| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| openAccess |  | 30-mar-2015 | Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation | Nozal, Pilar; Garrido, Sofía; Martínez-Ara, Jorge; Picazo, María Luz; Yébenes, Laura; Álvarez-Doforno, Rita; Pinto, Sheila CSIC; Rodríguez de Córdoba, Santiago ; López Trascasa, Margarita | artículo |
| openAccess |  | may-2022 | CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative | Luque, Juan M. CSIC; Mendes, Ingrid; Gómez, Beatriz; Morte, Beatriz CSIC ORCID; Heredia, Miguel CSIC; Lopez Herreras, Enrique; Corrochano, Virginia; Bueren, Juan; Gallano, Pia; Artuch, Rafael; Fillat, Cristina CSIC; Pérez-Jurado, Luis Alberto; Montoliu, Lluís CSIC ORCID ; Carracedo, Ángel; Millán, José María; Webb, Susan M.; Palau, Francesc; CIBERER Network; Lapunzina, Pablo; Albiñana, Virginia CSIC; Arjona, Emilia CSIC ORCID ; Bernabéu, Carmelo CSIC ORCID ; Botella, Luisa María CSIC ORCID ; Pinto, Sheila CSIC; Rodríguez de Córdoba, Santiago ; Ruiz, Ángela; Antiñolo, Guillermo CSIC ORCID; Borrego, Salud CSIC ORCID; Bravo-Gil, Nereida CSIC; González-del Pozo, María; Méndez-Vidal, Cristina CSIC ORCID; Arbones, Maria L. CSIC ORCID ; Caparrós-Martín, José A. CSIC; Cediel, Rafael CSIC; Contreras, Julio CSIC; Estañ, María Cristina CSIC; Guerrero-López, Rosa CSIC; Jiménez-Estrada, Juan Andrés CSIC; Manguan-García, Cristina CSIC ORCID; Murillo-Cuesta, Silvia CSIC ORCID; Palencia-Campos, Adrián CSIC; Perona Abellón, Rosario CSIC ORCID; Rivera-Barahona, Ana CSIC; Rodriguez-de la Rosa, Lourdes CSIC ORCID; Ruiz-Pérez, Victor L. CSIC ORCID; Sastre, Leandro CSIC ORCID; Valencia, María CSIC; Varela-Nieto, Isabel CSIC ORCID ; Cervera, Javier; Cima, Sergio de CSIC ORCID; Gougeard, Nadine CSIC ORCID; Heredia, Miguel CSIC; Llácer, José Luis CSIC ORCID ; Marco-Marín, Clara CSIC ORCID; Marina, Alberto CSIC ORCID ; Mollá, Belén CSIC ORCID; Moreno-Estellés, Mireia CSIC ORCID; Pérez-Jiménez, Eva CSIC ORCID; Rubio, Vicente CSIC ORCID ; Sanz, Pascual CSIC ORCID ; Cortés-Rodríguez, Ana; Navas, Plácido CSIC ORCID; Sánchez Cuesta, Ana María; Santos-Ocaña, Carlos CSIC ORCID ; Fraga, Mario F. CSIC ORCID; Nieto, M. Ángela CSIC ORCID | artículo de revisión |
| openAccess |  | ene-2012 | Complement factor H variants I890 and L1007 while commonly associated with atypical haemolytic uremic syndrome are polymorphisms with no functional significance | Tortajada, Agustín CSIC ORCID; Pinto, Sheila CSIC; Martínez-Ara, Jorge; López-Trascasa, Margarita; Sánchez-Corral, Pilar CSIC ORCID; Rodríguez de Córdoba, Santiago | artículo |
| openAccess |  | 18-sep-2014 | Complement mutations in Diacylglycerol Kinase-E-associated atypical hemolytic uremic syndrome. | Sánchez Chinchilla, Daniel; Pinto, Sheila CSIC; Hoppe, Bernd; Adragna, Marta; López, Laura; Roldán, María Luisa Justa; Peña, Antonia; López Trascasa, Margarita; Sánchez-Corral, Pilar CSIC ORCID; Rodríguez de Córdoba, Santiago | artículo |
| openAccess |  | feb-2018 | Complete functional characterization of disease-associated genetic variants in the complement factor H gene | Martín Merinero, Héctor CSIC ORCID; Pinto, Sheila CSIC; García-Fernández, Jesús CSIC ; Arjona, Emilia CSIC ORCID ; Tortajada, Agustín CSIC ORCID; Rodríguez de Córdoba, Santiago | artículo |
| openAccess |  | ene-2014 | Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene | Román-Ortiz, E.; Mendizabal Oteiza, S.; Pinto, Sheila CSIC; López Trascasa, Margarita; Sánchez-Corral, Pilar CSIC ORCID; Rodríguez de Córdoba, Santiago | artículo |
| openAccess |  | feb-2017 | Extravascular hemolysis and complement consumption in Paroxysmal Nocturnal Hemoglobinuria patients undergoing eculizumab treatment | Subías, Marta CSIC ; Martín Merinero, Héctor CSIC ORCID; López, Alicia; Anter, Jaouad CSIC; Pinto, Sheila CSIC; Rodríguez de Córdoba, Santiago | artículo |
| closedAccess |  | ene-2018 | Factor H competitor generated by gene conversion events associates with atypical hemolytic uremic syndrome | Goicoechea de Jorge, Elena CSIC ORCID; Tortajada, Agustín CSIC ORCID; Pinto, Sheila CSIC; Gastoldi, Sara; Martín Merinero, Héctor CSIC ORCID; García-Fernández, Jesús CSIC ; Arjona, Emilia CSIC ORCID ; Cao, Mercedes; Remuzzi, Giuseppe; Noris, Marina; Rodríguez de Córdoba, Santiago | artículo |
| openAccess |  | abr-2014 | Genetics of atypical hemolytic uremic syndrome (aHUS) | Rodríguez de Córdoba, Santiago ; Subías, Marta CSIC ; Pinto, Sheila CSIC; Tortajada, Agustín CSIC ORCID | artículo |
| openAccess |  | 13-sep-2010 | Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation | Martínez-Barricarte, Rubén CSIC; Heurich, Meike; Valdés-Cañedo, Francisco; Vázquez-Martul, Eduardo; Torreira, Eva CSIC; Montes, Tamara CSIC; Tortajada, Agustín CSIC ORCID; Pinto, Sheila CSIC; López-Trascasa, Margarita; Morgan, B. Paul; Llorca, Óscar CSIC ORCID; Harris, Claire L.; Rodríguez de Córdoba, Santiago | artículo |
| openAccess | | oct-2016 | Insight into the role of CFHR proteins in renal disease | Gutiérrez Tenorio, Josué; Pinto, Sheila CSIC; García-Fernández, Jesús CSIC ; Arjona, Emilia CSIC ORCID ; Rodríguez de Córdoba, Santiago ; Goicoechea de Jorge, Elena CSIC ORCID | comunicación de congreso |
| openAccess |  | 16-sep-2015 | Molecular basis of factor H R1210C association with ocular and renal diseases | Recalde, Sergio; Tortajada, Agustín CSIC ORCID; Subías, Marta CSIC ; Anter, Jaouad CSIC; Pinto, Sheila CSIC; Rodríguez de Córdoba, Santiago | artículo |
| openAccess | | oct-2016 | Prevalent FHR-1 mutant protein generated by gene conversion reveals crucial role of factor H polymorphisms in atypical Hemolytic Uremic Syndrome (aHUS) | Tortajada, Agustín CSIC ORCID; Pinto, Sheila CSIC; Gastoldi, Sara; García-Fernández, Jesús CSIC ; Merinero, Hector; Arjona, Emilia CSIC ORCID ; Noris, Marina; Rodríguez de Córdoba, Santiago | comunicación de congreso |
|  | 2015 | The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome | Martínez-Barricarte, Rubén CSIC; López-Perrote, Andrés CSIC ORCID; Tortajada, Agustín CSIC ORCID; Pinto, Sheila CSIC; Llorca, Óscar CSIC ORCID; Rodríguez de Córdoba, Santiago | artículo |
| openAccess | | oct-2016 | Towards a complete functional characterization of the disease-associated genetic variants found in the CFH gene. | Martín Merinero, Héctor CSIC ORCID; Pinto, Sheila CSIC; García-Fernández, Jesús CSIC ; Arjona, Emilia CSIC ORCID ; Tortajada, Agustín CSIC ORCID; Rodríguez de Córdoba, Santiago | comunicación de congreso |
