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Elisabetta Cosi

Showing results (1-10 of 25) with videos related to

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Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|April 26, 2018
Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and ThrombosisAntonio Girolami, Elisabetta Cosi, Silvia Ferrari, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 16, 2018
Cardiovascular diseases in congenital prekallikrein deficiency: comparison with other chance-associated morbiditiesAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Hematology (Amsterdam, Netherlands)|November 23, 2017
A structure-function analysis in patients with prekallikrein deficiencyAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Blood Cells, Molecules & Diseases|March 19, 2019
Heterozygous FXII deficiency is not associated with an increased incidence of thrombotic events: Results of a long term studyAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|August 5, 2017
Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting DisordersAntonio Girolami, Elisabetta Cosi, Silvia Ferrari, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|August 27, 2014
Myocardial infarctions and other acute coronary syndromes in rare congenital bleeding disorders: a critical analysis of all reported casesAntonio Girolami, Silvia Ferrari, Luisa Sambado, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 19, 2015
Prevalence of hypertension and its complications in congenital prekallikrein deficiency: analysis of all reported cases and clinical significanceAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Journal of Thrombosis and Thrombolysis|January 30, 2019
Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation periodAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Seminars in Thrombosis and Hemostasis|May 15, 2015
The Story of Serum Prothrombin Conversion Accelerator, Proconvertin, Stable Factor, Cothromboplastin, Prothrombin Accelerator or Autoprothrombin I, and Their Subsequent Merging into Factor VIIAntonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Seminars in Thrombosis and Hemostasis|April 16, 2015
Complex history of the discovery and characterization of congenital factor X deficiencyAntonio Girolami, Elisabetta Cosi, Luisa Sambado, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|April 26, 2018
Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and ThrombosisAntonio Girolami, Elisabetta Cosi, Silvia Ferrari, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 16, 2018
Cardiovascular diseases in congenital prekallikrein deficiency: comparison with other chance-associated morbiditiesAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Hematology (Amsterdam, Netherlands)|November 23, 2017
A structure-function analysis in patients with prekallikrein deficiencyAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Blood Cells, Molecules & Diseases|March 19, 2019
Heterozygous FXII deficiency is not associated with an increased incidence of thrombotic events: Results of a long term studyAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|August 5, 2017
Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting DisordersAntonio Girolami, Elisabetta Cosi, Silvia Ferrari, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|August 27, 2014
Myocardial infarctions and other acute coronary syndromes in rare congenital bleeding disorders: a critical analysis of all reported casesAntonio Girolami, Silvia Ferrari, Luisa Sambado, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 19, 2015
Prevalence of hypertension and its complications in congenital prekallikrein deficiency: analysis of all reported cases and clinical significanceAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Journal of Thrombosis and Thrombolysis|January 30, 2019
Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation periodAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Seminars in Thrombosis and Hemostasis|May 15, 2015
The Story of Serum Prothrombin Conversion Accelerator, Proconvertin, Stable Factor, Cothromboplastin, Prothrombin Accelerator or Autoprothrombin I, and Their Subsequent Merging into Factor VIIAntonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.
Seminars in Thrombosis and Hemostasis|April 16, 2015
Complex history of the discovery and characterization of congenital factor X deficiencyAntonio Girolami, Elisabetta Cosi, Luisa Sambado, et al.
Pageof 3