20654. UNC13A Y SU IMPACTO EN LA SUPERVIVENCIA EN PACIENTES CON ELA von Bea Sintes, M., Villarreal Miñano, J., Lombardo del Toro, P., Assialioui, A., Terrafeta Pastor, C., Farrero Muñoz, E., Prats Soro, E., Sarasate Azkona, M., Virgili Casas, M., Herrera Rodríguez, V., Romero Gangonells, E., Andrés Benito, P., Domínguez Rubio, R., Povedano Panadés, M., Caravaca Puchades, A.

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Persistence of respiratory and inflammatory responses after dermal sensitization to persulfate salts in a mouse model of non-atopic asthma von Cruz, M J, Olle-Monge, M, Vanoirbeek, J A, Assialioui, A, Gomez-Olles, S, Muñoz, X

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Persistence of respiratory and inflammatory responses after dermal sensitization to persulfate salts in a mouse model of non-atopic asthma von Cruz, Maria Jesus, Olle-Monge, Marta, Vanoirbeek, Jeroen, Assialioui, A, Gomez-Olles, Susana, Munoz, Xavier

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Calidad de vida en pacientes adultos con epilepsia generalizada idiopática. Estudio EPILAK von Salas Puig, Javier, Sopelana Garay, David, Quintana Luque, Manuel, Seijo Raposo, I., Abraira del Fresno, Laura, Fonseca, E., Santamarina Pérez, Estevo, Toledo Argany, Manuel

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ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization von Tazelaar, G.H.P, Boeynaems, S, De Decker, M, van Vugt, J.J.F.A, Kool, L, Goedee, H.S, McLaughlin, R.L, Sproviero, W, Iacoangeli, A, Moisse, M, Jacquemyn, M, Daelemans, D, Dekker, A.M, van der Spek, R.A, Westeneng, H-J, Kenna, K.P, Assialioui, A, Da Silva, N, Povedano, M, Pardina, J.S.M, Hardiman, O, Salachas, F, Millecamps, S, Vourc’h, P, Corcia, P, Couratier, P, Morrison, K.E, Shaw, P.J, Shaw, C.E, Pasterkamp, R.J, Landers, J.E, Van Den Bosch, L, Robberecht, W, Al-Chalabi, A, van den Berg, L.H, Van Damme, P, Veldink, J.H, van Es, M.A

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Mutations in the glycosyltransferase domain of GLT8D1 are associated with familial amyotrophic lateral sclerosis von Cooper-Knock, J, Moll, T, Ramesh, T, Castelli, L, Beer, A, Robins, H, Fox, I, Niedermoser, I, Van Damme, P, Moisse, M, Robberecht, W, Hardiman, O, Panades, M.P, Assialioui, A, Mora, J.S, Basak, A.N, Morrison, K.E, Shaw, C.E, Al-Chalabi, A, Landers, J.E, Wyles, M, Heath, P.R, Higginbottom, A, Walsh, T, Kazoka, M, McDermott, C.J, Hautbergue, G.M, Kirby, J, Shaw, P.J

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The corticobasal syndrome could be caused by TDP-43 pathology von Assialioui, Abdelilah, Jensen, Christian, Catena, Esther

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Elevated Cerebrospinal Fluid Proteins and Albumin Determine a Poor Prognosis for Spinal Amyotrophic Lateral Sclerosis von Assialioui, Abdelilah, Domínguez, Raúl, Ferrer, Isidro, Andrés-Benito, Pol, Povedano, Mónica

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Microvascular abnormalities in skin capillaries of individuals with amyotrophic lateral sclerosis von Assialioui, Abdelilah, Marco-Pascual, Carla, Torrente-Segarra, Vicenç, Domínguez, Raul, Santos, Naiara, Peñafiel, Judith, Juanola, Xavier, Povedano, Mónica, Ferrer, Isidro

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El Viaje fasí asociado a los ritos de la escuela mālikí. Escrito por el sabio Al-Ṭayyib b. Abī Bakr b. Kirān al-Fāsī (m. 1314 /1896). Estudio e investigación von Assialioui, Aziz

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El Viaje fasí asociado a los ritos de la escuela mālikí. Escrito por el sabio Al-Ṭayyib b. Abī Bakr b. Kirān al-Fāsī (m. 1314 /1896). Estudio e investigación von Assialioui, Aziz

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TDP-43 Vasculopathy in the Spinal Cord in Sporadic Amyotrophic Lateral Sclerosis (sALS) and Frontal Cortex in sALS/FTLD-TDP von Ferrer, Isidro, Andrés-Benito, Pol, Carmona, Margarita, Assialioui, Abdelilah, Povedano, Mónica

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Elevated Cerebrospinal Fluid Proteins and Albumin Determine a Poor Prognosis for Spinal Amyotrophic Lateral Sclerosis von Assialioui, Abdelilah, Domínguez, Raúl, Ferrer, Isidro, Andrés Benito, Pol, Povedano, Mónica

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Microvascular abnormalities in skin capillaries of individuals with amyotrophic lateral sclerosis von Domínguez, Raúl, Assialioui, Abdelilah, Marco Pascual, Carla, Torrente Segarra, Vicenç, Santos, Naiara, Peñafiel, Judith, Juanola, Xavier, Povedano, Mònica, Ferrer, Isidro (Ferrer Abizanda)

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Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral Sclerosis von Cooper-Knock, Johnathan, Moll, Tobias, Ramesh, Tennore, Castelli, Lydia, Beer, Alexander, Robins, Henry, Fox, Ian, Niedermoser, Isabell, Van Damme, Philip, Moisse, Matthieu, Robberecht, Wim, Hardiman, Orla, Panades, Monica P., Assialioui, Abdelilah, Mora, Jesus S., Basak, A. Nazli, Morrison, Karen E., Shaw, Christopher E., Al-Chalabi, Ammar, Landers, John E., Wyles, Matthew, Heath, Paul R., Higginbottom, Adrian, Walsh, Theresa, Kazoka, Mbombe, McDermott, Christopher J., Hautbergue, Guillaume M., Kirby, Janine, Shaw, Pamela J.

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Characterizing SOD1 mutations in Spain: The impact of genotype, age and sex in the natural history of the disease von Vázquez‐Costa, Juan F., Borrego‐Hernández, Daniel, Paradas, Carmen, Gómez‐Caravaca, María Teresa, Rojas‐Garcia, Ricardo, Varona, Luis, Povedano, Mónica, García‐Sobrino, Tania, Jericó Pascual, Ivonne, Gutiérrez, Antonio, Riancho, Javier, Turon‐Sans, Janina, Assialioui, Abdelilah, Pérez‐Tur, Jordi, Sevilla, Teresa, Esteban Pérez, Jesús, García‐Redondo, Alberto, López, Alberto Andrés, Calabria, M. Dolores, Díaz‐Marín, Carmen, Caravaca, Eva Fages, Dávila, Lucía Galán, Martínez, Alberto García, Gimenez‐Muñoz, Álvaro, Sola, Antonio Guerrero, Cadavid, Javier Mascías, Mora Pardina, Jesús S., Blanco, José Luis Muñoz, Juntas‐Morales, Raúl, Morgado, Yolanda, Pardo, Julio, Valladares, Amador, Vilar‐Ventura, Rosa Maria

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Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral Sclerosis von Cooper-Knock, Johnathan, Moll, Tobias, Ramesh, Tennore, Castelli, Lydia, Beer, Alexander, Robins, Henry, Fox, Ian, Niedermoser, Isabell, Van Damme, Philip, Moisse, Matthieu, Robberecht, Wim, Hardiman, Orla, Panades, Monica P, Assialioui, Abdelilah, Mora, Jesus S, Basak, A. Nazli, Morrison, Karen E, Shaw, Christopher E, Al-Chalabi, Ammar, Landers, John E, Wyles, Matthew, Heath, Paul R, Higginbottom, Adrian, Walsh, Theresa, Kazoka, Mbombe, McDermott, Christopher J, Hautbergue, Guillaume M, Kirby, Janine, Shaw, Pamela J

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ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization von Tazelaar, Gijs H.P, Boeynaems, Steven, De Decker, Mathias, van Vugt, Joke J.F.A, Kool, Lindy, Goedee, H. Stephan, McLaughlin, Russell L, Sproviero, William, Iacoangeli, Alfredo, Moisse, Matthieu, Jacquemyn, Maarten, Daelemans, Dirk, Dekker, Annelot M, van der Spek, Rick A, Westeneng, Henk-Jan, Kenna, Kevin P, Assialioui, Abdelilah, Da Silva, Nica, Povedano, Monica, Pardina, Jesus S. Mora, Hardiman, Orla, Salachas, Francois, Millecamps, Stephanie, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Morrison, Karen E, Shaw, Pamela J, Shaw, Christopher E, Pasterkamp, R. Jeroen, Landers, John E, Van den Bosch, Ludo, Robberecht, Wim, Al-Chalabi, Ammar, van den Berg, Leonard H, Van Damme, Philip, Veldink, Jan H, van Es, Michael A

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TDP-43 Vasculopathy in the Spinal Cord in Sporadic Amyotrophic Lateral Sclerosis (sALS) and Frontal Cortex in sALS/FTLD-TDP von Ferrer, Isidro (Ferrer Abizanda), Andrés Benito, Pol, Carmona Murillo, Margarita, Assialioui, Abdelilah, Povedano, Mònica

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ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization von Tazelaar, Gijs H. P, Boeynaems, Steven, Decker, Mathias De, Povedano, Mònica, Assialioui, Abdelilah, Project MinE ALS Sequencing Consortium

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