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Journal Article
Durmus, Hacer, Ayhan, Ozgecan, Cirak, Sebahattin, Deymeer, Feza, Parman, Yesim, Franke, Andre 
ORCID: 0000-0003-1530-5811, Eiber, Nane, Chevessier, Frederic, Schloetzer-Schrehardt, Ursula, Clemen, Christoph S., Hashemolhosseini, Said ORCID: 0000-0002-6564-5649, Schroeder, Rolf, Hemmrich-Stanisak, Georg, Tolun, Aslihan ORCID: 0000-0002-0328-6046 and Serdaroglu-Oflazer, Piraye
(2016).
Neuromuscular endplate pathology in recessive desminopathies: Lessons from man and mice.
Neurology, 87 (8).
S. 799 - 806.
PHILADELPHIA:
LIPPINCOTT WILLIAMS & WILKINS.
ISSN 1526-632X
Eiber, Nane, Frob, Franziska, Schowalter, Mirjam, Thiel, Christian, Clemen, Christoph S., Schroder, Rolf and Hashemolhosseini, Said (2020). Lack of Desmin in Mice Causes Structural and Functional Disorders of Neuromuscular Junctions. Front. Molec. Neurosci., 13. LAUSANNE: FRONTIERS MEDIA SA. ISSN 1662-5099
Spoerrer, Marina, Kah, Delf, Gerum, Richard C., Reischl, Barbara, Huraskin, Danyil, Dessalles, Claire A., Schneider, Werner, Goldmann, Wolfgang H., Herrmann, Harald, Thievessen, Ingo, Clemen, Christoph S., Friedrich, Oliver, Hashemolhosseini, Said, Schroeder, Rolf and Fabry, Ben (2022). The desmin mutation R349P increases contractility and fragility of stem cell-generated muscle micro-tissues. Neuropathol. Appl. Neurobiol., 48 (3). HOBOKEN: WILEY. ISSN 1365-2990