Cristina Santoro | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
OUTCOMES OF 65 PREGNANCIES IN 34 WOMEN WITH 5 DIFFERENT FORMS OF INHERITED PLATELET FUNCTION DISORDERS ENROLLED IN A RETROSPECTIVE AND MULTICENTRIC STUDY	HAEMATOLOGICA	2015
BLEEDING RISK OF SURGERY IN PATIENTS WITH INHERITED PLATELET FUNCTION DISORDERS (IPFD): OUTCOME OF 389 SURGERIES IN 205 PATIENTS	HAEMATOLOGICA	2015
HOW DIAGNOSTIC AND THERAPEUTIC APPROACHE CHANGED IN THE LAST DECADES IN THE PHILADELPHIA NEGATIVE MPN PATIENTS OF THE REGISTRO ITALIANO TROMBOCITEMIE (RIT)	HAEMATOLOGICA	2015
Predictors of success of immune tolerance induction in hemophilia a patients with high-responding inhibitors. A prognostic score from the Italian profit registry	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2015
Functional effects of F8 missense mutations on DDAVP response in nonsevere hemophilia A brothers	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2015
Investigating potential determinants of ITI success using immune gene expression profiling: a preliminary study	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2015
A case of thrombosis in congenital afibrinogenemia patient: a physiopathologic and management dilemma	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2015
Inhibitors in Hemophilia (HA): experience of a single center in the last 22 years	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2015
Cancers in patients with von Willebrand disease: a survey from the Italian association of hemophilia centres	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2015
Outcomes of 65 pregnancies in 34 women with 5 different forms of inherited platelet function disorders enrolled in a retrospective and multicentric study, on behalf of eha-swg on thrombocytopenias and platelet function disorders	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2015
Congenital FXI deficiency: preliminary results of phenotypic (clinical and laboratory) and genotypic characterization of a case series from a single center	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2015
Inhibitors in Haemophilia A: Experience of A Single Center in The Last 20 Years	HAEMOPHILIA	2015
A Case Of Thrombosis In Congenital Afibrinogenemia: A Physiopathologic And Management Dilemma	HAEMOPHILIA	2015
Congenital FXI Deficiency: Preliminary Results Of Phenotypic (Clinical And Laboratory) And Genotypic Characterization Of A Case Series From A Single Center	HAEMOPHILIA	2015
ROLE OF TREATMENT ON THE DEVELOPMENT OF SECONDARY MALIGNANCIES IN PATIENTS WITH ESSENTIAL THROMBOCYTEMIA	HAEMATOLOGICA	2015
IDO1 suppresses inhibitor development in hemophilia A treated with factor VIII	THE JOURNAL OF CLINICAL INVESTIGATION	2015
Inhibitor development and mortality in non-severe hemophilia A	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2015
Benefits of prophylaxis versus on-demand treatment in adolescents and adults with severe haemophilia A: The POTTER study	THROMBOSIS AND HAEMOSTASIS	2015
Bleeding phenotype and correlation with factor XI (FXI) activity in congenital FXI deficiency: Results of a retrospective study from a single centre	HAEMOPHILIA	2015
Rituximab for treating inhibitors in people with inherited severe hemophilia	COCHRANE DATABASE OF SYSTEMATIC REVIEWS	2015