Prof. Dr. Rolf Schröder



Organisationseinheit


Professur für Neuropathologie



Projektleitung


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). https://dx.doi.org/10.1186/s13023-019-1066-9
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. https://dx.doi.org/10.1111/nan.12516
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. https://dx.doi.org/10.1016/j.ejca.2018.09.033
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). https://dx.doi.org/10.1038/s41598-019-46723-6
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. https://dx.doi.org/10.1016/j.bbr.2018.11.035
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. https://dx.doi.org/10.1016/j.ebiom.2019.04.062
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. https://dx.doi.org/10.1016/j.nmd.2017.09.009
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. https://dx.doi.org/10.1016/j.nmd.2018.04.001
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). https://dx.doi.org/10.1242/dmm.033449
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. https://dx.doi.org/10.1055/s-0044-101033

Zuletzt aktualisiert 2017-13-10 um 02:00