Wintrobe's clinical hematology.
| Other Authors: | |
|---|---|
| Language: | English |
| Published: |
Philadelphia :
Wolters Kluwer Health/Lippincott Williams & Wilkins,
[2009], ©2009.
|
| Edition: | Twelfth edition / |
| Subjects: | |
| Physical Description: | 2 volumes (xxv, 2,606, I-47 pages) : illustrations (some color) ; 29 cm |
| Variant Title: |
Clinical hematology. |
| Format: | Book |
Contents:
- V. 1: Examination of the blood and bone marrow
- Clinical flow cytometry
- Cytogenetics
- Molecular biology and hematology
- Origin and development of blood cells
- Erythropoiesis
- The mature erythrocyte
- Destruction of erythrocytes
- Neutrophilic leukocytes
- The human eosinophil
- Basophilic leukocytes: mast cells and basophils
- Mononuclear phagocytes
- Phagocytosis
- Lymphocytes and lymphatic organs
- B lymphocytes
- T lymphocytes and natural killer cells
- Effector mechanisms in immunity
- Megakaryocytes
- Platelet structure and function in hemostasis and thrombosis
- Blood coagulation and fibrinolysis
- Endothelium: angiogenesis and the regulation of hemostasis
- Red cell, platelet, and white cell antigens
- Transfusion medicine
- Hematopoietic stem cell transplantation
- Gene therapy for hematologic disorders
- Anemia: general considerations
- Iron deficiency and related disorders
- Sideroblastic anemias
- Hemochromatosis
- Porphyria
- Hereditary spherocytosis, hereditary elliptocytosis, and other disorders associated with abnormalities of the erythrocyte membrane
- Hereditary hemolytic anemias due to red blood cell enzyme disorders
- Autoimmune hemolytic anemia
- Alloimmune hemolytic disease of the fetus and newborn
- Paroxysmal nocturnal hemoglobinuria
- Acquired nonimmune hemolytic disorders
- Sickle cell anemia and other sickling syndromes
- Thalassemias and related disorders: quantitative disorders of hemoglobin synthesis
- Hemoglobins with altered oxygen affinity, unstable hemoglobins, M-hemoglobins, and dyshemoglobinemias
- Megaloblastic anemias: disorders of impaired DNA synthesis
- Inherited aplastic anemia syndromes
- Acquired aplastic anemia
- Red cell aplasia
- Congenital dyserythropoietic anemias
- Anemias secondary to chronic disease
- Anemias during pregnancy and the postpartum period
- Amemias unique to the newborn period
- Erythrocytosis
- V. 2: Diagnostic approach to the bleeding disorders
- Thrombocytopenia: pathophysiology and classification
- Thrombocytopenia casued by immunologic platelet destruction
- Thrombotic thrombocytopenic purpura, hemolytic-uremic syndrome, and related disorders
- Miscellaneous causes of thrombocytopenia
- Bleeding disorders caused by vascular abnormalities
- Essential thrombocythemia and thrombocytosis
- Qualitative disorders of platelet function
- Inherited coagulation disorders
- Acquired coagulation disorders
- Thrombosis and antithrombotic therapy
- Diagnostic approach to malignant and nonmalignant disorders of the phagocytic and immune systems
- Neutropenia
- Qualitative disorders of leukocytes
- Abnormalities of the monocyte-marocphage system: the lysosomal storage diseases
- Langerhans cell histiocytosis
- Pathology of langerhans cell histiocytosis and other histiocytic proliferations
- Infectious mononucleosis and other Epstein-Barr virus-related disorders
- Primary immunodeficiency syndromes
- Acquired immunodeficiency syndrome
- Disorders of the spleen
- Tumors of the spleen
- Hematopoietic tumors: principles of pathologic diagnosis
- Complications of hematopoietic neoplasms
- Principles and pharmacology of chemotherapy
- Immunotherapy
- Supportive care in hematologic malignancies
- Molecular genetics of acute leukemia
- Diagnosis and classification of the acute leukemias and myelodysplastic syndrome
- Acute lymphoblastic leukemia in adults
- Acute myeloid leukemia in adults
- Acute lymphoblastic leukemia in children
- Acute myelogenous leukemia in children
- Acute promyelocytic leukemia
- Myelodysplastic syndromes
- Pathology of the myeloproliferative diseases
- Chronic myeloid leukemia
- Polycythemia vera
- Primary myelofibrosis
- Systemic mastocytosis
- Diagnosis and classification of lymphomas
- Molecular genetic aspects of non-hodgkin lymphomagenesis
- Non-Hodgkin lymphoma in adults
- Non-Hodgkin lymphoma in children
- Chronic lymphocytic leukemia
- Hairy cell leukemia
- Cutaneous T-cell lymphoma: mycosis fungoides and sézary syndrome
- Hodgkin lymphoma
- Practical aspects of the clinical approach to patients with monoclonal immunoglobulin disorders
- Monoclonal gammopathies of undetermined significance and smoldering multiple myeloma
- Multiple myeloma
- Immunoglobulin light-chain amyloidosis (primary amyloidosis)
- Waldenström macroglobulinemia
- Cryoglobulinemia and heavy chain disease.