-
1
-
-
0029016883
-
Resistance to activated protein C as an additional risk factor in hereditary deficiency of protein S
-
Zoller B, Bertsdotte A, Gareia de Frutos P, Duhlback B. Resistance to activated protein C as an additional risk factor in hereditary deficiency of protein S. Blood 1995; 85:3518-3523.
-
(1995)
Blood
, vol.85
, pp. 3518-3523
-
-
Zoller, B.1
Bertsdotte, A.2
Gareia De Frutos, P.3
Duhlback, B.4
-
2
-
-
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; 369:46-67.
-
(1994)
Nature
, vol.369
, pp. 46-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
De Ronde, H.6
-
3
-
-
0028810738
-
World distribution of factor V Leiden
-
Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet 1995; 346:1133-1134.
-
(1995)
Lancet
, vol.346
, pp. 1133-1134
-
-
Rees, D.C.1
Cox, M.2
Clegg, J.B.3
-
4
-
-
0032922667
-
High prevalence of factor V Leiden in healthy Jordanian Arabs
-
Awidi A, Shannak M, Bseiso A, Kailani M, Kailani MA, Omar N, Anshasi B. High prevalence of factor V Leiden in healthy Jordanian Arabs. Thromb Haemost 1999; 81:582-584.
-
(1999)
Thromb Haemost
, vol.81
, pp. 582-584
-
-
Awidi, A.1
Shannak, M.2
Bseiso, A.3
Kailani, M.4
Kailani, M.A.5
Omar, N.6
Anshasi, B.7
-
5
-
-
33645484927
-
Frequncy of factor V Leiden, prothrombin G20210A, and methyltetrahydrofolate reductase C677T mutations in 200 healthy individuals, and 150 thrombotic Jordanian patients
-
Eid S, Shubilat T, Habahba N, Rihani G. Frequncy of factor V Leiden, prothrombin G20210A, and methyltetrahydrofolate reductase C677T mutations in 200 healthy individuals, and 150 thrombotic Jordanian patients [Abstract]. Pathophysiol Haemost Thromb 2002; 32 (suppl 2): 135.
-
(2002)
Pathophysiol Haemost Thromb
, vol.32
, Issue.SUPPL. 2
, pp. 135
-
-
Eid, S.1
Shubilat, T.2
Habahba, N.3
Rihani, G.4
-
6
-
-
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 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; 88:3698-3703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
7
-
-
0033899336
-
Prevalence of factor V Leiden and prothrombin G20210A mutations in unselected patients with venous thromboembolism
-
De Moerloose P, Reber G, Perrier A, Perneger T, Bounameaux H. Prevalence of factor V Leiden and prothrombin G20210A mutations in unselected patients with venous thromboembolism. Br J Haematol 2000; 110:125-129.
-
(2000)
Br J Haematol
, vol.110
, pp. 125-129
-
-
De Moerloose, P.1
Reber, G.2
Perrier, A.3
Perneger, T.4
Bounameaux, H.5
-
8
-
-
0031981017
-
Geographic distribution of the 20210 G to a prothrombin variant
-
Rosendaal FR, Doggen CJM, Zivelin A, Arruda VR, Aiach M, Sis Covick DS, et al. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 1998; 79:706-708.
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.M.2
Zivelin, A.3
Arruda, V.R.4
Aiach, M.5
Sis Covick, D.S.6
-
9
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, et al. A candidate genetic risk factor for vascular disease:a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1994; 10:111-113.
-
(1994)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
-
10
-
-
0029655724
-
Molecular genetic analysis in mild hyperhomocysteinemia: A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease
-
Klojtmans LAJ, Van den Hevvel LP, Boers GHJ, Frosst P, Stevens EMB, Denheeijer M, et al. Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease. Am J Hum Genet 1996; 58:35-41.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 35-41
-
-
Klojtmans, L.A.J.1
Van Den Hevvel, L.P.2
Boers, G.H.J.3
Frosst, P.4
Stevens, E.M.B.5
Denheeijer, M.6
-
11
-
-
0032933161
-
Prevalence of prothrombin G20210 A, factor V G1691 a (Leiden), and methyltetrahydrofolate reductase (MTHFR) C 677T in seven different populations determined by multiple allele-specific PCR
-
Hessner MJ, Luhm RA, Pearson SL, Endean DJ, Friedman KD, Montgomery RR. Prevalence of prothrombin G20210 A, factor V G1691 A (Leiden), and methyltetrahydrofolate reductase (MTHFR) C 677T in seven different populations determined by multiple allele-specific PCR. Thromb Haemost 1999; 81:733-738.
-
(1999)
Thromb Haemost
, vol.81
, pp. 733-738
-
-
Hessner, M.J.1
Luhm, R.A.2
Pearson, S.L.3
Endean, D.J.4
Friedman, K.D.5
Montgomery, R.R.6
-
12
-
-
10544253846
-
Inherited thrombophilia: Part I
-
Lane DA, Manucci OM, Bauer KA, Bertina RM, Bochkov NP, Boulyjenkov V, et al. Inherited thrombophilia: Part I. Thromb Haemost 1996; 76:651-662.
-
(1996)
Thromb Haemost
, vol.76
, pp. 651-662
-
-
Lane, D.A.1
Manucci, O.M.2
Bauer, K.A.3
Bertina, R.M.4
Bochkov, N.P.5
Boulyjenkov, V.6
-
13
-
-
0002180743
-
Risk of venous thrombosis in carriers of a common mutation in the homocysteine regulatory enzyme methylteterahydrofolate reductase
-
Ocal IT, Sadeghi A, Press RD. Risk of venous thrombosis in carriers of a common mutation in the homocysteine regulatory enzyme methylteterahydrofolate reductase. Mol Diagnosis 1997; 2:61-68.
-
(1997)
Mol Diagnosis
, vol.2
, pp. 61-68
-
-
Ocal, I.T.1
Sadeghi, A.2
Press, R.D.3
-
14
-
-
0030717409
-
Prevalence of Factor V-Leiden mutation in four distinct American ethnic populations
-
Gregg JP, Yamane AJ, Grody WW. Prevalence of Factor V-Leiden mutation in four distinct American ethnic populations. Am J Med Genet 1997; 73:334-336.
-
(1997)
Am J Med Genet
, vol.73
, pp. 334-336
-
-
Gregg, J.P.1
Yamane, A.J.2
Grody, W.W.3
-
15
-
-
0030747763
-
Prevalence of factor V Leiden mutation in various population
-
Herrman FH, Koesling M, Schoeder W, Latman R, Jimenez-Bonilla R, Lopacciuk S, et al. Prevalence of factor V Leiden mutation in various population. Genet Epidemiol 1997; 14:403-411.
-
(1997)
Genet Epidemiol
, vol.14
, pp. 403-411
-
-
Herrman, F.H.1
Koesling, M.2
Schoeder, W.3
Latman, R.4
Jimenez-Bonilla, R.5
Lopacciuk, S.6
-
16
-
-
0031059758
-
Prevalence of factor V Leiden mutation in Non-European populations
-
Pepe G, Rickards O, Camacho V, Brunelli T, Gori Ann, Giusti B, et al. Prevalence of factor V Leiden mutation in Non-European populations. Thromb Haemost 1997; 77:329-331.
-
(1997)
Thromb Haemost
, vol.77
, pp. 329-331
-
-
Pepe, G.1
Rickards, O.2
Camacho, V.3
Brunelli, T.4
Ann, G.5
Giusti, B.6
-
17
-
-
0034898551
-
High prevalence of factor V Leiden mutation among healthy individuals and patients with deep venous thrombosis in Lebanon
-
7 Taher A, Khalil I, Shamseddine A, El-Ahdab F, Bazarbchi A. High prevalence of factor V Leiden mutation among healthy individuals and patients with deep venous thrombosis in Lebanon. Thromb Haemost 2001; 86:723-724.
-
(2001)
Thromb Haemost
, vol.86
, pp. 723-724
-
-
Taher, A.1
Khalil, I.2
Shamseddine, A.3
El-Ahdab, F.4
Bazarbchi, A.5
-
18
-
-
0030955080
-
4047 Men and women: Implications for venous thromboembolism screening
-
Ridker PM, Miletich JP, Hennekens CH, Buring JE. 4047 men and women: implications for venous thromboembolism screening [Abstract]. JAMA 1997; 277:1305-1307.
-
(1997)
JAMA
, vol.277
, pp. 1305-1307
-
-
Ridker, P.M.1
Miletich, J.P.2
Hennekens, C.H.3
Buring, J.E.4
-
19
-
-
0031903390
-
Prevalence of 20210A allele of the prothrombin gene in venous thromboembolism patients
-
Leroyer C, Mercier B, Oger E, Chenu E, Abgrall JF, Ferec C, Moltier D. Prevalence of 20210A allele of the prothrombin gene in venous thromboembolism patients. Thromb Haemost 1998; 80:49-51.
-
(1998)
Thromb Haemost
, vol.80
, pp. 49-51
-
-
Leroyer, C.1
Mercier, B.2
Oger, E.3
Chenu, E.4
Abgrall, J.F.5
Ferec, C.6
Moltier, D.7
-
20
-
-
0033946578
-
Coagulation factor II activity determination is not usefull as a screening tool for the G20210A prothrombin gene allele
-
Grenewald M, Germowitz A, Beneke H, Guethner C, Gricsshammer M. Coagulation factor II activity determination is not usefull as a screening tool for the G20210A prothrombin gene allele. Thromb Haemost 2000; 84:141-142.
-
(2000)
Thromb Haemost
, vol.84
, pp. 141-142
-
-
Grenewald, M.1
Germowitz, A.2
Beneke, H.3
Guethner, C.4
Gricsshammer, M.5
-
21
-
-
0037954204
-
High prevalence of prothrombin G20210A mutation among patients with deep venous thrombosis in Lebanon
-
Taher A, Khalil I, Abou-Merhi R, Shamseddine A, Bazarbachi A. High prevalence of prothrombin G20210A mutation among patients with deep venous thrombosis in Lebanon. Thromb Haemost 2003; 89:945-946.
-
(2003)
Thromb Haemost
, vol.89
, pp. 945-946
-
-
Taher, A.1
Khalil, I.2
Abou-Merhi, R.3
Shamseddine, A.4
Bazarbachi, A.5
-
22
-
-
0032750381
-
Prevalence of prothrombin gene G20210A mutation in thrombophilic and healthy Algerian subjects
-
Helley D, Chafa O, Yaker NL, Reghits A, Fisher AM. Prevalence of prothrombin gene G20210A mutation in thrombophilic and healthy Algerian subjects. Thromb Haemost 1999; 82:1554-1555.
-
(1999)
Thromb Haemost
, vol.82
, pp. 1554-1555
-
-
Helley, D.1
Chafa, O.2
Yaker, N.L.3
Reghits, A.4
Fisher, A.M.5
-
23
-
-
0036893569
-
Factor V G1691A and factor II G20210A mutations
-
Finan RR, Tamin H, Amen G, Sharide HE, Rasid M, Alunen WY. Factor V G1691A and factor II G20210A mutations. Am J Hematol 2002; 71:300-305.
-
(2002)
Am J Hematol
, vol.71
, pp. 300-305
-
-
Finan, R.R.1
Tamin, H.2
Amen, G.3
Sharide, H.E.4
Rasid, M.5
Alunen, W.Y.6
-
24
-
-
0032852675
-
Factor V leiden and factor II G20210A mutations in patients with recurrent abortion
-
Sovza SS, Ferriani RA, Pontes AG, Zago MA, Franco RF. Factor V leiden and factor II G20210A mutations in patients with recurrent abortion. Hum Reprod 1999; 14:2448-2550.
-
(1999)
Hum Reprod
, vol.14
, pp. 2448-2550
-
-
Sovza, S.S.1
Ferriani, R.A.2
Pontes, A.G.3
Zago, M.A.4
Franco, R.F.5
-
25
-
-
0037633079
-
Common C677T polymorphism of the methyltetrahydrofolate reductase gene and the risk of venous thromboembolism: Meta-analysis of 31 studies
-
Ray JG, Shmorgun D, Chan WS. Common C677T polymorphism of the methyltetrahydrofolate reductase gene and the risk of venous thromboembolism: meta-analysis of 31 studies. Pathophysiol Haemost Thromb 2002; 32:51-58.
-
(2002)
Pathophysiol Haemost Thromb
, vol.32
, pp. 51-58
-
-
Ray, J.G.1
Shmorgun, D.2
Chan, W.S.3
-
26
-
-
0031713550
-
Effect of the MTHFR C677T variant and risk of venous thromboembolism: Interaction with factor V Leiden and prothrombin (G20210A) mutations
-
Brown K, Luddington R, Baglin T. Effect of the MTHFR C677T variant and risk of venous thromboembolism: interaction with factor V Leiden and prothrombin (G20210A) mutations. Br J Haematol 1998; 103:42-44.
-
(1998)
Br J Haematol
, vol.103
, pp. 42-44
-
-
Brown, K.1
Luddington, R.2
Baglin, T.3
|