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  • Marie-Agnès Dragon-Durey, Sidharth Kumar Sethi, +12 authors Véronique Frémeaux-Bacchi
  • Medicine
  • Journal of the American Society of Nephrology…
  • 2010 (First Published: 1 December 2010)
  • Atypical hemolytic uremic syndrome (aHUS) is a rare form of thrombotic microangiopathy that associates, in 70% of cases, with genetic or acquired disorders leading to dysregulation of the alternativeContinue Reading
  • Aditi Sinha, Ashima Gulati, +24 authors Arvind Bagga
  • Medicine
  • Kidney international
  • 2014 (First Published: 1 May 2014)
  • Antibodies to complement factor H are an uncommon cause of hemolytic uremic syndrome (HUS). Information on clinical features and outcomes in children is limited. In order to explore this we studied aContinue Reading
  • Caroline Blanc, Lubka T. Roumenina, +12 authors M-A Dragon-Durey
  • Biology, Medicine
  • Journal of immunology
  • 2012 (First Published: 1 October 2012)
  • Complement is a major innate immune surveillance system. One of its most important regulators is the plasma protein factor H (FH). FH inactivation by mutations or by autoantibodies is associated withContinue Reading
  • Jennifer G. Jetton, Louis J. Boohaker, +12 authors David J. Askenazi
  • Medicine
  • The Lancet. Child & adolescent health
  • 2017 (First Published: 1 November 2017)
  • Background Single-center studies suggest that neonatal acute kidney injury (AKI) is associated with poor outcomes. However, inferences regarding the association between AKI, mortality, and hospitalContinue Reading
  • Marie-Agnès Dragon-Durey, Caroline Blanc, Arnaud Garnier, Johannes Hofer, Sidharth Kumar Sethi, Lothar-Bernd Zimmerhackl
  • Medicine
  • Seminars in thrombosis and hemostasis
  • 2010 (First Published: 1 September 2010)
  • Non-Shiga toxin-associated hemolytic uremic syndrome (atypical HUS) is a rare form of thrombotic microangiopathy that associates hemolytic anemia, thrombocytopenia, and acute renal failure. TheContinue Reading