ArTS Archivio della ricerca di Trieste

Sfoglia per Rivista  HAEMATOLOGICA

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Mostrati risultati da 10 a 29 di 131
Titolo Data di pubblicazione Autori File
B-cell compartment as the selective target for the treatment of immune thrombocytopenias 1-gen-2003 ZAJA, FrancescoDE VITA, SalvatoreFANIN, Renato +
B-cell depletion with rituximab as treatment for autoimmune thrombocytopenia 1-gen-2002 ZAJA, FRANCESCODE VITA, Salvatore +
B-cell depletion with rituximab as treatment for immune hemolytic anemia and chronic thrombocytopenia 1-gen-2002 Zaja F +
B-cell depletion with rituximab as treatment for immune hemolytic anemia and chronic thrombocytopenia 1-gen-2002 ZAJA, FrancescoDE VITA, SalvatoreFANIN, Renato +
A B-cell receptor-related gene signature predicts response to ibrutinib treatment in mantle cell lymphoma cell lines 1-gen-2019 Zucchetto A.Vit F.Bittolo T.Zaja F. +
Benign Idiopathic Hypereosinophilia: A Feeble Masquerader Or A Smouldering Form Of The Hypereosinophilic Syndrome? 1-gen-1995 Marco Confalonieri +
Biological and clinical implications of BIRC3 mutations in chronic lymphocytic leukemia 1-gen-2020 De Paoli L.Zaja F. +
Blood donation and iron deficiency: Another possible face of celiac disease 1-gen-2007 Cannizzaro RCanzonieri V +
Brentuximab vedotin in relapsed/refractory Hodgkin's lymphoma: the Italian experience and results of its use in daily clinical practice outside clinical trials 1-gen-2013 ZAJA, Francesco +
Chlorambucil plus rituximab as front-line therapy for elderly and/or unfit chronic lymphocytic leukemia patients: Correlation with biologically-based risk stratification 1-gen-2017 Pozzato G. +
Chronic GVHD and sequential study of cytokine patterns and lymphocyte subsets in patients underwent allogeneic stem cell transplantation with reduced intensity conditioning 1-gen-2006 DAMIANI, DanielaZAJA, Francesco +
Clinical and genetic aspects Bernard-Soulier syndrome: searching for genotype/phenotype correlations. 1-gen-2011 SAVOIA, ANNADE ROCCO, DANIELADI STAZIO, MARIATERESABOTTEGA, ROBERTA +
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb{alpha} (Bolzano mutation). 1-gen-2012 BOTTEGA, ROBERTADE ROCCO, DANIELASAVOIA, ANNA +
Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia 1-gen-2016 DE ROCCO, DANIELAGNAN, CHIARAFALESCHINI, MICHELASAVOIA, ANNA +
CLL TRANSFORMING TO RICHTER'S SYNDROME CARRY STEROTYPED HCDR3S AT VERY HIGH FREQUENCY (> 50%) AND DISPLAY BIASED USAGE OF HOMOLOGOUS IGHV4-39 GENES 1-gen-2008 Canzonieri V +
Computed tomography, magnetic resonance and gallium 67 scintigraphy for the imaging of residual lymphoma 1-gen-1995 ZAJA, FrancescoFANIN, RenatoZUIANI, Chiara +
Computed tomography, magnetic resonance and gallium 67 scintigraphy for the imaging of residual lymphoma. 1-gen-1995 Zaja F +
Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations 1-gen-2007 SAVOIA, ANNADI STAZIO, MARIATERESA +
Danazol therapy in myelodisplastic syndromes 1-gen-1992 POZZATO, GABRIELE +
Defective expression of GPIb/IX/V complex in platelets from patients with May-Hegglin anomaly and Sebastian syndrome 1-gen-2002 SAVOIA, ANNA +
Mostrati risultati da 10 a 29 di 131
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