LRRK2 delays degradative receptor trafficking by impeding late endosomal budding through decreasing Rab7 activity von Gómez-Suaga, Patricia, Rivero-Ríos, Pilar, Fdez, Elena, Blanca Ramírez, Marian, Ferrer, Isidro, Aiastui, Ana, López De Munain, Adolfo, Hilfiker, Sabine

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Genealogy of the neurodegenerative diseases based on a meta-analysis of age-stratified incidence data von Gerovska, Daniela, Irizar, Haritz, Otaegi, David, Ferrer, Isidre, López de Munain, Adolfo, Araúzo-Bravo, Marcos J.

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Progranulin deficiency induces overactivation of WNT5A expression via TNF-α/NF-κB pathway in peripheral cells from frontotemporal dementia-linked granulin mutation carriers von Alquézar, Carolina, de la Encarnación, Ana, Moreno, Fermín, López de Munain, Adolfo, Martín-Requero, Ángeles

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ALS: A bucket of genes, environment, metabolism and unknown ingredients von Zufiría, Mónica, Gil-Bea, Francisco Javier, Fernández-Torrón, Roberto, Poza, Juan José, Muñoz-Blanco, Jose Luis, Rojas-García, Ricard, Riancho, Javier, López de Munain, Adolfo

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Association between total, processed, red and white meat consumption and all-cause, CVD and IHD mortality: a meta-analysis of cohort studies von Abete, Itziar, Romaguera, Dora, Vieira, Ana Rita, Lopez de Munain, Adolfo, Norat, Teresa

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Clinical Correlations With Lewy Body Pathology in LRRK2-Related Parkinson Disease von Kalia, Lorraine V, Lang, Anthony E, Hazrati, Lili-Naz, Fujioka, Shinsuke, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A, Van Deerlin, Vivianna M, Trojanowski, John Q, Hurtig, Howard I, Alcalay, Roy N, Marder, Karen S, Clark, Lorraine N, Gaig, Carles, Tolosa, Eduardo, Ruiz-Martínez, Javier, Marti-Masso, Jose F, Ferrer, Isidre, López de Munain, Adolfo, Goldman, Samuel M, Schüle, Birgitt, Langston, J. William, Aasly, Jan O, Giordana, Maria T, Bonifati, Vincenzo, Puschmann, Andreas, Canesi, Margherita, Pezzoli, Gianni, Maues De Paula, Andre, Hasegawa, Kazuko, Duyckaerts, Charles, Brice, Alexis, Stoessl, A. Jon, Marras, Connie

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Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy von Freyermuth, Fernande, Rau, Frédérique, Kokunai, Yosuke, Linke, Thomas, Sellier, Chantal, Nakamori, Masayuki, Kino, Yoshihiro, Arandel, Ludovic, Jollet, Arnaud, Thibault, Christelle, Philipps, Muriel, Vicaire, Serge, Jost, Bernard, Udd, Bjarne, Day, John W., Duboc, Denis, Wahbi, Karim, Matsumura, Tsuyoshi, Fujimura, Harutoshi, Mochizuki, Hideki, Deryckere, François, Kimura, Takashi, Nukina, Nobuyuki, Ishiura, Shoichi, Lacroix, Vincent, Campan-Fournier, Amandine, Navratil, Vincent, Chautard, Emilie, Auboeuf, Didier, Horie, Minoru, Imoto, Keiji, Lee, Kuang-Yung, Swanson, Maurice S., de Munain, Adolfo Lopez, Inada, Shin, Itoh, Hideki, Nakazawa, Kazuo, Ashihara, Takashi, Wang, Eric, Zimmer, Thomas, Furling, Denis, Takahashi, Masanori P., Charlet-Berguerand, Nicolas

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Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2 von Martí-Massó, José-Félix, Ruiz-Martínez, Javier, Bolaño, Maria J., Ruiz, Irune, Gorostidi, Ana, Moreno, Fermin, Ferrer, Isidre, de Munain, Adolfo López

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Assessing the role of TUBA4A gene in frontotemporal degeneration von Dols-Icardo, Oriol, Iborra, Oriol, Valdivia, Jessica, Pastor, Pau, Ruiz, Agustín, López de Munain, Adolfo, Sánchez-Valle, Raquel, Álvarez, Victoria, Sánchez-Juan, Pascual, Lleó, Alberto, Fortea, Juan, Blesa, Rafael, Cardona, Fernando, Baquero, Miquel, Alonso, María Dolores, Ortega-Cubero, Sara, Pastor, María A, Razquin, Cristina, Boada, Mercè, Hernández, Isabel, Gorostidi, Ana, Moreno, Fermín, Zulaika, Miren, Lladó, Albert, Coto, Eliecer, Combarros, Onofre, Pérez-Tur, Jordi, Clarimón, Jordi

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Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy von Beijer, Danique, Deconinck, Tine, De Bleecker, Jan L, Dotti, Maria Teresa, Malandrini, Alessandro, Urtizberea, J Andoni, Zulaica, Miren, López de Munain, Adolfo, Asselbergh, Bob, De Jonghe, Peter, Baets, Jonathan

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Altered tubulin detyrosination due to SVBP malfunction induces cytokinesis failure and senescence, underlying a complex hereditary spastic paraplegia von Launay, Nathalie, Espinosa-Alcantud, Maria, Verdura, Edgard, Fernández-Eulate, Gorka, Ondaro, Jon, Iruzubieta, Pablo, Marsal, Maria, Schlüter, Agatha, Ruiz, Montserrat, Fourcade, Stephane, Rodríguez-Palmero, Agustí, Zulaica, Miren, Sistiaga, Andone, Labayru, Garazi, Loza-Alvarez, Pablo, Vaquero, Alejandro, Lopez de Munain, Adolfo, Pujol, Aurora

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Genetic Mutation Analysis of Parkinson’s Disease Patients Using Multigene Next-Generation Sequencing Panels von Gorostidi, Ana, Martí-Massó, José Félix, Bergareche, Alberto, Rodríguez-Oroz, Mari Cruz, López de Munain, Adolfo, Ruiz-Martínez, Javier

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Genetic and epigenetic modifications of Sox2 contribute to the invasive phenotype of malignant gliomas von Alonso, Marta M, Diez-Valle, Ricardo, Manterola, Lorea, Rubio, Angel, Liu, Dan, Cortes-Santiago, Nahir, Urquiza, Leire, Jauregi, Patricia, Lopez de Munain, Adolfo, Sampron, Nicolás, Aramburu, Ander, Tejada-Solís, Sonia, Vicente, Carmen, Odero, María D, Bandrés, Eva, García-Foncillas, Jesús, Idoate, Miguel A, Lang, Frederick F, Fueyo, Juan, Gomez-Manzano, Candelaria

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Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia von Marti-Masso, Jose Felix, Ruiz-Martínez, Javier, Makarov, Vladimir, de Munain, Adolfo López, Gorostidi, Ana, Bergareche, Alberto, Yoon, Seungtai, Buxbaum, Joseph D., Paisán-Ruiz, Coro

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Common Characteristics Between Frailty and Myotonic Dystrophy Type 1: A Narrative Review von Garmendia, Joana, Labayru, Garazi, Souto Barreto, Philipe de, Vergara, Itziar, de Munain, Adolfo López, Sistiaga, Andone

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Neurogenetic Disorders in the Basque Population von Massó, José Félix Martí, Zarranz, Juan José, Otaegui, David, López de Munain, Adolfo

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Metabolic alterations in plasma from patients with familial and idiopathic Parkinson's disease von Yakhine-Diop, Sokhna M S, Morales-García, José A, Niso-Santano, Mireia, González-Polo, Rosa A, Uribe-Carretero, Elisabet, Martinez-Chacon, Guadalupe, Durand, Sylvere, Maiuri, Maria Chiara, Aiastui, Ana, Zulaica, Miren, Ruíz-Martínez, Javier, López de Munain, Adolfo, Pérez-Tur, Jordi, Pérez-Castillo, Ana, Kroemer, Guido, Bravo-San Pedro, José M, Fuentes, José M

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Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia von Alvarez, Victoria, Sánchez-Ferrero, Elena, Beetz, Christian, Díaz, Marta, Alonso, Belén, Corao, Ana I, Gámez, Josep, Esteban, Jesús, Gonzalo, Juan F, Pascual-Pascual, Samuel I, López de Munain, Adolfo, Moris, Germán, Ribacoba, Renne, Márquez, Celedonio, Rosell, Jordi, Marín, Rosario, García-Barcina, Maria J, Del Castillo, Emilia, Benito, Carmen, Coto, Eliecer

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Targeting TDP-43 phosphorylation by Casein Kinase-1δ inhibitors: a novel strategy for the treatment of frontotemporal dementia von Alquezar, Carolina, Salado, Irene G, de la Encarnación, Ana, Pérez, Daniel I, Moreno, Fermín, Gil, Carmen, de Munain, Adolfo López, Martínez, Ana, Martín-Requero, Ángeles

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T cells and immune functions of plasma extracellular vesicles are differentially modulated from adults to centenarians von Alberro, Ainhoa, Osorio-Querejeta, Iñaki, Sepúlveda, Lucía, Fernández-Eulate, Gorka, Mateo-Abad, Maider, Muñoz-Culla, Maider, Carregal-Romero, Susana, Matheu, Ander, Vergara, Itziar, López de Munain, Adolfo, Sáenz-Cuesta, Matías, Otaegui, David

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