Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Nikolas Ruffer"'
Autor:
Martin Krusche, Ina Kötter, Lennard Ostendorf, Nikolas Ruffer, Marie-Therese Holzer, Tobias B. Huber
Publikováno v:
RMD Open, Vol 9, Iss 4 (2023)
Objective Refractory autoimmune diseases remain a significant challenge in clinical practice and new therapeutic options are needed. This systematic review evaluates the existing reported data on the CD38-targeting antibody daratumumab as a new thera
Externí odkaz:
https://doaj.org/article/91dfbff184434bdfb5678d0265ef3692
Autor:
Martin Krusche, Nikolas Ruffer
Publikováno v:
RMD Open, Vol 9, Iss 3 (2023)
The VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) is an adult-onset systemic autoinflammatory condition that is caused by an acquired deficiency of the UBA1 gene in hematopoietic progenitor cells. The clinical spectrum of
Externí odkaz:
https://doaj.org/article/0f62d31b9cfe4ddba612b2a525fa147a
Autor:
Anna Kernder, Tim Filla, Kirsten de Groot, Bernhard Hellmich, Julia Holle, Peter Lamprecht, Frank Moosig, Nikolas Ruffer, Christof Specker, Stefan Vordenbäumen, Matthias Schneider, Gamal Chehab
Publikováno v:
Frontiers in Medicine, Vol 9 (2023)
ObjectiveTo analyze the impact of the COVID-19 pandemic on medical care and vaccination acceptance of vasculitis patients in Germany.MethodsA web-based national survey was developed by rheumatology centers and vasculitis patient advocacy groups. The
Externí odkaz:
https://doaj.org/article/1e603fd00537450ba3aa2e66f9634044
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
IntroductionAutoinflammatory diseases (AID) are rare diseases presenting with episodes of sterile inflammation. These involve multiple organs and can cause both acute organ damage and serious long-term effects, like amyloidosis. Disease-specific anti
Externí odkaz:
https://doaj.org/article/2f3d9ad01a63487eae5e2adceaffdfbe
Autor:
Nikolas Ruffer, Marie-Therese Holzer, Lukas Can Bal, Simon Melderis, Martin Krusche, Tobias B. Huber, Ina Kötter
Publikováno v:
Rheumatology International. 43:551-557
Immune-mediated thrombotic thrombocytopenic purpura (iTTP) is a potentially fatal acquired thrombotic microangiopathy syndrome that frequently develops in the context of infectious diseases or systemic autoimmune conditions including connective tissu
Autor:
Martin Krusche, Nikolas Ruffer
Publikováno v:
Arthritis und Rheuma. 42:241-246
ZUSAMMENFASSUNGDie idiopathische rekurrierende Perikarditis (IRP) umfasst rezidivierende Perikarditis-Episoden, für die keine anderen Ursachen bzw. Auslöser gefunden werden können. Aufgrund ihres inflammatorischen Charakters (meist akute Schmerzat
Autor:
Tim Oqueka, Sören Galow, Marcel Simon, Anna Weidmann, Nicole Stübiger, Elvin Zengin-Sahm, Christoph Sinning, Martin Krusche, Nikolas Ruffer, Stefan Steurer, Xenia Schick-Bengardt, Marcial Sebode, Ludwig Jesse Horst, Oliver M. Steinmetz, Simon Melderis, Sina Cathérine Rosenkranz, Katharina Möller, Holger Jantke, Hans Klose
Publikováno v:
Zeitschrift für Rheumatologie. 81:535-548
Publikováno v:
Rheumatology.
Objectives To evaluate the effectiveness and safety of current treatment strategies for the vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome. Methods A protocolized systematic review according to PRISMA guidelines was perform
Publikováno v:
Rheumatology.
ObjectiveTo investigate the differential diagnostic spectrum in patients with suspected Behçet’s syndrome (BS) in low prevalence regions. In addition, the number of patients fulfilling the ICBD criteria despite not having BS was evaluated.MethodsT
Publikováno v:
Zeitschrift für Rheumatologie. 81:240-243
Die viszerale Leishmaniasis (VL) ist eine chronische Parasitose, die durch Erreger der Gattung Leishmania ausgelost wird und zahlreiche Erkrankungen imitieren kann. Die Leitsymptome der VL (Splenomegalie, Panzytopenie, Fieber) konnen insbesondere bei