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Volumn 16, Issue 6, 2005, Pages 417-421

Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR G677A among 594 thrombotic Jordanian patients

Author keywords

Factor V Leiden; MTHFR C677T; Prothrombin G20210A; Thrombophilia

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5 LEIDEN; PROTHROMBIN;

EID: 24044478750     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.mbc.0000175478.46831.52     Document Type: Article
Times cited : (17)

References (27)
  • 1
    • 0029016883 scopus 로고
    • 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
  • 3
    • 0028810738 scopus 로고
    • 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
  • 5
    • 33645484927 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 9
    • 0029049553 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 13
    • 0002180743 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 17
    • 0034898551 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 20
    • 0033946578 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 24
    • 0032852675 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.