Search Results - "Gill, Joan C"
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Efficacy and safety of rVIII-SingleChain: results of a phase 1/3 multicenter clinical trial in severe hemophilia A
Published in Blood (04-08-2016)“…Recombinant VIII (rVIII)-SingleChain is a novel B-domain–truncated recombinant factor VIII (rFVIII), comprised of covalently bonded factor VIII (FVIII) heavy…”
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Full-length sucrose-formulated recombinant factor VIII for treatment of previously untreated or minimally treated young children with severe haemophilia A: results of an international clinical investigation
Published in Thrombosis and haemostasis (01-03-2005)“…The safety and efficacy of a full-length sucrose-formulated recombinant factor VIII product (rFVIII-FS; Kogenate FS; Kogenate Bayer) was evaluated in…”
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Hemostatic efficacy, safety, and pharmacokinetics of a recombinant von Willebrand factor in severe von Willebrand disease
Published in Blood (22-10-2015)“…This phase 3 trial evaluated the safety and hemostatic efficacy of a recombinant von Willebrand factor (rVWF) for treatment of bleeds in severe von Willebrand…”
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Hepatitis C Virus Induces Regulatory T Cells by Naturally Occurring Viral Variants to Suppress T Cell Responses
Published in Clinical & developmental immunology (01-01-2011)“…Regulatory T cell markers are increased in chronically infected individuals with the hepatitis C virus (HCV), but to date, the induction and maintenance of…”
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Measurement of plasma and platelet tissue factor pathway inhibitor, factor V and Protein S in people with haemophilia
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-11-2019)“…Introduction Tissue factor pathway inhibitor (TFPI) is a naturally occurring anticoagulant found in plasma, where it circulates bound to lipoproteins, factor V…”
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The pharmacokinetic diversity of two von Willebrand factor (VWF)/ factor VIII (FVIII) concentrates in subjects with congenital von Willebrand disease. Results from a prospective, randomised crossover study
Published in Thrombosis and haemostasis (01-08-2011)“…The pharmacokinetic (PK) profiles of von Willebrand factor (VWF) /factor VIII (FVIII) concentrates are important for treatment efficacy and safety of von…”
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Rituximab for treatment of inhibitors in haemophilia A. A Phase II study
Published in Thrombosis and haemostasis (02-09-2014)“…The development of antibodies against infused factor VIII (FVIII) in patients with haemophilia A is a serious complication leading to poorly controlled…”
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Eptifibatide-induced thrombocytopenia and thrombosis in humans require FcγRIIa and the integrin β3 cytoplasmic domain
Published in The Journal of clinical investigation (01-03-2009)“…Thrombocytopenia and thrombosis following treatment with the integrin αIIbβ3 antagonist eptifibatide are rare complications caused by patient antibodies…”
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The effect of secondary prophylaxis versus episodic treatment on the range of motion of target joints in patients with haemophilia
Published in British journal of haematology (01-05-2013)“…Summary This study prospectively compared the effect of secondary prophylaxis to episodic treatment on target joint (TJ) range of motion (ROM), number of joint…”
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Naturally occurring CD4+ T-cell epitope variants act as altered peptide ligands leading to impaired helper T-cell responses in hepatitis C virus infection
Published in Human immunology (01-05-2011)“…Abstract Hepatitis C virus (HCV) has a high rate of replication and lacks RNA-proofreading capabilities, thereby leading to variant or mutant viruses…”
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Bleeding disorders: A common cause of menorrhagia in adolescents
Published in The Journal of pediatrics (01-06-2001)“…Objective: To determine the frequency of underlying bleeding disorders in adolescents with menorrhagia. Study design: We retrospectively reviewed the charts of…”
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Thromboelastography in the Assessment of Bleeding Following Surgery for Congenital Heart Disease
Published in World journal for pediatric & congenital heart surgery (01-10-2012)“…Background: Perioperative bleeding is common in pediatric cardiac surgery patients. Traditional laboratory tests do not adequately characterize coagulation…”
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Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitors
Published in Thrombosis and haemostasis (01-12-1998)“…To assess the safety and efficacy of a fixed dose of recombinant activated factor VII (rFVIIa; NovoSeven) in the home setting for mild to moderately severe…”
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Prediction of Warfarin Dose in Pediatric Patients: An Evaluation of the Predictive Performance of Several Models
Published in The journal of pediatric pharmacology and therapeutics (01-05-2016)“…The objective of this study was to evaluate the performance of pediatric pharmacogenetic-based dose prediction models by using an independent cohort of…”
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Identification of FcγRIIa as the ITAM-bearing receptor mediating αIIbβ3 outside-in integrin signaling in human platelets
Published in Blood (01-10-2008)“…Immunoreceptor tyrosine-based activation motif (ITAM)–containing proteins have recently been demonstrated in macrophages and neutrophils to be required for…”
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Interferon-gamma secretion defects in haemophilia A patients receiving highly purified plasma-derived or recombinant factor VIII
Published in British journal of haematology (01-12-1996)“…The outcome of developing immune responses is influenced by interactions among a large and complex network of secreted cytokines. T-cell secretion of…”
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Epitopes of the NS3 protein of hepatitis C virus: Recognition in HLA-DR4 transgenic mice
Published in Immunology and cell biology (01-02-2002)“…Hepatitis C virus (HCV) infects more than 180 million of the world's population and causes a persistent infection that over decades can result in cirrhosis and…”
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A study of prospective surveillance for inhibitors among persons with haemophilia in the United States
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-03-2014)“…Summary Inhibitors are a rare but serious complication of treatment of patients with haemophilia. Phase III clinical trials enrol too few patients to…”
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T-lymphocyte subpopulations in patients with classic hemophilia treated with cryoprecipitate and lyophilized concentrates
Published in The New England journal of medicine (13-01-1983)Get more information
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