-
1
-
-
0033519051
-
Venous thrombosis: A multicausal disease
-
10.1016/S0140-6736(98)10266-0
-
Rosendaal FR. Venous thrombosis: A multicausal disease. Lancet 1999;353:1167-1173. 10.1016/S0140-6736(98)10266-0
-
(1999)
Lancet
, vol.353
, Issue.1
, pp. 1167-1173
-
-
Rosendaal, F.R.1
-
2
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
10.1038/369064a0
-
Bertina RM, Koeleman BPC, Koster T, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994;369:64-67. 10.1038/369064a0
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
-
3
-
-
0032921209
-
Born to clot: The European burden
-
10233439
-
Rees DC, Chapman NH, Webster MT, Guerreiro JF, Rochette J, Clegg JB. Born to clot: The European burden. Br J Haematol. 1999;105:564-566. 10233439
-
(1999)
Br. J. Haematol.
, vol.105
, pp. 564-566
-
-
Rees, D.C.1
Chapman, N.H.2
Webster, M.T.3
Guerreiro, J.F.4
Rochette, J.5
Clegg, J.B.6
-
4
-
-
0344255725
-
Absence of Factor V Leiden, thrombomodulin and prothrombin gene variants in Black South African women with pre-eclampsia and eclampsia
-
12628278
-
Hira B, Pegoraro RJ, Rom L, Moodley J. Absence of Factor V Leiden, thrombomodulin and prothrombin gene variants in Black South African women with pre-eclampsia and eclampsia. BJOG. 2003;110:327-328. 12628278
-
(2003)
BJOG
, vol.110
, pp. 327-328
-
-
Hira, B.1
Pegoraro, R.J.2
Rom, L.3
Moodley, J.4
-
5
-
-
0031569558
-
Absence of the factor V Leiden mutation in Ethiopians
-
10.1016/S0049-3848(97)00061-3
-
Abdulkadir J, Feleke Y, Berg JP, Falch JA, Odegaard OR. Absence of the factor V Leiden mutation in Ethiopians. Thromb Res. 1997;86:181-182. 10.1016/S0049-3848(97)00061-3
-
(1997)
Thromb. Res.
, vol.86
, pp. 181-182
-
-
Abdulkadir, J.1
Feleke, Y.2
Berg, J.P.3
Falch, J.A.4
Odegaard, O.R.5
-
6
-
-
0042701681
-
Factor V Leiden and prothrombin G20210A mutations in Thai patients awaiting kidney transplant
-
12757241
-
Arnutti P, Nathalang O, Cowawintaweewat S, Prayoonwiwat W, Choovichian P. Factor V Leiden and prothrombin G20210A mutations in Thai patients awaiting kidney transplant. Southeast Asian J Trop Med Public Health. 2002;33:869-871. 12757241
-
(2002)
Southeast Asian J. Trop. Med. Public Health
, vol.33
, pp. 869-871
-
-
Arnutti, P.1
Nathalang, O.2
Cowawintaweewat, S.3
Prayoonwiwat, W.4
Choovichian, P.5
-
7
-
-
0032239152
-
Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Korean patients with deep venous thrombosis
-
9886165
-
Kim TW, Kim WK, Lee JH, et al. Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Korean patients with deep venous thrombosis. J Korean Med Sci. 1998;13:587-590. 9886165
-
(1998)
J. Korean Med. Sci.
, vol.13
, pp. 587-590
-
-
Kim, T.W.1
Kim, W.K.2
Lee, J.H.3
-
8
-
-
0036544888
-
Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population
-
10.1016/S0049-3848(02)00064-6
-
Lu Y, Zhao Y, Liu G, et al. Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population. Thromb Res. 2002;106:7-12. 10.1016/S0049-3848(02)00064-6
-
(2002)
Thromb. Res.
, vol.106
, pp. 7-12
-
-
Lu, Y.1
Zhao, Y.2
Liu, G.3
-
9
-
-
0033843870
-
The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese
-
10.1002/1096-8652(200009)65:1<45::AID-AJH8>3.0.CO;2-V
-
Irani-Hakime N, Tamim H, Kreidy R, Almawi WY. The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese. Am J Hematol. 2000;65:45-49. 10.1002/ 1096-8652(200009)65:1<45::AID-AJH8>3.0.CO;2-V
-
(2000)
Am. J. Hematol.
, vol.65
, pp. 45-49
-
-
Irani-Hakime, N.1
Tamim, H.2
Kreidy, R.3
Almawi, W.Y.4
-
10
-
-
0036796224
-
Prevalence of two thrombophilia predisposing mutations: Factor V G1691A (R506Q; Leiden) and prothrombin G20210A, among healthy Lebanese
-
12362248
-
Tamim H, Finan RR, Almawi, WY. Prevalence of two thrombophilia predisposing mutations: Factor V G1691A (R506Q; Leiden) and prothrombin G20210A, among healthy Lebanese. Thromb Haemost. 2002;88:691-692. 12362248
-
(2002)
Thromb. Haemost.
, vol.88
, pp. 691-692
-
-
Tamim, H.1
Finan, R.R.2
Almawi, W.Y.3
-
11
-
-
0037743910
-
Factor V Leiden and prothrombin gene G20210A mutations in ocular Behcet disease
-
10.1034/j.1600-0420.2003.00068.x
-
Batioglu F, Atmaca LS, Karabulut HG, Beyza Sayin D. Factor V Leiden and prothrombin gene G20210A mutations in ocular Behcet disease. Acta Ophthalmol Scand. 2003;81:283-285. 10.1034/j.1600-0420.2003.00068.x
-
(2003)
Acta Ophthalmol. Scand.
, vol.81
, pp. 283-285
-
-
Batioglu, F.1
Atmaca, L.S.2
Karabulut, H.G.3
Beyza Sayin, D.4
-
12
-
-
0034111630
-
Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population
-
10775032
-
Angelopoulou K, Nicolaides A, Constantinou Deltas C. Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population. Clin Appl Thromb Hemost. 2000;6:104-107. 10775032
-
(2000)
Clin. Appl. Thromb. Hemost.
, vol.6
, pp. 104-107
-
-
Angelopoulou, K.1
Nicolaides, A.2
Constantinou Deltas, C.3
-
13
-
-
0037418247
-
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age
-
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group
-
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group. No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age. Circulation. 2003;107:1117-1122.
-
(2003)
Circulation
, vol.107
, pp. 1117-1122
-
-
-
14
-
-
0034780697
-
Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke
-
11697722
-
Lopaciuk S, Bykowska K, Kwiecinski H, et al. Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke. Clin Appl Thromb Hemost. 2001;7:346-350. 11697722
-
(2001)
Clin. Appl. Thromb. Hemost.
, vol.7
, pp. 346-350
-
-
Lopaciuk, S.1
Bykowska, K.2
Kwiecinski, H.3
-
15
-
-
0034866037
-
Prevalence and association of the factor V Leiden and prothrombin G20210A in healthy subjects and patients with venous thromboembolism
-
11471205
-
Coen D, Zadro R, Honovic L, Banfic L, Stavljenic Rukavina A. Prevalence and association of the factor V Leiden and prothrombin G20210A in healthy subjects and patients with venous thromboembolism. Croat Med J. 2001;42:488-492. 11471205
-
(2001)
Croat Med. J.
, vol.42
, pp. 488-492
-
-
Coen, D.1
Zadro, R.2
Honovic, L.3
Banfic, L.4
Stavljenic Rukavina, A.5
-
16
-
-
0034511765
-
Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives
-
11114134
-
Aznar J, Vaya A, Estelles A, et al. Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives. Haematologica. 2000;85:1271-1276. 11114134
-
(2000)
Haematologica
, vol.85
, pp. 1271-1276
-
-
Aznar, J.1
Vaya, A.2
Estelles, A.3
-
17
-
-
0031023757
-
A single genetic origin for a common Caucasian risk factor for venous thrombosis
-
9002940
-
Zivelin A, Griffin JH, Xu X, et al. A single genetic origin for a common Caucasian risk factor for venous thrombosis. Blood. 1997;89:397-402. 9002940
-
(1997)
Blood
, vol.89
, pp. 397-402
-
-
Zivelin, A.1
Griffin, J.H.2
Xu, X.3
-
18
-
-
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
-
8916933
-
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. 8916933
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
19
-
-
0030850713
-
Resistance to activated protein C as risk factor for thrombosis; molecular mechanism, laboratory investigation and clinical management
-
Dahlbäck B. Resistance to activated protein C as risk factor for thrombosis; molecular mechanism, laboratory investigation and clinical management. Sem Haematol. 1997;34:217-34.
-
(1997)
Sem. Haematol.
, vol.34
, pp. 217-234
-
-
Dahlbäck, B.1
-
20
-
-
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
-
11583312 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;86:809-816. 11583312
-
(2001)
Thromb. Haemost.
, vol.86
, pp. 809-816
-
-
Emmerich, J.1
Rosendaal, F.R.2
Cattaneo, M.3
-
21
-
-
16544393963
-
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians
-
15559724
-
Eid SS, Rihani G. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians. Clin Lab Sci. 2004;17:200-202. 15559724
-
(2004)
Clin. Lab. Sci.
, vol.17
, pp. 200-202
-
-
Eid, S.S.1
Rihani, G.2
-
22
-
-
12244274332
-
Absence of factor V Leiden mutation and low prothrombin G 20210 A mutation prevalence in a healthy Moroccan population
-
12529766
-
Mathonnet F, Nadifi S, Serazin-Leroy V, Dakouane M, Giudicelli Y. Absence of factor V Leiden mutation and low prothrombin G 20210 A mutation prevalence in a healthy Moroccan population. Thromb Haemost. 2002;88:1073-1074. 12529766
-
(2002)
Thromb. Haemost.
, vol.88
, pp. 1073-1074
-
-
Mathonnet, F.1
Nadifi, S.2
Serazin-Leroy, V.3
Dakouane, M.4
Giudicelli, Y.5
-
23
-
-
0031004312
-
Prevalence of the FVQ506 (factor V Leiden) mutation in the normal and thrombophilic Algerian population
-
9207426
-
Chafa O, Reghis A, Aubert A, Fischer AM. Prevalence of the FVQ506 (factor V Leiden) mutation in the normal and thrombophilic Algerian population. Br J Haematol. 1997;97:688-689. 9207426
-
(1997)
Br. J. Haematol.
, vol.97
, pp. 688-689
-
-
Chafa, O.1
Reghis, A.2
Aubert, A.3
Fischer, A.M.4
-
24
-
-
0032922667
-
High prevalence of factor V Leiden in healthy Jordanian Arabs
-
10235443
-
Awidi A, Shannak M, Bseiso A, et al. High prevalence of factor V Leiden in healthy Jordanian Arabs. Thromb Haemost. 1999;81:582-584. 10235443
-
(1999)
Thromb. Haemost.
, vol.81
, pp. 582-584
-
-
Awidi, A.1
Shannak, M.2
Bseiso, A.3
-
25
-
-
0032723944
-
High frequency of factor V Leiden in a population of Israeli Arabs
-
10613668
-
Rosen E, Renbaum P, Heyd J, Levy-Lahad E. High frequency of factor V Leiden in a population of Israeli Arabs. Thromb Haemost. 1999;82:1768. 10613668
-
(1999)
Thromb. Haemost.
, vol.82
, pp. 1768
-
-
Rosen, E.1
Renbaum, P.2
Heyd, J.3
Levy-Lahad, E.4
-
26
-
-
0030824411
-
New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians
-
9308750
-
Castoldi E, Lunghi B, Mingozzi F, Ioannou P, Marchetti G, Bernardi F. New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians. Thromb Haemost. 1997;78:1037-1041. 9308750
-
(1997)
Thromb. Haemost.
, vol.78
, pp. 1037-1041
-
-
Castoldi, E.1
Lunghi, B.2
Mingozzi, F.3
Ioannou, P.4
Marchetti, G.5
Bernardi, F.6
-
27
-
-
0028371802
-
New data for AG haplotype frequencies in Caucasoid populations and selective neutrality of the AG polymorphism
-
8157263
-
Sanchez-Mazas A, Butler-Brunner E, Excoffier L, et al. New data for AG haplotype frequencies in Caucasoid populations and selective neutrality of the AG polymorphism. Hum Biol. 1994;66:27-48. 8157263
-
(1994)
Hum. Biol.
, vol.66
, pp. 27-48
-
-
Sanchez-Mazas, A.1
Butler-Brunner, E.2
Excoffier, L.3
-
28
-
-
0031963298
-
Relation of three genetic traits to venous thrombosis in an African-American population
-
9440395
-
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;147:30-35. 9440395
-
(1998)
Am. J. Epidemiol.
, vol.147
, pp. 30-35
-
-
Dilley, A.1
Austin, H.2
Hooper, W.C.3
-
29
-
-
0032933161
-
Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylene-tetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR
-
10365746
-
Hessner MJ, Luhm RA, Pearson SL, Endean DJ, Friedman KD, Montgomery RR. Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylene-tetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR. Thromb Haemost. 1999;81:733-738. 10365746
-
(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
-
30
-
-
0030031847
-
World distribution of factor V Leiden mutation
-
10.1016/S0140-6736(96)91590-1
-
de Maat MP, Kluft C, Jespersen J, Gram J. World distribution of factor V Leiden mutation. Lancet. 1996;347:58. 10.1016/S0140-6736(96)91590-1
-
(1996)
Lancet
, vol.347
, pp. 58
-
-
de Maat, M.P.1
Kluft, C.2
Jespersen, J.3
Gram, J.4
-
31
-
-
2442637355
-
Prothrombin G20210A is not prevalent in North India
-
10.1046/j.1538-7836.2003.00430.x
-
Garewal G, Das R, Ahluwalia J, Mittal N, Varma S. Prothrombin G20210A is not prevalent in North India. J Thromb Haemost. 2003;1:2253-2254. 10.1046/j.1538-7836.2003.00430.x
-
(2003)
J. Thromb. Haemost.
, vol.1
, pp. 2253-2254
-
-
Garewal, G.1
Das, R.2
Ahluwalia, J.3
Mittal, N.4
Varma, S.5
-
32
-
-
0036893569
-
Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population
-
10.1002/ajh.10223
-
Finan RR, Tamim H, Ameen G, Sharida HE, Rashid M, Almawi WY. Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population. Am J Hematol. 2002;71:300-305. 10.1002/ajh.10223
-
(2002)
Am. J. Hematol.
, vol.71
, pp. 300-305
-
-
Finan, R.R.1
Tamim, H.2
Ameen, G.3
Sharida, H.E.4
Rashid, M.5
Almawi, W.Y.6
-
33
-
-
16244399522
-
Prevalence of antiphospholipid antibodies, factor V G1691A (Leiden) and prothrombin G20210A mutations in first and second trimester recurrent pregnancy loss
-
10.1016/j.ejogrb.2004.07.003
-
Mtiraoui N, Borgi L, Hizem S, et al. Prevalence of antiphospholipid antibodies, factor V G1691A (Leiden) and prothrombin G20210A mutations in first and second trimester recurrent pregnancy loss. Eur J Obstet Gynecol Reprod Biol. 2005;119:164-170. 10.1016/j.ejogrb.2004.07.003
-
(2005)
Eur. J. Obstet. Gynecol. Reprod. Biol.
, vol.119
, pp. 164-170
-
-
Mtiraoui, N.1
Borgi, L.2
Hizem, S.3
|