SOM0226, a repositioned compound for the treatment of TTR amyloidosis

por Reig, Núria, Ventura, Salvador, Salvadó, Maria, Gámez, Josep, Insa, Raúl
Publicado 2015

Haplotype Analysis of the First A4V-SOD1 Spanish Family: Two Separate Founders or a Single Common Founder?

por Garcia, Cecilia, Vidal-Taboada, Jose Manuel, Syriani, Enrique, Salvado, Maria, Morales, Miguel, Gamez, Josep
Publicado 2019

CX3CR1 Is a Modifying Gene of Survival and Progression in Amyotrophic Lateral Sclerosis

por Lopez-Lopez, Alan, Gamez, Josep, Syriani, Emilio, Morales, Miguel, Salvado, Maria, Rodríguez, Manuel J., Mahy, Nicole, Vidal-Taboada, Jose M.
Publicado 2014

Intravenous immunoglobulin to prevent myasthenic crisis after thymectomy and other procedures can be omitted in patients with well-controlled myasthenia gravis

por Gamez, Josep, Salvadó, María, Carmona, Francesc, de Nadal, Miriam, Romero, Laura, Ruiz, Daniel, Jáuregui, Alberto, Martínez, Olga, Pérez, Javier, Suñé, Pilar, Deu, María
Publicado 2019

Long-term survival analysis of masitinib in amyotrophic lateral sclerosis

por Mora, Jesus S., Bradley, Walter G., Chaverri, Delia, Hernández-Barral, María, Mascias, Javier, Gamez, Josep, Gargiulo-Monachelli, Gisella M., Moussy, Alain, Mansfield, Colin D., Hermine, Olivier, Ludolph, Albert C.
Publicado 2021

Variably protease‐sensitive prionopathy presenting within ALS/FTD spectrum

por Vicente‐Pascual, Mikel, Rossi, Marcello, Gámez, Josep, Lladó, Albert, Valls, Josep, Grau‐Rivera, Oriol, Ávila Polo, Rainiero, Llorens, Franc, Zerr, Inga, Ferrer, Isidre, Nos, Carlos, Parchi, Piero, Sánchez‐Valle, Raquel, Gelpí, Ellen
Publicado 2018

Influence of early neurological complications on clinical outcome following lung transplant

por Gamez, Josep, Salvado, Maria, Martinez-de La Ossa, Alejandro, Deu, Maria, Romero, Laura, Roman, Antonio, Sacanell, Judith, Laborda, Cesar, Rochera, Isabel, Nadal, Miriam, Carmona, Francesc, Santamarina, Estevo, Raguer, Nuria, Canela, Merce, Solé, Joan
Publicado 2017

Consensus-based care recommendations for adults with myotonic dystrophy type 2

por Schoser, Benedikt, Montagnese, Federica, Bassez, Guillaume, Fossati, Barbara, Gamez, Josep, Heatwole, Chad, Hilbert, James, Kornblum, Cornelia, Kostera-Pruszczyk, Anne, Krahe, Ralf, Lusakowska, Anna, Meola, Giovanni, Moxley, Richard, Thornton, Charles, Udd, Bjarne, Formaker, Paul
Publicado 2019

Cognitive decline in amyotrophic lateral sclerosis: Neuropathological substrate and genetic determinants

por Borrego‐Écija, Sergi, Turon‐Sans, Janina, Ximelis, Teresa, Aldecoa, Iban, Molina‐Porcel, Laura, Povedano, Mónica, Rubio, Miguel Angel, Gámez, Josep, Cano, Antonio, Paré‐Curell, Martí, Bajo, Lorena, Sotoca, Javier, Clarimón, Jordi, Balasa, Mircea, Antonell, Anna, Lladó, Albert, Sánchez‐Valle, Raquel, Rojas‐García, Ricard, Gelpi, Ellen
Publicado 2021

Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia

por Álvarez, Victoria, Sánchez-Ferrero, Elena, Beetz, Christian, Díaz, Marta, Alonso, Belén, Corao, Ana I, Gámez, Josep, Esteban, Jesús, Gonzalo, Juan F, Pascual-Pascual, Samuel I, de Munain, Adolfo López, Moris, Germán, Ribacoba, Renne, Márquez, Celedonio, Rosell, Jordi, Marín, Rosario, García-Barcina, Maria J, del Castillo, Emilia, Benito, Carmen, Coto, Eliecer
Publicado 2010

Long-term efficacy and safety of inotersen for hereditary transthyretin amyloidosis: NEURO-TTR open-label extension 3-year update

por Brannagan, Thomas H., Coelho, Teresa, Wang, Annabel K., Polydefkis, Michael J., Dyck, Peter J., Berk, John L., Drachman, Brian, Gorevic, Peter, Whelan, Carol, Conceição, Isabel, Plante-Bordeneuve, Violaine, Merlini, Giampaolo, Obici, Laura, Plana, Josep Maria Campistol, Gamez, Josep, Kristen, Arnt V., Mazzeo, Anna, Gentile, Luca, Narayana, Arvind, Olugemo, Kemi, Aquino, Peter, Benson, Merrill D., Gertz, Morie
Publicado 2022

Dystrophinopathy Phenotypes and Modifying Factors in DMD Exon 45–55 Deletion

por Poyatos‐García, Javier, Martí, Pilar, Liquori, Alessandro, Muelas, Nuria, Pitarch, Inmaculada, Martinez‐Dolz, Luis, Rodríguez, Benjamin, Gonzalez‐Quereda, Lidia, Damiá, Maria, Aller, Elena, Selva‐Gimenez, Marta, Vilchez, Roger, Diaz‐Manera, Jordi, Alonso‐Pérez, Jorge, Barcena, José Eulalio, Jauregui, Amaia, Gámez, Josep, Aladrén, Jesus Angel, Fernández, Ariadna, Montolio, Marisol, Azorin, Inmaculada, Hervas, David, Casasús, Ana, Nieto, Marisa, Gallano, Pia, Sevilla, Teresa, Vilchez, Juan Jesus
Publicado 2022

Randomized phase 2 study of ACE‐083, a muscle‐promoting agent, in facioscapulohumeral muscular dystrophy

por Statland, Jeffrey M., Campbell, Craig, Desai, Urvi, Karam, Chafic, Díaz‐Manera, Jordi, Guptill, Jeffrey T., Korngut, Lawrence, Genge, Angela, Tawil, Rabi N., Elman, Lauren, Joyce, Nanette C., Wagner, Kathryn R., Manousakis, Georgios, Amato, Anthony A., Butterfield, Russell J., Shieh, Perry B., Wicklund, Matthew, Gamez, Josep, Bodkin, Cynthia, Pestronk, Alan, Weihl, Conrad C., Vilchez‐Padilla, Juan J., Johnson, Nicholas E., Mathews, Katherine D., Miller, Barry, Leneus, Ashley, Fowler, Marcie, van de Rijn, Marc, Attie, Kenneth M.
Publicado 2022