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Volumn 15, Issue 4, 2009, Pages 415-420

Prevalence of thrombophilic mutations and ACE i/d polymorphism in turkish ischemic stroke patients

Author keywords

Coagulation factors; Ischemic stroke

Indexed keywords

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

EID: 69749107078     PISSN: 10760296     EISSN: None     Source Type: Journal    
DOI: 10.1177/1076029608315163     Document Type: Article
Times cited : (20)

References (42)
  • 1
    • 0037153045 scopus 로고    scopus 로고
    • New players in the genetic of stroke
    • Tournier-Laserve E. New players in the genetic of stroke. N Eng J Med. 2002 ; 347: 1711-1712.
    • (2002) N Eng J Med , vol.347 , pp. 1711-1712
    • Tournier-Laserve, E.1
  • 2
    • 33646339153 scopus 로고    scopus 로고
    • Association studies of genetic polymorphism, environmental factors and their interaction in ischemic stroke
    • Gao X., Yang H., ZhiPing T. Association studies of genetic polymorphism, environmental factors and their interaction in ischemic stroke. Neurosci Lett. 2006 ; 398: 172-177.
    • (2006) Neurosci Lett , vol.398 , pp. 172-177
    • Gao, X.1    Yang, H.2    Zhiping, T.3
  • 3
    • 34047266657 scopus 로고    scopus 로고
    • Predictive genetic variants for venous thrombosis: What's new
    • Bezemer ID, Rosendaal FR Predictive genetic variants for venous thrombosis: what's new ? Semin Hematol. 2007 ; 44: 85-92.
    • (2007) Semin Hematol , vol.44 , pp. 85-92
    • Bezemer, I.D.1    Rosendaal, F.R.2
  • 4
    • 0027446268 scopus 로고
    • Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C
    • Dahlb̈k B., Carlsson M., Svensson PJ Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C. Proc Natl Acad Sci. 1993 ; 90: 1004-1008.
    • (1993) Proc Natl Acad Sci , vol.90 , pp. 1004-1008
    • Dahlb̈k, B.1    Carlsson, M.2    Svensson, P.J.3
  • 5
    • 0036756202 scopus 로고    scopus 로고
    • Role of genetic mutations in vascular access thrombosis among hemodialysis patients waiting for renal transplantation
    • Atac B., Yakupoglu U., Ozbek N., Ozdemir FN, Bilgin N. Role of genetic mutations in vascular access thrombosis among hemodialysis patients waiting for renal transplantation. Transplant Proc. 2002 ; 34: 2030-2032.
    • (2002) Transplant Proc , vol.34 , pp. 2030-2032
    • Atac, B.1    Yakupoglu, U.2    Ozbek, N.3    Ozdemir, F.N.4    Bilgin, N.5
  • 7
    • 0034955889 scopus 로고    scopus 로고
    • Aspects of gene polymorphism in cardiovascular disease: The renin-angiotensin system
    • Carluccio M., Soccio M., de Caterina R. Aspects of gene polymorphism in cardiovascular disease: the renin-angiotensin system. Eur J Clin Invest. 2001 ; 31: 476-488.
    • (2001) Eur J Clin Invest , vol.31 , pp. 476-488
    • Carluccio, M.1    Soccio, M.2    De Caterina, R.3
  • 8
    • 0027514354 scopus 로고
    • Classification of ischemic stroke: Definition for use in a multicenter clinical trial
    • Adams HP, Bendixen BH, Keppelle J., et al. Classification of ischemic stroke: definition for use in a multicenter clinical trial. Stroke. 1993 ; 24: 35-41.
    • (1993) Stroke , vol.24 , pp. 35-41
    • Adams, H.P.1    Bendixen, B.H.2    Keppelle, J.3
  • 9
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HS A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988 ; 16: 1215.
    • (1988) Nucleic Acids Res , vol.16 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.S.3
  • 10
    • 0032824284 scopus 로고    scopus 로고
    • Prevalence of mild hyperhomocysteinaemia and association with thrombophilic genotypes (factor v Leiden and prothrombin G20210A) in Italian patients with venous thromboembolic disease
    • De Stefano V., Zappacosta B., Persichilli S., et al. Prevalence of mild hyperhomocysteinaemia and association with thrombophilic genotypes (factor V Leiden and prothrombin G20210A) in Italian patients with venous thromboembolic disease. Br J Haematol. 1999 ; 106: 564-568.
    • (1999) Br J Haematol , vol.106 , pp. 564-568
    • De Stefano, V.1    Zappacosta, B.2    Persichilli, S.3
  • 11
    • 0033621632 scopus 로고    scopus 로고
    • Effect of methylenetetrahydrofolate reductase 677 C-T, 1298 A-C, and 1317 T-C on factor v 1691 mutation in Turkish deep vein thrombosis patients
    • Akar N., Akar E., Akçay R., Avcu F., Yalççn A., Cin S. Effect of methylenetetrahydrofolate reductase 677 C-T, 1298 A-C, and 1317 T-C on factor V 1691 mutation in Turkish deep vein thrombosis patients. Thromb Res. 2000 ; 97: 163-167.
    • (2000) Thromb Res , vol.97 , pp. 163-167
    • Akar, N.1    Akar, E.2    Akçay, R.3    Avcu, F.4    Yalççn, A.5    Cin, S.6
  • 12
    • 0034963230 scopus 로고    scopus 로고
    • Genetic polymorphisms of the renin-angiotensin-aldosterone system in end-stage renal disease
    • Lovati E., Richard A., Frey BM, Frey FJ, Ferrari P. Genetic polymorphisms of the renin-angiotensin-aldosterone system in end-stage renal disease. Kidney Int. 2001 ; 60: 46-54.
    • (2001) Kidney Int , vol.60 , pp. 46-54
    • Lovati, E.1    Richard, A.2    Frey, B.M.3    Frey, F.J.4    Ferrari, P.5
  • 14
    • 17744410104 scopus 로고    scopus 로고
    • Prothrombin gene 20210 G-A mutation in the Turkish population
    • Akar N., Mlslrlloglu M., Akar E. Prothrombin gene 20210 G-A mutation in the Turkish population. Am J Haematol. 1998 ; 58: 249.
    • (1998) Am J Haematol , vol.58 , pp. 249
    • Akar, N.1    Mlslrlloglu, M.2    Akar, E.3
  • 15
    • 0032723473 scopus 로고    scopus 로고
    • Factor V1691 G-A, prothrombin 20210 G-A, and methylenetetrahydrofolate reductase 677 C-T variants in Turkish children with cerebral infarct
    • Akar N., Akar E., Deda G., Sipahi T., Orsal A. Factor V1691 G-A, prothrombin 20210 G-A, and methylenetetrahydrofolate reductase 677 C-T variants in Turkish children with cerebral infarct. J Child Neurol. 1999 ; 14: 749-1751.
    • (1999) J Child Neurol , vol.14 , pp. 749-1751
    • Akar, N.1    Akar, E.2    Deda, G.3    Sipahi, T.4    Orsal, A.5
  • 16
    • 0031734222 scopus 로고    scopus 로고
    • Deletion polymorphism at the angiotensin-converting enzyme gene in Turkish patients with coronary artery disease
    • Akar N., Aras Ö., Ömürlü K., Cin S. Deletion polymorphism at the angiotensin-converting enzyme gene in Turkish patients with coronary artery disease. Scand J Clin Lab Invest. 1998 ; 58: 491-496.
    • (1998) Scand J Clin Lab Invest , vol.58 , pp. 491-496
    • Akar, N.1    Aras, Ö.2    Ömürlü, K.3    Cin, S.4
  • 17
    • 1342288363 scopus 로고    scopus 로고
    • Early risk of recurrence by subtype of ischemic stroke in population-based incidence studies
    • Lovett JK, Coull AJ, Rothwell PM Early risk of recurrence by subtype of ischemic stroke in population-based incidence studies. Neurology. 2004: 62 ; 569-573.
    • (2004) Neurology , vol.62 , pp. 569-573
    • Lovett, J.K.1    Coull, A.J.2    Rothwell, P.M.3
  • 18
    • 0031898124 scopus 로고    scopus 로고
    • Meta-analysis of the ACE gene ischaemic stroke
    • Sharma P. Meta-analysis of the ACE gene ischaemic stroke. J Neurol Neurosurg Psychiatry. 1998 ; 64: 227-230.
    • (1998) J Neurol Neurosurg Psychiatry , vol.64 , pp. 227-230
    • Sharma, P.1
  • 19
    • 0029094165 scopus 로고
    • Angiotensin converting enzyme gene deletion polymorphism: A new risk factor for lacuner stroke but no carotid atheroma
    • Markus HS, Barley J., Lunt R., et al. Angiotensin converting enzyme gene deletion polymorphism: a new risk factor for lacuner stroke but no carotid atheroma. Stroke. 1995 ; 26: 1329-1333.
    • (1995) Stroke , vol.26 , pp. 1329-1333
    • Markus, H.S.1    Barley, J.2    Lunt, R.3
  • 20
    • 0031408002 scopus 로고    scopus 로고
    • Polymorphism of angiotensin-converting enzyme, angiotensinogen, and Apolipoprotein e genes in a Japanese population with cerebrovascular disease
    • Nakata Y., Katsuya T., Rakugi H., et al. Polymorphism of angiotensin-converting enzyme, angiotensinogen, and Apolipoprotein E genes in a Japanese population with cerebrovascular disease. Am J Hypertens. 1997 ; 12: 1391-1395.
    • (1997) Am J Hypertens , vol.12 , pp. 1391-1395
    • Nakata, Y.1    Katsuya, T.2    Rakugi, H.3
  • 21
    • 0030758043 scopus 로고    scopus 로고
    • Polymorphism in the angiotensin- converting enzyme (ACE) gene in patients with thrombotic brain infarction
    • Doi Y., Yoshinari M., Yoshizumi H., Ibayashi S., Wakisaka M., Fujishima M. Polymorphism in the angiotensin- converting enzyme (ACE) gene in patients with thrombotic brain infarction. Atherosclerosis. 1997 ; 132: 145-150.
    • (1997) Atherosclerosis , vol.132 , pp. 145-150
    • Doi, Y.1    Yoshinari, M.2    Yoshizumi, H.3    Ibayashi, S.4    Wakisaka, M.5    Fujishima, M.6
  • 22
    • 0029877404 scopus 로고    scopus 로고
    • Ischemic stroke and the gene for angiotensin-converting enzyme in Japanese hypertensives
    • Kario K., Kanai N., Saito K., Nago N., Takefumi M., Shimada K. Ischemic stroke and the gene for angiotensin-converting enzyme in Japanese hypertensives. Circulation. 1996 ; 93: 1630-1633. (Pubitemid 26131337)
    • (1996) Circulation , vol.93 , Issue.9 , pp. 1630-1633
    • Kario, K.1    Kanai, N.2    Saito, K.3    Nago, N.4    Matsuo, T.5    Shimada, K.6
  • 23
    • 0030862539 scopus 로고    scopus 로고
    • Angiotensin-converting enzyme gene I/D polymorphism and carotid plaques in Japanese
    • Watanabe Y., Ishigami T., Kawano Y., et al. Angiotensin-converting enzyme gene I/D polymorphism and carotid plaques in Japanese. Hypertension. 1997 ; 30: 569-573.
    • (1997) Hypertension , vol.30 , pp. 569-573
    • Watanabe, Y.1    Ishigami, T.2    Kawano, Y.3
  • 24
    • 0029071460 scopus 로고
    • Angiotensin-converting enzyme I/D polymorphism and arterial wall thickness in a general population
    • Castellano M., Muiesan ML, Rizzoni D., et al. Angiotensin-converting enzyme I/D polymorphism and arterial wall thickness in a general population. Circulation. 1995 ; 91: 2721-2724.
    • (1995) Circulation , vol.91 , pp. 2721-2724
    • Castellano, M.1    Muiesan, M.L.2    Rizzoni, D.3
  • 25
    • 0028810738 scopus 로고
    • World distribution of factor v Leiden
    • Reed DC, Cox M., Clegg JB World distribution of factor V Leiden. Lancet. 1995 ; 346: 1133-1134.
    • (1995) Lancet , vol.346 , pp. 1133-1134
    • Reed, D.C.1    Cox, M.2    Clegg, J.B.3
  • 26
    • 0028931717 scopus 로고
    • High risk of thrombosis in patients homozygous for factor v Leiden (activated protein C resistance)
    • Rosendaal FR, Koster T., Vandenbroucke JP, Reistma PH High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance). Blood. 1995 ; 85: 1504-1508.
    • (1995) Blood , vol.85 , pp. 1504-1508
    • Rosendaal, F.R.1    Koster, T.2    Vandenbroucke, J.P.3    Reistma, P.H.4
  • 27
    • 0029958969 scopus 로고    scopus 로고
    • Frequency of resistance to activated protein C due to factor v mutation in young patients with ischaemic stroke (letter)
    • Alboucher JF, Guirand-Chaumeil B., Chollet F., Cadroy Y., Sie P. Frequency of resistance to activated protein C due to factor V mutation in young patients with ischaemic stroke (letter). Stroke. 1996 ; 27: 766-767.
    • (1996) Stroke , vol.27 , pp. 766-767
    • Alboucher, J.F.1    Guirand-Chaumeil, B.2    Chollet, F.3    Cadroy, Y.4    Sie, P.5
  • 28
    • 0000730663 scopus 로고    scopus 로고
    • Factor v mutation and cryptogenic stroke in the young [abstract]
    • Chimowitz M., Mansbach H., Schmaier A. Factor V mutation and cryptogenic stroke in the young [abstract]. Stroke. 1996 ; 27: 188.
    • (1996) Stroke , vol.27 , pp. 188
    • Chimowitz, M.1    Mansbach, H.2    Schmaier, A.3
  • 29
    • 0028998202 scopus 로고
    • Factor v Leiden gene mutation and thrombin generation in relation to the development of acute stroke
    • Catto A., Carter A., Ireland H., et al. Factor V Leiden gene mutation and thrombin generation in relation to the development of acute stroke. Arterioscler Thromb Vasc Biol. 1995 ; 15: 783-785.
    • (1995) Arterioscler Thromb Vasc Biol , vol.15 , pp. 783-785
    • Catto, A.1    Carter, A.2    Ireland, H.3
  • 30
    • 0028910906 scopus 로고
    • Mutation in the gene coding for coagulation factor v and the risk of myocardial infarction, stroke and venous thrombosis in apparently healthy men
    • Ridker PM, Hennekens CH, Lidpaintner K., Stampfer MJ, Elsenberg PR, Miletich JP Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke and venous thrombosis in apparently healthy men. N Engl J Med. 1995 ; 332: 912-917.
    • (1995) N Engl J Med , vol.332 , pp. 912-917
    • Ridker, P.M.1    Hennekens, C.H.2    Lidpaintner, K.3    Stampfer, M.J.4    Elsenberg, P.R.5    Miletich, J.P.6
  • 31
    • 0029886290 scopus 로고    scopus 로고
    • Activated protein C resistance in ischemic stroke not due to factor v arginine506ĝ†'glutamine mutation
    • Fisher M., Fernandez JA, Ameriso SF, et al. Activated protein C resistance in ischemic stroke not due to factor V arginine506ĝ† 'glutamine mutation. Stroke. 1996 ; 27: 1163-1166.
    • (1996) Stroke , vol.27 , pp. 1163-1166
    • Fisher, M.1    Fernandez, J.A.2    Ameriso, S.F.3
  • 32
    • 0030060241 scopus 로고    scopus 로고
    • Ischemic stroke in the elderly: Role of the common factor v mutation causing resistance to activated protein C
    • Press RD, Liu XY, Beamer N., Coull BM Ischemic stroke in the elderly: role of the common factor V mutation causing resistance to activated protein C. Stroke. 1996 ; 27: 44-48.
    • (1996) Stroke , vol.27 , pp. 44-48
    • Press, R.D.1    Liu, X.Y.2    Beamer, N.3    Coull, B.M.4
  • 33
    • 1842333859 scopus 로고    scopus 로고
    • Low prevalance of the factor v Leiden among patients with ischemic stroke
    • Sánchez J., Román J., de la Torre M., Velasco F., Torres A. Low prevalance of the factor V Leiden among patients with ischemic stroke. Haemostasis. 1997 ; 27: 9-15.
    • (1997) Haemostasis , vol.27 , pp. 9-15
    • Snchez, J.1    Romn, J.2    De La Torre, M.3    Velasco, F.4    Torres, A.5
  • 34
    • 0344765521 scopus 로고    scopus 로고
    • Risk of stroke in young women and two prothrombotic mutation: Factor v Leiden and prothrombin gene variant (G20210A)
    • Longstreth WT, Rosendaal FR, Siscovick DS, et al. Risk of stroke in young women and two prothrombotic mutation: factor V Leiden and prothrombin gene variant (G20210A). Stroke. 1998 ; 29: 577-580.
    • (1998) Stroke , vol.29 , pp. 577-580
    • Longstreth, W.T.1    Rosendaal, F.R.2    Siscovick, D.S.3
  • 35
    • 0029827076 scopus 로고    scopus 로고
    • Screening for the factor v Arg506 Gln mutation in patients with TIA and stroke
    • Markus HS, Zhang Y., Jeffery S. Screening for the factor V Arg506 Gln mutation in patients with TIA and stroke. Cerebrovasc Dis. 1996 ; 6: 360-362.
    • (1996) Cerebrovasc Dis , vol.6 , pp. 360-362
    • Markus, H.S.1    Zhang, Y.2    Jeffery, S.3
  • 36
    • 0031981017 scopus 로고    scopus 로고
    • Geographic distribution of the 20210 G to A prothrombin variant
    • Rosendaal FR, Doggen CJ, Zivelin A., 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.2    Zivelin, A.3
  • 37
    • 0030792668 scopus 로고    scopus 로고
    • The prothrombin gene G20210A variant: Prevalance in a U.K. anticoagulant clinic population
    • Cumming AM, Keeney S., Salden A., Bhavnani M., Shwe K., Hay CRM. The prothrombin gene G20210A variant: prevalance in a U.K. anticoagulant clinic population. Br J Haemotol. 1997 ; 98: 353-355.
    • (1997) Br J Haemotol , vol.98 , pp. 353-355
    • Cumming, A.M.1    Keeney, S.2    Salden, A.3    Bhavnani, M.4    Shwe, K.5    Hay, C.R.M.6
  • 38
    • 0032525101 scopus 로고    scopus 로고
    • Prothrombin G20210A mutation genotype is a risk factor for cerebrovascular ischemic disease in young patients
    • De Stefano V., Chiusulo P., Paciaroni K., et al. Prothrombin G20210A mutation genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood. 1998 ; 91: 3562-3565.
    • (1998) Blood , vol.91 , pp. 3562-3565
    • De Stefano, V.1    Chiusulo, P.2    Paciaroni, K.3
  • 39
    • 0030736412 scopus 로고    scopus 로고
    • The transition G to A at position 20210 in the 3' untranslated region of the prothrombin gene is not associated with cerebral ischaemia
    • Martinelli I., Franchi F., Akwan S., Bettini P., Merati G., Mannucci PM The transition G to A at position 20210 in the 3' untranslated region of the prothrombin gene is not associated with cerebral ischaemia. Blood. 1997 ; 29: 3806.
    • (1997) Blood , vol.29 , pp. 3806
    • Martinelli, I.1    Franchi, F.2    Akwan, S.3    Bettini, P.4    Merati, G.5    Mannucci, P.M.6
  • 41
    • 0030880665 scopus 로고    scopus 로고
    • A common polymorphism in the methylentetrahydrofolate reductase gene, homocysteine, and ischemic cerebrovascular disease
    • Markus HS, Ali N., Swaminathan R., Sankaralingam A., Molloy J., Powell J. A common polymorphism in the methylentetrahydrofolate reductase gene, homocysteine, and ischemic cerebrovascular disease. Stroke. 1997 ; 28: 1739-1743.
    • (1997) Stroke , vol.28 , pp. 1739-1743
    • Markus, H.S.1    Ali, N.2    Swaminathan, R.3    Sankaralingam, A.4    Molloy, J.5    Powell, J.6
  • 42
    • 0031847010 scopus 로고    scopus 로고
    • Methylenetetrahydrofolate reductase gene polymorphism: Relation to blood pressure and cerebrovascular disease
    • Nakata Y., Katsuya T., Takami S., et al. Methylenetetrahydrofolate reductase gene polymorphism: relation to blood pressure and cerebrovascular disease. Am J Hypertens. 1998 ; 11: 1019-1023.
    • (1998) Am J Hypertens , vol.11 , pp. 1019-1023
    • Nakata, Y.1    Katsuya, T.2    Takami, S.3


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