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carriers. A person with hemophilia lacks the genetic information to produce one of the proteins needed for blood clotting. Most hemophiliacs have a;
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identification with Queen Victoria, the world's most renowned carrier, hemophilia is a genetic disease whose sufferers had little recourse until the mid;
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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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carriers. A person with hemophilia lacks the genetic information to produce one of the proteins needed for blood clotting. Most hemophiliacs have 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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Textbook of Hemophilia, 3rd edition Edited by Christine A. Lee, MA, MD, DSc, FRCP, FRCPath, FRCOG Emeritus Professor of Haemophilia;
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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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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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There is a general need amongst healthcare professionals for practical advice on the management of patients with bleeding disorders. This;
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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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About 31% of the patients with a factor VIII replacement therapy develop a factor VIII inhibitor.From these are 23% low-responder ( 5BE) [8;
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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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Living with haemophilia has established itself as the complete guide to haemophilia and related disorders. Written primarily for affected;
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Among the topics covered are: - Adrenal Gland - Amniocentesis - Botany - Cell Membrane - Down Syndrome - Fossils - Hemophilia - Molecule;
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This issue will provide a current update on diagnosis, treatment, and management of children with being hematological disorders. Dr;
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is provided by comprehensive care haemophilia centres where staff of all specialities concerned with treatment- haematologists, paediatricians, nurses;
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The latest edition of this practical handbook provides a concise yet comprehensive overview of common and rare problems with hemostasis and;
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; Sickle Cell; Anticoagulants; Aplastic anemia & MDS; Hereditary Hemochromatosis and Pernicious Anemia; Hemophilia; Blood book: cells, products;
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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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leukemia, which remains the most common form of pediatric cancer. Specifically, articles address ALL, AML, and leukemia in patients with Down;
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. World Federation of Hemophilia. Copenhagen. June 25th. 1963. War can come to an oasis, peace can come to the trenches. With this book, Dr Peter;
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/Thalessemia; Muscle dystrophy; Spinal muscular atrophy; Wilson Disease; Hemophilia; National and International Accreditation; Blood Banking;
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Hematology is a branch of medicine. It studies the diseases of blood along with their causes, treatment, prevention and prognosis. Some;
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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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to any online entitlements included with the product. One of the most practical resources for diagnosis and treatment;
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