versus nocturnal polysomnographic respiratory parameters in cystic fibrosis during early adolescence
|
Waters, K.A.
|
|
2017
|
16 |
2 |
p. 250-257
|
artikel
|
| 2 |
Agreement between multiple-breath nitrogen washout systems in children and adults
|
Poncin, William
|
|
2017
|
16 |
2 |
p. 258-266
|
artikel
|
| 3 |
Chest imaging in CF studies - Commentary
|
Eichler, Irmgard
|
|
2017
|
16 |
2 |
p. 173-174
|
artikel
|
| 4 |
Chest imaging in cystic fibrosis studies: What counts, and can be counted?
|
Szczesniak, Rhonda
|
|
2017
|
16 |
2 |
p. 175-185
|
artikel
|
| 5 |
Clostridium difficile carriage in adult cystic fibrosis (CF); implications for patients with CF and the potential for transmission of nosocomial infection
|
Burke, D.G.
|
|
2017
|
16 |
2 |
p. 291-298
|
artikel
|
| 6 |
Counterpoint: Confronting the challenge of non-adherence: Building patient-provider relationships — a patient's perspective
|
Kvam, Christopher M.
|
|
2017
|
16 |
2 |
p. 306-307
|
artikel
|
| 7 |
Counterpoint: Too little care or too little collaboration: Approaches to treatment refusal in CF
|
Sawicki, Gregory S.
|
|
2017
|
16 |
2 |
p. 304-305
|
artikel
|
| 8 |
Cystic fibrosis radiographic biomarkers - Commentary
|
Durmowicz, Anthony G.
|
|
2017
|
16 |
2 |
p. 172
|
artikel
|
| 9 |
Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: A longitudinal study
|
Barr, Helen L.
|
|
2017
|
16 |
2 |
p. 230-238
|
artikel
|
| 10 |
Editorial Board
|
|
|
2017
|
16 |
2 |
p. ii
|
artikel
|
| 11 |
Effect of bronchodilators in healthy individuals receiving lumacaftor/ivacaftor combination therapy
|
Marigowda, Gautham
|
|
2017
|
16 |
2 |
p. 246-249
|
artikel
|
| 12 |
Effect of probiotics on respiratory, gastrointestinal and nutritional outcomes in patients with cystic fibrosis: A systematic review
|
Anderson, Jacqueline L.
|
|
2017
|
16 |
2 |
p. 186-197
|
artikel
|
| 13 |
Fatal disseminated Rasamsonia infection in cystic fibrosis post-lung transplantation
|
Hong, Gina
|
|
2017
|
16 |
2 |
p. e3-e7
|
artikel
|
| 14 |
Hyperpolarized 129Xe for investigation of mild cystic fibrosis lung disease in pediatric patients
|
Thomen, Robert P.
|
|
2017
|
16 |
2 |
p. 275-282
|
artikel
|
| 15 |
MRI accelerating progress in functional assessment of cystic fibrosis lung disease
|
Wielpütz, Mark O.
|
|
2017
|
16 |
2 |
p. 165-167
|
artikel
|
| 16 |
News
|
|
|
2017
|
16 |
2 |
p. 168-169
|
artikel
|
| 17 |
Non-invasive prenatal diagnosis (NIPD) of cystic fibrosis: an optimized protocol using MEMO fluorescent PCR to detect the p.Phe508del mutation
|
Guissart, C.
|
|
2017
|
16 |
2 |
p. 198-206
|
artikel
|
| 18 |
Oxidized glutathione and uric acid as biomarkers of early cystic fibrosis lung disease
|
Dickerhof, Nina
|
|
2017
|
16 |
2 |
p. 214-221
|
artikel
|
| 19 |
Phenotypic shift in Pseudomonas aeruginosa populations from cystic fibrosis lungs after 2-week antipseudomonal treatment
|
Fernández-Barat, Laia
|
|
2017
|
16 |
2 |
p. 222-229
|
artikel
|
| 20 |
Preliminary comparison of normalized T1 and non-contrast perfusion MRI assessments of regional lung disease in cystic fibrosis patients
|
Donnola, Shannon B.
|
|
2017
|
16 |
2 |
p. 283-290
|
artikel
|
| 21 |
The challenges of maintaining momentum in CF drug development and approval - Commentary
|
Flume, Patrick A.
|
|
2017
|
16 |
2 |
p. 170-171
|
artikel
|
| 22 |
The expansion and performance of national newborn screening programmes for cystic fibrosis in Europe
|
Barben, Jürg
|
|
2017
|
16 |
2 |
p. 207-213
|
artikel
|
| 23 |
The impact of cystic fibrosis on work attendance and performance in adults living in rural and remote Western Australia
|
Wood, Jamie
|
|
2017
|
16 |
2 |
p. e1-e2
|
artikel
|
| 24 |
Use of hyperpolarized helium-3 MRI to assess response to ivacaftor treatment in patients with cystic fibrosis
|
Altes, Talissa A.
|
|
2017
|
16 |
2 |
p. 267-274
|
artikel
|
| 25 |
When is too little care, too much harm in cystic fibrosis? Psychological and ethical approaches to the problem
|
Massie, John
|
|
2017
|
16 |
2 |
p. 299-303
|
artikel
|
| 26 |
Year to year change in FEV1 in patients with cystic fibrosis and different mutation classes
|
De Boeck, K
|
|
2017
|
16 |
2 |
p. 239-245
|
artikel
|
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