Basic Concepts Of Hemostasis Routledge Revivals Series
Coordonnateurs : Murano Genesio, Bick Rodger L.
First published in 1980, Murano and Bick provide well rounded accounts into the effects of Hemostasis and Thrombosis as well as a guide to the general physiology, associated disorders and therapeutic techniques used to address them. This book is ideal for students and practicioners of Hematology as well as those with a general interest in medicine.
PHYSIOLOGY AND BIOCHEMISTRY OF HEMOSTASIS Introduction The Three Hemostatic Compartments. 3. Chapter 1. Vascular Function in Hemostasis, 5. Chapter 2. Platelet Funstion in Hemostasis, 17. Chapter 3. Plasma Protein Function in Hemostasis, 43. CLINICAL DISORDERS OF HEMOSTASIS Chapter 4. A Systematic Approach to the Diagnosis of Bleeding Disorders, 81. Chapter 5. Vascular Disorders, 89. Chapter 6. Platelet Disorders,95. Chapter 7. Hereditary Plasma Protein Disorders. Chapter 8. Disseminated Intravascular Coagulation (DIC) and Related Syndromes, 163.Chapter 9. Primary Hyperfibrino(geno)lytic Syndromes, 181. Chapter 10. Acquired Circulating Anticoagulants and Defective Hemostasis in Malignant Paraprotein Disorders, 205. Chapter 11. Alterations of Hemostasis Associated with Malignancy, 213. Chapter 12. Malignancy and Anticoagulation, 227. HYPERCOAGULABILITY, THROMBOSIS, AND THERAPY Chapter 13. Hypercoagulability and Thrombosis, 237. Chapter 14. Anticoagulant and Antiplatelet Therapy, 245. Chapter 15. Thrombolytic Therapy, 259. Glossary, 269. Index, 271.
Date de parution : 03-2021
17.8x25.4 cm
Disponible chez l'éditeur (délai d'approvisionnement : 12 jours).
Prix indicatif 42,77 €
Ajouter au panierDate de parution : 08-2019
17.8x25.4 cm
Disponible chez l'éditeur (délai d'approvisionnement : 12 jours).
Prix indicatif 154,17 €
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Mots-clés :
Euglobulin Lysis Time; clinical evaluation; High Molecular Weight Kininogen; hemostasis disorder; Hemolytic Transfusion Reactions; platelet thrombosis; Platelet Function; therapeutic techniques; Factor VIII; thrombohemorrhagic syndromes; Factor XIII Deficiency; AHF; Classical Hemophilia; Template Bleeding Time; Prothrombin Complex Concentrate; Factor XII; Factor Viii; Factor Xi; Factor XI; Soluble Fibrin Monomer; Factor IX; Platelet Release Reaction; Fibrin Monomer; Factor XIII; Osler Weber Rendu Disease; HHT; Hemostasis