The Japanese experience with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome.
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Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpuraThe von Willebrand factor-cleaving protease (ADAMTS-13) and the diagnosis of thrombotic thrombocytopenic purpura (TTP)Shigatoxin triggers thrombotic thrombocytopenic purpura in genetically susceptible ADAMTS13-deficient mice.Von Willebrand factor-cleaving protease activity remains at the intermediate level in thrombotic thrombocytopenic purpura.Thrombotic thrombocytopenic purpura and its diagnosis.Thrombotic thrombocytopenic purpura: a thrombotic disorder caused by ADAMTS13 deficiencyA case report of thrombotic thrombocytopenic purpura and severe acute renal failure post non-myeloablative allogeneic peripheral blood stem cell transplantation treated with plasma exchange and hemodialysis.Thrombotic thrombocytopenic purpura and bone marrow necrosis as the initial presentation of lung cancer.The effectiveness of measuring for fragmented red cells using an automated hematology analyzer in patients with thrombotic microangiopathy.Mechanisms of microvascular thrombosis in thrombotic thrombocytopenic purpura.Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic microangiopathies: the French TMA reference center experienceElevated Von Willebrand factor propeptide for the diagnosis of thrombotic microangiopathy and for predicting a poor outcome.Clinical features of severe acquired ADAMTS13 deficiency in thrombotic thrombocytopenic purpura: the Korean TTP registry experience.Investigational drugs in thrombotic thrombocytopenic purpura.ADAMTS-13 activity and autoantibodies classes and subclasses as prognostic predictors in acquired thrombotic thrombocytopenic purpura.Children and adults with thrombotic thrombocytopenic purpura associated with severe, acquired Adamts13 deficiency: comparison of incidence, demographic and clinical features.CD(+)(4)CD(+)(25) Treg cells in thrombotic thrombocytopenic purpura associated with systemic lupus erythematosus patients.Impact of severe ADAMTS13 deficiency on clinical presentation and outcomes in patients with thrombotic microangiopathies: the experience of the Harvard TMA Research Collaborative.Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura.Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) 2017 in Japan.Thrombotic microangiopathy in haematopoietic cell transplantation: an update.Historical perspective and future directions in platelet research.Measurement of ADAMTS13.Thrombotic thrombocytopenic purpuraThrombotic thrombocytopenic purpura
P2860
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P2860
The Japanese experience with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome.
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
name
The Japanese experience with t ...... ura-hemolytic uremic syndrome.
@ast
The Japanese experience with t ...... ura-hemolytic uremic syndrome.
@en
type
label
The Japanese experience with t ...... ura-hemolytic uremic syndrome.
@ast
The Japanese experience with t ...... ura-hemolytic uremic syndrome.
@en
prefLabel
The Japanese experience with t ...... ura-hemolytic uremic syndrome.
@ast
The Japanese experience with t ...... ura-hemolytic uremic syndrome.
@en
P2093
P1476
The Japanese experience with t ...... ura-hemolytic uremic syndrome.
@en
P2093
Hideo Wada
Hideo Yagi
Hiromichi Ishizashi
Masanori Matsumoto
Yoshihiro Fujimura
P356
10.1053/J.SEMINHEMATOL.2003.10.009
P577
2004-01-01T00:00:00Z