nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An aerobiological model of aerosol survival of different strains of Pseudomonas aeruginosa isolated from people with cystic fibrosis
|
Clifton, I.J. |
|
2010 |
9 |
1 |
p. 64-68 5 p. |
artikel |
2 |
A 10-year large-scale cystic fibrosis carrier screening in the Italian population
|
Picci, Luigi |
|
2010 |
9 |
1 |
p. 29-35 7 p. |
artikel |
3 |
Can Burkholderia cepacia complex be eradicated with nebulised Amiloride and TOBIĀ®?
|
Ball, R. |
|
2010 |
9 |
1 |
p. 73-74 2 p. |
artikel |
4 |
Constipation in pediatric Cystic Fibrosis patients: An underestimated medical condition
|
van der Doef, H.P.J. |
|
2010 |
9 |
1 |
p. 59-63 5 p. |
artikel |
5 |
Cystic fibrosis transmembrane conductance regulator (CFTR) regulates the production of osteoprotegerin (OPG) and prostaglandin (PG) E2 in human bone
|
Le Heron, Louis |
|
2010 |
9 |
1 |
p. 69-72 4 p. |
artikel |
6 |
Entry of Burkholderia organisms into respiratory epithelium: CFTR, microfilament and microtubule dependence
|
Taylor, Jane B. |
|
2010 |
9 |
1 |
p. 36-43 8 p. |
artikel |
7 |
Inflammation in Achromobacter xylosoxidans infected cystic fibrosis patients
|
Hansen, C.R. |
|
2010 |
9 |
1 |
p. 51-58 8 p. |
artikel |
8 |
Long-term daily high and low doses of azithromycin in children with cystic fibrosis: A randomized controlled trial
|
Kabra, S.K. |
|
2010 |
9 |
1 |
p. 17-23 7 p. |
artikel |
9 |
Measuring and improving respiratory outcomes in cystic fibrosis lung disease: Opportunities and challenges to therapy
|
Zemanick, Edith T. |
|
2010 |
9 |
1 |
p. 1-16 16 p. |
artikel |
10 |
Prevalence of dyslipidemia in adults with cystic fibrosis
|
Rhodes, Bronwen |
|
2010 |
9 |
1 |
p. 24-28 5 p. |
artikel |
11 |
Pulmonary outcome differences in U.S. and French cystic fibrosis cohorts diagnosed through newborn screening
|
Walsh, Aimee C. |
|
2010 |
9 |
1 |
p. 44-50 7 p. |
artikel |