Sfoglia per Autore
Spectrum of 5’UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected
2017 Ferrari, Silvia; Lombardi, ANNA-MARIA; Putti, Maria Caterina; Bertomoro, Antonella; Cortella, Irene; Barzon, Isabella; Girolami, Antonio; Fabris, Fabrizio
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.; Girolami, B.; Lombardi, A. M.
Thrombotic Events in Asymptomatic FXII Deficiency versus Symptomatic FXI Deficiency: Surprising Observations.
2016 Girolami, Antonio; Cosi, Elisabetta; Santarossa, Claudia; Ferrari, Silvia; Lombardi, ANNA MARIA; Ferrari, Silvia
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, Antonio; Molina, Ma; Lopez Galletti, Ml; Ferrari, Silvia; Sambado, Luisa; Guglielmone, H.
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, Antonio; Cosi, Elisabetta; Santarossa, Claudia; Ferrari, Silvia; Girolami, B; Lombardi, ANNA MARIA
Drug-Induced Thrombophilic or Prothrombotic States: An Underestimated Clinical Problem That Involves Both Legal and Illegal Compounds
2016 Girolami, Antonio; Cosi, Elisabetta; Tasinato, V; Santarossa, Claudia; Ferrari, Silvia; Girolami, B.
Ischemic strokes in congenital bleeding disorders: comparison with myocardial infarction and other acute coronary syndromes
2016 Girolami, Antonio; Ferrari, Silvia; Cosi, Elisabetta; Peroni, Edoardo; Fabris, Fabrizio
Pulmonary embolism in congenital bleeding disorders: Intriguing discrepancies among different clotting factors deficiencies
2016 Girolami, A.; Cosi, E.; Tasinato, V.; Peroni, E.; Girolami, B.; Lombardi, A. M.
A forgotten or minimized head trauma, rather than a mild FVII deficiency, is the most likely cause of a subdural hematoma
2016 Girolami, Antonio; Ferrari, Silvia; Cosi, Elisabetta; Lombardi, A. M.
Prevalence of hypertension and its complications in congenital Prekallikrein deficiency: analysis of all reported cases and clinical significance.
2015 Girolami, Antonio; Ferrari, Silvia; Cosi, Elisabetta; Sambado, Luisa; Girolami, B.
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, Antonio; Cosi, Elisabetta; Santarossa, Claudia; Ferrari, Silvia; Randi, MARIA LUIGIA
Venous thrombosis in von Willebrand disease as observed in one centre and as reported in the literature.
2015 Girolami, Antonio; Tasinato, V; Sambado, Luisa; Peroni, Edoardo; Casonato, Sandra
Complex History of the Discovery and Characterization of Congenital Factor X Deficiency.
2015 Girolami, Antonio; Cosi, Elisabetta; Sambado, Luisa; Girolami, B; Randi, MARIA LUIGIA
Congenital FXI and FVII deficiencies assure an apparent opposite protection against arterial or venous thrombosis: an intriguing observation.
2015 Girolami, A.; Peroni, E.; Girolami, B.; Ferrari, S.; Lombardi, A. M
Acquired Isolated FVII Deficiency An Underestimated and Potentially Important Laboratory Finding.
2015 Girolami, Antonio; Santarossa, Claudia; Cosi, Elisabetta; Ferrari, Silvia; Lombardi, Anna Maria
Bleeding manifestations apparently unrelated to coagulation or other organic disorders: A tentative classification and diagnostic clues
2014 Girolami, Antonio; Bertozzi, Irene; Tasinato, Valentina; Sambado, Luisa; Treleani, Martina
Myocardial Infarctions and Other Acute Coronary Syndromes in Rare Congenital Bleeding Disorders: A Critical Analysis of All Reported Cases.
2014 Girolami, Antonio; Ferrari, Silvia; Sambado, Luisa; Peroni, Edoardo; Cosi, Elisabetta
Associated risk factors and arterial occlusions in patients with von Willebrand disease: Analysis of the literature and report of two cases
2014 Girolami, Antonio; Ferrari, Silvia; Bertomoro, Antonella; Peroni, Edoardo; Sambado, Luisa; Casonato, Sandra
Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease.
2014 Pontara, Elena; Gresele, Paolo; PELOSO CATTINI, MARIA GRAZIA; Daidone, Viviana; Barbon, Giovanni; Girolami, Antonio; Zanonato, Elisa; Casonato, Sandra
Discrepant ratios of arterial versus venous thrombosis in hemophilia A as compared with hemophilia B
2014 Girolami, Antonio; Bertozzi, Irene; De Marinis, Giulia Berti; Tasinato, Valentina; Sambado, Luisa
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