COSI, ELISABETTA

COSI, ELISABETTA  

Dipartimento di Medicina - DIMED  

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Risultati 1 - 20 di 54 (tempo di esecuzione: 0.072 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding 2020 Girolami A.Cosi E. + JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
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 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 - -
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 - -
Antibiotic use and associated factors in a large sample of hospitalised older people 2019 Fabris FBertozzi IBogoni GCosi EPrandini T + JOURNAL OF GLOBAL ANTIMICROBIAL RESISTANCE - -
Antihypertensive treatment changes and related clinical outcomes in older hospitalized patients 2023 Piano S.Randi ML.Bertozzi I.Cosi E. + EUROPEAN JOURNAL OF CLINICAL INVESTIGATION - -
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 - -
Complex History of the Discovery and Characterization of Congenital Factor X Deficiency. 2015 GIROLAMI, ANTONIOCOSI, ELISABETTASAMBADO, LUISARANDI, MARIA LUIGIA + SEMINARS IN THROMBOSIS AND 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 - -
Disability, and not diabetes, is a strong predictor of mortality in oldest old patients hospitalized with pneumonia 2018 Fabris FBERTOZZI IBogoni GCosi EPrandini T + EUROPEAN JOURNAL OF INTERNAL MEDICINE - -
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 - -
Drug–drug interactions involving CYP3A4 and p-glycoprotein in hospitalized elderly patients 2019 Fabris FBERTOZZI IBogoni GCosi EPrandini T + EUROPEAN JOURNAL OF INTERNAL MEDICINE - -
Effect of busulfan on JAK2V617F allele burden. 2014 RANDI, MARIA LUIGIASANTAROSSA, CLAUDIAPERONI, EDOARDOCOSI, ELISABETTADUNER, ELENABERTOZZI, IRENEFABRIS, FABRIZIO HAEMATOLOGICA - -
Factor X Friuli coagulation disorder: Almost 50 Years Later 2018 Girolami A.Cosi E.Santarossa C.Ferrari S. + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations 2019 Lombardi, Anna MCosi, ElisabettaBiagetti, GiacomoRandi, Maria L + BRITISH JOURNAL OF HAEMATOLOGY - -
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 - -