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درصورت عدم همخوانی توضیحات با کتاب
از ساعت 7 صبح تا 10 شب
ویرایش: 10.
نویسندگان: Marshall A. Lichtman (editor)
سری:
ISBN (شابک) : 9781264269204, 126426920X
ناشر:
سال نشر: 2022
تعداد صفحات: 655
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 73 مگابایت
در صورت تبدیل فایل کتاب Williams manual of hematology به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب کتابچه راهنمای خون شناسی ویلیامز نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
Cover Williams Manual of Hematology Title Copyright Preface PART I INITIAL CLINICAL EVALUATION Approach to the Patient PART II DISORDERS OF RED CELLS Classification of Anemias and Erythrocytoses Aplastic Anemia: Acquired and Inherited Pure Red Cell Aplasia Anemia of Chronic (Inflammatory, Neoplastic, and Renal) Disease Erythropoietic Effects of Endocrine Disorders Congenital Dyserythropoietic Anemias Folate, Cobalamin, and Megaloblastic Anemias Iron Deficiency and Iron Overload Anemia Resulting from Other Nutritional Deficiencies Hereditary and Acquired Sideroblastic Anemias Anemia Resulting from Marrow Infiltration Erythrocyte Membrane Disorders Hemolytic Anemia Related to Red Cell Enzyme Defects The Thalassemias The Sickle Cell Diseases and Other Hemoglobinopathies Unstable Hemoglobins and Hemoglobins with Altered Oxygen Affinity Methemoglobinemia and Other Dyshemoglobinemias Fragmentation Hemolytic Anemia Hemolytic Anemia Resulting from a Chemical or Physical Agent Hemolytic Anemia Resulting from Infectious Agents Hemolytic Anemia Resulting from Warm-Reacting Antibodies Cryopathic Hemolytic Anemia Drug-Induced Hemolytic Anemia Alloimmune Hemolytic Disease of the Newborn Hypersplenism and Hyposplenism Polyclonal Erythrocytoses (Primary and Secondary) The Porphyrias PART III DISORDERS OF GRANULOCYTES Classification and Clinical Manifestations of Neutrophil Disorders Neutropenia and Neutrophilia Disorders of Neutrophil Function Eosinophils and Their Disorders Basophils, Mast Cells and Their Disorders PART IV DISORDERS OF MONOCYTES AND MACROPHAGES Classification and Clinical Manifestations of Monocyte and Macrophage Disorders Monocytosis and Monocytopenia Inflammatory and Malignant Histiocytosis Gaucher Disease and Related Lysosomal Storage Diseases PART V PRINCIPLES OF THERAPY FOR NEOPLASTIC HEMATOLOGIC DISORDERS Pharmacology and Toxicity of Antineoplastic Drugs Principles of Hematopoietic Cell Transplantation Immune Cell Therapy: Genetically Engineered T Cells PART VI THE CLONAL MYELOID DISORDERS Classification and Clinical Manifestations of the Clonal Myeloid Disorders Polycythemia Vera Essential Thrombocythemia Paroxysmal Nocturnal Hemoglobinuria Myelodysplastic Syndromes The Acute Myelogenous Leukemias The Chronic Myelogenous Leukemias Primary Myelofibrosis PART VII THE POLYCLONAL LYMPHOID DISEASES Classification and Clinical Manifestations of Polyclonal Lymphocyte and Plasma Cell Disorders Lymphocytosis and Lymphocytopenia Primary Immunodeficiency Syndrome Hematologic Manifestations of the Acquired Immunodeficiency Syndrome The Mononucleosis Syndromes PART VIII THE CLONAL LYMPHOID ANDPLASMA CELL DISEASES Classification and Clinical Manifestations of the Neoplastic Lymphocytic Disorders The Acute Lymphoblastic Leukemias The Chronic Lymphocytic Leukemias Hairy Cell Leukemia Large Granular Lymphocytic Leukemia General Considerations of Lymphoma: Epidemiology, Etiology, Heterogeneity, and Primary Extranodal Disease Hodgkin Lymphoma Diffuse Large B-Cell Lymphoma and Related Diseases Follicular Lymphoma Mantle Cell Lymphoma Marginal Zone B-Cell Lymphoma Burkitt Lymphoma Cutaneous T-Cell Lymphoma Mature T-Cell and Natural Killer Cell Lymphomas Essential Monoclonal Gammopathy Myeloma Macroglobulinemia Heavy-Chain Diseases Amyloidosis PART IX DISORDERS OF PLATELETS AND HEMOSTASIS Clinical Manifestations, Evaluation and Classification of Disorders of Hemostasis Thrombocytopenia Hereditary and Reactive (Secondary) Thrombocytosis Hereditary Platelet Disorders Acquired Platelet Disorders The Vascular Purpuras PART X DISORDERS OF COAGULATION PROTEINS Hemophilia A and B von Willebrand Disease Hereditary Disorders of Fibrinogen Inherited Deficiencies of Coagulation Factors II, V, VII, X, XI, and XIII and Combined Deficiencies of Factor V and VIII and of Antibody-Mediated Coagulation Factor Deficiencies Hemostatic Dysfunction Related to Liver Diseases The Antiphospholipid Syndrome Disseminated Intravascular Coagulation Fibrinolysis and Thrombolysis PART XI THROMBOSIS AND ANTITHROMBOTIC THERAPY Principles of Antithrombotic and Antifibrinolytic Therapy Hereditary Thrombophilia Venous Thromboembolism Antibody-Mediated Thrombotic Disorders: Thrombotic Thrombocytopenic Purpura and Heparin-Induced Thrombocytopenia PART XII TRANSFUSION AND HEMAPHERESIS Red Cell Transfusion Transfusion of Platelets Plasma and Plasma Component Therapy Therapeutic Hemapheresis Table of Normal Values