[PDF] from hematologylibrary.orgMS Kumar, A Narla, A Nonami… - …, 2011 - bloodjournal.hematologylibrary.org ... Page 4. 4 Introduction The 5q- syndrome is a subtype of myelodysplastic syndrome (MDS) characterized by a macrocyticanemia, a normal or elevated platelet count, and hypolobated micromegakaryocytes. 1 ...macrocyticanemia. 4 ... View as HTML
[PDF] from pagepress.orgJ Boultwood - Pediatric Reports, 2011 - pagepress.org ... diseases including DBA and Treacher Collins syndrome.24,26 We have recently generated a mouse model of the 5q- syndrome using large-scale chromo- somal engineering.27 Haploinsufficiency of the Cd74-Nid67 interval caused macrocyticanemia, prominent erythroid ... Related articles
[PDF] from hvsch.orgRB Sommerville… - Clinical Chemistry, 2011 - Am Assoc Clin Chem ... In addition, 5 months before the onset of his paresthesias, he was discovered to have a macrocyticanemia that did not respond to treatment with vitamin B 12 and folate. He ... What are some causes of macrocyticanemia? Could ...
P Amireault, S Hatia, E Bayard… - Proceedings of the …, 2011 - National Acad Sciences ... The combination of these two defects causes TPH1 −/− animals to develop a phenotype of macrocyticanemia. ... 1. TPH1 −/− mice display a phenotype of aregenerative macrocyticanemia. (A–C) A significant decrease in the number of RBCs (7.5 ± 0.2 vs. ...
[HTML] from hematologylibrary.orgSR Ellis - Blood, 2011 - bloodjournal.hematologylibrary.org ... Diamond-Blackfan anemia is a rare congenital hypoplastic macrocyticanemia that typically presents in the first year of life. The hypoplastic ... inactivation. 8 Yet, unlike DBA and 5q−, individuals with TCS do not exhibit a macrocyticanemia. 9 ... Related articles - All 3 versions
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