Results 1 to 10 of about 10,754 (217)

Pure red cell aplasia [PDF]

open access: bronzeBritish Journal of Haematology, 2000
Paul Fisch   +2 more
openalex   +4 more sources

Muco-Cutaneous Lichen Planus in a Patient with Thymoma and Pure Red Cell Aplasia. [PDF]

open access: diamondIndian Dermatol Online J
Meena A   +5 more
europepmc   +2 more sources

Pure Red Cell Aplasia Caused by Acute Hepatitis A [PDF]

open access: yes, 2011
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]

open access: yes, 1993
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

Pure Red Cell Aplasia [PDF]

open access: yesBlood, 2016
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

Rituximab therapy for pure red cell aplasia due to anti-epoetin antibodies in a woman treated with epoetin-alfa: a case report [PDF]

open access: yes, 2009
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]

open access: yes, 2011
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

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