nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Cystic fibrosis gene mutations and gastrointestinal diseases
|
Bahmanyar, Shahram |
|
2010 |
9 |
4 |
p. 288-291 4 p. |
artikel |
2 |
Effect of Th2 type cytokines on hCLCA1 and mucus expression in cystic fibrosis airways
|
Hauber, Hans-Peter |
|
2010 |
9 |
4 |
p. 277-279 3 p. |
artikel |
3 |
High dose intermittent ticarcillin–clavulanate administration in pediatric cystic fibrosis patients
|
Zobell, Jeffery T. |
|
2010 |
9 |
4 |
p. 280-283 4 p. |
artikel |
4 |
Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: Three areas for future research
|
Rottier, Bart L. |
|
2010 |
9 |
4 |
p. 296-297 2 p. |
artikel |
5 |
Lung transplantation in patients with cystic fibrosis and Mycobacterium abscessus infection
|
Gilljam, Marita |
|
2010 |
9 |
4 |
p. 272-276 5 p. |
artikel |
6 |
Opportunities for quality improvement in cystic fibrosis newborn screening
|
Groose, Molly K. |
|
2010 |
9 |
4 |
p. 284-287 4 p. |
artikel |
7 |
Osteopenia in Cftr-deltaF508 mice
|
Paradis, Josée |
|
2010 |
9 |
4 |
p. 239-245 7 p. |
artikel |
8 |
Pneumothorax in cystic fibrosis: Prevalence and outcomes in Scotland
|
MacDuff, A. |
|
2010 |
9 |
4 |
p. 246-249 4 p. |
artikel |
9 |
Renal impairment in children with cystic fibrosis
|
Andrieux, Annick |
|
2010 |
9 |
4 |
p. 263-268 6 p. |
artikel |
10 |
Report of two patients with associated conditions in addition to cystic fibrosis
|
Jambhekar, Supriya K. |
|
2010 |
9 |
4 |
p. 269-271 3 p. |
artikel |
11 |
Serum-surfactant SP-D correlates inversely to lung function in cystic fibrosis
|
Olesen, Hanne Vebert |
|
2010 |
9 |
4 |
p. 257-262 6 p. |
artikel |
12 |
Serum tobramycin levels following delivery of tobramycin (Tobi®) via eFlow® advanced nebuliser in children with cystic fibrosis
|
Guy, E.L. |
|
2010 |
9 |
4 |
p. 292-295 4 p. |
artikel |
13 |
Year-to-year changes in lung function in individuals with cystic fibrosis
|
Liou, Theodore G. |
|
2010 |
9 |
4 |
p. 250-256 7 p. |
artikel |