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Hemophilia and Von Willebrand Disease

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

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

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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Benign Hematologic Disorders in Children, An Issue of Pediatric Clinics of North America

HUS; von Willebrand Disease; Female bleeding; Functional platelet disorders; Hemolytic anemia; Advocacy in hematology; ITP; and Acquired;

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100 Questions & Answers About Von Willebrand Disease

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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Pediatric Hematology , An Issue of Hematology/Oncology Clinics of North America

Secondary Immune cytopenias, Disorders of Iron overload, Disorders of Iron metabolism, Approach to Hemophilia in a Changing Treatment Landscape, Von;

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Blood Saga

-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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Hematologic Disorders in Pregnancy,An Issue of Hematology/Oncology Clinics of North America

to delivery. Hematologic disorders covered include anemia, myeloproliferative disorders, von Willebrand disease, leukemia and lymphoma;

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The Bleeding Disease - Hemophilia and the Unintended Consequences of Medical Progress

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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Surviving hemophilia

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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Inherited Bleeding Disorders in Women

von Willebrand disease, rare bleeding disorders and inherited platelet disorders. This important resource: Offers an updated guide for;

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Surviving Hemophilia: A Road Trip Through the Worl

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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37th Hemophilia Symposium Hamburg 2006

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

Linked by Blood: Hemophilia and AIDS recounts the factors responsible for the widespread infection of people with hemophilia by Human;

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Textbook of Hemophilia

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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Hemophilia

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Laboratory Medicine in India, An Issue of Clinics in Laboratory Medicine

/Thalessemia; Muscle dystrophy; Spinal muscular atrophy; Wilson Disease; Hemophilia; National and International Accreditation; Blood Banking;

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Royal Maladies

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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Hemophilia and Other Hemorrhagic States

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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An Update on Pediatric Oncology and Hematology , An Issue of Hematology/Oncology Clinics of North America

aspects that most clinicians see on a regular basis-sickle cell disease, thalassemia, and hemophilia, and ITP.;

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Hemophilia and Hemostasis

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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Chronic Illnesses, Syndromes, and Rare Disorders

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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Health Technology Assessments and Rare Diseases

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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31st Hemophilia Symposium

Some 23. 5% of all members and patients of treatment centers completed the questionnaire. One striking fact is that participation;

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36th Hemophilia Symposium Hamburg 2005

].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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Coagulopathy, An Issue of Oral and Maxillofacial Surgery Clinics of North America

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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Vertebrate and Invertebrate Respiratory Proteins, Lipoproteins and other Body Fluid Proteins

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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