Thrombotic microangiopathy is featured by microangiopathic haemolytic anaemia, thrombocytopenia and the presence of peripheral fragmented red cells. Thrombotic thrombocytopenic purpura (TTP) is the major disease entity of concern, which is caused by a congenital or acquired deficiency of a von Willebrand factor (vWF) cleaving protease known as ADAMTS13 (A Disintegrin And Metalloprotease with Thrombospondin type 1 motif, member 13). Deficiency of this protease, leads to accumulation of uncleaved ultra-large hyperactive vWF multimers in peripheral circulation causing the extensive microvascular platelet aggregation in a TTP event. However, the differential diagnosis is sometimes difficult because symptoms and signs can be non-specific and ...
The von Willebrand factor cleaving protease (ADAMTS-13) hydrolyses a peptide bond in the plasma mult...
Thrombotic thrombocytopenic purpura (TTP) is a disorder characterized by disseminated thrombotic occ...
BACKGROUND: The recently discovered plasma enzyme ADAMTS-13 cleaves the A2-domain of von Willebrand ...
ADAMTS-13, the thirteenth member of the ADAMTS (A Disintegrin And Metalloprotease with Thrombo-Spond...
The last 10 years witnessed the publication of many studies on the pathophysiology of thrombotic thr...
Thrombotic microangiopathy can be caused by several conditions which are difficult to diagnose from ...
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease characterized by acute...
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease, disease, characterise...
BACKGROUND: ADAMTS13 deficiency causes accumulation of unusually large von Willebrand factor molecul...
ADAMTS13 (a disintegrin-like and metallo-proteinase with thrombospondin type 1 motif), the metallopr...
The congenital or acquired deficiency of the von Willebrand factor (VWF) cleaving protease, ADAMTS-1...
Thrombotic thrombocytopenic purpura (TTP) is a life-threatening thrombotic microangiopathic (TMA) di...
A finding of an ADAMTS13 (a disintegrin-like and metalloprotease with thrombospondin type 1 motif, m...
13), a plasma metalloprotease, cleaves von Willebrand factor (VWF) [1,2]. This cleavage is crucial f...
Summary Background: ADAMTS13 deficiency causes accumulation of unusually large von Willebrand factor...
The von Willebrand factor cleaving protease (ADAMTS-13) hydrolyses a peptide bond in the plasma mult...
Thrombotic thrombocytopenic purpura (TTP) is a disorder characterized by disseminated thrombotic occ...
BACKGROUND: The recently discovered plasma enzyme ADAMTS-13 cleaves the A2-domain of von Willebrand ...
ADAMTS-13, the thirteenth member of the ADAMTS (A Disintegrin And Metalloprotease with Thrombo-Spond...
The last 10 years witnessed the publication of many studies on the pathophysiology of thrombotic thr...
Thrombotic microangiopathy can be caused by several conditions which are difficult to diagnose from ...
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease characterized by acute...
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease, disease, characterise...
BACKGROUND: ADAMTS13 deficiency causes accumulation of unusually large von Willebrand factor molecul...
ADAMTS13 (a disintegrin-like and metallo-proteinase with thrombospondin type 1 motif), the metallopr...
The congenital or acquired deficiency of the von Willebrand factor (VWF) cleaving protease, ADAMTS-1...
Thrombotic thrombocytopenic purpura (TTP) is a life-threatening thrombotic microangiopathic (TMA) di...
A finding of an ADAMTS13 (a disintegrin-like and metalloprotease with thrombospondin type 1 motif, m...
13), a plasma metalloprotease, cleaves von Willebrand factor (VWF) [1,2]. This cleavage is crucial f...
Summary Background: ADAMTS13 deficiency causes accumulation of unusually large von Willebrand factor...
The von Willebrand factor cleaving protease (ADAMTS-13) hydrolyses a peptide bond in the plasma mult...
Thrombotic thrombocytopenic purpura (TTP) is a disorder characterized by disseminated thrombotic occ...
BACKGROUND: The recently discovered plasma enzyme ADAMTS-13 cleaves the A2-domain of von Willebrand ...