| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A prospective analysis of unplanned patient-initiated contacts in an adult cystic fibrosis centre
|
Burnet, Espérie
|
|
2018
|
17 |
5 |
p. 636-642
|
artikel
|
| 2 |
Children with cystic fibrosis demonstrate no respiratory immunological, infective or physiological, consequences of vitamin D deficiency
|
Thursfield, Rebecca M.
|
|
2018
|
17 |
5 |
p. 657-665
|
artikel
|
| 3 |
Combination potentiator (‘co-potentiator’) therapy for CF caused by CFTR mutants, including N1303K, that are poorly responsive to single potentiators
|
Phuan, Puay-Wah
|
|
2018
|
17 |
5 |
p. 595-606
|
artikel
|
| 4 |
Cystic fibrosis epithelial cells are primed for apoptosis as a result of increased Fas (CD95)
|
Chen, Qiwei
|
|
2018
|
17 |
5 |
p. 616-623
|
artikel
|
| 5 |
Development and electronic validation of the revised Cystic Fibrosis Questionnaire (CFQ-R Teen/Adult)
|
Solé, Amparo
|
|
2018
|
17 |
5 |
p. 672-679
|
artikel
|
| 6 |
Editorial Board
|
|
|
2018
|
17 |
5 |
p. ii
|
artikel
|
| 7 |
Hypertonic saline has a prolonged effect on mucociliary clearance in adults with cystic fibrosis
|
Trimble, Aaron T.
|
|
2018
|
17 |
5 |
p. 650-656
|
artikel
|
| 8 |
Initial development and pilot testing of observer-reported outcomes (ObsROs) for children with cystic fibrosis ages 0–11years
|
Edwards, T.C.
|
|
2018
|
17 |
5 |
p. 680-686
|
artikel
|
| 9 |
Mast cell tryptase changes with Aspergillus fumigatus – Host crosstalk in cystic fibrosis patients
|
Gomez, Carine
|
|
2018
|
17 |
5 |
p. 631-635
|
artikel
|
| 10 |
News
|
|
|
2018
|
17 |
5 |
p. 562-565
|
artikel
|
| 11 |
N1303K: Leaving no stone unturned in the search for transformational therapeutics
|
Noel, Sabrina
|
|
2018
|
17 |
5 |
p. 555-557
|
artikel
|
| 12 |
Patient-reported outcomes: Time for a new approach?
|
Abbott, Janice
|
|
2018
|
17 |
5 |
p. 560-561
|
artikel
|
| 13 |
Physiological and pharmacological characterization of the N1303K mutant CFTR
|
DeStefano, Samantha
|
|
2018
|
17 |
5 |
p. 573-581
|
artikel
|
| 14 |
Primary sclerosing cholangitis is associated with abnormalities in CFTR
|
Werlin, Steven
|
|
2018
|
17 |
5 |
p. 666-671
|
artikel
|
| 15 |
Rescue of CFTR NBD2 mutants N1303K and S1235R is influenced by the functioning of the autophagosome
|
Liu, Qiangni
|
|
2018
|
17 |
5 |
p. 582-594
|
artikel
|
| 16 |
Resolvin D1 regulates epithelial ion transport and inflammation in cystic fibrosis airways
|
Ringholz, Fiona C.
|
|
2018
|
17 |
5 |
p. 607-615
|
artikel
|
| 17 |
Risk factors for persistent Aspergillus respiratory isolation in cystic fibrosis
|
Hong, Gina
|
|
2018
|
17 |
5 |
p. 624-630
|
artikel
|
| 18 |
The choice of lung function reference equation affects clinical trial eligibility: Results from a cystic fibrosis cohort
|
Mathiesen, Inger Hee
|
|
2018
|
17 |
5 |
p. e46-e47
|
artikel
|
| 19 |
The open door policy - An important and under-recognised activity of the adult CF centre
|
Tai, Anna Sze
|
|
2018
|
17 |
5 |
p. 558-559
|
artikel
|
| 20 |
The Q359K/T360K mutation causes cystic fibrosis in Georgian Jews
|
Mei-Zahav, M.
|
|
2018
|
17 |
5 |
p. e41-e45
|
artikel
|
| 21 |
Using registry data to improve quality of care
|
McIntyre, Kieran
|
|
2018
|
17 |
5 |
p. 566-572
|
artikel
|
| 22 |
Young patients with cystic fibrosis demonstrate subtle alterations of the cardiovascular system
|
Eising, Jacobien B.
|
|
2018
|
17 |
5 |
p. 643-649
|
artikel
|
Tijdschrift beschrijving