-
1
-
-
0033519051
-
Venous thrombosis: A multicausal disease
-
FR Rosendaal 1999 Venous thrombosis: a multicausal disease Lancet 353 1167 1173
-
(1999)
Lancet
, vol.353
, pp. 1167-1173
-
-
Rosendaal, F.R.1
-
2
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
RM Bertina BPC Koeleman T Koster FR Rosendaal RJ Dirven H de Ronde PA van der Velden PH Reitsma 1994 Mutation in blood coagulation factor V associated with resistance to activated protein C Nature 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
Van Der Velden, P.A.7
Reitsma, P.H.8
-
4
-
-
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
-
SR Poort FR Rosendaal PH Reitsma RM Bertina 1996 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 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
-
5
-
-
0029153954
-
The polymerase chain reaction with sequence specific primers for the detection of the factor V mutation associated with activated protein C resistance
-
NE Kirschbaum PA Foster 1995 The polymerase chain reaction with sequence specific primers for the detection of the factor V mutation associated with activated protein C resistance Thromb Haemost 74 874 878
-
(1995)
Thromb Haemost
, vol.74
, pp. 874-878
-
-
Kirschbaum, N.E.1
Foster, P.A.2
-
6
-
-
0032068646
-
Multiplex ASA PCR for a simultaneous determination of factor V Leiden gene, G-A 20210 prothrombin gene and C-T 677 MTHFR gene mutations
-
N Hezard P Cornillet-Lefebvre L Gillot G Potron P Nguyen 1998 Multiplex ASA PCR for a simultaneous determination of factor V Leiden gene, G-A 20210 prothrombin gene and C-T 677 MTHFR gene mutations Thromb Haemost 79 1054 1055
-
(1998)
Thromb Haemost
, vol.79
, pp. 1054-1055
-
-
Hezard, N.1
Cornillet-Lefebvre, P.2
Gillot, L.3
Potron, G.4
Nguyen, P.5
-
7
-
-
0023753018
-
Diagnosis of sickle cell anemia and beta-thalassemia with enzymatically amplified DNA and nonradioactive allele-specific oligonucleotide probes
-
RK Saiki CA Chang CH Levenson TC Warren CD Boehm HH Kazazian Jr HA Erlich 1988 Diagnosis of sickle cell anemia and beta-thalassemia with enzymatically amplified DNA and nonradioactive allele-specific oligonucleotide probes N Engl J Med 319 537 541
-
(1988)
N Engl J Med
, vol.319
, pp. 537-541
-
-
Saiki, R.K.1
Chang, C.A.2
Levenson, C.H.3
Warren, T.C.4
Boehm, C.D.5
Kazazian Jr., H.H.6
Erlich, H.A.7
-
8
-
-
0343517715
-
Evaluation of the Roche diagnostics LightCycler-Factor V Leiden mutation detection kit and the LightCycler-Prothrombin mutation detection kit
-
M Nauck M Marz H Weiland 2000 Evaluation of the Roche diagnostics LightCycler-Factor V Leiden mutation detection kit and the LightCycler- Prothrombin mutation detection kit Clin Biochem 33 213 216
-
(2000)
Clin Biochem
, vol.33
, pp. 213-216
-
-
Nauck, M.1
Marz, M.2
Weiland, H.3
-
9
-
-
0032921340
-
Rapid detection of prothrombotic mutations of prothrombin (G20210A), factor V (G1691A), and methylenetetrahydrofolate Reductase (C677T) by real-time fluorescence PCR with the LightCycler
-
N von Ahsen E Schutz VW Armstrong M Oellerich 1999 Rapid detection of prothrombotic mutations of prothrombin (G20210A), factor V (G1691A), and methylenetetrahydrofolate Reductase (C677T) by real-time fluorescence PCR with the LightCycler Clin Chem 45 694 696
-
(1999)
Clin Chem
, vol.45
, pp. 694-696
-
-
Von Ahsen, N.1
Schutz, E.2
Armstrong, V.W.3
Oellerich, M.4
-
10
-
-
0031451539
-
Real-time fluorescence genotyping of factor V Leiden during rapid-cycle PCR
-
MJ Lay CT Wittwer 1997 Real-time fluorescence genotyping of factor V Leiden during rapid-cycle PCR Clin Chem 43 2262 2267
-
(1997)
Clin Chem
, vol.43
, pp. 2262-2267
-
-
Lay, M.J.1
Wittwer, C.T.2
-
11
-
-
0031981017
-
Geographic distribution of the 20210 G to a prothrombin variant
-
FR Rosendaal CJM Doggen A Zivelin VR Arruda M Aiach DS Siscovick A Hillarp HH Watzke F Bernardi AM Cumming FE Preston PH Reitsma 1998 Geographic distribution of the 20210 G to A prothrombin variant Thromb Haemost 79 700
-
(1998)
Thromb Haemost
, vol.79
, pp. 700
-
-
Rosendaal, F.R.1
Doggen, C.J.M.2
Zivelin, A.3
Arruda, V.R.4
Aiach, M.5
Siscovick, D.S.6
Hillarp, A.7
Watzke, H.H.8
Bernardi, F.9
Cumming, A.M.10
Preston, F.E.11
Reitsma, P.H.12
-
12
-
-
0030810628
-
Risk of venous thromboembolism associated with a G to a transition at position 20210 in the 38-untranslated region of the prothrombin gene
-
K Brown R Luddington D Williamson P Baker T Baglin 1997 Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 38-untranslated region of the prothrombin gene Br J Haematol 98 907
-
(1997)
Br J Haematol
, vol.98
, pp. 907
-
-
Brown, K.1
Luddington, R.2
Williamson, D.3
Baker, P.4
Baglin, T.5
-
14
-
-
0030845360
-
The 20210 a allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep vein thrombosis
-
A Hillarp B Zoller PJ Svensson B Dahlback 1997 The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep vein thrombosis Thromb Haemost 78 990
-
(1997)
Thromb Haemost
, vol.78
, pp. 990
-
-
Hillarp, A.1
Zoller, B.2
Svensson, P.J.3
Dahlback, B.4
-
15
-
-
0032946813
-
The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease
-
M Vargas I Soto CR Pinto MF Urgelles A Batalla J Rodriguez-Reguero A Cortina V Alvarez E Coto 1999 The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease Blood Coagul Fibrinolysis 10 39 41
-
(1999)
Blood Coagul Fibrinolysis
, vol.10
, pp. 39-41
-
-
Vargas, M.1
Soto, I.2
Pinto, C.R.3
Urgelles, M.F.4
Batalla, A.5
Rodriguez-Reguero, J.6
Cortina, A.7
Alvarez, V.8
Coto, E.9
-
16
-
-
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
-
M Cattaneo V Chantarangkul E Taioli JH Santos L Tagliabue 1999 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 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
-
17
-
-
0032840589
-
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors
-
T Antoniadi T Hatzis C Kroupis E Economou-Petersen MB Petersen 1999 Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors Am J Hematol 61 265 267
-
(1999)
Am J Hematol
, vol.61
, pp. 265-267
-
-
Antoniadi, T.1
Hatzis, T.2
Kroupis, C.3
Economou-Petersen, E.4
Petersen, M.B.5
-
19
-
-
0343168063
-
Prothrombin G20210A, factor V Leiden, and factor XIII Val34Leu: Common mutations of blood coagulation factors and deep vein thrombosis in Austria
-
W Renner H Koppel C Hoffmann K Schallmoser O Stanger H Toplak TC Wascher E Pilger 2000 Prothrombin G20210A, factor V Leiden, and factor XIII Val34Leu: common mutations of blood coagulation factors and deep vein thrombosis in Austria Thromb Res 99 35 39
-
(2000)
Thromb Res
, vol.99
, pp. 35-39
-
-
Renner, W.1
Koppel, H.2
Hoffmann, C.3
Schallmoser, K.4
Stanger, O.5
Toplak, H.6
Wascher, T.C.7
Pilger, E.8
-
20
-
-
0034866037
-
Prevalence and association of the factor V Leiden and prothrombin G20210A in healthy subjects and patients with venous thromboembolism
-
D Coen R Zadro L Honović L Banfić A Stavljenić Rukavina 2001 Prevalence and association of the factor V Leiden and prothrombin G20210A in healthy subjects and patients with venous thromboembolism Croat Med J 42 488 492
-
(2001)
Croat Med J
, vol.42
, pp. 488-492
-
-
Coen, D.1
Zadro, R.2
Honović, L.3
Banfić, L.4
Stavljenić Rukavina, A.5
-
22
-
-
0344918993
-
Heterogeneous distribution of the 20210G=A prothrombin and 677C=T methylenetetrahydrofolate reductase mutations in different human populations: Relevance for vascular disease risk
-
RF Franco J Elion MH Tavella AG Araujo MA Zago 1997 Heterogeneous distribution of the 20210G=A prothrombin and 677C=T methylenetetrahydrofolate reductase mutations in different human populations: relevance for vascular disease risk Blood 90 3130a
-
(1997)
Blood
, vol.90
-
-
Franco, R.F.1
Elion, J.2
Tavella, M.H.3
Araujo, A.G.4
Zago, M.A.5
-
23
-
-
0031618374
-
Frequencies of prothrombin 20210 G=A mutation may be different among races studies on Japanese populations with various forms of thrombotic disorders and healthy subjects
-
I Isshiki M Murata R Watanabe Y Matsubara K Kawano N Aoki H Yoshino K Ishikawa G Watanabe Y Ikeda 1998 Frequencies of prothrombin 20210 G=A mutation may be different among races studies on Japanese populations with various forms of thrombotic disorders and healthy subjects Blood Coagul Fibrinol 9 105
-
(1998)
Blood Coagul Fibrinol
, vol.9
, pp. 105
-
-
Isshiki, I.1
Murata, M.2
Watanabe, R.3
Matsubara, Y.4
Kawano, K.5
Aoki, N.6
Yoshino, H.7
Ishikawa, K.8
Watanabe, G.9
Ikeda, Y.10
-
24
-
-
0032933161
-
Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR
-
MJ Hessner RA Luhm SL Pearson DJ Endean KD Friedman RR Montgomery 1999 Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR Thromb Haemost 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
-
25
-
-
0031694967
-
The prothrombin 20210 G to a variation and thrombosis
-
RM Bertina 1998 The prothrombin 20210 G to A variation and thrombosis Curr Opin Hematol 5 339 342
-
(1998)
Curr Opin Hematol
, vol.5
, pp. 339-342
-
-
Bertina, R.M.1
-
26
-
-
0031856405
-
Prevalence of the G20210A polymorphism in the 3′-untranslated region of the prothrombin gene in different human populations
-
RF Franco SE Santos J Elion MH Tavella MA Zago 1998 Prevalence of the G20210A polymorphism in the 3′-untranslated region of the prothrombin gene in different human populations Acta Haematol 100 9 12
-
(1998)
Acta Haematol
, vol.100
, pp. 9-12
-
-
Franco, R.F.1
Santos, S.E.2
Elion, J.3
Tavella, M.H.4
Zago, M.A.5
-
27
-
-
0037321317
-
Prothrombin G20210A mutation, antithrombin, heparin cofactor II, protein C, and protein S defects
-
RL Bick 2003 Prothrombin G20210A mutation, antithrombin, heparin cofactor II, protein C, and protein S defects Hematol Oncol Clin North Am 17 9 36
-
(2003)
Hematol Oncol Clin North Am
, vol.17
, pp. 9-36
-
-
Bick, R.L.1
-
28
-
-
30644474960
-
An Arab selective gradient in the distribution of factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase (MTHFR) C677T
-
G Ameen N Irani-Hakime NA Fawaz T Mahjoub WY Almawi 2005 An Arab selective gradient in the distribution of factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase (MTHFR) C677T J Thromb Haemost 3 2126 2127
-
(2005)
J Thromb Haemost
, vol.3
, pp. 2126-2127
-
-
Ameen, G.1
Irani-Hakime, N.2
Fawaz, N.A.3
Mahjoub, T.4
Almawi, W.Y.5
-
30
-
-
0036796224
-
Prevalence of two thrombophilia predisposing mutations: Factor V G1691A (R506Q; Leiden) and prothrombin G20210A, among healthy Lebanese
-
H Tamim RR Finan WY Almawi 2002 Prevalence of two thrombophilia predisposing mutations: factor V G1691A (R506Q; Leiden) and prothrombin G20210A, among healthy Lebanese Thromb Haemost 88 691 692
-
(2002)
Thromb Haemost
, vol.88
, pp. 691-692
-
-
Tamim, H.1
Finan, R.R.2
Almawi, W.Y.3
-
31
-
-
0037954204
-
High prevalence of prothrombin G20210A mutation among patients with deep venous thrombosis in Lebanon
-
A Taher I Khalil R Abou-Merhi A Shamseddine A Bazarbachi 2003 High prevalence of prothrombin G20210A mutation among patients with deep venous thrombosis in Lebanon Thromb Haemost 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
-
32
-
-
0033501907
-
Prothrombin and the prothrombin 20210 G to a polymorphism: Their relationship with hypercoagulability and thrombosis
-
A Girolami P Simioni L Scarano G Carraro 1999 Prothrombin and the prothrombin 20210 G to A polymorphism: their relationship with hypercoagulability and thrombosis Blood Rev 13 205 210
-
(1999)
Blood Rev
, vol.13
, pp. 205-210
-
-
Girolami, A.1
Simioni, P.2
Scarano, L.3
Carraro, G.4
-
33
-
-
4344685226
-
Prothrombin G20210A gene mutation with LightCycler polymerase chain reaction in venous thrombosis and healthy population in the southeast of Turkey
-
O Ayyildiz S Kalkanli S Batun M Aybak A Isikdogan N Tiftik Z Bolaman M Soker E Muftuoglu 2004 Prothrombin G20210A gene mutation with LightCycler polymerase chain reaction in venous thrombosis and healthy population in the southeast of Turkey Heart Vessels 19 164 166
-
(2004)
Heart Vessels
, vol.19
, pp. 164-166
-
-
Ayyildiz, O.1
Kalkanli, S.2
Batun, S.3
Aybak, M.4
Isikdogan, A.5
Tiftik, N.6
Bolaman, Z.7
Soker, M.8
Muftuoglu, E.9
-
34
-
-
33845268445
-
Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population
-
JD Torres H Cardona L Alvarez W Cardona-Maya SA Castañeda F Quintero-Rivera A Cadavid G Bedoya L Tobón 2006 Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population Am J Hematol 81 933 937
-
(2006)
Am J Hematol
, vol.81
, pp. 933-937
-
-
Torres, J.D.1
Cardona, H.2
Alvarez, L.3
Cardona-Maya, W.4
Castañeda, S.A.5
Quintero-Rivera, F.6
Cadavid, A.7
Bedoya, G.8
Tobón, L.9
-
35
-
-
0031851759
-
The prothrombin gene G20210A mutation is not found among Japanese patients with deep vein thrombosis and healthy individuals
-
T Miyata T Kawasaki H Fujimura K Uchida M Tsushima H Kato 1998 The prothrombin gene G20210A mutation is not found among Japanese patients with deep vein thrombosis and healthy individuals Blood Coagul Fibrinolysis 9 451 452
-
(1998)
Blood Coagul Fibrinolysis
, vol.9
, pp. 451-452
-
-
Miyata, T.1
Kawasaki, T.2
Fujimura, H.3
Uchida, K.4
Tsushima, M.5
Kato, H.6
-
36
-
-
0032239152
-
Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Korean patients with deep vein thrombosis
-
TW Kim WK Kim JH Lee SB Kim SW Kim C Suh KH Lee JS Lee EJ Seo HS Chi SH Kim 1998 Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Korean patients with deep vein thrombosis J Korean Med Sci 13 587 590
-
(1998)
J Korean Med Sci
, vol.13
, pp. 587-590
-
-
Kim, T.W.1
Kim, W.K.2
Lee, J.H.3
Kim, S.B.4
Kim, S.W.5
Suh, C.6
Lee, K.H.7
Lee, J.S.8
Seo, E.J.9
Chi, H.S.10
Kim, S.H.11
-
38
-
-
0032529506
-
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene
-
A Zivelin N Rosenberg S Faier N Kornbrot H Peretz C Mannhalter MH Horellou U Seligsohn 1998 A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene Blood 92 1119 1124
-
(1998)
Blood
, vol.92
, pp. 1119-1124
-
-
Zivelin, A.1
Rosenberg, N.2
Faier, S.3
Kornbrot, N.4
Peretz, H.5
Mannhalter, C.6
Horellou, M.H.7
Seligsohn, U.8
-
39
-
-
0036403373
-
Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease
-
F Burzotta K Paciaroni V De Stefano P Chiusolo A Manzoli I Casorelli AM Leone E Rossi G Leone A Maseri F Andreotti 2002 Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease Eur Heart J 23 26 30
-
(2002)
Eur Heart J
, vol.23
, pp. 26-30
-
-
Burzotta, F.1
Paciaroni, K.2
De Stefano, V.3
Chiusolo, P.4
Manzoli, A.5
Casorelli, I.6
Leone, A.M.7
Rossi, E.8
Leone, G.9
Maseri, A.10
Andreotti, F.11
-
41
-
-
0030845360
-
The 20210 a allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
-
A Hillarp B Zöller PJ Svensson B Dahlbäck 1997 The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis Thromb Haemost 78 990 992
-
(1997)
Thromb Haemost
, vol.78
, pp. 990-992
-
-
Hillarp, A.1
Zöller, B.2
Svensson, P.J.3
Dahlbäck, B.4
-
42
-
-
33746025917
-
Distinct association of factor V-Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisia and Lebanon
-
L Bouaziz-Borgi WY Almawi N Mtiraoui B Nsiri SH Keleshian R Kreidy B Louzir N Hezard T Mahjoub 2006 Distinct association of factor V-Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisia and Lebanon Am J Hematol 81 641 643
-
(2006)
Am J Hematol
, vol.81
, pp. 641-643
-
-
Bouaziz-Borgi, L.1
Almawi, W.Y.2
Mtiraoui, N.3
Nsiri, B.4
Keleshian, S.H.5
Kreidy, R.6
Louzir, B.7
Hezard, N.8
Mahjoub, T.9
|