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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
Weitere Informationen
Publikationsverlauf
Received
14. März 2003
Accepted after resubmission
27. Juli 2003
Publikationsdatum:
05. Dezember 2017 (online)

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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.