Patient and Caregiver Perceptions of Airway Clearance Methods Used for Cystic Fibrosis

Comparison of Physical Activity and Sedentary Behaviour between Schoolchildren with Cystic Fibrosis and Healthy Controls: A Gender Analysis

(2021) Alexandra Valencia-Peris et al.   International Journal of Environmental Research and Public Health

MRSA strains with distinct accessory genes predominate at different ages in cystic fibrosis

(2021) Harry S. Porterfield et al.   PEDIATRIC PULMONOLOGY

Cystic fibrosis 2019: Year in review

(2020) Iolo Doull   Paediatric Respiratory Reviews

Sustained Coinfections with Staphylococcus aureus and Pseudomonas aeruginosa in Cystic Fibrosis

(2020) Anthony J Fischer et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Objective Measures of Vest Therapy Adherence Among Pediatric Subjects With Cystic Fibrosis

(2020) Christine M Benoit et al.   Respiratory Care

Exercise as a substitute for traditional airway clearance in cystic fibrosis: a systematic review

(2020) Nathan Ward et al.   THORAX

Effects of exercise and airway clearance (PEP) on mucus clearance in cystic fibrosis: a randomised cross-over trial

(2019) Tiffany J. Dwyer et al.   EUROPEAN RESPIRATORY JOURNAL

Oscillating Positive Expiratory Pressure Therapy May Be Performed Poorly by Children With Cystic Fibrosis

(2019) Kevin J O'Sullivan et al.   Respiratory Care

Can exercise replace airway clearance techniques in cystic fibrosis? A survey of patients and healthcare professionals

(2019) N.J. Rowbotham et al.   Journal of Cystic Fibrosis

Answering the call to address cystic fibrosis treatment burden in the era of highly effective CFTR modulator therapy

(2019) Alex H. Gifford et al.   Journal of Cystic Fibrosis

Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial

(2019) Harry G M Heijerman et al.   LANCET

Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele

(2019) Peter G. Middleton et al.   NEW ENGLAND JOURNAL OF MEDICINE

Objective Versus Self-Reported Adherence to Airway Clearance Therapy in Cystic Fibrosis

(2018) Gabriela R Oates et al.   Respiratory Care

Exercise is commonly used as a substitute for traditional airway clearance techniques by adults with cystic fibrosis in Australia: a survey

(2018) Nathan Ward et al.   Journal of Physiotherapy

Development and electronic validation of the revised Cystic Fibrosis Questionnaire (CFQ-R Teen/Adult)

(2017) Amparo Solé et al.   Journal of Cystic Fibrosis

Tezacaftor–Ivacaftor in Residual-Function Heterozygotes with Cystic Fibrosis

(2017) Steven M. Rowe et al.   NEW ENGLAND JOURNAL OF MEDICINE

Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del

(2017) Jennifer L. Taylor-Cousar et al.   NEW ENGLAND JOURNAL OF MEDICINE

Objective Measurement of Adherence to Out-Patient Airway Clearance Therapy by High-Frequency Chest Wall Compression in Cystic Fibrosis

(2017) Christina L Mikesell et al.   Respiratory Care

Origins of Cystic Fibrosis Lung Disease

(2015) David A. Stoltz et al.   NEW ENGLAND JOURNAL OF MEDICINE

Airway clearance techniques used by people with cystic fibrosis in the UK

(2015) Z.H. Hoo et al.   Physiotherapy

A Functional Anatomic Defect of the Cystic Fibrosis Airway

(2014) Susan E. Birket et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Physiotherapy and cystic fibrosis

(2014) Maggie Patricia McIlwaine et al.   CURRENT OPINION IN PULMONARY MEDICINE

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis

(2014) M. J. Hoegger et al.   SCIENCE

Long-term multicentre randomised controlled study of high frequency chest wall oscillation versus positive expiratory pressure mask in cystic fibrosis

(2013) Maggie Patricia McIlwaine et al.   THORAX

A CFTR Potentiator in Patients with Cystic Fibrosis and theG551DMutation

(2011) Bonnie W. Ramsey et al.   NEW ENGLAND JOURNAL OF MEDICINE