| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestations
|
Darrah, Rebecca J.
|
|
2019
|
18 |
1 |
p. 127-134
|
artikel
|
| 2 |
Anaemia and iron deficiency in relation to fatigue in cystic fibrosis
|
Talbot, Nick P.
|
|
2019
|
18 |
1 |
p. e5
|
artikel
|
| 3 |
Authors’ response: Letter to the Editor ‘Anaemia and iron deficiency in relation to fatigue in cystic fibrosis’
|
Nap-van der Vlist, M.M.
|
|
2019
|
18 |
1 |
p. e6-e7
|
artikel
|
| 4 |
Breathlessness catastrophizing relates to poorer quality of life in adults with cystic fibrosis
|
Maras, Danijela
|
|
2019
|
18 |
1 |
p. 150-157
|
artikel
|
| 5 |
CFTR modulator theratyping: Current status, gaps and future directions
|
Clancy, John Paul
|
|
2019
|
18 |
1 |
p. 22-34
|
artikel
|
| 6 |
Continuous glucose monitoring in youth with cystic fibrosis treated with lumacaftor-ivacaftor
|
Li, Angel
|
|
2019
|
18 |
1 |
p. 144-149
|
artikel
|
| 7 |
Editorial Board
|
|
|
2019
|
18 |
1 |
p. ii
|
artikel
|
| 8 |
Editor in Chief Job Description for JCF_ElsevierDec18_Final
|
|
|
2019
|
18 |
1 |
p. v-vi
|
artikel
|
| 9 |
Effectiveness of ivacaftor in cystic fibrosis patients with non-G551D gating mutations
|
Guimbellot, Jennifer
|
|
2019
|
18 |
1 |
p. 102-109
|
artikel
|
| 10 |
Emergence of livestock-associated MRSA isolated from cystic fibrosis patients: Result of a Belgian national survey
|
Dodémont, M.
|
|
2019
|
18 |
1 |
p. 86-93
|
artikel
|
| 11 |
Eradication of early P. aeruginosa infection in children <7 years of age with cystic fibrosis: The early study
|
Ratjen, Felix
|
|
2019
|
18 |
1 |
p. 78-85
|
artikel
|
| 12 |
Establishment of a ΔF508-CF promyelocytic cell line for cystic fibrosis research and drug screening
|
Jennings, Scott
|
|
2019
|
18 |
1 |
p. 44-53
|
artikel
|
| 13 |
Higher Interleukin-7 serum concentrations in patients with cystic fibrosis correlate with impaired lung function
|
Seyfarth, Julia
|
|
2019
|
18 |
1 |
p. 71-77
|
artikel
|
| 14 |
How to live a long and healthy life with cystic fibrosis: Lessons from the CF ferret
|
Wine, Jeffrey J.
|
|
2019
|
18 |
1 |
p. 8-9
|
artikel
|
| 15 |
Investigating the effects of long-term dornase alfa use on lung function using registry data
|
Newsome, S.J.
|
|
2019
|
18 |
1 |
p. 110-117
|
artikel
|
| 16 |
Italian and North American dietary intake after ivacaftor treatment for Cystic Fibrosis Gating Mutations
|
Sainath, Nina N.
|
|
2019
|
18 |
1 |
p. 135-143
|
artikel
|
| 17 |
JCF – progress in 2018
|
Bell, Scott C.
|
|
2019
|
18 |
1 |
p. 1-5
|
artikel
|
| 18 |
Lumacaftor/Ivacaftor reduces pulmonary exacerbations in patients irrespective of initial changes in FEV1
|
McColley, Susanna A.
|
|
2019
|
18 |
1 |
p. 94-101
|
artikel
|
| 19 |
Newborn blood spot screening for cystic fibrosis with a four-step screening strategy in the Netherlands
|
Dankert-Roelse, Jeannette E.
|
|
2019
|
18 |
1 |
p. 54-63
|
artikel
|
| 20 |
News
|
|
|
2019
|
18 |
1 |
p. 10-12
|
artikel
|
| 21 |
Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung function
|
Forrest, Osric A.
|
|
2019
|
18 |
1 |
p. 64-70
|
artikel
|
| 22 |
Respiratory rate in infants with cystic fibrosis throughout the first year of life and association with lung clearance index measured shortly after birth
|
Korten, Insa
|
|
2019
|
18 |
1 |
p. 118-126
|
artikel
|
| 23 |
Successful Lung Re-transplant in a Patient with Cepacia Syndrome due to Burkholderia ambifaria
|
Goodlet, Kellie J.
|
|
2019
|
18 |
1 |
p. e1-e4
|
artikel
|
| 24 |
Take it personally: how personal we reach when we are so different from each other?
|
Kerem, Eitan
|
|
2019
|
18 |
1 |
p. 6-7
|
artikel
|
| 25 |
The CF Canada-Sick Kids Program in individual CF therapy: A resource for the advancement of personalized medicine in CF
|
Eckford, Paul D.W.
|
|
2019
|
18 |
1 |
p. 35-43
|
artikel
|
| 26 |
The lung and gut microbiome: what has to be taken into consideration for cystic fibrosis?
|
Héry-Arnaud, Geneviève
|
|
2019
|
18 |
1 |
p. 13-21
|
artikel
|
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