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Page 1
A new β(0) frameshift mutation, HBB: c.44delT (p.Leu14ArgfsX5), identified in an Argentinean family associated with secondary genetic modifiers of β-thalassemia.
Pepe C, Eberle SE, Chaves A, Milanesio B, Aguirre FM, Gómez VA, Diaz L, Mansini AP, Fernandez DA, Sciuccati G, Candas A, Cervio C, Bonduel M, Feliú-Torres A. Pepe C, et al. Among authors: eberle se. Hemoglobin. 2014;38(6):444-6. doi: 10.3109/03630269.2014.964361. Epub 2014 Sep 30. Hemoglobin. 2014. PMID: 25268796
[Erythrocyte indexes in hereditary spherocytosis].
Eberle SE, Sciuccati G, Bonduel M, Díaz L, Staciuk R, Torres AF. Eberle SE, et al. Medicina (B Aires). 2007;67(6 Pt 2):698-700. Medicina (B Aires). 2007. PMID: 18422060 Clinical Trial. Spanish.
[Effect of hydroxyurea on hemoglobin S].
Torres AF, Eberle SE, Sciuccati G, Bonduel M. Torres AF, et al. Among authors: eberle se. Medicina (B Aires). 2003;63(2):140-2. Medicina (B Aires). 2003. PMID: 12793083 Spanish.
Lineage switch in childhood acute leukemia: an unusual event with poor outcome.
Rossi JG, Bernasconi AR, Alonso CN, Rubio PL, Gallego MS, Carrara CA, Guitter MR, Eberle SE, Cocce M, Zubizarreta PA, Felice MS. Rossi JG, et al. Among authors: eberle se. Am J Hematol. 2012 Sep;87(9):890-7. doi: 10.1002/ajh.23266. Epub 2012 Jun 8. Am J Hematol. 2012. PMID: 22685031 Free article.
Persistent pain alters AMPA receptor subunit levels in the nucleus accumbens.
Su C, D'amour J, Lee M, Lin HY, Manders T, Xu D, Eberle SE, Goffer Y, Zou AH, Rahman M, Ziff E, Froemke RC, Huang D, Wang J. Su C, et al. Among authors: eberle se. Mol Brain. 2015 Aug 12;8:46. doi: 10.1186/s13041-015-0140-z. Mol Brain. 2015. PMID: 26260133 Free PMC article.
14 results