P119 An 8-week open-label interventional multi-centre study to evaluate the Lung Clearance Index as endpoint for clinical trials in cystic fibrosis patients ≥6 years of age, chronically infected with Pseudomonas aeruginosa
Welsner, M., Nährig, S., Mellies, U., Sieder, C., Ziegler, J.
Published in Journal of cystic fibrosis (01.06.2018)
Published in Journal of cystic fibrosis (01.06.2018)
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Journal Article
P242 Small colony variants of Staphylococcus aureus often exhibit a mucoid phenotype in the airways of people with cystic fibrosis
Rumpf, C., Schwartbeck, B., Janssen, T., Hait, R.J., Decker, C., Romme, K., Dübbers, A., Große-Onnebrink, J., Küster, P., Graepler-Mainka, U., Hebestreit, H., van Koningsbruggen-Rietschel, S., Renner, S., Wollschläger, B., Nährig, S., Stehling, F., Schlegtendal, A., Ballmann, M., Junge, S., Sutharsan, S., Deiwick, S., Kahl, B.C.
Published in Journal of cystic fibrosis (01.06.2023)
Published in Journal of cystic fibrosis (01.06.2023)
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Journal Article
Volumenabhängigkeit des ganzkörperplethysmographisch bestimmten Atemwegswiderstandes – Differenzierung von Übergewicht und Atemwegsobstruktion
Dressel, H, Jobst, A, de la Motte, D, Huber, R, Gamarra, F, Stratakis, D, Nährig, S, Seißler, J, Smith, H, Steinhäusser, W, Nowak, D, Jörres, R
Published in Pneumologie (07.04.2008)
Published in Pneumologie (07.04.2008)
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Conference Proceeding
Geringe Erythropoetin-Antwort auf Hypoxie bei Mukoviszidose (CF)-Patienten
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Conference Proceeding