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High prevalence of risk factors for cardiovascular disease in parents of IDDM patients with albuminuria. 1-gen-1997 De Cosmo, S; Bacci, S; Piras, Gp; Cignarelli, Mauro; Placentino, G; Margaglione, Maurizio; Colaizzo, D; Di Minno, G; Giorgino, R; Liuzzi, A; Viberti, G. C.
An alternative method for PAI-1 promoter polymorphism (4G/5G) typing. 1-gen-1997 Margaglione, Maurizio; Grandone, E; Cappucci, G; Colaizzo, D; Giuliani, N; Vecchione, G; D’Addedda, M; Di Minno, G.
Hemostatic variables and ischemic cardiovascular disease: do we need a concerted effort for more profitable future clinical investigations? 1-gen-1997 Di Minno, G; Mancini, Fp; Margaglione, Maurizio
Thrombotic thrombocytopenic purpura in pregnancy: a multifaceted disease. 1-gen-1997 Grandone, E; Margaglione, Maurizio; Pavone, G.
Factor V Leiden is associated with repeated and recurrent unexplained fetal losses. 1-gen-1997 Grandone, E; Margaglione, Maurizio; Colaizzo, D; D’Addedda, M; Cappucci, G; Vecchione, G; Sciannamé, N; Pavone, G; Di Minno, G.
Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia 1-gen-1997 Grandone, E; Margaglione, Maurizio; Colaizzo, D; Cappucci, G; Paladini, D; Martinelli, P; Montanaro, S; Pavone, G; Di Minno, G.
Clinical relevance of polymorphic markers of arterial thrombosis. 1-gen-1997 Di Minno, G; Grandone, E; Margaglione, Maurizio
Plasminogen activator inhibitor-1 (PAI-1) antigen plasma levels in subjects attending a metabolic ward. Relation to polymorphism of the PAI-1 and Angiotensin Converting Enzyme (ACE) genes. 1-gen-1997 Margaglione, Maurizio; Grandone, E; Vecchione, G; Cappucci, G; Giuliani, N; Colaizzo, D; Celentano, E; Panico, S; Di Minno, G.
Presence of Factor V Leiden and MTHFR mutation in a patient with complicated pregnancies. 1-gen-1997 Grandone, E; Margaglione, Maurizio; Colaizzo, D; Pavone, G; Di Minno, G.
Prevalence of apolipoprotein E alleles in healthy subjects and survivors of ischemic stroke. An Italian case-control study. 1-gen-1998 Margaglione, Maurizio; Seripa, D; Gravina, C; Grandone, E; Vecchione, G; Cappucci, G; Merla, G; Papa, S; Postiglione, A; DI MINNO, G; Fazio, Vm
A fast and accurate method for genotyping the angiotensin-converting enzyme I/D polymorphism. 1-gen-1998 Mancini, Fp; Margaglione, Maurizio; Tufano, A; Celentano, A; Ferrara, La; Colantuoni, V; Di Minno, G.
Relation between PAI-1 gene locus polymorphism and family history of coronary artery disease. 1-gen-1998 Margaglione, Maurizio; Grandone, E; Di Minno, G.
The PAI-1 gene locus 4G/5G polymorphism is associated with a family history of coronary artery disease. 1-gen-1998 Margaglione, Maurizio; Cappucci, G; Colaizzo, D; Giuliani, N; Vecchione, G; Grandone, E; Pennelli, O; Di Minno, G.
Fibrinogen plasma levels in an apparently healthy general population. Relation to environmental and genetic determinants. 1-gen-1998 Margaglione, Maurizio; Cappucci, G; Colaizzo, D; Pirro, L; Vecchione, G; Grandone, E; Di Minno, G.
Reduction of mononuclear cytokine production in hemodialysis patients treated with steam-sterilized low-flux polysulphone membranes. 1-gen-1998 Aucella, F; Vigilante, M; Grandone, E; Colaizzo, D; Margaglione, Maurizio; Modoni, S; Orlandini, G; Stallone, C.
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 1-gen-1998 Grandone, E.; Margaglione, Maurizio; Colaizzo, D.; D'Andrea, Giovanna; Cappucci, G.; Brancaccio, V.; DI MINNO, G.
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 1-gen-1998 Ames, P. R; Tommasino, C; D'Andrea, Giovanna; Iannaccone, L; Brancaccio, V; Margaglione, Maurizio
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 1-gen-1998 Margaglione, Maurizio; D'Andrea, Giovanna; D'Addedda, M; Giuliani, N; Cappucci, G; Iannaccone, L; Vecchione, G; Grandone, E; Brancaccio, V; DI MINNO, G.
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 1-gen-1998 Margaglione, Maurizio; Brancaccio, V; Giuliani, N; D'Andrea, Giovanna; Cappucci, G; Iannaccone, L; Vecchione, G; Grandone, E; DI MINNO, G.
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 1-gen-1998 Margaglione, Maurizio; Brancaccio, V; Giuliani, N; D'Andrea, Giovanna; Cappucci, G; Iannaccone, L; Vecchione, G; Grandone, E; ANN INTERN MED, DI MINNO G. INCREASED RISK OF VENOUS THROMBOSIS IN CARRIERS OF THE PROTHROMBIN A. GENE V. A. R. I. A. N. T.; .,
Mostrati risultati da 21 a 40 di 365
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