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It has not been associated with autoimmune hemolytic anemia of the fetus.
Case report of warm-antibody autoimmune hemolytic anemia with typical laboratory findings.
Direct Coombs test, used to test for autoimmune hemolytic anemia.
Another serious adverse effect is autoimmune hemolytic anemia.
This condition is called autoimmune hemolytic anemia.
Spherocytes are found in hereditary spherocytosis and autoimmune hemolytic anemia.
RA may cause a warm autoimmune hemolytic anemia.
The disease is usually non-progressive and self-limited, but patients can manifest autoimmune hemolytic anemia.
Acquired autoimmune hemolytic anemia is a disorder that occurs in individuals who previously had a normal red blood cell system.
There is no known prevention for idiopathic autoimmune hemolytic anemia, because the cause is unknown.
Fludarabine is associated with the development of severe autoimmune hemolytic anemia in a proportion of patients.
Idiopathic autoimmune hemolytic anemia is a drop in the number of red blood cells due to increased destruction by the body's defense (immune) system.
Idiopathic autoimmune hemolytic anemia is an acquired disease that occurs when antibodies form against a person's own red blood cells.
It is a form of autoimmune hemolytic anemia, specifically one in which antibodies only bind red blood cells at low body temperatures, typically 28-31 C.
Autoimmune hemolytic anemia.
In autoimmune hemolytic anemia, concentrations of hemoglobin A1 (HbA1) is undetectable.
Drug-induced autoimmune hemolytic anemia is a form of hemolytic anemia.
Autoimmune hemolytic anemia and/or thrombocytopenia can occur in patients with any stage of CLL.
Its overall pathology resembles a combination of autoimmune hemolytic anemia and idiopathic thrombocytopenic purpura.
Idiopathic autoimmune hemolytic anemia accounts for one-half of all immune hemolytic anemias.
Autoimmune hemolytic anemia: In people with this condition, an overactive immune system destroys the body's own red blood cells, causing anemia.
If the direct Coombs test is positive, hemolysis is caused by an immune process (e.g. autoimmune hemolytic anemia).
Autoimmune hemolytic anemia is a condition in which the red blood cells that normally carry oxygen and carbon dioxide are destroyed by an autoimmune process.
It has been variously reported that between 10% and 23% of patients who have autoimmune hemolytic anemia, will also have thrombocytopenia and thus Evans syndrome.
Hematologic causes of death were divided between autoimmune hemolytic anemia and immune-mediated thrombocytopenia (ITP).