Lung clearance index response in patients with CF with class III CFTR mutations

Thorax. 2016 May;71(5):476-7. doi: 10.1136/thoraxjnl-2015-207894. Epub 2016 Mar 4.

¹ Division of Respiratory Medicine, Department of Pediatrics, Toronto, Ontario, Canada Physiology & Experimental Medicine, The Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada.
² Physiology & Experimental Medicine, The Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada Division of Gastroenterology and Nutrition, Department of Pediatrics, Toronto, Ontario, Canada Department of Pediatrics, University of Toronto, Ontario, Canada.
³ Division of Respiratory Medicine, Department of Pediatrics, Toronto, Ontario, Canada Physiology & Experimental Medicine, The Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada Division of Gastroenterology and Nutrition, Department of Pediatrics, Toronto, Ontario, Canada.
⁴ Division of Respiratory Medicine, Department of Pediatrics, Toronto, Ontario, Canada Physiology & Experimental Medicine, The Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada Institute of Health Policy, Management and Evaluation, University of Toronto, Ontario, Canada.
⁵ Division of Respiratory Medicine, Department of Pediatrics, Toronto, Ontario, Canada Physiology & Experimental Medicine, The Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada Department of Pediatrics, University of Toronto, Ontario, Canada.

No abstract available

Keywords: Cystic Fibrosis.

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