Removal of Eroded Gastric Bands Using a Transgastric SILS Device von Spitali, C., De Vogelaere, Kristel, Delvaux, G.

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Dysphagia after Colon Interposition Graft for Esophageal Carcinoma von Spitali, C., De Vogelaere, Kristel, Delvaux, Georges

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The impact of cognitive function deficits and their recovery on functional outcome in subjects affected by ischemic subacute stroke: results from the Italian multicenter longitudin... von MANCUSO, Mauro, IOSA, Marco, ABBRUZZESE, Laura, MATANO, Alessandro, COCCIA, Michela, BAUDO, Silvia, BENEDETTI, Adonella, GAMBARELLI, Carmen, SPACCAVENTO, Simona, AMBIVERI, Giordano, MEGNA, Marisa, TOGNETTI, Paola, MAIETTI, Alessandra, RINALDESI, Maria L., GAMBERINI, Giulia, VARALTA, Valentina, MORONE, Giovanni, CIANCARELLI, Irene

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Upper limb telerehabilitation with Home Care and Activity Desk (HCAD) system von Zampolini, M., Baratta, S., Schifini, F., Spitali, C., Todeschini, E., Bernabeu, M., Tormos, JM, Opisso, E., Magni, R., Magnino, F., Huijgen, BCH, Vollenbroek-Hutten, MMR, Hermens, HJ, Nieuwenhoven, van J, Ilsbroukx, S, Scattareggia, Marchese S., Macellari, V, Giacomozzi, C

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Low dystrophin variability between muscles and stable expression over time in Becker muscular dystrophy using capillary Western immunoassay von Koeks, Z., Janson, A. A., Beekman, C., Signorelli, M., van Duyvenvoorde, H. A., van den Bergen, J. C., Hooijmans, M. T., Alleman, I., Hegeman, I. M., Verschuuren, J. J. G. M., v. Deutekom, J. C., Spitali, P., Datson, N. A., Niks, E. H.

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293P Evaluation of creatine/creatinine ratio and myostatin as monitoring biomarkers for DMD patients using real-world data von Degan, C., Vries, S., Ikelaar, N., Tsonaka, R., Niks, E., Spitali, P.

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Affinity proteomics within rare diseases: a BIO‐NMD study for blood biomarkers of muscular dystrophies von Ayoglu, Burcu, Chaouch, Amina, Lochmüller, Hanns, Politano, Luisa, Bertini, Enrico, Spitali, Pietro, Hiller, Monika, Niks, Eric H, Gualandi, Francesca, Pontén, Fredrik, Bushby, Kate, Aartsma‐Rus, Annemieke, Schwartz, Elena, Le Priol, Yannick, Straub, Volker, Uhlén, Mathias, Cirak, Sebahattin, ‘t Hoen, Peter A C, Muntoni, Francesco, Ferlini, Alessandra, Schwenk, Jochen M, Nilsson, Peter, Al‐Khalili Szigyarto, Cristina

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A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures von Hiller, Monika, Falzarano, Maria Sofia, Garcia-Jimenez, Iker, Sardone, Valentina, Verheul, Ruurd C, Popplewell, Linda, Anthony, Karen, Ruiz-Del-Yerro, Estibaliz, Osman, Hana, Goeman, Jelle J, Mamchaoui, Kamel, Dickson, George, Ferlini, Alessandra, Muntoni, Francesco, Aartsma-Rus, Annemieke, Arechavala-Gomeza, Virginia, Datson, Nicole A, Spitali, Pietro

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284P Suspension bead array profiling of 1018 serum proteins in search for disease progression biomarkers for Duchenne muscular dystrophy von Carrasco, A. Jiménez-Requena, Ajeenah, A., Johansson, C., Naveed, A., Tobin, R., Degan, C., de Vries, S., van der Burgt, Y., Diaz-Manera, J., Guglieri, M., Dang, U., Tsonaka, R., Spitali, P., Hathout, Y., Szigyarto, C. Al-Khalili

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296P Development of monitoring biomarker signatures in Duchenne muscular dystrophy von De Vries, S., Degan, C., Tobin, R., Jimenéz-Requena, A., Ajeenah, A., Johansson, C., Van der Burgt, Y., Diaz-Manera, J., Guglieri, M., Szigyarto, C. Al-Khalili, Spitali, P., Hathout, Y., Tsonaka, R., Dang, U.

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300P Brain involvement in Duchenne muscular dystrophy (BIND) von Tetorou, K., Aghaeipour, A., Gileadi, T., Ma, S., Quinteiro, P. Perdomo, Saoudi, A., Ceschi, L., Zarrouki, F., Mitsogiannis, M., Fergus, C., Kelly, V., Zhang, L., Spitali, P., Aoki, Y., Morgan, J., Montanaro, F., Vaillend, C., Goyenvalle, A., Muntoni, F.

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Evaluation of serum MMP-9 as predictive biomarker for antisense therapy in Duchenne von Lourbakos, A., Yau, N., de Bruijn, P., Hiller, M., Kozaczynska, K., Jean-Baptiste, R., Reza, M., Wolterbeek, R., Koeks, Z., Ayoglu, B., de Klerk, D., Campion, G., Zaharieva, I., Nadarajah, V. D., Nilsson, P., Al-Khalili Szigyarto, C., Muntoni, F., Lochmüller, H., Verschuuren, J. J., Goemans, N., Tulinius, M., Niks, E. H., de Kimpe, S., Aartsma-Rus, A., ’t Hoen, Peter A. C., Spitali, P.

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Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy von Previtali, Stefano C., Gidaro, Teresa, Díaz-Manera, Jordi, Zambon, Alberto, Carnesecchi, Stephanie, Roux-Lombard, Pascale, Spitali, Pietro, Signorelli, Mirko, Szigyarto, Cristina Al-Khalili, Johansson, Camilla, Gray, Julian, Labolle, Delphine, Porte Thomé, Florence, Pitchforth, Jacqueline, Domingos, Joana, Muntoni, Francesco

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Reduced cerebral gray matter and altered white matter in boys with Duchenne muscular dystrophy von Doorenweerd, Nathalie, Straathof, Chiara S., Dumas, Eve M., Spitali, Pietro, Ginjaar, Ieke B., Wokke, Beatrijs H., Schrans, Debby G., van den Bergen, Janneke C., van Zwet, Erik W., Webb, Andrew, van Buchem, Mark A., Verschuuren, Jan J., Hendriksen, Jos G., Niks, Erik H., Kan, Hermien E.

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Fibronectin is a serum biomarker for Duchenne muscular dystrophy von Cynthia Martin, F., Hiller, Monika, Spitali, Pietro, Oonk, Stijn, Dalebout, Hans, Palmblad, Magnus, Chaouch, Amina, Guglieri, Michela, Straub, Volker, Lochmüller, Hanns, Niks, Erik H., Verschuuren, Jan J. G. M., Aartsma-Rus, Annemieke, Deelder, André M., van der Burgt, Yuri E. M., 't Hoen, Peter A. C.

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609P Integration of healthcare and research to optimize treatment and collect real-world data in neuromuscular disorders von Verschoof, M., Slingerland, F., Roest, A., de Vreede, I., Warmenhoven, N., van Beek, C., de Witte, P., Bot, D., van Wageningen, H., Atsma, D., Straathof, C., Kan, H., Spitali, P., Snijder, R., Hoek, R., van der Holst, M., Meijer-Krom, Y., Niks, E.

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Validation of genetic modifiers for Duchenne muscular dystrophy: a multicentre study assessing SPP1 and LTBP4 variants von van den Bergen, Janneke C, Hiller, Monika, Böhringer, Stefan, Vijfhuizen, Linda, Ginjaar, Hendrika B, Chaouch, Amina, Bushby, Kate, Straub, Volker, Scoto, Mariacristina, Cirak, Sebahattin, Humbertclaude, Véronique, Claustres, Mireille, Scotton, Chiara, Passarelli, Chiara, Lochmüller, Hanns, Muntoni, Francesco, Tuffery-Giraud, Sylvie, Ferlini, Alessandra, Aartsma-Rus, Annemieke M, Verschuuren, Jan J G M, 't Hoen, Peter AC, Spitali, Pietro

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TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy von Spitali, Pietro, Zaharieva, Irina, Bohringer, Stefan, Hiller, Monika, Chaouch, Amina, Roos, Andreas, Scotton, Chiara, Claustres, Mireille, Bello, Luca, McDonald, Craig M, Hoffman, Eric P, Koeks, Zaida, Eka Suchiman, H, Cirak, Sebahattin, Scoto, Mariacristina, Reza, Mojgan, 't Hoen, Peter A C, Niks, Erik H, Tuffery-Giraud, Sylvie, Lochmüller, Hanns, Ferlini, Alessandra, Muntoni, Francesco, Aartsma-Rus, Annemieke

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Value of Global Longitudinal Strain for Identification and Monitoring of Left Ventricular Dysfunction in Becker Muscular Dystrophy von van de Velde, Nienke M., Gegenava, Tea, Koeks, Zaïda, Butcher, Steele C., Roest, Arno Aw, Bax, Jeroen J., Atsma, Douwe E., Spitali, Pietro, Ajmone Marsan, Nina, Niks, Erik H.

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Accurate quantification of dystrophin mRNA and exon skipping levels in Duchenne Muscular Dystrophy von Spitali, Pietro, Heemskerk, Hans, Vossen, Rolf HAM, Ferlini, Alessandra, den Dunnen, Johan T, 't Hoen, Peter AC, Aartsma-Rus, Annemieke

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