Pathogenesis of Atypical Hemolytic Uremic Syndrome
Author:
Affiliation:
1. Division of Nephrology and Endocrinology, the University of Tokyo Hospital
2. Department of Prevention of Diabetes and Lifestyle-Related Diseases Graduate School of Medicine, the University of Tokyo
Publisher
Japan Atherosclerosis Society
Subject
Biochemistry (medical),Cardiology and Cardiovascular Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/jat/26/2/26_RV17026/_pdf
Reference98 articles.
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3. 3) Kokame K, Matsumoto M, Soejima K, Yagi H, Ishizashi H, Funato M, Tamai H, Konno M, Kamide K, Kawano Y, Miyata T, Fujimura Y: Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci U S A, 2002; 99: 11902-11907
4. 4) Huang J, Motto DG, Bundle DR, Sadler JE: Shiga toxin B subunits induce VWF secretion by human endothelial cells and thrombotic microangiopathy in ADAMTS13-deficient mice. Blood, 2010; 116: 3653-3659
5. 5) Kato H, Nangaku M, Hataya H, Sawai T, Ashida A, Fujimaru R, Hidaka Y, Kaname S, Maruyama S, Yasuda T, Yoshida Y, Ito S, Hattori M, Miyakawa Y, Fujimura Y, Okada H, Kagami S: Clinical guides for atypical hemolytic uremic syndrome in Japan. Clin Exp Nephrol, 2016; 20: 536-543
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