The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force von Beaudin, Marie, Matilla-Dueñas, Antoni, Soong, Bing-Weng, Pedroso, Jose Luiz, Barsottini, Orlando G., Mitoma, Hiroshi, Tsuji, Shoji, Schmahmann, Jeremy D., Manto, Mario, Rouleau, Guy A, Klein, Christopher, Dupre, Nicolas

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Molecular pathogenesis of spinocerebellar ataxias von Dueñas, Antoni Matilla, Goold, Robert, Giunti, Paola

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Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37 von Corral-Juan, Marc, Serrano-Munuera, Carmen, Rábano, Alberto, Cota-González, Daniel, Segarra-Roca, Anna, Ispierto, Lourdes, Cano-Orgaz, Antonio Tomás, Adarmes, Astrid D, Méndez-del-Barrio, Carlota, Jesús, Silvia, Mir, Pablo, Volpini, Victor, Alvarez-Ramo, Ramiro, Sánchez, Ivelisse, Matilla-Dueñas, Antoni

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The Ever Expanding Spinocerebellar Ataxias. Editorial von Matilla-Dueñas, Antoni

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POLR3A-related spastic ataxia: new mutations and a look into the phenotype von Infante, Jon, Serrano-Cárdenas, Karla M., Corral‐Juan, Marc, Farré, Xavier, Sánchez, Ivelisse, de Lucas, Enrique M., García, Antonio, Martín-Gurpegui, José Luis, Berciano, José, Matilla-Dueñas, Antoni

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New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32 von Serrano-Munuera, Carmen, Corral-Juan, Marc, Stevanin, Giovanni, San Nicolás, Hector, Roig, Carles, Corral, Jordi, Campos, Berta, de Jorge, Laura, Morcillo-Suárez, Carlos, Navarro, Arcadi, Forlani, Sylvie, Durr, Alexandra, Kulisevsky, Jaime, Brice, Alexis, Sánchez, Ivelisse, Volpini, Victor, Matilla-Dueñas, Antoni

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Perrault syndrome with neurological features in a compound heterozygote for two TWNK mutations: overlap of TWNK-related recessive disorders von Domínguez-Ruiz, María, García-Martínez, Alberto, Corral-Juan, Marc, Pérez-Álvarez, Ángel I, Plasencia, Ana M, Villamar, Manuela, Moreno-Pelayo, Miguel A, Matilla-Dueñas, Antoni, Menéndez-González, Manuel, Del Castillo, Ignacio

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Ataxia and Action Myoclonus Related to Novel Mutations in ATP13A2 Gene von Manrique, Leire, Sánchez‐Rodríguez, Antonio, Pelayo‐Negro, Ana L., Corral‐Juan, Marc, Matilla‐Dueñas, Antoni, Infante, Jon

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Cellular and Molecular Pathways Triggering Neurodegeneration in the Spinocerebellar Ataxias von Matilla-Dueñas, Antoni, Sánchez, Ivelisse, Corral-Juan, Marc, Dávalos, Antoni, Alvarez, Ramiro, Latorre, Pilar

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Characterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia von López, Eva, Casasnovas, Carlos, Giménez, Javier, Matilla-Dueñas, Antoni, Sánchez, Ivelisse, Volpini, Víctor

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Novel genotype–phenotype correlations, differential cerebellar allele-specific methylation, and a common origin of the (ATTTC)n insertion in spinocerebellar ataxia type 37 von Sanchez-Flores, Marina, Corral-Juan, Marc, Gasch-Navalón, Esther, Cirillo, Davide, Sanchez, Ivelisse, Matilla-Dueñas, Antoni

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Genotype of an individual single nucleotide polymorphism regulates DNA methylation at the TRPC3 alternative promoter von Martin-Trujillo, Alex, Iglesias-Platas, Isabel, Coto, Eliecer, Corral-Juan, Marc, San Nicolás, Hector, Corral, Jordi, Volpini, Victor, Matilla-Dueñas, Antoni, Monk, David

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Correction to: Characterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia von López, Eva, Casasnovas, Carlos, Giménez, Javier, Matilla-Dueñas, Antoni, Sánchez, Ivelisse, Volpini, Víctor

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Machado-Joseph disease in a Sudanese family links East Africa to Portuguese families and allows reestimation of ancestral age of the Machado lineage von Martins, Sandra, Yahia, Ashraf, Costa, Inês P. D., Siddig, Hassab E., Abubaker, Rayan, Koko, Mahmoud, Corral-Juan, Marc, Matilla-Dueñas, Antoni, Brice, Alexis, Durr, Alexandra, Leguern, Eric, Ranum, Laura P. W., Amorim, António, Elsayed, Liena E. O., Stevanin, Giovanni, Sequeiros, Jorge

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Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1 von Matilla-Dueñas, Antoni, Goold, Robert, Giunti, Paola

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A novel function of Ataxin-1 in the modulation of PP2A activity is dysregulated in the spinocerebellar ataxia type 1 von Sánchez, Ivelisse, Piñol, Patricia, Corral-Juan, Marc, Pandolfo, Massimo, Matilla-Dueñas, Antoni

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New spinocerebellar ataxia subtype caused by SAMD9L mutation triggering mitochondrial dysregulation (SCA49) von Corral-Juan, Marc, Casquero, Pilar, Giraldo-Restrepo, Natalia, Laurie, Steve, Martinez-Piñeiro, Alicia, Mateo-Montero, Raidili Cristina, Ispierto, Lourdes, Vilas, Dolores, Tolosa, Eduardo, Volpini, Victor, Alvarez-Ramo, Ramiro, Sánchez, Ivelisse, Matilla-Dueñas, Antoni

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Ataxia Rating Scales—Psychometric Profiles, Natural History and Their Application in Clinical Trials von Saute, Jonas Alex Morales, Donis, Karina Carvalho, Serrano-Munuera, Carmen, Genis, David, Ramirez, Luís Torres, Mazzetti, Pilar, Pérez, Luis Velázquez, Latorre, Pilar, Sequeiros, Jorge, Matilla-Dueñas, Antoni, Jardim, Laura Bannach

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A novel SGCE variant is associated with myoclonus-dystonia with phenotypic variability von Delgado-Alvarado, Manuel, Matilla-Dueñas, Antoni, Altadill-Bermejo, Antonio, Setién, Sonia, Misiego-Peral, Mercedes, Sánchez-de la Torre, José Ramón, Corral-Juan, Marc, Riancho, Javier

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FMR1 Premutation: Basic Mechanisms and Clinical Involvement von Milà, Montserrat, Rodriguez-Revenga, Laia, Matilla-Dueñas, Antoni

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