| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Association between the introduction of a new cystic fibrosis inhaled antibiotic class and change in prevalence of patients receiving multiple inhaled antibiotic classes
|
Dasenbrook, Elliott C.
|
|
2015
|
14 |
3 |
p. 370-375
6 p.
|
artikel
|
| 2 |
Costs and health-related quality of life of patients with cystic fibrosis and their carers in France
|
Chevreul, Karine
|
|
2015
|
14 |
3 |
p. 384-391
8 p.
|
artikel
|
| 3 |
Cystic fibrosis (cf) and ovarian reserve: A cross-sectional study examining serum anti-mullerian hormone (amh) in young women
|
Schram, C.A.
|
|
2015
|
14 |
3 |
p. 398-402
5 p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
2015
|
14 |
3 |
p. ii-
1 p.
|
artikel
|
| 5 |
Emerging bacterial pathogens and changing concepts of bacterial pathogenesis in cystic fibrosis
|
Parkins, Michael D.
|
|
2015
|
14 |
3 |
p. 293-304
12 p.
|
artikel
|
| 6 |
Genotyping of Pseudomonas aeruginosa reveals high diversity, stability over time and good outcome of eradication
|
Johansson, E.
|
|
2015
|
14 |
3 |
p. 353-360
8 p.
|
artikel
|
| 7 |
Improved repeatability of nasal potential difference with a larger surface catheter
|
Vermeulen, François
|
|
2015
|
14 |
3 |
p. 317-323
7 p.
|
artikel
|
| 8 |
Initial evaluation of the Parent Cystic Fibrosis Questionnaire—Revised (CFQ-R) in infants and young children
|
Alpern, Adrianne N.
|
|
2015
|
14 |
3 |
p. 403-411
9 p.
|
artikel
|
| 9 |
Is infection with hypermutable Pseudomonas aeruginosa clinically significant?
|
Auerbach, Adi
|
|
2015
|
14 |
3 |
p. 347-352
6 p.
|
artikel
|
| 10 |
Ivacaftor and sinonasal pathology in a cystic fibrosis patient with genotype deltaF508/S1215N
|
Vreede, C.L.
|
|
2015
|
14 |
3 |
p. 412-413
2 p.
|
artikel
|
| 11 |
Microbiology review series: CF microbiology — Towards 2020 and beyond
|
Rogers, Geraint B.
|
|
2015
|
14 |
3 |
p. 289-290
2 p.
|
artikel
|
| 12 |
Nasal potential difference: Best or average result for CFTR function as diagnostic criteria for cystic fibrosis?
|
Keenan, Katherine
|
|
2015
|
14 |
3 |
p. 310-316
7 p.
|
artikel
|
| 13 |
News
|
|
|
2015
|
14 |
3 |
p. 291-292
2 p.
|
artikel
|
| 14 |
Protease–antiprotease imbalances differ between Cystic Fibrosis patients' upper and lower airway secretions
|
Hentschel, Julia
|
|
2015
|
14 |
3 |
p. 324-333
10 p.
|
artikel
|
| 15 |
Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years
|
Kidd, Timothy J.
|
|
2015
|
14 |
3 |
p. 361-369
9 p.
|
artikel
|
| 16 |
Pseudomonas aeruginosa in CF and non-CF homes is found predominantly in drains
|
Purdy-Gibson, M.E.
|
|
2015
|
14 |
3 |
p. 341-346
6 p.
|
artikel
|
| 17 |
Pulmonary function outcomes for assessing cystic fibrosis care
|
Wagener, Jeffrey S.
|
|
2015
|
14 |
3 |
p. 376-383
8 p.
|
artikel
|
| 18 |
Serum retinol levels and pulmonary function in children and adolescents with cystic fibrosis
|
Woestenenk, J.W.
|
|
2015
|
14 |
3 |
p. 392-397
6 p.
|
artikel
|
| 19 |
Sputum club cell protein concentration is associated with pulmonary exacerbation in cystic fibrosis
|
Laguna, Theresa A.
|
|
2015
|
14 |
3 |
p. 334-340
7 p.
|
artikel
|
| 20 |
The p.Gly622Asp (G622D) mutation, frequently found in Reunion Island and in black populations, is associated with a wide spectrum of CF and CFTR-RD phenotypes
|
Marion, Heller
|
|
2015
|
14 |
3 |
p. 305-309
5 p.
|
artikel
|
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