| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A false positive newborn screening result due to a complex allele carrying two frequent CF-causing variants
|
Bergougnoux, Anne
|
|
2016
|
15 |
3 |
p. 309-312
4 p.
|
artikel
|
| 2 |
A longitudinal analysis of chronic MRSA and Pseudomonas aeruginosa co-infection in cystic fibrosis: A single-center study
|
Maliniak, Maret L.
|
|
2016
|
15 |
3 |
p. 350-356
7 p.
|
artikel
|
| 3 |
A small molecule neutrophil elastase inhibitor, KRP-109, inhibits cystic fibrosis mucin degradation
|
Chillappagari, Shashi
|
|
2016
|
15 |
3 |
p. 325-331
7 p.
|
artikel
|
| 4 |
Bronchopulmonary infection–colonization patterns in Spanish cystic fibrosis patients: Results from a national multicenter study
|
de Dios Caballero, Juan
|
|
2016
|
15 |
3 |
p. 357-365
9 p.
|
artikel
|
| 5 |
CFTR potentiator therapy ameliorates impaired insulin secretion in CF patients with a gating mutation
|
Tsabari, Reuven
|
|
2016
|
15 |
3 |
p. e25-e27
nvt p.
|
artikel
|
| 6 |
Comparing the harmful effects of nontuberculous mycobacteria and Gram negative bacteria on lung function in patients with cystic fibrosis
|
Qvist, Tavs
|
|
2016
|
15 |
3 |
p. 380-385
6 p.
|
artikel
|
| 7 |
Creation and characterization of an airway epithelial cell line for stable expression of CFTR variants
|
Gottschalk, Laura B.
|
|
2016
|
15 |
3 |
p. 285-294
10 p.
|
artikel
|
| 8 |
Editorial Board
|
|
|
2016
|
15 |
3 |
p. ii-
1 p.
|
artikel
|
| 9 |
Epidemic Pseudomonas aeruginosa infection in patients with cystic fibrosis is not a risk factor for poor clinical Outcomes following lung transplantation
|
Pritchard, Julia
|
|
2016
|
15 |
3 |
p. 392-399
8 p.
|
artikel
|
| 10 |
High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia
|
Petrova, N.V.
|
|
2016
|
15 |
3 |
p. e28-e32
nvt p.
|
artikel
|
| 11 |
Hypoglycaemia in cystic fibrosis in the absence of diabetes: A systematic review
|
Armaghanian, N.
|
|
2016
|
15 |
3 |
p. 274-284
11 p.
|
artikel
|
| 12 |
Implementation of newborn screening for cystic fibrosis in Norway. Results from the first three years
|
Lundman, Emma
|
|
2016
|
15 |
3 |
p. 318-324
7 p.
|
artikel
|
| 13 |
Implementing ICMH-CF (International Committee on Mental Health in CF) guidance on screening for depression and anxiety symptoms: A feasibility and pilot study
|
Duff, A.J.A.
|
|
2016
|
15 |
3 |
p. e33-e34
nvt p.
|
artikel
|
| 14 |
Infant lung function tests as endpoints in the ISIS multicenter clinical trial in cystic fibrosis
|
Davis, Stephanie D.
|
|
2016
|
15 |
3 |
p. 386-391
6 p.
|
artikel
|
| 15 |
Interferon response of the cystic fibrosis bronchial epithelium to major and minor group rhinovirus infection
|
Schögler, Aline
|
|
2016
|
15 |
3 |
p. 332-339
8 p.
|
artikel
|
| 16 |
IV-treated pulmonary exacerbations in the prior year: An important independent risk factor for future pulmonary exacerbation in cystic fibrosis
|
VanDevanter, Donald R.
|
|
2016
|
15 |
3 |
p. 372-379
8 p.
|
artikel
|
| 17 |
Low sodium status in cystic fibrosis—as assessed by calculating fractional Na+ excretion—is associated with decreased growth parameters
|
Knepper, Christiane
|
|
2016
|
15 |
3 |
p. 400-405
6 p.
|
artikel
|
| 18 |
Measurement of fecal elastase improves performance of newborn screening for cystic fibrosis
|
Barben, Juerg
|
|
2016
|
15 |
3 |
p. 313-317
5 p.
|
artikel
|
| 19 |
Microbial colonization and lung function in adolescents with cystic fibrosis
|
Hector, Andreas
|
|
2016
|
15 |
3 |
p. 340-349
10 p.
|
artikel
|
| 20 |
News
|
|
|
2016
|
15 |
3 |
p. 272-273
2 p.
|
artikel
|
| 21 |
Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucus
|
Gianotti, Ambra
|
|
2016
|
15 |
3 |
p. 295-301
7 p.
|
artikel
|
| 22 |
Streptococcus pneumoniae oropharyngeal colonization in children and adolescents with cystic fibrosis
|
Esposito, Susanna
|
|
2016
|
15 |
3 |
p. 366-371
6 p.
|
artikel
|
| 23 |
The benefits of newborn screening for cystic fibrosis: The Canadian experience
|
Mak, D.Y.F.
|
|
2016
|
15 |
3 |
p. 302-308
7 p.
|
artikel
|
| 24 |
Toward quality improvement in cystic fibrosis newborn screening: Progress and continuing challenges
|
Farrell, Philip M.
|
|
2016
|
15 |
3 |
p. 267-269
3 p.
|
artikel
|
| 25 |
Understanding the natural history and clinical implications of airways infections in CF — Moving beyond the classics
|
Parkins, Michael D.
|
|
2016
|
15 |
3 |
p. 270-271
2 p.
|
artikel
|
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