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Hematology

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Coagulation, Hemostasis, and Disorders

Acquired Hemophilia

Acute Lymphoblastic Leukemia (ALL) Guidelines

Acute Myelogenous Leukemia (AML) Guidelines

Alpha2-Plasmin Inhibitor Deficiency

Antithrombin Deficiency

Arsine Poisoning

Disseminated Intravascular Coagulation

Dysfibrinogenemia

Esophageal Hematoma

Factor II

Factor IX Deficiency

Factor V Deficiency

Factor VII

Factor X

Factor XI Deficiency

Factor XIII

Glanzmann Thrombasthenia

Hemolytic-Uremic Syndrome

Hemophilia A

Hemophilia B

Heparin-Induced Thrombocytopenia

Hypercoagulability - Hereditary Thrombophilia and Lupus Anticoagulants Associated With Venous Thrombosis and Emboli

Idiopathic Thrombocytopenic Purpura

Immune Thrombocytopenia and Pregnancy

Immune Thrombocytopenic Purpura (ITP)

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

Thromboembolism

Thrombotic Thrombocytopenic Purpura

von Willebrand Disease

Disorders of Lymphocytic Function

Combined B-Cell and T-Cell Disorders

Pure B-Cell Disorders

Heme Synthesis and Disorders

Acute Intermittent Porphyria

ALA Dehydratase Deficiency Porphyria

Chester Porphyria

Hereditary Coproporphyria

Porphyria Overview

Immune System and Disorders

Eosinophilia

Hypereosinophilic Syndrome

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

Extramedullary Plasmacytoma

Familial Renal Amyloidosis

Gamma Heavy Chain Disease

Hematopoietic Stem Cell Transplantation

Immunoglobulin-Related Amyloidosis

Light Chain-Associated Renal Disorders

Light-Chain Deposition Disease

Monoclonal Gammopathies of Uncertain Origin

Mu Heavy Chain Disease

Multiple Myeloma

Waldenstrom Macroglobulinemia

Red Blood Cells and Disorders

Anemia

Anemia in Elderly Persons

Anemia of Chronic Disease and Renal Failure

Aplastic Anemia

Argyria

Beta Thalassemia

Bone Marrow Failure

Cold Agglutinin Disease

Folic Acid Deficiency

Glucose-6-Phosphate Dehydrogenase Deficiency

Hemoglobin C Disease

Hemoglobinopathy Retinopathy

Hemolytic Anemia

Hereditary Spherocytosis

Iron Deficiency Anemia

Macrocytosis

Megaloblastic Anemia

Methemoglobinemia

Myelophthisic Anemia

Paroxysmal Nocturnal Hemoglobinuria

Pernicious Anemia

Pure Red Cell Aplasia

Sickle Cell Anemia

Sideroblastic Anemias

Transfusion-Induced Iron Overload

Valsalva Retinopathy

Stem Cells and Disorders

Acute Lymphoblastic Leukemia

Acute Myelogenous Leukemia

Acute Promyelocytic Leukemia

AIDS-Related Lymphomas

Anaplastic Large Cell Lymphoma

B-Cell Lymphoma

Chronic Lymphocytic Leukemia

Chronic Myelogenous Leukemia

Chronic Myelogenous Leukemia (CML) Guidelines

Cutaneous T-Cell Lymphoma

Diffuse Large Cell Lymphoma

Erythroleukemia

Erythromelalgia

Essential Thrombocytosis

Follicular Lymphoma

Hairy Cell Leukemia

High-Grade Malignant Immunoblastic Lymphoma

Hodgkin Lymphoma

Hyperviscosity Syndrome

Lymphoblastic Lymphoma

Mantle Cell Lymphoma

Mediastinal Lymphoma

Mucosa-Associated Lymphoid Tissue

Myelodysplastic Syndrome

Myeloproliferative Disease

Non-Hodgkin Lymphoma

Polycythemia Vera

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

Spur Cell Anemia

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