The management of patients with hemolytic uremic syndrome is challenging, and strategies for accurate diagnosis and effective treatment are needed. Intensive research over the past several years has revealed dysregulation of the complement system to be the main underlying cause of the syndrome, making this system the target of promising novel diagnostic and treatment strategies.
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Atypical hemolytic uremic syndrome
Orphanet Journal of Rare Diseases Open Access 08 September 2011
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Acknowledgements
The authors' work cited in this commentary was supported by ÖNB (Austrian Research Fund), Medical University Innsbruck and GPN (German Pediatric Nephrology Society).
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L. B. Zimmerhackl declares an association with the following company: Alexion Pharmaceuticals, as consultant, recipient of speakers bureau honoraria and recipient of grant/research support. The other authors declare no competing interests.
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Rosales, A., Riedl, M. & Zimmerhackl, L. Atypical HUS: current diagnostic and therapeutic approaches. Nat Rev Nephrol 6, 504–506 (2010). https://doi.org/10.1038/nrneph.2010.98
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DOI: https://doi.org/10.1038/nrneph.2010.98
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Atypical hemolytic uremic syndrome
Orphanet Journal of Rare Diseases (2011)