Automatic bronchus and artery analysis on chest computed tomography to evaluate the effect of inhaled hypertonic saline in children aged 3-6 years with cystic fibrosis in a randomized clinical trial.
暂无分享,去创建一个
R. Kronmal | M. Rosenfeld | E. Andrinopoulou | J. Charbonnier | H. Tiddens | F. Ratjen | S. Davis | D. Caudri | L. Gallardo-Estrella | Q. Lv | Richard A. Kronmal | S. Stick | Yuxin Chen | Eleni-Rosalina Andrinopoulou | Leticia Gallardo-Estrella | Jean-Paul Charbonnier | Daan Caudri | Margaret Rosenfeld | Felix Ratjen | Karen D. Hinckley Stukovsky | Harm A.W.M. Tiddens | K. D. Stukovsky
[1] C. Boylan,et al. Luminal mucus plugs are spatially associated with airway wall thickening in severe COPD and asthma: A single-centered, retrospective, observational study. , 2022, Respiratory medicine.
[2] Marleen de Bruijne,et al. WS19.06 Validation of airway-artery algorithm to detect and monitor airway disease on chest computed tomography in the ataluren cystic fibrosis cohort , 2022, Journal of Cystic Fibrosis.
[3] R. Kronmal,et al. The effect of inhaled hypertonic saline on lung structure in children aged 3-6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trial. , 2022, The Lancet. Respiratory medicine.
[4] E. Andrinopoulou,et al. Sensitive automated airway-artery method to monitor progression of CF airway disease , 2021, Paediatric cystic fibrosis (CF).
[5] J. Davies,et al. Cystic fibrosis , 2021, The Lancet.
[6] J. Davies,et al. Utility of lung clearance index in CF: What we know, what we don't know and musings on how to bridge the gap. , 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[7] M. Skov,et al. Prospective longitudinal association between repeated multiple breath washout measurements and computed tomography scores in children with cystic fibrosis. , 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[8] M. M. van der Eerden,et al. The radiological diagnosis of bronchiectasis: what's in a name? , 2020, European Respiratory Review.
[9] H. Tiddens,et al. Diagnosis and quantification of bronchiectasis using computed tomography or magnetic resonance imaging: A systematic review. , 2020, Respiratory medicine.
[10] C. Wainwright,et al. Health-related quality-of-life in children with cystic fibrosis aged 5-years and associations with health outcomes. , 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[11] H. Tiddens,et al. Structural determinants of long-term functional outcomes in young children with cystic fibrosis , 2020, European Respiratory Journal.
[12] E. Andrinopoulou,et al. Airway disease on chest computed tomography of preschool children with cystic fibrosis is associated with school‐age bronchiectasis , 2019, Pediatric pulmonology.
[13] S. Stanojevic,et al. Inhaled hypertonic saline in preschool children with cystic fibrosis (SHIP): a multicentre, randomised, double-blind, placebo-controlled trial. , 2019, The Lancet. Respiratory medicine.
[14] Amir Pourmorteza,et al. Photon-counting CT: Technical Principles and Clinical Prospects. , 2018, Radiology.
[15] E. Andrinopoulou,et al. Quantitative assessment of airway dimensions in young children with cystic fibrosis lung disease using chest computed tomography , 2017, Pediatric pulmonology.
[16] P. Sly,et al. Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It? , 2017, American journal of respiratory and critical care medicine.
[17] Marleen de Bruijne,et al. Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification , 2017, European Radiology.
[18] A. Althouse. Adjust for Multiple Comparisons? It's Not That Simple. , 2016, The Annals of thoracic surgery.
[19] Marleen de Bruijne,et al. Multicentre chest computed tomography standardisation in children and adolescents with cystic fibrosis: the way forward , 2016, European Respiratory Journal.
[20] S. Stick,et al. Lung Clearance Index and Structural Lung Disease on Computed Tomography in Early Cystic Fibrosis. , 2015, American journal of respiratory and critical care medicine.
[21] Marleen de Bruijne,et al. PRAGMA-CF. A Quantitative Structural Lung Disease Computed Tomography Outcome in Young Children with Cystic Fibrosis. , 2015, American journal of respiratory and critical care medicine.
[22] H. Tiddens,et al. What did we learn from two decades of chest computed tomography in cystic fibrosis? , 2014, Pediatric Radiology.
[23] Peter D Sly,et al. Assessment of early bronchiectasis in young children with cystic fibrosis is dependent on lung volume. , 2013, Chest.
[24] R. Boucher,et al. Hypertonic saline is effective in the prevention and treatment of mucus obstruction, but not airway inflammation, in mice with chronic obstructive lung disease. , 2013, American journal of respiratory cell and molecular biology.
[25] F. Ratjen,et al. Early lung disease in cystic fibrosis. , 2013, The Lancet. Respiratory medicine.
[26] S. Stanojevic,et al. Multi-ethnic reference values for spirometry for the 3–95-yr age range: the global lung function 2012 equations , 2012, European Respiratory Journal.
[27] J. Carlin,et al. Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: a randomized trial. , 2011, JAMA.
[28] M. Rosenfeld,et al. Bronchiectasis and pulmonary exacerbations in children and young adults with cystic fibrosis. , 2011, Chest.
[29] M. Goddard. Histopathology of bronchiectasis , 2011 .
[30] S. Stanojevic,et al. Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF , 2011, Thorax.
[31] A. Bush,et al. Airway remodelling and its relationship to inflammation in cystic fibrosis , 2010, Thorax.
[32] Scott H. Donaldson,et al. Cystic fibrosis lung disease starts in the small airways: Can we treat it more effectively? , 2010, Pediatric pulmonology.
[33] H. Tiddens,et al. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis , 2007, Thorax.
[34] R. Boucher. Cystic fibrosis: a disease of vulnerability to airway surface dehydration. , 2007, Trends in molecular medicine.
[35] R. Boucher. Airway surface dehydration in cystic fibrosis: pathogenesis and therapy. , 2007, Annual review of medicine.
[36] R. Boucher,et al. Evidence for airway surface dehydration as the initiating event in CF airway disease , 2007, Journal of internal medicine.
[37] M. Knowles,et al. Mucus clearance and lung function in cystic fibrosis with hypertonic saline. , 2006, The New England journal of medicine.
[38] N L Müller,et al. Computed tomographic imaging of the airways: relationship to structure and function , 2005, European Respiratory Journal.
[39] W. Hop,et al. Cartilaginous airway wall dimensions and airway resistance in cystic fibrosis lungs. , 2000, The European respiratory journal.
[40] J. Charbonnier,et al. WS06.5 Validation of automated airway-artery method to diagnosis of cystic fibrosis-related bronchiectasis and airway wall thickening , 2021 .