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Automatic airway segmentation from computed tomography using robust and efficient 3-D convolutional neural networks

Scientific reports, 2021-08, Vol.11 (1), p.16001-16001, Article 16001

2021

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Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification

European radiology, 2017-11, Vol.27 (11), p.4680-4689

2017

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Monitoring Cystic Fibrosis Lung Disease by Computed Tomography: Radiation Risk in Perspective

American journal of respiratory and critical care medicine, 2014-06, Vol.189 (11), p.1328-1336

2014

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Chest radiography and computed tomography imaging in cystic fibrosis: current challenges and new perspectives

Pediatric radiology, 2023-04, Vol.53 (4), p.649-659

2023

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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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Chest computed tomography outcomes in a randomized clinical trial in cystic fibrosis: Lessons learned from the first ataluren phase 3 study

PloS one, 2020-11, Vol.15 (11), p.e0240898-e0240898

2020

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Inhaled antibiotics: dry or wet?

The European respiratory journal, 2014-11, Vol.44 (5), p.1308-1318

2014

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Crowdsourcing airway annotations in chest computed tomography images

PloS one, 2021-04, Vol.16 (4), p.e0249580-e0249580

2021

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Maximum inspiratory pressure as a clinically meaningful trial endpoint for neuromuscular diseases: a comprehensive review of the literature

Orphanet journal of rare diseases, 2017-03, Vol.12 (1), p.52-52, Article 52

2017

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Congenital lung abnormalities on magnetic resonance imaging: the CLAM study

European radiology, 2023-07, Vol.33 (7), p.4767-4779

2023

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Cystic fibrosis lung disease starts in the small airways: Can we treat it more effectively?

Pediatric pulmonology, 2010-02, Vol.45 (2), p.107-117

2010

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Patient-specific modeling of regional antibiotic concentration levels in airways of patients with cystic fibrosis: are we dosing high enough?

PloS one, 2015-03, Vol.10 (3), p.e0118454-e0118454

2015

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Quantification of Diaphragm Mechanics in Pompe Disease Using Dynamic 3D MRI

PloS one, 2016-07, Vol.11 (7), p.e0158912-e0158912

2016

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Magnetic resonance imaging in children: common problems and possible solutions for lung and airways imaging

Pediatric Radiology, 2015-12, Vol.45 (13), p.1901-1915

2015

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MRI changes in diaphragmatic motion and curvature in Pompe disease over time

European radiology, 2022-12, Vol.32 (12), p.8681-8691

2022

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What did we learn from two decades of chest computed tomography in cystic fibrosis?

Pediatric radiology, 2014-12, Vol.44 (12), p.1490-1495

2014

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The development of bronchiectasis on chest computed tomography in children with cystic fibrosis: can pre-stages be identified?

European radiology, 2016-12, Vol.26 (12), p.4563-4569

2016

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Diffusion weighted imaging in cystic fibrosis disease: beyond morphological imaging

European radiology, 2016-11, Vol.26 (11), p.3830-3839

2016

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Creating a training set for artificial intelligence from initial segmentations of airways

European radiology experimental, 2021-11, Vol.5 (1), p.54-54, Article 54

2021

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Annual Vaccination against Influenza Virus Hampers Development of Virus-Specific CD8+ T Cell Immunity in Children

Journal of Virology, 2011-11, Vol.85 (22), p.11995-12000

2011

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Chest MRI to diagnose early diaphragmatic weakness in Pompe disease

Orphanet journal of rare diseases, 2021-01, Vol.16 (1), p.21-21, Article 21

2021

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Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn screening to 5 years of age

Thorax, 2013-07, Vol.68 (7), p.643-651

2013

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Structural and Functional Lung Disease in Primary Ciliary Dyskinesia

Chest, 2008-08, Vol.134 (2), p.351-357

2008

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Automatic airway–artery analysis on lung CT to quantify airway wall thickening and bronchiectasis

Medical physics (Lancaster), 2016-10, Vol.43 (10), p.5736-5744

2016

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Chest Computed Tomography Scores Are Predictive of Survival in Patients with Cystic Fibrosis Awaiting Lung Transplantation

American journal of respiratory and critical care medicine, 2012-05, Vol.185 (10), p.1096-1103

2012

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Automatic airway segmentation from computed tomography using robust and efficient 3-D convolutional neural networks

Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification

Monitoring Cystic Fibrosis Lung Disease by Computed Tomography: Radiation Risk in Perspective

Chest radiography and computed tomography imaging in cystic fibrosis: current challenges and new perspectives

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

Chest computed tomography outcomes in a randomized clinical trial in cystic fibrosis: Lessons learned from the first ataluren phase 3 study

Inhaled antibiotics: dry or wet?

Crowdsourcing airway annotations in chest computed tomography images

Maximum inspiratory pressure as a clinically meaningful trial endpoint for neuromuscular diseases: a comprehensive review of the literature

Congenital lung abnormalities on magnetic resonance imaging: the CLAM study

Cystic fibrosis lung disease starts in the small airways: Can we treat it more effectively?

Patient-specific modeling of regional antibiotic concentration levels in airways of patients with cystic fibrosis: are we dosing high enough?

Quantification of Diaphragm Mechanics in Pompe Disease Using Dynamic 3D MRI

Magnetic resonance imaging in children: common problems and possible solutions for lung and airways imaging

MRI changes in diaphragmatic motion and curvature in Pompe disease over time

What did we learn from two decades of chest computed tomography in cystic fibrosis?

The development of bronchiectasis on chest computed tomography in children with cystic fibrosis: can pre-stages be identified?

Diffusion weighted imaging in cystic fibrosis disease: beyond morphological imaging

Creating a training set for artificial intelligence from initial segmentations of airways

Annual Vaccination against Influenza Virus Hampers Development of Virus-Specific CD8+ T Cell Immunity in Children

Chest MRI to diagnose early diaphragmatic weakness in Pompe disease

Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn screening to 5 years of age

Structural and Functional Lung Disease in Primary Ciliary Dyskinesia

Automatic airway–artery analysis on lung CT to quantify airway wall thickening and bronchiectasis

Chest Computed Tomography Scores Are Predictive of Survival in Patients with Cystic Fibrosis Awaiting Lung Transplantation

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