Search Results - "Rajpurkar, M."
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Lupus anticoagulant acquired hypoprothrombinemia syndrome in childhood: two distinct patterns and review of the literature
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-11-2015)“…Introduction Lupus anticoagulant associated with acquired prothrombin deficiency also known as ‘lupus anticoagulant hypoprothrombinemia syndrome’ (LAHS) is an…”
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Inhibitors in factor IX deficiency a report of the ISTH-SSC international FIX inhibitor registry (1997-2006)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2009)“…Haemophilia B is an X‐linked disorder resulting in coagulation factor IX deficiency. Patients with severe deficiency (<1% factor IX activity) may have…”
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Use of recombinant activated factor VII in patients with Glanzmann's thrombasthenia: a review of the literature
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-07-2014)“…Summary Glanzmann's thrombasthenia (GT) is a rare bleeding disorder characterized by a quantitative or qualitative defect of glycoprotein IIb/IIIa on the…”
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Transition of care for pediatric and adult patients with venous thromboembolism: A National Quality Improvement Project from the American Thrombosis and Hemostasis Network (ATHN)
Published in Thrombosis research (01-04-2021)“…Transition of care (TOC) for management of anticoagulation from inpatient to outpatient setting for patients with acute venous thromboembolism (VTE) poses…”
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Results of a multinational survey of diagnostic and management practices of thromboembolic pulmonary embolism in children
Published in Thrombosis research (01-11-2019)“…The incidence of thromboembolic (TE)-pediatric pulmonary embolism (PPE) is increasing. We sought to evaluate current practice patterns and gaps in the…”
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Recommendations for future research in relation to pediatric pulmonary embolism: communication from the SSC of the ISTH
Published in Journal of thrombosis and haemostasis (01-02-2018)Get full text
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Laboratory variability in the diagnosis of type 2 VWD variants
Published in Journal of thrombosis and haemostasis (01-01-2021)“…Essentials Patients with von Willebrand disease were enrolled in our study. Type 2 VWD diagnoses were based on original test results. Repeat evaluation…”
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Thromboelastography identifies children with rare bleeding disorders and predicts bleeding phenotype
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2015)“…Summary Rare bleeding disorders (RBDs) comprise 3–5% of all congenital bleeding disorders. They can evade typical coagulation screening tests and there is a…”
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Recommendations for the assessment of non‐extremity venous thromboembolism outcomes: communication from the SSC of the ISTH
Published in Journal of thrombosis and haemostasis (01-03-2015)Get full text
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Immune tolerance induction in 31 children with haemophilia A: is ITI less successful in African Americans?
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-05-2011)“…Inhibitor development continues to be a major problem in the treatment of haemophilia. Immune tolerance induction (ITI) continues to be the most effective…”
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Therapeutic and prophylactic ethanol lock therapy in patients with bleeding disorders
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2014)“…Summary Obtaining a reliable venous access is a limiting factor for early initiation of clotting factor prophylaxis and immune tolerance induction. To…”
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Need for a new paediatric post thrombotic sequelae outcome measure for non-extremity thrombosis
Published in Thrombosis and haemostasis (01-06-2011)Get more information
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Ethanol lock therapy for the treatment of catheter-related infections in haemophilia patients
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-11-2009)“…Central venous access devices (CVAD) are increasingly being used for optimal delivery of clotting factor concentrates in patients with haemophilia with poor…”
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Crucial role for the VWF A1 domain in binding to type IV collagen
Published in Blood (02-04-2015)“…Von Willebrand factor (VWF) contains binding sites for platelets and for vascular collagens to facilitate clot formation at sites of injury. Although previous…”
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Molecular pathogenesis and heterogeneity in type 3 VWD families in U.S. Zimmerman program
Published in Journal of thrombosis and haemostasis (01-07-2022)“…Background Type 3 von Willebrand Disease (VWD) is a rare and severe form of VWD characterized by the absence of von Willebrand factor (VWF). Objectives As part…”
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Multicenter randomized controlled trial on Duration of Therapy for Thrombosis in Children and Young Adults (the Kids‐DOTT trial): pilot/feasibility phase findings
Published in Journal of thrombosis and haemostasis (01-09-2015)“…Summary Background Randomized controlled trials (RCTs) on pediatric venous thromboembolism (VTE) treatment have been challenged by unsubstantiated design…”
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PB0649 Results from the RESIST Study for Tolerance Induction in Patients with Poor Prognosis for ITI Success
Published in Research and practice in thrombosis and haemostasis (01-10-2023)Get full text
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Thrombotic events with recombinant activated factor VII (rFVIIa) in approved indications are rare and associated with older age, cardiovascular disease, and concomitant use of activated prothrombin complex concentrates (aPCC)
Published in Journal of blood medicine (01-01-2019)“…Recombinant activated factor VII (rFVIIa; NovoSeven RT; Novo Nordisk A/S, Bagsvaerd, Denmark) is approved in the United States for the treatment of bleeding…”
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