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Items where Author is "Sinnreich, M."

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Number of items: 12.

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.

Herrendorff, R. and Faleschini, M. T. and Stiefvater, A. and Erne, B. and Wiktorowicz, T. and Kern, F. and Hamburger, M. and Potterat, O. and Kinter, J. and Sinnreich, M.. (2016) Identification of plant-derived alkaloids with therapeutic potential for myotonic dystrophy type I. Journal of Biological Chemistry, 291 (33). pp. 17165-17177.

Hafner, P. and Bonati, U. and Erne, B. and Schmid, M. and Rubino, D. and Pohlman, U. and Peters, T. and Rutz, E. and Frank, S. and Neuhaus, C. and Deuster, S. and Gloor, M. and Bieri, O. and Fischmann, A. and Sinnreich, M. and Gueven, N. and Fischer, D.. (2016) Improved Muscle Function in Duchenne Muscular Dystrophy through L-Arginine and Metformin: An Investigator-Initiated, Open-Label, Single-Center, Proof-Of-Concept-Study. PLoS ONE, 11 (1). e0147634.

Probstel, A. K. and Schaller, A. and Lieb, J. and Hench, J. and Frank, S. and Fuhr, P. and Kappos, L. and Sinnreich, M.. (2016) Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimic. Neurol Genet, 2 (6). e121.

Athanasopoulou, I. M. and Rasenack, M. and Grimm, C. and Axer, H. and Sinnreich, M. and Decard, B. F. and Grimm, A.. (2016) Ultrasound of the nerves — An appropriate addition to nerve conduction studies to differentiate paraproteinemic neuropathies. Journal of the Neurological Sciences, 362. pp. 188-195.

2013

O'Ferrall, E. K. and Gendron, D. and Guiot, M. C. and Hall, J. and Sinnreich, M.. (2013) Lower motor neuron syndrome due to cauda equina hypertrophy with onion bulbs. Muscle & nerve, Vol. 48, H. 2. pp. 301-305.

Peyer, A. K. and Kinter, J. and Hench, J. and Frank, S. and Fuhr, P. and Thomann, S. and Fischmann, A. and Kneifel, S. and Camano, P. and Munain, A. L. and Sinnreich, M. and Renaud, S.. (2013) Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia. Neuromuscular disorders, Vol. 23, H. 2. pp. 149-154.

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.

Ozcelik, S. and Fraser, G. and Castets, P. and Schaeffer, V. and Skachokova, Z. and Breu, K. and Clavaguera, F. and Sinnreich, M. and Kappos, L. and Goedert, M. and Tolnay, M. and Winkler, D. T.. (2013) Rapamycin attenuates the progression of tau pathology in P301S tau transgenic mice. PLoS ONE, Vol. 8, H. 5 , e62459.

2012

Azakir, B. A. and Di Fulvio, S. and Salomon, S. and Brockhoff, M. and Therrien, C. and Sinnreich, M.. (2012) Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules. Journal of biological chemistry, Vol. 287, H. 33. pp. 27629-27636.

Azakir, B. A. and Di Fulvio, S. and Kinter, J. and Sinnreich, M.. (2012) Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells. Journal of biological chemistry, Vol. 287, H. 13. pp. 10344-10354.

2011

Di Fulvio, S. and Azakir, B. A. and Therrien, C. and Sinnreich, M.. (2011) Dysferlin interacts with histone deacetylase 6 and increases alpha-tubulin acetylation. PLoS ONE, Vol. 6, H. 12 , e28563.

This list was generated on Fri Mar 29 06:43:01 2024 CET.