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Mostrati risultati da 21 a 40 di 361
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
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 - -
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 - -
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 - -
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 - -
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 - -
Pulmonary embolism in congenital bleeding disorders: Intriguing discrepancies among different clotting factors deficiencies 2016 Girolami A.Cosi E.Tasinato V.Peroni E. + BLOOD COAGULATION & FIBRINOLYSIS - -
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 - -
Thrombotic Events in Asymptomatic FXII Deficiency versus Symptomatic FXI Deficiency: Surprising Observations. 2016 GIROLAMI, ANTONIOCOSI, ELISABETTASANTAROSSA, CLAUDIAFERRARI, SILVIALOMBARDI, ANNA MARIA + ACTA HAEMATOLOGICA - -
Ischemic strokes in congenital bleeding disorders: comparison with myocardial infarction and other acute coronary syndromes 2016 GIROLAMI, ANTONIOFERRARI, SILVIACOSI, ELISABETTAPERONI, EDOARDOFABRIS, FABRIZIO Cardiovascular & Hematological Disorders-Drug Targets - -
Acquired Isolated FVII Deficiency An Underestimated and Potentially Important Laboratory Finding. 2015 GIROLAMI, ANTONIOSANTAROSSA, CLAUDIACOSI, ELISABETTAFERRARI, SILVIA + CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
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 - -
Venous thrombosis in von Willebrand disease as observed in one centre and as reported in the literature. 2015 GIROLAMI, ANTONIOSAMBADO, LUISAPERONI, EDOARDOCASONATO, SANDRA + 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 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 - -
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 - -
Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease. 2014 PONTARA, ELENAGRESELE, PAOLOPELOSO CATTINI, MARIA GRAZIADAIDONE, VIVIANABARBON, GIOVANNIGIROLAMI, ANTONIOZANONATO, ELISACASONATO, SANDRA BLOOD COAGULATION & FIBRINOLYSIS - -
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 - -
Associated risk factors and arterial occlusions in patients with von Willebrand disease: Analysis of the literature and report of two cases 2014 GIROLAMI, ANTONIOFERRARI, SILVIABERTOMORO, ANTONELLAPERONI, EDOARDOSAMBADO, LUISACASONATO, SANDRA CASE REPORTS IN INTERNAL MEDICINE - -
Bleeding manifestations apparently unrelated to coagulation or other organic disorders: A tentative classification and diagnostic clues 2014 Girolami, AntonioBertozzi, Irene + HEMATOLOGY - -
Discrepant ratios of arterial versus venous thrombosis in hemophilia A as compared with hemophilia B 2014 Girolami, AntonioBertozzi, Irene + JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
Mostrati risultati da 21 a 40 di 361
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