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September 15, 2001BloodOpen Access

Specific von Willebrand factor–cleaving protease in thrombotic microangiopathies: a study of 111 cases

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Authors

AVAgnès VeyradierDélégation Paris 5BOBernadette ObertUniversité Paris-SudAHAnne HoullierInserm

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Veyradier et al. (2001) studied this question.

synapsesocial.com/papers/6a74492f2ea79cdc4d61ae75https://doi.org/10.1182/blood.v98.6.1765
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Also Consider

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

  1. 1Increased Fragmentation of von Willebrand Factor, Due to Abnormal Cleavage of the Subunit, Parallels Disease Activity in Recurrent Hemolytic Uremic Syndrome and Thrombotic Thrombocytopenic Purpura and Discloses Predisposition in Families1999 · 49 citations
  2. 2Unusually Large Plasma Factor VIII: von Willebrand Factor Multimers in Chronic Relapsing Thrombotic Thrombocytopenic Purpura1982 · 1,118 citations
  3. 3Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type IIA von Willebrand factor.1990 · 337 citations
  4. 4Estimation of the von Willebrand Factor-cleaving Protease in Plasma Using Monoclonal Antibodies to vWF1999 · 112 citations
  5. 5von Willebrand Factor–Cleaving Protease in Thrombotic Thrombocytopenic Purpura and the Hemolytic–Uremic Syndrome1998 · 1,674 citations