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Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis

Thorax, 2008-02, Vol.63 (2), p.129-134

2008

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Improved treatment response to dornase alfa in cystic fibrosis patients using controlled inhalation

The European respiratory journal, 2011-12, Vol.38 (6), p.1328-1335

2011

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Lung parenchyma and structure visualisation in paediatric chest MRI: a comparison of different short and ultra-short echo time protocols

Clinical radiology, 2023-04, Vol.78 (4), p.e319-e327

2023

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Model of mucociliary clearance in cystic fibrosis lungs

Journal of theoretical biology, 2015-05, Vol.372, p.81-88

2015

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Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis

The European respiratory journal, 2004-01, Vol.23 (1), p.93-97

2004

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Progression of lung disease on computed tomography and pulmonary function tests in children and adults with cystic fibrosis

Thorax, 2006-01, Vol.61 (1), p.80-85

2006

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Imaging of respiratory muscles in neuromuscular disease: A review

Neuromuscular disorders : NMD, 2018-03, Vol.28 (3), p.246-256

2018

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Recombinant human DNase nebulisation in children with cystic fibrosis: before bedtime or after waking up?

The European respiratory journal, 2007-10, Vol.30 (4), p.763-768

2007

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Pharmacokinetics of inhaled monodisperse beclomethasone as a function of particle size

British journal of clinical pharmacology, 2007-09, Vol.64 (3), p.328-334

2007

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Pharmacokinetics and Tolerability of Once Daily Double Dose Tobramycin Inhalation in Cystic Fibrosis Using Controlled and Conventional Nebulization

Journal of aerosol medicine and pulmonary drug delivery, 2016-06, Vol.29 (3), p.273-280

2016

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Small airway deposition of dornase alfa during exacerbations in cystic fibrosis; a randomized controlled clinical trial

Pediatric pulmonology, 2014-02, Vol.49 (2), p.154-161

2014

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Development of a core outcome set for congenital pulmonary airway malformations: study protocol of an international Delphi survey

BMJ open, 2021-04, Vol.11 (4), p.e044544-e044544

2021

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Lung disease in FLNA mutation: Confirmatory report

European journal of medical genetics, 2011-05, Vol.54 (3), p.299-300

2011

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Determining presence of lung disease in young children with cystic fibrosis: Lung clearance index, oxygen saturation and cough frequency

Journal of cystic fibrosis, 2012-05, Vol.11 (3), p.223-230

2012

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Assessment of CF lung disease using motion corrected PROPELLER MRI: a comparison with CT

European radiology, 2016-03, Vol.26 (3), p.780-787

2016

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Novel strategies in newborn screening for cystic fibrosis: a prospective controlled study

Thorax, 2012-04, Vol.67 (4), p.289-295

2012

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Cost-effectiveness of newborn screening for cystic fibrosis determined with real-life data

Journal of cystic fibrosis, 2015-03, Vol.14 (2), p.194-202

2015

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Spirometer-controlled cine magnetic resonance imaging used to diagnose tracheobronchomalacia in paediatric patients

The European respiratory journal, 2014, Vol.43 (1), p.115-124

2014

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Bronchodilation in infants with malacia or recurrent wheeze

Archives of disease in childhood, 2003-03, Vol.88 (3), p.246-249

2003

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Annual lung function changes in young patients with chronic lung disease

The European respiratory journal, 2002-05, Vol.19 (5), p.886-891

2002

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Automatic Airway Segmentation in Chest CT Using Convolutional Neural Networks

Image Analysis for Moving Organ, Breast, and Thoracic Images, p.238-250

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Variability of aerosol delivery via spacer devices in young asthmatic children in daily life

The European respiratory journal, 1999-04, Vol.13 (4), p.787-791

1999

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Aerosol delivery from spacers in wheezy infants: a daily life study

The European respiratory journal, 2000-11, Vol.16 (5), p.850-856

2000

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Effect of a facemask leak on aerosol delivery from a pMDI-spacer system

Journal of aerosol medicine, 2004-03, Vol.17 (1), p.1-6

2004

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Cartilaginous airway wall dimensions and airway resistance in cystic fibrosis lungs

The European respiratory journal, 2000-04, Vol.15 (4), p.735-742

2000

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Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis

Improved treatment response to dornase alfa in cystic fibrosis patients using controlled inhalation

Lung parenchyma and structure visualisation in paediatric chest MRI: a comparison of different short and ultra-short echo time protocols

Model of mucociliary clearance in cystic fibrosis lungs

Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis

Progression of lung disease on computed tomography and pulmonary function tests in children and adults with cystic fibrosis

Imaging of respiratory muscles in neuromuscular disease: A review

Recombinant human DNase nebulisation in children with cystic fibrosis: before bedtime or after waking up?

Pharmacokinetics of inhaled monodisperse beclomethasone as a function of particle size

Pharmacokinetics and Tolerability of Once Daily Double Dose Tobramycin Inhalation in Cystic Fibrosis Using Controlled and Conventional Nebulization

Small airway deposition of dornase alfa during exacerbations in cystic fibrosis; a randomized controlled clinical trial

Development of a core outcome set for congenital pulmonary airway malformations: study protocol of an international Delphi survey

Lung disease in FLNA mutation: Confirmatory report

Determining presence of lung disease in young children with cystic fibrosis: Lung clearance index, oxygen saturation and cough frequency

Assessment of CF lung disease using motion corrected PROPELLER MRI: a comparison with CT

Novel strategies in newborn screening for cystic fibrosis: a prospective controlled study

Cost-effectiveness of newborn screening for cystic fibrosis determined with real-life data

Spirometer-controlled cine magnetic resonance imaging used to diagnose tracheobronchomalacia in paediatric patients

Bronchodilation in infants with malacia or recurrent wheeze

Annual lung function changes in young patients with chronic lung disease

Automatic Airway Segmentation in Chest CT Using Convolutional Neural Networks

Variability of aerosol delivery via spacer devices in young asthmatic children in daily life

Aerosol delivery from spacers in wheezy infants: a daily life study

Effect of a facemask leak on aerosol delivery from a pMDI-spacer system

Cartilaginous airway wall dimensions and airway resistance in cystic fibrosis lungs

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