Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anja Kerstein-Stähle"'
Autor:
Sebastian Klapa, Antje Müller, Andreas Koch, Anja Kerstein‐Stähle, Wataru Kähler, Harald Heidecke, Susanne Schinke, Markus Huber‐Lang, Martin Nitschke, Silke Pitann, Solveig Augustin, Christian M. Karsten, Gabriela Riemekasten, Peter Lamprecht
Publikováno v:
Arthritis & Rheumatology. 75:760-767
Autor:
Sabrina Arnold, Sebastian Klapa, Konstanze Holl-Ulrich, Antje Müller, Anja Kerstein-Stähle, Peter Lamprecht
Publikováno v:
Zeitschrift für Rheumatologie. 81:558-566
Autor:
Sabrina, Arnold, Sebastian, Klapa, Konstanze, Holl-Ulrich, Antje, Müller, Anja, Kerstein-Stähle, Peter, Lamprecht
Publikováno v:
Zeitschrift fur RheumatologieLiteratur. 81(7)
Vasculitides are inflammatory diseases of blood vessels caused by autoimmune or infectious processes, which are associated with alterations and destruction of the vascular wall. From a histopathological point of view, granulomatous vasculitides can b
Autor:
Katja Bieber, Jennifer E. Hundt, Xinhua Yu, Marc Ehlers, Frank Petersen, Christian M. Karsten, Jörg Köhl, Khalaf Kridin, Kathrin Kalies, Anika Kasprick, Stephanie Goletz, Jens Y. Humrich, Rudolf A. Manz, Axel Künstner, Christoph M. Hammers, Reza Akbarzadeh, Hauke Busch, Christian D. Sadik, Tanja Lange, Hanna Grasshoff, Alexander M. Hackel, Jeanette Erdmann, Inke König, Walter Raasch, Mareike Becker, Anja Kerstein-Stähle, Peter Lamprecht, Gabriela Riemekasten, Enno Schmidt, Ralf J. Ludwig
Publikováno v:
Autoimmunity Reviews. 22:103236
Approximately 5% of the world-wide population is affected by autoimmune diseases. Overall, autoimmune diseases are still difficult to treat, impose a high burden on patients, and have a significant economic impact. Like other complex diseases, e.g.,
Autor:
Sebastian Ullrich, Sara Comdühr, Anja Kerstein-Stähle, Konstanze Holl-Ulrich, Peter Lamprecht, Sebastian Klapa, Antje Müller, Bettina Krause
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 6474, p 6474 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
ANCA-associated vasculitis (AAV) comprises granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA). While systemic vasculitis is a hallmark of all AAV, GPA is characterized by e