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Coexistent sickle cell anemia and autoimmune hemolytic anemia in two adolescents. [PDF]

open access: yesEinstein (Sao Paulo)
Soares VR   +3 more
europepmc   +1 more source

Phase I study of pomalidomide in relapsed or refractory Waldenström macroglobulinaemia

open access: yes
British Journal of Haematology, Volume 207, Issue 1, Page 244-248, July 2025.
Karan L. Chohan   +9 more
wiley   +1 more source
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Congenital Hemolytic Anemia.

Medical Clinics of North America, 2017
Red blood cell (RBC) destruction can be secondary to intrinsic disorders of the RBC or to extrinsic causes. In the congenital hemolytic anemias, intrinsic RBC enzyme, RBC membrane, and hemoglobin disorders result in hemolysis. The typical clinical presentation is a patient with pallor, anemia, jaundice, and often splenomegaly.
K. Haley
semanticscholar   +4 more sources

Autoimmune Hemolytic Anemia.

Medical Clinics of North America, 2017
Autoimmune hemolytic anemia is an acquired autoimmune disorder resulting in the production of antibodies directed against red blood cell antigens causing shortened erythrocyte survival. The disorders can present as a primary disorder (idiopathic) or secondary to other autoimmune disorders, malignancies, or infections.
Howard A Liebman, Ilene C Weitz
semanticscholar   +3 more sources

Hemolytic Anemia with Hemoglobinuria

American Journal of Clinical Pathology, 1948
Hemolytic anemia with hemoglobinuria is frequently a striking clinical event indicative of extensive intravascular hemolysis. The condition lends itself to detailed study because of the morphologic abnormalities in the blood and bone marrow, the marked accumulation of hemoglobin and its derivatives in the blood plasma and urine, the aberrations of ...
Daniel Stats   +2 more
openaire   +5 more sources

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