Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Peter Küster"'
Autor:
Sivagurunathan Sutharsan, Stefanie Dillenhoefer, Matthias Welsner, Florian Stehling, Folke Brinkmann, Manuel Burkhart, Helmut Ellemunter, Anna-Maria Dittrich, Christina Smaczny, Olaf Eickmeier, Matthias Kappler, Carsten Schwarz, Sarah Sieber, Susanne Naehrig, Lutz Naehrlich, Klaus Tenbrock, Claus Pfannenstiel, Dirk Steffen, Jochen Meister, Britta Welzenbach, Anette Scharschinger, Markus Kratz, Maike Pincus, Tobias Tenenbaum, Mirjam Stahl, Kerstin Landwehr, Stefanie Dillenhöfer, Hans Kössel, Petra Kaiser, Manfred Käding, Simone Stolz, Stefan Blaas, Jutta Hammermann, Monika Gappa, Antje Schuster, Dana Spittel, Sabine Zirlik, Sabina Schmitt, Joachim Bargon, Malte Cremer, Sebastian Fähndrich, Andrea Heinzmann, Lutz Nährlich, Stefan Kuhnert, Sebastian Schmidt, Bettina Wollschläger, Anna Nolde, Inka Held, Wolfgang Kamin, Felix C. Ringshausen, Sabine Wege, Olaf Sommerburg, Norbert Geier, Sara Lisa Fleser, Heinrike Wilkens, Michael Lorenz, Paul Vöhringer, Martin Schebek, Christian Timke, Ingrid Bobis, Thomas Nüßlein, Doris Dieninghoff, Ernst Rietschel, Bastian Klinkhammer, Freerk Prenzel, Alexandra Wald, Axel Kempa, Eva Lücke, Ines Adams, Krystyna Poplawska, Simone Lehmkühler, Monika Bauck, Anne Pfülb, Rainald Fischer, Gudrun Schopper, Susanne Nährig, Matthias Griese, Jörg Grosse, Peter Küster, Birte KinderHolger Köster, Susanne Büsing, Margarethe Pohl, Andreas Artlich, Alexander Kiefer, Manfred Ballmann, Nikola Gjorgjevski, Markus A. Rose, Friederike Ruf, Rolf Mahlberg, Wolfgang Thomas, Ute Graepler, Sebastian Bode, hilipp Meyn, Josef Rosenecker, Cordula Koerner, Klaus-Michael Keller, Tina Teßmer, Helge Hebestreit, Gerhild Lohse
Publikováno v:
The Lancet Regional Health. Europe, Vol 32, Iss , Pp 100690- (2023)
Summary: Background: Treatment with elexacaftor/tezacaftor/ivacaftor (ETI) improves multiple clinical outcomes in people with cystic fibrosis (pwCF) with at least one F508del allele. This study evaluated the real-world impact of ETI on lung function,
Externí odkaz:
https://doaj.org/article/cb7f1132ad9145b4909f1a838def4b95
Autor:
Marie K. Wieneke, Felix Dach, Claudia Neumann, Dennis Görlich, Lena Kaese, Theo Thißen, Angelika Dübbers, Christina Kessler, Jörg Große-Onnebrink, Peter Küster, Holger Schültingkemper, Bianca Schwartbeck, Johannes Roth, Jerzy-Roch Nofer, Janina Treffon, Julia Posdorfer, Josefine Marie Boecken, Mariele Strake, Miriam Abdo, Sophia Westhues, Barbara C. Kahl
Publikováno v:
mSphere, Vol 6, Iss 3 (2021)
Staphylococcus aureusS. aureus
Externí odkaz:
https://doaj.org/article/38d616b2390b499d8616ab454ab11d91
Autor:
Corinna Westphal, Dennis Görlich, Stefanie Kampmeier, Susann Herzog, Nadja Braun, Carina Hitschke, Alexander Mellmann, Georg Peters, Barbara C. Kahl, Staphylococcal CF Study Group, Sibylle Junge., Burkhard Tümmler., Helmut Ellermunter, Angelika Dübbers, Peter Küster, Manfred Ballmann, Cordula Koerner-Rettberg, Jörg Große-Onnebrink, Eberhardt Heuer, Wolfgang Sextro, Jochen G, Jutta Hammermann, Ute Graepler-Mainka, Doris Staab, Bettina Wollschläger, Antje Schuster, Friedrich-Karl Tegtmeyer, Sivagurunathan Sutharsan, Alexandra Wald
Publikováno v:
Frontiers in Microbiology, Vol 11 (2020)
BackgroundStaphylococcus aureus is one of the most isolated pathogens from the airways of cystic fibrosis (CF) patients. There is a lack of information about the clonal nature of S. aureus cultured from CF patients and their impact on disease. We hyp
Externí odkaz:
https://doaj.org/article/984c7a7dfba141388d61877eb8766f77
Autor:
Susann Herzog, Felix Dach, Nicole de Buhr, Silke Niemann, Jannik Schlagowski, Diego Chaves-Moreno, Claudia Neumann, Jonas Goretzko, Vera Schwierzeck, Alexander Mellmann, Angelika Dübbers, Peter Küster, Holger Schültingkemper, Ursula Rescher, Dietmar H. Pieper, Maren von Köckritz-Blickwede, Barbara C. Kahl
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Staphylococcus aureus is one of the first and most prevalent pathogens cultured from the airways of cystic fibrosis (CF) patients, which can persist there for extended periods. Airway infections in CF patients are characterized by a strong inflammato
Externí odkaz:
https://doaj.org/article/d2bcd5f29662432aad134ee62a51d8fe
Autor:
Bianca Schwartbeck, Johannes Birtel, Janina Treffon, Lars Langhanki, Alexander Mellmann, Devika Kale, Janina Kahl, Nina Hirschhausen, Claudia Neumann, Jean C Lee, Friedrich Götz, Holger Rohde, Hanae Henke, Peter Küster, Georg Peters, Barbara C Kahl
Publikováno v:
PLoS Pathogens, Vol 12, Iss 11, p e1006024 (2016)
Cystic fibrosis (CF) is associated with chronic bacterial airway infections leading to lung insufficiency and decreased life expectancy. Staphylococcus aureus is one of the most prevalent pathogens isolated from the airways of CF patients. Mucoid col
Externí odkaz:
https://doaj.org/article/115eac6277384925803e40396e57d6fa
Autor:
Sibylle Junge, Dennis Görlich, Martijn den Reijer, Bärbel Wiedemann, Burkhard Tümmler, Helmut Ellemunter, Angelika Dübbers, Peter Küster, Manfred Ballmann, Cordula Koerner-Rettberg, Jörg Große-Onnebrink, Eberhardt Heuer, Wolfgang Sextro, Jochen G Mainz, Jutta Hammermann, Joachim Riethmüller, Ute Graepler-Mainka, Doris Staab, Bettina Wollschläger, Rüdiger Szczepanski, Antje Schuster, Friedrich-Karl Tegtmeyer, Sivagurunathan Sutharsan, Alexandra Wald, Jerzy-Roch Nofer, Willem van Wamel, Karsten Becker, Georg Peters, Barbara C Kahl
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0166220 (2016)
Staphylococcus aureus is an important pathogen in cystic fibrosis (CF). However, it is not clear which factors are associated with worse lung function in patients with persistent S. aureus airway cultures. Our main hypothesis was that patients with h
Externí odkaz:
https://doaj.org/article/2fd170f46763453f9678ccb54294c200
Autor:
Vera Eickel, Barbara Kahl, Beatrice Reinisch, Angelika Dübbers, Peter Küster, Claudia Brandt, Barbara Spellerberg
Publikováno v:
PLoS ONE, Vol 4, Iss 2, p e4650 (2009)
Streptococcus agalactiae is a well-known pathogen for neonates and immunocompromized adults. Beyond the neonatal period, S. agalactiae is rarely found in the respiratory tract. During 2002-2008 we noticed S. agalactiae in respiratory secretions of 30
Externí odkaz:
https://doaj.org/article/3cad0a680d2e4262aefe016cdf1c3085
Autor:
Julia Posdorfer, Josefine Marie Boecken, Jörg Große-Onnebrink, Johannes Roth, Angelika Dübbers, Mariele Strake, Jerzy-Roch Nofer, Felix Dach, Holger Schültingkemper, Claudia Neumann, Peter Küster, Bianca Schwartbeck, Sophia Westhues, Miriam Abdo, Marie K Wieneke, Dennis Görlich, Lena Kaese, Theo Thißen, Christina Kessler, Barbara C. Kahl, Janina Treffon
Publikováno v:
mSphere
mSphere, Vol 6, Iss 3 (2021)
mSphere, Vol 6, Iss 3 (2021)
Staphylococcus aureus is one of the most common pathogens isolated from the airways of cystic fibrosis (CF) patients and often persists for extended periods. There is limited knowledge about the diversity of S. aureus in CF. We hypothesized that incr
Autor:
Holger Schültingkemper, Farina E. Lennartz, Peter Küster, Christina Kessler, Georg Peters, Jörg Große-Onnebrink, Angelika Dübbers, Barbara C. Kahl, Bianca Schwartbeck
Publikováno v:
International Journal of Medical Microbiology. 309:283-287
Background: Staphylococcus aureus is one of the most frequently isolated pathogens in the respiratory tract of CF patients. Recently, we characterized peculiar mucoid S. aureus isolates, which are excessive biofilm formers and which carried a 5bp-del
Autor:
Bianca Schwartbeck, Holger Schültingkemper, Georg Peters, Angelika Dübbers, Christina Kessler, Mathias Schwerdt, Janina Treffon, Jörg Große-Onnebrink, Stefanie Kampmeier, Claudia Neumann, Susann Herzog, Peter Küster, Dennis Görlich, Barbara C. Kahl
Publikováno v:
International Journal of Medical Microbiology. 308:631-639
Background Cystic fibrosis (CF) is an autosomal recessive disease associated with chronic airway infections by Staphylococcus aureus as one of the earliest and most prevalent pathogens. We conducted a retrospective study to determine the S. aureus in