All Stories

  1. Malignant hypertension due to defective complement regulation
  2. Acquired Thrombotic Thrombocytopenic Purpura
  3. A Mechanistic Approach to the Diagnosis and Management of Atypical Hemolytic Uremic Syndrome
  4. Repair of Nanodefects in a Two-Dimensional Crystal Anticoagulant Shield in the Antiphospholipid Syndrome
  5. Eculizumab Therapy Leads to Rapid Resolution of Thrombocytopenia in Atypical Hemolytic Uremic Syndrome
  6. Thrombotic Thrombocytopenic Purpura and the Atypical Hemolytic Uremic Syndrome
  7. Concurrent atypical hemolytic uremic syndrome in a case of "refractory" thrombocytopenic purpura
  8. Untying the Knot of Thrombotic Thrombocytopenic Purpura and Atypical Hemolytic Uremic Syndrome
  9. Thrombotic Thrombocytopenic Purpura and the Hemolytic-Uremic Syndrome
  10. Autoimmune Thrombotic Microangiopathy: Advances in Pathogenesis, Diagnosis, and Management
  11. von Willebrand Factor, Shear Stress, and ADAMTS13 in Hemostasis and Thrombosis
  12. Excessive activation of the complement system in atypical hemolytic uremic syndrome: is it ready for prime time?
  13. Pathophysiology of thrombotic thrombocytopenic purpura
  14. Mechanisms of microvascular thrombosis in thrombotic thrombocytopenic purpura
  15. Thrombotic Thrombocytopenic Purpura: A Thrombotic Disorder Caused by ADAMTS13 Deficiency
  16. ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpura
  17. ADAMTS13 and microvascular thrombosis
  18. Multifunctional Composite Nanoparticles:  Magnetic, Luminescent, and Mesoporous
  19. ADAMTS13-binding IgG are present in patients with thrombotic thrombocytopenic purpura
  20. Current Concepts in Thrombotic Thrombocytopenic Purpura
  21. ADAMTS13 is expressed in hepatic stellate cells
  22. Why Do We Need ADAMTS13?
  23. Molecular Mechanisms in Thrombotic Thrombocytopenic Purpura
  24. Thrombocytopenia and Severe Hyperbilirubinemia in the Neonatal Period Secondary to Congenital Thrombotic Thrombocytopenic Purpura and ADAMTS13 Deficiency
  25. An enzyme immunoassay of ADAMTS13 distinguishes patients with thrombotic thrombocytopenic purpura from normal individuals and carriers of ADAMTS13 mutations
  26. Rituximab for chronic recurring thrombotic thrombocytopenic purpura: a case report and review of the literature
  27. Rituximab induces remission of cerebral ischemia caused by thrombotic thrombocytopenic purpura
  28. Thrombotic Thrombocytopenic Purpura in a Newborn
  29. Presence of ADAMTS13 Activity in a Patient with Metastatic Cancer and Thrombotic Microangiopathy
  30. Ultralarge von Willebrand factor multimers and normal ADAMTS13 activity in the umbilical cord blood
  31. Deficiency of ADAMTS13 and thrombotic thrombocytopenic purpura
  32. Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura
  33. Inhibitors of ADAMTS13: a potential factor in the cause of thrombotic microangiopathy in a renal allograft recipient
  34. Transfusion of polymerised human haemoglobin in a patient with severe sickle-cell anaemia
  35. Deficiency of ADAMTS13 in thrombotic thrombocytopenic purpura
  36. Warm-Antibody Autoimmune Hemolytic Anemia Developing after Thrombotic Thrombocytopenic Purpura
  37. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
  38. Von Willebrand Factor and Von Willebrand Factor-Cleaving Metalloprotease Activity in Escherichia coli O157:H7-Associated Hemolytic Uremic Syndrome
  39. A comparison of von Willebrand Factor antigen with platelet activity in vitro in normal and venous occlusion blood
  40. Von Willebrand factor-cleaving protease activity and proteolysis of von Willebrand factor in bone marrow transplant-associated thrombotic microangiopathy
  41. Surface dependent structures of von Willebrand factor observed by AFM under aqueous conditions
  42. Thrombotic Thrombocytopenic Purpura Associated with Clopidogrel
  43. Role of A and B blood group antigens in the expression of adhesive activity of von Willebrand factor
  44. Antibody Inhibitors to von Willebrand Factor Metalloproteinase and Increased Binding of von Willebrand Factor to Platelets in Ticlopidine-Associated Thrombotic Thrombocytopenic Purpura
  45. High titers of inhibitors of von Willebrand factor-cleaving metalloproteinase in a fatal case of acute thrombotic thrombocytopenic purpura
  46. Antibodies to von Willebrand Factor–Cleaving Protease in Acute Thrombotic Thrombocytopenic Purpura
  47. The high molecular weight form of endothelial cell von Willebrand factor is released by the regulated pathway
  48. Subunit composition of plasma von Willebrand factor multimers: Evidence for a non-proteolytic mechanism resulting in apparent increase in proteolytic fragments
  49. Endothelial cell-derived high molecular weight von Willebrand factor is converted into the plasma multimer pattern by granulocyte proteases
  50. ADAMTS-13