-
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 SW, Rosendaal FR, Reitsma PH, Bertina RM. 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.W.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
2
-
-
0018966649
-
Incidence of acute deep vein thrombosis in two districts. A phlebographic study
-
Kierkegaard A. Incidence of acute deep vein thrombosis in two districts. A phlebographic study. Acta Chir Scand 1980; 146: 267-9.
-
(1980)
Acta Chir Scand
, vol.146
, pp. 267-269
-
-
Kierkegaard, A.1
-
3
-
-
0022973304
-
Epidemiology and pathogenesis of venous thrombosis
-
Hirsch J, Hull RD, Raskob GE. Epidemiology and pathogenesis of venous thrombosis. J Am Coll Cardiol 1986; 8 (Suppl. B): 104B-13B.
-
(1986)
J Am Coll Cardiol
, vol.8
, Issue.SUPPL. B
-
-
Hirsch, J.1
Hull, R.D.2
Raskob, G.E.3
-
4
-
-
0028877613
-
Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC subcommittee on Fibrinogen
-
Haverkate F, Samama M. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC subcommittee on Fibrinogen. Thromb Haemost 1995; 73:151-61.
-
(1995)
Thromb Haemost
, vol.73
, pp. 151-161
-
-
Haverkate, F.1
Samama, M.2
-
5
-
-
0025241268
-
Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep-vein thrombosis
-
Heijboer H, Brandjes D, Büller HR et al. Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep-vein thrombosis. N Engl J Med 1990; 323: 1512-6.
-
(1990)
N Engl J Med
, vol.323
, pp. 1512-1516
-
-
Heijboer, H.1
Brandjes, D.2
Büller, H.R.3
-
6
-
-
0026695880
-
Thromboembolic disease - Critical evaluation of laboratory investigation
-
Malm J, Laurell M, Nilsson IM, Dahlbäck B. Thromboembolic disease - critical evaluation of laboratory investigation. Thromb Haemost 1992; 68: 7-13.
-
(1992)
Thromb Haemost
, vol.68
, pp. 7-13
-
-
Malm, J.1
Laurell, M.2
Nilsson, I.M.3
Dahlbäck, B.4
-
7
-
-
0027446268
-
Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C
-
Dahlbäck B, Carlsson M, Svensson PJ. Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C. Proc Natl Acad Sci USA 1993; 90: 1004-8.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 1004-1008
-
-
Dahlbäck, B.1
Carlsson, M.2
Svensson, P.J.3
-
8
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, van der Velden PA, Reitsma PH. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369: 64-7.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
De Ronde, H.6
Van Der Velden, P.A.7
Reitsma, P.H.8
-
9
-
-
0028352460
-
Activated protein C resistance caused by Arg506Gln mutation in factor Va
-
Greengard JS, Sun X, Xu X, Fernandez JA, Griffin JH, Evatt BL. Activated protein C resistance caused by Arg506Gln mutation in factor Va. Lancet 1994; 343: 1362-3.
-
(1994)
Lancet
, vol.343
, pp. 1362-1363
-
-
Greengard, J.S.1
Sun, X.2
Xu, X.3
Fernandez, J.A.4
Griffin, J.H.5
Evatt, B.L.6
-
10
-
-
0028243401
-
Association of idiopathic thromboembolism with single point mutation at Arg506 of factor V
-
Voorberg J, Roelse J, Koopman R, Büller H, Berends F, ten Cate JW, Mertens K, van Mourik JA. Association of idiopathic thromboembolism with single point mutation at Arg506 of factor V. Lancet 1994; 343: 1535-6.
-
(1994)
Lancet
, vol.343
, pp. 1535-1536
-
-
Voorberg, J.1
Roelse, J.2
Koopman, R.3
Büller, H.4
Berends, F.5
Ten Cate, J.W.6
Mertens, K.7
Van Mourik, J.A.8
-
11
-
-
0028291210
-
Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis
-
Zöller B, Dahlbäck B. Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis. Lancet 1996; 343: 1536-8.
-
(1996)
Lancet
, vol.343
, pp. 1536-1538
-
-
Zöller, B.1
Dahlbäck, B.2
-
12
-
-
0027428481
-
Anticoagulant protein C pathway defective in a majority of thrombophilic patients
-
Griffin JH, Evatt BL, Wideman C, Fernandez JA. Anticoagulant protein C pathway defective in a majority of thrombophilic patients. Blood 1993; 82: 1989-93.
-
(1993)
Blood
, vol.82
, pp. 1989-1993
-
-
Griffin, J.H.1
Evatt, B.L.2
Wideman, C.3
Fernandez, J.A.4
-
13
-
-
0027520285
-
Venous thrombosis due to poor response to activated protein C: Leiden thrombophilia study
-
Koster T, Rosendaal FR, de Ronde F, Briët E, Vandenbroucke JP, Bertina RM. Venous thrombosis due to poor response to activated protein C: Leiden thrombophilia study. Lancet 1993; 342: 1503-6.
-
(1993)
Lancet
, vol.342
, pp. 1503-1506
-
-
Koster, T.1
Rosendaal, F.R.2
De Ronde, F.3
Briët, E.4
Vandenbroucke, J.P.5
Bertina, R.M.6
-
14
-
-
0028098210
-
Resistance to activated protein C as a basis for venous thrombosis
-
Svensson PJ, Dahlbäck B. Resistance to activated protein C as a basis for venous thrombosis. N Engl J Med 1994; 330: 517-21.
-
(1994)
N Engl J Med
, vol.330
, pp. 517-521
-
-
Svensson, P.J.1
Dahlbäck, B.2
-
15
-
-
0023230641
-
Nucleotide sequence of the gene for human prothrombin
-
Degen SJF, Davie EW. Nucleotide sequence of the gene for human prothrombin. Biochemistry 1987; 26: 6165-77.
-
(1987)
Biochemistry
, vol.26
, pp. 6165-6177
-
-
Degen, S.J.F.1
Davie, E.W.2
-
16
-
-
0023175705
-
Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively
-
Royle NJ, Irwin DM, Koschinsky ML, MacGillivray RTA, Hamerton JL. Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively. Somat Cell Mol Genet 1987; 13: 285-92.
-
(1987)
Somat Cell Mol Genet
, vol.13
, pp. 285-292
-
-
Royle, N.J.1
Irwin, D.M.2
Koschinsky, M.L.3
MacGillivray, R.T.A.4
Hamerton, J.L.5
-
17
-
-
0001630993
-
Physiology and biochemistry of prothrombin
-
Bloom AL, Forbes CD, Thoraas DP, Tuddenham EGD, eds. Churchill Livingstone, Edinburgh, UK
-
Jackson CM. Physiology and biochemistry of prothrombin. In: Haemostasis and Thrombosis. Bloom AL, Forbes CD, Thoraas DP, Tuddenham EGD, eds. Churchill Livingstone, Edinburgh, UK 1994, pp 397-438.
-
(1994)
Haemostasis and Thrombosis
, pp. 397-438
-
-
Jackson, C.M.1
-
18
-
-
0027057084
-
Thrombin, a link between coagulation activation and fibrinolysis
-
Bertina RM, van Tilburg NH, de Fouw NJ, Haverkate F. Thrombin, a link between coagulation activation and fibrinolysis. Ann NY Acad Sci 1992; 667: 239-48.
-
(1992)
Ann NY Acad Sci
, vol.667
, pp. 239-248
-
-
Bertina, R.M.1
Van Tilburg, N.H.2
De Fouw, N.J.3
Haverkate, F.4
-
19
-
-
0029014036
-
An allosteric switch controls the procoagulant and anticoagulant activities of thrombin
-
Dang QD, Vindigni A, Di Cera E. An allosteric switch controls the procoagulant and anticoagulant activities of thrombin. Proc Natl Acad Sci USA 1995; 92: 5977-81.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 5977-5981
-
-
Dang, Q.D.1
Vindigni, A.2
Di Cera, E.3
-
20
-
-
0030609926
-
The factor V:R506Q mutation causing APC resistance is highly prevalent among unselected outpatients with clinically suspected deep venous thrombosis
-
Svensson PJ, Zöller B, Mattiasson I, Dahlbäck B. The factor V:R506Q mutation causing APC resistance is highly prevalent among unselected outpatients with clinically suspected deep venous thrombosis. J Intern Med 1997; 241: 379-86.
-
(1997)
J Intern Med
, vol.241
, pp. 379-386
-
-
Svensson, P.J.1
Zöller, B.2
Mattiasson, I.3
Dahlbäck, B.4
-
21
-
-
0028037137
-
Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C
-
Zöller B, Svensson PJ, He X, Dahlback B. Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C. J Clin Invest 1994; 94: 2521-4.
-
(1994)
J Clin Invest
, vol.94
, pp. 2521-2524
-
-
Zöller, B.1
Svensson, P.J.2
He, X.3
Dahlback, B.4
-
22
-
-
0029878085
-
Elevated levels of prothrombin activation fragment 1+2 in plasma from patients with inherited APC-resistance and/or protein S deficiency
-
Zöller B, Holm J, Svensson PJ, Dahlback B. Elevated levels of prothrombin activation fragment 1+2 in plasma from patients with inherited APC-resistance and/or protein S deficiency. Thromb Haemost 1996; 75: 270-4.
-
(1996)
Thromb Haemost
, vol.75
, pp. 270-274
-
-
Zöller, B.1
Holm, J.2
Svensson, P.J.3
Dahlback, B.4
-
23
-
-
0030054356
-
Prothrombin fragment 1+2 and thrombin-antithrombin complex levels in patients with inherited APC-resistance due to factor V Leiden mutation
-
Simioni P, Scarano L, Gavasso S, Sardella C, Girolami B, Scudeller A, Girolami A. Prothrombin fragment 1+2 and thrombin-antithrombin complex levels in patients with inherited APC-resistance due to factor V Leiden mutation. Br J Haematol 1996; 92: 435-41.
-
(1996)
Br J Haematol
, vol.92
, pp. 435-441
-
-
Simioni, P.1
Scarano, L.2
Gavasso, S.3
Sardella, C.4
Girolami, B.5
Scudeller, A.6
Girolami, A.7
-
24
-
-
0028505212
-
New markers for in vivo coagulation
-
Bauer KA. New markers for in vivo coagulation. Current opinion in Hematology 1994; 1: 341-6.
-
(1994)
Current Opinion in Hematology
, vol.1
, pp. 341-346
-
-
Bauer, K.A.1
-
25
-
-
0027949265
-
Mechanisms, markers and management of coagulation activation
-
Mannucci PM. Mechanisms, markers and management of coagulation activation. Br Med Bull 1994; 50: 851-70.
-
(1994)
Br Med Bull
, vol.50
, pp. 851-870
-
-
Mannucci, P.M.1
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