5PSQ-171 Tocilizumab in patients with COVID-19: results in clinical practice von Barcia Martin, MI, Sanchez Suarez, S, Aguilar Guisado, C, Garcia Gimeno, MM

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Patterns of physical activity progression in patients with COPD von Koreny, M, Demeyer, H, Benet, M, Arbillaga-Etxarri, A, Balcells, E, Barberan-Garcia, A, Gimeno-Santos, E, Hopkinson, NS, De Jong, C, Karlsson, N, Louvaris, Z, Polkey, MI, Puhan, MA, Rabinovich, RA, Rodríguez-Roisin, R, Vall-Casas, P, Vogiatzis, I, Troosters, T, Garcia-Aymerich, J, Urban Training Study Group and PROactive Consortium members, Urban Training Study Group, Delgado, A, Torrent-Pallicer, J, Vilaró, J, Chiaradía, DAR, Marín, A, Ortega, P, Celorrio, N, Teagudo, MM, Montellà, N, Muñoz, L, Toran, P, Simonet, P, Jané, C, Martín-Cantera, C, Borrell, E, PROactive Consortium members, Ivanoff, N, Corriol-Rohou, S, Jarrod, I, Erzen, D, Brindicci, C, Higenbottam, T, Scuri, M, McBride, P, Kamel, N, Tabberer, M, Dobbels, F, De Boer, P, Kulich, K, Glendenning, A, Rudell, K, Wilson, FJ, Nikai, E, Van der Molen, T, MacNee, B, Frei, A

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International variations in associations of allergic markers and diseases in children: ISAAC Phase Two von Weinmayr, G, Genuneit, J, Nagel, G, Björkstén, B, van Hage, M, Priftanji, A, Cooper, P, Rijkjärv, M.-A, von Mutius, E, Tsanakas, J, Forastiere, F, Doekes, G, Garrido, J.B, Suarez-Varela, M.M, Bråbäck, L, Strachan, D.P

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Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene von Akhtar, MM, Lorenzini, M, Cicerchia, M, Ochoa, JP, Hey, TM, Sabater Molina, M, Restrepo-Cordoba, MA, Dal Ferro, M, Stolfo, D, Johnson, R, Larrañaga-Moreira, JM, Robles-Mezcua, A, Rodriguez-Palomares, JF, Casas, G, Peña-Peña, ML, Lopes, LR, Gallego-Delgado, M, Franaszczyk, M, Laucey, G, Rangel-Sousa, D, Basurte, M, Palomino-Doza, J, Villacorta, E, Bilinska, Z, Limeres Freire, J, Garcia Pinilla, JM, Barriales-Villa, R, Fatkin, D, Sinagra, G, Garcia-Pavia, P, Gimeno, JR, Mogensen, J, Monserrat, L, Elliott, PM, European Genetic Cardiomyopathies Initiative Investigators

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Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy von Ochoa, JP, Sabater-Molina, M, García-Pinilla, JM, Mogensen, J, Restrepo-Córdoba, A, Palomino-Doza, J, Villacorta, E, Martinez-Moreno, M, Ramos-Maqueda, J, Zorio, E, Peña-Peña, ML, García-Granja, PE, Rodríguez-Palomares, JF, Cárdenas-Reyes, IJ, de la Torre-Carpente, MM, Bautista-Pavés, A, Akhtar, MM, Cicerchia, MN, Bilbao-Quesada, R, Mogollón-Jimenez, MV, Salazar-Mendiguchía, J, Mesa Latorre, JM, Arnaez, B, Olavarri-Miguel, I, Fuentes-Cañamero, ME, Lamounier, A, Pérez Ruiz, JM, Climent-Payá, V, Pérez-Sanchez, I, Trujillo-Quintero, JP, Lopes, LR, Repáraz-Andrade, A, Marín-Iglesias, R, Rodriguez-Vilela, A, Sandín-Fuentes, M, Garrote, JA, Cortel-Fuster, A, Lopez-Garrido, M, Fontalba-Romero, A, Ripoll-Vera, T, Llano-Rivas, I, Fernandez-Fernandez, X, Isidoro-García, M, Garcia-Giustiniani, D, Barriales-Villa, R, Ortiz-Genga, M, García-Pavía, P, Elliott, PM, Gimeno, JR, Monserrat, L

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