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DerechosPreviewFecha Public.TítuloAutor(es)Tipo
openAccessoct-2016Database of complement gene variants: a comprehensive database providing insights on function, structure and allele frequency for genetic variants identified in complement-mediated diseasesOsborne, Amy J.; Rodríguez de Córdoba, Santiago ; Fremeaux-Bacchi, Veronique; Noris, Marina; Smith, Richard; van den Heuvel, Bert; Goodship, Timothy H.J.; Perkins, Stephencomunicación de congreso
closedAccessrestringido.pdf.jpgmar-2006De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndromeHeinen, Stephan; Sánchez-Corral, Pilar CSIC ORCID; Jackson, Michael; Strain, Lisa; Goodship, Judith A.; Kemp, Elizabeth J.; Skerka, Christine; Jokiranta, T. Sakari; Meyers, Kevin; Wagner, Eric; Robitaille, Pierre; Esparza-Gordillo, Jorge CSIC; Rodríguez de Córdoba, Santiago ; Zipfel, Peter F.; Goodship, Timothy H.J.artículo
closedAccessaccesoRestringido.pdf.jpg1-nov-2012Sensitive and specific assays for C3 nephritic factors permit dissection of mechanisms underlying complement dysregulationPaixao-Cavalcante, Danielle; López-Trascasa, Margarita; Skattum, Lillemor; Giclas, Patricia C.; Goodship, Timothy H.J.; Rodríguez de Córdoba, Santiago ; Truedsson, Lennart; Morgan, B. Paul; Harris, Claire L.artículo
openAccess2008_Martinez-Barricarte et al_JASN.pdf.jpgmar-2008The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndromeMartínez-Barricarte, Rubén CSIC; Pianetti, Gaia; Gautard, Ruxandra; Misselwitz, Joachim; Strain, Lisa; Fremeaux-Bacchi, Veronique; Skerka, Christine; Zipfel, Peter F.; Goodship, Timothy H.J.; Noris, Marina; Remuzzi, Giuseppe; Rodríguez de Córdoba, Santiago artículo
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