| no |
title |
author |
magazine |
year |
volume |
issue |
page(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
|
article
|
| 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
|
article
|
| 3 |
Attention deficit hyperactivity disorder symptoms in patients with cystic fibrosis
|
Cohen-Cymberknoh, Malena
|
|
2018
|
17 |
2 |
p. 281-285
|
article
|
| 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
|
article
|
| 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
|
article
|
| 6 |
ECFS best practice guidelines: the 2018 revision
|
Castellani, Carlo
|
|
2018
|
17 |
2 |
p. 153-178
|
article
|
| 7 |
Editorial Board
|
|
|
2018
|
17 |
2 |
p. ii
|
article
|
| 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
|
article
|
| 9 |
Exploring probiotic use in a regional cystic fibrosis consortium
|
Gonzalez, K.D.
|
|
2018
|
17 |
2 |
p. e20-e21
|
article
|
| 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
|
article
|
| 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
|
article
|
| 12 |
Ivacaftor restores CFTR-dependent sweat gland fluid secretion in cystic fibrosis subjects with S945L alleles
|
Kim, Jeeyeon
|
|
2018
|
17 |
2 |
p. 179-185
|
article
|
| 13 |
Ivacaftor withdrawal syndrome in cystic fibrosis patients with the G551D mutation
|
Trimble, Aaron T.
|
|
2018
|
17 |
2 |
p. e13-e16
|
article
|
| 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
|
article
|
| 15 |
Mechanisms of humoral immune response against Pseudomonas aeruginosa biofilm infection in cystic fibrosis
|
Mauch, Renan Marrichi
|
|
2018
|
17 |
2 |
p. 143-152
|
article
|
| 16 |
New directions on lung clearance index variability and feasibility
|
O’Neill, Katherine
|
|
2018
|
17 |
2 |
p. 137-139
|
article
|
| 17 |
News
|
|
|
2018
|
17 |
2 |
p. 140-142
|
article
|
| 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
|
article
|
| 19 |
Ratiometric sweat secretion optical test in cystic fibrosis, carriers and healthy subjects
|
Bergamini, Gabriella
|
|
2018
|
17 |
2 |
p. 186-189
|
article
|
| 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
|
article
|
| 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
|
article
|
| 22 |
The effect of enteral tube feeding in cystic fibrosis: A registry based study
|
Libeert, Denis
|
|
2018
|
17 |
2 |
p. 264-270
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 26 |
Variability of monthly nitrogen multiple-breath washout during one year in children with cystic fibrosis
|
Green, Kent
|
|
2018
|
17 |
2 |
p. 242-248
|
article
|
Journal description