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Autor:
Gebhard Feierl, Ernst Eber, Andrea J. Grisold, Clemens Kittinger, Tanja Kaschnigg, Lilian Masoud-Landgraf, Gernot Zarfel, Ute Wagner-Eibel, Simone Friedl
Publikováno v:
Current Microbiology
Cystic fibrosis (CF) is the most common hereditary lung disease in the Caucasian population, characterized by viscous bronchial secretion, consecutive defective mucociliary clearance, and unavoidable colonization with microorganisms. Besides Pseudomo