| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acute effects of viral respiratory tract infections on sputum bacterial density during CF pulmonary exacerbations
|
Chin, Melanie
|
|
2015
|
14 |
4 |
p. 482-489
8 p.
|
artikel
|
| 2 |
Altered intestinal bile salt biotransformation in a cystic fibrosis (Cftr−/− ) mouse model with hepato-biliary pathology
|
Bodewes, Frank A.J.A.
|
|
2015
|
14 |
4 |
p. 440-446
7 p.
|
artikel
|
| 3 |
Alternative outcomes for the multiple breath washout in children with CF
|
Stanojevic, Sanja
|
|
2015
|
14 |
4 |
p. 490-496
7 p.
|
artikel
|
| 4 |
An unusual cause of growth failure in cystic fibrosis: A salutary reminder of the interaction between glucocorticoids and cytochrome P450 inhibiting medication
|
Albert, Benjamin B.
|
|
2015
|
14 |
4 |
p. e9-e11
nvt p.
|
artikel
|
| 5 |
A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT-1026) versus tobramycin inhalation solution in stable cystic fibrosis patients
|
Stuart Elborn, J.
|
|
2015
|
14 |
4 |
p. 507-514
8 p.
|
artikel
|
| 6 |
Breaking bad news, the diagnosis of cystic fibrosis in childhood
|
Havermans, Trudy
|
|
2015
|
14 |
4 |
p. 540-546
7 p.
|
artikel
|
| 7 |
Clinical expression of patients with the D1152H CFTR mutation
|
Terlizzi, Vito
|
|
2015
|
14 |
4 |
p. 447-452
6 p.
|
artikel
|
| 8 |
Clinical relevance of Pseudomonas aeruginosa hypermutation in cystic fibrosis chronic respiratory infection
|
Oliver, Antonio
|
|
2015
|
14 |
4 |
p. e1-e2
nvt p.
|
artikel
|
| 9 |
Clinical relevance of Pseudomonas aeruginosa hypermutation in cystic fibrosis chronic respiratory infection
|
Bar-Meir, Maskit
|
|
2015
|
14 |
4 |
p. e3-
1 p.
|
artikel
|
| 10 |
Cystic Fibrosis Foundation and European Cystic Fibrosis Society Survey of cystic fibrosis mental health care delivery
|
Abbott, J.
|
|
2015
|
14 |
4 |
p. 533-539
7 p.
|
artikel
|
| 11 |
Cystic fibrosis — From basic science to clinical benefit: A review series
|
Hartl, Dominik
|
|
2015
|
14 |
4 |
p. 415-416
2 p.
|
artikel
|
| 12 |
Editorial Board
|
|
|
2015
|
14 |
4 |
p. ii-
1 p.
|
artikel
|
| 13 |
Equivalent substrates enable simultaneous study of gastrointestinal pH and CF-related diabetes
|
Borowitz, Drucy
|
|
2015
|
14 |
4 |
p. e6-e8
nvt p.
|
artikel
|
| 14 |
Experience of care from the perspective of individuals with cystic fibrosis and families: Results from 70 CF Foundation accredited programs in the USA
|
Homa, Karen
|
|
2015
|
14 |
4 |
p. 515-522
8 p.
|
artikel
|
| 15 |
Host-pathogen interplay in the respiratory environment of cystic fibrosis
|
Yonker, Lael M.
|
|
2015
|
14 |
4 |
p. 431-439
9 p.
|
artikel
|
| 16 |
Impact of storage conditions on metabolite profiles of sputum samples from persons with cystic fibrosis
|
Zhao, Jiangchao
|
|
2015
|
14 |
4 |
p. 468-473
6 p.
|
artikel
|
| 17 |
Implications of multiple freeze-thawing on respiratory samples for culture-independent analyses
|
Cuthbertson, Leah
|
|
2015
|
14 |
4 |
p. 464-467
4 p.
|
artikel
|
| 18 |
Inflammation in cystic fibrosis lung disease: Pathogenesis and therapy
|
Cantin, André M.
|
|
2015
|
14 |
4 |
p. 419-430
12 p.
|
artikel
|
| 19 |
Intraductal papillary mucinous neoplasm of the pancreas in an adult patient with cystic fibrosis after double-lung transplantation
|
Eigner, W.
|
|
2015
|
14 |
4 |
p. 523-525
3 p.
|
artikel
|
| 20 |
Ivacaftor as salvage therapy in a patient with cystic fibrosis genotype F508del/R117H/IVS8-5T
|
Carter, S.
|
|
2015
|
14 |
4 |
p. e4-e5
nvt p.
|
artikel
|
| 21 |
Molecular epidemiology of Aspergillus collected from cystic fibrosis patients
|
Sabino, Raquel
|
|
2015
|
14 |
4 |
p. 474-481
8 p.
|
artikel
|
| 22 |
News
|
|
|
2015
|
14 |
4 |
p. 417-418
2 p.
|
artikel
|
| 23 |
Osteopontin is increased in cystic fibrosis and can skew the functional balance between ELR-positive and ELR-negative CXC-chemokines
|
Jovic, Sandra
|
|
2015
|
14 |
4 |
p. 453-463
11 p.
|
artikel
|
| 24 |
Trends in bone mineral density in young adults with cystic fibrosis over a 15year period
|
Putman, Melissa S.
|
|
2015
|
14 |
4 |
p. 526-532
7 p.
|
artikel
|
| 25 |
Vitamin D deficiency is associated with pulmonary dysfunction in cystic fibrosis
|
Sexauer, William P.
|
|
2015
|
14 |
4 |
p. 497-506
10 p.
|
artikel
|
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