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| Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases MA Dragon-Durey, V Fremeaux-Bacchi, C Loirat, J Blouin, P Niaudet, ... Journal of the American Society of Nephrology 15 (3), 787-795, 2004 | 436 | 2004 |
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| Atypical aHUS: state of the art CM Nester, T Barbour, SR de Cordoba, MA Dragon-Durey, ... Molecular immunology 67 (1), 31-42, 2015 | 314 | 2015 |
| Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome EA Moulton, D Kavanagh, J Blouin, A Caudy, N Arzouk, R Cleper, ... Journal of the American Society of Nephrology 17 (7), 2017-2025, 2006 | 277 | 2006 |
| Prompt plasma exchanges and immunosuppressive treatment improves the outcomes of anti-factor H autoantibody-associated hemolytic uremic syndrome in children A Sinha, A Gulati, S Saini, C Blanc, A Gupta, BS Gurjar, H Saini, ... Kidney international 85 (5), 1151-1160, 2014 | 228 | 2014 |
| Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome F Bienaime, MA Dragon-Durey, CH Regnier, SC Nilsson, WH Kwan, ... Kidney international 77 (4), 339-349, 2010 | 218 | 2010 |
| Y402H complement factor H polymorphism associated with exudative age-related macular degeneration in the French population EH Souied, N Leveziel, F Richard, MA Dragon-Durey, G Coscas, ... Mol Vis 11 (131-32), 1135-1140, 2005 | 216 | 2005 |
| Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome LT Roumenina, M Jablonski, C Hue, J Blouin, JD Dimitrov, ... Blood, The Journal of the American Society of Hematology 114 (13), 2837-2845, 2009 | 193 | 2009 |
| Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet … P Coppo, D Bengoufa, A Veyradier, M Wolf, A Bussel, GA Millot, S Malot, ... Medicine 83 (4), 233-244, 2004 | 191 | 2004 |
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| The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome MA Dragon-Durey, C Blanc, F Marliot, C Loirat, J Blouin, ... Journal of medical genetics 46 (7), 447-450, 2009 | 170 | 2009 |
