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Mostrati risultati da 1 a 20 di 361
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
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. + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
African and African-American Contribution to the Knowledge of the FVII Padua (Arg304Gln) Defect 2020 Girolami A.Ferrari S.Cosi E. JOURNAL OF THE NATIONAL MEDICAL ASSOCIATION - -
A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding 2020 Girolami A.Cosi E. + JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
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. CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Heterozygous FXII deficiency is not associated with an increased incidence of thrombotic events: Results of a long term study 2019 Girolami, AntonioFerrari, SilviaCosi, ElisabettaRandi, Maria Luigia BLOOD CELLS, MOLECULES, & DISEASES - -
New data on FII, FV, FIX and thrombomodulin defects: blood keeps clotting in normal and in peculiar ways 2019 Girolami, AntonioFerrari, SilviaRandi, Maria Luigia + HEMATOLOGY - -
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, AntonioCosi, ElisabettaFerrari, SilviaRandi, Maria Luigia + CARDIOVASCULAR & HAEMATOLOGICAL DISORDERS - DRUG TARGETS - -
Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period 2019 Girolami, AntonioFerrari, SilviaCosi, ElisabettaRandi, Maria Luigia + JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis 2018 Girolami A.Cosi E.Ferrari S. + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Factor X Friuli coagulation disorder: Almost 50 Years Later 2018 Girolami A.Cosi E.Santarossa C.Ferrari S. + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders 2018 Girolami, AntonioCosi, ElisabettaFerrari, SilviaLombardi, AnnamariaFabris, Fabrizio CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
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. + HEMATOLOGY - -
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. + JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
A structure–function analysis in patients with prekallikrein deficiency 2018 Girolami A.Ferrari S.Cosi E. + HEMATOLOGY - -
Cardiovascular diseases in congenital prekallikrein deficiency: Comparison with other chanceassociated morbidities 2018 Girolami A.Ferrari S.Cosi E. + BLOOD COAGULATION & FIBRINOLYSIS - -
Vitamin K-Dependent Coagulation Factors That May be Responsible for Both Bleeding and Thrombosis (FII, FVII, and FIX) 2018 Girolami, AntonioFerrari, SilviaCosi, ElisabettaSantarossa, ClaudiaRandi, Maria Luigia CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
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. + BLOOD COAGULATION & FIBRINOLYSIS - -
Prethrombotic, prothrombotic, thrombophilic states, hypercoagulable state, thrombophilia etc.: semantics should be respected even in medical papers 2017 Girolami A.Cosi E. + JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
Role of replacement therapy in the evaluation of thrombosis occurring in congenital bleeding conditions 2017 Girolami A.Ferrari S.Cosi E. + THROMBOSIS AND HAEMOSTASIS - -
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. + HEMATOLOGY - -
Mostrati risultati da 1 a 20 di 361
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