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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O.5 Mutations in MuRF1 and MuRF3 cause a novel protein aggregate myopathy and cardiomyopathy von Olivé, M, Abdul-Hussein, S, Oldfors, A, Fürst, D.O, van der Ven, P.F.M, Gonzalez-Mera, L, Gonzalez-Costello, J, Torrejon-Escribano, B, Alio, J, Pou, A, Ferrer, I, Tajsharghi, H

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G.O.5 Deciphering protein aggregates in myofibrillar myopathies – A proteomics approach von Kley, R.A, Maerkens, A, Olive, M, Claeys, K.G, Hanisch, F, van der Ven, P.F.M, Fuerst, D.O, Mueller, T, Marcus, K, Vorgerd, M

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P5.56 Myofibrillar myopathy associated with filamin C mutations: Refining the phenotype and new insights in pathogenesis von Vorgerd, M, Kley, R.A, Serdaroglu-Oflazer, P, Odgerel, Z, Olive, M, Lee, H.S, Hahn, Y, van der Ven, P.F.M, Höhfeld, J, Kirschner, J, Bilbao, J.M, Goldfarb, L.G, Fürst, D.O

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G.O.7 Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency von Guergueltcheva, V, Peeters, K, Baets, J, Ceuterick-de Groote, C, Martin, J.J, Suls, A, Vriendt, E.D, Mihaylova, V, Chamova, T, Almeida-Souza, L, Ydens, E, Tzekov, C, Hadjidekov, G, Gospodinova, M, Storm, K, Reyniers, E, Bichev, S, van der Ven, P.F.M, Furst, D.O, Mitev, V, Lochmuller, H, Timmerman, V, Tournev, I, De Jonghe, P, Jordanova, A

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D.P.3.01 Immunohistochemical and ultrastructural findings in myofibrillar myopathies von Claeys, K.G, Fardeau, M, Fürst, D.O, van der Ven, P.F.M, Behin, A, Brochier, G, Dubourg, O, Eymard, B, Faulkner, G, Guidy, C, Kley, R, Maisonobe, T, Manere, L, Richard, P, Schröder, R, Stojkovic, T, Suominen, T, Tolksdorf, K, Vicart, P, Udd, B, Voit, T, Stoltenburg, G

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Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency von Guergueltcheva, V, Peeters, K, Baets, J, Ceuterick-de Groote, C, Martin, J J, Suls, A, De Vriendt, E, Mihaylova, V, Chamova, T, Almeida-Souza, L, Ydens, E, Tzekov, C, Hadjidekov, G, Gospodinova, M, Storm, K, Reyniers, E, Bichev, S, van der Ven, P F M, Fürst, D O, Mitev, V, Lochmüller, H, Timmerman, V, Tournev, I, De Jonghe, P, Jordanova, A

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A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2 von Palenzuela, L, Andreu, A L, Gàmez, J, Vilà, M R, Kunimatsu, T, Meseguer, A, Cervera, C, Fernandez Cadenas, I, van der Ven, P F M, Nygaard, T G, Bonilla, E, Hirano, M

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Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscle von Bönnemann, C.G, Thompson, T.G, van der Ven, P.F.M, Goebel, H.H, Warlo, I, Vollmers, B, Reimann, J, Herms, J, Gautel, M, Takada, F, Beggs, A.H, Fürst, D.O, Kunkel, L.M, Hanefeld, F, Schröder, R

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Induction of corticospinal target finding by release of a diffusible, chemotropic factor in cervical spinal grey matter von Joosten, E.A.J., van der Ven, P.F.M., Hooiveld, M.H.W., ten Donkelaar, H.J.

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83 In vitro analysis of the functional impact of a MLP missense mutation associated with hypertrophic cardiomyopathy von Geier, C., Perrot, A., Gehmlich, K., Van der Ven, P.F.M., Fürst, D.O., Osterziel, K.J.

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Real-world effectiveness of reslizumab in patients with severe eosinophilic asthma: first Iinitiators and switchers von Hashimoto, S., Kroes, J.A., Eger, K.A., Asam, P.F.M., Hofstee, H.B., Bendien, S.A., Braunstahl, G.J., Broeders, M.E.A.C., Imming, L.M., Langeveld, B., Maitland-Van der Zee, A.H., Oud, K.T.M., Patberg, K.W., Smeenk, F.W.J.M., Romme, E.A.P.M., Bezouw, M.J. van, Ven, M.J. van de, Veen, A. van, Velzen, E. van, Veen, I.H.P.A.A. van, Weersink, E.J.M., Brinke, A. ten, Sont, J.K., Bel, E.H.

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