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American Journal of Hematology, ISSN 0361-8609, 11/2014, Volume 89, Issue 11, pp. 1055 - 1062
Chronic lymphocytic leukemia (CLL) is frequently complicated by secondary autoimmune cytopenias (AIC) represented by autoimmune hemolytic anemia (AIHA), immune... 
FAILURE SYNDROME GROUP | HEMOLYTIC-ANEMIA | NEUTROPENIA COMMITTEE | CONSENSUS GUIDELINES | IMMUNE THROMBOCYTOPENIC PURPURA | REGULATORY T-CELLS | TOLL-LIKE RECEPTORS | DIRECT ANTIGLOBULIN-TEST | PROGNOSTIC-SIGNIFICANCE | HEMATOLOGY | RED-CELL APLASIA | T-Lymphocyte Subsets - immunology | Prognosis | Humans | Immunosuppressive Agents - therapeutic use | Red-Cell Aplasia, Pure - etiology | Neoplastic Stem Cells - immunology | Paraneoplastic Syndromes - diagnosis | Agranulocytosis - blood | Adrenal Cortex Hormones - therapeutic use | Anemia, Hemolytic, Autoimmune - blood | Immunoglobulin M - immunology | Leukemia, Lymphocytic, Chronic, B-Cell - complications | Blood Cells - immunology | Purpura, Thrombocytopenic, Idiopathic - blood | Purpura, Thrombocytopenic, Idiopathic - etiology | Splenectomy | Purpura, Thrombocytopenic, Idiopathic - therapy | Agranulocytosis - therapy | Antigen Presentation | Anemia, Hemolytic, Autoimmune - therapy | Immunoglobulin G - immunology | Clone Cells - immunology | Anemia, Hemolytic, Autoimmune - diagnosis | Agranulocytosis - etiology | Leukemia, Lymphocytic, Chronic, B-Cell - immunology | Anemia, Hemolytic, Autoimmune - etiology | Paraneoplastic Syndromes - therapy | Risk Factors | Agranulocytosis - diagnosis | Combined Modality Therapy | Paraneoplastic Syndromes - etiology | Receptors, Antigen, B-Cell - immunology | Red-Cell Aplasia, Pure - blood | Blood Component Transfusion | Autoantibodies - immunology | Models, Immunological | Purpura, Thrombocytopenic, Idiopathic - diagnosis | Paraneoplastic Syndromes - blood | Red-Cell Aplasia, Pure - therapy | Leukemia, Lymphocytic, Chronic, B-Cell - drug therapy | Immunoglobulin Heavy Chains - genetics | Red-Cell Aplasia, Pure - diagnosis | Lymphocytic leukemia | Chemotherapy | Cancer
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British Journal of Haematology, ISSN 0007-1048, 11/2011, Volume 155, Issue 4, pp. 498 - 508
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