LOMBARDI, ANNA MARIA

LOMBARDI, ANNA MARIA  

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Risultati 1 - 7 di 7 (tempo di esecuzione: 0.01 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Bagliori nel vuoto. Dall'uovo elettrico ai raggi X, un percorso tra elettricità  e pneumatica dal Seicento a oggi 2003 LOMBARDI, ANNA MARIAPERUZZI, GIULIOTALAS, SOFIA - - -
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 - -
Thrombotic Events in Asymptomatic FXII Deficiency versus Symptomatic FXI Deficiency: Surprising Observations. 2016 GIROLAMI, ANTONIOCOSI, ELISABETTASANTAROSSA, CLAUDIAFERRARI, SILVIALOMBARDI, ANNA MARIA + ACTA HAEMATOLOGICA - -
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 - -
Familial acquired thrombotic thrombocytopenic purpura: immunogenetic link with HLA-DRB1*11 and DQB1*03 antigens 2017 Lombardi, Anna MFabris, FabrizioVianello, Fabrizio + BRITISH JOURNAL OF HAEMATOLOGY - -
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 - -
Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations 2019 Lombardi, Anna MCosi, ElisabettaBiagetti, GiacomoRandi, Maria L + BRITISH JOURNAL OF HAEMATOLOGY - -