Lower exhaled nitric oxide in infants with Cystic Fibrosis compared to healthy controls

Author:

Korten Insa,Liechti Margot,Singer Florian,Hafen Gaudenz,Rochat Isabelle,Anagnostopoulou Pinelopi,Müller-Suter Dominik,Usemann Jakob,Moeller Alexander,Frey Urs,Latzin Philipp,Casaulta Carmen

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference22 articles.

1. Exhaled nitric oxide in pulmonary diseases: a comprehensive review;Barnes;Chest,2010

2. Nitric oxide in cystic fibrosis;de Winter-de Groot;J Cyst Fibros,2005

3. Biomarkers in exhaled breath condensate indicate presence and severity of cystic fibrosis in children;Robroeks;Pediatr Allergy Immunol,2008

4. Low levels of exhaled nitric oxide are associated with impaired lung function in cystic fibrosis;Keen;Pediatr Pulmonol,2010

5. Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis;Grasemann;Respir Res,2006

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