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The Journal of Pediatrics|December 10, 1999
Decreased levels of nitrosothiols in the lower airways of patients with cystic fibrosis and normal pulmonary functionH Grasemann, B Gaston, K Fang, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|December 8, 2000
Airway nitric oxide in infants with acute wheezy bronchitisF Ratjen, I Kavuk, S Gärtig, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 27, 2024
SPLUNC1 as a biomarker of pulmonary exacerbations in children with cystic fibrosisE Ben-Meir, L Perrem, M Shaw, et al.The European Respiratory Journal|December 21, 2007
Effect of growth hormone therapy on nitric oxide formation in cystic fibrosis patientsC Grasemann, F Ratjen, D Schnabel, et al.American Journal of Respiratory and Critical Care Medicine|December 9, 2000
Airway nitric oxide levels in cystic fibrosis patients are related to a polymorphism in the neuronal nitric oxide synthase geneH Grasemann, N Knauer, R Büscher, et al.The European Respiratory Journal|January 11, 2005
Oral L-arginine supplementation in cystic fibrosis patients: a placebo-controlled studyH Grasemann, C Grasemann, F Kurtz, et al.The European Respiratory Journal|June 3, 2000
Effect of L-arginine infusion on airway NO in cystic fibrosis and primary ciliary dyskinesia syndromeH Grasemann, S S Gärtig, H G Wiesemann, et al.Archives of Disease in Childhood|April 16, 1998
Nitric oxide metabolites in cystic fibrosis lung diseaseH Grasemann, I Ioannidis, R P Tomkiewicz, et al.Nitric Oxide : Biology and Chemistry|March 14, 2002
Nasal nitric oxide levels in cystic fibrosis patients are associated with a neuronal NO synthase (NOS1) gene polymorphismH Grasemann, K Storm van's Gravesande, S Gärtig, et al.The Journal of Antimicrobial Chemotherapy|January 7, 2006
Pharmacokinetics of inhaled colistin in patients with cystic fibrosisF Ratjen, E Rietschel, D Kasel, et al.Pageof 9