| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Bordetella bronchiseptica in a pediatric Cystic Fibrosis center
|
Brady, Cynthia
|
|
2014
|
13 |
1 |
p. 43-48
6 p.
|
artikel
|
| 2 |
Clinical presentation of mild cystic fibrosis in a Serbian patient homozygous for the CFTR mutation c.1393-1G>A
|
Nikolic, Aleksandra
|
|
2014
|
13 |
1 |
p. 111-113
3 p.
|
artikel
|
| 3 |
Comparison of different IRT-PAP protocols to screen newborns for cystic fibrosis in three central European populations
|
Sommerburg, Olaf
|
|
2014
|
13 |
1 |
p. 15-23
9 p.
|
artikel
|
| 4 |
Complicated Clostridium difficile colitis in children with cystic fibrosis: Association with gastric acid suppression?
|
Com, G.
|
|
2014
|
13 |
1 |
p. 37-42
6 p.
|
artikel
|
| 5 |
Corrigendum to: “Update on cystic fibrosis-related diabetes” [Journal of Cystic Fibrosis 12 (2013) 318-331]
|
Kelly, Andrea
|
|
2014
|
13 |
1 |
p. 119-
1 p.
|
artikel
|
| 6 |
Culture-based diagnostic microbiology in cystic fibrosis: Can we simplify the complexity?
|
Burns, Jane L.
|
|
2014
|
13 |
1 |
p. 1-9
9 p.
|
artikel
|
| 7 |
Cystic fibrosis and pregnancy in the modern era: A case control study
|
Ahluwalia, Monica
|
|
2014
|
13 |
1 |
p. 69-73
5 p.
|
artikel
|
| 8 |
Editorial Board
|
|
|
2014
|
13 |
1 |
p. ii-
1 p.
|
artikel
|
| 9 |
Effect of ivacaftor on CFTR forms with missense mutations associated with defects in protein processing or function
|
Van Goor, Fredrick
|
|
2014
|
13 |
1 |
p. 29-36
8 p.
|
artikel
|
| 10 |
Evaluating the predictive ability of sweat chloride
|
Heltshe, Sonya L.
|
|
2014
|
13 |
1 |
p. 118-
1 p.
|
artikel
|
| 11 |
Evaluation of specific immune response in early P. aeruginosa infection in cystic fibrosis patients
|
Dolce, Daniela
|
|
2014
|
13 |
1 |
p. 116-117
2 p.
|
artikel
|
| 12 |
Hemoglobin≤12.9g/dl predicts risk of antibiotic treatment in cystic fibrosis
|
Gifford, A.H.
|
|
2014
|
13 |
1 |
p. 114-115
2 p.
|
artikel
|
| 13 |
Induced sputum compared to bronchoalveolar lavage in young, non-expectorating cystic fibrosis children
|
Blau, Hannah
|
|
2014
|
13 |
1 |
p. 106-110
5 p.
|
artikel
|
| 14 |
Inflammatory and immunological biomarkers are not related to survival in adults with Cystic Fibrosis
|
Moffitt, K.L.
|
|
2014
|
13 |
1 |
p. 63-68
6 p.
|
artikel
|
| 15 |
Interval exercise training in cystic fibrosis — Effects on exercise capacity in severely affected adults
|
Gruber, Wolfgang
|
|
2014
|
13 |
1 |
p. 86-91
6 p.
|
artikel
|
| 16 |
Investigating the role of matrix components in protection of Burkholderia cepacia complex biofilms against tobramycin
|
Messiaen, Anne-Sophie
|
|
2014
|
13 |
1 |
p. 56-62
7 p.
|
artikel
|
| 17 |
Nasal potential difference measurements in diagnosis of cystic fibrosis: An international survey
|
Naehrlich, Lutz
|
|
2014
|
13 |
1 |
p. 24-28
5 p.
|
artikel
|
| 18 |
[No title]
|
|
|
2014
|
13 |
1 |
p. 120-122
3 p.
|
artikel
|
| 19 |
Predictors for future cystic fibrosis-related diabetes by oral glucose tolerance test
|
Schmid, Kerstin
|
|
2014
|
13 |
1 |
p. 80-85
6 p.
|
artikel
|
| 20 |
Pulmonary exacerbations in CF patients with early lung disease
|
Anstead, Michael
|
|
2014
|
13 |
1 |
p. 74-79
6 p.
|
artikel
|
| 21 |
Reduced fat oxidation rates during submaximal exercise in boys with cystic fibrosis
|
Nguyen, Thanh
|
|
2014
|
13 |
1 |
p. 92-98
7 p.
|
artikel
|
| 22 |
Relationship between sweat chloride, sodium, and age in clinically obtained samples
|
Traeger, Nadav
|
|
2014
|
13 |
1 |
p. 10-14
5 p.
|
artikel
|
| 23 |
Respiratory physicians and clinic coordinators' attitudes to population-based cystic fibrosis carrier screening
|
Cunningham, Fiona
|
|
2014
|
13 |
1 |
p. 99-105
7 p.
|
artikel
|
| 24 |
The role of respiratory viruses in adult patients with cystic fibrosis receiving intravenous antibiotics for a pulmonary exacerbation
|
Etherington, C.
|
|
2014
|
13 |
1 |
p. 49-55
7 p.
|
artikel
|
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