Items where Author is "Fischer, D."

2013

Peyer, A. K. and Abicht, A. and Heinimann, K. and Sinnreich, M. and Fischer, D.. (2013) Quinine sulfate as a therapeutic option in a patient with slow channel congenital myasthenic syndrome. Neuromuscular disorders, Vol. 23, H. 7. pp. 571-574.

2012

Gensicke, H. and Datta, A. N. and Dill, P. and Schindler, C. and Fischer, D.. (2012) Increased incidence of Guillain-Barré syndrome after surgery. European journal of neurology, Vol. 19, H. 9. pp. 1239-1244.

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.

Treves, S. and Vukcevic, M. and Jeannet, P. Y. and Levano, S. and Girard, T. and Urwyler, A. and Fischer, D. and Voit, T. and Jungbluth, H. and Lillis, S. and Muntoni, F. and Quinlivan, R. and Sarkozy, A. and Bushby, K. and Zorzato, F.. (2011) Enhanced excitation-coupled Ca(2+) entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with central core disease. Human Molecular Genetics, 20 (3). pp. 589-600.

Hilbert, P. and Frank, S. and Raheem, O. and Suominen, T. and Penttilä, S. and Udd, B. and Fischer, D.. (2011) Normal muscle MRI does not preclude increased connective tissue in muscle of recessive myotonia congenita. Acta neurologica scandinavica, 124. pp. 146-147.

2009

Niemann, H. and Fischer, D. and Graffe, D. and Knittel, K. and Montiel, A. and Heilmeyer, O. and Nöthen, K. and Pape, T. and Kasten, S. and Bohrmann, G. and Boetius, A. and Gutt, J.. (2009) Biogeochemistry of a low-activity cold seep in the Larsen B area, western Weddell Sea, Antarctica. Biogeosciences, Vol. 6 , S. 2383–2395.

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.

Dierick, I. and Baets, J. and Irobi, J. and Jacobs, A. and De Vriendt, E. and Deconinck, T. and Merlini, L. and Van den Bergh, P. and Rasic, V. M. and Robberecht, W. and Fischer, D. and Morales, R. J. and Mitrovic, Z. and Seeman, P. and Mazanec, R. and Kochanski, A. and Jordanova, A. and Auer-Grumbach, M. and Helderman-van den Enden, A. T. and Wokke, J. H. and Nelis, E. and De Jonghe, P. and Timmerman, V.. (2008) Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies : a genotype-phenotype correlation study. Brain, Vol. 131, H. 5. pp. 1217-1227.