Results 1 to 10 of about 10,754 (217)
Erythropoietin‐induced pure red cell aplasia
Vivian K. P. Yeung
openalex +4 more sources
Muco-Cutaneous Lichen Planus in a Patient with Thymoma and Pure Red Cell Aplasia. [PDF]
Meena A +5 more
europepmc +2 more sources
Pure Red Cell Aplasia Caused by Acute Hepatitis A [PDF]
Pure red cell aplasia is characterized as a normocytic anemia associated with reticulocytopenia and the absence of erythroblasts in the bone marrow. Pure red cell aplasia can be induced by various causes such as thymoma, connective tissue disease, viral ...
Chehal +14 more
core +2 more sources
Parvovirus B19 infection in pediatric transplant patients [PDF]
Evidence of recent parvovirus virus infection (as determined by the presence of a positive IgM antibody titer) without other identified causes of anemia was found in 5 of 26 pediatric solid-organ transplant recipients evaluated for moderate-to-severe ...
Gartner, JC +7 more
core +1 more source
AbstractPure red cell aplasia (PRCA) is a syndrome defined by a normocytic normochromic anemia with severe reticulocytopenia and marked reduction or absence of erythroid precursors from the bone marrow. Diamond-Blackfan anemia is a congenital form of PRCA.
openaire +7 more sources
Neuromyelitis Optica spectrum disorder complicated with pure red cell aplasia: a case report. [PDF]
Jiang W +9 more
europepmc +3 more sources
Pure red cell aplasia secondary to erythropoietin therapy. [PDF]
Edwards GM, Alejmi AA.
europepmc +2 more sources
Rituximab therapy for pure red cell aplasia due to anti-epoetin antibodies in a woman treated with epoetin-alfa: a case report [PDF]
Introduction Pure red cell aplasia due to anti-epoetin antibodies is a known complication of epoetin therapy for anemia due to chronic kidney disease. This disease has not previously been well described in the setting of therapy for chronic hepatitis C ...
Behler, Caroline M +3 more
core +3 more sources
Aplastic Crisis as Primary Manifestation of Systemic Lupus Erythematosus [PDF]
Aplastic crisis is an unusual feature of systemic lupus erythematosus (SLE). We report the case of a 54-year-old woman presenting with both (extravascular) Coombs-positive hemolytic anemia and laboratory findings of bone marrow hyporegeneration with ...
Alger M +23 more
core +1 more source

