Search Results - "Knoebl, Paul"
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Redefining outcomes in immune TTP: an international working group consensus report
Published in Blood (08-04-2021)“…Immune-mediated thrombotic thrombocytopenic purpura (iTTP) is a potentially fatal thrombotic microangiopathy caused by autoantibody-mediated severe deficiency…”
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Emicizumab for the treatment of acquired hemophilia A
Published in Blood (21-01-2021)“…Acquired hemophilia A (AHA) is a severe bleeding disorder caused by inhibiting autoantibodies to coagulation factor VIII (FVIII). For hemostatic treatment,…”
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International recommendations on the diagnosis and treatment of acquired hemophilia A
Published in Haematologica (Roma) (01-07-2020)“…Acquired hemophilia A (AHA), a rare bleeding disorder caused by neutralizing autoantibodies against coagulation factor VIII (FVIII), occurs in both men and…”
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Acquired hemophilia A: Updated review of evidence and treatment guidance
Published in American journal of hematology (01-07-2017)“…Acquired hemophilia A (AHA) is a rare disease resulting from autoantibodies (inhibitors) against endogenous factor VIII (FVIII) that leads to bleeding, which…”
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Long-term follow-up after successful treatment of vaccine-induced prothrombotic immune thrombocytopenia
Published in Thrombosis research (01-11-2021)“…Cases of ChAdOx1 nCoV-19 (AstraZeneca) vaccinated patients with thrombocytopenia, elevated D-dimer, and elevated platelet factor 4 (PF4) antibody levels with-…”
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Caplacizumab prevents refractoriness and mortality in acquired thrombotic thrombocytopenic purpura: integrated analysis
Published in Blood advances (27-04-2021)“…The efficacy and safety of caplacizumab in individuals with acquired thrombotic thrombocytopenic purpura (aTTP) have been established in the phase 2 TITAN and…”
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The path of uncovering a prothrombotic thrombocytopenic syndrome after viral vector‐based COVID‐19 vaccination: Where there is much light, the shadow is deep
Published in Research and practice in thrombosis and haemostasis (01-10-2021)“…During the following weeks and months, further clinical and experimental data were published at an impressive pace, setting the ground for evidence-based…”
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Concizumab prophylaxis in persons with hemophilia A or B with inhibitors: patient-reported outcome results from the phase 3 explorer7 study
Published in Research and practice in thrombosis and haemostasis (01-05-2024)“…Patient-reported outcomes (PROs) reflect patient perceptions of disease and treatment and are important for evaluating new therapies. Evaluate the effects of…”
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INTEGRATED EFFICACY RESULTS FROM THE PHASE 2 AND PHASE 3 STUDIES WITH CAPLACIZUMAB IN PATIENTS WITH ACQUIRED THROMBOTIC THROMBOCYTOPENIC PURPURA
Published in Hematology, Transfusion and Cell Therapy (01-11-2021)“…Objective: An integrated analysis based on the Phase 2 TITAN (NCT01151423) and Phase 3 HERCULES (NCT02553317) studies with caplacizumab (CPLZ) in acquired…”
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Is there an association between hemostatic abnormalities and the outcome of acute lung injury?
Published in Critical care medicine (01-08-2007)Get full text
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Severe congenital protein C deficiency : the use of protein C concentrates (human) as replacement therapy for life-threatening blood-clotting complications
Published in Biologics (01-06-2008)“…Summarizes the current knowledge on protein C replacement therapy in congenital protein C deficiency. Source: National Library of New Zealand Te Puna…”
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Prevention and Management of Bleeding Episodes in Patients with Acquired Hemophilia A
Published in Drugs (New York, N.Y.) (01-12-2018)“…Acquired hemophilia A (AHA) is a rare autoimmune disease caused by autoantibodies inhibiting the function of coagulation factor VIII. It is characterized by…”
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Should emicizumab be used in patients with acquired hemophilia A?
Published in Journal of thrombosis and haemostasis (01-03-2021)“…Emicizumab is currently approved to prevent bleeding in patients with congenital hemophilia A with or without neutralizing antibodies (inhibitors) against…”
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Inherited and acquired thrombotic thrombocytopenic purpura (TTP) in adults
Published in Seminars in thrombosis and hemostasis (01-06-2014)“…Thrombotic thrombocytopenic purpura (TTP) is a clearly defined entity of thrombotic microangiopathies (TMAs), a heterogeneous group of disorders characterized…”
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Thrombotic thrombocytopenic purpura
Published in Memo - Magazine of European medical oncology (2018)“…Summary Thrombotic thrombocytopenic purpura (TTP) is a clearly defined entity of the thrombotic microangiopathies (TMA), a heterogeneous group of disorders…”
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Management of acquired haemophilia A in severe Covid‐19: Haemostatic bridging with emicizumab to keep the balance between bleeding and thrombosis
Published in British journal of clinical pharmacology (01-02-2023)“…Acquired haemophilia A (AHA) is an autoimmune bleeding disorder caused by autoantibodies blocking coagulation factor VIII (FVIII). Haemostatic management of…”
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Acquired haemophilia: an overview for clinical practice
Published in European journal of haematology (01-12-2015)“…Acquired haemophilia is a potentially life‐threatening bleeding disorder caused by the development of autoantibodies against coagulation factors, most commonly…”
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Bleeding and response to hemostatic therapy in acquired hemophilia A: results from the GTH-AH 01/2010 study
Published in Blood (16-07-2020)“…Acquired hemophilia A (AHA) is due to autoantibodies against coagulation factor VIII (FVIII) and most often presents with unexpected bleeding. In contrast to…”
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