Coverart for item
The Resource Wintrobe's clinical hematology

Wintrobe's clinical hematology

Label
Wintrobe's clinical hematology
Title
Wintrobe's clinical hematology
Title variation
Clinical hematology
Contributor
Subject
Language
eng
Member of
Cataloging source
UV0
Dewey number
616.1/5
Illustrations
illustrations
Index
index present
LC call number
RB145
LC item number
.W74 2009
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
http://library.link/vocab/relatedWorkOrContributorDate
1901-1986
http://library.link/vocab/relatedWorkOrContributorName
  • Wintrobe, Maxwell M.
  • Greer, John P
http://library.link/vocab/subjectName
  • Hematology
  • Blood
  • Blood
  • Hematologic Diseases
  • Hematology
Label
Wintrobe's clinical hematology
Instantiates
Publication
Bibliography note
Includes bibliographical references and index
Carrier category
online resource
Carrier category code
  • cr
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
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 caused 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
Dimensions
unknown
Edition
  • 12th ed. /
  • editors, John P. Greer [and others].
Extent
1 online resource (2 volumes (xxv, 2606, I-47 pages))
Form of item
online
Lccn
2008036157
Media category
computer
Media MARC source
rdamedia
Media type code
  • c
Other physical details
illustrations (some color)
Specific material designation
remote
System details
Mode of access: World Wide Web
Label
Wintrobe's clinical hematology
Publication
Bibliography note
Includes bibliographical references and index
Carrier category
online resource
Carrier category code
  • cr
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
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 caused 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
Dimensions
unknown
Edition
  • 12th ed. /
  • editors, John P. Greer [and others].
Extent
1 online resource (2 volumes (xxv, 2606, I-47 pages))
Form of item
online
Lccn
2008036157
Media category
computer
Media MARC source
rdamedia
Media type code
  • c
Other physical details
illustrations (some color)
Specific material designation
remote
System details
Mode of access: World Wide Web

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