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The American Journal of Medicine|September 5, 2002
Prevalence of monoclonal gammopathy in patients presenting with acquired angioedema type 2Véronique Frémeaux-Bacchi, Marie-Thérèse Guinnepain, Patrice Cacoub, et al.Journal of the American Society of Nephrology : JASN|June 10, 2006
Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndromeVéronique Fremeaux-Bacchi, Elizabeth A Moulton, David Kavanagh, et al.Journal of the American Society of Nephrology : JASN|November 6, 2010
Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndromeMarie-Agnès Dragon-Durey, Sidharth Kumar Sethi, Arvind Bagga, et al.International Journal of Nephrology and Renovascular Disease|June 23, 2011
Atypical hemolytic uremic syndrome and mutation analysis of factor H gene in two Tunisian familiesImen Habibi, Imen Sfar, Walid Ben Alaya, et al.Kidney International|December 18, 2009
Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndromeFrank Bienaime, Marie-Agnes Dragon-Durey, Catherine H Regnier, et al.Blood|July 9, 2009
Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndromeLubka T Roumenina, Mathieu Jablonski, Christophe Hue, et al.Blood|September 18, 2008
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndromeVeronique Frémeaux-Bacchi, Elizabeth C Miller, M Kathryn Liszewski, et al.Pageof 2