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This volume, based on the second international symposium on hemophilia held in Rome, includes not only the presented material but also;
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of inhibitors in hemophiliacs, hemophilic arthropathy and synovitis, relevant hemophilia treatment 2006, and pediatric hemostasiology. The volume;
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, Alkhurma, and Omsk hemorrhagic fever viruses and other flaviviruses with hemorrhagic potential Virologists, clinicians, biomedical;
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, Alkhurma, and Omsk hemorrhagic fever viruses and other flaviviruses with hemorrhagic potential Virologists, clinicians, biomedical;
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Hemophilia is one of the most well-known rare diseases in the world. It is a genetic disease, where men have hemophilia and women are;
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providers, and many others. Gene insertion therapy now holds the promise of a cure for hemophilia in the near future. Scientific breakthroughs;
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Hemophilia is one of the most well-known rare diseases in the world. It is a genetic disease, where men have hemophilia and women are;
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An intensive historical study of the hereditary diseases hemophilia and porphyria in the personal and political lives of the European royal;
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of Hemophilia, 3rd edition * Features eight new chapters, covering individualised dosing, vCJD and haemophilia, new drugs in the pipeline, and surgery;
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Ebola virus and Marburg virus are related viruses that cause hemorrhagic fevers illnesses marked by severe bleeding, organ failure, and;
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Hemophilia and Von Willebrand Disease: Factor VIII and Von Willebrand Factor serves as a must-have reference on the important role;
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of persons with hemophilia brought unexpectedly fatal results in the 1980s when people with the disease contracted HIV-AIDS and Hepatitis C;
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Linked by Blood: Hemophilia and AIDS recounts the factors responsible for the widespread infection of people with hemophilia by Human;
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Viral hemorrhagic fevers (VHFs) represent a collection of illnesses caused by several distinct viral families. While some types;
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practice. Real-life cases are used to depict a wide range of clinical scenarios and to highlight significant aspects of management of hemorrhagic;
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].In the case of severe hemophilia B,about 10.5% of the patients develop inhibitory antibodies [9]. Anti-factor VIII-antibodies are also seen in 15;
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examination of joints and muscles, documentation of product batches, laboratory tests and good cooperation with other faculties. As many as 68. 9;
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might encounter in diagnosing, managing and treating hemophilia and hemostasis. It provides a practical and informative guide to the broad range;
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Oral Surgeon Needs to Know; ASA, Plavix, and Other Antiplatelet Medications: What the Oral Surgeon Needs to Know; Heparin and Lovenox: What the;
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include: Lymphangioleiomyomatosis, Pulmonary Lymphangiomatosis, Langerhans Cell Histiocytosis and other Histiocytic Diseases of the Lung;
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of substance use in veteran twins, hemorrhagic fever with renal syndrome, the psychological effects of military captivity, and dioxin in adipose tissue;
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of clean water, insect-borne diseases, and viral hemorrhagic fever.;
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) is impaired. Acquired hemophilia is a rare disorder characterized by spontaneous bleeding in a patient with no previous personal or family hemorrhagic;
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White matter injury can result from both ischemic and hemorrhagic stroke as well as a host of other CNS diseases and conditions such as;
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trauma and hemorrhagic shock. The nitric oxide pathway and nitric oxide synthesis regulation are also discussed.;
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