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The New England Journal of Medicine, ISSN 0028-4793, 04/2019, Volume 380, Issue 16, p. e23
Journal Article
Blood, ISSN 0006-4971, 01/2013, Volume 121, Issue 1, pp. 38 - 47
A mild thrombocytopenia is relatively frequent during pregnancy and has generally no consequences for either the mother or the fetus. Although representing no... 
POSTPARTUM PLASMA-EXCHANGE | PLATELET COUNTS | VON-WILLEBRAND-DISEASE | IMMUNE THROMBOCYTOPENIA | OBSTETRIC PATIENTS | PURPURA | ACUTE FATTY LIVER | HELLP HEMOLYSIS | ELEVATED LIVER-ENZYMES | HEMATOLOGY | FACTOR-CLEAVING PROTEASE | HELLP Syndrome - drug therapy | Recurrence | Humans | Immunosuppressive Agents - therapeutic use | Hemolytic-Uremic Syndrome - blood | Plasma Exchange | Pregnancy Complications, Hematologic - drug therapy | Contraindications | Purpura, Thrombocytopenic, Idiopathic - blood | Purpura, Thrombocytopenic, Idiopathic - drug therapy | Young Adult | Purpura, Thrombocytopenic, Idiopathic - therapy | HELLP Syndrome - diagnosis | Thrombocytopenia - drug therapy | Purpura, Thrombotic Thrombocytopenic - drug therapy | Adult | Female | Hemolytic-Uremic Syndrome - therapy | Hemolytic-Uremic Syndrome - diagnosis | Infant, Newborn | Diagnosis, Differential | Antibodies, Monoclonal, Murine-Derived | Thrombocytopenia - etiology | HELLP Syndrome - blood | Purpura, Thrombotic Thrombocytopenic - congenital | Thrombocytopenia - congenital | Rituximab | Anticoagulants - therapeutic use | Combined Modality Therapy | Purpura, Thrombotic Thrombocytopenic - diagnosis | Anticoagulants - adverse effects | Purpura, Thrombotic Thrombocytopenic - prevention & control | Danazol | Algorithms | Purpura, Thrombocytopenic, Idiopathic - diagnosis | Pre-Eclampsia - blood | Immunosuppressive Agents - adverse effects | Thrombocytopenia - diagnosis | Disease Management | Pregnancy - blood | Purpura, Thrombotic Thrombocytopenic - blood | Fetal Monitoring
Journal Article
Lancet, The, ISSN 0140-6736, 02/2008, Volume 371, Issue 9610, pp. 395 - 403
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
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Journal Article