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Information about topics related to the pathophysiology, pharmacology, and clinical aspects of bleeding, coagulation, and hemostasis, including information about recombinant coagulation Factor VIIa.
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Date Added: Jan 1, 2006 Hits: 0 Rating: 0.00 Votes: 0
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Introduction and methods, manufacture of therapeutic coagulation factor concentrates, safety data on which recommendations are based, licensing status, therapeutic guidelines, clinical audit and a review of the guidelines.
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Date Added: Jan 1, 2006 Hits: 0 Rating: 0.00 Votes: 0
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Also known as Hageman factor, this is a congenital coagulation disorder that causes prolonged coagulation in a test tube but does not cause abnormal bleeding. Includes brief information.
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Date Added: Jan 1, 2006 Hits: 0 Rating: 0.00 Votes: 0
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Brief information about this inherited bleeding disorder including causes, symptoms, and prognosis.
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Date Added: Jan 1, 2006 Hits: 0 Rating: 0.00 Votes: 0
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Provides brief information about this inherited bleeding disorder, which is similar to hemophilia. Includes causes, symptoms, and prognosis.
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Date Added: Jan 1, 2006 Hits: 0 Rating: 0.00 Votes: 0
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Information about this inherited disorder that causes abnormal bleeding including causes, treatment, and prognosis.
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Date Added: Jan 1, 2006 Hits: 0 Rating: 0.00 Votes: 0
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Brief information about these hypercoagulability disorders including causes, treatment, and prognosis.
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Date Added: Jan 1, 2006 Hits: 1 Rating: 0.00 Votes: 0
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Information about these rare medical conditions, anticoagulant therapy, research and online forum.
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Date Added: Jan 1, 2006 Hits: 0 Rating: 0.00 Votes: 0
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David Ginsburg, M.D: An article covering von Willebrand Factor, coagulation factor V, plasminogen activator inhibitor-1, primary pulmonary hypertension and bone marrow transplantation.
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Date Added: Jan 1, 2007 Hits: 0 Rating: 0.00 Votes: 0
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Features diagrams and information about the various thrombophilic genetic markers, general information about clotting, glossary, and list of research sources.
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Date Added: Jan 1, 2007 Hits: 0 Rating: 0.00 Votes: 0
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