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Hemorrhage disorders --- Hemorrhagic diathesis --- Treatment. --- Therapy.
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HEMORRHAGIC DIATHESIS --- HEMOSTASIS --- FIBRINOLYSIS --- THROMBOSIS --- HEMORRHAGE --- NEOPLASMS --- CARDIOLIPINS --- SERPINS
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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 these essential blood-clotting proteins play in research and clinical medicine. Clinicians and researchers face the daily challenge of staying current on the vast amounts of research that is now generated. The reference to Janus in the title refers to the two roles of the Factor VIII/Von Willebrand Factor Complex: initiation of coagulation and propagation of clot formation. The complex prevents bleeding in hemophilia and Von Willebrand disease but also augments arterial and venous thrombosis. Presents one source of information on Hemophilia and Von Willebrand Disease, as well as Factor VIII and Von Willebrand Factor, eliminating the search through hundreds of journal articles.--
Hemophilia. --- Classic hemophilia --- Factor VIII deficiency --- Haemophilia --- Hematophilia --- Hemophilia A --- Hemorrhagic diathesis --- Blood coagulation disorders
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This book demonstrates the great efforts aimed at further improving the care of the hemophilia, which may bring further improvement in the quality of life of hemophilia persons and their families.
Hemophilia. --- Classic hemophilia --- Factor VIII deficiency --- Haemophilia --- Hematophilia --- Hemophilia A --- Hemorrhagic diathesis --- Blood coagulation disorders --- Haematology
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BLOOD COAGULATION DISORDERS --- HEMORRHAGE --- FACTOR IX --- HEMORRHAGIC DIATHESIS --- VON WILLEBRAND FACTOR --- INFECTION --- THROMBOSIS --- DRUG THERAPY
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Hemorrhagic Diathesis --- Thrombosis --- Blood --- Cardiovascular system --- Sang --- Appareil cardiovasculaire --- periodicals --- Circulation --- Periodicals --- Périodiques --- Hemorrhagic Disorders --- periodicals. --- Périodiques --- MDCARDIO MDHEMATO
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The book Hemophilia - Recent Advances covers various rapid advances being made in this field. The authors have produced state-of-the art chapters. Over some decades, management of hemophilia has progressed from episode based to prophylaxis. It has moved from plasma and cryoprecipitate to new generations of recombinant coagulation factors. Efforts have been made to cover recent advances in the field. The intricacies of genotype and phenotype of hemophilia are explained. Management with recombinant factors has added to problems like inhibitors, which require more skillful handling. Perioperative management of hemophilia is also explained. Every chapter of this book is peer reviewed and evidence based. The information provided in this book makes the readers well informed and more inquisitive, thereby raising new issues, innovation, and research.
Hemophilia --- Management. --- Classic hemophilia --- Factor VIII deficiency --- Haemophilia --- Hematophilia --- Hemophilia A --- Hemorrhagic diathesis --- Blood coagulation disorders --- Haematology
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Hemophilia --- Genetic aspects. --- Treatment. --- Classic hemophilia --- Factor VIII deficiency --- Haemophilia --- Hematophilia --- Hemophilia A --- Hemorrhagic diathesis --- Blood coagulation disorders
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AIDS (Disease) --- Hemophilia. --- Classic hemophilia --- Factor VIII deficiency --- Haemophilia --- Hematophilia --- Hemophilia A --- Hemorrhagic diathesis --- Blood coagulation disorders --- Acquired immune deficiency syndrome --- Acquired immunodeficiency syndrome --- Acquired immunological deficiency syndrome --- HIV infections --- Immunological deficiency syndromes --- Virus-induced immunosuppression
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