| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Addressing the burden of illness in adults with cystic fibrosis with screening and triage: An early intervention model of palliative care
|
Dhingra, Lara
|
|
|
19 |
2 |
p. 262-270
|
artikel
|
| 2 |
Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis
|
Bilton, Diana
|
|
|
19 |
2 |
p. 284-291
|
artikel
|
| 3 |
An end to casual sexism
|
Bush, Andrew
|
|
|
19 |
2 |
p. 332
|
artikel
|
| 4 |
A smartphone application for reporting symptoms in adults with cystic fibrosis improves the detection of exacerbations: Results of a randomised controlled trial
|
Wood, Jamie
|
|
|
19 |
2 |
p. 271-276
|
artikel
|
| 5 |
At the forefront of cystic fibrosis Basic Science research: 16th ECFS Basic Science Conference
|
Taggart, Clifford C.
|
|
|
19 |
2 |
p. 169-170
|
artikel
|
| 6 |
CF: There's an app for that!
|
Nasr, Samya Z.
|
|
|
19 |
2 |
p. 172-173
|
artikel
|
| 7 |
Cystic fibrosis related diabetes in Europe: Prevalence, risk factors and outcome; Olesen et al
|
Olesen, Hanne V
|
|
|
19 |
2 |
p. 321-327
|
artikel
|
| 8 |
Developing a smartphone application to support social connectedness and wellbeing in young people with cystic fibrosis
|
Francis, Jacinta
|
|
|
19 |
2 |
p. 277-283
|
artikel
|
| 9 |
Dissociation of systemic and mucosal autoimmunity in cystic fibrosis
|
Theprungsirikul, J.
|
|
|
19 |
2 |
p. 196-202
|
artikel
|
| 10 |
Distribution and outcomes of infection of Mycobacterium avium complex species in cystic fibrosis
|
Azar, Michelle
|
|
|
19 |
2 |
p. 232-235
|
artikel
|
| 11 |
Dysregulated insulin in pancreatic insufficient cystic fibrosis with post-prandial hypoglycemia
|
Kilberg, Marissa J.
|
|
|
19 |
2 |
p. 310-315
|
artikel
|
| 12 |
Editorial Board
|
|
|
|
19 |
2 |
p. ii
|
artikel
|
| 13 |
Gender Equity
|
Polineni, Deepika
|
|
|
19 |
2 |
p. 328-329
|
artikel
|
| 14 |
GLPG2737 in lumacaftor/ivacaftor-treated CF subjects homozygous for the F508del mutation: A randomized phase 2A trial (PELICAN)
|
van Koningsbruggen-Rietschel, Silke
|
|
|
19 |
2 |
p. 292-298
|
artikel
|
| 15 |
‘Go for it, dream big, work hard and persist’: A message to the next generation of CF leaders in recognition of International Women's Day 2020
|
Langawi, Mona Al
|
|
|
19 |
2 |
p. 184-193
|
artikel
|
| 16 |
Guidance for computed tomography (CT) imaging of the lungs for patients with cystic fibrosis (CF) in research studies
|
van Straten, Marcel
|
|
|
19 |
2 |
p. 176-183
|
artikel
|
| 17 |
Healthcare reassessment in a pandemics time: challenges for CF
|
Castellani, Carlo
|
|
|
19 |
2 |
p. 194-195
|
artikel
|
| 18 |
Human cystic fibrosis monocyte derived macrophages display no defect in acidification of phagolysosomes when measured by optical nanosensors
|
Law, Sheonagh M.
|
|
|
19 |
2 |
p. 203-210
|
artikel
|
| 19 |
Infection with Prevotella nigrescens induces TLR2 signalling and low levels of p65 mediated inflammation in Cystic Fibrosis bronchial epithelial cells
|
Bertelsen, A.
|
|
|
19 |
2 |
p. 211-218
|
artikel
|
| 20 |
Investigating transmission of Mycobacterium abscessus amongst children in an Australian cystic fibrosis centre
|
Yan, Jennifer
|
|
|
19 |
2 |
p. 219-224
|
artikel
|
| 21 |
Mutation-specific dual potentiators maximize rescue of CFTR gating mutants
|
Veit, Guido
|
|
|
19 |
2 |
p. 236-244
|
artikel
|
| 22 |
News Article
|
|
|
|
19 |
2 |
p. 174-175
|
artikel
|
| 23 |
Peak OGTT glucose is associated with lower lung function in young children with cystic fibrosis
|
Prentice, Bernadette J.
|
|
|
19 |
2 |
p. 305-309
|
artikel
|
| 24 |
Pilot study to test inhaled nitric oxide in cystic fibrosis patients with refractory Mycobacterium abscessus lung infection
|
Bentur, Lea
|
|
|
19 |
2 |
p. 225-231
|
artikel
|
| 25 |
Pursuit of Equity
|
Flume, Patrick
|
|
|
19 |
2 |
p. 171
|
artikel
|
| 26 |
Regarding the article entitled “A smartphone application for reporting symptoms in adults with cystic fibrosis improves the detection of exacerbations: Results of a randomised controlled trial”
|
Hoo, Zhe Hui
|
|
|
19 |
2 |
p. e9
|
artikel
|
| 27 |
Single dose escalation studies with inhaled POL6014, a potent novel selective reversible inhibitor of human neutrophil elastase, in healthy volunteers and subjects with cystic fibrosis
|
Barth, P.
|
|
|
19 |
2 |
p. 299-304
|
artikel
|
| 28 |
The association of pediatric cystic fibrosis-related diabetes screening on clinical outcomes by center: A CF patient registry study
|
Franck Thompson, Elizabeth
|
|
|
19 |
2 |
p. 316-320
|
artikel
|
| 29 |
To be or not to be on CFTR modulators during pregnancy: Risks to be considered
|
Vekaria, Sona
|
|
|
19 |
2 |
p. e7-e8
|
artikel
|
| 30 |
Variation in lung function and nutritional decline in cystic fibrosis by genotype: An analysis of the Canadian cystic fibrosis registry
|
Leung, Garvin J.
|
|
|
19 |
2 |
p. 255-261
|
artikel
|
| 31 |
Whole-blood transcriptomic responses to lumacaftor/ivacaftor therapy in cystic fibrosis
|
Kopp, Benjamin T.
|
|
|
19 |
2 |
p. 245-254
|
artikel
|
| 32 |
Why women need to “Work hard(er) and persist” to succeed in the clinic and the lab
|
Davies, Janet M.
|
|
|
19 |
2 |
p. 330-331
|
artikel
|
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