Results 11 to 20 of about 66,503 (250)

Development of New Drugs for Autoimmune Hemolytic Anemia

open access: yesPharmaceutics, 2022
Autoimmune hemolytic anemia (AIHA) is a rare disorder characterized by the autoantibody-mediated destruction of red blood cells, and treatments for it still remain challenging.
Zhengrui Xiao, Irina Murakhovskaya
doaj   +2 more sources

The choice of new treatments in autoimmune hemolytic anemia: how to pick from the basket?

open access: yesFrontiers in Immunology, 2023
Autoimmune hemolytic anemia (AIHA) is defined by increased erythrocyte turnover mediated by autoimmune mechanisms. While corticosteroids remain first-line therapy in most cases of warm-antibody AIHA, cold agglutinin disease is treated by targeting the ...
S. Berentsen, B. Fattizzo, W. Barcellini
semanticscholar   +1 more source

Severe autoimmune hemolytic anemia; epidemiology, clinical management, outcomes and knowledge gaps

open access: yesFrontiers in Immunology, 2023
Autoimmune hemolytic anemia (AIHA) is an acquired hemolytic disorder, mediated by auto-antibodies, and has a variable clinical course ranging from fully compensated low grade hemolysis to severe life-threatening cases.
Femke V. M. Mulder   +7 more
semanticscholar   +1 more source

Autoimmune hemolytic anemia: causes and consequences

open access: yesExpert Review of Clinical Immunology, 2022
Introduction Autoimmune hemolytic anemia (AIHA) is classified according to the direct antiglobulin test (DAT) and thermal characteristics of the autoantibody into warm and cold forms, and in primary versus secondary depending on the presence of ...
B. Fattizzo, W. Barcellini
semanticscholar   +1 more source

How I treat warm autoimmune hemolytic anemia.

open access: yesBlood, 2021
Warm autoimmune hemolytic anemia (wAIHA) is caused by increased erythrocyte destruction by IgG autoantibodies, with or without complement activation.
W. Barcellini, B. Fattizzo
semanticscholar   +1 more source

Autoimmune Hemolytic Anemia After mRNA COVID Vaccine

open access: yesJournal of Investigative Medicine High Impact Case Reports, 2022
Discussion of the hematologic complications of vaccination for severe acute respiratory syndrome coronavirus-2 (COVID-19) has primarily focused on the development of vaccine-associated immune thrombosis with thrombocytopenia (VITT).
Z. Fatima   +3 more
semanticscholar   +1 more source

Intravascular hemolysis and multitreatment predict thrombosis in patients with autoimmune hemolytic anemia

open access: yesJournal of Thrombosis and Haemostasis, 2022
Thrombosis may complicate autoimmune hemolytic anemia (AIHA), but its predictors are still lacking, and no clear‐cut indications for anticoagulant prophylaxis are available.
B. Fattizzo   +5 more
semanticscholar   +1 more source

Warm autoimmune hemolytic anemia and the best treatment strategies.

open access: yesHematology. American Society of Hematology. Education Program, 2022
Warm autoimmune hemolytic anemia (wAIHA) is characterized by evidence of red blood cell (RBC) hemolysis and a direct antiglobulin test positive for IgG and sometimes complement. While varying with the extent of the compensatory increase in RBC production,
D. Kuter
semanticscholar   +1 more source

Survival in autoimmune hemolytic anemia remains poor, results from a nationwide cohort with 37 years of follow‐up

open access: yesEuropean Journal of Haematology, 2022
Autoimmune hemolytic anemia (AIHA) is considered a chronic disease, with an overall good prognosis. However, recent reports indicate pre‐mature mortality. Causes of death have not been evaluated previously.
D. Hansen, S. Möller, H. Frederiksen
semanticscholar   +1 more source

Autoimmune Hemolytic Anemia in the Pediatric Setting

open access: yesJournal of Clinical Medicine, 2021
Autoimmune hemolytic anemia (AIHA) is a rare disease in children, presenting with variable severity. Most commonly, warm-reactive IgG antibodies bind erythrocytes at 37 °C and induce opsonization and phagocytosis mainly by the splenic macrophages ...
Aikaterini Voulgaridou, T. Kalfa
semanticscholar   +1 more source

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