Now showing items 1-3 of 3

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      Espectro de la neuromielitis óptica. Revisión bibliográfica y descripción de la serie de casos de la OSI-Araba 

      Pérez Bacigalupe, Laura (2023-09-13)
      [ES] Introducción: Los desórdenes del espectro de la neuromielitis óptica (NMOSD) son entidades autoinmunes desmielinizantes que afectan principalmente al nervio óptico y a la médula espinal en brotes recurrentes. Son ...
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      Exploring Genetic Factors Involved in Huntington Disease Age of Onset: E2F2 as a New Potential Modifier Gene 

      Valcárcel Ocete, Leire; Alkorta Aranburu, Gorka; Iriondo Orensanz, Mikel ORCID; Fullaondo Elordui-Zapaterieche, Asier ORCID; García-Barcina, María; Fernández-García, José Manuel; Lezcano-García, Elena; Losada-Domingo, José María; Ruiz-Ojeda, Javier; Álvarez de Arcaya, Amaia; Pérez- Ramos, José María; Roos, Raymund A. C.; Nielsen, Jørgen E.; Saft, Carsten; REGISTRY investigators of the European Huntington's Disease Network; Zubiaga Elordieta, Ana María ORCID; Aguirre Escobal, Ana Isabel ORCID (Public Library Science, 2015-07-06)
      Age of onset (AO) of Huntington disease (HD) is mainly determined by the length of the CAG repeat expansion (CAGexp) in exon 1 of the HTT gene. Additional genetic variation has been suggested to contribute to AO, although ...
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      Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55-IL6ST Gene Region in Immature Dendritic Cells 

      Mena Lucía, Jorge; Alloza Moral, Iraide; Tulloch Navarro, Raquel; Aldekoa Etxabe, Ane; Díez-García, Javier ORCID; Villanueva Etxebarria, Ane; Lindskog, Cecilia; Antigüedad, Alfredo; Boyero, Sabas; Mendibe Bilbao, María del Mar; Álvarez de Arcaya, Amaia; Sánchez Menoyo, José Luis; Midaglia, Luciana; Villarrubia, Noelia; Malhotra, Sunny; Montalbán, Xavier; Villar, Luisa M.; Comabella, Manuel; Vandenbroeck, Koen (Frontiers Media, 2022)
      [EN] Intronic single-nucleotide polymorphisms (SNPs) in the ANKRD55 gene are associated with the risk for multiple sclerosis (MS) and rheumatoid arthritis by genome-wide association studies (GWAS). The risk alleles have ...