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1987 1
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2006 3
2007 4
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30 results

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Page 1
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 …
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. ...Including 2 patients in this study, 13 patients with RPS10 mutations and 38 …
INTRODUCTION: Diamond-Blackfan anemia (DBA) is a rare congenital bone marrow failure syndrome characterized by erythroi …
Critical Issues in Diamond-Blackfan Anemia and Prospects for Novel Treatment.
Li H, Lodish HF, Sieff CA. Li H, et al. Hematol Oncol Clin North Am. 2018 Aug;32(4):701-712. doi: 10.1016/j.hoc.2018.04.005. Epub 2018 Jun 5. Hematol Oncol Clin North Am. 2018. PMID: 30047421 Free PMC article. Review.
Diamond-Blackfan anemia (DBA) is a severe congenital hypoplastic anemia caused by mutation in a ribosomal protein gene. ...
Diamond-Blackfan anemia (DBA) is a severe congenital hypoplastic anemia caused by mutation in a ribosomal protei
The functions of RPS19 and their relationship to Diamond-Blackfan anemia: a review.
Morimoto K, Lin S, Sakamoto K. Morimoto K, et al. Mol Genet Metab. 2007 Apr;90(4):358-62. doi: 10.1016/j.ymgme.2006.11.004. Epub 2006 Dec 18. Mol Genet Metab. 2007. PMID: 17178250 Review.
RPS19 is a ribosomal protein linked to Diamond-Blackfan anemia whose functions have begun to be elucidated. We review here the known roles of RPS19 in both ribosome construction and other extra-ribosomal functions and discuss their relationship to Diamond
RPS19 is a ribosomal protein linked to Diamond-Blackfan anemia whose functions have begun to be elucidated. We review h …
Diamond-blackfan anemia: etiology, pathophysiology, and treatment.
Halperin DS, Freedman MH. Halperin DS, et al. Am J Pediatr Hematol Oncol. 1989 Winter;11(4):380-94. Am J Pediatr Hematol Oncol. 1989. PMID: 2694854 Review.
Diamond-Blackfan anemia (DBA) is manifested by a wide variety of clinical and in vitro abnormalities. Despite this biological diversity, the hematological phenotype is remarkably similar for all patients and consists of a normochromic-macrocytic anemia
Diamond-Blackfan anemia (DBA) is manifested by a wide variety of clinical and in vitro abnormalities. Despite this biol
Diamond-Blackfan anemia: erythropoiesis lost in translation.
Flygare J, Karlsson S. Flygare J, et al. Blood. 2007 Apr 15;109(8):3152-4. doi: 10.1182/blood-2006-09-001222. Epub 2006 Dec 12. Blood. 2007. PMID: 17164339 Free article. Review.
Diamond-Blackfan anemia (DBA) is a congenital erythroid aplasia that usually presents as macrocytic anemia during infancy. ...Recent studies and emerging findings suggest that a malfunctioning translational machinery may be a cause of anemia in
Diamond-Blackfan anemia (DBA) is a congenital erythroid aplasia that usually presents as macrocytic anemia durin
Diamond-Blackfan anemia and nutritional deficiency-induced anemia in children.
Gelbart D. Gelbart D. JAAPA. 2014 Apr;27(4):36-44. doi: 10.1097/01.JAA.0000442702.95598.fc. JAAPA. 2014. PMID: 24662257 Review.
Diamond-Blackfan anemia is a rare, inherited disease that characteristically presents as a chronic, normochromic macrocytosis due to red cell lineage bone marrow failure. Although studies are elaborating on the genetic basis for its associated comorbidities,
Diamond-Blackfan anemia is a rare, inherited disease that characteristically presents as a chronic, normochromic macroc
The genomics of inherited bone marrow failure: from mechanism to the clinic.
Wegman-Ostrosky T, Savage SA. Wegman-Ostrosky T, et al. Br J Haematol. 2017 May;177(4):526-542. doi: 10.1111/bjh.14535. Epub 2017 Feb 17. Br J Haematol. 2017. PMID: 28211564 Free article. Review.
Herein we review the clinical features, underlying biology, and new genomic discoveries in the IBMFS, including Fanconi anaemia, dyskeratosis congenita, Diamond Blackfan anaemia, Shwachman Diamond syndrome and some disorders of the myeloid and megakary …
Herein we review the clinical features, underlying biology, and new genomic discoveries in the IBMFS, including Fanconi anaemia, dyskeratosi …
Anemia as the Main Manifestation of Myelodysplastic Syndromes.
Santini V. Santini V. Semin Hematol. 2015 Oct;52(4):348-56. doi: 10.1053/j.seminhematol.2015.06.002. Epub 2015 Jun 30. Semin Hematol. 2015. PMID: 26404446 Review.
These progenitors show distinctive dysplastic features that consent diagnosis, and are recognizable and differentiated, although not easily, from other morphologic alterations present in other types of anemia. Reaching the diagnosis of MDS in a macrocytic anemia and …
These progenitors show distinctive dysplastic features that consent diagnosis, and are recognizable and differentiated, although not easily, …
Diamond-blackfan anemia and cyclosporine therapy revisited.
Alessandri AJ, Rogers PC, Wadsworth LD, Davis JH. Alessandri AJ, et al. J Pediatr Hematol Oncol. 2000 Mar-Apr;22(2):176-9. doi: 10.1097/00043426-200003000-00020. J Pediatr Hematol Oncol. 2000. PMID: 10779036 Review.
A girl with Diamond-Blackfan anemia diagnosed in infancy started cyclosporine A (CSA) therapy at 9 years and 8 months of age after experiencing unacceptable side effects while receiving prednisone. ...A trial of CSA therapy should be considered in patients wi …
A girl with Diamond-Blackfan anemia diagnosed in infancy started cyclosporine A (CSA) therapy at 9 years and 8 months o …
30 results