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Perioperative management of Evans Syndrome for free tissue transfer: Case report and recommendations. [PDF]
JPRAS OpenWillborg BE +4 more
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[Hemolytic anemia. 1. Autoimmune hemolytic anemia].
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 2007 openaire +1 more source
Anemia. II. Hemolytic anemia. IV. Acquired hemolytic anemia.
Indian journal of medical sciences, 1971 openaire +1 more source
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American Journal of Hematology, 2002
AbstractRed blood cell (RBC) autoantibodies are a relatively uncommon cause of anemia. However, autoimmune hemolytic anemia (AIHA) must be considered in the differential diagnosis of hemolytic anemias, especially if the patient has a concomitant lymphoproliferative disorder, autoimmune disease, or viral or mycoplasmal infection. Classifications of AIHA
Bradley C, Gehrs, Richard C, Friedberg
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AbstractRed blood cell (RBC) autoantibodies are a relatively uncommon cause of anemia. However, autoimmune hemolytic anemia (AIHA) must be considered in the differential diagnosis of hemolytic anemias, especially if the patient has a concomitant lymphoproliferative disorder, autoimmune disease, or viral or mycoplasmal infection. Classifications of AIHA
Bradley C, Gehrs, Richard C, Friedberg
exaly +3 more sources
Cancer Treatment Reviews, 1996
One of the most fundamental tenets of medical diagnosis is that when presented with a complex problem, the clinician attempts to make a single, unifying diagnosis. In approaching the problem of hemolytic anemia in the patient with cancer, it is often difficult to adhere to this tenet.
L F, Diehl, C D, Bolan, R B, Weiss
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One of the most fundamental tenets of medical diagnosis is that when presented with a complex problem, the clinician attempts to make a single, unifying diagnosis. In approaching the problem of hemolytic anemia in the patient with cancer, it is often difficult to adhere to this tenet.
L F, Diehl, C D, Bolan, R B, Weiss
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Medical Clinics of North America, 1980
Immune hemolytic anemia is an acquired anemia resulting from the premature destruction of red cells caused by the presence of antibody and/or complement on the red cell surface. The Coombs test, modified and improved, remains the mainstay of diagnosis.
J A, Axelson, A F, LoBuglio
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Immune hemolytic anemia is an acquired anemia resulting from the premature destruction of red cells caused by the presence of antibody and/or complement on the red cell surface. The Coombs test, modified and improved, remains the mainstay of diagnosis.
J A, Axelson, A F, LoBuglio
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The Indian Journal of Pediatrics, 1998
Immune hemolytic anemia can be either isoimmune or autoimmune. Autoimmune hemolytic anemias (AIHA) consist of group of disorders whose common characteristics are the presence of an antibody which in turn causes short red blood cell (RBC) life. The rate and site of hemolysis and hence the clinical manifestations depends on the type of antibody attached ...
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Immune hemolytic anemia can be either isoimmune or autoimmune. Autoimmune hemolytic anemias (AIHA) consist of group of disorders whose common characteristics are the presence of an antibody which in turn causes short red blood cell (RBC) life. The rate and site of hemolysis and hence the clinical manifestations depends on the type of antibody attached ...
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The American Journal of Medicine, 1964
Abstract Results of investigations in twenty-four cases of acute hemolytic anemia are presented. Among the associated conditions which appeared to be causally related to the anemia were infections, ingestion of drugs and chemicals, malignant diseases, acute glomerulonephritis, thrombotic thrombocytopenic purpura, idiopathic autoimmune hemolytic ...
R O, WALLERSTEIN, P M, AGGELER
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Abstract Results of investigations in twenty-four cases of acute hemolytic anemia are presented. Among the associated conditions which appeared to be causally related to the anemia were infections, ingestion of drugs and chemicals, malignant diseases, acute glomerulonephritis, thrombotic thrombocytopenic purpura, idiopathic autoimmune hemolytic ...
R O, WALLERSTEIN, P M, AGGELER
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