Professur für Neuropathologie


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

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Abstract

Journal

Treatment of keratinocytes with 4-phenylbutyrate in epidermolysis bullosa: Lessons for therapies in keratin disorders (2019) Spörrer M, Prochnicki A, Tölle RC, Nyström A, Esser PR, Homberg M, Athanasiou I, 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 Loss of the novel Vcp (valosin containing protein) interactor Washc4 interferes with autophagy-mediated proteostasis in striated muscle and leads to myopathy in vivo (2018) Kustermann M, Manta L, Paone C, Kustermann J, Lausser L, Wiesner C, Eichinger L, et al. Journal article Expression of N471D strumpellin leads to defects in the endolysosomal system (2018) Song L, Rijal R, Karow M, Stumpf M, Hahn O, Park L, Insall R, et al. Journal article Inclusion Body Myopathy, Paget's Disease, and Fronto-temporal Dementia: a VCP-related Multi-systemic Proteinopathy (2018) Mengel D, Librizzi D, Schoser B, Glaeser D, Clemen CS, Dodel R, Schröder R 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
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