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Volumn 112, Issue 3, 2003, Pages 143-146

Genetic assessment of cardiovascular risk factors in the Greek Cypriot population

Author keywords

Cardiovascular risk factors; Greek Cypriot; Thrombophilia

Indexed keywords

APOLIPOPROTEIN B; APOLIPOPROTEIN E; BLOOD CLOTTING FACTOR 13; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 5 LEIDEN; DIHYDROFOLATE REDUCTASE; FIBRINOGEN; GLYCOPROTEIN IIIA; PLASMINOGEN ACTIVATOR INHIBITOR; PROTHROMBIN;

EID: 1042275520     PISSN: 00493848     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.thromres.2003.12.012     Document Type: Article
Times cited : (4)

References (22)
  • 1
    • 0034649257 scopus 로고    scopus 로고
    • Genetics of cardiovascular disease
    • Milewicz D.M., Seidman C.E. Genetics of cardiovascular disease. Circulation. 102:2000;IV103-IV111.
    • (2000) Circulation , vol.102
    • Milewicz, D.M.1    Seidman, C.E.2
  • 2
    • 0037375566 scopus 로고    scopus 로고
    • Polymorphisms in coagulation factor genes and their impact on arterial and venous thrombosis
    • Endler G., Mannhalter C. Polymorphisms in coagulation factor genes and their impact on arterial and venous thrombosis. Clin. Chim. Acta. 330:2003;31-55.
    • (2003) Clin. Chim. Acta , vol.330 , pp. 31-55
    • Endler, G.1    Mannhalter, C.2
  • 3
    • 0034111630 scopus 로고    scopus 로고
    • Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population
    • Angelopoulou K., Nicolaides A., Constantinou Deltas C. Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population. Clin. Appl. Thromb. Hemost. 6:2000;104-107.
    • (2000) Clin. Appl. Thromb. Hemost. , vol.6 , pp. 104-107
    • Angelopoulou, K.1    Nicolaides, A.2    Constantinou Deltas, C.3
  • 5
    • 0034995296 scopus 로고    scopus 로고
    • The factor V HR2 haplotype: Prevalence and association of the A4070G and A6755G polymorphisms
    • Pecheniuk N.M., Morris C.P., Walsh T.P., Marsh N.A. The factor V HR2 haplotype: prevalence and association of the A4070G and A6755G polymorphisms. Blood Coagul. Fibrinolysis. 12:2001;201-206.
    • (2001) Blood Coagul. Fibrinolysis , vol.12 , pp. 201-206
    • Pecheniuk, N.M.1    Morris, C.P.2    Walsh, T.P.3    Marsh, N.A.4
  • 6
    • 0032840589 scopus 로고    scopus 로고
    • Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors
    • Antoniadi T., Hatzis T., Kroupis C., Economou-Petersen E., Petersen M.B. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors. Am. J. Hematol. 61:1999;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
  • 7
    • 0034866037 scopus 로고    scopus 로고
    • Prevalence and association of the factor V Leiden and prothrombin G20210A in healthy subjects and patients with venous thromboembolism
    • 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. 42:2001;488-492.
    • (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
  • 8
    • 0032729370 scopus 로고    scopus 로고
    • The VITA project: Prothrombin G20210A mutation and venous thromboembolism in the general population
    • Tosetto A., Missiaglia E., Frezzato M., Rodeghiero F. The VITA project: prothrombin G20210A mutation and venous thromboembolism in the general population. Thromb. Haemost. 82:1999;1395-1398.
    • (1999) Thromb. Haemost. , vol.82 , pp. 1395-1398
    • Tosetto, A.1    Missiaglia, E.2    Frezzato, M.3    Rodeghiero, F.4
  • 9
    • 0032946813 scopus 로고    scopus 로고
    • The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease
    • Vargas M., Soto I., Pinto C.R., Urgelles M.F., Batalla A., Rodriguez-Reguero J.et al. The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease. Blood Coagul. Fibrinolysis. 10:1999;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
  • 10
    • 0142165021 scopus 로고    scopus 로고
    • Relationships between fibrinogen, plasminogen activator inhibitor-1, and their gene polymorphisms in current smokers with essential hypertension
    • Jastrzebska M., Goracy I., Naruszewicz M. Relationships between fibrinogen, plasminogen activator inhibitor-1, and their gene polymorphisms in current smokers with essential hypertension. Thromb. Res. 110:2003;339-344.
    • (2003) Thromb. Res. , vol.110 , pp. 339-344
    • Jastrzebska, M.1    Goracy, I.2    Naruszewicz, M.3
  • 11
    • 0028810738 scopus 로고
    • World distribution of factor V Leiden
    • Rees D.C., Cox M., Clegg J.B. World distribution of factor V Leiden. Lancet. 346:1995;1133-1134.
    • (1995) Lancet , vol.346 , pp. 1133-1134
    • Rees, D.C.1    Cox, M.2    Clegg, J.B.3
  • 12
    • 0343168063 scopus 로고    scopus 로고
    • Prothrombin G20210A, factor V Leiden, and factor XIII Val34Leu: Common mutations of blood coagulation factors and deep vein thrombosis in Austria
    • Renner W., Koppel H., Hoffmann C., Schallmoser K., Stanger O., Toplak H.et al. Prothrombin G20210A, factor V Leiden, and factor XIII Val34Leu: common mutations of blood coagulation factors and deep vein thrombosis in Austria. Thromb. Res. 99:2000;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
  • 14
    • 0027384932 scopus 로고
    • Genetic polymorphisms of the a and B subunits of coagulation factor XIII in the Chinese population
    • Zhang L., Stradmann-Bellinghausen B., Schneider P.M., Rittner C. Genetic polymorphisms of the A and B subunits of coagulation factor XIII in the Chinese population. Exp. Clin. Immunogenet. 10:1993;137-140.
    • (1993) Exp. Clin. Immunogenet. , vol.10 , pp. 137-140
    • Zhang, L.1    Stradmann-Bellinghausen, B.2    Schneider, P.M.3    Rittner, C.4
  • 16
    • 0032736545 scopus 로고    scopus 로고
    • Factor V Leiden and the common haemochromatosis mutation HFE C282Y: Is there an association in familial venous thromboembolic disease?
    • MacLean R.M., Feeney G.P., Bowley S.J., Bowen D.J., Worwood M., Collins P.W. Factor V Leiden and the common haemochromatosis mutation HFE C282Y: is there an association in familial venous thromboembolic disease? Br. J. Haematol. 107:1999;210-212.
    • (1999) Br. J. Haematol. , vol.107 , pp. 210-212
    • MacLean, R.M.1    Feeney, G.P.2    Bowley, S.J.3    Bowen, D.J.4    Worwood, M.5    Collins, P.W.6
  • 17
    • 0032891959 scopus 로고    scopus 로고
    • Risk of venous thromboembolism associated with the common hereditary haemochromatosis Hfe gene (C282Y) mutation
    • Brown K., Luddington R., Taylor S.A., Lillicrap D.P., Baglin T.P. Risk of venous thromboembolism associated with the common hereditary haemochromatosis Hfe gene (C282Y) mutation. Br. J. Haematol. 105:1999;95-97.
    • (1999) Br. J. Haematol. , vol.105 , pp. 95-97
    • Brown, K.1    Luddington, R.2    Taylor, S.A.3    Lillicrap, D.P.4    Baglin, T.P.5
  • 18
  • 19
    • 0036840683 scopus 로고    scopus 로고
    • The apolipoprotein B R3500Q gene mutation in Spanish subjects with a clinical diagnosis of familial hypercholesterolemia
    • Castillo S., Tejedor D., Mozas P., Reyes G., Civeira F., Alonso R.et al. The apolipoprotein B R3500Q gene mutation in Spanish subjects with a clinical diagnosis of familial hypercholesterolemia. Atherosclerosis. 165:2002;127-135.
    • (2002) Atherosclerosis , vol.165 , pp. 127-135
    • Castillo, S.1    Tejedor, D.2    Mozas, P.3    Reyes, G.4    Civeira, F.5    Alonso, R.6
  • 20
    • 0035012625 scopus 로고    scopus 로고
    • The mutation APOB-100 R3500Q in Eastern Europe
    • Horvath A., Ganev V. The mutation APOB-100 R3500Q in Eastern Europe. Atherosclerosis. 156:2001;241-242.
    • (2001) Atherosclerosis , vol.156 , pp. 241-242
    • Horvath, A.1    Ganev, V.2
  • 21
    • 0035864632 scopus 로고    scopus 로고
    • Apolipoprotein e genotype and cardiovascular disease in the Framingham Heart Study
    • Lahoz C., Schaefer E.J., Cupples L.A., Wilson P.W., Levy D., Osgood D.et al. Apolipoprotein E genotype and cardiovascular disease in the Framingham Heart Study. Atherosclerosis. 154:2001;529-537.
    • (2001) Atherosclerosis , vol.154 , pp. 529-537
    • Lahoz, C.1    Schaefer, E.J.2    Cupples, L.A.3    Wilson, P.W.4    Levy, D.5    Osgood, D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.