
Dr Han Mou Tsai
Current affiliation: Han Mou Tsai
Subject: Medicine And Medical Sciences
Primary location: United States
Ultralarge von Willebrand factor multimers and normal ADAMTS13 activity in the umbilical cord blood
Published in:Thrombosis Research
Publication date:2002-11-01
Subunit composition of plasma von Willebrand factor multimers: Evidence for a non-proteolytic mechanism resulting in apparent increase in proteolyt...
Published in:Thrombosis Research
Publication date:1991-07-01
Multifunctional Composite Nanoparticles: Magnetic, Luminescent, and Mesoporous
Published in:Chemistry of Materials
Publication date:2006-10-01
Malignant hypertension due to defective complement regulation
Published in:Journal of Clinical Hypertension
Publication date:2015-09-11What's it about?This report describes the case of a patient who presented with severe, wildly unstable hypertension, often accompanied with the symptoms of headach...
Acquired Thrombotic Thrombocytopenic Purpura
Published in:ADAMTS13
Publication date:2015-01-01
Thrombotic Thrombocytopenic Purpura and the Hemolytic-Uremic Syndrome
Published in:Platelets
Publication date:2013-01-01
ADAMTS-13
Published in:Proteases in Biology and Disease
Publication date:Not available
von Willebrand Factor, Shear Stress, and ADAMTS13 in Hemostasis and Thrombosis
Published in:ASAIO Journal
Publication date:2012-02-01
Pathophysiology of thrombotic thrombocytopenic purpura
Published in:International Journal of Hematology
Publication date:2010-01-01
Autoimmune Thrombotic Microangiopathy: Advances in Pathogenesis, Diagnosis, and Management
Published in:Seminars in Thrombosis and Hemostasis
Publication date:2012-04-03
Current Concepts in Thrombotic Thrombocytopenic Purpura
Published in:Annual Review of Medicine
Publication date:2006-02-01
Molecular Mechanisms in Thrombotic Thrombocytopenic Purpura
Published in:Seminars in Thrombosis and Hemostasis
Publication date:2004-10-01
Mechanisms of microvascular thrombosis in thrombotic thrombocytopenic purpura
Published in:Kidney International
Publication date:2009-02-01
Deficiency of ADAMTS13 in thrombotic thrombocytopenic purpura
Published in:International Journal of Hematology
Publication date:2002-03-01
Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura
Published in:Journal of Molecular Medicine
Publication date:2002-10-01
Thrombotic Thrombocytopenic Purpura in a Newborn
Published in:Journal of Perinatology
Publication date:2003-01-01
ADAMTS13 and microvascular thrombosis
Published in:Expert Review of Cardiovascular Therapy
Publication date:2006-11-01
Deficiency of ADAMTS13 and thrombotic thrombocytopenic purpura
Published in:Transfusion
Publication date:2002-11-01
Why Do We Need ADAMTS13?
Published in:Japanese Journal of Thrombosis and Hemostasis
Publication date:2005-01-01
Antibodies to von Willebrand Factor–Cleaving Protease in Acute Thrombotic Thrombocytopenic Purpura
Published in:New England Journal of Medicine
Publication date:1998-11-26
Transfusion of polymerised human haemoglobin in a patient with severe sickle-cell anaemia
Published in:The Lancet
Publication date:2002-08-01
Warm-Antibody Autoimmune Hemolytic Anemia Developing after Thrombotic Thrombocytopenic Purpura
Published in:Acta Haematologica
Publication date:2002-01-01
Presence of ADAMTS13 Activity in a Patient with Metastatic Cancer and Thrombotic Microangiopathy
Published in:Acta Haematologica
Publication date:2003-01-01
ADAMTS13 is expressed in hepatic stellate cells
Published in:Laboratory Investigation
Publication date:2005-04-04
ADAMTS13-binding IgG are present in patients with thrombotic thrombocytopenic purpura
Published in:Thrombosis and Haemostasis
Publication date:2006-04-12
Antibody Inhibitors to von Willebrand Factor Metalloproteinase and Increased Binding of von Willebrand Factor to Platelets in Ticlopidine-Associate...
Published in:Annals of Internal Medicine
Publication date:2000-05-16
An enzyme immunoassay of ADAMTS13 distinguishes patients with thrombotic thrombocytopenic purpura from normal individuals and carriers of ADAMTS13 ...
Published in:Thrombosis and Haemostasis
Publication date:2004-02-27
Untying the Knot of Thrombotic Thrombocytopenic Purpura and Atypical Hemolytic Uremic Syndrome
Published in:The American Journal of Medicine
Publication date:2013-03-01
Thrombotic Thrombocytopenic Purpura and the Atypical Hemolytic Uremic Syndrome
Published in:Hematology/Oncology Clinics of North America
Publication date:2013-06-01
Rituximab induces remission of cerebral ischemia caused by thrombotic thrombocytopenic purpura
Published in:European Journal Of Haematology
Publication date:2003-03-01
Thrombotic Thrombocytopenic Purpura: A Thrombotic Disorder Caused by ADAMTS13 Deficiency
Published in:Hematology/Oncology Clinics of North America
Publication date:2007-08-01
A comparison of von Willebrand Factor antigen with platelet activity in vitro in normal and venous occlusion blood
Published in:Platelets
Publication date:2001-01-01
Excessive activation of the complement system in atypical hemolytic uremic syndrome: is it ready for prime time?
Published in:Kidney International
Publication date:2010-02-01
Use of eculizumab in the treatment of a case of refractory, ADAMTS13-deficient thrombotic thrombocytopenic purpura: additional data and clinical fo...
Published in:British Journal of Haematology
Publication date:2013-05-21
High titers of inhibitors of von Willebrand factor-cleaving metalloproteinase in a fatal case of acute thrombotic thrombocytopenic purpura
Published in:American Journal of Hematology
Publication date:2000-01-01
Eculizumab Therapy Leads to Rapid Resolution of Thrombocytopenia in Atypical Hemolytic Uremic Syndrome
Published in:Advances in Hematology
Publication date:2014-01-01
A Mechanistic Approach to the Diagnosis and Management of Atypical Hemolytic Uremic Syndrome
Published in:Transfusion Medicine Reviews
Publication date:2014-10-01
Surface dependent structures of von Willebrand factor observed by AFM under aqueous conditions
Published in:Colloids and Surfaces B Biointerfaces
Publication date:2000-12-01
Endothelial cell-derived high molecular weight von Willebrand factor is converted into the plasma multimer pattern by granulocyte proteases
Published in:Biochemical and Biophysical Research Communications
Publication date:1989-02-01
Thrombotic Thrombocytopenic Purpura Associated with Clopidogrel
Published in:New England Journal of Medicine
Publication date:2000-06-15
Repair of Nanodefects in a Two-Dimensional Crystal Anticoagulant Shield in the Antiphospholipid Syndrome
Published in:NanoCellBiology
Publication date:2014-04-10Novel Molecular Strategies Assessed by Atomic Force Microscopy
Thrombocytopenia and Severe Hyperbilirubinemia in the Neonatal Period Secondary to Congenital Thrombotic Thrombocytopenic Purpura and ADAMTS13 Defi...
Published in:Journal of Pediatric Hematology/Oncology
Publication date:2004-08-01
Von Willebrand factor-cleaving protease activity and proteolysis of von Willebrand factor in bone marrow transplant-associated thrombotic microangi...
Published in:The Hematology Journal
Publication date:2001-01-01
Von Willebrand Factor and Von Willebrand Factor-Cleaving Metalloprotease Activity in Escherichia coli O157:H7-Associated Hemolytic Uremic Syndrome
Published in:Pediatric Research
Publication date:2001-05-01
Inhibitors of ADAMTS13: a potential factor in the cause of thrombotic microangiopathy in a renal allograft recipient
Published in:Transplantation Journal
Publication date:2002-10-01
ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpura
Published in:European Journal of Pediatrics
Publication date:2006-12-24
The high molecular weight form of endothelial cell von Willebrand factor is released by the regulated pathway
Published in:British Journal of Haematology
Publication date:1991-10-01
Role of A and B blood group antigens in the expression of adhesive activity of von Willebrand factor
Published in:British Journal of Haematology
Publication date:2000-06-01
Rituximab for chronic recurring thrombotic thrombocytopenic purpura: a case report and review of the literature
Published in:British Journal of Haematology
Publication date:2004-03-01
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
Published in:Nature
Publication date:2001-10-04