Recent data and developments in myositis

por Stenzel, Werner, Goebel, Hans H.
Publicado 2021

Biomarkers in Inflammatory Myopathies—An Expanded Definition

por Benveniste, Olivier, Goebel, Hans-Hilmar, Stenzel, Werner
Publicado 2019

Identification of the Endogenous Key Substrates of the Human Organic Cation Transporter OCT2 and Their Implication in Function of Dopaminergic Neurons

por Taubert, Dirk, Grimberg, Gundula, Stenzel, Werner, Schömig, Edgar
Publicado 2007

Editorial: Inflammatory muscle diseases: an update

por Tanboon, Jantima, Needham, Merrilee, Mozaffar, Tahseen, Stenzel, Werner, Nishino, Ichizo
Publicado 2023

A case of inflammatory peripheral nerve destruction antedating anti-NMDA receptor encephalitis

por Prüss, Harald, Hoffmann, Christian, Stenzel, Werner, Saschenbrecker, Sandra, Ebinger, Martin
Publicado 2014

The Liver-Stage Plasmodium Infection Is a Critical Checkpoint for Development of Experimental Cerebral Malaria

por Sato, Yuko, Ries, Stefanie, Stenzel, Werner, Fillatreau, Simon, Matuschewski, Kai
Publicado 2019

Inclusion body myositis and associated diseases: an argument for shared immune pathologies

por Nelke, Christopher, Kleefeld, Felix, Preusse, Corinna, Ruck, Tobias, Stenzel, Werner
Publicado 2022

Proteomic Profiling Unravels a Key Role of Specific Macrophage Subtypes in Sporadic Inclusion Body Myositis

por Roos, Andreas, Preusse, Corinna, Hathazi, Denisa, Goebel, Hans-Hilmar, Stenzel, Werner
Publicado 2019

Neuropathologie II: Erkrankungen des zentralen und peripheren Nervensystems: Ausblick auf neue Techniken in der Elektronenmikroskopie

por Schänzer, Anne, Dittmayer, Carsten, Weis, Joachim, Stenzel, Werner, Goebel, Hans-Hilmar
Publicado 2023

Neuropathologie I: Muskuläre Erkrankungen

por Schänzer, Anne, Dittmayer, Carsten, Porubsky, Stefan, Weis, Joachim, Goebel, Hans-Hilmar, Stenzel, Werner
Publicado 2022

Sequestration of cholesterol within the host late endocytic pathway restricts liver-stage Plasmodium development

por Petersen, Wiebke, Stenzel, Werner, Silvie, Olivier, Blanz, Judith, Saftig, Paul, Matuschewski, Kai, Ingmundson, Alyssa
Publicado 2017

Performance of ENMC and EULAR/ACR classification systems applied to a single tertiary center cohort of dermatomyositis patients

por Zoske, Jan, Schneider, Udo, Siegert, Elise, Kleefeld, Felix, Preuße, Corinna, Stenzel, Werner, Hahn, Katrin
Publicado 2021

Amyloid deposits and inflammatory infiltrates in sporadic inclusion body myositis: the inflammatory egg comes before the degenerative chicken

por Benveniste, Olivier, Stenzel, Werner, Hilton-Jones, David, Sandri, Marco, Boyer, Olivier, van Engelen, Baziel G. M.
Publicado 2015

Complement deposition at the neuromuscular junction in seronegative myasthenia gravis

por Hoffmann, Sarah, Harms, Lutz, Schuelke, Markus, Rückert, Jens-Carsten, Goebel, Hans-Hilmar, Stenzel, Werner, Meisel, Andreas
Publicado 2020

Anaplastic lymphoma kinase inhibitor-associated myositis

por Uruha, Akinori, Kliesch, Stefan, Schmid, Simone, Dittmayer, Carsten, Goebel, Hans-Hilmar, Dressel, Alexander, Stenzel, Werner, Handreka, Robert
Publicado 2020

Inflammatory features in sporadic late‐onset nemaline myopathy are independent from monoclonal gammopathy

por Tanboon, Jantima, Uruha, Akinori, Arahata, Yukie, Dittmayer, Carsten, Schweizer, Leonille, Goebel, Hans‐Hilmar, Nishino, Ichizo, Stenzel, Werner
Publicado 2021

The Deubiquitinating Enzyme Cylindromatosis Dampens CD8(+) T Cell Responses and Is a Critical Factor for Experimental Cerebral Malaria and Blood–Brain Barrier Damage

por Schmid, Ursula, Stenzel, Werner, Koschel, Josephin, Raptaki, Maria, Wang, Xu, Naumann, Michael, Matuschewski, Kai, Schlüter, Dirk, Nishanth, Gopala
Publicado 2017

ANO5-related muscle diseases: From clinics and genetics to pathology and research strategies

por Christiansen, Jon, Güttsches, Anne-Katrin, Schara-Schmidt, Ulrike, Vorgerd, Matthias, Heute, Christoph, Preusse, Corinna, Stenzel, Werner, Roos, Andreas
Publicado 2022

Atypical presentation of Arts syndrome due to a novel hemizygous loss-of-function variant in the PRPS1 gene

por Puusepp, Sanna, Reinson, Karit, Pajusalu, Sander, van Kuilenburg, André B.P., Dobritzsch, Doreen, Roelofsen, Jeroen, Stenzel, Werner, Õunap, Katrin
Publicado 2020

Novel bi-allelic variants expand the SPTBN4-related genetic and phenotypic spectrum

por Buelow, Markus, Süßmuth, David, Smith, Laurie D., Aryani, Omid, Castiglioni, Claudia, Stenzel, Werner, Bertini, Enrico, Schuelke, Markus, Knierim, Ellen
Publicado 2021