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Acta Neuropathologica|April 17, 2021
Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathologyElise Siegert, Akinori Uruha, Hans-Hilmar Goebel, et al.Acta Neuropathologica|January 19, 2024
Multi-level profiling unravels mitochondrial dysfunction in myotonic dystrophy type 2Felix Kleefeld, Rita Horvath, Iago Pinal-Fernandez, et al.Journal of Neurology|June 26, 2025
Mitochondrial pathology in inflammatory myopathies: a marker of worse clinical outcomeAntonio Lauletta, Luca Bosco, Gioia Merlonghi, et al.Journal of Neurology|June 6, 2023
Morphological and molecular comparison of HIV-associated and sporadic inclusion body myositisSinja Vogt, Felix Kleefeld, Corinna Preusse, et al.Acta Neuropathologica|September 29, 2023
Senescent fibro-adipogenic progenitors are potential drivers of pathology in inclusion body myositisChristopher Nelke, Christina B Schroeter, Lukas Theissen, et al.Scientific Reports|October 3, 2024
Molecular composition of skeletal muscle in infants and adults: a comparative proteomic and transcriptomic studyAlexander Schaiter, Andreas Hentschel, Felix Kleefeld, et al.Skeletal Muscle|February 12, 2026
Unveiling FLNC variants: iPSC-derived myogenic cells as a model to study disease mechanismsNassam M Daya, Anne Schänzer, Andreas Hentschel, et al.Rheumatology (Oxford, England)|October 24, 2025
Identification of a distinctive gene signature associated with disease activity in granulomatous myositisIago Pinal-Fernandez, Nikolas Ruffer, Maria Casal-Dominguez, et al.Medrxiv : the Preprint Server for Health Sciences|June 26, 2025
Identification of a distinctive gene signature in granulomatous myositisIago Pinal-Fernandez, Nikolas Ruffer, Maria Casal-Dominguez, et al.Brain : a Journal of Neurology|September 13, 2022
Methylation of the 4q35 D4Z4 repeat defines disease status in facioscapulohumeral muscular dystrophyHannes Erdmann, Florentine Scharf, Stefanie Gehling, et al.Pageof 4