Results 211 to 220 of about 16,341 (256)
Some of the next articles are maybe not open access.
Journal of pediatric hematology/oncology, 2019
Acquired pure red cell aplasia and acquired amegakaryocytic thrombocytopenic purpura are rare in children. Similarly, clonal expansion of T-cell large granular lymphocytes is infrequently seen in pediatrics.
M. Rajpurkar +5 more
semanticscholar +1 more source
Acquired pure red cell aplasia and acquired amegakaryocytic thrombocytopenic purpura are rare in children. Similarly, clonal expansion of T-cell large granular lymphocytes is infrequently seen in pediatrics.
M. Rajpurkar +5 more
semanticscholar +1 more source
Pure Red-Cell Aplasia and Epoetin Therapy
New England Journal of Medicine, 2004Between 1988 and 1998, antibody-associated pure red-cell aplasia was reported in three patients who had undergone treatment with recombinant human erythropoietin (epoetin). Between 1998 and 2000, 13 such cases were reported from France--12 in patients who had received the Eprex formulation of epoetin alfa and 1 in a patient who had received Neorecormon
Bennett CL +17 more
openaire +3 more sources
Eltrombopag restores erythropoiesis in refractory adult acquired pure red cell aplasia
International journal of hematology, 2021Xiaoqing Liu +8 more
semanticscholar +1 more source
Acquired pure red cell aplasia
American Journal of Hematology, 1987S S, Ammus, A A, Yunis
openaire +2 more sources
Medical Journal of Australia, 1982
This paper describes a case of pure red-cell aplasia in a child whose mother and grandfather also had the disorder. A raised haemoglobin F level was documented in the child and his mother in remission, and in a sibling who was not anaemic. Further support is provided for the theory that this disorder is inherited as a autosomal dominant with variable ...
openaire +2 more sources
This paper describes a case of pure red-cell aplasia in a child whose mother and grandfather also had the disorder. A raised haemoglobin F level was documented in the child and his mother in remission, and in a sibling who was not anaemic. Further support is provided for the theory that this disorder is inherited as a autosomal dominant with variable ...
openaire +2 more sources