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Drugs and Diseases
Articles on
Hematology
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Coagulation, Hemostasis, and Disorders
Acquired Hemophilia
Alpha2-Plasmin Inhibitor Deficiency
Antithrombin Deficiency
Arsine Poisoning
Disseminated Intravascular Coagulation (DIC)
Dysfibrinogenemia
Esophageal Hematoma
Factor II Deficiency
Factor V Deficiency
Factor VII Deficiency
Factor X Deficiency
Factor XI Deficiency
Factor XIII Deficiency
Glanzmann Thrombasthenia
Hemolytic-Uremic Syndrome
Hemophilia A (Factor VIII Deficiency)
Hemophilia B (Factor IX Deficiency)
Heparin-Induced Thrombocytopenia
Hereditary and Acquired Hypercoagulability
Immune Thrombocytopenia (ITP)
Immune Thrombocytopenia (ITP) in Emergency Medicine
Immune Thrombocytopenia and Pregnancy
Internal Jugular Vein Thrombosis
Miscarriages Caused by Blood Coagulation Protein or Platelet Deficits
Nonplatelet Hemostatic Disorders
Paradoxical Embolism
Platelet Disorders
Protein C Deficiency
Protein S Deficiency
Renal Vein Thrombosis
Secondary Thrombocytosis
Superficial Thrombophlebitis
Thrombotic Thrombocytopenic Purpura (TTP)
Venous Thromboembolism (VTE)
von Willebrand Disease
Disorders of Lymphocytic Function
Pure B-Cell Disorders
Severe Combined Immunodeficiency (SCID)
Heme Synthesis and Disorders
Acute Intermittent Porphyria
ALA Dehydratase Deficiency Porphyria
Chester Porphyria
Hereditary Coproporphyria
Porphyria Overview
Immune System and Disorders
Eosinophilia
Hypereosinophilic Syndrome
Hyperviscosity Syndrome
Immunology of Transplant Rejection
Kikuchi Disease
Neutropenia
Neutropenic Fever Empiric Therapy
Neutrophilia
Paroxysmal Cold Hemoglobinuria
Splenomegaly
Systemic Mastocytosis
Lymphoproliferative Disorders
Burkitt Lymphoma and Burkitt-like Lymphoma
Castleman Disease
Plasma Cell Disorders
Familial Renal Amyloidosis
Gamma Heavy Chain Disease
Immunoglobulin-Related Amyloidosis
Light Chain-Associated Renal Disorders
Light-Chain Deposition Disease
Monoclonal Gammopathies of Undetermined Significance (MGUS)
Mu Heavy Chain Disease
Multiple Myeloma
Solitary Plasmacytoma
Waldenstrom Macroglobulinemia
Red Blood Cells and Disorders
Anemia
Anemia in Elderly Persons
Anemia of Chronic Disease and Kidney Failure
Aplastic Anemia
Argyria
Beta Thalassemia
Bone Marrow Failure
Cold Agglutinin Disease
Folate Deficiency
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
Hemoglobin C Disease
Hemoglobinopathy Retinopathy
Hemolytic Anemia
Iron Deficiency Anemia
Macrocytosis
Megaloblastic Anemia
Methemoglobinemia
Myelophthisic Anemia
Paroxysmal Nocturnal Hemoglobinuria
Pernicious Anemia
Pure Red Cell Aplasia
Sickle Cell Disease (SCD)
Sideroblastic Anemias
Thalassemia Intermedia
Transfusion-Induced Iron Overload
Valsalva Retinopathy
Stem Cells and Disorders
Acute Lymphoblastic Leukemia (ALL)
Acute Myeloid Leukemia (AML)
Acute Promyelocytic Leukemia (APL)
AIDS-Related Lymphomas
Anaplastic Large Cell Lymphoma
B-Cell Lymphoma
Chronic Lymphocytic Leukemia (CLL)
Chronic Myelogenous Leukemia (CML)
Cutaneous T-Cell Lymphoma
Diffuse Large B-Cell Lymphoma (DLBCL)
Erythroleukemia
Erythromelalgia
Essential Thrombocytosis
Follicular Lymphoma
Graft Versus Host Disease (GVHD)
Hairy Cell Leukemia
Hematopoietic Stem Cell Transplantation (HSCT)
Hodgkin Lymphoma
Lymphoblastic Lymphoma
Mantle Cell Lymphoma
Mediastinal Lymphoma
Mucosa-Associated Lymphoid Tissue Lymphomas (MALTomas)
Myelodysplastic Syndrome (MDS)
Myeloproliferative Disease
Non-Hodgkin Lymphoma (NHL)
Non-Hodgkin Lymphoma Guidelines
Polycythemia Vera
Posttransplant Lymphoproliferative Disease (PTLD)
Primary Myelofibrosis
Secondary Polycythemia
Thyroid Lymphoma
X-linked Lymphoproliferative Syndrome
Transfusion Medicine
Alloimmunization From Transfusions
Blood Substitutes
Intravenous Immunoglobulin
Transfusion Reactions
Transfusion-Transmitted Diseases
Uncommon RBC Membrane Disorders
Hereditary Elliptocytosis
Hereditary Pyropoikilocytosis
Hereditary Spherocytosis
Spur Cell Anemia
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M
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O
P
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V
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X
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Z
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SWIPE FOR MORE
AIDS-Related Lymphomas
ALA Dehydratase Deficiency Porphyria
Acquired Hemophilia
Acute Intermittent Porphyria
Acute Lymphoblastic Leukemia (ALL)
Acute Myeloid Leukemia (AML)
Acute Promyelocytic Leukemia (APL)
Alloimmunization From Transfusions
Alpha2-Plasmin Inhibitor Deficiency
Anaplastic Large Cell Lymphoma
Anemia
Anemia in Elderly Persons
Anemia of Chronic Disease and Kidney Failure
Antithrombin Deficiency
Aplastic Anemia
Argyria
Arsine Poisoning
B-Cell Lymphoma
Beta Thalassemia
Blood Substitutes
Bone Marrow Failure
Burkitt Lymphoma and Burkitt-like Lymphoma
Castleman Disease
Chester Porphyria
Chronic Lymphocytic Leukemia (CLL)
Chronic Myelogenous Leukemia (CML)
Cold Agglutinin Disease
Cutaneous T-Cell Lymphoma
Diffuse Large B-Cell Lymphoma (DLBCL)
Disseminated Intravascular Coagulation (DIC)
Dysfibrinogenemia
Eosinophilia
Erythroleukemia
Erythromelalgia
Esophageal Hematoma
Essential Thrombocytosis
Factor II Deficiency
Factor V Deficiency
Factor VII Deficiency
Factor X Deficiency
Factor XI Deficiency
Factor XIII Deficiency
Familial Renal Amyloidosis
Folate Deficiency
Follicular Lymphoma
Gamma Heavy Chain Disease
Glanzmann Thrombasthenia
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency
Graft Versus Host Disease (GVHD)
Hairy Cell Leukemia
Hematopoietic Stem Cell Transplantation (HSCT)
Hemoglobin C Disease
Hemoglobinopathy Retinopathy
Hemolytic Anemia
Hemolytic-Uremic Syndrome
Hemophilia A (Factor VIII Deficiency)
Hemophilia B (Factor IX Deficiency)
Heparin-Induced Thrombocytopenia
Hereditary Coproporphyria
Hereditary Elliptocytosis
Hereditary Pyropoikilocytosis
Hereditary Spherocytosis
Hereditary and Acquired Hypercoagulability
Hodgkin Lymphoma
Hypereosinophilic Syndrome
Hyperviscosity Syndrome
Immune Thrombocytopenia (ITP)
Immune Thrombocytopenia (ITP) in Emergency Medicine
Immune Thrombocytopenia and Pregnancy
Immunoglobulin-Related Amyloidosis
Immunology of Transplant Rejection
Internal Jugular Vein Thrombosis
Intravenous Immunoglobulin
Iron Deficiency Anemia
Kikuchi Disease
Light Chain-Associated Renal Disorders
Light-Chain Deposition Disease
Lymphoblastic Lymphoma
Macrocytosis
Mantle Cell Lymphoma
Mediastinal Lymphoma
Megaloblastic Anemia
Methemoglobinemia
Miscarriages Caused by Blood Coagulation Protein or Platelet Deficits
Monoclonal Gammopathies of Undetermined Significance (MGUS)
Mu Heavy Chain Disease
Mucosa-Associated Lymphoid Tissue Lymphomas (MALTomas)
Multiple Myeloma
Myelodysplastic Syndrome (MDS)
Myelophthisic Anemia
Myeloproliferative Disease
Neutropenia
Neutropenic Fever Empiric Therapy
Neutrophilia
Non-Hodgkin Lymphoma (NHL)
Non-Hodgkin Lymphoma Guidelines
Nonplatelet Hemostatic Disorders
Paradoxical Embolism
Paroxysmal Cold Hemoglobinuria
Paroxysmal Nocturnal Hemoglobinuria
Pernicious Anemia
Platelet Disorders
Polycythemia Vera
Porphyria Overview
Posttransplant Lymphoproliferative Disease (PTLD)
Primary Myelofibrosis
Protein C Deficiency
Protein S Deficiency
Pure B-Cell Disorders
Pure Red Cell Aplasia
Renal Vein Thrombosis
Secondary Polycythemia
Secondary Thrombocytosis
Severe Combined Immunodeficiency (SCID)
Sickle Cell Disease (SCD)
Sideroblastic Anemias
Solitary Plasmacytoma
Splenomegaly
Spur Cell Anemia
Superficial Thrombophlebitis
Systemic Mastocytosis
Thalassemia Intermedia
Thrombotic Thrombocytopenic Purpura (TTP)
Thyroid Lymphoma
Transfusion Reactions
Transfusion-Induced Iron Overload
Transfusion-Transmitted Diseases
Valsalva Retinopathy
Venous Thromboembolism (VTE)
Waldenstrom Macroglobulinemia
X-linked Lymphoproliferative Syndrome
von Willebrand Disease
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Chief Editors
Emmanuel C Besa, MD
Sara J Grethlein, MD, FACP
Srikanth Nagalla, MBBS, MS, FACP
Perumal Thiagarajan, MD
