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

Year Number of Results
1983 1
1987 1
1989 2
1990 1
1992 2
1993 2
1994 1
1995 2
1996 3
1997 2
1998 4
1999 3
2000 4
2001 4
2002 2
2003 3
2004 4
2005 4
2006 8
2007 11
2008 6
2009 5
2010 11
2011 9
2012 7
2013 7
2014 10
2015 4
2016 10
2017 16
2018 14
2019 9
2020 12
2021 8
2022 6
2023 12
2024 3

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189 results

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Page 1
Diamond-Blackfan anemia.
Da Costa L, Leblanc T, Mohandas N. Da Costa L, et al. Blood. 2020 Sep 10;136(11):1262-1273. doi: 10.1182/blood.2019000947. Blood. 2020. PMID: 32702755 Free PMC article. Review.
Diamond-Blackfan anemia (DBA) was the first ribosomopathy described and is a constitutional inherited bone marrow failure syndrome. ...
Diamond-Blackfan anemia (DBA) was the first ribosomopathy described and is a constitutional inherited bone marrow failu …
Pure red cell aplasia.
Means RT Jr. Means RT Jr. Blood. 2016 Nov 24;128(21):2504-2509. doi: 10.1182/blood-2016-05-717140. Blood. 2016. PMID: 27881371 Free article. Review.
Pure 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. Acq …
Pure red cell aplasia (PRCA) is a syndrome defined by a normocytic normochromic anemia with severe reticulocytopenia and marked reduc …
Diamond-Blackfan anemia.
Krijanovski OI, Sieff CA. Krijanovski OI, et al. Hematol Oncol Clin North Am. 1997 Dec;11(6):1061-77. doi: 10.1016/s0889-8588(05)70483-4. Hematol Oncol Clin North Am. 1997. PMID: 9443046 Review.
Diamond-Blackfan anemia (DBA) is a rare, congenital, hypoplastic anemia that usually presents in early infancy. ...The disease is characterized by a moderate-to-severe macrocytic anemia, occasional neutropenia or thrombocytosis, a normocellular …
Diamond-Blackfan anemia (DBA) is a rare, congenital, hypoplastic anemia that usually presents in early infancy. …
Diamond-Blackfan anemia.
Willig TN, Gazda H, Sieff CA. Willig TN, et al. Curr Opin Hematol. 2000 Mar;7(2):85-94. doi: 10.1097/00062752-200003000-00003. Curr Opin Hematol. 2000. PMID: 10698294 Review.
Diamond Blackfan anemia is a rare congenital hypoplastic anemia that usually presents early in infancy. ...The disease is characterized by a moderate to severe macrocytic anemia, occasional neutropenia or thrombocytosis, a normocellular bone mar …
Diamond Blackfan anemia is a rare congenital hypoplastic anemia that usually presents early in infancy. ...The d …
Hereditary myeloid malignancies.
Rafei H, DiNardo CD. Rafei H, et al. Best Pract Res Clin Haematol. 2019 Jun;32(2):163-176. doi: 10.1016/j.beha.2019.05.001. Epub 2019 May 3. Best Pract Res Clin Haematol. 2019. PMID: 31203998 Free PMC article. Review.
Genetic predispositions to myeloid malignancies can be classified into three categories: familial cancer syndromes associated with increased risk of various malignancies including myelodysplasia and acute myeloid leukemia such as Li-Fraumeni syndrome and constitutional mismatch r …
Genetic predispositions to myeloid malignancies can be classified into three categories: familial cancer syndromes associated with increased …
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 …
Diamond-Blackfan anemia in adults: In pursuit of a common approach for a rare disease.
Iskander D, Roy NBA, Payne E, Drasar E, Hennessy K, Harrington Y, Christodoulidou C, Karadimitris A, Batkin L, de la Fuente J. Iskander D, et al. Blood Rev. 2023 Sep;61:101097. doi: 10.1016/j.blre.2023.101097. Epub 2023 May 8. Blood Rev. 2023. PMID: 37263874 Review.
Diamond-Blackfan anemia (DBA) is a rare bone marrow failure syndrome, usually caused by loss-of function variants in genes encoding ribosomal proteins. The hallmarks of DBA are anemia, congenital anomalies and cancer predisposition. Although DBA usuall …
Diamond-Blackfan anemia (DBA) is a rare bone marrow failure syndrome, usually caused by loss-of function variants in ge …
Identification of novel mutations in patients with Diamond-Blackfan anemia and literature review of RPS10 and RPS26 mutations.
Li J, Su Y, Chen L, Lin Y, Ru K. Li J, et al. Int J Lab Hematol. 2023 Oct;45(5):766-773. doi: 10.1111/ijlh.14126. Epub 2023 Jun 28. Int J Lab Hematol. 2023. PMID: 37376976 Review.
INTRODUCTION: Diamond-Blackfan anemia (DBA) is a rare congenital bone marrow failure syndrome characterized by erythroid aplasia, physical malformation, and cancer predisposition. ...
INTRODUCTION: Diamond-Blackfan anemia (DBA) is a rare congenital bone marrow failure syndrome characterized by erythroi …
Concise Review: Advanced Cell Culture Models for Diamond Blackfan Anemia and Other Erythroid Disorders.
Migliaccio AR, Varricchio L. Migliaccio AR, et al. Stem Cells. 2018 Feb;36(2):172-179. doi: 10.1002/stem.2735. Epub 2017 Dec 5. Stem Cells. 2018. PMID: 29124822 Free PMC article. Review.
Recent cell culture advances have greatly increased the number of human erythroid cells that can be generated in vitro and are used as experimental models to study diseases, such as Diamond Blackfan Anemia, which were previously poorly amenable to investigati …
Recent cell culture advances have greatly increased the number of human erythroid cells that can be generated in vitro and are used as exper …
Diamond-Blackfan Anemia: A Case Report and Review of the Literature.
Dorn KM, Burns KD, Trout MAR, Ward DI, Wagner KJ, Meyer LR, Baack ML, Rodel RL. Dorn KM, et al. Neonatology. 2021;118(4):500-504. doi: 10.1159/000516030. Epub 2021 May 18. Neonatology. 2021. PMID: 34004602 Review.
We report a case of a male neonate delivered urgently via cesarean at thirty-five 5/7 weeks gestation for non-reassuring fetal monitoring who was found to have severe anemia at birth that could not be explained by acute blood loss. He was born to a 24-year-old mother, whos …
We report a case of a male neonate delivered urgently via cesarean at thirty-five 5/7 weeks gestation for non-reassuring fetal monitoring wh …
189 results