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Low activity of von Willebrand factor-cleaving protease is not restricted to patients suffering from thrombotic thrombocytopenic purpura.

作者信息

Loof A H, van Vliet H H, Kappers-Klunne M C

出版信息

Br J Haematol. 2001 Mar;112(4):1087-8. doi: 10.1046/j.1365-2141.2001.02622-5.x.

DOI:10.1046/j.1365-2141.2001.02622-5.x
PMID:11324640
Abstract
摘要

相似文献

1
Low activity of von Willebrand factor-cleaving protease is not restricted to patients suffering from thrombotic thrombocytopenic purpura.血管性血友病因子裂解蛋白酶活性降低并不局限于血栓性血小板减少性紫癜患者。
Br J Haematol. 2001 Mar;112(4):1087-8. doi: 10.1046/j.1365-2141.2001.02622-5.x.
2
von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome.血栓性血小板减少性紫癜和溶血尿毒综合征中的血管性血友病因子裂解蛋白酶
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Deficient activity of von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura.血栓性血小板减少性紫癜中血管性血友病因子裂解蛋白酶活性缺乏。
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Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura.急性血栓性血小板减少性紫癜中针对血管性血友病因子裂解蛋白酶的抗体。
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Immunotherapy for thrombotic thrombocytopenic purpura.血栓性血小板减少性紫癜的免疫疗法。
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[A woman suffering from systemic lupus erythematosus and acquired thrombotic thrombocytopenic purpura].一名患有系统性红斑狼疮和获得性血栓性血小板减少性紫癜的女性
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Thrombotic thrombocytopenic purpura attributable to von Willebrand factor-cleaving protease inhibitor in an 8-year-old boy.一名8岁男孩因血管性血友病因子裂解蛋白酶抑制剂导致血栓性血小板减少性紫癜。
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[Thrombotic thrombocytopenic purpura and von Willebrand factor- specific-cleaving enzyme].
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