Sfoglia per Autore
Inherited prothrombotic conditions and premature ischemic stroke. sex difference in the association with factor V Leiden. Arterioscler Thromb Vasc Biol 19(7): 1751-6, 1999
1999-01-01 Margaglione, M; D’Andrea, G; Giuliani, N; Brancaccio, V; De Lucia, D; Grandone, E; De Stefano, V; Tonali, Pa; Di Minno, G
. Reply . Reply Am J Obstet Gynecol. 181(4):1041; 1999. 181(4):1041; 1999
1999-01-01 Grandone, E; Margaglione, M; Di Minno, G
. Compound heterozygosity (554-589 del, C515-T transition) in the platelet glycoprotein Ib gene in a patient with a severe bleeding tendency. Thromb Haemost 1999, 81(4): 486-92
1999-01-01 Margaglione, M; D’Andrea, G; Grandone, E; Brancaccio, V; Amoriello, A; Di Minno, G
Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (mthfr) gene in offspring of patients with myocardial infarction.
1999-01-01 Margaglione, Maurizio; Colaizzo, D; Cappucci, G; del Popolo, A; Vecchione, G; Grandone, E; Di Minno, G.
. C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives. Arterioscler Thromb Vasc Biol. 2000; 20(1):198-203
2000-01-01 Margaglione, M; Cappucci, G; Colaizzo, D; Vecchione, G; Grandone, E; Di Minno, G
.. A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing. Blood 2000; 96(7):2501-5
2000-01-01 Margaglione, M; Santacroce, R; Colaizzo, D; Seripa, D; Vecchione, G; Lupone, Mr; De Lucia, D; Fortina, P; Grandone, E; Perricone, C; Di Minno, G
Inherited thrombophilic risk factors and venous thromboembolism: distinct role in peripheral deep venous thrombosis and pulmonary embolism. Chest. 2000;118(5):1405-11
2000-01-01 Margaglione, M; Brancaccio, V; De Lucia, D; Martinelli, I; Ciampa, A; Grandone, E; Di Minno, G
.Polymorphism of the angiotensin-converting enzyme gene in end-stage renal failure patients. Nephron 2000; 85(1):54-9
2000-01-01 Aucella, F; Vigilante, M; Margaglione, M; Grandone, E; del Popolo, A; Forcella, M; Procaccini, D; Salatino, G; Passione, A; Ktena, M; De Min, A; Stallone, C
Genetic modulation of oral anticoagulation with warfarin. Thromb Haemost. 2000; 84(5):775-8
2000-01-01 Margaglione, M; Colaizzo, D; D'Andrea, G; Brancaccio, V; Ciampa, A; Grandone, E; Di Minno, G
A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo. Thromb Haemost.;86(6):1483-8. 2001
2001-01-01 Margaglione, M; Vecchione, G; Santacroce, R; D'Angelo, F; Casetta, B; Papa, Ml; Grandone, E; Di Minno, G
Inherited thrombophilic risk factors in a large cohort of individuals referred to Italian thrombophilia centers: distinct roles in different clinical settings. Haematologica. 2001; 86(6): 634-9
2001-01-01 Margaglione, M; Brancaccio, V; Ciampa, A; Papa, Ml; Grandone, E; Di Minno, G
Familial thrombophilia and the occurrence of fetal growth restriction. Haematologica. 2001, 86(4):428-31
2001-01-01 Martinelli, P; Grandone, E; Colaizzo, D; Paladini, D; Scianname, N; Margaglione, M; Di Minno, G
Risk of pregnancy-related venous thrombosis in carriers of severe inherited thrombophilia Thromb Haemost. 2001; 86(3):800-3
2001-01-01 Martinelli, I; Legnani, C; Bucciarelli, P; Grandone, E; De Stefano, V; Mannucci, Pm
Inherited thrombophilia and in vitro fertilization implantation failure. Fertil Steril. 2001, 76(1):201-2.
2001-01-01 Grandone, E; Colaizzo, D; Lo Bue, A; Checola, Mg; Cittadini, E; Margaglione, M
The effect of the interleukin-6 c/g-174 polymorphism and circulating interleukin-6 on fibrinogen plasma levels. Haematologica 2001; 86(2):199-204
2001-01-01 Margaglione, M; Bossone, A; Cappucci, G; Colaizzo, D; Grandone, E; Di Minno, G
. Impact of prothrombotic mutations and family history on the occurrence of intra-uterine fetal deaths. Haematologica 2002; 87(10):1118-9
2002-01-01 Grandone, E; Colaizzo, D; Brancaccio, V; Ciampa, A; Di Minno, G; Margaglione, M
. Maternal and fetal inherited thrombophilias. Am J Obstet Gynecol. 2002; 186(6):1376
2002-01-01 Grandone, E; Margaglione, M
. Occurrence of factor V Leiden mutation (Arg506Gln) and anticardiolipin antibodies in migraine patients. Neurol Sci , 2002; 22(6):455-8
2002-01-01 Intiso, D; Crociani, P; Fogli, D; Grandone, E; Cappucci, G; Di Rienzo, F; Di Viesti, P; Simone, P; Tonali, P
Lower birth-weight in neonates of mothers carrying factor V G1691A and factor II A(20210) mutations. Haematologica. 2002; 87(2):177-81
2002-01-01 Grandone, E; Margaglione, M; Colaizzo, D; Pavone, G; Paladini, D; Martinelli, P; Di Minno, G
.Preventing adverse obstetric outcomes in women with genetic thrombophilia. Fertil Steril. 2002; 78(2):371-5
2002-01-01 Grandone, E; Brancaccio, V; Colaizzo, D; Scianname, N; Pavone, G; Di Minno, G; Margaglione, M
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