Prof. Dr. Rolf Schröder


Professur für Neuropathologie


Biomechanical changes of skeletal muscle in desminopathies - a novel approach to unravel the causes of progressive weakness in inherited muscle diseases
Prof. Wolfgang Goldmann; Prof. Dr. Rolf Schröder; Prof. Dr. Dr. Oliver Friedrich
(01.07.2014 - 30.06.2015)

Publikationen (Download BibTeX)

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Dittrich, S., Graf, E., Trollmann, R., Neudorf, U., Schara, U., Heilmann, A.,... Eichhorn, J. (2019). Effect and safety of treatment with ACE-inhibitor Enalapril and β-blocker metoprolol on the onset of left ventricular dysfunction in Duchenne muscular dystrophy - A randomized, double-blind, placebo-controlled trial. Orphanet Journal of Rare Diseases, 14(1).
Winter, L., Unger, A., Berwanger, C., Spörrer, M., Türk, M., Chevessier, F.,... Schröder, R. (2019). Imbalances in protein homeostasis caused by mutant desmin. Neuropathology and Applied Neurobiology, 45(5), 476-494.
Moreira, A., Loquai, C., Pfoefer, C., Kaehler, K.C., Knauss, S., Heppt, M.V.,... Heinzerling, L. (2019). Myositis and neuromuscular side-effects induced by immune checkpoint inhibitors. European journal of cancer, 106, 12-23.
Haug, M., Meyer, C., Reischl, B., Prölß, G., Vetter, K., Iberl, J.,... Friedrich, O. (2019). The MyoRobot technology discloses a premature biomechanical decay of skeletal muscle fiber bundles derived from R349P desminopathy mice. Scientific Reports, 9(1).
Minakaki, G., Canneva, F., Chevessier, F., Bode, F., Menges, S., Timotius, I.,... Klucken, J. (2019). Treadmill exercise intervention improves gait and postural control in alpha-synuclein mouse models without inducing cerebral autophagy. Behavioural Brain Research, 363, 199-215.
Spörrer, M., Prochnicki, A., Tölle, R.C., Nyström, A., Esser, P.R., Homberg, M.,... Kiritsi, D. (2019). Treatment of keratinocytes with 4-phenylbutyrate in epidermolysis bullosa: Lessons for therapies in keratin disorders. EBioMedicine.
Brackmann, F., Türk, M., Gratzki, N., Rompel, O., Jungbluth, H., Schröder, R., & Trollmann, R. (2018). Compound heterozygous RYR1 mutations in a preterm with arthrogryposis multiplex congenita and prenatal CNS bleeding. Neuromuscular Disorders, 28(1), 54-58.
Türk, M., Weber, I., Vogt-Ladner, G., Schröder, R., & Winterholler, M. (2018). Diaphragmatic dysfunction as the presenting symptom in neuromuscular disorders: A retrospective longitudinal study of etiology and outcome in 30 German patients. Neuromuscular Disorders, 28(6), 484-490.
Song, L., Rijal, R., Karow, M., Stumpf, M., Hahn, O., Park, L.,... Eichinger, L. (2018). Expression of N471D strumpellin leads to defects in the endolysosomal system. Disease Models & Mechanisms, 11(9).
Mengel, D., Librizzi, D., Schoser, B., Glaeser, D., Clemen, C.S., Dodel, R., & Schröder, R. (2018). Inclusion Body Myopathy, Paget's Disease, and Fronto-temporal Dementia: a VCP-related Multi-systemic Proteinopathy. Fortschritte der Neurologie, Psychiatrie, 86(7), 434-438.

Zuletzt aktualisiert 2017-13-10 um 02:00