Browsing by Author Visconte, Valeria

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PreviewIssue DateTitleAuthor(s)AdvisorType
2014Familial Systemic Mastocytosis With Germline Kit K509i Mutation Is Sensitive To Treatment With Imatinib, Dasatinib And Pkc412.de Melo Campos, Paula; Machado-Neto, João A; Scopim-Ribeiro, Renata; Visconte, Valeria; Tabarroki, Ali; Duarte, Adriana S S; Barra, Flávia F C; Vassalo, José; Rogers, Heesun J; Lorand-Metze, Irene; Tiu, Ramon V; Costa, Fernando F; Olalla Saad, Sara T; Traina, Fabiola-Artigo de periódico
2012SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromesVisconte, Valeria; Rogers, Heesun J.; Singh, Jarnail; Barnard, John; Bupathi, Manoj; Traina, Fabiola; McMahon, James; Makishima, Hideki; Szpurka, Hadrian; Jankowska, Anna; Jerez, Andres; Sekeres, Mikkael A.; Saunthararajah, Yogen; Advani, Anjali S.; Copelan, Edward; Koseki, Haruhiko; Isono, Kyoichi; Padgett, Richard A.; Osman, Sami; Koide, Kazunori; O'Keefe, Christine; Maciejewski, Jaroslaw P.; Tiu, Ramon V.-Artigo de periódico
2012Molecular Mutations in U2AF1 Are Most Commonly Found in Del20q Myelodysplastic Syndromes but Do Not Lead to Poor Prognosis in This Karyotypic SubtypeTabarroki, Ali; Zhang, Li; Visconte, Valeria; Bupathi, Manoj; Rogers, Heesun J.; Makishima, Hideki; Traina, Fabiola; Hamilton, Betty K.; Hasrouni, Edy; Clemente, Michael J.; Campos, Paula de Melo; Duong, Hien K.; Advani, Anjali; Sekeres, Mikkael A.; Copelan, Edward A.; Tiu, Ramon V.-Artigo de periódico