Olalla Saad ST - Search Results

1

The challenges of handling deferasirox in sickle cell disease patients older than 40 years.

Ribeiro LB, Soares EA, Costa FF, Gilli SCO, Olalla Saad ST, Benites BD. Ribeiro LB, et al. Among authors: olalla saad st. Hematology. 2019 Dec;24(1):596-600. doi: 10.1080/16078454.2019.1657667. Hematology. 2019. PMID: 31434554 Free article.

2

Molecular heterogeneity of G6PD deficiency in an Amazonian population and description of four new variants.

Hamel AR, Cabral IR, Sales TS, Costa FF, Olalla Saad ST. Hamel AR, et al. Among authors: olalla saad st. Blood Cells Mol Dis. 2002 May-Jun;28(3):399-406. doi: 10.1006/bcmd.2002.0524. Blood Cells Mol Dis. 2002. PMID: 12367584

3

Reduction of AHSP synthesis in hemin-induced K562 cells and EPO-induced CD34(+) cells leads to alpha-globin precipitation, impairment of normal hemoglobin production, and increased cell death.

Pinho FO, de Albuquerque DM, Olalla Saad ST, Costa FF. Pinho FO, et al. Among authors: olalla saad st. Exp Hematol. 2008 Mar;36(3):265-72. doi: 10.1016/j.exphem.2007.11.003. Epub 2008 Jan 7. Exp Hematol. 2008. PMID: 18179859 Free article.

4

Both interleukin-3 and interleukin-6 are necessary for better ex vivo expansion of CD133+ cells from umbilical cord blood.

Bordeaux-Rego P, Luzo A, Costa FF, Olalla Saad ST, Crosara-Alberto DP. Bordeaux-Rego P, et al. Among authors: olalla saad st. Stem Cells Dev. 2010 Mar;19(3):413-22. doi: 10.1089/scd.2009.0098. Stem Cells Dev. 2010. PMID: 19656071

5

Increased adhesive and inflammatory properties in blood outgrowth endothelial cells from sickle cell anemia patients.

Sakamoto TM, Lanaro C, Ozelo MC, Garrido VT, Olalla-Saad ST, Conran N, Costa FF. Sakamoto TM, et al. Among authors: olalla saad st. Microvasc Res. 2013 Nov;90:173-9. doi: 10.1016/j.mvr.2013.10.002. Epub 2013 Oct 18. Microvasc Res. 2013. PMID: 24144783

6

Stathmin 1 is involved in the highly proliferative phenotype of high-risk myelodysplastic syndromes and acute leukemia cells.

Machado-Neto JA, de Melo Campos P, Favaro P, Lazarini M, Lorand-Metze I, Costa FF, Olalla Saad ST, Traina F. Machado-Neto JA, et al. Among authors: olalla saad st. Leuk Res. 2014 Feb;38(2):251-7. doi: 10.1016/j.leukres.2013.11.013. Epub 2013 Dec 1. Leuk Res. 2014. PMID: 24355524

7

ANKHD1 silencing inhibits Stathmin 1 activity, cell proliferation and migration of leukemia cells.

Machado-Neto JA, Lazarini M, Favaro P, de Melo Campos P, Scopim-Ribeiro R, Franchi Junior GC, Nowill AE, Lima PR, Costa FF, Benichou S, Olalla Saad ST, Traina F. Machado-Neto JA, et al. Among authors: olalla saad st. Biochim Biophys Acta. 2015 Mar;1853(3):583-93. doi: 10.1016/j.bbamcr.2014.12.012. Epub 2014 Dec 16. Biochim Biophys Acta. 2015. PMID: 25523139 Free article.

8

Low Ten-eleven-translocation 2 (TET2) transcript level is independent of TET2 mutation in patients with myeloid neoplasms.

Scopim-Ribeiro R, Machado-Neto JA, de Melo Campos P, Niemann FS, Lorand-Metze I, Costa FF, Olalla Saad ST, Traina F. Scopim-Ribeiro R, et al. Among authors: olalla saad st. Diagn Pathol. 2016 Mar 16;11:28. doi: 10.1186/s13000-016-0476-4. Diagn Pathol. 2016. PMID: 26984174 Free PMC article.

9

Cytokine polymorphisms in sickle cell disease and the relationship with cytokine expression.

Olenscki Gilli SC, Pericole FV, Benites BD, Sippert EÂ, Castilho LM, Addas-Carvalho M, Olalla Saad ST. Olenscki Gilli SC, et al. Among authors: olalla saad st. Exp Hematol. 2016 Jul;44(7):583-9. doi: 10.1016/j.exphem.2016.03.008. Epub 2016 Mar 26. Exp Hematol. 2016. PMID: 27026283 Free article.

10

Amputations in Sickle Cell Disease: Case Series and Literature Review.

Maximo C, Olalla Saad ST, Thome E, Queiroz AM, Lobo C, Ballas SK. Maximo C, et al. Among authors: olalla saad st. Hemoglobin. 2016 Jun;40(3):150-5. doi: 10.3109/03630269.2016.1167736. Hemoglobin. 2016. PMID: 27117565 Review.

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