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