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EXPERT REVIEW OF HEMATOLOGY, ISSN 1747-4086, 06/2019, Volume 12, Issue 6, pp. 383 - 395
Journal Article
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 02/2017, Volume 15, Issue 2, pp. 312 - 322
Essentials An international collaboration provides a consensus for clinical definitions. This concerns thrombotic microangiopathies and thrombotic... 
diagnosis, differential | thrombotic thrombocytopenic purpura | thrombotic microangiopathy | thrombocytopenia | ADAMTS‐13 protein, human | ADAMTS-13 protein, human | MANAGEMENT | ANTI-ADAMTS13 ANTIBODIES | HEMOLYTIC-UREMIC-SYNDROME | IGG ANTIBODIES | FACTOR-CLEAVING PROTEASE | PLASMA-EXCHANGE | ACUTE EPISODES | ADAMTS13 ACTIVITY | RITUXIMAB | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | UPSHAW-SCHULMAN SYNDROME | Recurrence | Humans | ADAMTS13 Protein - blood | Fibrin - chemistry | Societies, Medical | Adult | Female | Hemolytic-Uremic Syndrome - diagnosis | Child | von Willebrand Factor - metabolism | Hemolysis | Diagnosis, Differential | Hematology - standards | Terminology as Topic | Treatment Outcome | Inflammation | Purpura, Thrombotic Thrombocytopenic - diagnosis | Remission Induction | Consensus | Complement System Proteins | Platelet Aggregation | Pregnancy | Platelet Count | Blood Platelets - metabolism | Erythrocytes - metabolism | Thrombotic Microangiopathies - diagnosis | Thrombocytopenic purpura | Enzymes | Terms and phrases | Anemia | Liver | Von Willebrand factor | Working groups | Standardization | Thrombocytopenia | Thrombotic microangiopathy | Clinical trials | Disseminated intravascular coagulation | Transplantation | Thrombotic thrombocytopenic purpura | Hemolytic anemia | Purpura | Eclampsia | Remission | Platelets | Autoimmune diseases
Journal Article
American Journal of Hematology, ISSN 0361-8609, 11/2017, Volume 92, Issue 11, pp. E644 - E646
Journal Article
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 10/2017, Volume 15, Issue 10, pp. 1889 - 1900
Summary Thrombotic thrombocytopenic purpura (TTP), a potentially fatal clinical syndrome, is primarily caused by autoantibodies against the von Willebrand... 
diagnosis | therapeutics | pathology | thrombotic microangiopathies | von Willebrand factor | HEMOLYTIC-UREMIC-SYNDROME | VON-WILLEBRAND-FACTOR | FACTOR-CLEAVING PROTEASE | MEDIATED GENE-THERAPY | PLASMA-EXCHANGE THERAPY | ADAMTS13 ACTIVITY | DISSEMINATED INTRAVASCULAR COAGULATION | ADVERSE-REACTIONS SONAR | RENAL-FAILURE | PERIPHERAL VASCULAR DISEASE | MALIGNANT HYPERTENSION | HEMATOLOGY | Recombinant Proteins - therapeutic use | Genetic Therapy | Predictive Value of Tests | Autoantibodies - blood | Humans | Plasma Exchange | ADAMTS13 Protein - blood | ADAMTS13 Protein - immunology | Hemostasis | Immunotherapy | Thrombocytopenia - therapy | Diagnosis, Differential | ADAMTS13 Protein - therapeutic use | Risk Factors | Treatment Outcome | Purpura, Thrombotic Thrombocytopenic - diagnosis | Purpura, Thrombotic Thrombocytopenic - epidemiology | Thrombocytopenia - blood | ADAMTS13 Protein - genetics | Anemia, Hemolytic - therapy | Anemia, Hemolytic - diagnosis | Thrombocytopenia - diagnosis | Purpura, Thrombotic Thrombocytopenic - therapy | Anemia, Hemolytic - blood | Purpura, Thrombotic Thrombocytopenic - blood | Autoimmunity | Autoantibodies | Anemia | Development and progression | Homeopathy | Materia medica and therapeutics | Thrombocytopenic purpura | Haptoglobin | Therapeutics | Von Willebrand factor | Hemoglobin | Diagnosis | Health aspects | Corticoids | Plasma | Cyclosporins | Pathogenesis | Prophylaxis | Antagonists | Splenectomy | Hemolytic anemia | Remission | Metalloproteinase | Thrombocytopenia | Thrombotic microangiopathy | Hemolytic uremic syndrome | Immunomodulation | Rituximab | Morbidity | L-Lactate dehydrogenase | Cyclophosphamide | Purpura | Lactic acid | Gene therapy | Platelets | Pathology | Thrombotic Microangiopathies | von Willebrand Factor
Journal Article