| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Bone health and disease in cystic fibrosis
|
Marquette, Malcolm
|
|
2016
|
20 |
S |
p. 2-5
4 p.
|
artikel
|
| 2 |
Cystic Fibrosis in Children and Adults
|
David, T.J.
|
|
2016
|
20 |
S |
p. 1-
1 p.
|
artikel
|
| 3 |
Cystic Fibrosis Papers of the Year 2015
|
Doull, Iolo
|
|
2016
|
20 |
S |
p. 18-20
3 p.
|
artikel
|
| 4 |
Electronic patient records, past, present and future
|
Peckham, Daniel
|
|
2016
|
20 |
S |
p. 8-11
4 p.
|
artikel
|
| 5 |
Is deafness mutation screening required in cystic fibrosis patients?
|
Abusamra, Rania
|
|
2016
|
20 |
S |
p. 24-26
3 p.
|
artikel
|
| 6 |
Lifestyle treatments in cystic fibrosis: The NHS should not pay
|
Hull, Jeremy
|
|
2016
|
20 |
S |
p. 15-17
3 p.
|
artikel
|
| 7 |
Lifestyle treatments in cystic fibrosis: The NHS should pay
|
Ketchell, Robert Ian
|
|
2016
|
20 |
S |
p. 12-14
3 p.
|
artikel
|
| 8 |
Phenotypic variability of R117H-CFTR expression within monozygotic twins
|
Waller, Michael D.
|
|
2016
|
20 |
S |
p. 21-23
3 p.
|
artikel
|
| 9 |
Pneumothorax in cystic fibrosis: beyond the guidelines
|
Lord, Robert W.
|
|
2016
|
20 |
S |
p. 30-33
4 p.
|
artikel
|
| 10 |
Severe Achromobacter xylosoxidans infection and loss of sputum bacterial diversity in an adult patient with cystic fibrosis
|
Talbot, Nick P.
|
|
2016
|
20 |
S |
p. 27-29
3 p.
|
artikel
|
| 11 |
Treatment of pulmonary exacerbations in cystic fibrosis – could do better?
|
Smyth, Alan
|
|
2016
|
20 |
S |
p. 6-7
2 p.
|
artikel
|
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