“…BACKGROUND: Autoimmune hemolytic anemia (AIHA) results from red cell destruction due to circulating autoantibodies against red cell membrane antigens. …”
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“…The transfusion-medicine specialists and physicians are often in a difficult situation when the patient has severe worsening anemia and all the blood is mismatched. This situation can arise in patients with red cell autoantibodies or alloantibodies due to previous transfusions. …”
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“…EPO is used widely for treating anemia of critical illness or anemia induced by chemotherapy. …”
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“…Transfusions should be administered as clinically indicated for patients with acute, ongoing blood loss and those who have objective signs and symptoms of anemia despite maintenance of euvolemia. The hemoglobin level at which serious morbidity or mortality occurs in critically ill patients with active ischemic heart disease is a subject of continued debate but it is likely that a set transfusion trigger will not provide an optimal risk–benefit profile in this population.…”
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“…IGS should be considered in patients with megaloblastic anemia not responding to oral vit B12 and associated proteinuria.…”
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“…The fifteen known Fanconi Anemia (FA) proteins cooperate in a pathway which regulates DNA interstrand crosslink repair. …”
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“…We report here on a 60-year-old male with alcohol-related macrocytic anemia. He was hospitalized on three occasions with hemoglobin < 9.0 g/dL and mean corpuscular volume > 130 fL. …”
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“…Recent evidence suggests anemia may be independently related to these falls. …”
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“…OBJECTIVE: The oxidative stress in 20 sickle cell anemia patients taking hydroxyurea and 13 sickle cell anemia patients who did not take hydroxyurea was compared with a control group of 96 individuals without any hemoglobinopathy. …”
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“…Anemia is a frequent comorbidity of heart failure and is associated with poor outcomes. …”
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“…The patient suffered from two side effects : membranous nephropathy and aplastic anemia. She was treated and the systemic effects of mercury were reversed after 4 years. …”
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“…Most importantly, these changes correlated with the inflammatory state of the patients and anemia of chronic disease. Taken together, altered iron handling, inflammation and anemia of chronic disease constitute an ominous triad in SLE.…”
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“…Sickle cell anemia is a genetically inherited disease in which the “SS” individual possesses an abnormal beta globin gene. …”
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“…Incidence of mild to moderate anemia was higher in BTT and SCT compared to non-BTT or non-SCT subjects. …”
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“…Urinary tract infections (UTI) in children with sickle cell anemia (SCA) may result in long term renal dysfunction. …”
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