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                             15 results found
no title author magazine year volume issue page(s) type
1 A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis Mayell, S.J.
2009
8 1 p. 71-78
8 p.
article
2 Common mutations in cuban cystic fibrosis patients Collazo, Teresa
2009
8 1 p. 47-49
3 p.
article
3 Diagnostic significance of measurements of specific IgG antibodies to Pseudomonas aeruginosa by three different serological methods Pressler, Tacjana
2009
8 1 p. 37-42
6 p.
article
4 Early referral to cystic fibrosis specialist centre impacts on respiratory outcome Lebecque, P.
2009
8 1 p. 26-30
5 p.
article
5 GFR estimates using cystatin C are superior to serum creatinine in adult patients with cystic fibrosis Beringer, Paul M.
2009
8 1 p. 19-25
7 p.
article
6 Highlights of a workshop to discuss targeting inflammation in cystic fibrosis Banner, Katharine H.
2009
8 1 p. 1-8
8 p.
article
7 Long-term, low-dose azithromycin treatment reduces the incidence but increases macrolide resistance in Staphylococcus aureus in Danish CF patients Hansen, C.R.
2009
8 1 p. 58-62
5 p.
article
8 Pancreatic enzyme replacement therapy for young cystic fibrosis patients Munck, Anne
2009
8 1 p. 14-18
5 p.
article
9 Pseudomonas aeruginosa lasR mutants are associated with cystic fibrosis lung disease progression Hoffman, Lucas R.
2009
8 1 p. 66-70
5 p.
article
10 Regimens for eradicating early Pseudomonas aeruginosa infection in children do not promote antibiotic resistance in this organism Ho, Sheng-Ang
2009
8 1 p. 43-46
4 p.
article
11 Respiratory muscle strength in stable adolescent and adult patients with cystic fibrosis Dunnink, M.A.
2009
8 1 p. 31-36
6 p.
article
12 The immediate effect of musculoskeletal physiotherapy techniques and massage on pain and ease of breathing in adults with cystic fibrosis Lee, Annemarie
2009
8 1 p. 79-81
3 p.
article
13 Time course and recovery of arterial blood gases during exacerbations in adults with Cystic Fibrosis Waterhouse, D.F.
2009
8 1 p. 9-13
5 p.
article
14 Urinary incontinence in 9–16 year olds with cystic fibrosis compared to other respiratory conditions and a normal group Browne, W.J.
2009
8 1 p. 50-57
8 p.
article
15 Wilson disease as a cause of liver injury in cystic fibrosis Kotalová, Radana
2009
8 1 p. 63-65
3 p.
article
                             15 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands