Thrombotic Thrombocytopenic Purpura Attributable to von Willebrand Factor-Cleaving Protease Inhibitor in an 8-Year-Old Boy
Author:
Affiliation:
1. University of Oklahoma Health Sciences Center Oklahoma City, OK 73104
2. Unified Division of Hematology Albert Einstein College of Medicine and Montefiore Medical Center Bronx, NY 10467
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology, and Child Health
Link
https://publications.aap.org/pediatrics/article-pdf/109/2/322/1113663/pe0202000322.pdf
Reference22 articles.
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2. Furlan M, Robles R, Galbusera M, et al. Von Willebrand factor—cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N Engl J Med.1998;339:1578–1584
3. Tsai HM, Lian ECY. Antibodies to Von Willebrand factor—cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med.1998;339:1585–1594
4. Moake J. Moschcowitz, multimers and metalloprotease. N Engl J Med.1998;339:1629–1631
5. Allford SL, Harrison P, Lawrie AS, Liesner R, MacKie IJ, Machin SJ. Von Willebrand factor–cleaving protease activity in congenital thrombotic thrombocytopenic purpura. Br J Haematol.2000;111:1215–1222
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