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Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus

American journal of human genetics, 2018-12, Vol.103 (6), p.984-994

2018

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Pulmonary function deficits in newborn screened infants with cystic fibrosis managed with standard UK care are mild and transient

The European respiratory journal, 2017-11, Vol.50 (5), p.1700326-1700326

2017

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Registries and collaborative studies for primary ciliary dyskinesia in Europe

ERJ open research, 2020-04, Vol.6 (2), p.5

2020

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Childhood bronchiectasis, so little is known

Archives of disease in childhood, 2022-06, Vol.107 (6), p.523-524

2022

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De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry

American journal of human genetics, 2019-11, Vol.105 (5), p.1030-1039

2019

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Eradication success for non-tuberculous mycobacteria in children with cystic fibrosis

The European respiratory journal, 2021-05, Vol.57 (5), p.2003636

2021

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Treatment Preference Among People With Cystic Fibrosis: The Importance of Reducing Treatment Burden

Chest, 2022-12, Vol.162 (6), p.1241-1254

2022

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Data Resource Profile: The UK Cystic Fibrosis Registry

International journal of epidemiology, 2018-02, Vol.47 (1), p.9-10e

2018

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Chronicity Counts: The Impact of Pseudomonas aeruginosa , Staphylococcus aureus , and Coinfection in Cystic Fibrosis

American journal of respiratory and critical care medicine, 2024-07, Vol.210 (2), p.240-242

2024

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Lung Clearance Index at 4 Years Predicts Subsequent Lung Function in Children with Cystic Fibrosis

American journal of respiratory and critical care medicine, 2011-03, Vol.183 (6), p.752-758

2011

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Pancreatic enzyme prescription following ivacaftor licensing: A retrospective analysis of the US and UK cystic fibrosis registries

Journal of cystic fibrosis, 2024-07, Vol.23 (4), p.746-753

2024

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Incidence and risk factors of cancer in individuals with cystic fibrosis in the UK; a case-control study

Journal of cystic fibrosis, 2022-03, Vol.21 (2), p.302-308

2022

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Trajectories of early growth and subsequent lung function in cystic fibrosis: An observational study using UK and Canadian registry data

Journal of cystic fibrosis, 2023-05, Vol.22 (3), p.388-394

2023

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Survival estimates in European cystic fibrosis patients and the impact of socioeconomic factors: a retrospective registry Cohort study

The European respiratory journal, 2021-09, Vol.58 (3), p.2002288

2021

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Using Negative Control Outcomes and Difference-in-Differences Analysis to Estimate Treatment Effects in an Entirely Treated Cohort: The Effect of Ivacaftor in Cystic Fibrosis

American journal of epidemiology, 2022-03, Vol.191 (3), p.505-515

2022

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Future therapies for cystic fibrosis

Nature communications, 2023-02, Vol.14 (1), p.693-693, Article 693

2023

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Are inhaled corticosteroids prescribed rationally in primary ciliary dyskinesia?

The European respiratory journal, 2018-03, Vol.51 (3), p.1702221-1702221

2018

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Recovery of baseline lung function after pulmonary exacerbation in children with primary ciliary dyskinesia

Pediatric pulmonology, 2016-12, Vol.51 (12), p.1362-1366

2016

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An observational study of the lung clearance index throughout childhood in cystic fibrosis: early years matter

The European respiratory journal, 2020-10, Vol.56 (4), p.2000006

2020

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Projecting the impact of triple CFTR modulator therapy on intravenous antibiotic requirements in cystic fibrosis using patient registry data combined with treatment effects from randomised trials

Thorax, 2022-09, Vol.77 (9), p.873-881

2022

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Non-invasive ventilation and clinical outcomes in cystic fibrosis: Findings from the UK CF registry

Journal of cystic fibrosis, 2019-09, Vol.18 (5), p.665-670

2019

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Impact of cystic fibrosis on birthweight: a population based study of children in Denmark and Wales

Thorax, 2019-05, Vol.74 (5), p.447-454

2019

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Combination antifungal therapy for Scedosporium species in cystic fibrosis

Pediatric pulmonology, 2020-08, Vol.55 (8), p.1993-1995

2020

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Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus

Pulmonary function deficits in newborn screened infants with cystic fibrosis managed with standard UK care are mild and transient

Registries and collaborative studies for primary ciliary dyskinesia in Europe

Pulmonary exacerbations in patients with primary ciliary dyskinesia: an expert consensus definition for use in clinical trials

Childhood bronchiectasis, so little is known

De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry

Eradication success for non-tuberculous mycobacteria in children with cystic fibrosis

Treatment Preference Among People With Cystic Fibrosis: The Importance of Reducing Treatment Burden

Data Resource Profile: The UK Cystic Fibrosis Registry

Chronicity Counts: The Impact of Pseudomonas aeruginosa , Staphylococcus aureus , and Coinfection in Cystic Fibrosis

Lung Clearance Index at 4 Years Predicts Subsequent Lung Function in Children with Cystic Fibrosis

Pancreatic enzyme prescription following ivacaftor licensing: A retrospective analysis of the US and UK cystic fibrosis registries

Incidence and risk factors of cancer in individuals with cystic fibrosis in the UK; a case-control study

Trajectories of early growth and subsequent lung function in cystic fibrosis: An observational study using UK and Canadian registry data

Survival estimates in European cystic fibrosis patients and the impact of socioeconomic factors: a retrospective registry Cohort study

Using Negative Control Outcomes and Difference-in-Differences Analysis to Estimate Treatment Effects in an Entirely Treated Cohort: The Effect of Ivacaftor in Cystic Fibrosis

Future therapies for cystic fibrosis

Are inhaled corticosteroids prescribed rationally in primary ciliary dyskinesia?

Recovery of baseline lung function after pulmonary exacerbation in children with primary ciliary dyskinesia

An observational study of the lung clearance index throughout childhood in cystic fibrosis: early years matter

Projecting the impact of triple CFTR modulator therapy on intravenous antibiotic requirements in cystic fibrosis using patient registry data combined with treatment effects from randomised trials

Non-invasive ventilation and clinical outcomes in cystic fibrosis: Findings from the UK CF registry

Clinical characteristics of SARS-CoV-2 infection in children with cystic fibrosis: An international observational study

Impact of cystic fibrosis on birthweight: a population based study of children in Denmark and Wales

Combination antifungal therapy for Scedosporium species in cystic fibrosis

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