Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sina Berenbrinker"'
Autor:
Ute Graepler-Mainka, Tobias Kirn, Matthias Kappler, Ingo B. Autenrieth, Michael Hogardt, Ernst Eber, Marlies Wagner, Anjali Ralhan, Joachim Riethmueller, Sina Berenbrinker, Matthias Griese, Peter Martus, Andreas Pfleger, Andreas Hector, Dominik Hartl
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 15(3)
With intensified antibiotic therapy and longer survival, patients with cystic fibrosis (CF) are colonized with a more complex pattern of bacteria and fungi. However, the clinical relevance of these emerging pathogens for lung function remains poorly
Autor:
Matthias Kappler, Matthias Griese, Ute Graepler-Mainka, Sina Berenbrinker, Joachim Riethmueller, T. Kirn, Andreas Hector, Dominik Hartl
Publikováno v:
Journal of Cystic Fibrosis. 13
Background and Objectives: Fungi, particularly Aspergillus and Candida species, are increasingly found in cystic fibrosis (CF) airway fluids. However, their association with other CF pathogens, medications and lung function, especially in CF children
Autor:
Dominik Hartl, Bojana Mirković, Laura Eichler, Anjai Ralhan, Michelle A. Murray, Matthias Griese, Markus Mezger, Regina Ensenauer, Ines Mack, N. Gerry McElvaney, Gillian M. Lavelle, Deirdre Horan, Anurag Singh, Sanjay H. Chotirmall, Andreas Hector, Sina Berenbrinker, Ute Graepler-Mainka, Joachim Riethmüller
Publikováno v:
Journal of Allergy and Clinical Immunology. 138:1183-1189.e4
Background Chitinases have recently gained attention in the field of pulmonary diseases, particularly in asthma and chronic obstructive pulmonary disease, but their potential role in patients with cystic fibrosis (CF)–associated lung disease remain
Autor:
Ute Graepler-Mainka, Andreas Hector, Martin Stern, Joachim Riethmueller, Sina Berenbrinker, Dominik Hartl
Publikováno v:
Journal of Cystic Fibrosis. :S39
Objectives: Fungi, particularly Aspergillus and Candida species, are increasingly found in cystic fibrosis (CF) airway fluids. However, their relationship to other CF pathogens, medications and lung function, especially in CF children, remains poorly