A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding von Girolami, Antonio, Ferrari, Silvia, Cosi, Elisabetta

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Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis von Girolami, Antonio, Cosi, Elisabetta, Ferrari, Silvia, Girolami, Bruno

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Vitamin K-Dependent Coagulation Factors That May be Responsible for Both Bleeding and Thrombosis (FII, FVII, and FIX) von Girolami, Antonio, Ferrari, Silvia, Cosi, Elisabetta, Santarossa, Claudia, Randi, Maria Luigia

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Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States von Girolami, Antonio, Ferrari, Silvia, Cosi, Elisabetta, Girolami, Bruno

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P1014: GERMINAL JAK2 MOLECULAR ALTERATIONS IN PATIENTS WITH IDIOPATHIC ERYTHROCYTOSIS von Benetti, Andrea, Bertozzi, Irene, Cosi, Elisabetta, Luigia Randi, Maria

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The Dysprothrombinemias due to Arg596 Mutations: A Conundrum With No Bleeding Tendency and Venous Thrombosis due to Antithrombin Resistance von Girolami, Antonio, Ferrari, Silvia, Cosi, Elisabetta, Randi, Maria Luigia

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Impact of HFE mutations on thrombotic risk in patients with idiopathic erythrocytosis: A single‐centre study von Bertozzi, Irene, Benetti, Andrea, Cosi, Elisabetta, Zerbinati, Martina, Fortino, Cecilia, Randi, Maria Luigia, Simioni, Paolo

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Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders von Girolami, Antonio, Cosi, Elisabetta, Ferrari, Silvia, Lombardi, Annamaria, Fabris, Fabrizio

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Coexistence of Multiple Gene Variants in Some Patients with Erythrocytoses von Benetti, Andrea, Bertozzi, Irene, Ceolotto, Giulio, Cortella, Irene, Regazzo, Daniela, Biagetti, Giacomo, Cosi, Elisabetta, Randi, Maria Luigia

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Factor X Friuli Coagulation Disorder: Almost 50 Years Later von Girolami, Antonio, Cosi, Elisabetta, Santarossa, Claudia, Ferrari, Silvia, Girolami, Bruno, Lombardi, Anna Maria

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Peculiar, poorly known, rare congenital bleeding disorders presenting thrombotic events: an understudied chapter of molecular, blood coagulation defects von Girolami, Antonio, Cosi, Elisabetta, Ferrari, Silvia, Santarossa, Claudia, Girolami, Bruno

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Systemic Mastocytosis and Essential Thrombocythemia: Case Report and Literature Overview von Cancian, Mauro, Cosi, Elisabetta, Pizzi, Marco, Giannini, Sandro, Bertozzi, Irene, Fabris, Fabrizio, Randi, Maria Luigia

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Myocardial Infarctions and Other Acute Coronary Syndromes in Rare Congenital Bleeding Disorders von Girolami, Antonio, Ferrari, Silvia, Sambado Luisa, Peroni Edoardo, Cosi Elisabetta

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Effect of busulfan on JAK2V617F allele burden von Randi, Maria Luigia, Santarossa, Claudia, Peroni, Edoardo, Cosi, Elisabetta, Duner, Elena, Bertozzi, Irene, Fabris, Fabrizio

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African and African-American Contribution to the Knowledge of the FVII Padua (Arg304Gln) Defect von Girolami, Antonio, Ferrari, Silvia, Cosi, Elisabetta

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Heterozygous FXII deficiency is not associated with an increased incidence of thrombotic events: Results of a long term study von Girolami, Antonio, Ferrari, Silvia, Cosi, Elisabetta, Randi, Maria Luigia

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Cardiovascular diseases in congenital prekallikrein deficiency: comparison with other chance-associated morbidities von Girolami, Antonio, Ferrari, Silvia, Cosi, Elisabetta, Girolami, Bruno

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Role of replacement therapy in the evaluation of thrombosis occurring in congenital bleeding conditions von Girolami, Antonio, Ferrari, Silvia, Cosi, Elisabetta, Girolami, Bruno

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Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period von Girolami, Antonio, Ferrari, Silvia, Cosi, Elisabetta, Girolami, Bruno, Randi, Maria Luigia

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HFE mutations in idiopathic erythrocytosis von Biagetti, Giacomo, Catherwood, Mark, Robson, Nuala, Bertozzi, Irene, Cosi, Elisabetta, McMullin, Mary F., Randi, Maria L.

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