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Browsing by Author Pinto, Sheila

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Showing results 1 to 14 of 14
RightsPreviewIssue DateTitleAuthor(s)Type
openAccessBMC Nephrology_S. Rodríguez de Córdoba_2015.pdf.jpg30-Mar-2015Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutationNozal, Pilar; Garrido, Sofía; Martínez-Ara, Jorge; Picazo, María Luz; Yébenes, Laura; Álvarez-Doforno, Rita; Pinto, Sheila ; Rodríguez de Córdoba, Santiago ; López Trascasa, Margaritaartículo
openAccess2012_Tortajada et al_Kidney Int.pdf.jpgJan-2012Complement factor H variants I890 and L1007 while commonly associated with atypical haemolytic uremic syndrome are polymorphisms with no functional significanceTortajada, Agustín ; Pinto, Sheila ; Martínez-Ara, Jorge; López-Trascasa, Margarita; Sánchez-Corral, Pilar ; Rodríguez de Córdoba, Santiago artículo
openAccess2014_Sanchez-Chinchilla et al_Clin J Am Soc Nephrol_complemento.pdf.jpg18-Sep-2014Complement mutations in Diacylglycerol Kinase-E-associated atypical hemolytic uremic syndrome.Sánchez Chinchilla, Daniel; Pinto, Sheila ; Hoppe, Bernd; Adragna, Marta; Lopez, Laura; Roldán, María Luisa Justa; Peña, Antonia; López Trascasa, Margarita; Sánchez-Corral, Pilar ; Rodríguez de Córdoba, Santiago artículo
openAccessFeb-2018Complete functional characterization of disease-associated genetic variants in the complement factor H geneMartín Merinero, Héctor; Pinto, Sheila ; García-Fernández, Jesús; Arjona, Emilia; Tortajada, Agustín ; Rodríguez de Córdoba, Santiago artículo
openAccessRoman-Ortiz et al_2014_Pediatric Nephrology.pdf.jpgJan-2014Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid geneRomán-Ortiz, E.; Mendizabal Oteiza, S.; Pinto, Sheila ; López Trascasa, Margarita; Sánchez-Corral, Pilar ; Rodríguez de Córdoba, Santiago artículo
openAccess2017-Immunobiology-Postprint_COMPLETO.pdf.jpgFeb-2017Extravascular hemolysis and complement consumption in Paroxysmal Nocturnal Hemoglobinuria patients undergoing eculizumab treatmentSubías, Marta; Martín Merinero, Héctor; López, Alicia; Anter, Jauoad; Pinto, Sheila ; Rodríguez de Córdoba, Santiago artículo
closedAccessrestringido.pdf.jpgJan-2018Factor H competitor generated by gene conversion events associates with atypical hemolytic uremic syndromeGoicoechea de Jorge, Elena ; Tortajada, Agustín ; Pinto, Sheila ; Gastoldi, Sara; Merinero, Hector; García-Fernández, Jesús; Arjona, Emilia; Cao, Mercedes; Remuzzi, Giuseppe; Noris, Marina; Rodríguez de Córdoba, Santiago artículo
openAccessRodriguez de Cordoba et al_2014_Sem Thromb Hem.pdf.jpgApr-2014Genetics of atypical hemolytic uremic syndrome (aHUS)Rodríguez de Córdoba, Santiago ; Subías, Marta; Pinto, Sheila ; Tortajada, Agustín artículo
openAccessJCI43343 v1.pdf.jpg13-Sep-2010Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulationMartínez-Barricarte, Rubén ; Heurich, Meike; Valdés-Cañedo, Francisco; Vázquez-Martul, Eduardo; Torreira, Eva ; Montes, Tamara ; Tortajada, Agustín ; Pinto, Sheila ; López-Trascasa, Margarita; Morgan, B. Paul; Llorca, Óscar ; Harris, Claire L.; Rodríguez de Córdoba, Santiago artículo
openAccessOct-2016Insight into the role of CFHR proteins in renal diseaseGutiérrez Tenorio, Josué; Pinto, Sheila ; García-Fernández, Jesús; Arjona, Emilia; Rodríguez de Córdoba, Santiago ; Goicoechea de Jorge, Elena comunicación de congreso
openAccess2015_Recalde et al_JASN.pdf.jpg16-Sep-2015Molecular basis of factor H R1210C association with ocular and renal diseasesRecalde, Sergio; Tortajada, Agustín ; Subías, Marta; Anter, Jauoad; Pinto, Sheila ; Rodríguez de Córdoba, Santiago artículo
openAccessOct-2016Prevalent FHR-1 mutant protein generated by gene conversion reveals crucial role of factor H polymorphisms in atypical Hemolytic Uremic Syndrome (aHUS)Tortajada, Agustín ; Pinto, Sheila ; Gastoldi, Sara; García-Fernández, Jesús; Merinero, Hector; Arjona, Emilia; Noris, Marina; Rodríguez de Córdoba, Santiago comunicación de congreso
Molecular Microbiology _S. R. de Córdoba_2015.pdf.jpg2015The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndromeMartínez-Barricarte, Rubén ; López-Perrote, Andrés ; Tortajada, Agustín ; Pinto, Sheila ; Llorca, Óscar ; Rodríguez de Córdoba, Santiago artículo
openAccessOct-2016Towards a complete functional characterization of the disease-associated genetic variants found in the CFH gene.Martín Merinero, Héctor; Pinto, Sheila ; García-Fernández, Jesús; Arjona, Emilia; Tortajada, Agustín ; Rodríguez de Córdoba, Santiago comunicación de congreso