Items where Author is "Walter, M. C."

2016

Sunderkotter, C. and Nast, A. and Worm, M. and Dengler, R. and Dorner, T. and Ganter, H. and Hohlfeld, R. and Melms, A. and Melzer, N. and Rosler, K. and Schmidt, J. and Sinnreich, M. and Walter, M. C. and Wanschitz, J. and Wiendl, H.. (2016) Guidelines on dermatomyositis-excerpt from the interdisciplinary S2k guidelines on myositis syndromes by the German Society of Neurology. J Dtsch Dermatol Ges, 14 (3). pp. 321-338.

2011

Ullrich, N. D. and Fischer, D. and Kornblum, C. and Walter, M. C. and Niggli, E. and Zorzato, F. and Treves, S.. (2011) Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle. Human Mutation, 32 (3). pp. 309-317.

2008

Strach, K. and Sommer, T. and Grohé, C. and Meyer, C. and Fischer, D. and Walter, M. C. and Vorgerd, M. and Reilich, P. and Bär, H. and Reimann, J. and Reuner, U. and Germing, A. and Goebel, H. H. and Lochmüller, H. and Wintersperger, B. and Schröder, R.. (2008) Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathies. Neuromuscular disorders, Vol. 18, H. 6. pp. 475-482.