Search Results - "Aljamali, Majed N."
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Successful treatment of canine hemophilia by continuous expression of canine FVIIa
Published in Blood (16-04-2009)“…Continuous expression of activated factor VII (FVIIa) via gene transfer is a potential therapeutic approach for hemophilia patients with or without inhibitory…”
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Long-term expression of murine activated factor VII is safe, but elevated levels cause premature mortality
Published in The Journal of clinical investigation (01-05-2008)“…Intravenous infusion of recombinant human activated Factor VII (FVIIa) has been used for over a decade in the successful management of bleeding episodes in…”
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66. Gene Transfer-Mediated Expression of Murine Factor VIIa Improves Clot Formation in a Mouse Model for Bernard-Soulier Syndrome
Published in Molecular therapy (01-05-2006)“…Moderate to severe bleeding occurs in Bernard-Soulier syndrome (BSS) patients due to a rare inherited dysfunction of their platelet GPIbα/β-IX-V receptor, a…”
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Lessons from Transgenic Mice Expressing Supra-Physiological Levels of Activated Murine Factor VII
Published in Blood (16-11-2005)“…A gene transfer approach using an engineered activated murine FVII (mVIIa) has previously shown efficacy in correcting the bleeding diathesis of hemophilia B…”
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Successful and Safe Treatment of Canine Hemophilia by Continuous Expression of Canine FVIIa: a Model for FVIII/FIX Gene-Based Bypassing Agents
Published in Blood (16-11-2008)“…Recombinant human activated Factor VII (rhFVIIa) is extensively used in the management of hemophilic inhibitor patients. However, the short plasma half-life…”
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Generation of Transgenic Mice Expressing High Levels of Activated Murine Coagulation Factor VII
Published in Blood (16-11-2004)“…Treatment of acute bleeding episodes in hemophilic patients with inhibitors can be successfully managed by the infusion of recombinant human factor VIIa…”
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606. Molecular Characterization of Hereditary Factor VII Deficiency in Beagles
Published in Molecular therapy (01-05-2005)“…Hereditary factor VII deficiency is the most common autosomal recessive inherited factor deficiency. Several mutations in the coding sequence of the human…”
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32. Efficacy and Safety of Mouse Coagulation Factor VIIa Gene Transfer in Hemophilia B Mice
Published in Molecular therapy (01-05-2004)“…One major complication of replacement therapy with clotting factors in patients with hemophilia A and B is the development of inhibitory antibodies that…”
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