Maurizio Margaglione
Maurizio Margaglione
Unknown affiliation
Verified email at unifg.it
TitleCited byYear
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin
G D'Andrea, RL D'Ambrosio, P Di Perna, M Chetta, R Santacroce, ...
Blood 105 (2), 645-649, 2005
8642005
Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis
L Amitrano, MA Guardascione, V Brancaccio, M Margaglione, F Manguso, ...
Journal of hepatology 40 (5), 736-741, 2004
5752004
Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism
J Emmerich, FR Rosendaal, M Cattaneo, M Margaglione, V De Stefano, ...
Thrombosis and haemostasis 86 (09), 809-816, 2001
4362001
Factor V Leiden is associated with repeated and recurrent unexplained fetal losses
E Grandone, M Margaglione, D Colaizzo, M d'Addedda, G Cappucci, ...
Thrombosis and haemostasis 77 (05), 0822-0824, 1997
3341997
Genetic modulation of oral anticoagulation with warfarin
M Margaglione, D Colaizzo, G D’Andrea, V Brancaccio, A Ciampa, ...
Thrombosis and haemostasis 84 (11), 775-778, 2000
3062000
Prothrombotic genetic risk factors in young survivors of myocardial infarction
D Ardissino, PM Mannucci, PA Merlini, F Duca, R Fetiveau, L Tagliabue, ...
Blood 94 (1), 46-51, 1999
3021999
Factor V Leiden, C> T MTHFR polymorphism and genetic susceptibility to preeclampsia
E Grandone, M Margaglione, D Colaizzo, G Cappucci, D Paladini, ...
Thrombosis and haemostasis 77 (06), 1052-1054, 1997
2991997
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis
L Amitrano, V Brancaccio, MA Guardascione, M Margaglione, ...
Hepatology 31 (2), 345-348, 2000
2862000
Increased risk for venous thrombosis in carriers of the prothrombin G→ A20210 gene variant
M Margaglione, V Brancaccio, N Giuliani, G D'Andrea, G Cappucci, ...
Annals of Internal Medicine 129 (2), 89-93, 1998
2811998
F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis
SC Gouw, HM van den Berg, J Oldenburg, J Astermark, PG de Groot, ...
Blood 119 (12), 2922-2934, 2012
2692012
Prognostic factors in noncirrhotic patients with splanchnic vein thromboses
L Amitrano, MA Guardascione, M Scaglione, L Pezzullo, N Sangiuliano, ...
The American journal of gastroenterology 102 (11), 2464, 2007
2422007
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations
E Grandone, M Margaglione, D Colaizzo, G D’Andrea, G Cappucci, ...
American journal of obstetrics and gynecology 179 (5), 1324-1328, 1998
2411998
Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and probucol-sensitive mechanism.
G Di Minno, G Davi, M Margaglione, F Cirillo, E Grandone, G Ciabattoni, ...
The Journal of clinical investigation 92 (3), 1400-1406, 1993
2151993
Plasma thrombin-activatable fibrinolysis inhibitor antigen concentration and genotype in relation to myocardial infarction in the north and south of Europe
I Juhan-Vague, PE Morange, H Aubert, M Henry, MF Aillaud, MC Alessi, ...
Arteriosclerosis, thrombosis, and vascular biology 22 (5), 867-873, 2002
2072002
Insight into the nature of the CRP–coronary event association using Mendelian randomization
JP Casas, T Shah, J Cooper, E Hawe, AD McMahon, D Gaffney, ...
International journal of epidemiology 35 (4), 922-931, 2006
1942006
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group
Circulation 107 (8), 1117-1122, 2003
1902003
The PAI-1 gene locus 4G/5G polymorphism is associated with a family history of coronary artery disease
M Margaglione, G Cappucci, D Colaizzo, N Giuliani, G Vecchione, ...
Arteriosclerosis, thrombosis, and vascular biology 18 (2), 152-156, 1998
1871998
Low-grade inflammation may play a role in the etiology of the metabolic syndrome in patients with coronary heart disease: the HIFMECH study
JS Yudkin, I Juhan-Vague, E Hawe, SE Humphries, G Di Minno, ...
Metabolism 53 (7), 852-857, 2004
1842004
The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis
D Colaizzo, L Amitrano, GL Tiscia, G Scenna, E Grandone, ...
Journal of Thrombosis and Haemostasis 5 (1), 55-61, 2007
1832007
PAI-1 plasma levels in a general population without clinical evidence of atherosclerosis: relation to environmental and genetic determinants
M Margaglione, G Cappucci, M d’Addedda, D Colaizzo, N Giuliani, ...
Arteriosclerosis, thrombosis, and vascular biology 18 (4), 562-567, 1998
1801998
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