Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00035024.xml
Thromb Haemost 2003; 90(05): 955-956
DOI: 10.1160/TH03-03-0150
DOI: 10.1160/TH03-03-0150
Case Report
ADAMTS 13 genotype and vWF protease activity in an Italian family with TTP
Further Information
Publication History
Received
14 March 2003
Accepted after resubmission
27 July 2003
Publication Date:
05 December 2017 (online)
![](https://www.thieme-connect.de/media/10.1055-s-00035024/200305/lookinside/thumbnails/10-1160-th03-03-0150-1.jpg)
-
References
- 1 Levy GG, Nichols WC, Lian EC. et al Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 2001; 413: 488-94.
- 2 Kokame K, Matsumoto M, Sojima K. et al Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. PNAS 2002; 99: 11902-7.
- 3 Schneppenheim R, Budde U, Oyen F. et al Von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP. Blood 2003; 101: 1845-50.
- 4 Savasan S, Lee S-K, Ginsburg D. et al ADAMTS13 gene mutation in congenital thrombotic thrombocytopenic purpura with previously reported normal VWF cleaving protease activity. Blood 2003; 101 (11) 4449-51.
- 5 Gerritsen HE, Turecek PL, Schwartz HP. et al Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: a tool for the diagnosis of thrombotic thrombocytopenic purpura (TTP). Thromb Haemost 1999; 82: 1386-89.
- 6 Mc JR Minn, George JN. Evaluation of women with clinically suspected thrombotic thrombocytopenic purpura-hemolytic uremic syndrome during pregnancy. J Clin Apheresis 2001; 16: 202-9.