| The human complement factor H: functional roles, genetic variations and disease associations SR de Córdoba, J Esparza-Gordillo, EG de Jorge, M Lopez-Trascasa, ... Molecular immunology 41 (4), 355-367, 2004 | 748 | 2004 |
| Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome EG de Jorge, CL Harris, J Esparza-Gordillo, L Carreras, EA Arranz, ... Proceedings of the National Academy of Sciences 104 (1), 240-245, 2007 | 539 | 2007 |
| Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome D Pérez-Caballero, C González-Rubio, ME Gallardo, M Vera, ... The American Journal of Human Genetics 68 (2), 478-484, 2001 | 354 | 2001 |
| Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32 J Esparza-Gordillo, EG Jorge, A Buil, LC Berges, M Lopez-Trascasa, ... Human Molecular Genetics 14 (5), 703-712, 2005 | 332 | 2005 |
| Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome P Sánchez-Corral, D Pérez-Caballero, O Huarte, AM Simckes, ... The American Journal of Human Genetics 71 (6), 1285-1295, 2002 | 273 | 2002 |
| Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in Spain O Roche, A Blanch, T Caballero, N Sastre, D Callejo, M López-Trascasa Annals of Allergy, Asthma & Immunology 94 (4), 498-503, 2005 | 266 | 2005 |
| Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation R Martínez-Barricarte, M Heurich, F Valdes-Cañedo, E Vazquez-Martul, ... The Journal of clinical investigation 120 (10), 3702-3712, 2010 | 257 | 2010 |
| High prevalence of anti-C1q antibodies in biopsy-proven active lupus nephritis M Trendelenburg, M Lopez-Trascasa, E Potlukova, S Moll, S Regenass, ... Nephrology Dialysis Transplantation 21 (11), 3115-3121, 2006 | 246 | 2006 |
| High prevalence of anti-C1q antibodies in biopsy-proven active lupus nephritis M Trendelenburg, M Lopez-Trascasa, E Potlukova, S Moll, S Regenass, ... Nephrology Dialysis Transplantation 21 (11), 3115-3121, 2006 | 246 | 2006 |
| Characterization of complement factor H–related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome C Abarrategui-Garrido, R Martínez-Barricarte, M López-Trascasa, ... Blood, The Journal of the American Society of Hematology 114 (19), 4261-4271, 2009 | 245 | 2009 |
| Functional analysis in serum from atypical Hemolytic Uremic Syndrome patients reveals impaired protection of host cells associated with mutations in factor H P Sánchez-Corral, C Gonzalez-Rubio, SR de Córdoba, ... Molecular immunology 41 (1), 81-84, 2004 | 210 | 2004 |
| The interactive factor h–atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and factor I mutations with … RE Saunders, C Abarrategui‐Garrido, V Frémeaux‐Bacchi, ... Human mutation 28 (3), 222-234, 2007 | 195 | 2007 |
| Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part I. Classification, epidemiology, pathophysiology, genetics, clinical … T Caballero, ML Baeza, R Cabañas, A Campos, S Cimbollek, ... Journal of investigational allergology & clinical immunology 21 (5), 333-47 …, 2011 | 181 | 2011 |
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| Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree J Esparza-Gordillo, EG de Jorge, CA Garrido, L Carreras, ... Molecular immunology 43 (11), 1769-1775, 2006 | 150 | 2006 |
| Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part II. Treatment, follow-up, and special situations T Caballero, ML Baeza, R Cabañas, A Campos, S Cimbollek, ... J Investig Allergol Clin Immunol 21 (6), 422-441, 2011 | 146 | 2011 |
| Metallopeptidase activities in hereditary angioedema: effect of androgen prophylaxis on plasma aminopeptidase P C Drouet, A Désormeaux, J Robillard, D Ponard, L Bouillet, L Martin, ... Journal of allergy and clinical immunology 121 (2), 429-433, 2008 | 130 | 2008 |
| Elevated factor H–related protein 1 and factor H pathogenic variants decrease complement regulation in IgA nephropathy A Tortajada, E Gutiérrez, EG de Jorge, J Anter, A Segarra, M Espinosa, ... Kidney international 92 (4), 953-963, 2017 | 108 | 2017 |
| Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation D Paixao-Cavalcante, M Lopez-Trascasa, L Skattum, PC Giclas, ... Kidney international 82 (10), 1084-1092, 2012 | 103 | 2012 |
| Hereditary angioedema: The mutation spectrum of SERPING1/C1NH in a large Spanish cohort O Roche, A Blanch, C Duponchel, G Fontán, M Tosi, M López‐Trascasa Human mutation 26 (2), 135-144, 2005 | 102 | 2005 |
Santiago Rodriguez de CordobaCentro de Investigaciones Biologicas Margarita Salas (CSIC)Geverifieerd e-mailadres voor cib.csic.es
