Francesco Barone | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Von Willebrand factor with increased binding capacity is associated with reduced platelet aggregation but enhanced agglutination in COVID-19 patients: another COVID-19 paradox?	JOURNAL OF THROMBOSIS AND THROMBOLYSIS	2021
Single centre experience on Acquired Haemophilia A patients: Diagnosis, clinical management and analysis of factors predictive of response and outcome	HAEMOPHILIA	2021
Effect of low or high doses of low‐molecular‐weight heparin on thrombin generation and other haemostasis parameters in critically ill patients with COVID‐19	BRITISH JOURNAL OF HAEMATOLOGY	2020
Acquired FXIII deficiency and AL amyloidosis: A case of a rare association	TRANSFUSION AND APHERESIS SCIENCE	2020
Application of Global Coagulation Assays in Hemophilia B Patients to Evaluate the Hemostatic Potential in Baseline Conditions	HAEMOPHILIA	2017
Application of global coagulation assays in hemophilia B patients to evaluate the hemostatic potential in baseline conditions and after FIX concentrate administration	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2016
Investigation of possible correlation between clinical and laboratory phenotype in congenital FXI deficiency: results from a single center	HAEMOPHILIA	2016
Application of global coagulation assays in Hemophilia B patients to evaluate the hemostatic potential in baseline conditions and after FIX concentrate administration	HAEMOPHILIA	2016
Investigation of possible correlation between clinical and laboratory phenotype in congenital FXI deficiency: results from a single center	JOURNAL OF THROMBOSIS AND HAEMOSTASIS	2016
Investigation of Possible Correlation Between Clinical and Laboratory Phenotype in Congenital FXI Deficiency: Results from a Single Center	HAEMOPHILIA	2016
THROMBOPOIETIN RECEPTOR AGONISTS IN PATIENTS AFFECTED BY PRIMARY IMMUNE THROMBOCYTOPENIA: ANALYSIS OF POSSIBLE PREDICTIVE FACTORS FOR SUSTAINED AND DURABLE RESPONSE FROM A RETROSPECTIVE CASE SERIES	HAEMATOLOGICA	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
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
Bleeding phenotype and correlation with factor XI (FXI) activity in congenital FXI deficiency: Results of a retrospective study from a single centre	HAEMOPHILIA	2015