-
1
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
1. Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369: 64-67.
-
(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
-
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
-
2. Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. 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.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
3
-
-
0030667686
-
Factor V Leiden mutation and the risks for thromboembolic disease: A clinical perspective
-
3. Price DT, Ridker PM. Factor V Leiden mutation and the risks for thromboembolic disease: a clinical perspective. Ann Intern Med 1997; 127: 895-903.
-
(1997)
Ann Intern Med
, vol.127
, pp. 895-903
-
-
Price, D.T.1
Ridker, P.M.2
-
4
-
-
0030870825
-
Factor V Leiden and other coagulation factor mutations affecting thrombotic risk
-
4. Bertina RM. Factor V Leiden and other coagulation factor mutations affecting thrombotic risk. Clin Chem 1997; 43: 1678-1683.
-
(1997)
Clin Chem
, vol.43
, pp. 1678-1683
-
-
Bertina, R.M.1
-
5
-
-
0002116036
-
Hypercoagulable states
-
Hoffman R, Benz EJ Jr, Shattil SJ, Furie B, Cohen HJ, Silberstein LE (editors). New York: Churchill Livingstone
-
5. Bauer KA. Hypercoagulable states. In: Hoffman R, Benz EJ Jr, Shattil SJ, Furie B, Cohen HJ, Silberstein LE (editors): Hematology: basic principles and clinical practice. 2nd edition. New York: Churchill Livingstone; 1995. pp. 1781-1795.
-
(1995)
Hematology: Basic Principles and Clinical Practice. 2nd Edition
, pp. 1781-1795
-
-
Bauer, K.A.1
-
6
-
-
0028910906
-
Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men
-
6. Ridker PM, Hennekens CH, Lindpaintner K, Stampfer MJ, Eisenberg PR, Miletich JP. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men. N Eng J Med 1995; 332: 912-917.
-
(1995)
N Eng J Med
, vol.332
, pp. 912-917
-
-
Ridker, P.M.1
Hennekens, C.H.2
Lindpaintner, K.3
Stampfer, M.J.4
Eisenberg, P.R.5
Miletich, J.P.6
-
7
-
-
0030845360
-
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep vein thrombosis
-
7. Hillarp A, Zöller B, Svensson P, Dahlbäck B. The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep vein thrombosis. Thromb Haemost 1997; 78: 990-992.
-
(1997)
Thromb Haemost
, vol.78
, pp. 990-992
-
-
Hillarp, A.1
Zöller, B.2
Svensson, P.3
Dahlbäck, B.4
-
8
-
-
0030714108
-
Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease
-
8. Arruda VR, Annichino-Bizzacchi JM, Gonçalves MS, Costa FF. Prevalence of the prothrombin gene variant (nt20210A) 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
Gonçalves, M.S.3
Costa, F.F.4
-
10
-
-
0030608645
-
Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia
-
10. 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: 1426-1429.
-
(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
-
11
-
-
0027447258
-
Inherited predisposition to thrombosis
-
11. Miletich JP, Prescott SM, White R, Majerus PW, Bovill EG. Inherited predisposition to thrombosis. Cell 1993; 72: 477-480.
-
(1993)
Cell
, vol.72
, pp. 477-480
-
-
Miletich, J.P.1
Prescott, S.M.2
White, R.3
Majerus, P.W.4
Bovill, E.G.5
-
12
-
-
0028577799
-
Hypercoagulable states: Molecular genetics to clinical practice
-
12. Schafer AI. Hypercoagulable states: molecular genetics to clinical practice. Lancet 1994; 344: 1739-1742.
-
(1994)
Lancet
, vol.344
, pp. 1739-1742
-
-
Schafer, A.I.1
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