Anti-Factor B Antibodies and Acute Postinfectious GN in Children von Chauvet, Sophie, Berthaud, Romain, Devriese, Magali, Mignotet, Morgane, Martins, Paula Vieira, Robe-Rybkine, Tania, Miteva, Maria A., Gyulkhandanyan, Aram, Ryckewaert, Amelie, Louillet, Ferielle, Merieau, Elodie, Mestrallet, Guillaume, Rousset-Rouviere, Caroline, Thervet, Eric, Hogan, Julien, Ulinski, Tim, Villoutreix, Bruno O., Roumenina, Lubka, Boyer, Olivia, Fremeaux-Bacchi, Veronique

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Impact of hypertensive emergency and rare complement variants on the presentation and outcome of atypical hemolytic uremic syndrome von El Karoui, Khalil, Boudhabhay, Idris, Petitprez, Florent, Vieira-Martins, Paula, Fakhouri, Fadi, Zuber, Julien, Aulagnon, Florence, Matignon, Marie, Rondeau, Eric, Mesnard, Laurent, Halimi, Jean-Michel, Frémeaux-Bacchi, Véronique

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Sheep Erythrocyte Preparation for Hemolytic Tests Exploring Complement Functional Activities von Chabannes, Melchior, Bordereau, Pauline, Martins, Paula Vieira, Dragon-Durey, Marie-Agnès

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C3 Glomerulopathy With Concurrent Thrombotic Microangiopathy: Clinical and Immunological Features von Chabannes, Melchior, Rabant, Marion, El Sissy, Carine, Dragon-Durey, Marie-Agnès, Vieira Martins, Paula, Meuleman, Marie Sophie, Karras, Alexandre, Buob, David, Bridoux, Frank, Daugas, Eric, Audard, Vincent, Caillard, Sophie, Olagne, Jérôme, Kandel, Christine, Ferlicot, Sophie, Philipponnet, Carole, Crepin, Thomas, Thervet, Eric, Ducloux, Didier, Frémeaux-Bacchi, Véronique, Chauvet, Sophie

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Rare germline complement factor H variants in patients with paroxysmal nocturnal hemoglobinuria von Prata, Pedro Henrique, Galimard, Jacques-Emmanuel, Sicre de Fontbrune, Flore, Duval, Anna, Vieira Martins, Paula, Roncelin, Stephane, Debureaux, Pierre-Édouard, Lepretre, Anne-Claire, Larcher, Lise, Birsen, Rudy, Benhamou, Ygal, Soulier, Jean, Socié, Gérard, Fremeaux-Bacchi, Véronique, Peffault de Latour, Régis

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Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome von Schramm, Elizabeth C., Roumenina, Lubka T., Rybkine, Tania, Chauvet, Sophie, Vieira-Martins, Paula, Hue, Christophe, Maga, Tara, Valoti, Elisabetta, Wilson, Valerie, Jokiranta, Sakari, Smith, Richard J.H., Noris, Marina, Goodship, Tim, Atkinson, John P., Fremeaux-Bacchi, Veronique

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Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies von El Sissy, Carine, Rosain, Jérémie, Vieira-Martins, Paula, Bordereau, Pauline, Gruber, Aurélia, Devriese, Magali, de Pontual, Loïc, Taha, Muhamed-Kheir, Fieschi, Claire, Picard, Capucine, Frémeaux-Bacchi, Véronique

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Defining the genetics of thrombotic microangiopathies von Vieira-Martins, Paula, El Sissy, Carine, Bordereau, Pauline, Gruber, Aurelia, Rosain, Jeremie, Fremeaux-Bacchi, Veronique

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C3 glomerulopathy is highly prevalent in French Polynesia von Candela, Nelly, Benichou, Nicolas, Lefebvre, Mathilde, Gueguen, Lorraine, Vieira-Martins, Paula, El Sissy, Carine, Sartelet, Hervé, Testevuide, Pascale, Delaval, Ronan, Faguer, Stanislas

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Complement deficiencies and human diseases von Rosain, Jérémie, Ngo, Stéphanie, Bordereau, Pauline, Poulain, Nelly, Roncelin, Stéphane, Vieira Martins, Paula, Dragon-Durey, Marie-Agnès, Frémeaux-Bacchi, Véronique

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Acquired and genetic drivers of C3 and C5 convertase dysregulation in C3 glomerulopathy and immunoglobulin-associated MPGN von Roquigny, Julia, Meuleman, Marie-Sophie, El Sissy, Carine, Martins, Paula Vieira, Meri, Seppo, Duval, Anna, Lequintrec, Moglie, Fakhouri, Fadi, Chauvet, Sophie, Frémeaux-Bacchi, Véronique

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Hot Spot of Complement Factor I Rare Variant p.Ile357Met in Patients With Hemolytic Uremic Syndrome von Schwotzer, Nora, Fakhouri, Fadi, Martins, Paula Vieira, Delmas, Yahsou, Caillard, Sophie, Zuber, Julien, Moranne, Olivier, Mesnard, Laurent, Frémeaux-Bacchi, Véronique, El-Sissy, Carine

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2639 Unraveling complement activation profiles on endothelial cells in healthy donors using an ex vivo model von Duval, Anna, Meuleman, Marie-Sophie, Grunenwald, Anne, Vieira-Martins, Paula, Apithy, Marie-Joelle, Benotmane, Ilies, Martzloff, Jonas, Lemonnier, Lisa, Chauvet, Sophie, Roumenina, Lubka, Caillard, Sophie, Bacchi, Veronique Fremeaux

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Assessing complement blockade in patients with paroxysmal nocturnal hemoglobinuria receiving eculizumab von Peffault de Latour, Régis, Fremeaux-Bacchi, Véronique, Porcher, Raphaël, Xhaard, Aliénor, Rosain, Jérémie, Castaneda, Diana Cadena, Vieira-Martins, Paula, Roncelin, Stéphane, Rodriguez-Otero, Paula, Plessier, Aurélie, Sicre de Fontbrune, Flore, Abbes, Sarah, Robin, Marie, Socié, Gérard

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Rapid Nephrogenomics in Intensive Care for Early Intervention in Adult Thrombotic Microangiopathies: SA-PO796 von Yousfi, Nadhir, Mille, Marie, Hamza, Abderaouf, Vandermeersch, Sophie, Beaumeunier, Sacha, Bertrand, Denis, Blum, Michael, Doudement, Julien, El Sissy, Carine, Vieira-Martins, Paula, Philippe, Nicolas, Bacchi, Veronique Fremeaux, Mesnard, Laurent

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COVID-19 as a potential trigger of complement-mediated atypical HUS von El Sissy, Carine, Saldman, Antonin, Zanetta, Gilbert, Martins, Paula Vieira, Poulain, Coralie, Cauchois, Raphaël, Kaplanski, Gilles, Venetz, Jean-Pierre, Bobot, Mickaël, Dobosziewicz, Hélène, Daniel, Laurent, Koubi, Marie, Sadallah, Salima, Rotman, Samuel, Mousson, Christiane, Pascual, Manuel, Frémeaux-Bacchi, Véronique, Fakhouri, Fadi

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Complement Gene Variants and Shiga Toxin-Producing Escherichia coli -Associated Hemolytic Uremic Syndrome: Retrospective Genetic and Clinical Study von Frémeaux-Bacchi, Véronique, Sellier-Leclerc, Anne-Laure, Vieira-Martins, Paula, Limou, Sophie, Kwon, Theresa, Lahoche, Annie, Novo, Robert, Llanas, Brigitte, Nobili, François, Roussey, Gwenaëlle, Cailliez, Mathilde, Ulinski, Tim, Deschênes, Georges, Alberti, Corinne, Weill, François-Xavier, Mariani, Patricia, Loirat, Chantal

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Complement biomarkers as predictors of disease outcome in C3 glomerulopathy von Hauer, Jill, Marinozzi, Maria-Chiara, Vieira-Martins, Paula, Roumenina, Lubka, Smith, Richard J.H., Frémeaux-Bacchi, Véronique, Chauvet, Sophie

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Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy von Roumenina, Lubka, Chadebech, Philippe, Bodivit, Gwellaouen, Vieira‐martins, Paula, Grunenwald, Anne, Boudhabhay, Idris, Poillerat, Victoria, Pakdaman, Sadaf, Kiger, Laurent, Jouard, Alicia, Audureau, Etienne, Pirenne, France, Galactéros, Frédéric, Frémeaux‐bacchi, Véronique, Bartolucci, Pablo

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Statistical validation of rare complement variants provides insights on the molecular basis of atypical haemolytic uraemic syndrome and C3 glomerulopathy von Osborne, Amy J., Breno, Matteo, Borsa, Nicolo Ghiringhelli, Bu, Fengxiao, Frémeaux-Bacchi, Véronique, Gale, Daniel P., van den Heuvel, Lambertus P., Kavanagh, David, Noris, Marina, Pinto, Sheila, Rallapalli, Pavithra M., Remuzzi, Giuseppe, de Cordoba, Santiago Rodríguez, Ruiz, Angela, Smith, Richard J. H., Vieira-Martins, Paula, Volokhina, Elena, Wilson, Valerie, Goodship, Timothy H. J., Perkins, Stephen J.

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