Familial and Recurrent Forms of Hemolytic Uremic Syndrome&amp;sol;Thrombotic Thrombocytopenic Purpura

Giuseppe Remuzzi, Miriam Galbusera, Marina Noris, Maria Teresa Canciani, Erica Daina, Elena Bresin, Silvia Contaretti, Jessica Caprioli, Sara Gamba, Piero Ruggenenti, Norberto Perico, Pier Mannuccio Mannucci

Familial and Recurrent Forms of Hemolytic Uremic Syndrome&amp;sol;Thrombotic Thrombocytopenic Purpura

Discussion(0)

Related publications

Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura

Molecular basis of familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.

Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura

Chapter 14 Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura

von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome

Familial and Recurrent Forms of Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura