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Jiménez-Reinoso A., Marín AV., Subías M., López-Lera A., Román-Ortíz E., Payne K., Ma CS., Arbore G., Kolev M., Freeley SJ., Kemper C., Tangye SG., Fernández-Malavé E., Rodríguez de Córdoba S., López-Trascasa M. and Regueiro JR.
[2017]. Human plasma C3 is essential for the development of memory B, but not T, lymphocytes. J Allergy Clin Immunol. 141:1151-1154.
Goicoechea de Jorge, E., Tortajada, A., Pinto, S., Gastoldi, S., Martín-Merinero, H., García-Fernández, J., Arjona, E., Cao, M., Remuzzi, G., Noris, M. and Rodríguez de Córdoba, S.
[2018]. Factor H competitor generated by gene conversion events associates with Atypical Hemolytic Uremic Syndrome. J. Am. Soc. Nephrol. 28:240-249..
Merinero, H.M., García, S.P., García-Fernández, J., Arjona, E., Tortajada, A., Rodríguez de Córdoba, S.
[2018]. Complete functional characterization of disease-associated genetic variants in the complement factor H gene. Kidney International. 93:470-481.
Huerta, A., Arjona, E., Portoles, J., Lopez-Sanchez, P., Rabasco, C., Espinosa, M., Cavero, T., Blasco, M., Cao, M., Manrique, J., Cabello-Chavez, V., Suñer, M., Heras, M., Fulladosa, X., Belmar, L., Sempere, A., Peralta, C., Castillo, L., Arnau, A., Praga, M., Rodriguez de Cordoba, S.
[2018]. A retrospective study of pregnancy-associated atypical hemolytic uremic syndrome. Kidney International. 93:450-459.
de Jorge, E.G., Yebenes, H., Serna, M., Tortajada, A., Llorca, O., de Córdoba, S.R.
[2018]. How novel structures inform understanding of complement function. Seminars in Immunopathology. 40:3-14.
Tortajada, A., Gutiérrez, E., Goicoechea de Jorge, E., Anter, J., Segarra, A., Espinosa, M., Blasco, M., Roman, E., Marco, H., Quintana, L.F., Gutiérrez, J., Pinto, S., Lopez-Trascasa, M., Praga, M., Rodriguez de Córdoba, S.
[2017]. Elevated factor H-related protein 1 and factor H pathogenic variants decrease complement regulation in IgA nephropathy. Kidney International. 92:953-963.
Nitschke, F., Sullivan, M.A., Wang, P., Zhao, X., Chown, E.E., Perri, A.M., Israelian, L., Juana-López, L., Bovolenta, P., Rodríguez de Córdoba, S., Steup, M., Minassian, B.A.
[2017]. Abnormal glycogen chain length pattern, not hyperphosphorylation, is critical in Lafora disease. EMBO Molecular Medicine. 9:909-917-.
Csincsi, Á.I., Szabó, Z., Bánlaki, Z., Uzonyi, B., Cserhalmi, M., Kárpáti, É., Tortajada, A., Caesar, J.J.E., Prohászka, Z., Jokiranta, T.S., Lea, S.M., De Córdoba, S.R., Józsi, M.
[2017]. FHR-1 binds to C-reactive protein and enhances rather than inhibits complement activation. Journal of Immunology. 199:292-303.
Cao, M., Ferreiro, T., Leite, N., Pita, F., Bolaños, L., Valdés, F., Alonso, A., Vázquez, E., Mosquera, J., Trigás, M., Rodríguez de Córdoba, S.
[2017]. Case Report: Two cases of atypical hemolytic uremic syndrome (aHUS) and eosinophilic granulomatosis with polyangiitis (EGPA): a possible relationship. CEN Case Rep. 6:91-97.
Querol-García, J., Fernández, F.J., Marin, A.V., Gómez, S., Fullà, D., Melchor-Tafur, C., Franco-Hidalgo, V., Albertí, S., Juanhuix, J., de Córdoba, S.R., Regueiro, J.R., Vega, M.C.
[2017]. Crystal structure of glyceraldehyde-3-phosphate dehydrogenase from the gram-positive bacterial pathogen A. vaginae, an immunoevasive factor that interacts with the human C5a anaphylatoxin. Frontiers in Microbiology. 8:541.
Cavero, T., Rabasco, C., López, A., Román, E., Ávila, A., Sevillano, Á., Huerta, A., Rojas-Rivera, J., Fuentes, C., Blasco, M., Jarque, A., García, A., Mendizabal, S., Gavela, E., Macía, M., Quintana, L.F., María Romera, A., Borrego, J., Arjona, E., Espinosa, M., Portolés, J., Gracia-Iguacel, C., González-Parra, E., Aljama, P., Morales, E., Cao, M., Rodríguez De Córdoba, S., Praga, M.
[2017]. Eculizumab in secondary atypical haemolytic uraemic syndrome. Nephrology Dialysis Transplantation. 32:466-474.
López-Perrote, A., Harrison, R.E.S., Subías, M., Alcorlo, M., Rodríguez de Córdoba, S., Morikis, D., Llorca, O.
[2017]. Ionic tethering contributes to the conformational stability and function of complement C3b. Molecular Immunology. 85:137-147.
Subías Hidalgo, M., Yébenes, H., Rodríguez-Gallego, C., Martín-Ambrosio, A., Domínguez, M., Tortajada, A., Rodríguez de Córdoba, S., Llorca, O.
[2017]. Functional and structural characterization of four mouse monoclonal antibodies to complement C3 with potential therapeutic and diagnostic applications. European Journal of Immunology. 47:504-515.
Subías Hidalgo, M., Martin Merinero, H., López, A., Anter, J., García, S.P., Ataúlfo Gonzalez-Fernández, F., Forés, R., Lopez-Trascasa, M., Villegas, A., Ojeda, E., Rodríguez de Córdoba, S.
[2017]. Extravascular hemolysis and complement consumption in Paroxysmal Nocturnal Hemoglobinuria patients undergoing eculizumab treatment. Immunobiology. 222:363-371.
Goodship, T.H.J., Cook, H.T., Fakhouri, F., Fervenza, F.C., Frémeaux-Bacchi, V., Kavanagh, D., Nester, C.M., Noris, M., Pickering, M.C., Rodríguez de Córdoba, S., Roumenina, L.T., Sethi, S., Smith, R.J.H., Alpers, C.E., Appel, G.B., Ardissino, G., Ariceta, G., Arici, M., Bagga, A., Bajema, I.M., Blasco, M., Burke, L., Cairns, T.D., Carratala, M., D'Agati, V.D., Daha, M.R., De Vriese, A.S., Dragon-Durey, M.-A., Fogo, A.B., Galbusera, M., Gale, D.P., Haller, H., Johnson, S., Józsi, M., Karpman, D., Lanning, L., Le Quintrec, M., Licht, C., Loirat, C., Monfort, F., Morgan, B.P., Noël, L.-H., O'Shaughnessy, M.M., Rabant, M., Rondeau, E., Ruggenenti, P., Sheerin, N.S., Smith, J., Spoleti, F., Thurman, J.M., van de Kar, N.C.A.J., Vivarelli, M., Zipfel, P.F.
[2017]. Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference. Kidney International. 91:539-551.
Laurence, J., Haller, H., Mannucci, P.M., Nangaku, M., Praga, M., de Cordoba, S.R.
[2016]. Atypical hemolytic uremic syndrome (aHUS): Essential aspects of an accurate diagnosis. Clinical Advances in Hematology and Oncology. 14:2-15.
Xiao X., Ghossein C., Tortajada A., Zhang Y., Meyer N., Jones M., Ghiringhelli Borsa N., Nester CM., Thomas CP., Rodríguez de Córdoba S. and Smith RJH.
[2016]. Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene. Mol. Immunol. 77:89-96
Rodríguez de Córdoba S.
[2016]. Alteraciones de la Inmunidad Natural; Genes del Complemento y Predisposición a la Enfermedad. Genómica Aplicada (Instituto Roche). Artículo divulgativo
Blom AM., Corvillo Rodríguez F., Magda M., Stasitojc G., Nozal P., Pérez-Valdivia MA., Cabello-Chaves V., Rodríguez de Córdoba S., López-Trascasa M. and Okrój M.
[2016]. Testing the activity of complement convertases in serum/plasma for diagnosis of C4NeF-mediated C3 glomerulonephritis, a case report." J. Clin. Immunol. 36:517-527
Olivar R., Luque A., Cárdenas-Brito S., Naranjo-Gómez M., Blom AM., Borrás F., Rodríguez de Córdoba S., Zipfel P. and Aran JM.
[2016]. The Complement Inhibitor Factor H Generates an Anti-inflammatory and Tolerogenic State in Monocyte-Derived Dendritic Cells. J. Immunol. 196:4274-4290
