Professur für Neuropathologie

Growing old too early: Skeletal muscle single fiber biomechanics in ageing r349p desmin knock-in mice using the myorobot technology (2020) Pollmann C, Haug M, Reischl B, Prölß G, Pöschel T, Rupitsch S, Clemen CS, et al. Journal article 246th ENMC International Workshop: Protein aggregate myopathies 24–26 May 2019, Hoofddorp, The Netherlands (2020) Olivé M, Winter L, Fürst DO, Schröder R Journal article Dual Functional States of R406W-Desmin Assembly Complexes Cause Cardiomyopathy with Severe Intercalated Disc Derangement in Humans and in Knock-In Mice (2020) Herrmann H, Cabet E, Chevalier NR, Moosmann J, Schultheis D, Haas J, Schowalter M, et al. Journal article Plectin-related scapuloperoneal myopathy with treatment-responsive myasthenic syndrome (2020) Argente-Escrig H, Schultheis D, Kamm L, Schowalter M, Thiel C, Türk M, Clemen CS, et al. Journal article AAV-mediated cardiac gene transfer of wild-type desmin in mouse models for recessive desminopathies (2020) Ruppert T, Heckmann MB, Rapti K, Schultheis D, Jungmann A, Katus HA, Winter L, et al. Journal article Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in mice (2020) Stöckigt F, Eichhorn L, Beiert T, Knappe V, Radecke T, Steinmetz M, Nickenig G, et al. Journal article The MyoRobot technology discloses a premature biomechanical decay of skeletal muscle fiber bundles derived from R349P desminopathy mice (2019) Haug M, Meyer C, Reischl B, Prölß G, Vetter K, Iberl J, Nübler S, et al. Journal article Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: A case report (2019) Türk M, Nagel AM, Roemer F, Schlötzer-Schrehardt U, Thiel C, Winterholler M, Schröder R Journal article Disruptive recessive TTN missense mutations cause a wide range of clinico-pathological features (2019) Rees M, Fukuzawa A, Nikoopour R, Kho A, Qi J, Fernandez-Garcia M, Wraige E, et al. Conference contribution Sarcomeric pathology induced by homozygous expression of the myofibrillar myopathy - associated p.W2711X filamin C mutant (2019) Schuld J, Orfanos Z, Chevessier F, Unger A, Kirfel G, Van Der Ven P, Linke W, et al. Conference contribution