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Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium

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Gut microbiota signatures in cystic fibrosis: Loss of host CFTR function drives the microbiota enterophenotype

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Prevalence, geographic risk factor, and development of a standardized protocol for fungal isolation in cystic fibrosis: Results from the international prospective study “MFIP”

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State-of-the-art review of lung imaging in cystic fibrosis with recommendations for pulmonologists and radiologists from the “iMAging managEment of cySTic fibROsis” (MAESTRO) consortium

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A web-based psychological support program for caregivers of children with cystic fibrosis: a pilot study

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A randomised, double-blind, placebo-controlled trial of repeated nebulisation of non-viral cystic fibrosis transmembrane conductance regulator (CFTR) gene therapy in patients with cystic fibrosis

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Chemoattractants and cytokines in primary ciliary dyskinesia and cystic fibrosis: key players in chronic respiratory diseases

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Organization of Patient Management and Fungal Epidemiology in Cystic Fibrosis

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Cystic Fibrosis Diagnosis in Newborns, Children, and Adults

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Economic Burden And Health-Related Quality Of Life Of Patients With Cystic Fibrosis In Bulgaria

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The Potential of Self-Management mHealth for Pediatric Cystic Fibrosis: Mixed-Methods Study for Health Care and App Assessment

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OUP accepted manuscript

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Systematic Review of Postural Assessment in Individuals With Obstructive Respiratory Conditions

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Diffusion weighted imaging in cystic fibrosis disease: beyond morphological imaging

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Adult Care in Cystic Fibrosis

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Tobramycin and Beta-Lactam Antibiotic Use in Cystic Fibrosis Exacerbations: A Pharmacist Approach

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Vancomycin Dosing and Monitoring in the Treatment of Cystic Fibrosis: Results of a National Practice Survey

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Ventilatory limitation and dynamic hyperinflation during exercise testing in Cystic Fibrosis

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Cystic fibrosis – Ten promising therapeutic approaches in the current era of care

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Physiological markers of exercise capacity and lung disease severity in cystic fibrosis

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Comparison of health-related quality of life among children with cystic fibrosis and their parents in two Eastern European countries

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Perceived burden of respiratory physiotherapy in people with cystic fibrosis taking elexacaftor–tezacaftor–ivacaftor combination: a 1-year observational study

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Current Practices and Potential Nanotechnology Perspectives for Pain Related to Cystic Fibrosis

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Standard (head-down tilt) versus modified (without head-down tilt) postural drainage in infants and young children with cystic fibrosis

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Electronic home monitoring of children with cystic fibrosis to detect and treat acute pulmonary exacerbations and its effect on 1-year FEV1

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