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Proteomic profiles in inclusion body myositis and polymyositis with mitochondrial pathology

Abstract Background Idiopathic inflammatory myopathies (IIMs) are autoimmune muscle diseases with distinct clinical, histopathological, and molecular features. Among them, inclusion body myositis (IBM) is refractory to immunotherapy and characterized by combined inflammatory and degenerative changes...

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Автори: Felix Kleefeld, Christina B. Schroeter, Donya Abdennebi, Vera Dobelmann, Sara Walli, Andreas Roos, Ute Distler, Stefan Tenzer, Tobias Bopp, Paula Quint, Linda-Isabell Schmitt, Markus Leo, Tim Hagenacker, Iago Pinal-Fernandez, Maria Casal-Dominguez, Andrew L. Mammen, Corinna Preuße, Lorenzo Maggi, Alexander Mensch, Sven G. Meuth, Werner Stenzel, Tobias Ruck, Christopher Nelke
Формат: Artigo
Мова:Inglês
Опубліковано: BMC 2026-02-01
Серія:Acta Neuropathologica Communications
Онлайн доступ:https://doi.org/10.1186/s40478-026-02243-9
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