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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: sciuccati g. Hemoglobin. 2014;38(6):444-6. doi: 10.3109/03630269.2014.964361. Epub 2014 Sep 30. Hemoglobin. 2014. PMID: 25268796
Familial idiopathic myelofibrosis and multiple hemangiomas.
Bonduel M, Sciuccati G, Torres AF, Pierini A, Gallo G. Bonduel M, et al. Among authors: sciuccati g. Am J Hematol. 1998 Oct;59(2):175-7. doi: 10.1002/(sici)1096-8652(199810)59:2<175::aid-ajh13>3.0.co;2-8. Am J Hematol. 1998. PMID: 9766805 Free article.
Factor V Leiden mutation in the Argentinian population.
Hepner M, Roldan A, Pieroni G, Frontroth JP, Serviddio RM, Torres AF, Sciuccati G, Bonduel M. Hepner M, et al. Among authors: sciuccati g. Thromb Haemost. 1999 Jun;81(6):989. Thromb Haemost. 1999. PMID: 10404780 No abstract available.
Prothrombotic abnormalities in children with venous thromboembolism.
Bonduel M, Hepner M, Sciuccati G, Torres AF, Pieroni G, Frontroth JP. Bonduel M, et al. Among authors: sciuccati g. J Pediatr Hematol Oncol. 2000 Jan-Feb;22(1):66-72. doi: 10.1097/00043426-200001000-00013. J Pediatr Hematol Oncol. 2000. PMID: 10695825
Prothrombotic disorders in children with moyamoya syndrome.
Bonduel M, Hepner M, Sciuccati G, Torres AF, Tenembaum S. Bonduel M, et al. Among authors: sciuccati g. Stroke. 2001 Aug;32(8):1786-92. doi: 10.1161/01.str.32.8.1786. Stroke. 2001. PMID: 11486106 Clinical Trial.
[Beta thalassemia major in Argentina].
Torres FA, Bonduel M, Sciuccati G, del Pozo A, Roldán A, Ciaccio M, Orazi V, Fano V, Ozuna B, Lejarraga H, Muriel SF. Torres FA, et al. Among authors: sciuccati g. Medicina (B Aires). 2002;62(2):124-34. Medicina (B Aires). 2002. PMID: 12038033 Spanish.
36 results