The PLASMIC score for the prediction of a likelihood of a severe ADAMTS13 deficiency represents a valid pre-test diagnostic tool to identify patients with thrombotic thrombocytopenic purpura.
Giovanni Tiscia+17 more
doaj +1 more source
Circulating immune complexes in thrombotic thrombocytopenic purpura (TTP) [letter] [PDF]
Antonio Celada, LH Perrin
openalex +1 more source
Pathophysiology of thrombotic thrombocytopenic purpura.
The discovery of a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, member 13 (ADAMTS13) revolutionized our approach to thrombotic thrombocytopenic purpura (TTP).
J. E. Sadler
semanticscholar +1 more source
Vitamin B12 Deficiency with Pseudothrombotic Microangiopathy and Thrombotic Thrombocytopenic Purpura: Similarities and Differences [PDF]
Buess, Charles+3 more
core +2 more sources
Objective: We present a rare case of pernicious anemia presented as multi-organ dysfunction syndrome, later found to have pseudo-thrombotic thrombocytopenic purpura.
Saroj Kandel+9 more
doaj +1 more source
Treatment of Thrombotic Thrombocytopenic Purpura With Antiplatelet Drugs [PDF]
Jacob Amir, Stephen Krauss
openalex +1 more source
Beyond plasma exchange: novel therapies for thrombotic thrombocytopenic purpura.
The advent of plasma exchange has dramatically changed the prognosis of acute thrombotic thrombocytopenic purpura (TTP). Recent insights into TTP pathogenesis have led to the development of novel therapies targeting pathogenic anti-ADAMTS13 antibody ...
Kathryn E. Dane, Shruti Chaturvedi
semanticscholar +1 more source
Thrombotic thrombocytopenic purpura and dose of plasma exchange [PDF]
EG Taft
openalex +1 more source
Pathologic effects of plasma from patients with thrombotic thrombocytopenic purpura on platelets and cultured vascular endothelial cells [PDF]
E. Robert Burns, D Zucker-Franklin
openalex +1 more source
The effect of single nucleotide polymorphisms and mutations on congenital thrombotic thrombocytopenic purpura phenotype [PDF]
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease with a reported incidence of 6 cases per million per year in the UK. It is characterised by episodes of microangiopathic haemolytic anaemia and thrombocytopenia, with the ...
Tate, H., Tate, H.
core