The landmark text that has guided generations of hematologists and related practitioners―updated with the latest research findings and improved format and presentation Long revered for its comprehensiveness and extraordinary depth of detail, Williams Hematology provides essential coverage of the origins, pathophysiological mechanisms, and management of benign and malignant disorders of blood and marrow cells and coagulation proteins. The text contains a wealth of basic science and translational pathophysiology for optimal, lifelong learning. Experts in research and clinical hematology, the editors are known worldwide for their contributions to the field. This new edition contains everything that has made Williams Hematology the go-to resource for decades and has been updated with new chapters and critical new research into the molecular mechanisms responsible for hematological disorders and the impact on diagnosis and treatment. And the new format enables you to access each chapter via content modules covering key topics, with summaries, infographics, and cases―all linked to review questions for self-assessment. The full-color presentation integrates images of blood and tissue findings where they are cited in the text. NEW TO THIS EDITION: Updated and revised content reflecting the latest research and developments Convenient format that streamlines the learning process and improves retention Additional chapters added on: Immune Checkpoint Inhibitors Immune Cell Therapy: Chimeric Antigen Receptor T Cell Therapy Immune Cell Therapy Dendritic Cell and Natural Killer Cell Therapy The processes of cell death and survival Application of Big Data and Deep Learning in Hematology Williams Hematology Cases with multiple-choice questions including detailed explanations—perfect preparation for the boards Continuously updated online content with comprehensive drug therapy database and other resources
Science 341(6148):1233158, 2013. Aiuti A, Biasco L, Scaramuzza S, et al: Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome. Science 341(6148):1233151, 2013. Lombardo A, Genovese P, Beausejour CM, ...
Sales Handle Concise and condensed content referenced to the classic main text of Williams Hematology, 10th edition. This book is perfect for use when time is tight on rounds or in the clinic.
A full-color quick reference distilled from the world's leading hematology text
A Doody's Core Title ESSENTIAL PURCHASE! After six editions, Williams Hematology remains the cornerstone text in the literature for hematology.
"This edition continues the tradition of providing a comprehensive, updated textbook of hematology. This very worthy objective is spectacularly met by this edition.
Prevost N, et al: Interactions between Eph kinases and ephrins provide a mechanism to support platelet aggregation once cell-to-cell contact has occurred. Proc Natl Acad Sci USA 99(14):9219–9224, 2002. Prevost N, et al: Signaling by ...
Trimble M, Caro J, Talalla A, et al. Secondary erythrocytosis due to a cerebellar hemangioblastoma: demonstration of erythropoietin mRNA in the tumor. Blood. 1991;78:599. 172. McFadzean AJS, Todd D, Tsang, KC.
- Concise coverage of the diagnosis and treatment makes the handbook ideal for quick reference, as well as for Board review! NEW to the Third Edition...- Emerging diagnostic and treatment strategies refine clinical decision-making.
The approach to hematoligic problems; The normal hematopoietic system; Basic cytology; Origin and development of the blood and blood-forming tissues; The erythrocyte; Morphology, intrinsic metabolism, function, laboratory evaluation; Production of...
Neville RWJ, Weir BJ, Lazarus NR. Hystricomorph insulins. Symp Zool Soc London. 1974;34:417-433. Opazo JC, Soto-Gamboa M, Bozinovic F. Blood glucose concentration in caviomorph rodents. Comp Biochem Physiol A Mol Integr Physiol.