A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis von Zisimopoulou, P, Evangelakou, P, Tzartos, J, Lazaridis, K, Zouvelou, V, Mantegazza, R, Antozzi, C, Andreetta, F, Evoli, A, Deymeer, F, Saruhan-Direskeneli, G, Durmus, H, Brenner, T, Vaknin, A, Berrih-Aknin, S, Frenkian Cuvelier, M, Stojkovic, T, DeBaets, M, Losen, M, Martinez-Martinez, P, Kleopa, K.A, Zamba-Papanicolaou, E, Kyriakides, T, Kostera-Pruszczyk, A, Szczudlik, P, Szyluk, B, Lavrnic, D, Basta, I, Peric, S, Tallaksen, C, Maniaol, A, Tzartos, S.J

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Clinical comparison of anti-MuSK-vs anti-AChR-positive and seronegative myasthenia gravis von DEYMEER, F, GUNGOR-TUNCER, O, YILMAZ, V, PARMAN, Y, SERDAROGLU, P, OZDEMIR, C, VINCENT, A, SARUHAN-DIRESKENELI, G

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The treatment effect on peripheral B cell markers in antibody positive myasthenia gravis patients von Yilmaz, V., Tuzun, E., Durmus, H., Oflazer, P., Aysal, F., Parman, Y., Gungor-Tuncer, O., Deymeer, F., Saruhan-Direskeneli, G.

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Relation of HLA‐DRB1 to IgG4 autoantibody and cytokine production in muscle‐specific tyrosine kinase myasthenia gravis (MuSK‐MG) von Çebi, M., Durmuş, H., Yılmaz, V., Yentür, S.P., Aysal, F., Oflazer, P., Parman, Y., Deymeer, F., Saruhan‐Direskeneli, G.

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Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling von Toksoy, G, Durmus, H, Aghayev, A, Bagirova, G, Sevinc Rustemoglu, B, Basaran, S, Avci, S, Karaman, B, Parman, Y, Altunoglu, U, Yapici, Z, Tekturk, P, Deymeer, F, Topaloglu, H, Kayserili, H, Oflazer-Serdaroglu, P, Uyguner, ZO

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Titin antibodies in “seronegative” myasthenia gravis — A new role for an old antigen von Stergiou, C, Lazaridis, K, Zouvelou, V, Tzartos, J, Mantegazza, R, Antozzi, C, Andreetta, F, Evoli, A, Deymeer, F, Saruhan-Direskeneli, G, Durmus, H, Brenner, T, Vaknin, A, Berrih-Aknin, S, Behin, A, Sharshar, T, De Baets, M, Losen, M, Martinez-Martinez, P, Kleopa, K.A, Zamba-Papanicolaou, E, Kyriakides, T, Kostera-Pruszczyk, A, Szczudlik, P, Szyluk, B, Lavrnic, D, Basta, I, Peric, S, Tallaksen, C, Maniaol, A, Gilhus, N.E, Casasnovas Pons, C, Pitha, J, Jakubíkova, M, Hanisch, F, Bogomolovas, J, Labeit, D, Labeit, S, Tzartos, S.J

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Nusinersen in SMA 2 and 3: Risks vs benefits von Nusinersen, Deymeer F.

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Oculopharyngodistal myopathy is a distinct entity: Clinical and genetic features of 47 patients von DURMUS, H, LAVAL, S. H, STRAUB, V, BUSHBY, K, LOCHMÜLLER, H, SERDAROGLU-OFLAZER, P, DEYMEER, F, PARMAN, Y, KIYAN, E, GOKYIGITI, M, ERTEKIN, C, ERCAN, I, SOLAKOGLU, S, KARCAGI, V

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MuSK autoantibodies in myasthenia gravis detected by cell based assay — A multinational study von Tsonis, A.I, Zisimopoulou, P, Lazaridis, K, Tzartos, J, Matsigkou, E, Zouvelou, V, Mantegazza, R, Antozzi, C, Andreetta, F, Evoli, A, Deymeer, F, Saruhan-Direskeneli, G, Durmus, H, Brenner, T, Vaknin, A, Berrih-Aknin, S, Behin, A, Sharshar, T, De Baets, M, Losen, M, Martinez-Martinez, P, Kleopa, K.A, Zamba-Papanicolaou, E, Kyriakides, T, Kostera-Pruszczyk, A, Szczudlik, P, Szyluk, B, Lavrnic, D, Basta, I, Peric, S, Tallaksen, C, Maniaol, A, Casasnovas Pons, C, Pitha, J, Jakubíkova, M, Hanisch, F, Tzartos, S.J

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The effect of interleukin (IL)‐21 and CD4+CD25++ T cells on cytokine production of CD4+ responder T cells in patients with myasthenia gravis von Alahgholi‐Hajibehzad, M., Durmuş, H., Aysal, F., Gülşen‐Parman, Y., Oflazer, P., Deymeer, F., Saruhan‐Direskeneli, G.

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Distribution and severity of weakness in patients with polymyositis and dermatomyositis: Different pathophysiology, different affected muscle groups von Durmus, H, Deymeer, F, Parman, Y, Oflazer-Serdaroğlu, P

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ID 181 – Does high-pass filtering proposed for concentric needle electrode recording affect the calculated neuromuscular jitter in myasthenia gravis? von Görkem Şirin, N, Kocasoy Orhan, E, Durmuş, H, Barış Baslo, M, Deymeer, F

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Evaluation of maximum oxygen utilization in McArdle patients before and after exercise training von Gelisin, O, Durmus, H, Yakal, S, Kasikcioglu, E, Parman, Y, Deymeer, F, Oflazer-Serdaroğlu, P

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G.P.8 von Ozcan, O, Durmus, H, Tarhan, O, Polat, Z, Deymeer, F, Parman, Y, Oflazer-Serdaroglu, P

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P420: EMG in pediatric population: was it worth it? von Kocasoy Orhan, E, Baysal Kirac, L, Yalınay Dikmen, P, Matur, Z, Baslo, M.B, Ertaş, M, Öge, A.E, Deymeer, F, Yazıcı, J

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An autosomal recessive CMT family with a new mutation in the NDRG1 gene von Goksungur, M.T, Okamoto, Y, Pehlivan, D, Akyüz, K, Battaloglu, E, Deymeer, F, Serdaroglu, P, Lupski, J.R, Parman, Y

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Late-onset non-thymomatous generalized myasthenia gravis von Durmus, H, Yilmaz, V, Serdaroglu-Oflazer, P, Gulsen-Parman, Y, Saruhan-Direskeneli, G, Deymeer, F

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S44-5 Chloride and sodium channel myotonias von Lehmann-Horn, F, Deymeer, F, Jurkat-Rott, K

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Myophosphorylase (PYGM) mutations in Turkish patients with McArdle disease: A next generation sequencing study von Inal Gültekin, G, Toptaş Hekimoğlu, B, Görmez, Z, Durmuş, H, Demirci, H, Sağıroğlu, M, Parman, Y, Deymeer, F, Yılmaz, H, Pençe, S, Kurt, C, Tan, E, Özdamar, S, Giger, U, Öztürk, O, Serdaroğlu-Oflazer, P

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135. Electrophysiological decrement and transient weakness in myotonic syndromes von Matur, Z, Ciftci, F.D, Kara, B, Serdaroglu-Oflazer, P, Parman, Y, Basak, N, Jurkat-Rott, K, Lehmann-Horn, F, Deymeer, F

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