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Page 1
Bridging to transplant with azacitidine in juvenile myelomonocytic leukemia: a retrospective analysis of the EWOG-MDS study group.
Cseh A, Niemeyer CM, Yoshimi A, Dworzak M, Hasle H, van den Heuvel-Eibrink MM, Locatelli F, Masetti R, Schmugge M, Groß-Wieltsch U, Candás A, Kulozik AE, Olcay L, Suttorp M, Furlan I, Strahm B, Flotho C. Cseh A, et al. Among authors: candas a. Blood. 2015 Apr 2;125(14):2311-3. doi: 10.1182/blood-2015-01-619734. Blood. 2015. PMID: 25838281 Free article. No abstract available.
Phenotypic and genotypic characterization of glucose-6-phosphate dehydrogenase deficiency in Argentina. Retrospective and descriptive study.
Eandi Eberle S, Pepe C, Chaves A, Aguirre F, Milanesio B, Fernández D, Ávalos Gómez V, Sciuccati G, Díaz LA, Candas A, Cervio C, Bonduel M, Feliu Torres A. Eandi Eberle S, et al. Among authors: candas a. Arch Argent Pediatr. 2019 Aug 1;117(4):263-270. doi: 10.5546/aap.2019.eng.267. Arch Argent Pediatr. 2019. PMID: 31339274 Free article. English, Spanish.
[Glucose 6 phosphate dehydrogenase deficiency: a case series].
Eandi Eberle S, García Rosolen N, Urtasun C, Sciuccati G, Díaz L, Savietto V, Candás A, Avalos Gómez V, Cervio C, Bonduel M, Feliú Torres A. Eandi Eberle S, et al. Among authors: candas a. Arch Argent Pediatr. 2011 Aug;109(4):354-6. doi: 10.5546/aap.2011.354. Arch Argent Pediatr. 2011. PMID: 21829878 Spanish.
[Severe hemolytic anemia due to hemoglobin Southampton: case report].
Avalos Gómez V, Eandi Eberle S, Pepe C, Sciuccati G, García Rosolen N, Cervio C, Díaz L, Candás A, Bonduel M, Piazza G, Chaves D, Feliú Torres A. Avalos Gómez V, et al. Among authors: candas a. Arch Argent Pediatr. 2012 Oct;110(5):e91-4. doi: 10.5546/aap.2012.e91. Arch Argent Pediatr. 2012. PMID: 23070193 Free article. Spanish.
[Beta thalassemia intermedia: clinical characteristics and molecular analysis. Case series].
Eandi Eberle S, Pepe C, Aguirre F, Milanesio B, Fernández D, Mansini A, Chávez A, Sciuccati G, Díaz L, Candás A, Avalos Gómez V, Bonduel M, Feliú Torres A. Eandi Eberle S, et al. Among authors: candas a. Arch Argent Pediatr. 2015 Oct;113(5):e294-8. doi: 10.5546/aap.2015.e294. Arch Argent Pediatr. 2015. PMID: 26294166 Free article. Spanish.
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: candas a. Hemoglobin. 2014;38(6):444-6. doi: 10.3109/03630269.2014.964361. Epub 2014 Sep 30. Hemoglobin. 2014. PMID: 25268796