A multimodal approach to detect and monitor early lung disease in cystic fibrosis

Author:

Mondéjar-López Pedro1,Horsley Alexander2,Ratjen Felix3,Bertolo Silvia4,de Vicente Helene5,Asensio de la Cruz Òscar6

Affiliation:

1. Pediatric Pulmonologist, Pediatric Pulmonology and Cystic Fibrosis Unit, University Hospital Virgen de la Arrixaca, Murcia, Spain

2. Honorary Consultant, Respiratory Research Group, Division of Infection, Immunity & Respiratory Medicine, University of Manchester, Manchester, UK

3. Head, Division of Respiratory Medicine, Department of Pediatrics, Translational Medicine, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada

4. Radiologist, Department of Radiology, Ca’Foncello Regional Hospital, Treviso, Italy

5. Medical Advisor, Vertex Pharmaceuticals Spain S.L., Madrid, Spain

6. Pediatric Pulmonologist, Pediatric Unit, University Hospital Parc Taulí de Sabadell, Sabadell, Spain

Funder

provided by Robert Furlong and Kerry Dechant of Content

Publisher

Informa UK Limited

Subject

Public Health, Environmental and Occupational Health,Pulmonary and Respiratory Medicine,Immunology and Allergy

Reference131 articles.

1. Cystic fibrosis

2. Origins of Cystic Fibrosis Lung Disease

3. Lessons learned from the cystic fibrosis pig

4. Early lung disease in cystic fibrosis

5. Cystic Fibrosis Foundation. 2018 patient registry: annual data report. 2019. [cited 2020 Jan 2]. Available from: https://www.cff.org/Research/Researcher-Resources/Patient-Registry/2018-Patient-Registry-Annual-Data-Report.pdf

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