Matthias Türk

Lehrstuhl für Neuropathologie

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 Imbalances in protein homeostasis caused by mutant desmin (2019) Winter L, Unger A, Berwanger C, Spörrer M, Türk M, Chevessier F, Strucksberg KH, et al. Journal article Myositis and neuromuscular side-effects induced by immune checkpoint inhibitors (2019) Moreira A, Loquai C, Pfoefer C, Kaehler KC, Knauss S, Heppt MV, Gutzmer R, et al. Journal article The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice? (2018) Clemen CS, Winter L, Strucksberg KH, Berwanger C, Türk M, Kornblum C, Florin A, et al. Journal article Diaphragmatic dysfunction as the presenting symptom in neuromuscular disorders: A retrospective longitudinal study of etiology and outcome in 30 German patients (2018) Türk M, Weber I, Vogt-Ladner G, Schröder R, Winterholler M Journal article Perivascular hemosiderin deposits in human skeletal muscle tissue (2018) Delbridge C, Türk M, Agaimy A, Winterholler M, Schröder R Journal article Compound heterozygous RYR1 mutations in a preterm with arthrogryposis multiplex congenita and prenatal CNS bleeding (2018) Brackmann F, Türk M, Gratzki N, Rompel O, Jungbluth H, Schröder R, Trollmann R Journal article Ephedrine and 3,4 diaminopyridine responsive myasthenic syndrome in plectin-related epidermolysis bullosa simplex with muscular dystrophy (2017) Argente-Escrig H, Gomez NM, Gomez L, Türk M, Thiel C, Schröder R, Vilchez JJ Conference contribution 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