Torti, Lorenza

Torti, Lorenza  

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Data di pubblicazione Titolo Autore(i) File
1-gen-2013 Hypoxia-inducible factor-1α(Pro-582-Ser) polymorphism prevents iron deprivation in healthy blood donors Torti, Lorenza; Teofili, Luciana; Capodimonti, Sara; Nuzzolo, Eugenia Rosa; Iachininoto, Maria Grazia; Massini, Giuseppina; Coluzzi, S; Tafuri, A; Fiorin, F; Girelli, G; Zini, Gina; Larocca, Luigi Maria
1-gen-2011 Endothelial progenitor cells are clonal and exhibit the JAK2(V617F) mutation in a subset of thrombotic patients with Ph-negative myeloproliferative neoplasms Teofili, Luciana; Martini, Maurizio; Iachininoto, Mg; Capodimonti, Sara; Nuzzolo, Er; Torti, Lorenza; Cenci, Tonia; Larocca, Luigi Maria; Leone, Giuseppe
1-gen-2010 Detrimental clinical interaction between ritonavir-boosted protease inhibitors and vinblastine in HIV-infected patients with Hodgkin's lymphoma Cingolani, Antonella; Torti, Lorenza; Pinnetti, Carmela; De Gaetano Donati, Katleen; Murri, Rita; Tacconelli, Evelina; Larocca, Luigi Maria; Teofili, Luciana
1-gen-2010 Endothelial progenitor cell trafficking in human immunodeficiency virus-infected persons Teofili, Luciana; Iachininoto, Mg; Capodimonti, Sara; Ucciferri, C; Nuzzolo, Er; Martini, Maurizio; Torti, Lorenza; Falasca, K; Vecchiet, J; Leone, Giuseppe; Larocca, Luigi Maria
1-gen-2010 Essential thrombocythemia as underlying cause of malabsorption syndrome. Teofili, Luciana; Torti, Lorenza; Cina, Alessandro; Gasbarrini, Antonio; Novi, Marialuisa; Leone, Giuseppe; Larocca, Luigi Maria
1-gen-2010 Hereditary thrombocytosis caused by MPLSer505Asn is associated with a high thrombotic risk, splenomegaly and progression to bone marrow fibrosis Teofili, Luciana; Giona, Fiorina; Torti, Lorenza; Cenci, Tonia; Ricerca, Bianca Maria; Rumi, Carlo; Nunes, V; Foa', R; Leone, Giuseppe; Martini, Maurizio; Larocca, Luigi Maria
1-gen-2010 Thrombopoietin receptor activation, thrombopoietin mimetic drugs, and hereditary thrombocytosis: remarks on bone marrow fibrosis Teofili, Luciana; Giona, F; Martini, Maurizio; Torti, Lorenza; Cenci, Tonia; Foa', R; Leone, Giuseppe; Larocca, Luigi Maria
1-gen-2009 The mutant JAK2 allele burden in children with essential thrombocythemia Teofili, Luciana; Cenci, Tonia; Martini, Maurizio; Capodimonti, Sara; Torti, Lorenza; Giona, Fiorina; Amendola, Angela; Randi, Maria Luigia; Putti, Maria Caterina; Scapin, Margherita; Leone, Giuseppe; Larocca, Luigi Maria
1-gen-2008 A novel heterozygous HIF2AM535I mutation reinforces the role of oxygen sensing pathway disturbances in the pathogenesis of familial erythrocytosis Martini, Maurizio; Teofili, Luciana; Cenci, Tonia; Giona, Fiorina; Torti, Lorenza; Rea, Massimiliano; Foà, Robin; Leone, Giuseppe; Larocca, Luigi Maria
1-gen-2008 Epigenetic alteration of SOCS family members is a possible pathogenetic mechanism in JAK2 wild type myeloproliferative diseases Teofili, Luciana; Martini, Maurizio; Cenci, Tonia; Guidi, Francesco; Torti, Lorenza; Giona, Fiorina; Foà, Robin; Leone, Giuseppe; Larocca, Luigi Maria
1-gen-2007 Different STAT-3 and STAT-5 phosphorylation discriminates among Ph-negative chronic myeloproliferative diseases and is independent of the V617F JAK-2 mutation. Teofili, Luciana; Martini, Maurizio; Cenci, Tonia; Petrucci, Giovanna; Torti, Lorenza; Storti, Sergio; Guidi, Francesco; Leone, Giuseppe; Larocca, Luigi Maria
1-gen-2007 The revised WHO diagnostic criteria for Ph-negative myeloproliferative diseases are not appropriate for the diagnostic screening of childhood polycythemia vera and essential thrombocythemia Teofili, Luciana; Giona, Fiorina; Martini, Maurizio; Cenci, Tonia; Guidi, Francesco; Torti, Lorenza; Palumbo, Giovanna; Amendola, Angela; Leone, Giuseppe; Foà, Robin; Larocca, Luigi Maria