nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Advance care planning in cystic fibrosis: Current practices, challenges, and opportunities
|
Dellon, Elisabeth P. |
|
2016 |
15 |
1 |
p. 96-101 6 p. |
artikel |
2 |
Alterations in blood leukocytes of G551D-bearing cystic fibrosis patients undergoing treatment with ivacaftor
|
Bratcher, Preston E. |
|
2016 |
15 |
1 |
p. 67-73 7 p. |
artikel |
3 |
An evaluation of different steam disinfection protocols for cystic fibrosis nebulizers
|
Hohenwarter, K. |
|
2016 |
15 |
1 |
p. 78-84 7 p. |
artikel |
4 |
A semi-blinded study comparing 2 methods of measuring nasal potential difference: Subcutaneous needle versus dermal abrasion
|
De Wachter, E. |
|
2016 |
15 |
1 |
p. 60-66 7 p. |
artikel |
5 |
Assessment of epithelial sodium channel variants in nonwhite cystic fibrosis patients with non-diagnostic CFTR genotypes
|
Brennan, Marie-Luise |
|
2016 |
15 |
1 |
p. 52-59 8 p. |
artikel |
6 |
A successful uncomplicated CF pregnancy while remaining on Ivacaftor
|
Kaminski, Rachel |
|
2016 |
15 |
1 |
p. 133-134 2 p. |
artikel |
7 |
CF healthcare workers feel unprepared in providing suitable end of life care and desire more education: Results of a nationwide survey
|
Goggin, Jessica |
|
2016 |
15 |
1 |
p. 85-89 5 p. |
artikel |
8 |
CFTR modulators and pregnancy: Our work has only just begun
|
Goss, Christopher H. |
|
2016 |
15 |
1 |
p. 6-7 2 p. |
artikel |
9 |
Characterization of patients with cystic fibrosis presenting an indeterminate glucose tolerance (INDET)
|
Coriati, Adèle |
|
2016 |
15 |
1 |
p. 127-132 6 p. |
artikel |
10 |
Comparative ex vivo, in vitro and in silico analyses of a CFTR splicing mutation: Importance of functional studies to establish disease liability of mutations
|
Ramalho, Anabela S. |
|
2016 |
15 |
1 |
p. 21-33 13 p. |
artikel |
11 |
Deleterious impact of hyperglycemia on cystic fibrosis airway ion transport and epithelial repair
|
Bilodeau, Claudia |
|
2016 |
15 |
1 |
p. 43-51 9 p. |
artikel |
12 |
Development and evaluation of a palliative care curriculum for cystic fibrosis healthcare providers
|
Linnemann, Rachel W. |
|
2016 |
15 |
1 |
p. 90-95 6 p. |
artikel |
13 |
Editorial Board
|
|
|
2016 |
15 |
1 |
p. ii- 1 p. |
artikel |
14 |
Effect of ivacaftor in patients with advanced cystic fibrosis and a G551D-CFTR mutation: Safety and efficacy in an expanded access program in the United States
|
Taylor-Cousar, Jennifer |
|
2016 |
15 |
1 |
p. 116-122 7 p. |
artikel |
15 |
End of Life: Have we got it right?
|
Madge, S. |
|
2016 |
15 |
1 |
p. 2-3 2 p. |
artikel |
16 |
Fungal contamination of nebuliser devices used by people with cystic fibrosis
|
Peckham, D. |
|
2016 |
15 |
1 |
p. 74-77 4 p. |
artikel |
17 |
Is the raised volume rapid thoracic compression technique ready for use in clinical trials in infants with cystic fibrosis?
|
Matecki, Stefan |
|
2016 |
15 |
1 |
p. 10-20 11 p. |
artikel |
18 |
JCF-2015
|
|
|
2016 |
15 |
1 |
p. 1- 1 p. |
artikel |
19 |
Lack of evidence of increased risk of bacterial transmission during cystic fibrosis educational programmes
|
Ridderberg, Winnie |
|
2016 |
15 |
1 |
p. 109-115 7 p. |
artikel |
20 |
Long-term improvement of lung clearance index in patients with mild cystic fibrosis lung disease: Does hypertonic saline play a role?
|
Ellemunter, Helmut |
|
2016 |
15 |
1 |
p. 123-126 4 p. |
artikel |
21 |
News
|
Flume, Patrick |
|
2016 |
15 |
1 |
p. 8-9 2 p. |
artikel |
22 |
Skeletal muscle contractility and fatigability in adults with cystic fibrosis
|
Gruet, Mathieu |
|
2016 |
15 |
1 |
p. e1-e8 nvt p. |
artikel |
23 |
The impact of Cystic Fibrosis Transmembrane Regulator Disruption on cardiac function and stress response
|
Jiang, Kai |
|
2016 |
15 |
1 |
p. 34-42 9 p. |
artikel |
24 |
The importance of the mundane—Nebuliser care and hygiene
|
Moore, John E. |
|
2016 |
15 |
1 |
p. 4-5 2 p. |
artikel |
25 |
Tigecycline-induced acute pancreatitis in a cystic fibrosis patient: A case report and literature review
|
Hemphill, Michael T. |
|
2016 |
15 |
1 |
p. e9-e11 nvt p. |
artikel |
26 |
Web-based symptom screening in cystic fibrosis patients: A feasibility study
|
Balzano, Julie |
|
2016 |
15 |
1 |
p. 102-108 7 p. |
artikel |