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October 30, 2002BloodOpen Access

Deficiency of ADAMTS13 and thrombotic thrombocytopenic purpura

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HTHan‐Mou TsaiState University of New York

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Han‐Mou Tsai (2002) studied this question.

synapsesocial.com/papers/6a70c4b5f44fa9f079de7702https://doi.org/10.1182/blood-2002-07-2241
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome2002 · 192 citations
  2. 2High titers of inhibitors of von Willebrand factor-cleaving metalloproteinase in a fatal case of acute thrombotic thrombocytopenic purpura2000 · 60 citations
  3. 3Antibodies to von Willebrand Factor–Cleaving Protease in Acute Thrombotic Thrombocytopenic Purpura1998 · 1,781 citations
  4. 4Predicting response to plasma exchange in patients with thrombotic thrombocytopenic purpura with measurement of vWF‐cleaving protease activity2002 · 134 citations
  5. 5Specific von Willebrand factor–cleaving protease in thrombotic microangiopathies: a study of 111 cases2001 · 384 citations