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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 ...
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      Quantifying the patients perspective in neuromyelitis optica spectrum disorder: Psychometric properties of the SymptoMScreen questionnaire 

      Meca Lallana, José E.; Maurino, Jorge; Pérez Miralles, Francisco; Forero, Lucía; Sepúlveda, María; Calles, Carmen; Martínez Ginés, María L.; González Suárez, Inés; Boyero, Sabas; Romero Pinel, Lucía; Sempere, Ángel P.; Meca Lallana, Virginia; Querol, Luis; Costa Frossard, Lucienne; Prefasi, Daniel; Gómez Ballesteros, Rocío; Ballesteros Rodríguez, Francisco Javier ORCID (Public Library Of Science, 2021-07-29)
      BACKGROUND: The assessment of self-reported outcomes in neuromyelitis optica spectrum disorder (NMOSD) is limited by the lack of validated disease-specific measures. The SymptoMScreen (SyMS) is a patient-reported questionnaire ...