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A diagnostic pitfall in iron-refractory microcytic hypochromic anemia with acquired ring sideroblasts initially treated as iron deficiency anemia-a case report. [PDF]
Front Med (Lausanne)Liu X +5 more
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Mitapivat metabolically reprograms human β-thalassemic erythroblasts, increasing their responsiveness to oxidation. [PDF]
Blood AdvSiciliano A +17 more
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Malaria and dyserythropoiesis: a mini review. [PDF]
Front Cell Infect MicrobiolLiu FF, Li K.
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Correction to "CD34dim Cells Identified as Pluripotent Stem Cell-Derived Definitive Hemogenic Endothelium Purified Using Bone Morphogenetic Protein 4". [PDF]
Cell Prolifeuropepmc +1 more source
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Erythroblastic islands in erythroleukemia
Journal of Pediatric Hematology/Oncology, 1981Erythroblastic islands are distinct anatomical units allowing direct transfer of ferritin molecule into developing erythroblasts. A patient with Fanconi's anemia who developed acute erythroleukemia and hypotransferrinemia exhibited numerous erythroblastic islands in the bone marrow. This unusual finding in our patient is thought to be in response to an
A, Taher, E, Gilbert, N T, Shahidi
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American Journal of Hematology, 1988
AbstractEight cases each of erythroleukemia (AML‐M6) and erythroblastic crisis of chronic granulocytic leukemia (CGLBC‐E) were immunophenotyped with the help of a panel of lineage‐associated monoclonal antibodies (McAbs). The latter included those reactive with erythroid progenitor (BFU‐E and CFU‐E) and erythroid precursors at different stages of ...
A D, Gupta, S R, Dhond
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AbstractEight cases each of erythroleukemia (AML‐M6) and erythroblastic crisis of chronic granulocytic leukemia (CGLBC‐E) were immunophenotyped with the help of a panel of lineage‐associated monoclonal antibodies (McAbs). The latter included those reactive with erythroid progenitor (BFU‐E and CFU‐E) and erythroid precursors at different stages of ...
A D, Gupta, S R, Dhond
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American Journal of Diseases of Children, 1932
In 1925, Cooley and Lee 1 described five cases of anemia in children having unusual roentgenographic changes in the bones. Since this original description and a later report by the same authors, 2 much interest has been directed toward this condition. As other cases have been reported, difficulty has arisen in classifying this type of anemia.
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In 1925, Cooley and Lee 1 described five cases of anemia in children having unusual roentgenographic changes in the bones. Since this original description and a later report by the same authors, 2 much interest has been directed toward this condition. As other cases have been reported, difficulty has arisen in classifying this type of anemia.
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American Journal of Hematology, 2021
Perla Vicari, Vitor de Carvalho Queiroz
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Perla Vicari, Vitor de Carvalho Queiroz
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Thymic Tumor and Erythroblastic Aplasia
JAMA, 1962THE ASSOCIATION of a thymic tumor with selective aplasia of erythrocytes has aroused considerable interest over the last decade. Our knowledge of the syndrome has recently been reviewed. One of the curious features of this association is that erythroblastic aplasia may follow some years after the removal of a symptomless thymic tumor, although this has
C W, HAVARD, J A, PARRISH
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