nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Age-related heterogeneity in dental caries and associated risk factors in individuals with cystic fibrosis ages 6–20 years: A pilot study
|
Chi, Donald L. |
|
2018 |
17 |
6 |
p. 747-759 |
artikel |
2 |
Antimicrobial resistance in cystic fibrosis: Does it matter?
|
Flume, Patrick A. |
|
2018 |
17 |
6 |
p. 687-689 |
artikel |
3 |
Attenuation of exacerbation
|
Ranganathan, Sarath C. |
|
2018 |
17 |
6 |
p. 692-693 |
artikel |
4 |
CFTR rescue with VX-809 and VX-770 favors the repair of primary airway epithelial cell cultures from patients with class II mutations in the presence of Pseudomonas aeruginosa exoproducts
|
Adam, Damien |
|
2018 |
17 |
6 |
p. 705-714 |
artikel |
5 |
Characteristics and outcomes of oral antibiotic treated pulmonary exacerbations in children with cystic fibrosis
|
Hoppe, Jordana E. |
|
2018 |
17 |
6 |
p. 760-768 |
artikel |
6 |
Continuous glucose monitoring abnormalities in cystic fibrosis youth correlate with pulmonary function decline
|
Chan, Christine L. |
|
2018 |
17 |
6 |
p. 783-790 |
artikel |
7 |
Continuous glucose monitoring guided insulin therapy is associated with improved clinical outcomes in cystic fibrosis-related diabetes
|
Frost, Freddy |
|
2018 |
17 |
6 |
p. 798-803 |
artikel |
8 |
Defining antimicrobial resistance in cystic fibrosis
|
Kidd, Timothy J. |
|
2018 |
17 |
6 |
p. 696-704 |
artikel |
9 |
Dietary intake of energy-dense, nutrient-poor and nutrient-dense food sources in children with cystic fibrosis
|
Sutherland, Rosie |
|
2018 |
17 |
6 |
p. 804-810 |
artikel |
10 |
Dysglycaemia in CF – Why are investigating it, what should we measure and how should we treat it?
|
Brennan, Amanda |
|
2018 |
17 |
6 |
p. 690-691 |
artikel |
11 |
Early detection using qPCR of Pseudomonas aeruginosa infection in children with cystic fibrosis undergoing eradication treatment
|
Blanchard, Ana C. |
|
2018 |
17 |
6 |
p. 723-728 |
artikel |
12 |
Editorial Board
|
|
|
2018 |
17 |
6 |
p. ii |
artikel |
13 |
Establishing the diagnosis of chronic colonization with Pseudomonas aeruginosa of cystic fibrosis patients: Comparison of the European consensus criteria with genotyping of P. aeruginosa isolates
|
Jonckheere, Leander |
|
2018 |
17 |
6 |
p. 729-735 |
artikel |
14 |
False-positive cannabinoid screens in adult cystic fibrosis patients treated with lumacaftor/ivacaftor
|
Kissner, Dana |
|
2018 |
17 |
6 |
p. e51-e53 |
artikel |
15 |
Impact of a program ensuring consistent response to acute drops in lung function in children with cystic fibrosis
|
Schechter, Michael S. |
|
2018 |
17 |
6 |
p. 769-778 |
artikel |
16 |
Implementing the International Committee on Mental Health in Cystic Fibrosis (ICMH) guidelines: Screening accuracy and referral-treatment pathways
|
Verkleij, Marieke |
|
2018 |
17 |
6 |
p. 821-827 |
artikel |
17 |
Interleukin-1 is associated with inflammation and structural lung disease in young children with cystic fibrosis
|
Montgomery, Samuel T. |
|
2018 |
17 |
6 |
p. 715-722 |
artikel |
18 |
Magnetic resonance elastography demonstrates elevated liver stiffness in cystic fibrosis patients
|
Hayes Jr, Don |
|
2018 |
17 |
6 |
p. e54-e56 |
artikel |
19 |
Measured fetal and neonatal exposure to Lumacaftor and Ivacaftor during pregnancy and while breastfeeding
|
Trimble, Aaron |
|
2018 |
17 |
6 |
p. 779-782 |
artikel |
20 |
News
|
Wilschanski, Michael |
|
2018 |
17 |
6 |
p. 694-695 |
artikel |
21 |
Quality of life and mood in children with cystic fibrosis: Associations with sleep quality
|
Vandeleur, Moya |
|
2018 |
17 |
6 |
p. 811-820 |
artikel |
22 |
Quantifying fluctuation in glucose levels to identify early changes in glucose homeostasis in cystic fibrosis
|
Brugha, Rossa |
|
2018 |
17 |
6 |
p. 791-797 |
artikel |
23 |
Rate and predictors of prescription of lumacaftor – Ivacaftor in the 18 months following approval in the United States
|
Sawicki, Gregory S. |
|
2018 |
17 |
6 |
p. 742-746 |
artikel |
24 |
Understanding of safety monitoring in clinical trials by individuals with CF or their parents: A qualitative analysis
|
Kern-Goldberger, Andrew S. |
|
2018 |
17 |
6 |
p. 736-741 |
artikel |
25 |
Use of telavancin in adolescent patients with cystic fibrosis and prior intolerance to vancomycin: A case series
|
Bernstein, Adam T. |
|
2018 |
17 |
6 |
p. e48-e50 |
artikel |