-
1
-
-
0035806950
-
The thrombophilias: Well-defined risk factors with uncertain therapeutic implications
-
Bauer KA. The thrombophilias: Well-defined risk factors with uncertain therapeutic implications. Ann Intern Med 2001; 135(5): 367-73.
-
(2001)
Ann Intern Med
, vol.135
, Issue.5
, pp. 367-373
-
-
Bauer, K.A.1
-
2
-
-
0030317949
-
Deletion polymorphism of the angiotensin I-converting enzyme gene is associated with increased plasma angiotensin-converting enzyme activity but not with increased risk for myocardial infarction and coronary artery disease
-
Winkelmann BR, Nauck M, Klein B, et al. Deletion polymorphism of the angiotensin I-converting enzyme gene is associated with increased plasma angiotensin-converting enzyme activity but not with increased risk for myocardial infarction and coronary artery disease. Ann Intern Med 1996; 125(1): 19-25.
-
(1996)
Ann Intern Med
, vol.125
, Issue.1
, pp. 19-25
-
-
Winkelmann, B.R.1
Nauck, M.2
Klein, B.3
-
3
-
-
0031835010
-
Nitric oxide and prostacyclin are involved in antithrombotic action of captopril in venous thrombosis in rats
-
Pawlak R, Chabielska E, Golatowski J, et al. Nitric oxide and prostacyclin are involved in antithrombotic action of captopril in venous thrombosis in rats. Thromb Haemost 1998; 79: 1208-12.
-
(1998)
Thromb Haemost
, vol.79
, pp. 1208-1212
-
-
Pawlak, R.1
Chabielska, E.2
Golatowski, J.3
-
4
-
-
0029902158
-
Angiotensin II receptor antagonists in the prevention of radiation nephropathy
-
Moulder JE, Fish BL, Cohen EP, et al. Angiotensin II receptor antagonists in the prevention of radiation nephropathy. Radiat Res 1996; 146(1): 106-10.
-
(1996)
Radiat Res
, vol.146
, Issue.1
, pp. 106-110
-
-
Moulder, J.E.1
Fish, B.L.2
Cohen, E.P.3
-
5
-
-
0031963298
-
Relation of three genetic traits to venous thrombosis in an African-American population
-
Dilley A, Austin H, Hooper WC, et al. Relation of three genetic traits to venous thrombosis in an African-American population. Am J Epidemiol 1998; 147(1): 30-5.
-
(1998)
Am J Epidemiol
, vol.147
, Issue.1
, pp. 30-35
-
-
Dilley, A.1
Austin, H.2
Hooper, W.C.3
-
6
-
-
0033860279
-
Risk of venous thromboembolism associated with the insertion/deletion polymorphism in the angiotensin-converting enzyme gene
-
Gonzalez Ordonez AJ, Fernandez Carreira JM, Medina Rodriguez JM, et al. Risk of venous thromboembolism associated with the insertion/deletion polymorphism in the angiotensin-converting enzyme gene. Blood Coagul Fibrinolysis 2000; 11(5): 485-90.
-
(2000)
Blood Coagul Fibrinolysis
, vol.11
, Issue.5
, pp. 485-490
-
-
Gonzalez Ordonez, A.J.1
Fernandez Carreira, J.M.2
Medina Rodriguez, J.M.3
-
7
-
-
0035352321
-
Insertion/deletion polymorphism of the angiotensin I converting enzyme gene and pulmonary thromboembolism in Chinese population
-
Lu Y, Hui R, Zhao Y. Insertion/deletion polymorphism of the angiotensin I converting enzyme gene and pulmonary thromboembolism in Chinese population. Zhonghua Jie He He Hu Xi Za Zhi 2001; 24(5): 265-8.
-
(2001)
Zhonghua Jie He He Hu Xi Za Zhi
, vol.24
, Issue.5
, pp. 265-268
-
-
Lu, Y.1
Hui, R.2
Zhao, Y.3
-
8
-
-
0031762928
-
Deletion polymorphism in the angiotensin-converting enzyme gene as a thrombophilic risk factor after hip arthroplasty
-
Philipp CS, Dilley A, Saidi P, et al. Deletion polymorphism in the angiotensin-converting enzyme gene as a thrombophilic risk factor after hip arthroplasty. Thromb Haemost 1998; 80: 869-873.
-
(1998)
Thromb Haemost
, vol.80
, pp. 869-873
-
-
Philipp, C.S.1
Dilley, A.2
Saidi, P.3
-
9
-
-
0034533214
-
Effect of the angiotensin-converting enzyme gene deletion polymorphism on the risk of venous thromboembolism
-
Jackson A, Brown K, Langdown J, et al. Effect of the angiotensin-converting enzyme gene deletion polymorphism on the risk of venous thromboembolism. Br J Haematol 2000; 111(2): 562-4.
-
(2000)
Br J Haematol
, vol.111
, Issue.2
, pp. 562-564
-
-
Jackson, A.1
Brown, K.2
Langdown, J.3
-
10
-
-
0010260321
-
Treatment of deep vein thrombosis
-
Couturaud F, Kearon C. Treatment of deep vein thrombosis. Sem Vasc Med 2002; 1(1): 43-54.
-
(2002)
Sem Vasc Med
, vol.1
, Issue.1
, pp. 43-54
-
-
Couturaud, F.1
Kearon, C.2
-
11
-
-
0028814316
-
Role of clotting factor VIII an effect of von Willebrand factor on occurrence of DVT
-
Koster T, Blann AD, Briet E, et al. Role of clotting factor VIII an effect of von Willebrand factor on occurrence of DVT. Lancet 1995; 345: 152-5.
-
(1995)
Lancet
, vol.345
, pp. 152-155
-
-
Koster, T.1
Blann, A.D.2
Briet, E.3
-
12
-
-
0033519051
-
Venous thrombosis: A multicausal disease
-
Rosendaal FR. Venous thrombosis: A multicausal disease. Lancet 1999; 353: 1167-73.
-
(1999)
Lancet
, vol.353
, pp. 1167-1173
-
-
Rosendaal, F.R.1
-
13
-
-
0032934812
-
Increased levels of factor VIII and fibrinogen in patients with venous thrombosis are not caused by acute phase reactions
-
Kamphuisen PW, Eikenboom JCJ, Vos HL, et al. Increased levels of factor VIII and fibrinogen in patients with venous thrombosis are not caused by acute phase reactions. Thromb Haemost 1999; 81: 680-3.
-
(1999)
Thromb Haemost
, vol.81
, pp. 680-683
-
-
Kamphuisen, P.W.1
Eikenboom, J.C.J.2
Vos, H.L.3
-
14
-
-
0032543761
-
Venous thrombosis - The interaction of genes and the environment
-
Bertina RM, Rosendaal FR. Venous thrombosis - The interaction of genes and the environment. N Engl J Med 1998; 338(25): 1840-1.
-
(1998)
N Engl J Med
, vol.338
, Issue.25
, pp. 1840-1841
-
-
Bertina, R.M.1
Rosendaal, F.R.2
-
15
-
-
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 of Epidemiol 1996; 143(12): 1257-65.
-
(1996)
Am J of Epidemiol
, vol.143
, Issue.12
, pp. 1257-1265
-
-
Frezzato, M.1
Tosetto, A.2
Rodeghiero, F.3
-
16
-
-
0032976023
-
Genetic determinants of heritable venous thrombosis: Genotyping methods for factor V(Leiden)A1691G, methylenetetrahydrofolate reductase C677T, prothrombin G20210A mutation, and algorithms for venous thrombosis investigations
-
Donnelly JG, Rock GA. Genetic determinants of heritable venous thrombosis: Genotyping methods for factor V(Leiden)A1691G, methylenetetrahydrofolate reductase C677T, prothrombin G20210A mutation, and algorithms for venous thrombosis investigations. Clin Biochem 1999; 32(3): 223-228.
-
(1999)
Clin Biochem
, vol.32
, Issue.3
, pp. 223-228
-
-
Donnelly, J.G.1
Rock, G.A.2
-
17
-
-
0026581089
-
PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1)
-
Rigat B, Hubert C, Corvol P, et al. PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1). Nucleic Acids Res 1992; 20(6): 1433.
-
(1992)
Nucleic Acids Res
, vol.20
, Issue.6
, pp. 1433
-
-
Rigat, B.1
Hubert, C.2
Corvol, P.3
-
19
-
-
0032520087
-
Relation of Factor V Leiden genotype to risk for acute deep venous thrombosis after joint replacement surgery
-
Ryan DH, Crowther MA, Ginsberg JS, et al. Relation of Factor V Leiden genotype to risk for acute deep venous thrombosis after joint replacement surgery. Ann Intern Med 1998; 128(4): 270-6.
-
(1998)
Ann Intern Med
, vol.128
, Issue.4
, pp. 270-276
-
-
Ryan, D.H.1
Crowther, M.A.2
Ginsberg, J.S.3
-
20
-
-
0033602514
-
Extended anticoagulation compared to placebo after three months of therapy for a first episode of idiopathic venous thromboembolism
-
Kearon C, Gent M, Hirsh J, et al. Extended anticoagulation compared to placebo after three months of therapy for a first episode of idiopathic venous thromboembolism. N Engl J Med 1999; 340(12): 901-7.
-
(1999)
N Engl J Med
, vol.340
, Issue.12
, pp. 901-907
-
-
Kearon, C.1
Gent, M.2
Hirsh, J.3
-
21
-
-
0025284083
-
Intraoperative venous dilation and subsequent development of deep vein thrombosis in patients undergoing total hip or knee replacement
-
Stewart GJ, Lachman JW, Alburger PD, et al. Intraoperative venous dilation and subsequent development of deep vein thrombosis in patients undergoing total hip or knee replacement. Ultrasound Med Biol 1990; 16(2): 133-40.
-
(1990)
Ultrasound Med Biol
, vol.16
, Issue.2
, pp. 133-140
-
-
Stewart, G.J.1
Lachman, J.W.2
Alburger, P.D.3
-
22
-
-
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, et al. 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(10): 3698-703.
-
(1996)
Blood
, vol.88
, Issue.10
, pp. 3698-3703
-
-
Poort, S.W.1
Rosendaal, F.R.2
Reitsma, P.H.3
-
23
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BP, Koster T, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369(6475): 64-7.
-
(1994)
Nature
, vol.369
, Issue.6475
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.2
Koster, T.3
-
24
-
-
0034840147
-
Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism-pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism
-
Emmerich J, Rosendaal FR, Cattaneo M, et al. Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism-pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism. Thromb Haemost 2001; 86(3): 809-16.
-
(2001)
Thromb Haemost
, vol.86
, Issue.3
, pp. 809-816
-
-
Emmerich, J.1
Rosendaal, F.R.2
Cattaneo, M.3
-
25
-
-
0033602514
-
A comparison of three months of anticoagulation with extended anticoagulation for a first episode of idiopathic venous thromboembolism
-
Kearon C, Gent M, Hirsh J, et al. A comparison of three months of anticoagulation with extended anticoagulation for a first episode of idiopathic venous thromboembolism. N Engl J Med 1999; 340(12): 901-7.
-
(1999)
N Engl J Med
, vol.340
, Issue.12
, pp. 901-907
-
-
Kearon, C.1
Gent, M.2
Hirsh, J.3
-
26
-
-
0035913237
-
Three months versus one year of oral anticoagulant therapy for idiopathic deep venous thrombosis. Warfarin Optimal Duration Italian Trial Investigators
-
Agnelli G, Prandoni P, Santamaria MG, et al. Three months versus one year of oral anticoagulant therapy for idiopathic deep venous thrombosis. Warfarin Optimal Duration Italian Trial Investigators. N Engl J Med 2001; 345(3): 165-9.
-
(2001)
N Engl J Med
, vol.345
, Issue.3
, pp. 165-169
-
-
Agnelli, G.1
Prandoni, P.2
Santamaria, M.G.3
-
27
-
-
0030978253
-
Age-specific incidence rates of venous thromboembolism among heterozygous carriers of Factor V Leiden mutation
-
Ridker PM, Glynn RJ, Miletich JP, et al. Age-specific incidence rates of venous thromboembolism among heterozygous carriers of Factor V Leiden mutation. Ann Intern Med 1997; 126(7): 528-31.
-
(1997)
Ann Intern Med
, vol.126
, Issue.7
, pp. 528-531
-
-
Ridker, P.M.1
Glynn, R.J.2
Miletich, J.P.3
-
28
-
-
0029016883
-
Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S
-
Zoller B, Berntsdotter A, Garcia de Frutos P, et al. Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S. Blood 1995; 85(12): 3518-23.
-
(1995)
Blood
, vol.85
, Issue.12
, pp. 3518-3523
-
-
Zoller, B.1
Berntsdotter, A.2
Garcia De Frutos, P.3
-
29
-
-
0030968543
-
Mortality and causes of death in inherited antithrombin deficiency
-
Van Boven HH, Vandenbroucke JP, Westendorp RGJ, et al. Mortality and causes of death in inherited antithrombin deficiency. Thromb Haemost 1997; 77(3): 452-5.
-
(1997)
Thromb Haemost
, vol.77
, Issue.3
, pp. 452-455
-
-
Van Boven, H.H.1
Vandenbroucke, J.P.2
Westendorp, R.G.J.3
-
30
-
-
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, 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
-
31
-
-
0002440652
-
Case-control studies
-
In: Rothman KJ, Greenland S, editors; Philadelphia, PA: Lippincott Williams & Wilkins
-
Rothman KJ, Greenland S. Case-control studies. In: Rothman KJ, Greenland S, editors. Modern Epidemiology. Philadelphia, PA: Lippincott Williams & Wilkins, 1998: 93-114.
-
(1998)
Modern Epidemiology.
, pp. 93-114
-
-
Rothman, K.J.1
Greenland, S.2
|