Results 161 to 168 of about 78,032 (168)
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Transfusion, 2020
The PLASMIC score was developed to identify patients with thrombotic microangiopathy who are most likely to have immune thrombotic thrombocytopenic purpura (TTP) and benefit from therapeutic plasma exchange (TPE).
Koosha Paydary+4 more
semanticscholar +1 more source
The PLASMIC score was developed to identify patients with thrombotic microangiopathy who are most likely to have immune thrombotic thrombocytopenic purpura (TTP) and benefit from therapeutic plasma exchange (TPE).
Koosha Paydary+4 more
semanticscholar +1 more source
First‐in‐patient study of hetrombopag in patients with chronic idiopathic thrombocytopenic purpura
Journal of Thrombosis and Haemostasis, 2020Idiopathic thrombocytopenic purpura (ITP) especially refractory and (or) relapsed ITP, is a serious and global health burden and its clinical treatment is far from being satisfied.
Zhenlei Wang+10 more
semanticscholar +1 more source
An update on pathogenesis and diagnosis of thrombotic thrombocytopenic purpura
Expert Review of Hematology, 2019Introduction: Thrombotic thrombocytopenic purpura (TTP) is a rare and life-threatening thrombotic microangiopathy characterized by microangiopathic hemolytic anemia, consumption thrombocytopenia, and organ injury. TTP pathophysiology is based on a severe
B. Joly, P. Coppo, A. Veyradier
semanticscholar +1 more source
Pembrolizumab-induced thrombotic thrombocytopenic purpura
Journal of Oncology Pharmacy Practice, 2019Introduction Pembrolizumab is a humanised monoclonal antibody targeting the receptor programmed cell death protein-1 (PD-1), with anti-tumour activity demonstrated for many malignancies.
M. Dickey+6 more
semanticscholar +1 more source
The role of N-acetylcysteine in the treatment of thrombotic thrombocytopenic purpura
Journal of Thrombosis and Thrombolysis, 2016A. Rottenstreich+3 more
semanticscholar +1 more source
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
Nature, 2001G. Levy+18 more
semanticscholar +1 more source