Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Tilman, Schmidt"'
Autor:
Dominik Nell, Robert Wolf, Przemyslaw Marek Podgorny, Tobias Kuschnereit, Rieke Kuschnereit, Thomas Dabers, Sylvia Stracke, Tilman Schmidt
Publikováno v:
Biomedicines, Vol 12, Iss 2, p 455 (2024)
The nephrotic syndrome holds significant clinical importance and is characterized by a substantial protein loss in the urine. Damage to the glomerular basement membrane or podocytes frequently underlies renal protein loss. There is an increasing beli
Externí odkaz:
https://doaj.org/article/a29eb33d87c048e8b9923eae0d55eeb7
Autor:
Tilman Schmidt, Sara Afonso, Luce Perie, Karin Heidenreich, Sonia Wulf, Christian F. Krebs, Peter F. Zipfel, Thorsten Wiech
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Since the re-classification of membranoproliferative glomerulonephritis the new disease entity C3 glomerulopathy is diagnosed if C3 deposition is clearly dominant over immunoglobulins in immunohistochemistry or immunofluorescence. Although this new d
Externí odkaz:
https://doaj.org/article/790b4967f01b4ebab91eca8d0437d45e
Autor:
Tilman Schmidt, MD, Markus Gödel, MD, Maida Mahmud, MD, Lutz Fischer, MD, Tobias B. Huber, MD, Malte A. Kluger, MD, Florian Grahammer, MD
Publikováno v:
Transplantation Direct, Vol 8, Iss 2, p e1289 (2022)
Externí odkaz:
https://doaj.org/article/f752557d03364a608f235bf5b30cb7d5
Autor:
Linus A. Völker, Jessica Kaufeld, Gesa Balduin, Lena Merkel, Lucas Kühne, Dennis A. Eichenauer, Thomas Osterholt, Holger Hägele, Martin Kann, Franziska Grundmann, Benedikt Kolbrink, Kevin Schulte, Anja Gäckler, Andreas Kribben, Kristina Boss, Sebastian A. Potthoff, Lars C. Rump, Tilman Schmidt, Anja S. Mühlfeld, Karsten Schulmann, Matthias Hermann, Jens Gaedeke, Kristin Sauerland, Jörn Bramstedt, Ulrich P. Hinkel, Wolfgang Miesbach, Frederic Bauer, Timm H. Westhoff, Heike Bruck, Veronika Buxhofer-Ausch, Tobias J. Müller, Ralph Wendt, Ana Harth, Adrian Schreiber, Evelyn Seelow, Markus Tölle, Christopher Gohlisch, Markus Bieringer, Gesa Geuther, Wolfram J. Jabs, Michael Fischereder, Anke von Bergwelt-Baildon, Ulf Schönermarck, Paul Knoebl, Jan Menne, Paul T. Brinkkoetter, Fedai Özcan, Silke Markau, Matthias Girndt, Helmut Felten, Martin Hausberg, Marcus Brand, Jens Gerth, Martin Bommer, Stefan Zschiedrich, Johanna Schneider, Saban Elitok, Alexander Gawlik, Vedat Schwenger, Maximilian Roeder, Jörg Radermacher, Anke Morgner, Regina Herbst, Charis von Auer
Publikováno v:
Journal of Thrombosis and Haemostasis. 21:559-572
BACKGROUND: The von Willebrand factor-directed nanobody caplacizumab has greatly changed the treatment of immune thrombotic thrombocytopenic purpura (iTTP) in recent years. Data from randomized controlled trials established efficacy and safety. OBJEC
Autor:
Tilman Schmidt, Tobias B. Huber
Publikováno v:
Medizinische Klinik - Intensivmedizin und Notfallmedizin. 118:14-20
Autor:
Sven Pischke, Sarah Tamanaei, Maria Mader, Julian Schulze zur Wiesch, Christine Petersen-Benz, Munif Haddad, Marylyn M. Addo, Tilman Schmidt, Tobias B. Huber, Christian F. Krebs, Oliver M. Steinmetz, Jan E. Turner, Elion Hoxha, Thomas Horvatits
Publikováno v:
Pathogens, Vol 11, Iss 1, p 18 (2021)
Among numerous other immune-mediated diseases, glomerulonephritis has also been suspected to be an extrahepatic manifestation of HEV infection. In this prospective study, we tested 108 patients with glomerulonephritis and 108 age- and sex-matched hea
Externí odkaz:
https://doaj.org/article/dbb7081c77ac4069acc53f6fd4d5300c
Autor:
Elisa M. Alba Schmidt, Nicola Tomas, Tobias Huber, Thorsten Wiech, Tilman Schmidt, Ulrich Otto Wenzel
The complement system represents an ancient part of innate immunity and is comprised of multiple serum proteins. In several pathological conditions, including atypical hemolytic syndrome (aHUS), complement activation is contributing to disease progre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6b7815f2a9cbe15d773578b56783049
https://doi.org/10.1101/2023.01.27.23284929
https://doi.org/10.1101/2023.01.27.23284929
Autor:
Jan-Hendrik Riedel, Alina Borchers, Nariaki Asada, Anett Peters, Tilman Schmidt, Ulf Panzer, Pauline Ginsberg, Hans-Joachim Paust, Samuel Huber, Tobias B. Huber, Christian Krebs, Nicola Gagliani, Ning Song, Richard A. Flavell, Anna Kaffke, Jonas Luebbe, Jan-Eric Turner, Lennart Robben, Penelope Pelzcar, Sonja Hiekmann, Christoph Kilian
Publikováno v:
J Am Soc Nephrol
BACKGROUND: IL-17A–producing CD4(+) T helper (T(H)17) cells play a critical role in autoimmune and chronic inflammatory diseases, such as crescentic GN. The proinflammatory effects of IL-17 are mediated by the activation of the IL-17RA/IL-17RC comp
Publikováno v:
Journal of Nephrology
Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults. The disease is induced by antibodies, which are directed against the podocyte protein phospholipase A2 receptor 1 (PLA2R1-ab) in 80% of cases. B cell depleting treatments,
Publikováno v:
Molecular Immunology. 104:90-99
Immune-mediated glomerular diseases (glomerulonephritis) encompass a heterogeneous collection of diseases that cause inflammation within the glomerulus and other renal compartments with significant morbidity and mortality. In general, CD4+ T cells or