nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A comorbidity of CF in need of our attention and activity: Attention Deficit Hyperactivity Disorder!
|
Lemiere, Jurgen |
|
2018 |
17 |
2 |
p. 135-136 |
artikel |
2 |
A guide to interpreting estimated median age of survival in cystic fibrosis patient registry reports
|
Keogh, Ruth H. |
|
2018 |
17 |
2 |
p. 213-217 |
artikel |
3 |
Attention deficit hyperactivity disorder symptoms in patients with cystic fibrosis
|
Cohen-Cymberknoh, Malena |
|
2018 |
17 |
2 |
p. 281-285 |
artikel |
4 |
Blood flow regulation and oxidative stress during submaximal cycling exercise in patients with cystic fibrosis
|
Tucker, Matthew A. |
|
2018 |
17 |
2 |
p. 256-263 |
artikel |
5 |
Colistin resistance in Pseudomonas aeruginosa and Achromobacter spp. cultured from Danish cystic fibrosis patients is not related to plasmid-mediated expression of mcr-1
|
Pedersen, Maya G. |
|
2018 |
17 |
2 |
p. e22-e23 |
artikel |
6 |
ECFS best practice guidelines: the 2018 revision
|
Castellani, Carlo |
|
2018 |
17 |
2 |
p. 153-178 |
artikel |
7 |
Editorial Board
|
|
|
2018 |
17 |
2 |
p. ii |
artikel |
8 |
Effect of Lumacaftor/Ivacaftor on glucose metabolism and insulin secretion in Phe508del homozygous cystic fibrosis patients
|
Thomassen, Jan C. |
|
2018 |
17 |
2 |
p. 271-275 |
artikel |
9 |
Exploring probiotic use in a regional cystic fibrosis consortium
|
Gonzalez, K.D. |
|
2018 |
17 |
2 |
p. e20-e21 |
artikel |
10 |
FAM13A is a modifier gene of cystic fibrosis lung phenotype regulating rhoa activity, actin cytoskeleton dynamics and epithelial-mesenchymal transition
|
Corvol, Harriet |
|
2018 |
17 |
2 |
p. 190-203 |
artikel |
11 |
In statistics we trust: Towards the careful derivation and interpretation of meaningful survival estimates in cystic fibrosis
|
Mayer-Hamblett, N. |
|
2018 |
17 |
2 |
p. 133-134 |
artikel |
12 |
Ivacaftor restores CFTR-dependent sweat gland fluid secretion in cystic fibrosis subjects with S945L alleles
|
Kim, Jeeyeon |
|
2018 |
17 |
2 |
p. 179-185 |
artikel |
13 |
Ivacaftor withdrawal syndrome in cystic fibrosis patients with the G551D mutation
|
Trimble, Aaron T. |
|
2018 |
17 |
2 |
p. e13-e16 |
artikel |
14 |
Lumacaftor/ivacaftor in patients with cystic fibrosis and advanced lung disease homozygous for F508del-CFTR
|
Taylor-Cousar, Jennifer L. |
|
2018 |
17 |
2 |
p. 228-235 |
artikel |
15 |
Mechanisms of humoral immune response against Pseudomonas aeruginosa biofilm infection in cystic fibrosis
|
Mauch, Renan Marrichi |
|
2018 |
17 |
2 |
p. 143-152 |
artikel |
16 |
New directions on lung clearance index variability and feasibility
|
O’Neill, Katherine |
|
2018 |
17 |
2 |
p. 137-139 |
artikel |
17 |
News
|
|
|
2018 |
17 |
2 |
p. 140-142 |
artikel |
18 |
Rare cases of Blastobotrys raffinosifermentans as cause of FEV1 decline in two CF patients – Whole genome sequencing to exclude transmission
|
Jahn, K. |
|
2018 |
17 |
2 |
p. e17-e19 |
artikel |
19 |
Ratiometric sweat secretion optical test in cystic fibrosis, carriers and healthy subjects
|
Bergamini, Gabriella |
|
2018 |
17 |
2 |
p. 186-189 |
artikel |
20 |
Screening for ADHD in adults with cystic fibrosis: Prevalence, health-related quality of life, and adherence
|
Georgiopoulos, Anna M. |
|
2018 |
17 |
2 |
p. 276-280 |
artikel |
21 |
16S rRNA gene sequencing reveals site-specific signatures of the upper and lower airways of cystic fibrosis patients
|
Lucas, Sarah K. |
|
2018 |
17 |
2 |
p. 204-212 |
artikel |
22 |
The effect of enteral tube feeding in cystic fibrosis: A registry based study
|
Libeert, Denis |
|
2018 |
17 |
2 |
p. 264-270 |
artikel |
23 |
Three-center feasibility of lung clearance index in infants and preschool children with cystic fibrosis and other lung diseases
|
Stahl, Mirjam |
|
2018 |
17 |
2 |
p. 249-255 |
artikel |
24 |
Up-to-date and projected estimates of survival for people with cystic fibrosis using baseline characteristics: A longitudinal study using UK patient registry data
|
Keogh, Ruth H. |
|
2018 |
17 |
2 |
p. 218-227 |
artikel |
25 |
Variability of lung clearance index in clinically stable cystic fibrosis lung disease in school age children
|
Svedberg, Marcus |
|
2018 |
17 |
2 |
p. 236-241 |
artikel |
26 |
Variability of monthly nitrogen multiple-breath washout during one year in children with cystic fibrosis
|
Green, Kent |
|
2018 |
17 |
2 |
p. 242-248 |
artikel |