Digitale Bibliotheek
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                             26 gevonden resultaten
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
                             26 gevonden resultaten
 
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