Distinct muscle imaging patterns in myofibrillar myopathies von FISCHER, D, KLEY, R. A, HEYER, C. M, GROSSMANN, A, HUEBNER, A, KRESS, W, REIMANN, J, SCHRÖDER, R, EYMARD, B, FARDEAU, M, UDD, B, GOLDFARB, L, STRACH, K, VORGERD, M, OLIVE, M, MEYER, C, SOMMER, T, EGER, K, ROLFS, A, MEYER, W, POU, A, PRADAS, J

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Muscle diffusion tensor imaging in glycogen storage disease V (McArdle disease) von Rehmann, R., Schlaffke, L., Froeling, M., Kley, R. A., Kühnle, E., De Marées, M., Forsting, J., Rohm, M., Tegenthoff, M., Schmidt-Wilcke, T., Vorgerd, M.

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Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathy von Maerkens, A., Kley, R.A., Olivé, M., Theis, V., van der Ven, P.F.M., Reimann, J., Milting, H., Schreiner, A., Uszkoreit, J., Eisenacher, M., Barkovits, K., Güttsches, A.K., Tonillo, J., Kuhlmann, K., Meyer, H.E., Schröder, R., Tegenthoff, M., Fürst, D.O., Müller, T., Goldfarb, L.G., Vorgerd, M., Marcus, K.

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New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analyses von Maerkens, A, Olivé, M, Schreiner, A, Feldkirchner, S, Schessl, J, Uszkoreit, J, Barkovits, K, Güttsches, A K, Theis, V, Eisenacher, M, Tegenthoff, M, Goldfarb, L G, Schröder, R, Schoser, B, van der Ven, P F M, Fürst, D O, Vorgerd, M, Marcus, K, Kley, R A

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Autoimmune rippling muscle disease: IgG antibodies bind to human muscle fibers von Güttsches, A, Tegenthoff, M, Kley, R, Vorgerd, M

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Creatine for treating muscle disorders von Kley, R A, Vorgerd, M, Tarnopolsky, M A

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A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy von Vorgerd, Matthias, van der Ven, Peter F.M., Bruchertseifer, Vera, Löwe, Thomas, Kley, Rudolf A., Schröder, Rolf, Lochmüller, Hanns, Himmel, Mirko, Koehler, Katrin, Fürst, Dieter O., Huebner, Angela

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Gentamicin treatment in McArdle disease : Failure to correct myophosphorylase deficiency von SCHROERS, A, KLEY, R. A, STACHON, A, HORVATH, R, LOCHMÜLLER, H, ZANGE, J, VORGERD, M

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Creatine treatment in muscle disorders: a meta-analysis of randomised controlled trials von Kley, R A, Tarnopolsky, M A, Vorgerd, M

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Immune-mediated rippling muscle disease von SCHULTE-MATTLER, W. J, KLEY, R. A, ROTHENFUSSER-KORBER, E, BÖHM, S, BRÜNING, T, HACKEMANN, J, STEINBRECHER, A, DÜRING, M. V, VOSS, B, VORGERD, M

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Myofibrillar myopathies: new developments von Olivé, Montse, Kley, Rudolf A, Goldfarb, Lev G

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P.99 - Reliability of DTI-based muscle-volumetry as compared to conventional T1-based manual segmentation von Rehmann, R., Schlaffke, L., Kley, R., Vorgerd, M., Tegenthoff, M.

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Reliability of DTI-based muscle-volumetry as compared to conventional T1-based manual segmentation von Rehmann, R., Schlaffke, L., Kley, R., Vorgerd, M., Tegenthoff, M.

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Diffusion tensor imaging reveals changes in non-fat infiltrated muscles in Late Onset Pompe Disease von Rehmann, R, Froeling, M, Rohm, M, Forsting, J, Kley, R A, Schmidt-Wilcke, T, Karabul, N, Meyer-Frießem, C H, Vollert, J, Tegenthoff, M, Vorgerd, M, Schlaffke, L

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INFLAMMATORY MYOPATHIES von Weihl, C., Ciryam, P., Guttsches, A., Marcus, K., Morimoto, R., Vendruscolo, M., Kley, R.

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INFLAMMATORY MYOPATHIES: P.160A bioinformatics approach to define the aggregation capacity of the myofiber proteome in inclusion body myositis von Weihl, C., Ciryam, P., Guttsches, A., Marcus, K., Morimoto, R., Vendruscolo, M., Kley, R.

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P.396 - Autoimmune rippling muscle disease: IgG antibodies bind to human muscle fibers von Güttsches, A., Tegenthoff, M., Kley, R., Vorgerd, M.

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Identification of first Swiss desminopathy families using systematic muscle imaging in myofibrillar myopathies von Fischer, D, Olive, M, Kley, R, Strach, K, Hübner, A, Udd, B, Fardeau, M, Goldfarb, L, Studer, A, Weber, M

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Th2-M2 immunity in lesions of muscular sarcoidosis and macrophagic myofasciitis von Preusse, Corinna, Goebel, Hans-H., Pehl, Debora, Rinnenthal, Jan L., Kley, Rudolf A., Allenbach, Yves, Heppner, Frank L., Vorgerd, Matthias, Authier, François Jerôme, Gherardi, Romain, Stenzel, Werner

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Widening the spectrum of filamin-C myopathy: Predominantly proximal myopathy due to the p.A193T mutation in the actin-binding domain of FLNC von Van den Bogaart, F, Claeys, Kristl, Kley, R, Kusters, B, Schrading, S, Kamsteeg, E, Voermans, N

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