Occurence of thrombotic thrombocytopenic purpura in a systemic lupus erythematosus patient with antiphospholipid antibodies in association with a decreased activity of von Willebrand factor-cleaving protease
Author:
Affiliation:
1. Department of Medicine, Teikyo University School of Medicine, Tokyo, Japan
2. Department of Blood Transfusion, Nara Medical University, Nara, Japan
Publisher
SAGE Publications
Subject
Rheumatology
Link
http://journals.sagepub.com/doi/pdf/10.1191/0961203302lu230xx
Reference5 articles.
1. Acquired Deficiency of von Willebrand Factor-Cleaving Protease in a Patient With Thrombotic Thrombocytopenic Purpura
2. Antibodies to von Willebrand Factor–Cleaving Protease in Acute Thrombotic Thrombocytopenic Purpura
3. Catastrophic Antiphospholipid Syndrome: Clinical and Laboratory Features of 50 Patients
4. Upshaw-Schulman Syndrome Revisited: A Concept of Congenital Thrombotic Thrombocytopenic Purpura
5. Multiple thromboses in major arteries in a patient with antiphospholipid syndrome associated with excess of a large multimer of von Willebrand factor
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1. Catastrophic antiphospholipid syndrome: current aspects of pathogenesis, diagnosis and treatment;Modern Rheumatology Journal;2023-07-10
2. Changes in Plasma Levels of ADAMTS13 and von Willebrand Factor in Patients Undergoing Elective Joint Arthroplasty;Journal of Clinical Medicine;2022-10-30
3. Diagnosis and management of catastrophic antiphospholipid syndrome;Expert Review of Hematology;2017-03-13
4. Beta2-glycoprotein I Expression in Lupus Nephritis Patients with Antiphospholipid-associated Nephropathy;The Journal of Rheumatology;2016-09-15
5. Antiphospholipid Antibody-Mediated Thrombotic Mechanisms in Antiphospholipid Syndrome: Towards Pathophysiology-Based Treatment;Current Pharmaceutical Design;2016-09-01
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