Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P von Walter, M. C., Reilich, P., Huebner, A., Fischer, D., Schröder, R., Vorgerd, M., Kress, W., Born, C., Schoser, B. G., Krause, K. H., Klutzny, U., Bulst, S., Frey, J. R., Lochmüller, H.

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Alterations in the trapezius muscle in young patients with migraine – A pilot case series with MRI von Landgraf, M.N, Ertl-Wagner, B, Koerte, I.K, Thienel, J, Langhagen, T, Straube, A, von Kries, R, Reilich, P, Pomschar, A, Heinen, F

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High-dose immunoglobulin therapy in sporadic inclusion body myositis : a double-blind, placebo-controlled study von WALTER, M. C, LOCHMÜLLER, H, TOEPFER, M, SCHLOTTER, B, REILICH, P, SCHRÖDER, M, MÜLLER-FELBER, W, PONGRATZ, D

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P541: The impact of spinal muscular atrophies with regard to patients’ quality of life: a socio-economic analysis of a German patient cohort von Schreiber, O, Klug, C, Thiele, S, Herrmann, C, Zowe, J, Reilich, P, Nagels, K, Walter, M.C

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G.P.166 von Schreiber, O, Klug, C, Thiele, S, Schorling, E, Zowe, J, Reilich, P, Nagels, K, Walter, M.C

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Evaluation of Cost Of Illness (COI) and health care burden in Spinal Muscular Atrophies (SMA) von Klug, C, Thiele, S, Herrmann, C, Zowe, J, Reilich, P, Nagels, K, Walter, M.C

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Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degeneration von Schessl, J., Schuberth, M., Reilich, P., Schneiderat, P., Strigl-Pill, N., Walter, M. C., Schlotter-Weigel, B., Schoser, B.

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Seronegative myasthenic syndrome? von Selge, C., Kuempfel, T., Havla, J., Schoeberl, F., Danek, A., Reilich, P.

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Creatine monohydrate in muscular dystrophies : A double-blind, placebo-controlled clinical study von WALTER, M. C, LOCHMÜLLER, H, REILICH, P, KLOPSTOCK, T, HUBER, R, HARTARD, M, HENNIG, M, PONGRATZ, D, MÜLLER-FELBER, W

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P75 Muscle MRI findings in LGMD2L von Sarkozy, A, Hicks, P, Miller, J, Walter, M.C, Reilich, P, Radunovic, A, Vaidya, S.S, Lochmüller, H, Bushby, K, Straub, V

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P4.27 Muscle MRI findings in anoctaminopathy von Sarkozy, A, Hicks, D, Miller, J, Walter, M.C, Reilich, P, Lochmuller, H, Bushby, K, Straub, V

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P.47 - Congenital centronuclear myopathy and epidermolysis bullosa due to two novel mutations in the plectin gene von Walter, M., Reilich, P., Krause, S., Abicht, A., Schoser, B.

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Congenital centronuclear myopathy and epidermolysis bullosa due to two novel mutations in the plectin gene von Walter, M., Reilich, P., Krause, S., Abicht, A., Schoser, B.

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P64 Neutral lipid storage myopathy due to PNPLA2 mutations may respond to beta-adrenergic treatment von Horvath, R, Reilich, P, Krause, S, Turnbull, D.M, Trenell, M, Hollingsworth, K.G, Gorman, G.S, Czermin, B, Holinski-Feder, E, Walter, M.C, Schoser, B, Lochmüller, H

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Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial von Walter, Maggie C, Reilich, Peter, Thiele, Simone, Schessl, Joachim, Schreiber, Herbert, Reiners, Karlheinz, Kress, Wolfram, Müller-Reible, Clemens, Vorgerd, Matthias, Urban, Peter, Schrank, Bertold, Deschauer, Marcus, Schlotter-Weigel, Beate, Kohnen, Ralf, Lochmüller, Hanns

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FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients von Walter, M C, Petersen, J A, Stucka, R, Fischer, D, Schröder, R, Vorgerd, M, Schroers, A, Schreiber, H, Hanemann, C O, Knirsch, U, Rosenbohm, A, Huebner, A, Barisic, N, Horvath, R, Komoly, S, Reilich, P, Müller-Felber, W, Pongratz, D, Müller, J S, Auerswald, E A, Lochmüller, H

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De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy von Durling, H.J, Reilich, P, Müller-Höcker, J, Mendel, B, Pongratz, D, Wallgren-Pettersson, C, Gunning, P, Lochmüller, H, Laing, N.G

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G.P.166: Comparative economic impact of therapeutic innovation on health care burden of Duchenne Muscular Dystrophy (DMD) using Becker Muscular Dystrophy (BMD) as a comparator for... von Schreiber, O., Klug, C., Thiele, S., Schorling, E., Zowe, J., Reilich, P., Nagels, K., Walter, M.C.

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Seronegatives myasthenes Syndrom? von Selge, C., Kümpfel, T., Havla, J., Schöberl, F., Danek, A., Reilich, P.

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Muscle pathology in 57 patients with myotonic dystrophy type 2 von Schoser, Benedikt G.H., Schneider-Gold, Christiane, Kress, Wolfram, Goebel, Hans-Hilmar, Reilich, Peter, Koch, Manuela C., Pongratz, Dieter E., Toyka, Klaus V., Lochmüller, Hanns, Ricker, Kenneth

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