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This book contains the contribution to the 37th Hemophilia Symposium, Hamburg 2006. The main topics are epidemiolgy, treatment;
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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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For thousands of years boys known as 'bleeders' faced an early, painful death from hemophilia. Dubbed 'the Royal Disease' because of its;
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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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Textbook of Hemophilia, 3rd edition Edited by Christine A. Lee, MA, MD, DSc, FRCP, FRCPath, FRCOG Emeritus Professor of Haemophilia;
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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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By the 1970s, a therapeutic revolution, decades in the making, had transformed hemophilia from an obscure hereditary malady into a;
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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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Linked by Blood: Hemophilia and AIDS recounts the factors responsible for the widespread infection of people with hemophilia by Human;
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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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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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].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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Among the topics covered are: - Adrenal Gland - Amniocentesis - Botany - Cell Membrane - Down Syndrome - Fossils - Hemophilia - Molecule;
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was highest amongst elderly patients with severe hemophilia, whereas only 12. 2% of family members responded. Evaluation of the results revealed that;
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/Thalessemia; Muscle dystrophy; Spinal muscular atrophy; Wilson Disease; Hemophilia; National and International Accreditation; Blood Banking;
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As haemophilia is a life-long condition, continuing supervision by a group of medical personnel is r;...
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is an important topic for most patients with hemophilia. References 1. Neuntes Sozialgesetzbuch (SGB IX) - Rehabilitation und Teilhabe;
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; Sickle Cell; Anticoagulants; Aplastic anemia & MDS; Hereditary Hemochromatosis and Pernicious Anemia; Hemophilia; Blood book: cells, products;
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, including multiple novel coagulation factors for hemophilia, the increasing use of novel anticoagulants and their reversal agents, and the;
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topics: Hemophilia; Sickle cell acute chest; Sickle cell drugs; Sickle cell gene therapy; Sickle cell menses and pain; Pediatric DVT; Atypical;
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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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common blood diseases are blood clots, lymphoma, hemophilia, leukemia, among others. Hematopathologists are pathologists whose expertise lies;
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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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Balkan queens and of the scandalous Carol II of Romania; Victoria Eugenie, Spain's very English queen who, like Alexandra, introduced hemophilia;
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Needs to Know; Hemophilia: What the Oral Surgeon Needs to Know; Damage Control Resuscitation: What the Oral Surgeon Needs to Know; Hemostasis;
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, inpatient and outpatient *2 new chapters on heritable blood disorders *expert coverage of hemophilia *latest advances in thrombosis research;
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