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                             24 results found
no title author magazine year volume issue page(s) type
1 Benign outcome among positive cystic fibrosis newborn screen children with non-CF-causing variants Salinas, Danieli Barino
2015
14 6 p. 714-719
6 p.
article
2 Comparison of health-related quality of life among children with cystic fibrosis and their parents in two Eastern European countries Borawska-Kowalczyk, Urszula
2015
14 6 p. 798-804
7 p.
article
3 Concentration of fractional excretion of nitric oxide (FENO): A potential airway biomarker of restored CFTR function Kotha, Kavitha
2015
14 6 p. 733-740
8 p.
article
4 Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A new designation and management recommendations for infants with an inconclusive diagnosis following newborn screening Munck, A.
2015
14 6 p. 706-713
8 p.
article
5 Editorial Board 2015
14 6 p. ii-
1 p.
article
6 Effect of ivacaftor therapy on exhaled nitric oxide in patients with cystic fibrosis Grasemann, Hartmut
2015
14 6 p. 727-732
6 p.
article
7 Estimating body composition from skinfold thicknesses and bioelectrical impedance analysis in cystic fibrosis patients Alicandro, Gianfranco
2015
14 6 p. 784-791
8 p.
article
8 Factors associated with response to treatment of pulmonary exacerbations in cystic fibrosis patients Waters, Valerie J.
2015
14 6 p. 755-762
8 p.
article
9 Finding new drugs to enhance anion secretion in cystic fibrosis: Toward suitable systems for better drug screening. Report on the pre-conference meeting to the 12th ECFS Basic Science Conference, Albufeira, 25–28 March 2015 Verkman, Alan S.
2015
14 6 p. 700-705
6 p.
article
10 Hallmarks of therapeutic management of the cystic fibrosis functional landscape Amaral, Margarida D.
2015
14 6 p. 687-699
13 p.
article
11 Insulin secretion abnormalities in exocrine pancreatic sufficient cystic fibrosis patients Wooldridge, Jamie L.
2015
14 6 p. 792-797
6 p.
article
12 News Quittner, Alexandra
2015
14 6 p. 685-686
2 p.
article
13 Physical activity assessment in cystic fibrosis: A position statement Bradley, Judy
2015
14 6 p. e25-e32
nvt p.
article
14 Prolongation of antibiotic treatment for cystic fibrosis pulmonary exacerbations Waters, Valerie
2015
14 6 p. 770-776
7 p.
article
15 Proximity to blue spaces and risk of infection with Pseudomonas aeruginosa in cystic fibrosis: A case–control analysis Goeminne, Pieter C.
2015
14 6 p. 741-747
7 p.
article
16 Randomized trial of efficacy and safety of dornase alfa delivered by eRapid nebulizer in cystic fibrosis patients Sawicki, Gregory S.
2015
14 6 p. 777-783
7 p.
article
17 Should we monitor exhaled NO to assess the restoration of CFTR function in CF patients? Dinh-Xuan, Anh Tuan
2015
14 6 p. 683-684
2 p.
article
18 Sorting out the gray zone: Cystic fibrosis newborn screening McColley, Susanna A.
2015
14 6 p. 681-682
2 p.
article
19 The epidemiology of poor outcomes after pulmonary exacerbations Sanders, Don B.
2015
14 6 p. 679-680
2 p.
article
20 The ideal and the real world of mental health care delivery Ullrich, Gerald
2015
14 6 p. e33-e34
nvt p.
article
21 The influence of breathing mode on tobramycin serum levels using the I-neb AAD system in adults with cystic fibrosis van Velzen, A.J.
2015
14 6 p. 748-754
7 p.
article
22 The microbiology of the cystic fibrosis upper and lower airway Dosanjh, Amrita
2015
14 6 p. e35-
1 p.
article
23 Treatment and demographic factors affecting time to next pulmonary exacerbation in cystic fibrosis VanDevanter, Donald R.
2015
14 6 p. 763-769
7 p.
article
24 Use of ibuprofen to assess inflammatory biomarkers in induced sputum: Implications for clinical trials in cystic fibrosis Chmiel, James F.
2015
14 6 p. 720-726
7 p.
article
                             24 results found
 
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