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44P Novel TTN mutation causing a congenital onset, slowly progressive myopathy with contractures in two siblings by Bonaparte, S. Figueroa, Martinez-Viguera, A., Juanola-Mayos, E., Lucente, G., Almendrote, M., Gasch-Navalon, E., Corral-Juan, M., Matilla-Dueñas, A., Martinez-Piñeiro, A.

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Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert by Gutiérrez Gutiérrez, G., Díaz-Manera, J., Almendrote, M., Azriel, S., Eulalio Bárcena, J., Cabezudo García, P., Camacho Salas, A., Casanova Rodríguez, C., Cobo, A.M., Díaz Guardiola, P., Fernández-Torrón, R., Gallano Petit, M.P., García Pavía, P., Gómez Gallego, M., Gutiérrez Martínez, A.J., Jericó, I., Kapetanovic García, S., López de Munaín Arregui, A., Martorell, L., Morís de la Tassa, G., Moreno Zabaleta, R., Muñoz-Blanco, J.L., Olivar Roldán, J., Pascual Pascual, S.I., Peinado Peinado, R., Pérez, H., Poza Aldea, J.J., Rabasa, M., Ramos, A., Rosado Bartolomé, A., Rubio Pérez, M.Á., Urtizberea, J.A., Zapata-Wainberg, G., Gutiérrez-Rivas, E.

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Impacto de un centro terciario de ictus en la atención de pacientes con ictus isquémico agudo por disección de arterias cervicales by Almendrote, M, Millán, M, Prats, L.A, Pérez de la Ossa, N, López-Cancio, E, Gomis, M, Dorado, L, Hernández-Pérez, M, Hidalgo, C, García-Bermejo, P, Castaño, C, Domenech, S, Dávalos, A

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P.395Spanish Pompe registry: baseline characteristics of first 49 patients with adult onset of Pompe disease by Alonso-Perez, J., Segovia-Simon, S., Dominguez-Gonzalez, C., Olive-Plana, M., Mendoza-Grimon, D., Fernandez-Torron, R., Lopez-Munain, A., Muñoz-Blanco, J., Ramos-Fransi, A., Almendrote, M., Illa-Sendra, I., Diaz-Manera, J.

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Intravenous alteplase for stroke with unknown time of onset guided by advanced imaging: systematic review and meta-analysis of individual patient data by Schwamm, Lee H, Leys, Didier, Schellinger, Peter D, Thijs, Vincent, Wahlgren, Nils, Toyoda, Kazunori, Albiker, Christian, Almendrote, Miriam, Amiri, Hemasse, Bodechtel, Ulf, Bojaryn, Urszula, Cho, Tae-Hee, Choy, Lillian, Christensen, Hanne, De Hollander, Isabel, De Smedt, Ann, Dittrich, Ralf, Dusart, Anne, Ebinger, Martin, Fandler, Simon, Foerch, Christian, Gerner, Stefan, Harmel, Peter, Hennerici, Michael, Hermans, Sylvia, Hohenbichler, Katharina, Kallmünzer, Bernd, Kellert, Lars, Kraft, Peter, Lovelock, Caroline, Marzina, Annika, Møller, Anette, Moynihan, Barry, Nederkoorn, Paul, Oberndorfer, Stefan, Oppel, Lorenz, Pérez de la Ossa, Natalia, Remmers, Michel, Sagnier, Sharmilla, Soors, Peter, Turc, Guillaume, Vallet, Pauline, van Eendenburg, Cecile, von Weitzel, Paul, Weber, Claudia, Wollboldt, Christian, Ziemann, Ulf, Zuber, Mathieu, Egashira, Yusuke, Gotoh, Seiji, Ide, Toshihiro, Igarashi, Shuichi, Kanai, Haruka, Koga, Masatoshi, Kusumi, Masayoshi, Nagakane, Yoshinari, Sozu, Takashi, Tanaka, Eijiro, Terada, Tomoaki, Todo, Kenichi, Toyoda, Kazunori, Tsujino, Akira, Yonehara, Toshiro, Chen, W.H., Churilov, L., Coote, S., Coulton, B., Day, S., Desmond, P.M., Huang, H.Y., Jeng, J.S., Kasari, O., Kyndt, C., Lau, C.L., Lim, J.C., Lin, D., Loh, P.S., Low, E., Lu, C.J., Lu, M.K., Ng, J-L., Parsons, M.W., Phan, T., Sturm, J., Tatlisumak, T., Tsai, H.T., Tseng, L.T., Tu, H., Tu, H.T-H., Zhao, H., Bluhmki, Erich, Kala, Lalit, Laage, Rico, Nuñez, Xavier, Carandang, Raphael A., Drake, Kendra, Harris, Gordon J., Muzikansky, Alona, Song, Shlee S., Starkman, Sidney

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The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1 by Ballester-Lopez, Alfonsina, Linares-Pardo, Ian, Koehorst, Emma, Núñez-Manchón, Judit, Pintos-Morell, Guillem, Coll-Cantí, Jaume, Almendrote, Miriam, Lucente, Giuseppe, Arbex, Andrea, Magaña, Jonathan J, Murillo-Melo, Nadia M, Lucia, Alejandro, Monckton, Darren G, Cumming, Sarah A, Ramos-Fransi, Alba, Martínez-Piñeiro, Alicia, Nogales-Gadea, Gisela

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