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Volatile biomarkers of Pseudomonas aeruginosa in cystic fibrosis and noncystic fibrosis bronchiectasis

Letters in applied microbiology, 2011-06, Vol.52 (6), p.610-613

2011

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234 The outcome of referrals for lung transplantation in patients with cystic fibrosis (CF); a single centre experience

Journal of cystic fibrosis, 2016-06, Vol.15, p.S110-S110

2016

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P414 Providing advice and information to women with cystic fibrosis on their reproductive choices

Journal of cystic fibrosis, 2024-06, Vol.23, p.S194-S195

2024

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61 Comparison of two chromogenic media for isolation of Staphylococcus aureus from respiratory samples from patients with cystic fibrosis

Journal of cystic fibrosis, 2015-06, Vol.14, p.S73-S73

2015

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Assessment of sample handling practices on microbial activity in sputum samples from patients with cystic fibrosis

Letters in applied microbiology, 2010-09, Vol.51 (3), p.272-277

2010

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29 Ivacaftor treatment is associated with a decline in symptoms of extra-oesophageal reflux in patients with cystic fibrosis and the G551D mutation

Journal of cystic fibrosis, 2016-06, Vol.15, p.S58-S59

2016

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P344 Weight and wellbeing on elexacaftor/tezacaftor/ivacaftor

Journal of cystic fibrosis, 2024-06, Vol.23, p.S173-S174

2024

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P441 Virtualwards for providing hospital-at-home care for adults with cystic fibrosis

Journal of cystic fibrosis, 2024-06, Vol.23, p.S202-S202

2024

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A comprehensive study of the polymicrobial nature of lower respiratory tract infections in patients with cystic fibrosis (CF)

Journal of cystic fibrosis, 2010, Vol.9, p.S25-S25

2010

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P200 The prevalence of laryngopharyngeal reflux and sino-nasal symptoms in adults with cystic fibrosis

Journal of cystic fibrosis, 2022-06, Vol.21, p.S122

2022

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WS04.06 Neoplastic disease and treatment in cystic fibrosis (CF): a comprehensive single centre case series

Journal of cystic fibrosis, 2022-06, Vol.21, p.S9

2022

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Outreach clinics for the provision of specialist cystic fibrosis (CF) care to remote areas

Journal of cystic fibrosis, 2009, Vol.8, p.S109-S109

2009

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The effects of lung transplantation on the nutritional status of patients with cystic fibrosis

Journal of cystic fibrosis, 2009, Vol.8, p.S86-S86

2009

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P244 Fertility and fatherhood in men with cystic fibrosis (CF)

Journal of cystic fibrosis, 2018-06, Vol.17, p.S128-S128

2018

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WS12.3 Telehealth monitoring for home intravenous antibiotics in cystic fibrosis

Journal of cystic fibrosis, 2018-06, Vol.17, p.S22-S22

2018

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Anxiety and depression in adult patients with cystic fibrosis

Journal of cystic fibrosis, 2008-06, Vol.7, p.S106-S106

2008

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The increasing range and complexity of surgery in patients with cystic fibrosis

Journal of cystic fibrosis, 2008-06, Vol.7, p.S121-S121

2008

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P147 “What options are available for those not able to take current CFTR modulators?”: an answer hidden in plain sight?

Journal of cystic fibrosis, 2023-06, Vol.22, p.S110-S110

2023

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Hypersensitivity pneumonitis: current concepts

The European respiratory journal, 2001-09, Vol.18 (Supplement 32), p.81S

2001

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The Late Neolithic/Early Chalcolithic Transition at Teleilat Ghassul: Context, Chronology and Culture

Paléorient, 2007, Vol.33 (1), p.15-32

Bourke, S.J.

2007

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Assessment of sample handling practices on microbial activity in sputum samples from patients with cystic fibrosis: Sample handling of CF sputum

Letters in applied microbiology, 2010-09, Vol.51 (3), p.272-277

2010

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Volatile biomarkers of Pseudomonas aeruginosa in cystic fibrosis and noncystic fibrosis bronchiectasis: Volatile biomarkers of Ps. aeruginosa

Letters in applied microbiology, 2011-06, Vol.52 (6), p.610-613

2011

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Interstitial lung disease induced by exogenous agents: factors governing susceptibility

The European respiratory journal, 2001-09, Vol.18 (Supplement 32), p.30S

2001

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Endobronchial metastases simulating primary carcinoma of the lung

Respiratory medicine, 1989-03, Vol.83 (2), p.151-152

1989

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Cyclophosphamide in severe steroid-resistant bronchiolitis obliterans organizing pneumonia

Respiratory medicine, 1997-03, Vol.91 (3), p.175-177

1997

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Volatile biomarkers of Pseudomonas aeruginosa in cystic fibrosis and noncystic fibrosis bronchiectasis

234 The outcome of referrals for lung transplantation in patients with cystic fibrosis (CF); a single centre experience

P414 Providing advice and information to women with cystic fibrosis on their reproductive choices

61 Comparison of two chromogenic media for isolation of Staphylococcus aureus from respiratory samples from patients with cystic fibrosis

Assessment of sample handling practices on microbial activity in sputum samples from patients with cystic fibrosis

29 Ivacaftor treatment is associated with a decline in symptoms of extra-oesophageal reflux in patients with cystic fibrosis and the G551D mutation

P344 Weight and wellbeing on elexacaftor/tezacaftor/ivacaftor

P441 Virtualwards for providing hospital-at-home care for adults with cystic fibrosis

A comprehensive study of the polymicrobial nature of lower respiratory tract infections in patients with cystic fibrosis (CF)

P200 The prevalence of laryngopharyngeal reflux and sino-nasal symptoms in adults with cystic fibrosis

WS04.06 Neoplastic disease and treatment in cystic fibrosis (CF): a comprehensive single centre case series

Outreach clinics for the provision of specialist cystic fibrosis (CF) care to remote areas

The effects of lung transplantation on the nutritional status of patients with cystic fibrosis

P244 Fertility and fatherhood in men with cystic fibrosis (CF)

WS12.3 Telehealth monitoring for home intravenous antibiotics in cystic fibrosis

Anxiety and depression in adult patients with cystic fibrosis

The increasing range and complexity of surgery in patients with cystic fibrosis

P147 “What options are available for those not able to take current CFTR modulators?”: an answer hidden in plain sight?

Hypersensitivity pneumonitis: current concepts

The Late Neolithic/Early Chalcolithic Transition at Teleilat Ghassul: Context, Chronology and Culture

Assessment of sample handling practices on microbial activity in sputum samples from patients with cystic fibrosis: Sample handling of CF sputum

Volatile biomarkers of Pseudomonas aeruginosa in cystic fibrosis and noncystic fibrosis bronchiectasis: Volatile biomarkers of Ps. aeruginosa

Interstitial lung disease induced by exogenous agents: factors governing susceptibility

Endobronchial metastases simulating primary carcinoma of the lung

Cyclophosphamide in severe steroid-resistant bronchiolitis obliterans organizing pneumonia

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