| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Accurate assessment of systemic iron status in cystic fibrosis will avoid the hazards of inappropriate iron supplementation
|
Smith, D.J.
|
|
2013
|
12 |
3 |
p. 303-304
2 p.
|
artikel
|
| 2 |
Acknowledgment to reviewers 2012
|
|
|
2013
|
12 |
3 |
p. 305-307
3 p.
|
artikel
|
| 3 |
Antibiotic susceptibility testing in early and chronic respiratory infections with Pseudomonas aeruginosa
|
Foweraker, Juliet E.
|
|
2013
|
12 |
3 |
p. 302-
1 p.
|
artikel
|
| 4 |
Calculation of the capnographic index based on expiratory molar mass–volume-curves — A suitable tool to screen for cystic fibrosis lung disease
|
Fuchs, Susanne I.
|
|
2013
|
12 |
3 |
p. 277-283
7 p.
|
artikel
|
| 5 |
Characterization of a recurrent 3.8kb deletion involving exons 17a and 17b within the CFTR gene
|
Tang, Sha
|
|
2013
|
12 |
3 |
p. 290-294
5 p.
|
artikel
|
| 6 |
Dysbiosis of bifidobacteria and Clostridium cluster XIVa in the cystic fibrosis fecal microbiota
|
Duytschaever, Gwen
|
|
2013
|
12 |
3 |
p. 206-215
10 p.
|
artikel
|
| 7 |
Effect of allergy and inflammation on eicosanoid gene expression in CFTR deficiency
|
Bickford, Justin S.
|
|
2013
|
12 |
3 |
p. 258-265
8 p.
|
artikel
|
| 8 |
Hypertriglyceridemia is associated with insulin levels in adult cystic fibrosis patients
|
Ishimo, Marie-Claire
|
|
2013
|
12 |
3 |
p. 271-276
6 p.
|
artikel
|
| 9 |
Identification and distribution of Achromobacter species in cystic fibrosis
|
Spilker, Theodore
|
|
2013
|
12 |
3 |
p. 298-301
4 p.
|
artikel
|
| 10 |
Lung transplantation in cystic fibrosis normalizes essential fatty acid profiles
|
Witters, Peter
|
|
2013
|
12 |
3 |
p. 222-228
7 p.
|
artikel
|
| 11 |
Measures of body habitus are associated with lung function in adults with cystic fibrosis: A population-based study
|
Forrester, Doug L.
|
|
2013
|
12 |
3 |
p. 284-289
6 p.
|
artikel
|
| 12 |
Molecular detection of CF lung pathogens: Current status and future potential
|
Pattison, Sally H.
|
|
2013
|
12 |
3 |
p. 194-205
12 p.
|
artikel
|
| 13 |
Nasal polyposis in lung transplant recipients with cystic fibrosis
|
Vital, Domenic
|
|
2013
|
12 |
3 |
p. 266-270
5 p.
|
artikel
|
| 14 |
Poor growth in an infant with cystic fibrosis due to an antenatal perforation and incomplete bowel obstruction
|
Brookes, Isobel
|
|
2013
|
12 |
3 |
p. 295-297
3 p.
|
artikel
|
| 15 |
Positive parental attitudes to participating in research involving newborn screened infants with CF
|
Chudleigh, Jane
|
|
2013
|
12 |
3 |
p. 234-240
7 p.
|
artikel
|
| 16 |
Progression of structural lung disease on CT scans in children with cystic fibrosis related diabetes
|
Widger, John
|
|
2013
|
12 |
3 |
p. 216-221
6 p.
|
artikel
|
| 17 |
Reduced physical activity associated with work and transport in adults with cystic fibrosis
|
Rasekaba, Tshepo M.
|
|
2013
|
12 |
3 |
p. 229-233
5 p.
|
artikel
|
| 18 |
Safety and early treatment effects of the CXCR2 antagonist SB-656933 in patients with cystic fibrosis
|
Moss, Richard B.
|
|
2013
|
12 |
3 |
p. 241-248
8 p.
|
artikel
|
| 19 |
Soluble inflammation markers in nasal lavage from CF patients and healthy controls
|
Beiersdorf, Natalie
|
|
2013
|
12 |
3 |
p. 249-257
9 p.
|
artikel
|
| 20 |
What is the clinical significance of filamentous fungi positive sputum cultures in patients with cystic fibrosis?
|
Liu, Jane C.
|
|
2013
|
12 |
3 |
p. 187-193
7 p.
|
artikel
|
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