-
1
-
-
0029850530
-
A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort SR, Rosendaal FR, Reitsma PH, Bertina R. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.4
-
2
-
-
0031981017
-
Geographic distribution of the 20210G to A prothrombin variant
-
Abstract
-
Rosendaal FR, Doggen CJ, Zivelin A, Arruda VA, Aiach M, Siscovick DS, et al. Geographic distribution of the 20210G to A prothrombin variant. Thromb Haemost 1998; 79: 706-8. Abstract.
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.2
Zivelin, A.3
Arruda, V.A.4
Aiach, M.5
Siscovick, D.S.6
-
3
-
-
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: 990-2.
-
(1997)
Thromb Haemost
, vol.78
, pp. 990-992
-
-
Hillarp, A.1
Zoller, B.2
Svensson, P.J.3
Dahlback, B.4
-
4
-
-
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: 907-9.
-
(1997)
Br J Haematol
, vol.98
, pp. 907-909
-
-
Brown, K.1
Luddington, R.2
Williamson, D.3
Baker, P.4
Baglin, T.5
-
5
-
-
0030792668
-
The prothrombin gene G20210A variant: Prevalence in a U.K. Anticoagulant clinic population
-
Cumming AM, Keeney S, Salden A, Bhavnani M, Shwe KH, Hay CR. The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population. Br J Haematol 1997; 98: 353-5.
-
(1997)
Br J Haematol
, vol.98
, pp. 353-355
-
-
Cumming, A.M.1
Keeney, S.2
Salden, A.3
Bhavnani, M.4
Shwe, K.H.5
Hay, C.R.6
-
6
-
-
0031847816
-
Increased risk for venous thrombosis in carriers of the prothrombin G → A20210 gene variant
-
Margaglione M, Brancaccio V, Giuliani N, D'Andrea G, Cappucci G, Iannaccone L, et al. Increased risk for venous thrombosis in carriers of the prothrombin G → A20210 gene variant. Ann Int. Med 1998; 129: 89-93.
-
(1998)
Ann Int. Med
, vol.129
, pp. 89-93
-
-
Margaglione, M.1
Brancaccio, V.2
Giuliani, N.3
D'Andrea, G.4
Cappucci, G.5
Iannaccone, L.6
-
7
-
-
0030714108
-
Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease
-
Arruda VA, Annichinio-Bizzacchi JM, Goncalves MS, Costa F. Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease. Thromb Haemost 1997; 78: 1430-3.
-
(1997)
Thromb Haemost
, vol.78
, pp. 1430-1433
-
-
Arruda, V.A.1
Annichinio-Bizzacchi, J.M.2
Goncalves, M.S.3
Costa, F.4
-
8
-
-
0031825902
-
Prevalence of the factor II G20210A mutation in symptomatic patients with inherited thrombophilia
-
De Stefano V, Chiusolo P, Paciaroni K, Casorelli I, Di Mario A, Rossi E, et al. Prevalence of the Factor II G20210A mutation in symptomatic patients with inherited thrombophilia. Thromb Haemos. 1998; 80: 342-3.
-
(1998)
Thromb Haemos.
, vol.80
, pp. 342-343
-
-
De Stefano, V.1
Chiusolo, P.2
Paciaroni, K.3
Casorelli, I.4
Di Mario, A.5
Rossi, E.6
-
9
-
-
0030790061
-
The epidemiology of inherited thrombophilia: The VITA project
-
Rodeghiero F, Tosetto A. The epidemiology of inherited thrombophilia: the VITA Project. Thromb Haemost 1997; 78: 636-40.
-
(1997)
Thromb Haemost
, vol.78
, pp. 636-640
-
-
Rodeghiero, F.1
Tosetto, A.2
-
10
-
-
0030757480
-
The vita project: Phenotypic resistance to activated protein C and FV Leiden mutation in the general population
-
Tosetto A, Missiaglia E, Gatto E, Rodeghiero F. The Vita Project: phenotypic resistance to activated protein C and FV Leiden mutation in the general population. Thromb Haemost 1997; 78: 859-63.
-
(1997)
Thromb Haemost
, vol.78
, pp. 859-863
-
-
Tosetto, A.1
Missiaglia, E.2
Gatto, E.3
Rodeghiero, F.4
-
11
-
-
0029837881
-
The VITA project: Population-based distribution of protein C, antithrombin III, heparin cofactor II and plasminogen. Relationship with physiological variables and establishment of reference ranges
-
Rodeghiero F, Tosetto A. The VITA Project: Population-based distribution of protein C, antithrombin III, heparin cofactor II and plasminogen. Relationship with physiological variables and establishment of reference ranges. Thromb Haemost 1996; 76: 226-33.
-
(1996)
Thromb Haemost
, vol.76
, pp. 226-233
-
-
Rodeghiero, F.1
Tosetto, A.2
-
12
-
-
0029893568
-
Validated questionnaire for the identification of previous personal or familial venous thromboembolism
-
Frezzato M, Tosetto A, Rodeghiero F. Validated questionnaire for the identification of previous personal or familial venous thromboembolism. Am J Epidemiol 1996; 143: 1257-65.
-
(1996)
Am J Epidemiol
, vol.143
, pp. 1257-1265
-
-
Frezzato, M.1
Tosetto, A.2
Rodeghiero, F.3
-
14
-
-
0018676582
-
Spectrophotometric assays of prothrombin in plasma of patients using oral anticoagulants
-
Abstract
-
Bertina RM, van der Marel-Nieuwkoop W, Loeliger EA. Spectrophotometric assays of prothrombin in plasma of patients using oral anticoagulants. Thromb Haemost 1979; 42: 1296-305. Abstract.
-
(1979)
Thromb Haemost
, vol.42
, pp. 1296-1305
-
-
Bertina, R.M.1
Van Der Marel-Nieuwkoop, W.2
Loeliger, E.A.3
-
16
-
-
0025981009
-
The effect of non-differential outcome misclassification on estimates of the attributable and prevented fraction
-
Hsieh CC. The effect of non-differential outcome misclassification on estimates of the attributable and prevented fraction. Stat Med 1991; 10: 361-73.
-
(1991)
Stat Med
, vol.10
, pp. 361-373
-
-
Hsieh, C.C.1
-
20
-
-
0032005263
-
The prothrombin gene 3′-untranslated region mutation is frequently associated with factor V Leiden in thrombophilic patients and shows ethnic-specific variation in allele frequency
-
Abstract
-
Howard T, Marusa M, Boisza J, Young A, Sequeira J, Channel C, et al. The prothrombin gene 3′-untranslated region mutation is frequently associated with Factor V Leiden in thrombophilic patients and shows ethnic-specific variation in allele frequency. Blood 1998; 91: 1092. Abstract.
-
(1998)
Blood
, vol.91
, pp. 1092
-
-
Howard, T.1
Marusa, M.2
Boisza, J.3
Young, A.4
Sequeira, J.5
Channel, C.6
-
21
-
-
0031761182
-
Additional genetic risk factors for venous thromboembolism in carriers of FV Leiden
-
Tosetto A, Missiaglia E, Martinelli I, De Stefano V, Rodeghiero F. Additional genetic risk factors for venous thromboembolism in carriers of FV Leiden. Br J Haematol 1998; 103: 871-6.
-
(1998)
Br J Haematol
, vol.103
, pp. 871-876
-
-
Tosetto, A.1
Missiaglia, E.2
Martinelli, I.3
De Stefano, V.4
Rodeghiero, F.5
-
22
-
-
0031442537
-
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in arterial 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 arterial disease. Arterioscler Thromb Vase Biol 1997; 17: 2418-22.
-
(1997)
Arterioscler Thromb Vase Biol
, vol.17
, pp. 2418-2422
-
-
Ferraresi, P.1
Marchetti, G.2
Legnani, C.3
Cavallari, E.4
Castoldi, E.5
Mascoli, F.6
-
23
-
-
0030608645
-
Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia
-
Makris M, Preston FE, Beauchamp NJ, Cooper PC, Daly ME, Hampton KK, et al. Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia. Thromb Haemost 1997; 78: 1426-9.
-
(1997)
Thromb Haemost
, vol.78
, pp. 1426-1429
-
-
Makris, M.1
Preston, F.E.2
Beauchamp, N.J.3
Cooper, P.C.4
Daly, M.E.5
Hampton, K.K.6
-
24
-
-
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: 1793-7.
-
(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
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