Digitale Bibliotheek
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                             25 gevonden resultaten
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
                             25 gevonden resultaten
 
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