Prof. Dr. Rolf Schröder

Institute of Neuropathology Professur für Neuropathologie

Preaged remodeling of myofibrillar cytoarchitecture in skeletal muscle expressing R349P mutant desmin (2017) Diermeier S, Buttgereit A, Schürmann S, Winter L, Xu H, Murphy RM, Clemen CS, et al. Journal article Genetic analysis of VCP and WASH complex genes in a German cohort of sporadic ALS-FTD patients (2017) Türk M, Schröder R, Khuller K, Hofmann A, Berwanger C, Ludolph AC, Dekomien G, et al. Journal article VCP-related multisystem proteinopathy presenting as early-onset Parkinson disease (2017) Regensburger M, Türk M, Pagenstecher A, Schröder R, Winkler J Journal article Aging-related progressive skeletal muscle weakness in mutant DesR349P muscles: a matter of compromised cytoarchitecture (2016) Diermeier S, Buttgereit A, Clemen C, Schröder R, Friedrich O Journal article, other DesR349P Mutation Results in Ultrastructural Disruptions and Compromise of Skeletal Muscle Biomechanics Already at Preclinical Stages in Young Mice before the Onset of Protein Aggregation (2016) Diermeier S, Haug M, Reischl B, Buttgereit A, Schürmann S, Spörrer M, Goldmann W, et al. Conference contribution, Abstract of a poster Neuromuscular endplate pathology in recessive desminopathies: Lessons from man and mice (2016) Durmus H, Ayhan O, Cirak S, Deymeer F, Parman Y, Franke A, Eiber N, et al. Journal article Stroke in Duchenne Muscular Dystrophy: A Retrospective Longitudinal Study in 54 Patients (2016) Winterholler M, Hollaender C, Kerling F, Weber I, Dittrich S, Türk M, Schröder R Journal article New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analyses (2016) Maerkens A, Olive M, Schreiner A, Feldkirchner S, Schessl J, Uszkoreit J, Barkovits K, et al. Journal article Mutant p97 exhibits species-specific changes of its ATPase activity and compromises the UBXD9-mediated monomerisation of p97 hexamers (2016) Rijal R, Arhzaouy K, Strucksberg KH, Cross M, Hofmann A, Schröder R, Clemen CS, Eichinger L Journal article Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy (2016) Winter L, Türk M, Harter PN, Mittelbronn M, Kornblum C, Norwood F, Jungbluth H, et al. Journal article