Sfoglia per Rivista
The coagulopathy of cirrhosis assessed by thromboelastography and its correlation with conventional coagulation parameters
2008 V. Chantarangkul, A. Tripodi, Y. Viscardi, M. Primignani, A. Dell'Era, F.M. Fabris, L. Padovan, P.M. Mannucci
Combination of deferasirox and deferoxamine in clinical practice : alternative schemes of chelation in Thalassemia major (TM) patients
2013 E. Cassinerio, L. Zanaboni, A. Roghi, E. Poggiali, I. Gandolfi, M. Mazzoleni, L. Duca, N. Orofino, M. Cappellini
Combined lamivudine and adefovir dipivoxil treatment allows safe and long-term compath-1H therapy in refractory B-cell chronic lymphocytic leukemia with HBV reactivation
2005 A. Cortelezzi, M. Viganò, V.R. Zilioli, N.N. Fantini, M.C. Pasquini, M. Colombo, G. Lambertenghi Deliliers, P. Lampertico
Comparative transcript profiling of human platelets from patients with stable angina and acute coronary syndromes
2008 K. Gertow, G. Colombo, M. Brambilla, G. Marenzi, L. Ruggiero, M. De Metrio, D. Colnago, R. Bonzi, P. Biglioli, E. Tremoli, M. Camera
Comparison between spontaneously occurring and post-transplant metabolic syndrome
2009 C. Annaloro, L. Airaghi, S. Forti, P. Usardi, F. Onida, A. Della Volpe, E. Tagliaferri, G. Lambertenghi Deliliers
Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects
2019 M.M. Gorski, A. Lecchi, E.A. Femia, S. La Marca, A. Cairo, E. Pappalardo, L.A. Lotta, A. Artoni, F. Peyvandi
Comportamento delle mutazioni driver e non driver nei pazienti con Mielofibrosi in trattamento con Ruxolitinib
2018 S. Galimberti, S. Balducci, F. Guerrini, S. Grassi, M.G. Massantini, F. Ricci, D. Cattaneo, A. Iurlo, P. Vigneri, M. Petrini, G.A. Palumbo, C. Baratè
Conditions influencing the expansion of the circulating hemopoietic progenitor cell compartment
1990 C. Tarella, D. Ferrero, S. Siena, E. Gallo, P. Bondesan, M. Bregni, A. Pileri, A. Gianni
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran
2006 L. Monaldini, R. Asselta, S. Duga, F. Peyvandi, M. Malcovati, M.L. Tenchini
Congenital bleeding disorders and pregnancy
2005 A. Gringeri
Congenital deficiencies of anticoagulant proteins (Antithrombin III and Protein C)
1984 P.M. Mannucci, A. Tripodi, D. Mari
Conjunctival hemorrhagic events associated with imatinib
2007 F. Radaelli, C. Vener, F. Ripamonti, A. Iurlo, M. Colombi, A. Artoni, G. Reda, G. Lambertenghi Deliliers
Conjunctival hemorrhagic events associated with imatinib mesylate
2009 F. Radaelli, C. Vener, F. Grifoni, D. Vincenti, A. Iurlo, M. Colombi, A.S.A. Ciani, A. Artoni, A. Zanella, G. Lambertenghi Deliliers
Constitutively released adenosine diphosphate regulates proplatelet formation by human megakaryocytes
2012 A. Balduini, C.A. Di Buduo, A. Malara, A. Lecchi, P. Rebuzzini, M. Currao, I. Pallotta, J.A. Jakubowski, M. Cattaneo
Continued improvement in cardiac T2* with deferasirox treatment over 2 years : results from the extension of epic cardiac substudy in beta-thalassaemia patients with myocardial siderosis
2010 D. Pennell, J. Porter, M.D. Cappellini, L.L. Chan, A. El Beshlawy, Y. Aydinok, H. Ibrahim, C.K. Li, V. Viprakasit, M. Elalfy, A. Kattamis, G. Smith, D. Habr, B. Roubert, A. Taher
Continued improvement in myocardial T2* over two years of deferasirox therapy in β-thalassemia major patients with cardiac iron overload
2011 D. J. Pennell, J. B. Porter, M. D. Cappellini, L. L. Chan, A. El-Beshlawy, Y. Aydinok, H. Ibrahim, C. K. Li, V. Viprakasit, M. S. Elalfy, A. Kattamis, G. Smith, D. Habr, G. Domokos, B. Roubert, A. Taher
Contribution of bone marrow derived cell angiogenesis in bcr/abl negative chronic myeloproliferative disease
2009 G. Gritti, A. Cortelezzi, U. Gianelli, S. Lonati, I. Silvestris, C. Vener, F. Radaelli, G. Lambertenghi Deliliers
Control of iron homeostasis as a key component of macrophage polarization
2010 G. Cairo, M. Locati, A. Mantovani
Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency
2013 R. Bottega, A. Pecci, E. De Candia, N. Pujol Moix, P.G. Heller, P. Noris, D. De Rocco, G.M. Podda, A.C. Glembotsky, M. Cattaneo, C.L. Balduini, A. Savoia
Correlation of genomic aberrations with the mutational status of immunoglobulin heavy-chain variable region, ZAP-70 and CD38 expression in chronic lymphocytic leukemia
2005 F. Morabito, S. Fabris, G. Cutrona, S. Matis, C. Sleitano, M. Brugiatelli, C. Mammi, M. Spriano, E. Rossi , V. Callea, S. Zupo, M. Ferrarini, A. Neri
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