FERRARI, SILVIA

FERRARI, SILVIA  

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Titolo Data di pubblicazione Autore(i) Rivista Serie Titolo libro
Pathogenetic Role of Factor VII Deficiency and Thrombosis in Cross-Reactive Material Positive Patients 2013 GIROLAMI, ANTONIOSAMBADO, LUISABONAMIGO, EMANUELAFERRARI, SILVIALombardi, Am LABORATORY HEMATOLOGY - -
Myocardial Infarctions and Other Acute Coronary Syndromes in Rare Congenital Bleeding Disorders: A Critical Analysis of All Reported Cases. 2014 GIROLAMI, ANTONIOFERRARI, SILVIASAMBADO, LUISAPERONI, EDOARDOCOSI, ELISABETTA CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
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 - -
Prevalence of hypertension and its complications in congenital Prekallikrein deficiency: analysis of all reported cases and clinical significance. 2015 GIROLAMI, ANTONIOFERRARI, SILVIACOSI, ELISABETTASAMBADO, LUISAGirolami, B. BLOOD COAGULATION & FIBRINOLYSIS - -
Acquired Isolated FVII Deficiency An Underestimated and Potentially Important Laboratory Finding. 2015 GIROLAMI, ANTONIOSANTAROSSA, CLAUDIACOSI, ELISABETTAFERRARI, SILVIA + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
The story of serum prothrombin conversion accelerator, proconvertin, stable factor, cothromboplastin, prothrombin accelerator or autoprothrombin I, and their subsequent merging into factor VII 2015 GIROLAMI, ANTONIOCOSI, ELISABETTASANTAROSSA, CLAUDIAFERRARI, SILVIARANDI, MARIA LUIGIA SEMINARS IN THROMBOSIS AND HEMOSTASIS - -
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 - -
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 - -
Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched vs 128 unaffected family members, during a long sequential observation period (23.5 years). 2016 GIROLAMI, ANTONIOCOSI, ELISABETTASANTAROSSA, CLAUDIAFERRARI, SILVIALOMBARDI, ANNA MARIA + EUROPEAN JOURNAL OF HAEMATOLOGY - -
Aspetti clinici, epidemiologici e genetici delle diverse forme di trombocitopenie ereditarie 2016 Ferrari, Silvia - - -
Spectrum of 5’UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected 2017 FERRARI, SILVIALOMBARDI, ANNA-MARIABERTOMORO, ANTONELLACORTELLA, IRENEBARZON, ISABELLAGIROLAMI, ANTONIOFABRIS, FABRIZIO + PLATELETS - -
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 - -
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 - -
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. + JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
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 - -
Role of replacement therapy in the evaluation of thrombosis occurring in congenital bleeding conditions 2017 Girolami A.Ferrari S.Cosi E. + THROMBOSIS AND HAEMOSTASIS - -
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 - -
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 - -