Sfoglia per Autore
A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding
2020 Girolami, A.; Ferrari, S.; Cosi, E.
Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States
2020 Girolami, A.; Ferrari, S.; Cosi, E.; Girolami, B.
African and African-American Contribution to the Knowledge of the FVII Padua (Arg304Gln) Defect
2020 Girolami, A.; Ferrari, S.; Cosi, E.
The Dysprothrombinemias due to Arg596 Mutations: A Conundrum With No Bleeding Tendency and Venous Thrombosis due to Antithrombin Resistance
2019 Girolami, A.; Ferrari, S.; Cosi, E.; Randi, M. L.
Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period
2019 Girolami, Antonio; Ferrari, Silvia; Cosi, Elisabetta; Girolami, Bruno; Randi, Maria Luigia
Heterozygous FXII deficiency is not associated with an increased incidence of thrombotic events: Results of a long term study
2019 Girolami, Antonio; Ferrari, Silvia; Cosi, Elisabetta; Randi, Maria Luigia
New data on FII, FV, FIX and thrombomodulin defects: blood keeps clotting in normal and in peculiar ways
2019 Girolami, Antonio; Ferrari, Silvia; Girolami, Bruno; Randi, Maria Luigia
Thrombotic events in homozygotes with a proven or highly probable Arg304Gln Factor VII mutation (FVII Padua) 1): only limited replacement therapy is needed in case of surgery
2019 Girolami, Antonio; Cosi, Elisabetta; Ferrari, Silvia; Girolami, Bruno; Randi, Maria Luigia
Vitamin K-Dependent Coagulation Factors That May be Responsible for Both Bleeding and Thrombosis (FII, FVII, and FIX)
2018 Girolami, Antonio; Ferrari, Silvia; Cosi, Elisabetta; Santarossa, Claudia; Randi, Maria Luigia
Heparin, coumarin, protein C, antithrombin, fibrinolysis and other clotting related resistances: old and new concepts in blood coagulation
2018 Girolami, A.; Cosi, E.; Ferrari, S.; Girolami, B.
Cardiovascular diseases in congenital prekallikrein deficiency: Comparison with other chanceassociated morbidities
2018 Girolami, A.; Ferrari, S.; Cosi, E.; Girolami, B.
Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed
2018 Girolami, A.; Ferrari, S.; Cosi, E.; Girolami, B.; Lombardi, A. M.
A structure–function analysis in patients with prekallikrein deficiency
2018 Girolami, A.; Ferrari, S.; Cosi, E.; Lombardi, A. M.
Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis
2018 Girolami, A.; Cosi, E.; Ferrari, S.; Girolami, B.
Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders
2018 Girolami, Antonio; Cosi, Elisabetta; Ferrari, Silvia; Lombardi, Annamaria; Fabris, Fabrizio
Factor X Friuli coagulation disorder: Almost 50 Years Later
2018 Girolami, A.; Cosi, E.; Santarossa, C.; Ferrari, S.; Girolami, B.; Lombardi, A. M.
Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period*
2017 Girolami, A.; Cosi, E.; Ferrari, S.; Girolami, B.; Lombardi, A. M.
New clotting disorders that cast new light on blood coagulation and may play a role in clinical practice
2017 Girolami, A.; Cosi, E.; Ferrari, S.; Lombardi, A. M.; Girolami, B.
Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study
2017 Girolami, A.; Santarossa, C.; Cosi, E.; Ferrari, S.; Lombardi, A. M.; Girolami, B.
Spectrum of 5’UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected
2017 Ferrari, Silvia; Lombardi, ANNA-MARIA; Putti, Maria Caterina; Bertomoro, Antonella; Cortella, Irene; Barzon, Isabella; Girolami, Antonio; Fabris, Fabrizio
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