-
1
-
-
33645296094
-
Prevalence of factor v Leiden and prothrombin G20210A mutations in Chinese patients with deep venous thrombosis and pulmonary embolism
-
Jun ZJ, Ping T, Lei Y, Li L, Ming SY, Jing W. Prevalence of factor V Leiden and prothrombin G20210A mutations in Chinese patients with deep venous thrombosis and pulmonary embolism. Clin Lab Haem 2006; 28:111-116.
-
(2006)
Clin Lab Haem
, vol.28
, pp. 111-116
-
-
Jun, Z.J.1
Ping, T.2
Lei, Y.3
Li, L.4
Ming, S.Y.5
Jing, W.6
-
2
-
-
40949145685
-
Gene variants associated with deep vein thrombosis
-
Bezemer ID, Bare LA, Doggen CJM, Arellano AR, Tong C, Rowland CM, et al. Gene variants associated with deep vein thrombosis. JAMA 2008; 299:1306-1314.
-
(2008)
JAMA
, vol.299
, pp. 1306-1314
-
-
Bezemer, I.D.1
Bare, L.A.2
Cjm, D.3
Arellano, A.R.4
Tong, C.5
Rowland, C.M.6
-
3
-
-
35748974858
-
Molecular analysis of factor v Leiden, factor v Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients
-
Dölek B, Eraslan S, Eroglu S, Kesim BE, Ulutin T, Yalçiner A, et al. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients. Clin Appl Thromb Hemost 2007; 13:435-438.
-
(2007)
Clin Appl Thromb Hemost
, vol.13
, pp. 435-438
-
-
Dölek, B.1
Eraslan, S.2
Eroglu, S.3
Kesim, B.E.4
Ulutin, T.5
Yalçiner, A.6
-
4
-
-
0028910906
-
Mutation in the gene coding for coagulation factor v and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men
-
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 Engl J Med 1995; 332:912-917.
-
(1995)
N Engl 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
-
5
-
-
20244369707
-
The risk of recurrent venous thromboembolism in patients with and without factor v Leiden
-
Eichinger S, Pabinger I, Stumpflen A, Hirschl M, Bialonczyk C, Schneider B, et al. The risk of recurrent venous thromboembolism in patients with and without factor V Leiden. Thromb Haemost 1997; 77:624-628.
-
(1997)
Thromb Haemost
, vol.77
, pp. 624-628
-
-
Eichinger, S.1
Pabinger, I.2
Stumpflen, A.3
Hirschl, M.4
Bialonczyk, C.5
Schneider, B.6
-
6
-
-
0032897895
-
The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: Prevalence and association with factor v G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels
-
Cattaneo M, Chantarangkul V, Taioli E, Santos JH, Tagliabue L. The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels. Thromb Res 1999; 93:1-8.
-
(1999)
Thromb Res
, vol.93
, pp. 1-8
-
-
Cattaneo, M.1
Chantarangkul, V.2
Taioli, E.3
Santos, J.H.4
Tagliabue, L.5
-
7
-
-
0029850530
-
A common genetic variation in the 30-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 RM. A common genetic variation in the 30-untranslated region of the prothrombin gene is associated with elevated plasma 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
-
8
-
-
0002804385
-
Gene analysis
-
Weatherall DJ, editor. London: Churchill Livingstone
-
Old JM, Higgs DR. Gene analysis. In: Weatherall DJ, editor. Methods in hematology. The thalassemias. Vol.6. London: Churchill Livingstone; 1983. pp. 74-101.
-
(1983)
Methods in Hematology. The Thalassemias
, vol.6
, pp. 74-101
-
-
Old, J.M.1
Higgs, D.R.2
-
9
-
-
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, 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
Bpc, K.2
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
De Ronde, H.6
-
10
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyatte P, Sheppard CA, Mathews RG, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10:111-113.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyatte, P.4
Sheppard, C.A.5
Mathews, R.G.6
-
11
-
-
44649129978
-
Prevalence of factor v Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran
-
Rahimi Z, Vaisi-Raygani A, Mozafari H, Kharrazi H, Rezaei M, Nagel RL. Prevalence of factor V Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran. J Thromb Thrombolysis 2008; 25:280-283.
-
(2008)
J Thromb Thrombolysis
, vol.25
, pp. 280-283
-
-
Rahimi, Z.1
Vaisi-Raygani, A.2
Mozafari, H.3
Kharrazi, H.4
Rezaei, M.5
Nagel, R.L.6
-
12
-
-
0028931717
-
High risk of thrombosis in patients homozygous for factor v Leiden (activated protein C resistance)
-
Rosendaal FR, Koster T, Vandenbroucke JP, Reitsma PH. High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance). Blood 1995; 85:1504-1508.
-
(1995)
Blood
, vol.85
, pp. 1504-1508
-
-
Rosendaal, F.R.1
Koster, T.2
Vandenbroucke, J.P.3
Reitsma, P.H.4
-
13
-
-
23844551772
-
A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis
-
Almawi WY, Tamim H, Kreidy R, Timson G, Rahal E, NabulsiM, et al. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis. J Thromb Thrombolysis 2005; 19:189-196.
-
(2005)
J Thromb Thrombolysis
, vol.19
, pp. 189-196
-
-
Almawi, W.Y.1
Tamim, H.2
Kreidy, R.3
Timson, G.4
Nabulsim, R.E.5
-
14
-
-
35448932323
-
Increased factor v Leiden frequency is associated with venous thrombotic events among young Brazilian patients
-
Sabino AP, Guimaraes DAM, Ribeiro DD, Paiva SG, Dusse LMS, Carvalho MG, Fernandes AP. Increased factor V Leiden frequency is associated with venous thrombotic events among young Brazilian patients. J Thromb Thrombolysis 2007; 24:261-266.
-
(2007)
J Thromb Thrombolysis
, vol.24
, pp. 261-266
-
-
Sabino, A.P.1
Dam, G.2
Ribeiro, D.D.3
Paiva, S.G.4
Lms, D.5
Carvalho, M.G.6
Fernandes, A.P.7
-
15
-
-
40549119459
-
Hereditary thrombophilic risk factors and venous thromboembolism in Istanbul, Turkey: The role in different clinical manifestations of venous thromboembolism
-
Okumus G, Kiyan E, Arseven O, Tabak L, Diz-Kucukkaya R, Unlucerci Y, et al. Hereditary thrombophilic risk factors and venous thromboembolism in Istanbul, Turkey: the role in different clinical manifestations of venous thromboembolism. Clin Appl Thromb Hemost 2008; 14: 168-173.
-
(2008)
Clin Appl Thromb Hemost
, vol.14
, pp. 168-173
-
-
Okumus, G.1
Kiyan, E.2
Arseven, O.3
Tabak, L.4
Diz-Kucukkaya, R.5
Unlucerci, Y.6
-
16
-
-
33645729527
-
Risk of recurrent venous thromboembolism in patients with common thrombophilia
-
Ho WH, Hankey GJ, Quinlan DJ, Eikelboom JW. Risk of recurrent venous thromboembolism in patients with common thrombophilia. Arch Intern Med 2006; 166:729-736.
-
(2006)
Arch Intern Med
, vol.166
, pp. 729-736
-
-
Ho, W.H.1
Hankey, G.J.2
Quinlan, D.J.3
Eikelboom, J.W.4
-
17
-
-
51849149604
-
Factor v Leiden prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients
-
Altinisik J, Ates O, Ulutin T, Cengiz M, Buyru N. Factor V Leiden, prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients. Clin Appl Thromb Hemost 2008; 14:415-420.
-
(2008)
Clin Appl Thromb Hemost
, vol.14
, pp. 415-420
-
-
Altinisik, J.1
Ates, O.2
Ulutin, T.3
Cengiz, M.4
Buyru, N.5
-
18
-
-
31644446683
-
Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor v Leiden mutation
-
Gonzalez-Porras JR, Garcia-Sanz R, Alberca I, Lopez ML, Balanzatequi A, Gutierrez O, et al. Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation. Blood Coagul Fibrinolysis 2006; 17:23-28.
-
(2006)
Blood Coagul Fibrinolysis
, vol.17
, pp. 23-28
-
-
Gonzalez-Porras, J.R.1
Garcia-Sanz, R.2
Alberca, I.3
Lopez, M.L.4
Balanzatequi, A.5
Gutierrez, O.6
-
19
-
-
0032969605
-
No evidence for an increased risk of venous thrombosis in patients with factor v Leiden by the homozygous 677C to T mutation in the methylene- tetrahydrofolate-reductase gene
-
Rintelen C, Mannhalter C, Lechner K, Eichinger S, Kyrle PA, Papagiannopoulos M, et al. No evidence for an increased risk of venous thrombosis in patients with factor V Leiden by the homozygous 677C to T mutation in the methylene-tetrahydrofolate-reductase gene. Blood Coagul Fibrinolysis 1999; 10:101-105.
-
(1999)
Blood Coagul Fibrinolysis
, vol.10
, pp. 101-105
-
-
Rintelen, C.1
Mannhalter, C.2
Lechner, K.3
Eichinger, S.4
Kyrle, P.A.5
Papagiannopoulos, M.6
-
20
-
-
0030760946
-
A common mutation in the methylenetetrahydrofolate reductase gene (C677T). increases the risk for deep-vein thrombosis in patients with mutant factor v (factor V:Q506)
-
Cattaneo M, Tsai MY, Bucciarelli P, Taioli E, Zighetti ML, Bignell M, Manaucci PM. A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506). Arterioscler Thromb Vasc Biol 1997; 17:1662-1666.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 1662-1666
-
-
Cattaneo, M.1
Tsai, M.Y.2
Bucciarelli, P.3
Taioli, E.4
Zighetti, M.L.5
Bignell, M.6
Manaucci, P.M.7
-
21
-
-
0031886677
-
Thermolabile methylenetetrahydrofolate reductase and factor v Leiden in the risk of deep-vein thrombosis
-
Kluijtmans LA, den Heijer M, Reitsma PH, Heil SG, Blom HJ, Rosendaal FR. Thermolabile methylenetetrahydrofolate reductase and factor V Leiden in the risk of deep-vein thrombosis. Thromb Haemost 1998; 79:254-258.
-
(1998)
Thromb Haemost
, vol.79
, pp. 254-258
-
-
Kluijtmans, L.A.1
Den Heijer, M.2
Reitsma, P.H.3
Heil, S.G.4
Blom, H.J.5
Rosendaal, F.R.6
-
22
-
-
33947251140
-
No association between the common MTHFR 677C!T polymorphism and venous thrombosis
-
Bezemer ID, Doggen CJM, Vos HL, Rosendaal FR. No association between the common MTHFR 677C!T polymorphism and venous thrombosis. Arch Intern Med 2007; 167:497-501.
-
(2007)
Arch Intern Med
, vol.167
, pp. 497-501
-
-
Bezemer, I.D.1
Cjm, D.2
Vos, H.L.3
Rosendaal, F.R.4
-
23
-
-
33846899709
-
Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South Indians
-
Naushad S, Jamal NJ, Angalena R, Prasad CK, Devi AR. Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South Indians. Blood Coagul Fibrinolysis 2007; 18:113-117.
-
(2007)
Blood Coagul Fibrinolysis
, vol.18
, pp. 113-117
-
-
Naushad, S.1
Jamal, N.J.2
Angalena, R.3
Prasad, C.K.4
Devi, A.R.5
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