ADAMTS13 content in plasma-derived factor VIII/von Willebrand factor concentrates-Reference-Cited by-同舟云学术

ADAMTS13 content in plasma-derived factor VIII/von Willebrand factor concentrates

Published:2013-08-30 Issue:10 Volume:88 Page:895-898
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Peyvandi Flora¹,Mannucci Pier M.²,Valsecchi Carla¹,Pontiggia Silvia¹,Farina Claudio³,Retzios Anastassios D.⁴

Affiliation:

1. Angelo Bianchi Bonomi Haemophilia and Thrombosis Center; Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico; Department of Pathophysiology and Transplantation; University of Milan, Luigi Villa Foundation; Milan Italy

2. Scientific Direction; Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico; Milan Italy

3. Kedrion S.p.A., R&D Department; Lucca Italy

4. Bay Clinical R&D Services; LLC; San Ramon California

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.23527/fullpdf

Reference19 articles.

1. Thrombotic thrombocytopenic purpura: A thrombotic disorder caused by ADAMTS13 deficiency;Tsai;Hematol Oncol Clin North Am,2007

2. von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurring and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome;Remuzzi;Blood,2002

3. von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpura;Peyvandi;Br J Haematol,2004

4. Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura;Rock;N Engl J Med,1991

5. The use of intermediate purity factor VIII concentrate BPL 8Y as prophylaxis and treatment in congenital thrombocytopenic purpura;Scully;Br J Hematol,2006

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