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Aetiology in adult patients with bronchiectasis

Respiratory medicine, 2007-06, Vol.101 (6), p.1163-1170

2007

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Twenty-year review of quantitative transmission electron microscopy for the diagnosis of primary ciliary dyskinesia

Journal of clinical pathology, 2012-03, Vol.65 (3), p.267-271

2012

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Impaired innate interferon induction in severe therapy resistant atopic asthmatic children

Mucosal immunology, 2013-07, Vol.6 (4), p.797-806

2013

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Pseudomonas aeruginosa, cyanide accumulation and lung function in CF and non-CF bronchiectasis patients

The European respiratory journal, 2008-09, Vol.32 (3), p.740-747

2008

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Bronchial and peripheral airway nitric oxide in primary ciliary dyskinesia and bronchiectasis

Respiratory medicine, 2009-05, Vol.103 (5), p.700-706

2009

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Lung Clearance Index (LCI) is Stable in Most Primary Ciliary Dyskinesia (PCD) Patients Managed in a Specialist Centre: a Pilot Study

Lung, 2017-08, Vol.195 (4), p.441-443

2017

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Primary Ciliary Dyskinesia Due to Microtubular Defects is Associated with Worse Lung Clearance Index

Lung, 2018-04, Vol.196 (2), p.231-238

2018

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93 Determining the impact of the T2R38 bitter taste receptor on P. aeruginosa infection in the cystic fibrosis airway

Journal of cystic fibrosis, 2017-06, Vol.16, p.S88-S88

2017

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Elevated peripheral airway nitric oxide in bronchiectasis reflects disease severity

Respiratory medicine, 2011-06, Vol.105 (6), p.885-891

2011

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Diagnosis and management of primary ciliary dyskinesia

Archives of Disease in Childhood, 2014-09, Vol.99 (9), p.850-856

2014

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Exhaled Breath Condensate pH as a Non-invasive Measure of Inflammation in Non-CF Bronchiectasis

ISRN pulmonology, 2011-11, Vol.2011, p.1-6

2011

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Phenotypic variability of CCDC103 mutation in British Pakistani children with Primary Ciliary Dyskinesia (PCD)

Cilia (London), 2015-07, Vol.4 (S1), p.P61-P61, Article P61

2015

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Procalcitonin in stable and unstable patients with bronchiectasis

Chronic respiratory disease, 2008-08, Vol.5 (3), p.155-160

2008

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P239 A role for polycystins in airway mucociliary clearance?

Thorax, 2013-12, Vol.68 (Suppl 3), p.A185-A185

2013

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P82 Lung clearance index (LCI) and genotype-phenotype correlations in Primary Ciliary Dyskinesia (PCD)

Thorax, 2015-12, Vol.70 (Suppl 3), p.A116-A117

2015

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S69 Development of an in vitro assay to detect chemically-induced changes in ciliary beat frequency

Thorax, 2015-12, Vol.70 (Suppl 3), p.A40-A41

2015

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S75 The T2R38 bitter taste receptor as a modifier of host response to pseudomonas aeruginosa in cystic fibrosis: does T2R38 genotype impact on clinical infection?

Thorax, 2016-12, Vol.71 (Suppl 3), p.A44-A44

2016

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S75The T2R38 bitter taste receptor as a modifier of host response to pseudomonas aeruginosa in cystic fibrosis: does T2R38 genotype impact on clinical infection?

Thorax, 2016-12, Vol.71 (Suppl 3), p.A44-A44

2016

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Lung Clearance Index Patients Managed in a Specialist Centre: a Pilot Study

Lung, 2017-08, Vol.195 (4), p.441

2017

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S125A retrospective study characterising ciliary ultrastructure, light microscopy and sputum microbiology associations with lung function decline in a large adult primary ciliary dyskinesia cohort

Thorax, 2013-12, Vol.68 (Suppl 3), p.A65-A65

2013

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S125 A retrospective study characterising ciliary ultrastructure, light microscopy and sputum microbiology associations with lung function decline in a large adult primary ciliary dyskinesia cohort

Thorax, 2013-12, Vol.68 (Suppl 3), p.A65-A65

2013

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S88 Electron Tomography Detects Ultrastructural Abnormalities In Patients With Pcd Due To A Dnah11 Defect

Thorax, 2014-12, Vol.69 (Suppl 2), p.A48-A49

2014

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S68 A longitudinal study characterising a large adult primary ciliary dyskinesia cohort

Thorax, 2015-12, Vol.70 (Suppl 3), p.A40-A40

2015

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Twenty-year review of quantitative transmission electron microscopy for the diagnosis of primary ciliary dyskinesia

Journal of clinical pathology, 2012, Vol.65 (3), p.269-273

2012

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ERS Task Force guideline for the diagnosis of primary ciliary dyskinesia

The European respiratory journal, 2017-01, Vol.49 (1)

2017

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Aetiology in adult patients with bronchiectasis

Twenty-year review of quantitative transmission electron microscopy for the diagnosis of primary ciliary dyskinesia

Impaired innate interferon induction in severe therapy resistant atopic asthmatic children

Pseudomonas aeruginosa, cyanide accumulation and lung function in CF and non-CF bronchiectasis patients

Bronchial and peripheral airway nitric oxide in primary ciliary dyskinesia and bronchiectasis

Lung Clearance Index (LCI) is Stable in Most Primary Ciliary Dyskinesia (PCD) Patients Managed in a Specialist Centre: a Pilot Study

Primary Ciliary Dyskinesia Due to Microtubular Defects is Associated with Worse Lung Clearance Index

93 Determining the impact of the T2R38 bitter taste receptor on P. aeruginosa infection in the cystic fibrosis airway

Elevated peripheral airway nitric oxide in bronchiectasis reflects disease severity

Diagnosis and management of primary ciliary dyskinesia

Exhaled Breath Condensate pH as a Non-invasive Measure of Inflammation in Non-CF Bronchiectasis

Phenotypic variability of CCDC103 mutation in British Pakistani children with Primary Ciliary Dyskinesia (PCD)

Procalcitonin in stable and unstable patients with bronchiectasis

P239 A role for polycystins in airway mucociliary clearance?

P82 Lung clearance index (LCI) and genotype-phenotype correlations in Primary Ciliary Dyskinesia (PCD)

S69 Development of an in vitro assay to detect chemically-induced changes in ciliary beat frequency

S75 The T2R38 bitter taste receptor as a modifier of host response to pseudomonas aeruginosa in cystic fibrosis: does T2R38 genotype impact on clinical infection?

S75The T2R38 bitter taste receptor as a modifier of host response to pseudomonas aeruginosa in cystic fibrosis: does T2R38 genotype impact on clinical infection?

Lung Clearance Index Patients Managed in a Specialist Centre: a Pilot Study

S125A retrospective study characterising ciliary ultrastructure, light microscopy and sputum microbiology associations with lung function decline in a large adult primary ciliary dyskinesia cohort

S125 A retrospective study characterising ciliary ultrastructure, light microscopy and sputum microbiology associations with lung function decline in a large adult primary ciliary dyskinesia cohort

S88 Electron Tomography Detects Ultrastructural Abnormalities In Patients With Pcd Due To A Dnah11 Defect

S68 A longitudinal study characterising a large adult primary ciliary dyskinesia cohort

Twenty-year review of quantitative transmission electron microscopy for the diagnosis of primary ciliary dyskinesia

ERS Task Force guideline for the diagnosis of primary ciliary dyskinesia

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