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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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Von Willebrand Disease: Basic and Clinical Aspects provides an insight into all aspects of the condition. Since its discovery, von;
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von Willebrand disease (VWD) is an inherited bleeding disorder that is caused by deficiency or dysfunction of von Willebrand factor (VWF;
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HUS; von Willebrand Disease; Female bleeding; Functional platelet disorders; Hemolytic anemia; Advocacy in hematology; ITP; and Acquired;
Vergelijkbare producten zoals Benign Hematologic Disorders in Children, An Issue of Pediatric Clinics of North America
to provide both the patient's and doctor's views, 100 Questions & Answers About Von Willebrand Disease provides a much needed primer for;
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Secondary Immune cytopenias, Disorders of Iron overload, Disorders of Iron metabolism, Approach to Hemophilia in a Changing Treatment Landscape, Von;
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-twentieth century. In the first book to chronicle the emergence and transformation of the hemophilia community, Susan Resnik sets her story within;
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to delivery. Hematologic disorders covered include anemia, myeloproliferative disorders, von Willebrand disease, leukemia and lymphoma;
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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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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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von Willebrand disease, rare bleeding disorders and inherited platelet disorders. This important resource: Offers an updated guide for;
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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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of inhibitors in hemophiliacs, hemophilic arthropathy and synovitis, relevant hemophilia treatment 2006, and pediatric hemostasiology. The volume;
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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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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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/Thalessemia; Muscle dystrophy; Spinal muscular atrophy; Wilson Disease; Hemophilia; National and International Accreditation; Blood Banking;
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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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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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aspects that most clinicians see on a regular basis-sickle cell disease, thalassemia, and hemophilia, and ITP.;
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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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attention simply due to the fewer number of those affected. Literature and online resources about these conditions are not only limited but;
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covered include hemophilia, primary immune deficiency and the use of orphan drugs in oncology and there is an examination of Comparative;
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Some 23. 5% of all members and patients of treatment centers completed the questionnaire. One striking fact is that participation;
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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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This issue of Oral and Maxillofacial Surgery Clinics of North America focuses on Coagulopathy, and is edited by Drs. Jeffrey Bennett and;
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and vertebrate immune complexes. It also discusses a number of other proteins, such as the hemerythrins; serum albumin; serum amyloid A; von;
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