| 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
|
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