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Diamond-Blackfan anemia.
Da Costa L, Willig TN, Fixler J, Mohandas N, Tchernia G. Da Costa L, et al. Curr Opin Pediatr. 2001 Feb;13(1):10-5. doi: 10.1097/00008480-200102000-00002. Curr Opin Pediatr. 2001. PMID: 11176237 Review.
Diamond-Blackfan Anemia (DBA) is a rare, congenital hypoplastic anemia often diagnosed early in infancy. A moderate to severe aregenerative anemia is found in association with erythroblastopenia in an otherwise normocellular bone marrow. ...
Diamond-Blackfan Anemia (DBA) is a rare, congenital hypoplastic anemia often diagnosed early in infancy. A moder
Emerging Therapeutic Approaches for Diamond Blackfan Anemia.
Aspesi A, Borsotti C, Follenzi A. Aspesi A, et al. Curr Gene Ther. 2018;18(6):327-335. doi: 10.2174/1566523218666181109124538. Curr Gene Ther. 2018. PMID: 30411682 Free PMC article. Review.
Diamond Blackfan Anemia (DBA) is an inherited erythroid aplasia with onset in childhood. Patients carry heterozygous mutations in one of 19 Ribosomal Protein (RP) genes, that lead to defective ribosome biogenesis and function. ...
Diamond Blackfan Anemia (DBA) is an inherited erythroid aplasia with onset in childhood. Patients carry heterozygous mu
Perspectives of current understanding and therapeutics of Diamond-Blackfan anemia.
Liu Y, Karlsson S. Liu Y, et al. Leukemia. 2024 Jan;38(1):1-9. doi: 10.1038/s41375-023-02082-w. Epub 2023 Nov 16. Leukemia. 2024. PMID: 37973818 Free PMC article. Review.
Diamond-Blackfan anemia (DBA) is a rare congenital bone marrow failure disorder characterized by erythroid hypoplasia. ...
Diamond-Blackfan anemia (DBA) is a rare congenital bone marrow failure disorder characterized by erythroid hypoplasia.
How I treat Diamond-Blackfan anemia.
Vlachos A, Muir E. Vlachos A, et al. Blood. 2010 Nov 11;116(19):3715-23. doi: 10.1182/blood-2010-02-251090. Epub 2010 Jul 22. Blood. 2010. PMID: 20651069 Free PMC article. Review.
Diamond-Blackfan anemia (DBA) is characterized by red cell failure, the presence of congenital anomalies, and cancer predisposition. ...
Diamond-Blackfan anemia (DBA) is characterized by red cell failure, the presence of congenital anomalies, and cancer pr
p53 in the Molecular Circuitry of Bone Marrow Failure Syndromes.
Rakotopare J, Toledo F. Rakotopare J, et al. Int J Mol Sci. 2023 Oct 6;24(19):14940. doi: 10.3390/ijms241914940. Int J Mol Sci. 2023. PMID: 37834388 Free PMC article. Review.
Further studies confirmed, in humans and mice, that germline mutations affecting TP53 or its regulator MDM4 may cause short telomeres and alter hematopoiesis, but also revealed features of Diamond-Blackfan anemia (DBA) or Fanconi anemia (FA), two BMFSs …
Further studies confirmed, in humans and mice, that germline mutations affecting TP53 or its regulator MDM4 may cause short telomeres and al …
Using the Zebrafish as a Genetic Model to Study Erythropoiesis.
Zhang Y, Chen M, Chen C. Zhang Y, et al. Int J Mol Sci. 2021 Sep 28;22(19):10475. doi: 10.3390/ijms221910475. Int J Mol Sci. 2021. PMID: 34638816 Free PMC article. Review.
Defects in erythropoiesis can lead to blood disorders such as congenital dyserythropoietic anemias, Diamond-Blackfan anemias, sideroblastic anemias, myelodysplastic syndrome, and porphyria. ...
Defects in erythropoiesis can lead to blood disorders such as congenital dyserythropoietic anemias, Diamond-Blackfan anemias, …
The Role of α1-Microglobulin (A1M) in Erythropoiesis and Erythrocyte Homeostasis-Therapeutic Opportunities in Hemolytic Conditions.
Kristiansson A, Gram M, Flygare J, Hansson SR, Åkerström B, Storry JR. Kristiansson A, et al. Int J Mol Sci. 2020 Sep 30;21(19):7234. doi: 10.3390/ijms21197234. Int J Mol Sci. 2020. PMID: 33008134 Free PMC article. Review.
In addition, in a recently published study, it was observed that mice lacking A1M (A1M-KO) developed a macrocytic anemia phenotype. Altogether, this suggests that A1M may have a role in RBC development, stability and turnover. ...Here, we provide an overview of A1M and its …
In addition, in a recently published study, it was observed that mice lacking A1M (A1M-KO) developed a macrocytic anemia phenotype. A …
[Research Progress on Pathogenesis of Congenital Pure Red Cell Aplasia---Review].
Liu WY, Wang HQ, Shao ZH. Liu WY, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021 Oct;29(5):1654-1657. doi: 10.19746/j.cnki.issn.1009-2137.2021.05.045. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021. PMID: 34627456 Review. Chinese.
Congenital pure red cell aplasia, also known as Diamond-Blackfan anemia (DBA), is a hereditary disease characterized by pure red cell aplasia and congenital malformation. Its main clinical features are anemia, dysplasia, and tumor susceptibility. Ribos …
Congenital pure red cell aplasia, also known as Diamond-Blackfan anemia (DBA), is a hereditary disease characterized by …
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