Lista de obras - Alex Horsley - Dominio Público Uruguay

A novel method for infant multiple breath washout: First report in clinical practice

scientific article published on 18 June 2019

A very breathless woman

artículo científico publicado en 2011

Accurate lung volume measurements in vitro using a novel inert gas washout method suitable for infants

artículo científico publicado en 2015

An immunocytochemical assay to detect human CFTR expression following gene transfer

artículo científico publicado en 2009

Antibiotic treatment for Burkholderia cepacia complex in people with cystic fibrosis experiencing a pulmonary exacerbation

artículo científico publicado en 2016

Antibiotic treatment for Burkholderia cepacia complex in people with cystic fibrosis experiencing a pulmonary exacerbation

artículo científico publicado en 2012

Antibiotic treatment for Burkholderia cepacia complex in people with cystic fibrosis experiencing a pulmonary exacerbation

artículo científico publicado en 2011

Aspergillosis and the role of mucins in cystic fibrosis

artículo científico publicado en 2016

Assessing arthritis in the context of cystic fibrosis

scientific article published on 05 March 2019

Author's response: heterogeneity of change in LCI in patients with cystic fibrosis following antibiotic treatment

artículo científico publicado en 2013

Book review: Hodson and Geddes’ Cystic Fibrosis

artículo científico publicado en 2016

Burkholderia latens infection in cystic fibrosis

scientific article published on 02 February 2011

Can early Burkholderia cepacia complex infection in cystic fibrosis be eradicated with antibiotic therapy?

artículo científico publicado en 2011

Challenge for a new era-importance of ensuring accuracy of genotype in cystic fibrosis registries

artículo científico publicado en 2016

Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation

artículo científico publicado en 2013

Chapter 1 Genetics and pathophysiology

article

Chapter 5 Management of respiratory exacerbations

Clinical characteristics with inflammation profiling of long COVID and association with 1-year recovery following hospitalisation in the UK: a prospective observational study

Closed circuit rebreathing to achieve inert gas wash-in for multiple breath wash-out

artículo científico publicado en 2016

Comment on Comparison of lung clearance index determined by washout of N2 and SF6 in infants and preschool children with cystic fibrosis

scientific article published on 02 March 2019

Commentaries on Viewpoint: Using the same cut-off for sulfur hexafluoride and nitrogen multiple-breath washout may not be appropriate

artículo científico publicado en 2015

Consensus statement for inert gas washout measurement using multiple- and single- breath tests.

artículo científico publicado en 2013

Detection of early subclinical lung disease in children with cystic fibrosis by lung ventilation imaging with hyperpolarised gas MRI.

artículo científico publicado en 2017

Discordance between clinical, physiological, and radiological measures in cystic fibrosis

artículo científico publicado en 2014

ERS International Congress, Madrid, 2019: highlights from the Paediatric Assembly

artículo científico publicado en 2020

Effect of intermittent inspiratory leaks on measurement of lung clearance index using nitrogen and sulfur hexafluoride

artículo científico publicado en 2018

Effects of cystic fibrosis lung disease on gas mixing indices derived from alveolar slope analysis

artículo científico publicado en 2008

Effects of ivacaftor in patients with cystic fibrosis who carry the G551D mutation and have severe lung disease

artículo científico publicado en 2014

Efficacy and complications of small-bore, wire-guided chest drains

artículo científico publicado en 2006

Enhanced photoacoustic gas analyser response time and impact on accuracy at fast ventilation rates during multiple breath washout

artículo científico publicado en 2014

Evaluation of the impact of alveolar nitrogen excretion on indices derived from multiple breath nitrogen washout

artículo científico publicado en 2013

Feasibility and challenges of using multiple breath washout in COPD

scientific article published on 10 July 2018

Gout and hyperuricaemia in adults with cystic fibrosis

artículo científico publicado en 2011

Handheld computers in medicine: the way forward. ⬇️

artículo científico publicado en 2005

Implications of fatherhood in cystic fibrosis

artículo científico publicado en 2019

Itraconazole and inhaled fluticasone causing hypothalamic-pituitary-adrenal axis suppression in adults with cystic fibrosis

artículo científico publicado en 2012

Longitudinal Assessment of Children with Mild Cystic Fibrosis Using Hyperpolarized Gas Lung Magnetic Resonance Imaging and Lung Clearance Index.

artículo científico publicado en 2017

Lung clearance index in adults with non-cystic fibrosis bronchiectasis.

artículo científico publicado en 2014

Lung clearance index in cystic fibrosis subjects treated for pulmonary exacerbations

artículo científico publicado en 2015

Lung clearance index in detection of post-transplant bronchiolitis obliterans syndrome

artículo científico publicado en 2019

Lung clearance index in healthy volunteers, measured using a novel portable system with a closed circuit wash-in

scientific article published on 25 February 2020

Lung clearance index in the assessment of airways disease

artículo científico publicado en 2009

Lung clearance index is a repeatable and sensitive indicator of radiological changes in bronchiectasis

artículo científico publicado en 2014

Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis

scientific article published on 03 August 2007

Modelling structural determinants of ventilation heterogeneity: A perturbative approach

artículo científico publicado en 2018

Modelling structural determinants of ventilation heterogeneity: a perturbative approach

Orkambi in patients with severe disease - Bumps in the road to CFTR modulation

artículo científico publicado en 2017

Patterns of regional lung physiology in cystic fibrosis using ventilation magnetic resonance imaging and multiple-breath washout

scholarly article by Laurie J. Smith et al published 25 October 2018 in European Respiratory Journal

Phase I Studies of Acebilustat: Biomarker Response and Safety in Patients with Cystic Fibrosis

artículo científico publicado en 2016

Physical, cognitive, and mental health impacts of COVID-19 after hospitalisation (PHOSP-COVID): a UK multicentre, prospective cohort study

Preschool Multiple-Breath Washout Testing. An Official American Thoracic Society Technical Statement

artículo científico publicado en 2018

Putting lung function and physiology into perspective: cystic fibrosis in adults

artículo científico

Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis

artículo científico publicado en 2013

Reply: lung clearance index in primary ciliary dyskinesia and bronchiectasis.

artículo científico publicado en 2014

Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study

artículo científico publicado en 2023

SARS-CoV-2-specific nasal IgA wanes 9 months after hospitalisation with COVID-19 and is not induced by subsequent vaccination

artículo científico publicado en 2023

Simultaneous sulfur hexafluoride and nitrogen multiple-breath washout (MBW) to examine inherent differences in MBW outcomes

scientific article published on 01 October 2019

Supine posture changes lung volumes and increases ventilation heterogeneity in cystic fibrosis.

artículo científico publicado en 2017

Sweat chloride is not a useful marker of clinical response to Ivacaftor.

artículo científico publicado en 2013

The assessment of short and long term changes in lung function in CF using 129Xe MRI

artículo científico publicado en 2020

Using social media to improve communication with people with cystic fibrosis

artículo científico publicado en 2016

VX-659-Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles

article

Ventilation heterogeneity and the benefits and challenges of multiple breath washout testing in patients with cystic fibrosis.

artículo científico

Ventilation heterogeneity in children with well controlled asthma with normal spirometry indicates residual airways disease.

artículo científico publicado en 2008

What is the importance of classifying Aspergillus disease in cystic fibrosis patients?

artículo científico publicado en 2014

Lista de obras de Alex Horsley

A novel method for infant multiple breath washout: First report in clinical practice

A very breathless woman

Accurate lung volume measurements in vitro using a novel inert gas washout method suitable for infants

An immunocytochemical assay to detect human CFTR expression following gene transfer

Antibiotic treatment for Burkholderia cepacia complex in people with cystic fibrosis experiencing a pulmonary exacerbation

Antibiotic treatment for Burkholderia cepacia complex in people with cystic fibrosis experiencing a pulmonary exacerbation

Antibiotic treatment for Burkholderia cepacia complex in people with cystic fibrosis experiencing a pulmonary exacerbation

Aspergillosis and the role of mucins in cystic fibrosis

Assessing arthritis in the context of cystic fibrosis

Author's response: heterogeneity of change in LCI in patients with cystic fibrosis following antibiotic treatment

Book review: Hodson and Geddes’ Cystic Fibrosis

Burkholderia latens infection in cystic fibrosis

Can early Burkholderia cepacia complex infection in cystic fibrosis be eradicated with antibiotic therapy?

Challenge for a new era-importance of ensuring accuracy of genotype in cystic fibrosis registries

Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation

Chapter 1 Genetics and pathophysiology

Chapter 5 Management of respiratory exacerbations

Clinical characteristics with inflammation profiling of long COVID and association with 1-year recovery following hospitalisation in the UK: a prospective observational study

Closed circuit rebreathing to achieve inert gas wash-in for multiple breath wash-out

Comment on Comparison of lung clearance index determined by washout of N2 and SF6 in infants and preschool children with cystic fibrosis

Commentaries on Viewpoint: Using the same cut-off for sulfur hexafluoride and nitrogen multiple-breath washout may not be appropriate

Consensus statement for inert gas washout measurement using multiple- and single- breath tests.

Detection of early subclinical lung disease in children with cystic fibrosis by lung ventilation imaging with hyperpolarised gas MRI.

Discordance between clinical, physiological, and radiological measures in cystic fibrosis

ERS International Congress, Madrid, 2019: highlights from the Paediatric Assembly

Effect of intermittent inspiratory leaks on measurement of lung clearance index using nitrogen and sulfur hexafluoride

Effects of cystic fibrosis lung disease on gas mixing indices derived from alveolar slope analysis

Effects of ivacaftor in patients with cystic fibrosis who carry the G551D mutation and have severe lung disease

Efficacy and complications of small-bore, wire-guided chest drains

Enhanced photoacoustic gas analyser response time and impact on accuracy at fast ventilation rates during multiple breath washout

Evaluation of the impact of alveolar nitrogen excretion on indices derived from multiple breath nitrogen washout

Feasibility and challenges of using multiple breath washout in COPD

Gout and hyperuricaemia in adults with cystic fibrosis

Handheld computers in medicine: the way forward. ⬇️

Implications of fatherhood in cystic fibrosis

Itraconazole and inhaled fluticasone causing hypothalamic-pituitary-adrenal axis suppression in adults with cystic fibrosis

Longitudinal Assessment of Children with Mild Cystic Fibrosis Using Hyperpolarized Gas Lung Magnetic Resonance Imaging and Lung Clearance Index.

Lung clearance index in adults with non-cystic fibrosis bronchiectasis.

Lung clearance index in cystic fibrosis subjects treated for pulmonary exacerbations

Lung clearance index in detection of post-transplant bronchiolitis obliterans syndrome

Lung clearance index in healthy volunteers, measured using a novel portable system with a closed circuit wash-in

Lung clearance index in the assessment of airways disease

Lung clearance index is a repeatable and sensitive indicator of radiological changes in bronchiectasis

Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis

Modelling structural determinants of ventilation heterogeneity: A perturbative approach

Modelling structural determinants of ventilation heterogeneity: a perturbative approach

Orkambi in patients with severe disease - Bumps in the road to CFTR modulation

Patterns of regional lung physiology in cystic fibrosis using ventilation magnetic resonance imaging and multiple-breath washout

Phase I Studies of Acebilustat: Biomarker Response and Safety in Patients with Cystic Fibrosis

Physical, cognitive, and mental health impacts of COVID-19 after hospitalisation (PHOSP-COVID): a UK multicentre, prospective cohort study

Preschool Multiple-Breath Washout Testing. An Official American Thoracic Society Technical Statement

Putting lung function and physiology into perspective: cystic fibrosis in adults

Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis

Reply: lung clearance index in primary ciliary dyskinesia and bronchiectasis.

Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study

SARS-CoV-2-specific nasal IgA wanes 9 months after hospitalisation with COVID-19 and is not induced by subsequent vaccination

Simultaneous sulfur hexafluoride and nitrogen multiple-breath washout (MBW) to examine inherent differences in MBW outcomes

Supine posture changes lung volumes and increases ventilation heterogeneity in cystic fibrosis.

Sweat chloride is not a useful marker of clinical response to Ivacaftor.

The assessment of short and long term changes in lung function in CF using 129Xe MRI

Using social media to improve communication with people with cystic fibrosis

VX-659-Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles

Ventilation heterogeneity and the benefits and challenges of multiple breath washout testing in patients with cystic fibrosis.

Ventilation heterogeneity in children with well controlled asthma with normal spirometry indicates residual airways disease.

What is the importance of classifying Aspergillus disease in cystic fibrosis patients?