Haemolytic‐uraemic syndrome and thrombotic thrombocytopenic purpura—new insights into underlying biochemical mechanisms
Author:
Publisher
Oxford University Press (OUP)
Subject
Transplantation,Nephrology
Link
http://academic.oup.com/ndt/article-pdf/15/8/1112/23367722/151112.pdf
Reference19 articles.
1. Ballermann BJ. Endothelial cell activation. Kidney Int1998; 53: 1810–1826
2. Pichette V, Quérin S, Schürch W, Brun G, Lehner‐Netsch G, Delâge JM. Familial hemolytic uremic syndrome and homozygous factor H deficiency. Am J Kidney Dis1994; 24: 936–941
3. Warwicker P, Goodship THJ, Donne RL, et al. Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney Int1998; 53: 836–844
4. Rougier N, Kazatchkine MD, Rougier JP, et al. Human complement factor H deficiency associated with hemolytic uremic syndrome. J Am Soc Nephrol1998; 9: 2318–2326
5. Ying L, Katz Y, Schlesinger M, et al. Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome. Am J Hum Genet1999; 65: 1538–1546
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