Impacto fisiológico de la musicoterapia en la depresión, ansiedad, y bienestar del paciente con demencia tipo Alzheimer. Valoración de la utilización de cuestionarios para cuantifi... von de la Rubia Ortí, José Enrique, Cabañés Iranzo, Carmen, Sancho Espinós, Paula

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Physiological Impact of Music Therapy on Depression, Anxiety and Well-Being of Patients with Dementia of Alzheimer's Type. Assessment of the Use of Questionnaires to Quantify it von de la Rubia Ortí, José Enrique, Espinós, Paula Sancho, Cabañés Iranzo, Carmen

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Mitochondrial Dysfunction, Oxidative Stress and Neuroinflammation in Neurodegeneration with Brain Iron Accumulation (NBIA) von Hinarejos, Isabel, Machuca, Candela, Sancho, Paula, Espinós, Carmen

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Characterization of molecular mechanisms underlying the axonal Charcot-Marie-Tooth neuropathy caused by MORC2 mutations von Sancho, Paula, Bartesaghi, Luca, Miossec, Olivia, García-García, Francisco, Ramírez-Jiménez, Laura, Siddell, Anna, Åkesson, Elisabet, Hedlund, Eva, Laššuthová, Petra, Pascual-Pascual, Samuel I, Sevilla, Teresa, Kennerson, Marina, Lupo, Vincenzo, Chrast, Roman, Espinós, Carmen

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Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy von Lupo, Vincenzo, García-García, Francisco, Sancho, Paula, Tello, Cristina, García-Romero, Mar, Villarreal, Liliana, Alberti, Antonia, Sivera, Rafael, Dopazo, Joaquín, Pascual-Pascual, Samuel I, Márquez-Infante, Celedonio, Casasnovas, Carlos, Sevilla, Teresa, Espinós, Carmen

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Expanding the β-III Spectrin-Associated Phenotypes toward Non-Progressive Congenital Ataxias with Neurodegeneration von Sancho, Paula, Andrés-Bordería, Amparo, Gorría-Redondo, Nerea, Llano, Katia, Martínez-Rubio, Dolores, Yoldi-Petri, María Eugenia, Blumkin, Luba, Rodríguez de la Fuente, Pablo, Gil-Ortiz, Fernando, Fernández-Murga, Leonor, Sánchez-Monteagudo, Ana, Lupo, Vincenzo, Pérez-Dueñas, Belén, Espinós, Carmen, Aguilera-Albesa, Sergio

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Protein misfolding and clearance in the pathogenesis of a new infantile onset ataxia caused by mutations in PRDX3 von Martínez-Rubio, Dolores, Rodríguez-Prieto, Ángela, Sancho, Paula, Navarro-González, Carmen, Gorría-Redondo, Nerea, Miquel-Leal, Javier, Marco-Marín, Clara, Jenkins, Alison, Soriano-Navarro, Mario, Hernández, Alberto, Pérez-Dueñas, Belén, Fazzari, Pietro, Aguilera-Albesa, Sergio, Espinós, Carmen

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Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease von Sevilla, Teresa, Lupo, Vincenzo, Martínez-Rubio, Dolores, Sancho, Paula, Sivera, Rafael, Chumillas, María J, García-Romero, Mar, Pascual-Pascual, Samuel I, Muelas, Nuria, Dopazo, Joaquín, Vílchez, Juan J, Palau, Francesc, Espinós, Carmen

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Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect von Correa‐Vela, Marta, Lupo, Vincenzo, Montpeyó, Marta, Sancho, Paula, Marcé‐Grau, Anna, Hernández‐Vara, Jorge, Darling, Alejandra, Jenkins, Alison, Fernández‐Rodríguez, Sandra, Tello, Cristina, Ramírez‐Jiménez, Laura, Pérez, Belén, Sánchez‐Montáñez, Ángel, Macaya, Alfons, Sobrido, María J., Martinez‐Vicente, Marta, Pérez‐Dueñas, Belén, Espinós, Carmen

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Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias von Martínez-Rubio, Dolores, Hinarejos, Isabel, Sancho, Paula, Gorría-Redondo, Nerea, Bernadó-Fonz, Raquel, Tello, Cristina, Marco-Marín, Clara, Martí-Carrera, Itxaso, Martínez-González, María Jesús, García-Ribes, Ainhoa, Baviera-Muñoz, Raquel, Sastre-Bataller, Isabel, Martínez-Torres, Irene, Duat-Rodríguez, Anna, Janeiro, Patrícia, Moreno, Esther, Pías-Peleteiro, Leticia, Gordo, Mar O’Callaghan, Ruiz-Gómez, Ángeles, Muñoz, Esteban, Martí, Maria Josep, Sánchez-Monteagudo, Ana, Fuster, Candela, Andrés-Bordería, Amparo, Pons, Roser Maria, Jesús-Maestre, Silvia, Mir, Pablo, Lupo, Vincenzo, Pérez-Dueñas, Belén, Darling, Alejandra, Aguilera-Albesa, Sergio, Espinós, Carmen

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A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutation von Sancho, Paula, Sánchez-Monteagudo, Ana, Collado, Antonio, Marco-Marín, Clara, Domínguez-González, Cristina, Camacho, Ana, Knecht, Erwin, Espinós, Carmen, Lupo, Vincenzo

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Complexity of the Hereditary Motor and Sensory Neuropathies: Clinical and Cellular Characterization of the MPZ p.D90E Mutation von Lupo, Vincenzo, Pascual-Pascual, Samuel I., Sancho, Paula, Calpena, Eduardo, Gutiérrez-Molina, Manuel, Mateo-Martínez, Gonzalo, Espinós, Carmen, Arriola-Pereda, Gema

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Expanding the β-III Spectrin-Associated Phenotypes toward Non-Progressive Congenital Ataxias with Neurodegeneration von Sancho, Paula, Andrés-Bordería, Amparo, Gorría-Redondo, Nerea, Llano, Katia, Martínez-Rubio, Dolores, Yoldi-Petri, María Eugenia, Blumkin, Luba, Rodríguez de la Fuente, Pablo, Gil-Ortiz, Fernando, Fernández-Murga, Leonor, Sánchez-Monteagudo, Ana, Lupo, Vincenzo, Pérez-Dueñas, Belén, Espinós, Carmen, Aguilera-Albesa, Sergio, Universitat Autònoma de Barcelona

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Expanding the β-III Spectrin-Associated Phenotypes toward Non-Progressive Congenital Ataxias with Neurodegeneration von Sancho, Paula, Andrés-Bordería, Amparo, Gorría-Redondo, Nerea, Llano, Katia, Martínez-Rubio, Dolores, Yoldi-Petri, María Eugenia, Blumkin, Luba, Rodríguez de la Fuente, Pablo, Gil-Ortiz, Fernando, Fernández-Murga, Leonor, Sánchez-Monteagudo, Ana, Lupo, Vincenzo, Pérez-Dueñas, Belén, Espinós, Carmen, Aguilera-Albesa, Sergio, Universitat Autònoma de Barcelona

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Characterization of molecular mechanisms underlying the axonal Charcot-Marie-Tooth neuropathy caused by MORC2 mutations von Sancho, Paula, Bartesaghi, Luca, Miossec, Olivia, García-García, Francisco, Ramírez-Jiménez, Laura, Siddell, Anna, Ajkesson, Elisabet, Hedlund, Eva, Lassuthova, Petra, Pascual-Pascual, Samuel I, Sevilla, Teresa, Kennerson, Marina, Lupo, Vincenzo, Chrast, Roman, Espinós-Armero, Carmen Ángeles

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Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect von Correa-Vela, Marta, Lupo, Vincenzo, Montpeyó Garcia-Moreno, Marta, Sancho, Paula, Marcé-Grau, Anna, Hernández-Vara, Jorge, Darling, Alejandra, Jenkins, Alison, Fernández-Rodríguez, Sandra, Tello, Cristina, Ramírez-Jiménez, Laura, Pérez, Belén, Sánchez-Montáñez, Ángel, Macaya Ruiz, Alfons, Sobrido, María J, Martinez-Vicente, Marta, Pérez-Dueñas, Belén, Espinós, Carmen, Universitat Autònoma de Barcelona

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Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect von Correa Vela, Marta, Lupo, Vincenzo, Montpeyó Garcia-Moreno, Marta, Sancho, Paula, Marcé-Grau, Anna, Hernández-Vara, Jorge, Darling, Alejandra, Jenkins, Alison, Fernández-Rodríguez, Sandra, Tello, Cristina, Ramírez-Jiménez, Laura, Pérez, Belén, Sánchez-Montáñez, Ángel, Macaya Ruiz, Alfons, Sobrido, María-Jesús, Martinez-Vicente, Marta, Pérez-Dueñas, Belén, Espinós, Carmen, Universitat Autònoma de Barcelona

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Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy von Lupo, Vincenzo, García-García, Francisco, Sancho, Paula, Tello, Cristina, García-Romero, Mar, Villarreal, Liliana, Alberti, Antonia, Sivera, Rafael, Pascual-Pascual, Samuel I, Márquez-Infante, Celedonio, Casasnovas, Carlos, Sevilla, Teresa, Espinós-Armero, Carmen Ángeles

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Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease von Sevilla, Teresa, Lupo, Vincenzo, Martínez-Rubio, Dolores, Sancho, Paula, Sivera, Rafael, Chumillas, María J, García-Romero, Mar, Pascual-Pascual, Samuel I, Muelas, Nuria, Dopazo, Joaquín, Vílchez, Juan J, Palau, Francesc, Espinós-Armero, Carmen Ángeles

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Characterization of the molecular basis of Charcot-Marie-Tooth neuropathy through exoma sequencing. Pathogenicity Analysis of Variants von Collado Padilla, Antonio

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