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Updated: Jun 25, 2026

Endothelialized Microfluidics for Studying Microvascular Interactions in Hematologic Diseases
Published on: June 22, 2012
[Hemolytic-uremic syndrome: what is the mechanism?]
Véronique Fremeaux-Bacchi1, Fadi Fakhouri, Chantal Loirat
1Service d'immunologie biologique, hôpital Européen Georges-Pompidou, 75908 Paris Cedex 15. veronique.fremeaux-bacchi@egp.aphp.fr
Abstract:
Many data suggest that improper regulation of the alternative complement pathway is involved in the pathophysiology of atypical hemolytic-uremic syndrome. Until a few years ago, research exclusively focused on protein assays, which did not help to identify precise genetic factors predisposing to atypical hemolytic-uremic syndrome. In this context, the introduction of gene study considerably accelerated advances.
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