FERRARI, SILVIA

FERRARI, SILVIA  

Mostra records
Risultati 1 - 20 di 37 (tempo di esecuzione: 0.027 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A family with factor x deficiency from Argentina: a compound heterozygosis due to the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys) 2016 GIROLAMI, ANTONIOMolina, MaFERRARI, SILVIASAMBADO, LUISA + BLOOD COAGULATION & FIBRINOLYSIS - -
A forgotten or minimized head trauma, rather than a mild FVII deficiency, is the most likely cause of a subdural hematoma 2016 GIROLAMI, ANTONIOFERRARI, SILVIACOSI, ELISABETTALombardi, A. M. Blood Cells, Molecules and Diseases - -
A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemia 2017 LOMBARDI, ANNA-MARIAFERRARI, SILVIABARZON, ISABELLAFABRIS, FABRIZIOVIANELLO, FABRIZIO + BLOOD CELLS, MOLECULES, & DISEASES - -
A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome 2020 Ferrari S.Regazzo D.Omenetto E.Scaroni C.Semenzato G.Fabris F.Vianello F. AGING CLINICAL AND EXPERIMENTAL RESEARCH - -
A structure–function analysis in patients with prekallikrein deficiency 2018 Girolami A.Ferrari S.Cosi E. + HEMATOLOGY - -
Acquired Isolated FVII Deficiency An Underestimated and Potentially Important Laboratory Finding. 2015 GIROLAMI, ANTONIOSANTAROSSA, CLAUDIACOSI, ELISABETTAFERRARI, SILVIA + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Activated Platelet-Derived and Leukocyte-Derived Circulating Microparticles and the Risk of Thrombosis in Heparin-Induced Thrombocytopenia: A Role for PF4-Bearing Microparticles? 2018 Campello, ElenaRadu, Claudia M.Duner, ElenaLombardi, Anna M.Spiezia, LucaBendo, RaffaeleFerrari, SilviaSimioni, PaoloFabris, Fabrizio CYTOMETRY. PART B, CLINICAL CYTOMETRY - -
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 - -
Aspetti clinici, epidemiologici e genetici delle diverse forme di trombocitopenie ereditarie 2016 Ferrari, Silvia - - -
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 - -
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 - -
Cardiovascular diseases in congenital prekallikrein deficiency: Comparison with other chanceassociated morbidities 2018 Girolami A.Ferrari S.Cosi E. + BLOOD COAGULATION & FIBRINOLYSIS - -
Congenital FXI and FVII deficiencies assure an apparent opposite protection against arterial or venous thrombosis: an intriguing observation. 2015 Girolami, A.Peroni, E.Ferrari, S.Lombardi, A. M + HEMATOLOGY - -
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 - -
Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patients 2016 BERTI DE MARINIS, GIULIANOVELLO, STEFANOFERRARI, SILVIABARZON, ISABELLACORTELLA, IRENEBUSINARO, MARIA ANTONIETTAFABRIS, FABRIZIOLOMBARDI, ANNA-MARIA JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
Drug-Induced Thrombophilic or Prothrombotic States: An Underestimated Clinical Problem That Involves Both Legal and Illegal Compounds 2016 GIROLAMI, ANTONIOCOSI, ELISABETTATasinato, VSANTAROSSA, CLAUDIAFERRARI, SILVIA + 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 - -
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 - -
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 - -
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 - -