Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency-Reference-Cited by-同舟云学术

Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency

Published:2016-02-01 Issue:3 Volume:103 Page:283-291
ISSN:0925-5710
Container-title:International Journal of Hematology
language:en
Short-container-title:Int J Hematol

Author:

Fan Xinping,Kremer Hovinga Johanna A.,Shirotani-Ikejima Hiroko,Eura Yuka,Hirai Hidenori,Honda Shigenori,Kokame Koichi,Taleghani Magnus Mansouri,von Krogh Anne-Sophie,Yoshida Yoko,Fujimura Yoshihiro,Lämmle Bernhard,Miyata Toshiyuki

Funder

a scholarship from the Takeda Science Foundation

grants-in-aid from the Ministry of Health, Labor, and Welfare of Japan

grants-in-aid from the Japan Society for the Promotion of Science

the Takeda Science Foundation

a research grant from Baxter Bioscience

a scholarship from the Association for Preventive Medicine of Japan

the Swiss National Science Foundation

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Link

http://link.springer.com/content/pdf/10.1007/s12185-015-1933-7.pdf

Reference35 articles.

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2. Kokame K, Matsumoto M, Soejima K, Yagi H, Ishizashi H, Funato M, et al. Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci. 2002;99:11902–7.

3. Furlan M, Lämmle B. Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome: the role of von Willebrand factor-cleaving protease. Best Pract Res Clin Haematol. 2001;14:437–54.

4. Fujimura Y, Matsumoto M, Isonishi A, Yagi H, Kokame K, Soejima K, et al. Natural history of Upshaw–Schulman syndrome based on ADAMTS13 gene analysis in Japan. J Thromb Haemost. 2011;9(Suppl 1):283–301.

5. Noris M, Remuzzi G. Atypical hemolytic-uremic syndrome. N Engl J Med. 2009;361:1676–87.

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