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                             26 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A single bout of maximal exercise improves lung function in patients with cystic fibrosis Tucker, Matthew A.
2017
16 6 p. 752-758
7 p.
artikel
2 A treatment evaluator tool to monitor the real-world effectiveness of inhaled aztreonam lysine in cystic fibrosis Plant, Barry J
2017
16 6 p. 695-701
7 p.
artikel
3 A 3-year prognostic score for adults with cystic fibrosis Nkam, L.
2017
16 6 p. 702-708
7 p.
artikel
4 Bicarbonate in cystic fibrosis Kunzelmann, Karl
2017
16 6 p. 653-662
10 p.
artikel
5 Bile salt stimulated lipase: Inhibition by phospholipids and relief by phospholipase A2 Venuti, Elena
2017
16 6 p. 763-770
8 p.
artikel
6 Comment on data sparsity - Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: A longitudinal study Ayubi, Erfan
2017
16 6 p. e19-e20
nvt p.
artikel
7 Corrigendum to “Does current reporting of lung function by the UK cystic fibrosis registry allow a fair comparison of adult centres?” [J Cyst Fibros (2017) 585–591] Nightingale, J.A.
2017
16 6 p. e24-
1 p.
artikel
8 Corrigendum to “WS04.1 The effect of Orkambi® on exercise capacity and muscle strength” [J Cyst Fibros, volume 16, supplement 1, June 2017, pages S6–S7] Buckley, R.
2017
16 6 p. e25-
1 p.
artikel
9 Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: A longitudinal study; response to comments Barr, H.L.
2017
16 6 p. e21-
1 p.
artikel
10 Editorial Board 2017
16 6 p. ii-
1 p.
artikel
11 Effect of posture on lung ventilation distribution and associations with structure in children with cystic fibrosis Ramsey, Kathryn A.
2017
16 6 p. 713-718
6 p.
artikel
12 Exercise assessment and training in cystic fibrosis: Can less achieve more? Cox, Narelle S.
2017
16 6 p. 649-650
2 p.
artikel
13 Increased prevalence of colonic adenomas in patients with cystic fibrosis Hegagi, Mehdi
2017
16 6 p. 759-762
4 p.
artikel
14 Increased risk of PTLD in lung transplant recipients with cystic fibrosis Lowery, Erin M.
2017
16 6 p. 727-734
8 p.
artikel
15 Inhaled ENaC antisense oligonucleotide ameliorates cystic fibrosis-like lung disease in mice Crosby, Jeff R.
2017
16 6 p. 671-680
10 p.
artikel
16 Learning’s from the Editors Desk – 2017 Bell, Scott C.
2017
16 6 p. 645-646
2 p.
artikel
17 New Comorbidities in the Changing Face of Cystic Fibrosis Care Bonk, Michael
2017
16 6 p. 647-648
2 p.
artikel
18 News Bilton, Diana
2017
16 6 p. 651-652
2 p.
artikel
19 Pregnancy among cystic fibrosis women in the era of CFTR modulators Heltshe, Sonya L.
2017
16 6 p. 687-694
8 p.
artikel
20 Real-life acute lung function changes after lumacaftor/ivacaftor first administration in pediatric patients with cystic fibrosis Labaste, Aurélie
2017
16 6 p. 709-712
4 p.
artikel
21 Risk factors for persistent methicillin-resistant Staphylococcus aureus infection in cystic fibrosis Jennings, Mark T.
2017
16 6 p. 681-686
6 p.
artikel
22 The 1-min sit-to-stand test in cystic fibrosis — Insights into cardiorespiratory responses Radtke, Thomas
2017
16 6 p. 744-751
8 p.
artikel
23 The potential of phage therapy in cystic fibrosis: Essential human-bacterial-phage interactions and delivery considerations for use in Pseudomonas aeruginosa-infected airways Trend, Stephanie
2017
16 6 p. 663-670
8 p.
artikel
24 Tracheal diverticula in advanced cystic fibrosis: Prevalence, features, and outcomes after lung transplantation Kapnadak, Siddhartha G.
2017
16 6 p. 735-743
9 p.
artikel
25 Validation of multiple breath washout devices Raaijmakers, Lena
2017
16 6 p. e22-e23
nvt p.
artikel
26 What keeps children with cystic fibrosis awake at night? Vandeleur, Moya
2017
16 6 p. 719-726
8 p.
artikel
                             26 gevonden resultaten
 
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