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721.
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722.
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A novel antibody against human factor B that blocks formation of the C3bB proconvertase and inhibits complement activation in disease models. [electronic resource] by
- Subías, Marta
- Tortajada, Agustín
- Gastoldi, Sara
- Galbusera, Miriam
- López-Perrote, Andrés
- Lopez, Lucia de Juana
- González-Fernández, Fernando Ataúlfo
- Villegas-Martínez, Ana
- Dominguez, Mercedes
- Llorca, Oscar
- Noris, Marina
- Morgan, B Paul
- Rodríguez de Córdoba, Santiago
Producer: 20150416
In:
Journal of immunology (Baltimore, Md. : 1950) vol. 193
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723.
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An international consensus approach to the management of atypical hemolytic uremic syndrome in children. [electronic resource] by
- Loirat, Chantal
- Fakhouri, Fadi
- Ariceta, Gema
- Besbas, Nesrin
- Bitzan, Martin
- Bjerre, Anna
- Coppo, Rosanna
- Emma, Francesco
- Johnson, Sally
- Karpman, Diana
- Landau, Daniel
- Langman, Craig B
- Lapeyraque, Anne-Laure
- Licht, Christoph
- Nester, Carla
- Pecoraro, Carmine
- Riedl, Magdalena
- van de Kar, Nicole C A J
- Van de Walle, Johan
- Vivarelli, Marina
- Frémeaux-Bacchi, Véronique
Producer: 20160829
In:
Pediatric nephrology (Berlin, Germany) vol. 31
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724.
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725.
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Heme Drives Susceptibility of Glomerular Endothelium to Complement Overactivation Due to Inefficient Upregulation of Heme Oxygenase-1. [electronic resource] by
- May, Olivia
- Merle, Nicolas S
- Grunenwald, Anne
- Gnemmi, Viviane
- Leon, Juliette
- Payet, Cloé
- Robe-Rybkine, Tania
- Paule, Romain
- Delguste, Florian
- Satchell, Simon C
- Mathieson, Peter W
- Hazzan, Marc
- Boulanger, Eric
- Dimitrov, Jordan D
- Fremeaux-Bacchi, Veronique
- Frimat, Marie
- Roumenina, Lubka T
Producer: 20191119
In:
Frontiers in immunology vol. 9
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726.
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727.
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The MFHR1 Fusion Protein Is a Novel Synthetic Multitarget Complement Inhibitor with Therapeutic Potential. [electronic resource] by
- Michelfelder, Stefan
- Fischer, Friedericke
- Wäldin, Astrid
- Hörle, Kim V
- Pohl, Martin
- Parsons, Juliana
- Reski, Ralf
- Decker, Eva L
- Zipfel, Peter F
- Skerka, Christine
- Häffner, Karsten
Producer: 20190916
In:
Journal of the American Society of Nephrology : JASN vol. 29
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728.
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A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function. [electronic resource] by
- Roumenina, Lubka T
- Frimat, Marie
- Miller, Elizabeth C
- Provot, Francois
- Dragon-Durey, Marie-Agnes
- Bordereau, Pauline
- Bigot, Sylvain
- Hue, Christophe
- Satchell, Simon C
- Mathieson, Peter W
- Mousson, Christiane
- Noel, Christian
- Sautes-Fridman, Catherine
- Halbwachs-Mecarelli, Lise
- Atkinson, John P
- Lionet, Arnaud
- Fremeaux-Bacchi, Veronique
Producer: 20120717
In:
Blood vol. 119
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729.
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Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome. [electronic resource] by
- Hofer, Johannes
- Janecke, Andreas R
- Zimmerhackl, L B
- Riedl, Magdalena
- Rosales, Alejandra
- Giner, Thomas
- Cortina, Gerard
- Haindl, Carola J
- Petzelberger, Barbara
- Pawlik, Miriam
- Jeller, Verena
- Vester, Udo
- Gadner, Bettina
- van Husen, Michael
- Moritz, Michael L
- Würzner, Reinhard
- Jungraithmayr, Therese
Producer: 20130826
In:
Clinical journal of the American Society of Nephrology : CJASN vol. 8
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730.
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Atypical and secondary hemolytic uremic syndromes have a distinct presentation and no common genetic risk factors. [electronic resource] by
- Le Clech, Alice
- Simon-Tillaux, Noémie
- Provôt, François
- Delmas, Yahsou
- Vieira-Martins, Paula
- Limou, Sophie
- Halimi, Jean-Michel
- Le Quintrec, Moglie
- Lebourg, Ludivine
- Grangé, Steven
- Karras, Alexandre
- Ribes, David
- Jourde-Chiche, Noémie
- Rondeau, Eric
- Frémeaux-Bacchi, Véronique
- Fakhouri, Fadi
Producer: 20200921
In:
Kidney international vol. 95
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731.
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732.
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