Prof. Dr. Rolf Schröder



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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Unpublished / Preprint

Publication year

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Abstract

Journal

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 Early signs of architectural and biomechanical failure in isolated myofibers and immortalized myoblasts from desmin-mutant knock-in mice (2017) Diermeier S, Iberl J, Vetter K, Haug M, Pollmann C, Reischl B, Buttgereit A, et al. Journal article Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function (2017) Unger A, Beckendorf L, Boehme P, Kley R, Von Frieling-Salewsky M, Lochmueller H, Schröder R, et al. Journal article 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
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