All Resources

This page provides filters and search facilities across all types of CF resources contained within the ECFS website.

Additionally, you can visit the specific resource type pages as follows:

More information on CF publications can be found here: Publications

October 2016

Title: Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: a longitudinal study
Authors
Helen L. Barr, Nigel Halliday, David A. Barrett, Paul Williams, Douglas L. Forrester, Daniel Peckham, Kate Williams, Alan R. Smyth, David Honeybourne, Joanna L.Whitehouse, Edward F. Nash, Jane Dewar, Andrew Clayton, Alan J. Knox , Miguel Cámara , and Andrew W. Fogarty
References
J Cyst Fibros. 2016 Oct 20. pii: S1569-1993(16)30617-8
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Scientific abstract

October 2016

Title: Coronary artery disease in Cystic Fibrosis: An Emerging Concern?
Authors
Kate Skolnik, Robert D. Levy, Pearce G. Wilcox, Bradley S. Quon
References
J Cyst Fibros. 2016 Oct 14. pii: S1569-1993(16)30612-9
Keywords
Atherosclerosis, Coronary artery disease, Diabetes, Dyslipidemia, Heart disease
PDF icon CF Research News article
Scientific abstract
Title: Coronary artery disease in Cystic Fibrosis: An Emerging Concern?
Authors
Kate Skolnik, Robert D. Levy, Pearce G. Wilcox, Bradley S. Quon
References
J Cyst Fibros. 2016 Oct 14. pii: S1569-1993(16)30612-9
Keywords
Atherosclerosis, Coronary artery disease, Diabetes, Dyslipidemia, Heart disease
PDF icon CF Research News article
Scientific abstract

October 2016

Title: Year to year change in FEV1 in patients with cystic fibrosis and different mutation classes
Authors
K De Boeck, A Zolin
References
J Cyst Fibros. 2016 Oct 11. pii: S1569-1993(16)30611-7.
Keywords
Age distribution, Lung function, Mutation class
Theme
Epidemiology/Models of care
PDF icon CF Research News article
Scientific abstract
Title: Year to year change in FEV1 in patients with cystic fibrosis and different mutation classes
Authors
K De Boeck, A Zolin
References
J Cyst Fibros. 2016 Oct 11. pii: S1569-1993(16)30611-7.
Keywords
Age distribution, Lung function, Mutation class
Theme
Epidemiology/Models of care
PDF icon CF Research News article
Scientific abstract

October 2016

Title: Bone demineralization is improved by ivacaftor in patients with cystic fibrosis carrying the p.Gly551Asp mutation
Authors
Isabelle Sermet-Gaudelus, Martial Delion, Isabelle Durieu, Jacky Jacquot, Dominique Hubert
References
J Cyst Fibros. 2016 Oct 10. pii: S1569-1993(16)30605-1
Keywords
Bone density, CFTR corrector, RANKL
Theme
CFTR/Basic Science
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Scientific abstract

October 2016

Title: A cross-sectional analysis of daytime versus nocturnal polysomnographic respiratory parameters in cystic fibrosis during early adolescence.
Authors
Waters KA, Lowe A, Cooper P, Vella S, Selvadurai H
References
J Cyst Fibros. 2016 Oct 8. pii: S1569-1993(16)30609-9
Keywords
Adolescent, Child, Exercise test, Pulmonary, Sleep study
Theme
Pulmonology
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Scientific abstract

October 2016

Title: Therapeutic benefit observed with the CFTR potentiator, ivacaftor, in a CF patient homozygous for the W1282X CFTR nonsense mutation
Authors
Venkateshwar Mutyam, Emily Falk Libby, Ning Peng, Denis Hadjiliadis, Michael Bonk, George M. Solomon, Steven M. Rowe
References
J Cyst Fibros. 2016 Oct 1. pii: S1569-1993(16)30607-5
Keywords
CFTR potentiator, Ivacaftor, PTC mutations, Readthrough, W1282X
PDF icon CF Research News article
Scientific abstract