Search Results - "Spiezia, L."

Peripapillary Vessel Density as Early Biomarker in Multiple Sclerosis by Cennamo, Gilda, Carotenuto, Antonio, Montorio, Daniela, Petracca, Maria, Moccia, Marcello, Melenzane, Antonietta, Tranfa, Fausto, Lamberti, Anna, Spiezia, Antonio L., Servillo, Giuseppe, De Angelis, Marcello, Petruzzo, Martina, Criscuolo, Chiara, Lanzillo, Roberta, Brescia Morra, Vincenzo

“…Background: To evaluate retinal vessel density (VD) in macular and in peripapillary regions in patients with recent onset of multiple sclerosis, at initial…”
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“In vitro” correction of the severe factor V deficiency‐related coagulopathy by a novel plasma‐derived factor V concentrate by Bulato, C., Novembrino, C., Anzoletti, M. Boscolo, Spiezia, L., Gavasso, S., Berbenni, C., Tagariello, G., Farina, C., Nardini, I., Campello, E., Peyvandi, F., Simioni, P.

“…Introduction Severe congenital factor V (FV) deficiency is a rare bleeding disorder characterized by very low/undetectable levels of FV. Fresh frozen plasma is…”
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The haemostatic system in acromegaly: a single-centre case–control study by Campello, E., Marobin, M., Barbot, M., Radu, C. M., Voltan, G., Spiezia, L., Gavasso, S., Ceccato, F., Scaroni, C., Simioni, P.

“…Purpose Although the mortality from acromegaly is due in most cases to an increased cardiovascular risk, no study has globally evaluated the haemostatic…”
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“Hypocoagulable” thromboelastography profiles in patients with cyanotic congenital heart disease: Facts or technical artifacts? by Spiezia, L, Campello, E, Simioni, P

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Hyperfibrinolysis during liver transplantation detected by classical parameters and thromboelastometry by Maggiolo, S, Campello, E, Spiezia, L, Tredese, A, Saggiorato, G, Gavasso, S, Feltracco, P, Simioni, P

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Homozygous F5 deep‐intronic splicing mutation resulting in severe factor V deficiency and undetectable thrombin generation in platelet‐rich plasma by CASTOLDI, E., DUCKERS, C., RADU, C., SPIEZIA, L., ROSSETTO, V., TAGARIELLO, G., ROSING, J., SIMIONI, P.

“…Background: Coagulation factor (F) V deficiency is associated with a bleeding tendency of variable severity, but phenotype determinants are largely unknown…”
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Circulating microparticles in pregnant patients with primary anti-phospholipid syndrome: an exploratory study by Campello, E, Radu, CM, Tonello, M, Kuzenko, A, Bulato, C, Hoxha, A, Mattia, E, Spiezia, L, Ruffatti, A, Simioni, P

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P-047: Circulating microparticles in women with polycystic ovary syndrome: preliminary results by Campello, E, Mioni, R, Dalla Cà, A, Spiezia, L, Maggiolo, S, Radu, C.M, Bulato, C, Simioni, P

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P-046: Circulating microparticles in pregnant patients with primary antiphospholipid antibody syndrome by Campello, E, Radu, C.M, Tonello, M, Kuzenko, A, Bulato, C, Mattia, E, Spiezia, L, Ruffatti, A, Simioni, P

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Decreased hypercoagulable state in hepatitis C virus-cirrhotic patients treated with DAA: the outcome revolution by Zanetto, A, Campello, E, Spiezia, L, Shalaby, S, Franceschet, E, Tessari, M, Ferrarese, A, Frigo, A.C, Bortoluzzi, I, Gambato, M, Germani, G, Floreani, A, Farinati, F, Senzolo, M, Burra, P, Simioni, P, Russo, F.P

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Circulating Microparticles and Risk of Portal Vein Thrombosis in Patients with Liver Cirrhosis and Hepatocellular Carcinoma by Zanetto, A, Ferrarese, A, Nadal, E, Bortoluzzi, I, Campello, E, Spiezia, L, Cillo, U, Vitale, A, Farinati, F, Germani, G, Russo, F.P, Simioni, P, Burra, P, Senzolo, M

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Whole Blood Coagulation Tests are not Equally able to Detect Haemostatic Prothrombotic Alterations in Patients with Liver Cirrhosis and Hepatocellular Carcinoma: Rotational Thromboelastometry versus Thrombingeneration Test by Zanetto, A, Ferrarese, A, Nadal, E, Bortoluzzi, I, Campello, E, Spiezia, L, Cillo, U, Vitale, A, Farinati, F, Germani, G, Russo, F.P, Gavasso, S, Simioni, P, Burra, P, Senzolo, M

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Thrombophilia and the risk of post‐thrombotic syndrome: retrospective cohort observation by SPIEZIA, L., CAMPELLO, E., GIOLO, E., VILLALTA, S., PRANDONI, P.

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Efficacy and safety of treatment of acute nonmalignant portal vein thrombosis with subcutaneous fondaparinux in patients with cirrhosis and marked thrombocytopenia by Tonon, M, Piano, S, Sacerdoti, D, Dalla Valle, F, Spiezia, L, Bolognesi, M, Simioni, P, Angeli, P

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Thromboelastographic evaluation of hemostatic balance in cirrhotic patients with infection by Nadal, E, Simioni, P, Spiezia, L, Angeli, P, Fasolato, S, Zanetto, A, Ferrarese, A, Shalaby, S, Germani, G, Russo, F.P, Burra, P, Senzolo, M

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Thrombin generation in Cushing’s Syndrome: do the conventional clotting indices tell the whole truth? by Koutroumpi, S., Spiezia, L., Albiger, N., Barbot, M., Bon, M., Maggiolo, S., Gavasso, S., Simioni, P., Frigo, A., Mantero, F., Scaroni, C.

“…Cushing’s Syndrome (CS) is associated with an increased mortality, where hypercoagulability seems to have a crucial role in both arterial and venous…”
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Differential effects of high prothrombin levels on thrombin generation depending on the cause of the hyperprothrombinemia by CASTOLDI, E., SIMIONI, P., TORMENE, D., THOMASSEN, M. C. L. G. D., SPIEZIA, L., GAVASSO, S., ROSING, J.

“…Background: Hyperprothrombinemia, resulting from the prothrombin G20210A mutation or other causes, is associated with activated protein C (APC) resistance and…”
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Thrombin Activatable Fibrinolysis inhibitor in Cancer Patients with and without Venous Thromboembolism by Radu, C.M, Spiezia, L, Campello, E, Gavasso, S, Woodhams, B, Simioni, P

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High dose of human plasma-derived FVIII-VWF as first-line therapy in patients affected by acquired haemophilia A and concomitant cardiovascular disease: four case reports and a literature review by Zanon, E., Milan, M., Brandolin, B., Barbar, S., Spiezia, L., Saggiorato, G., Simioni, P., Baudo, F.

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Whole blood rotation thromboelastometry (ROTEM®) in nine severe factor V deficient patients and evaluation of the role of intraplatelets factor V by SPIEZIA, L., RADU, C., CAMPELLO, E., BULATO, C., BERTINI, D., BARILLARI, G., DE ANGELIS, V., PRADELLA, P., ZANON, E., SIMIONI, P.

“…Severe factor V (FV) deficiency (parahaemophilia) is a rare congenital hemorrhagic disorder characterized by very low or undetectable plasma FV levels and…”
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