Sfoglia per Rivista
[Clinical use of hematopoietic growth factors]
1991 A. M. Gianni, M. Bregni, S. Siena, C. Tarella, M. DiNicola, G. Bonadonna
Clinico-biological characterization of a subset of variant B-CLL, defined according to a combined cytofluorimetric/fish diagnostic approach
2009 A. Ferrario, L. Cro, L. Baldini, N. Zucal, R.L. Nobili, A. Neri, M. Lionetti, S. Fabris, F. Bertoni, F. Morabito, G. Cutrona, A. Cortelezzi, A. Guffanti, M. Goldaniga, L. Marcheselli, M. Ferrarini, G. Lambertenghi Deliliers
The clinico-biological features of a B-CLL variant, defined according to a combined cytofluorimetric/fish diagnostic approach
2007 L. Cro, L. Baldini, N. Zucal, A. Ferrario, L. Nobili, A. Neri, M. Lionetti, F. Bertoni, F. Morabito, G. Cutrona, A. Cortelezzi, A. Guffanti, M. Goldaniga, S. Luminari, M. Ferrarini, G. Lambertenghi Deliliers
Clinico-biological implications of adiponectin serum levels in chronic lymphocytic leukemia
2010 S. Molica, G. Di Giesi, G. Cutrona, K. Todoerti, R. Mirabelli, D. Giannarelli, I. Sperduti, M. Gentile, F. Morabito, A. Neri, M. Ferrarini, A. Vacca, D. Ribatti
Clinico-prognostic relevance of serum and cellular expression of adiponectin in early b-cell chronic lymphocytic leukemia
2007 S. Molica, G. Vitelli, G. Cutrona, K. Todoerti, R. Mirabelli, G. Digiesi, D. Giannarelli, I. Sperduti, F. Morabito, A. Neri, M. Ferrarini
Clonal eosinophils are a morphologic hallmark of ETV6/ABL1 positive acute myeloid leukemia
2002 R. La Starza, M. Trubia, N. Testoni, E. Ottaviani, E. Belloni, B. Crescenzi, M. Martelli, G. Flandrin, P. G. Pelicci, C. Mecucci
Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activity
2018 I. Donadon, J.H. Mcvey, I. Garagiola, A. Branchini, M. Mortarino, F. Peyvandi, F. Bernardi, M. Pinotti
Coagulation and platelet activation after retinal vein occlusion
1982 D. Mari, M. Santori, F. Bertoni, P.M Mannucci
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions
2006 R. Asselta, C. Dall'Osso, S. Duga, M. Spreafico, R. Saxena, M.L. Tenchini
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
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