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American Journal of Respiratory and Critical Care Medicine|November 14, 1997
Controlled trial of inhaled budesonide in patients with cystic fibrosis and chronic bronchopulmonary Psuedomonas aeruginosa infectionH Bisgaard, S S Pedersen, K G Nielsen, et al.
International Journal of Cardiology|January 22, 2013
Arrhythmia and exercise intolerance in Fontan patients: current status and future burdenL Idorn, K Juul, A S Jensen, et al.
Forensic Science International|November 1, 1988
Electrically-induced collagen calcification in pig skin. A histopathologic and histochemical studyT Karlsmark, L Danielsen, O Aalund, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 6, 2018
Initiating transitional care for adolescents with cystic fibrosis at the age of 12 is both feasible and promisingM Skov, G Teilmann, I N Damgaard, et al.
The European Respiratory Journal|June 10, 2010
Factors influencing age at diagnosis of primary ciliary dyskinesia in European childrenC E Kuehni, T Frischer, M-P F Strippoli, et al.
The European Respiratory Journal|December 2, 2009
Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in childrenA Barbato, T Frischer, C E Kuehni, et al.
Journal of Inherited Metabolic Disease|March 16, 2013
Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose studyL Borgwardt, C I Dali, J Fogh, et al.
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