Hematopoietic SCT for the Black African and non-Black African variants of sickle cell anemia von Lucarelli, G, Isgrò, A, Sodani, P, Marziali, M, Gaziev, J, Paciaroni, K, Gallucci, C, Cardarelli, L, Ribersani, M, Alfieri, C, De Angelis, G, Armiento, D, Andreani, M, Testi, M, Amato, A, Akinyanju, O O, Wakama, T T

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Pathogenesis of chronic rhinosinusitis in patients affected by β-thalassemia major and sickle cell anaemia post allogenic bone marrow transplant von Martino, F., Di Mauro, R., Paciaroni, K., Gaziev, J., Alfieri, C., Greco, L., Floris, R., Di Girolamo, S., Di Girolamo, M.

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Allogeneic cellular gene therapy in hemoglobinopathies-evaluation of hematopoietic SCT in sickle cell anemia von Lucarelli, G, Gaziev, J, Isgrò, A, Sodani, P, Paciaroni, K, Alfieri, C, De Angelis, G, Marziali, M, Simone, M D, Gallucci, C, Roveda, A, Saltarelli, F, Torelli, F, Andreani, M

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Higher CD3 and CD34 cell doses in the graft increase the incidence of acute GVHD in children receiving BMT for thalassemia von Gaziev, J, Isgrò, A, Marziali, M, Daniele, N, Gallucci, C, Sodani, P, Simone, M D, Adorno, G, Paciaroni, K, Andreani, M, Lanti, A, Del Proposto, G, Testi, M, De Angelis, G, Roveda, A, Alfieri, C, Saltarelli, F, Lucarelli, G

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Second hematopoietic SCT in patients with thalassemia recurrence following rejection of the first graft von Gaziev, J, Sodani, P, Lucarelli, G, Polchi, P, Marktel, S, Paciaroni, K, Marziali, M, Isgrò, A, Simone, M D, Roveda, A, Montuoro, A, Lanti, A, Alfieri, C, De Angelis, G, Gallucci, C, Ciceri, F, Roncarolo, M G

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G20210A Prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects von Burzotta, F, Paciaroni, K, De Stefano, V, Crea, F, Maseri, A, Leone, G, Andreotti, F

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Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease von Burzotta, F., Paciaroni, K., De Stefano, V., Chiusolo, P., Manzoli, A., Casorelli, I., Leone, A.M., Rossi, E., Leone, G., Maseri, A., Andreotti, F.

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The Risk of Recurrent Deep Venous Thrombosis among Heterozygous Carriers of Both Factor V Leiden and the G20210A Prothrombin Mutation von De Stefano, Valerio, Martinelli, Ida, Mannucci, Pier Mannuccio, Paciaroni, Katia, Chiusolo, Patrizia, Casorelli, Ida, Rossi, Elena, Leone, Giuseppe

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Screening for inherited thrombophilia: indications and therapeutic implications von De Stefano, V, Rossi, E, Paciaroni, K, Leone, G

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Recurrent deep vein thrombosis after the insertion of two vascular accesses in a 13-year-old thalassemic girl waiting for a haploidentical marrow transplant von Roveda, A, Sodani, P, Paciaroni, K, Gallucci, C, Lucarelli, G, Tenze, G

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Inherited Thrombophilia and First Venous Thromboembolism during Pregnancy and Puerperium von Martinelli, Ida, De Stefano, Valerio, Taioli, Emanuela, Paciaroni, Katia, Rossi, Elena, Pier, Mannucci Mannuccio

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Prevalence of the C536T Mutation in the Tissue Factor Pathway Inhibitor (TFPI) Gene among Patients with Venous Thromboembolic Disease von Paciaroni, Katia, Rossi, Elena, Bazzan, Mario, Ireland, Helen, Stefano, Valerio De

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Different Risks of Thrombosis in Four Coagulation Defects Associated With Inherited Thrombophilia: A Study of 150 Families von Martinelli, Ida, Mannucci, Pier Mannuccio, De Stefano, Valerio, Taioli, Emanuela, Rossi, Valentina, Crosti, Francesca, Paciaroni, Katia, Leone, Giuseppe, Faioni, Elena M.

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Prevalence of factor V Leiden and the G20210A prothrombin-gene mutation in inflammatory bowel disease von Papa, A, De Stefano, V, Gasbarrini, A, Chiusolo, P, Cianci, R, Casorelli, I, Paciaroni, K, Cammarota, G, Leone, G, Gasbarrini, G

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G20210A Prothrombin Gene Polymorphism and Extent of Coronary Disease von Burzotta, Francesco, Paciaroni, Katia, Andreotti, Felicita, Casorelli, Ida, De Stefano, Valerio

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807CC genotype of the platelet Gp Ia could represent a protective factor for recurrences of acute coronary events in acute coronary syndromes von Leone, Antonio Maria, Casorelli, I., Burzotta, F., Paciaroni, K., Sciahbasi, A., De Stefano, V., Leone, G., Andreotti, F., Maseri, A.

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Prothrombin G20210A Mutant Genotype Is a Risk Factor for Cerebrovascular Ischemic Disease in Young Patients von De Stefano, Valerio, Chiusolo, Patrizia, Paciaroni, Katia, Casorelli, Ida, Rossi, Elena, Molinari, Marco, Servidei, Serenella, Tonali, Pietro A., Leone, Giuseppe

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Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients von DE STEFANO, V, CHIUSOLO, P, PACIARONI, K, CASORELLI, I, ROSSI, E, MOLINARI, M, SERVIDEI, S, TONALI, P. A, LEONE, G

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Epidemiology of Factor V Leiden: Clinical Implications von de Stefano, Valerio, Chiusolo, Patrizia, Paciaroni, Katia, Leone, Giuseppe

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The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation von De Stefano, Valerio, Martinelli, Ida, Mannucci, Pier Mannuccio, Paciaroni, Katia, Rossi, Elena, Chiusolo, Patrizia, Casorelli, Ida, Leone, Giuseppe

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