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                             26 results found
no title author magazine year volume issue page(s) type
1 Aminoglycosides: old friend…new foe? Simmonds, N.J.
2016
15 4 p. 411-412
2 p.
article
2 A phase 3, multi-center, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of levofloxacin inhalation solution (APT-1026) in stable cystic fibrosis patients Flume, Patrick A.
2016
15 4 p. 495-502
8 p.
article
3 Beyond the lungs: The new GI frontier Freedman, Steven D.
2016
15 4 p. 409-410
2 p.
article
4 Bilateral midshaft femoral fractures in an adolescent baseball player Ju, D.G.
2016
15 4 p. e41-e43
nvt p.
article
5 Bronchial epithelial cell lines and primary nasal epithelial cells from cystic fibrosis respond differently to cigarette smoke exposure Williams, Mark Thomas Shaw
2016
15 4 p. 467-472
6 p.
article
6 CF end point commentary Durmowicz, Anthony G.
2016
15 4 p. 424-
1 p.
article
7 Colonoscopic screening shows increased early incidence and progression of adenomas in cystic fibrosis Niccum, David E.
2016
15 4 p. 548-553
6 p.
article
8 Diagnostic accuracy and distress associated with oropharyngeal suction in cystic fibrosis Doumit, Michael
2016
15 4 p. 473-478
6 p.
article
9 Distribution of the species of Achromobacter in a French Cystic Fibrosis Centre and multilocus sequence typing analysis reveal the predominance of A. xylosoxidans and clonal relationships between some clinical and environmental isolates Amoureux, Lucie
2016
15 4 p. 486-494
9 p.
article
10 d-Methionine reduces tobramycin-induced ototoxicity without antimicrobial interference in animal models Fox, Daniel J.
2016
15 4 p. 518-530
13 p.
article
11 Editorial Board 2016
15 4 p. ii-
1 p.
article
12 Efficacy measures for clinical trials: A review series Flume, Patrick A.
2016
15 4 p. 415-
1 p.
article
13 Evaluation of a systems biology approach to identify pharmacological correctors of the mutant CFTR chloride channel Pesce, Emanuela
2016
15 4 p. 425-435
11 p.
article
14 Gastric emptying and gastro-oesophageal reflux in children with cystic fibrosis Hauser, Bruno
2016
15 4 p. 540-547
8 p.
article
15 Highlighting the impact of cascade carrier testing in cystic fibrosis families Duguépéroux, Ingrid
2016
15 4 p. 452-459
8 p.
article
16 International prospective study of distal intestinal obstruction syndrome in cystic fibrosis: Associated factors and outcome Munck, Anne
2016
15 4 p. 531-539
9 p.
article
17 Newborn bloodspot screening for cystic fibrosis: What do antenatal and postnatal women know about cystic fibrosis? Fitzgerald, C.
2016
15 4 p. 436-442
7 p.
article
18 Newborn screening and population carrier screening for cystic fibrosis: Two ends of the same rope Massie, John
2016
15 4 p. 407-408
2 p.
article
19 Newborn screening for cystic fibrosis — The parent perspective Rueegg, Corina S.
2016
15 4 p. 443-451
9 p.
article
20 News 2016
15 4 p. 413-414
2 p.
article
21 Physiologic endpoints for clinical studies for cystic fibrosis Stanojevic, Sanja
2016
15 4 p. 416-423
8 p.
article
22 The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screening Stafler, Patrick
2016
15 4 p. 460-466
7 p.
article
23 The pharmacokinetics and toxicity of morning vs. evening tobramycin dosing for pulmonary exacerbations of cystic fibrosis: A randomised comparison Prayle, A.P.
2016
15 4 p. 510-517
8 p.
article
24 Tracheal diverticula in cystic fibrosis—A potentially important underreported finding on chest CT Gayer, Gabriela
2016
15 4 p. 503-509
7 p.
article
25 Ultrasound and magnetic resonance imaging assessment of joint disease in symptomatic patients with cystic fibrosis arthropathy Fitch, G.
2016
15 4 p. e35-e40
nvt p.
article
26 Use of nrdA gene sequence clustering to estimate the prevalence of different Achromobacter species among Cystic Fibrosis patients in the UK Coward, Amy
2016
15 4 p. 479-485
7 p.
article
                             26 results found
 
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