-
1
-
-
0029876985
-
Inherited thrombophilia: Pathogenesis, clinical syndromes and management
-
De Stefano V, Finazzi G, Mannucci PM. Inherited thrombophilia: pathogenesis, clinical syndromes and management. Blood 1996; 87: 3531-3544.
-
(1996)
Blood
, vol.87
, pp. 3531-3544
-
-
De Stefano, V.1
Finazzi, G.2
Mannucci, P.M.3
-
2
-
-
0029850530
-
A common genetic variation in the 3'untranslated region of the prothrombin gene is associated with elevated prothrombin levels and an increase in venous thrombosis
-
Poort S, Rosendaal E, Reitsma P, Bertina R. A common genetic variation in the 3'untranslated region of the prothrombin gene is associated with elevated prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-3703
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.1
Rosendaal, E.2
Reitsma, P.3
Bertina, R.4
-
3
-
-
0030810628
-
Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3'untranslated region of the prothrombin gene
-
Brown K, Luddington R, Williamson D, Baker P, Baglin T. Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3'untranslated region of the prothrombin gene. Br J Haematol 1997; 98: 907-909.
-
(1997)
Br J Haematol
, vol.98
, pp. 907-909
-
-
Brown, K.1
Luddington, R.2
Williamson, D.3
Baker, P.4
Baglin, T.5
-
4
-
-
0030845360
-
The 20210 A allele of the prothrombin gene is a common risk factor among swedish outpatients with verified deep venous thrombosis
-
Hillarp A, Zoller B, Svensson PJ, Dahlback B. The 20210 A allele of the prothrombin gene is a common risk factor among swedish outpatients with verified deep venous thrombosis. Thromb Haemost 1997; 78: 990-992.
-
(1997)
Thromb Haemost
, vol.78
, pp. 990-992
-
-
Hillarp, A.1
Zoller, B.2
Svensson, P.J.3
Dahlback, B.4
-
5
-
-
0030664938
-
The venous thrombosis risk factor 20210 A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease
-
Corral J, González-Conejero R, Lozano ML, Rivera J, Heras I, Vicente V. The venous thrombosis risk factor 20210 A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease. Br J Haematol 1997; 99: 304-307.
-
(1997)
Br J Haematol
, vol.99
, pp. 304-307
-
-
Corral, J.1
González-Conejero, R.2
Lozano, M.L.3
Rivera, J.4
Heras, I.5
Vicente, V.6
-
6
-
-
0030744832
-
The A20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic families
-
Alhenc-Gelas M, Le Cam-Duchez V, Emmerich J, Frebourg T, Fiessinger JN, Borg JYet al. The A20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic families. Blood 1997; 90: 1711.
-
(1997)
Blood
, vol.90
, pp. 1711
-
-
Alhenc-Gelas, M.1
Le Cam-Duchez, V.2
Emmerich, J.3
Frebourg, T.4
Fiessinger, J.N.5
Borg, J.Y.6
-
7
-
-
0030921663
-
A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women
-
Rosendaal FR, Siscovick DS, Schwartz SM, Psaty BM, Raghunathan TE, Vos HL. A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women. Blood 1997; 90: 1747-1750.
-
(1997)
Blood
, vol.90
, pp. 1747-1750
-
-
Rosendaal, F.R.1
Siscovick, D.S.2
Schwartz, S.M.3
Psaty, B.M.4
Raghunathan, T.E.5
Vos, H.L.6
-
8
-
-
0030736412
-
The transition G to A at position 20210 in the 3′-untranslated region of the prothrombin gene is not associated with cerebral ischaemia
-
Martinelli I, Franchi F, Akwan S, Bettini P, Merati G, Mannucci PM. The transition G to A at position 20210 in the 3′-Untranslated region of the prothrombin gene is not associated with cerebral ischaemia. Blood 1997; 90: 3806.
-
(1997)
Blood
, vol.90
, pp. 3806
-
-
Martinelli, I.1
Franchi, F.2
Akwan, S.3
Bettini, P.4
Merati, G.5
Mannucci, P.M.6
-
9
-
-
0032525101
-
Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients
-
De Stefano V, Chiusolo P, Paciaroni K, Casorelli I, Rossi E, Molinari M et al. Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood 1998; 91: 3562-3565.
-
(1998)
Blood
, vol.91
, pp. 3562-3565
-
-
De Stefano, V.1
Chiusolo, P.2
Paciaroni, K.3
Casorelli, I.4
Rossi, E.5
Molinari, M.6
-
10
-
-
0030789617
-
A patient homozygous for a mutation in the prothrombin gene 3′-untranslated region associated with massive thrombosis
-
Howard TE, Marusa M, Channell C, Duncan A. A patient homozygous for a mutation in the prothrombin gene 3′-untranslated region associated with massive thrombosis. Blood Coag Fibrinol 1997; 8: 316-319.
-
(1997)
Blood Coag Fibrinol
, vol.8
, pp. 316-319
-
-
Howard, T.E.1
Marusa, M.2
Channell, C.3
Duncan, A.4
-
11
-
-
0032543748
-
High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives
-
Martinelli I, Sacchi E, Landi G, Taioli E, Duca F, Mannucci PM. High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives. N Engl J Med 1998; 338: 1793-1797.
-
(1998)
N Engl J Med
, vol.338
, pp. 1793-1797
-
-
Martinelli, I.1
Sacchi, E.2
Landi, G.3
Taioli, E.4
Duca, F.5
Mannucci, P.M.6
-
12
-
-
0028810738
-
World distribution of factor V Leiden
-
Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet 1995; 346: 1133-1134.
-
(1995)
Lancet
, vol.346
, pp. 1133-1134
-
-
Rees, D.C.1
Cox, M.2
Clegg, J.B.3
-
13
-
-
0031981017
-
Geographic distribution of the 20210 G to A prothrombin variant
-
Rosendaal FR, Dogen CJ, Zivelin A, Arruda VR, Aiach M, Siscovick DS et al. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 1998; 79: 706-708.
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Dogen, C.J.2
Zivelin, A.3
Arruda, V.R.4
Aiach, M.5
Siscovick, D.S.6
-
14
-
-
0031442537
-
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease
-
Ferraresi P, Marchetti G, Legnani C, Cavallari E, Castoldi E, Mascoli F et al. The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease. Arterioscler Thromb Vasc Biol 1997; 17: 2418-2422.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 2418-2422
-
-
Ferraresi, P.1
Marchetti, G.2
Legnani, C.3
Cavallari, E.4
Castoldi, E.5
Mascoli, F.6
-
15
-
-
0030714108
-
Prevalence of the prothrombin gene variant (nt 20210A) in venous thrombosis and arterial disease
-
Arruda VR, Annichino-Bizzacchi JM, Goncalves MS, Costa FF. Prevalence of the prothrombin gene variant (nt 20210A) in venous thrombosis and arterial disease. Thromb Haemost 1997; 78: 1430-1433.
-
(1997)
Thromb Haemost
, vol.78
, pp. 1430-1433
-
-
Arruda, V.R.1
Annichino-Bizzacchi, J.M.2
Goncalves, M.S.3
Costa, F.F.4
-
16
-
-
0031618374
-
Frequencies of prothrombin 20120 G-A mutation may be different among races-studies on Japanese populations with various forms of thrombotic disorders and healthy subjects
-
Isshiki I, Murata M, Watanabe R, Matsubara Y, Kawano K, Aoki N et al. Frequencies of prothrombin 20120 G-A mutation may be different among races-studies on Japanese populations with various forms of thrombotic disorders and healthy subjects. Blood Coag Fibrinol 1998; 9:105-106.
-
(1998)
Blood Coag Fibrinol
, vol.9
, pp. 105-106
-
-
Isshiki, I.1
Murata, M.2
Watanabe, R.3
Matsubara, Y.4
Kawano, K.5
Aoki, N.6
|