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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1976 1
1977 1
1978 1
1981 2
1982 1
1983 2
1985 1
1988 1
1989 2
1990 2
1992 2
1993 1
1995 3
1996 2
1997 2
1998 4
1999 4
2000 5
2001 1
2002 1
2003 3
2004 3
2005 2
2006 1
2007 3
2008 2
2009 3
2010 7
2011 3
2012 4
2013 8
2014 2
2015 1
2016 2
2017 3
2019 5
2020 6
2021 5
2022 1
2023 3
2024 3

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102 results

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Page 1
Beta-thalassemia.
Galanello R, Origa R. Galanello R, et al. Orphanet J Rare Dis. 2010 May 21;5:11. doi: 10.1186/1750-1172-5-11. Orphanet J Rare Dis. 2010. PMID: 20492708 Free PMC article. Review.
Thalassemia minor is clinically asymptomatic but some subjects may have moderate anemia. Beta-thalassemias are caused by point mutations or, more rarely, deletions in the beta globin gene on chromosome 11, leading to reduced (beta+) or absent (beta0) synthesis of the beta …
Thalassemia minor is clinically asymptomatic but some subjects may have moderate anemia. Beta-thalassemias are caused by point mutati …
Congenital dyserythropoietic anemias.
Iolascon A, Andolfo I, Russo R. Iolascon A, et al. Blood. 2020 Sep 10;136(11):1274-1283. doi: 10.1182/blood.2019000948. Blood. 2020. PMID: 32702750 Free article. Review.
Congenital dyserythropoietic anemias (CDAs) are a heterogeneous group of inherited anemias that affect the normal differentiation-proliferation pathways of the erythroid lineage. ...
Congenital dyserythropoietic anemias (CDAs) are a heterogeneous group of inherited anemias that affect the normal differentiat
Diagnosis and management of congenital dyserythropoietic anemias.
Gambale A, Iolascon A, Andolfo I, Russo R. Gambale A, et al. Expert Rev Hematol. 2016 Mar;9(3):283-96. doi: 10.1586/17474086.2016.1131608. Epub 2016 Jan 6. Expert Rev Hematol. 2016. PMID: 26653117 Review.
Congenital dyserythropoietic anemias (CDAs) are inherited disorders hallmarked by chronic hyporegenerative anemia, relative reticulocytopenia, hemolytic component and iron overload. ...
Congenital dyserythropoietic anemias (CDAs) are inherited disorders hallmarked by chronic hyporegenerative anemia, rela
Autoinflammatory bone disorders.
Morbach H, Hedrich CM, Beer M, Girschick HJ. Morbach H, et al. Clin Immunol. 2013 Jun;147(3):185-96. doi: 10.1016/j.clim.2012.12.012. Epub 2013 Jan 5. Clin Immunol. 2013. PMID: 23369460 Review.
GATA factor mutations in hematologic disease.
Crispino JD, Horwitz MS. Crispino JD, et al. Blood. 2017 Apr 13;129(15):2103-2110. doi: 10.1182/blood-2016-09-687889. Epub 2017 Feb 8. Blood. 2017. PMID: 28179280 Free PMC article. Review.
Acquired and inherited GATA1 mutations contribute to Diamond-Blackfan anemia, acute megakaryoblastic leukemia, transient myeloproliferative disorder, and a group of related congenital dyserythropoietic anemias with thrombocytopenia. ...
Acquired and inherited GATA1 mutations contribute to Diamond-Blackfan anemia, acute megakaryoblastic leukemia, transient myeloprolife …
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, …
Erythrocyte disorders in the perinatal period.
Steiner LA, Gallagher PG. Steiner LA, et al. Semin Perinatol. 2007 Aug;31(4):254-61. doi: 10.1053/j.semperi.2007.05.003. Semin Perinatol. 2007. PMID: 17825683 Free PMC article. Review.
Anemia is a commonly encountered problem in the fetal and neonatal period, and can lead to significant morbidity and mortality. Intrinsic disorders of the erythrocyte, such as the hemoglobinopathies, enzyme deficiencies, and membrane defects are common causes of neonatal
Anemia is a commonly encountered problem in the fetal and neonatal period, and can lead to significant morbidity and mortality. Intri
Autoinflammatory bone diseases.
Stern SM, Ferguson PJ. Stern SM, et al. Rheum Dis Clin North Am. 2013 Nov;39(4):735-49. doi: 10.1016/j.rdc.2013.05.002. Epub 2013 Aug 17. Rheum Dis Clin North Am. 2013. PMID: 24182852 Free PMC article. Review.
The COPII pathway and hematologic disease.
Khoriaty R, Vasievich MP, Ginsburg D. Khoriaty R, et al. Blood. 2012 Jul 5;120(1):31-8. doi: 10.1182/blood-2012-01-292086. Epub 2012 May 14. Blood. 2012. PMID: 22586181 Free PMC article. Review.
Multiple diseases, hematologic and nonhematologic, result from defects in the early secretory pathway. Congenital dyserythropoietic anemia type II (CDAII) and combined deficiency of coagulation factors V and VIII (F5F8D) are the 2 known hematologic diseases t …
Multiple diseases, hematologic and nonhematologic, result from defects in the early secretory pathway. Congenital dyserythropoieti
Congenital Hemolytic Anemias: Is There a Role for the Immune System?
Zaninoni A, Fermo E, Vercellati C, Marcello AP, Barcellini W, Bianchi P. Zaninoni A, et al. Front Immunol. 2020 Jun 23;11:1309. doi: 10.3389/fimmu.2020.01309. eCollection 2020. Front Immunol. 2020. PMID: 32655575 Free PMC article. Review.
They are characterized by variable degree of anemia, chronic extravascular hemolysis, reduced erythrocyte life span, splenomegaly, jaundice, biliary lithiasis, and iron overload. ...Median Hb increase is 3 g/dL in HS, 1.6-1.8 g/dL in pyruvate kinase deficiency (PKD), and 1 …
They are characterized by variable degree of anemia, chronic extravascular hemolysis, reduced erythrocyte life span, splenomegaly, ja …
102 results