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Results: 1-25/37
Authors:
Di Minno, G
Tufano, A
Cerbone, AM
Citation: G. Di Minno et al., Antithrombotic drugs for older subjects - Guidelines formulated jointly bythe Italian Societies of Haemostasis and Thrombosis (SISET) and of Gerontology and Geriatrics (SIGG), NUTR MET CA, 11(1), 2001, pp. 41-62
Authors:
Margaglione, M
Brancaccio, V
Ciampa, A
Papa, ML
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., Inherited thrombophilic risk factors in a large cohort of individuals referred to Italian thrombophilla centers: distinct roles in different clinicalsettings, HAEMATOLOG, 86(6), 2001, pp. 634-639
Authors:
Martinelli, P
Grandone, E
Colaizzo, D
Paladini, D
Scianname, N
Margaglione, M
Di Minno, G
Citation: P. Martinelli et al., Familial thrombophilia and the occurrence of fetal growth restriction, HAEMATOLOG, 86(4), 2001, pp. 428-431
Authors:
Margaglione, M
Bossone, A
Cappucci, G
Colaizzo, D
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., The effect of interleukin-6 C/G-174 polymorphism and circulating interleukin-6 on fibrinogen plasma levels, HAEMATOLOG, 86(2), 2001, pp. 199-204
Authors:
Margaglione, M
Brancaccio, V
Ciampa, A
Di Minno, G
Citation: M. Margaglione et al., Reply to Rebuttal: Gene variants of the cytochrome P450CYP2C9 affect oral anticoagulation with warfarin, THROMB HAEM, 86(3), 2001, pp. 938-938
Authors:
Postiglione, A
Milan, G
Ruocco, A
Gallotta, G
Guiotto, G
Di Minno, G
Citation: A. Postiglione et al., Plasma folate, vitamin B-12, and total homocysteine and homozygosity for the C677T mutation of the 5,10-methylene tetrahydrofolate reductase gene in patients with Alzheimer's dementia - A case-control study, GERONTOLOGY, 47(6), 2001, pp. 324-329
Authors:
Meh, DA
Mosesson, MW
Siebenlist, KR
Simpson-Haidaris, PJ
Brennan, SO
DiOrio, JP
Thompson, K
Di Minno, G
Citation: Da. Meh et al., Fibrinogen Naples I (B beta A68T) nonsubstrate thrombin-binding capacities, THROMB RES, 103(1), 2001, pp. 63-73
Authors:
Madonna, P
Piemontino, U
De Stefano, V
Albisinni, R
Cerbone, AM
Di Minno, G
Citation: P. Madonna et al., Coexistence of thrombophilic gene polymorphisms among 559 unrelated consecutive patients with a history of thrombosis, THROMB RES, 101(4), 2001, pp. 317-319
Authors:
Madonna, P
De Stefano, V
Coppola, A
Cerbone, AM
Di Minno, G
Citation: P. Madonna et al., G20210A prothrombin gene mutation anal other trombophilic polymorphisms inpatients with portal or hepatic venous thrombosis, GASTROENTY, 120(4), 2001, pp. 1059-1060
Authors:
Davi, G
Di Minno, G
Coppola, A
Andria, G
Cerbone, AM
Madonna, P
Tufano, A
Falco, A
Marchesani, P
Ciabattoni, G
Patrono, C
Citation: G. Davi et al., Oxidative stress and platelet activation in homozygous homocystinuria, CIRCULATION, 104(10), 2001, pp. 1124-1128
Authors:
Margaglione, M
Cappucci, G
Colaizzo, D
Vecchione, G
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives, ART THROM V, 20(1), 2000, pp. 198-203
Authors:
Napoli, C
Palinski, W
Di Minno, G
D'Armiento, FP
Citation: C. Napoli et al., Determination of atherogenesis in apolipoprotein E-knockout mice, NUTR MET CA, 10(4), 2000, pp. 209-215
Authors:
Margaglione, M
Bossone, A
Brancaccio, V
Ciampa, A
Di Minno, G
Citation: M. Margaglione et al., Factor XIII Val34Leu polymorphism and risk of deep vein thrombosis, THROMB HAEM, 84(6), 2000, pp. 1118-1119
Authors:
Margaglione, M
Colaizzo, D
D'Andrea, G
Brancaccio, V
Clampa, A
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., Genetic modulation of oral anticoagulation with warfarin, THROMB HAEM, 84(5), 2000, pp. 775-778
Authors:
de Franchis, R
Fermo, I
Mazzola, G
Sebastio, G
Di Minno, G
Coppola, A
Andria, G
D'Angelo, A
Citation: R. De Franchis et al., Contribution of the cystathionine beta-synthase gene (844ins68) polymorphism to the risk of early-onset venous and arterial occlusive disease and of fasting hyperhomocysteinemia, THROMB HAEM, 84(4), 2000, pp. 576-582
Authors:
Margaglione, M
Di Castelnuovo, A
Totaro, A
Iacoviello, L
Di Minno, G
Citation: M. Margaglione et al., Risk of myocardial infarction in carriers of mutations in the hemochromatosis-associated gene, THROMB HAEM, 84(4), 2000, pp. 726-727
Authors:
Coppola, A
Davi, G
De Stefano, V
Mancini, FP
Cerbone, AM
Di Minno, G
Citation: A. Coppola et al., Homocysteine, coagulation, platelet function, and thrombosis, SEM THROMB, 26(3), 2000, pp. 243-254
Authors:
De Stefano, V
Madonna, P
Giannino, A
Coppola, A
Cerbone, AM
Pauciullo, P
Di Minno, G
Citation: V. De Stefano et al., Idiopathic Budd-Chiari syndrome in a patient with homozygous Factor V Leiden and heterozygous factor II G20210A mutations, THROMB RES, 100(6), 2000, pp. 567-568
Authors:
Margaglione, M
Brancaccio, V
De Lucia, D
Martinelli, I
Ciampa, A
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., Inherited thrombophilic risk factors and venous thromboembolism - Distinctrole in peripheral deep venous thrombosis and pulmonary embolism, CHEST, 118(5), 2000, pp. 1405-1411
Authors:
Margaglione, M
Santacroce, R
Colaizzo, D
Seripa, D
Vecchione, G
Lupone, MR
De Lucia, D
Fortina, P
Grandone, E
Perricone, C
Di Minno, G
Citation: M. Margaglione et al., A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing, BLOOD, 96(7), 2000, pp. 2501-2505
Authors:
Rubba, P
Di Minno, G
Andria, G
Citation: P. Rubba et al., Vascular complications of homocystinuria: Incidence, clinical pattern and treatment, DEV CARD M, 230, 2000, pp. 117-133
Authors:
De Cosmo, S
Margaglione, M
Tassi, V
Garrubba, M
Thomas, S
Olivetti, C
Piras, GP
Trevisan, R
Vedovato, M
Perin, PC
Bacci, S
Colaizzo, D
Cisternino, C
Zucaro, L
Di Minno, G
Trischitta, V
Viberti, GC
Citation: S. De Cosmo et al., ACE, PAI-1, decorin and Warner helicase genes are not associated with the development of renal disease in European patients with Type 1 diabetes, DIABET M R, 15(4), 1999, pp. 247-253
Authors:
Margaglione, M
D'Andrea, G
Giuliani, N
Brancaccio, V
De Lucia, D
Grandone, E
De Stefano, V
Tonali, PA
Di Minno, G
Citation: M. Margaglione et al., Inherited prothrombotic conditions and premature ischemic stroke - Sex difference in the association with factor V Leiden, ART THROM V, 19(7), 1999, pp. 1751-1756
Authors:
Maresca, G
Di Blasio, A
Marchioli, R
Di Minno, G
Citation: G. Maresca et al., Measuring plasma fibrinogen to predict stroke and myocardial infarction - An update, ART THROM V, 19(6), 1999, pp. 1368-1377
Authors:
Margaglione, M
D'Andrea, G
Colaizzo, D
Cappucci, G
del Popolo, A
Brancaccio, V
Ciampa, A
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., Coexistence of Factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism, THROMB HAEM, 82(6), 1999, pp. 1583-1587