Search Results - "Gill, Joan C"

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    Hemostatic efficacy, safety, and pharmacokinetics of a recombinant von Willebrand factor in severe von Willebrand disease by Gill, Joan C., Castaman, Giancarlo, Windyga, Jerzy, Kouides, Peter, Ragni, Margaret, Leebeek, FrankW.G., Obermann-Slupetzky, Ortrun, Chapman, Miranda, Fritsch, Sandor, Pavlova, Borislava G., Presch, Isabella, Ewenstein, Bruce

    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 by Cusick, Matthew F., Schiller, Jennifer J., Gill, Joan C., Eckels, David D.

    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 by Ellery, Paul E. R., Hilden, Ida, Thyregod, Peter, Martinez, Nicholas D., Maroney, Susan A., Gill, Joan C., Mast, Alan E.

    “…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 by Kessler, Craig M, Friedman, Ken, Schwartz, Bruce A, Gill, Joan C, Powell, Jerry S

    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 by Leissinger, C, Josephson, C D, Granger, S, Konkle, B A, Kruse-Jarres, R, Ragni, M V, Journeycake, J M, Valentino, L, Key, N S, Gill, J C, McCrae, K R, Neufeld, E J, Manno, C, Raffini, L, Saxena, K, Torres, M, Marder, V, Bennett, C M, Assmann, S F

    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 by Gao, Cunji, Boylan, Brian, Bougie, Dan, Gill, Joan C, Birenbaum, Jessica, Newman, Debra K, Aster, Richard H, Newman, Peter J

    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 by Gupta, Sweta, Siddiqi, Azfar‐E‐Alam, Soucie, J. Michael, Manco‐Johnson, Marilyn, Kulkarni, Roshni, Lane, Heidi, Ingram‐Rich, Robina, Gill, Joan C.

    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 by Cusick, Matthew F, Yang, Meiying, Gill, Joan C, Eckels, David D

    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 by Bevan, Jennifer A., Maloney, Kelly W., Hillery, Cheryl A., Gill, Joan C., Montgomery, Robert R., Scott, J.Paul

    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 by Niebler, Robert A., Gill, Joan C., Brabant, Christopher P., Mitchell, Michael E., Nugent, Melodee, Simpson, Pippa, Tweddell, James S., Ghanayem, Nancy S.

    “…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 by Key, N S, Aledort, L M, Beardsley, D, Cooper, H A, Davignon, G, Ewenstein, B M, Gilchrist, G S, Gill, J C, Glader, B, Hoots, W K, Kisker, C T, Lusher, J M, Rosenfield, C G, Shapiro, A D, Smith, H, Taft, E

    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 by Marek, Elizabeth, Momper, Jeremiah D, Hines, Ronald N, Takao, Cheryl M, Gill, Joan C, Pravica, Vera, Gaedigk, Andrea, Burckart, Gilbert J, Neville, Kathleen A

    “…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 by Boylan, Brian, Gao, Cunji, Rathore, Vipul, Gill, Joan C., Newman, Debra K., Newman, Peter J.

    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 by Newton-Nash, D K, Tollerud, D, Guevarra, L, Gill, J C

    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 by Eckels, David D, Bian, Tonghua, Gill, Joan C, S⊘nderstrup, Grete

    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 by Soucie, J. M., Miller, C. H., Kelly, F. M., Payne, A. B., Creary, M., Bockenstedt, P. L., Kempton, C. L., Manco-Johnson, M. J., Neff, A. T.

    “…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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