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Volumn 111, Issue 12, 2011, Pages 3-9

Gene-determined hemocoagulation disease as a cause of ischemic stroke in children

Author keywords

Children; Gene polymorphism; Stroke

Indexed keywords

ALPHA2 INTEGRIN; FIBRINOGEN; PLASMINOGEN ACTIVATOR INHIBITOR 1;

EID: 84865076629     PISSN: 19977298     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (48)
  • 1
    • 52449090507 scopus 로고    scopus 로고
    • Writing Group of the American Heart Association Stroke Council and the Council on Cardiovascular Disease in the Young « Management of Stroke in Infants and Children. A Scientific Statement From a SpecialWriting Group of the American Heart Association Stroke Council and the Council on Cardiovascular Disease in the Young»
    • Writing Group of the American Heart Association Stroke Council and the Council on Cardiovascular Disease in the Young «Management of Stroke in Infants and Children.A Scientific Statement From a SpecialWriting Group of the American Heart Association Stroke Council and the Council on Cardiovascular Disease in the Young». Stroke 2008; 39: 2644-2691.
    • (2008) Stroke , vol.39 , pp. 2644-2691
  • 2
    • 33645698753 scopus 로고    scopus 로고
    • Cryptogenic stroke in children: Possible role of patent foramen ovale
    • Agnetti A., Carano N., Sani E. et al. Cryptogenic stroke in children: possible role of patent foramen ovale. Neuropediatrics 2006; 37: 53-56.
    • (2006) Neuropediatrics , vol.37 , pp. 53-56
    • Agnetti, A.1    Carano, N.2    Sani, E.3
  • 3
    • 33646400828 scopus 로고    scopus 로고
    • Paradoxical emboli in children and young adults: Role of atrial septal defect and patent foramen ovale device closure
    • Bartz P.J., Cetta F., Cabalka A.K. et al. Paradoxical emboli in children and young adults: role of atrial septal defect and patent foramen ovale device closure. Mayo Clin Proc 2006; 81: 615-618.
    • (2006) Mayo Clin Proc , vol.81 , pp. 615-618
    • Bartz, P.J.1    Cetta, F.2    Cabalka, A.K.3
  • 5
    • 62949139815 scopus 로고    scopus 로고
    • Arterial ischemic stroke: Common risk factors in newborns and children
    • Pavlakis S.G., Levinson K. Arterial ischemic stroke: common risk factors in newborns and children. Stroke 2009; 40: 79-81.
    • (2009) Stroke , vol.40 , pp. 79-81
    • Pavlakis, S.G.1    Levinson, K.2
  • 6
    • 0034711674 scopus 로고    scopus 로고
    • Stroke in children: The coexistence of multiple risk factors predicts poor outcome
    • Launthier S., Carmant L., David M. et al. Stroke in children: The coexistence of multiple risk factors predicts poor outcome. Neurology 2000; 54: 371-378.
    • (2000) Neurology , vol.54 , pp. 371-378
    • Launthier, S.1    Carmant, L.2    David, M.3
  • 7
    • 0036142385 scopus 로고    scopus 로고
    • Report of the National Institute of Neurological Disorders and Stroke Workshop on Perinatal and Childhood Stroke
    • Lynch J.K., Hirtz D.G., DeVeber G., Nelson K.B. Report of the National Institute of Neurological Disorders and Stroke Workshop on Perinatal and Childhood Stroke. Pediatrics 2002; 109: 234-242.
    • (2002) Pediatrics , vol.109 , pp. 234-242
    • Lynch, J.K.1    Hirtz, D.G.2    Deveber, G.3    Nelson, K.B.4
  • 8
    • 0037609678 scopus 로고    scopus 로고
    • Factor V Leiden and prothrombin gene G20210A mutation in children with cerebral thromboembolism
    • Bonduel M., Sciuccati G., Hepner M. et al. Factor V Leiden and prothrombin gene G20210A mutation in children with cerebral thromboembolism. Am J Hematol 2003; 73: 81-86.
    • (2003) Am J Hematol , vol.73 , pp. 81-86
    • Bonduel, M.1    Sciuccati, G.2    Hepner, M.3
  • 9
    • 77951767998 scopus 로고    scopus 로고
    • Impact of thrombophilia on risk of arterial ischemic stroke or cerebral sinovenous thrombosis in neonates and children: A systematic review and meta-analysis of observational studies
    • Kenet G., Lütkhoff L.K., Albisetti M., Bernard T. et al. Impact of thrombophilia on risk of arterial ischemic stroke or cerebral sinovenous thrombosis in neonates and children: a systematic review and meta-analysis of observational studies. Circulation 2010; 121: 1838-1847.
    • (2010) Circulation , vol.121 , pp. 1838-1847
    • Kenet, G.1    Lütkhoff, L.K.2    Albisetti, M.3    Bernard, T.4
  • 10
    • 4644342171 scopus 로고    scopus 로고
    • Ischemic stroke in children: A study of the associated alterations
    • Rotta N.T., Ranzan J. Ischemic stroke in children: a study of the associated alterations. Arquivos de Neuro-Psiquiatria 2004; 62: 618-625.
    • (2004) Arquivos De Neuro-Psiquiatria , vol.62 , pp. 618-625
    • Rotta, N.T.1    Ranzan, J.2
  • 11
    • 0344676391 scopus 로고    scopus 로고
    • Is there a genetic basis for pediatric stroke?
    • Kirkham F.J. Is there a genetic basis for pediatric stroke? Curr Opin Pediatr 2003; 15: 6: 547-558.
    • (2003) Curr Opin Pediatr , vol.15 , Issue.6 , pp. 547-558
    • Kirkham, F.J.1
  • 12
    • 79451474588 scopus 로고    scopus 로고
    • Guidelines for the prevention of stroke in patients with stroke or transient ischemic attack: A guideline for healthcare professionals from the american heart association/American stroke association
    • Furie K.L., Kasner S.E., Adams R.J. et al. Guidelines for the prevention of stroke in patients with stroke or transient ischemic attack: a guideline for healthcare professionals from the american heart association/American stroke association. Stroke 2011; 42: 1: 227-276.
    • (2011) Stroke , vol.42 , Issue.1 , pp. 227-276
    • Furie, K.L.1    Kasner, S.E.2    Adams, R.J.3
  • 13
    • 0036193054 scopus 로고    scopus 로고
    • Beta-fibrinogen gene -455A/G polymorphism and plasma fibrinogen level in Chinese stroke patients
    • Liu Y., Pan J., Wang S. et al. Beta-fibrinogen gene -455A/G polymorphism and plasma fibrinogen level in Chinese stroke patients. Chin Med J 2002; 115: 214-216.
    • (2002) Chin Med J , vol.115 , pp. 214-216
    • Liu, Y.1    Pan, J.2    Wang, S.3
  • 14
    • 33750951250 scopus 로고    scopus 로고
    • Candidate Gene Polymorphisms Do Not Differ Between Newborns With Stroke and Normal Controls
    • Steven P., Yvonne W.W., Janet Lee et al. Candidate Gene Polymorphisms Do Not Differ Between Newborns With Stroke and Normal Controls. Stroke 2006; 37: 2678.
    • Stroke , vol.2006 , pp. 37
    • Steven, P.1    Yvonne, W.W.2    Janet, L.3
  • 15
    • 0031743737 scopus 로고    scopus 로고
    • Factor V Leiden and prothrombin gene G 20210 A variant in children with ischemic stroke
    • Zenz W., Bodó Z., Plotho J. et al. Factor V Leiden and prothrombin gene G 20210 A variant in children with ischemic stroke. Thromb Haemost 1998; 80: 763-766.
    • (1998) Thromb Haemost , vol.80 , pp. 763-766
    • Zenz, W.1    Bodó, Z.2    Plotho, J.3
  • 16
    • 0034502488 scopus 로고    scopus 로고
    • Etiology of stroke in children
    • Roach E.S. Etiology of stroke in children. Semin Pediatr Neurol 2000; 7: 4: 244-260.
    • (2000) Semin Pediatr Neurol , vol.7 , Issue.4 , pp. 244-260
    • Roach, E.S.1
  • 17
    • 0034995461 scopus 로고    scopus 로고
    • Prothrombotic disorders and abnormal neurodevelopmental outcome in infants with neonatal cerebral infarction
    • Mercuri E., Cowan F., Gupte G. et al. Prothrombotic disorders and abnormal neurodevelopmental outcome in infants with neonatal cerebral infarction. R{cyrillic}ediatrics 2001; 107: 6: 1400-1404.
    • (2001) R{cyrillic}ediatrics , vol.107 , Issue.6 , pp. 1400-1404
    • Mercuri, E.1    Cowan, F.2    Gupte, G.3
  • 18
    • 0034919297 scopus 로고    scopus 로고
    • Thromboembolism in newborns, infants and children
    • Nowak-Göttl U., Kosch A., Schlegel N. Thromboembolism in newborns, infants and children. Thromb Haemost 2001; 86: 1: 464-474.
    • (2001) Thromb Haemost , vol.86 , Issue.1 , pp. 464-474
    • Nowak-Göttl, U.1    Kosch, A.2    Schlegel, N.3
  • 19
    • 0345633546 scopus 로고    scopus 로고
    • Lipoprotein (a) and GeneticPolymorphisms of Clotting Factor V, Prothrombin, and Methylentetrahydrofolate Reductase Are Risk Factors of Spontaneous Ischemic Stroke in Childhood
    • Nowak-Göttl U., Sträter R., Heinecke A. et al. Lipoprotein (a) and GeneticPolymorphisms of Clotting Factor V, Prothrombin, and Methylentetrahydrofolate Reductase Are Risk Factors of Spontaneous Ischemic Stroke in Childhood. Blood 1999; 94: 11: 3678-3682.
    • (1999) Blood , vol.94 , Issue.11 , pp. 3678-3682
    • Nowak-Göttl, U.1    Sträter, R.2    Heinecke, A.3
  • 20
    • 22044438499 scopus 로고    scopus 로고
    • Matched case-control study on factor V Leiden and the prothrombin G20210A mutation in patients with ischemic stroke/transient ischemic attack up to the age of 60 years
    • Lalouschek W., Schillinger M., Hsieh K. et al. Matched case-control study on factor V Leiden and the prothrombin G20210A mutation in patients with ischemic stroke/transient ischemic attack up to the age of 60 years. Stroke 2005; 36: 7: 1405-1409.
    • (2005) Stroke , vol.36 , Issue.7 , pp. 1405-1409
    • Lalouschek, W.1    Schillinger, M.2    Hsieh, K.3
  • 21
    • 38949111543 scopus 로고    scopus 로고
    • 3' end mRNA processing: Olecularmechanisms and implications for health and disease
    • Danckwardt S., Hentze M.W., Kulozik A.E. 3' end mRNA processing: olecularmechanisms and implications for health and disease. EMBO J 2008; 27: 482-498.
    • (2008) EMBO J , vol.27 , pp. 482-498
    • Danckwardt, S.1    Hentze, M.W.2    Kulozik, A.E.3
  • 22
    • 0032525101 scopus 로고    scopus 로고
    • ProthrombinG20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients
    • De Stefano V., Chiusolo P., Paciaroni K. et al. ProthrombinG20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood 1998; 91: 10: 3562-3565.
    • (1998) Blood , vol.91 , Issue.10 , pp. 3562-3565
    • de Stefano, V.1    Chiusolo, P.2    Paciaroni, K.3
  • 23
    • 0344926303 scopus 로고    scopus 로고
    • Thrombophilia and stroke
    • Green D. Thrombophilia and stroke. Top Stroke Rehabil 2003; 10: 3: 21-33.
    • (2003) Top Stroke Rehabil , vol.10 , Issue.3 , pp. 21-33
    • Green, D.1
  • 24
    • 0032726661 scopus 로고    scopus 로고
    • Co-existence of two prothrombotic mutations, factor V 1691 G-A and prothrombin gene 20210 G-A, and the risk of cerebral infarct in pediatric patients
    • Akar N., Akar E., Deda G. et al. Co-existence of two prothrombotic mutations, factor V 1691 G-A and prothrombin gene 20210 G-A, and the risk of cerebral infarct in pediatric patients. Pediat Hematol Oncol 1999; 16: 565-566.
    • (1999) Pediat Hematol Oncol , vol.16 , pp. 565-566
    • Akar, N.1    Akar, E.2    Deda, G.3
  • 25
    • 0030755337 scopus 로고    scopus 로고
    • Thrombophilia due to 20210 G-->A prothrombin polymorphism and cerebral ischemia in the young
    • Bentolila S., Ripoll L., Drouet L. et al. Thrombophilia due to 20210 G-->A prothrombin polymorphism and cerebral ischemia in the young. Stroke 1997; 28: 9: 1846-1847.
    • (1997) Stroke , vol.28 , Issue.9 , pp. 1846-1847
    • Bentolila, S.1    Ripoll, L.2    Drouet, L.3
  • 26
    • 0028901713 scopus 로고
    • Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction
    • Eriksson P., Kallin B., van 't Hooft F.M. et al. Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction. Proc Natl Acad Sci USA 1995; 92: 6: 1851-1855.
    • (1995) Proc Natl Acad Sci USA , vol.92 , Issue.6 , pp. 1851-1855
    • Eriksson, P.1    Kallin, B.2    van 't Hooft, F.M.3
  • 27
    • 18844375381 scopus 로고    scopus 로고
    • Pleiotropic functions of plasminogen activator inhibitor-1
    • Lijnen H.R. Pleiotropic functions of plasminogen activator inhibitor-1. J Thromb Haemost 2005; 3: 35-45.
    • (2005) J Thromb Haemost , vol.3 , pp. 35-45
    • Lijnen, H.R.1
  • 28
    • 28344445503 scopus 로고    scopus 로고
    • PAI-1 and atherothrombosis
    • Vaughan D.E. PAI-1 and atherothrombosis. J Thromb Haemost 2005; 3: 1879-1883.
    • (2005) J Thromb Haemost , vol.3 , pp. 1879-1883
    • Vaughan, D.E.1
  • 29
    • 34447253783 scopus 로고    scopus 로고
    • The PAI-1 4G/5G gene polymorphism and ischemic stroke: An association study andmeta-analysis
    • Attia J., Thakkinstian A., Wang Y. et al. The PAI-1 4G/5G gene polymorphism and ischemic stroke: an association study andmeta-analysis. J Stroke Cerebrovasc Dis 2007; 16: 4: 173-179.
    • (2007) J Stroke Cerebrovasc Dis , vol.16 , Issue.4 , pp. 173-179
    • Attia, J.1    Thakkinstian, A.2    Wang, Y.3
  • 30
    • 84875298550 scopus 로고    scopus 로고
    • Plasminogen activator inhibitor- 1-675 4G/5G andmethylenetetrahydrofolate reductase gene variants in young acute myocardial infarction and juvenile ischemic stroke
    • Bivona G., Bellia C., Cammarieri S. et al. Plasminogen activator inhibitor- 1-675 4G/5G andmethylenetetrahydrofolate reductase gene variants in young acute myocardial infarction and juvenile ischemic stroke. Res J Biol Sci 2009; 3: 11: 1341-1343.
    • (2009) Res J Biol Sci , vol.3 , Issue.11 , pp. 1341-1343
    • Bivona, G.1    Bellia, C.2    Cammarieri, S.3
  • 31
    • 0035658214 scopus 로고    scopus 로고
    • Fibrinogen polymorphisms and disease
    • Laffan M.A. Fibrinogen polymorphisms and disease. Eur Heart J 2001; 22: 24: 2224-2226.
    • (2001) Eur Heart J , vol.22 , Issue.24 , pp. 2224-2226
    • Laffan, M.A.1
  • 32
    • 0033387742 scopus 로고    scopus 로고
    • Two common, functional polymorphisms in the promoter region of the beta-fibrinogen gene contribute to regulation of plasma fibrinogen concentration
    • van't Hooft F.M., von Bahr S.J., Silveira A. et al. Two common, functional polymorphisms in the promoter region of the beta-fibrinogen gene contribute to regulation of plasma fibrinogen concentration. Arterioscler Thromb Vasc Biol 1999; 19: 12: 3063-3070.
    • (1999) Arterioscler Thromb Vasc Biol , vol.19 , Issue.12 , pp. 3063-3070
    • Van't hooft, F.M.1    von Bahr, S.J.2    Silveira, A.3
  • 33
    • 0037384474 scopus 로고    scopus 로고
    • Fibrinogen gene promoter-455 A allele as a risk factor for lacunar stroke
    • Martiskainen M., Pohjasvaara T., Mikkelsson J. et al. Fibrinogen gene promoter-455 A allele as a risk factor for lacunar stroke. Stroke 2003; 34: 4: 886-891.
    • (2003) Stroke , vol.34 , Issue.4 , pp. 886-891
    • Martiskainen, M.1    Pohjasvaara, T.2    Mikkelsson, J.3
  • 34
    • 23244440000 scopus 로고    scopus 로고
    • Association of the -92C/G and 807C/T polymorphisms of the alpha2 subunit gene with human platelets alpha2beta1 receptor density
    • Ajzenberg N., Berroeta C., Philip I. et al. Association of the -92C/G and 807C/T polymorphisms of the alpha2 subunit gene with human platelets alpha2beta1 receptor density. Arterioscler Thromb Vasc Biol 2005; 25: 1756-1760.
    • (2005) Arterioscler Thromb Vasc Biol , vol.25 , pp. 1756-1760
    • Ajzenberg, N.1    Berroeta, C.2    Philip, I.3
  • 35
    • 4444352570 scopus 로고    scopus 로고
    • Structures of integrin domains and concerted conformational changes in the bidirectional signaling mechanism of alphaIIbbeta3
    • Calvete J.J. Structures of integrin domains and concerted conformational changes in the bidirectional signaling mechanism of alphaIIbbeta3. Exp BiolMed (Maywood) 2004; 229: 8: 732-744.
    • (2004) Exp BiolMed (Maywood) , vol.229 , Issue.8 , pp. 732-744
    • Calvete, J.J.1
  • 36
    • 0042735242 scopus 로고    scopus 로고
    • Resistance in vitro to low-dose aspirin is associated with platelet PlA1 (GP IIIa) polymorphism but not with C807T(GP Ia/IIa) and C-5T Kozak (GP Ibalpha) polymorphisms
    • Macchi L., Christiaens L., Brabant S. et al. Resistance in vitro to low-dose aspirin is associated with platelet PlA1 (GP IIIa) polymorphism but not with C807T(GP Ia/IIa) and C-5T Kozak (GP Ibalpha) polymorphisms. J Am Coll Cardiol 2003; 42: 6: 1115-1119.
    • (2003) J Am Coll Cardiol , vol.42 , Issue.6 , pp. 1115-1119
    • Macchi, L.1    Christiaens, L.2    Brabant, S.3
  • 37
    • 0036846748 scopus 로고    scopus 로고
    • Aspirin resistance in cardiovascular disease: A review of prevalence, mechanisms, and clinical significance
    • McKee S.A., Sane D.C., Deliargyris E.N. Aspirin resistance in cardiovascular disease: a review of prevalence, mechanisms, and clinical significance. Thromb Haemost 2002; 88: 711-715.
    • (2002) Thromb Haemost , vol.88 , pp. 711-715
    • McKee, S.A.1    Sane, D.C.2    Deliargyris, E.N.3
  • 38
    • 0033873109 scopus 로고    scopus 로고
    • Platelet glycoprotein polymorphisms as a risk factor for thronbosis
    • Bray P.F. Platelet glycoprotein polymorphisms as a risk factor for thronbosis. Curr Opin Hematol 2000; 7: 5: 284-289.
    • (2000) Curr Opin Hematol , vol.7 , Issue.5 , pp. 284-289
    • Bray, P.F.1
  • 39
    • 0033137302 scopus 로고    scopus 로고
    • The alpha2 gene coding sequence T807/A873 of the platelet collagen receptor integrin alpha2beta1 might be a genetic risk factor for the development of stroke in younger patients
    • Carlsson L.E., Santoso S., Spitzer C. et al. The alpha2 gene coding sequence T807/A873 of the platelet collagen receptor integrin alpha2beta1 might be a genetic risk factor for the development of stroke in younger patients. Blood 1999; 93: 11: 3583-3586.
    • (1999) Blood , vol.93 , Issue.11 , pp. 3583-3586
    • Carlsson, L.E.1    Santoso, S.2    Spitzer, C.3
  • 40
    • 0033937685 scopus 로고    scopus 로고
    • Genetic variants of platelet glycoprotein receptors and risk of stroke in young women
    • Reiner A.P., Kumar P.N., Schwartz S.M. et al. Genetic variants of platelet glycoprotein receptors and risk of stroke in young women. Stroke 2000; 31: 7: 1628-1633.
    • (2000) Stroke , vol.31 , Issue.7 , pp. 1628-1633
    • Reiner, A.P.1    Kumar, P.N.2    Schwartz, S.M.3
  • 41
    • 74949085061 scopus 로고    scopus 로고
    • The T Allele of the 677C>T olymorphism of Methylenetetrahydrofolate Reductase Gene is Associated With an Increased Risk of Ischemic Stroke in Polish Children
    • Zak I., Sarecka-Hujar B., Kopyta I. et al. The T Allele of the 677C>T olymorphism of Methylenetetrahydrofolate Reductase Gene is Associated With an Increased Risk of Ischemic Stroke in Polish Children. J ChildNeurol 2009; 24: 10: 1226-1262.
    • (2009) J ChildNeurol , vol.24 , Issue.10 , pp. 1226-1262
    • Zak, I.1    Sarecka-Hujar, B.2    Kopyta, I.3
  • 42
    • 0031922936 scopus 로고    scopus 로고
    • Factor XIII Val 34 Leu: A novel association with primary intracerebral hemorrhage
    • Catto A.J., Kohler H.P., Bannan S. et al. Factor XIII Val 34 Leu: a novel association with primary intracerebral hemorrhage. Stroke 1998; 29: 4: 813-816.
    • (1998) Stroke , vol.29 , Issue.4 , pp. 813-816
    • Catto, A.J.1    Kohler, H.P.2    Bannan, S.3
  • 43
    • 0034651014 scopus 로고    scopus 로고
    • The association between the Val34Leu polymorphism in the factor XIII gene and brain infarction
    • Elbaz A., Poirier O., Canaple S. et al. The association between the Val34Leu polymorphism in the factor XIII gene and brain infarction. Blood 2000; 95: 2: 586-591.
    • (2000) Blood , vol.95 , Issue.2 , pp. 586-591
    • Elbaz, A.1    Poirier, O.2    Canaple, S.3
  • 44
    • 0034648734 scopus 로고    scopus 로고
    • Polymorphisms in the factor gene and the risk of myocardial infarction in the patients with coronary artery disease
    • Girelli D., Russo C., Ferraresi P., Olivieri O. Polymorphisms in the factor gene and the risk of myocardial infarction in the patients with coronary artery disease. N Engl JMed 2000; 14: 343: 11: 774-780.
    • (2000) N Engl JMed , vol.343 , Issue.11 , pp. 774-780
    • Girelli, D.1    Russo, C.2    Ferraresi, P.3    Olivieri, O.4
  • 45
    • 0031725574 scopus 로고    scopus 로고
    • A common coding polymorphism in the FXIII A-subunit gene (FXIIIVal34Leu) affects crosslinking activity
    • Kohler H.P., Ariëns R.A., Whitaker P., Grant P.J. A common coding polymorphism in the FXIII A-subunit gene (FXIIIVal34Leu) affects crosslinking activity. Thromb Haemost 1998; 80: 4: 704.
    • (1998) Thromb Haemost , vol.80 , Issue.4 , pp. 704
    • Kohler, H.P.1    Ariëns, R.A.2    Whitaker, P.3    Grant, P.J.4
  • 46
    • 0033028586 scopus 로고    scopus 로고
    • Hyperhomocysteinemia, atherosclerosis and thrombosis
    • Cattaneo M. Hyperhomocysteinemia, atherosclerosis and thrombosis. Thromb Haemost 1999; 81: 165-176.
    • (1999) Thromb Haemost , vol.81 , pp. 165-176
    • Cattaneo, M.1
  • 47
    • 0037310672 scopus 로고    scopus 로고
    • Investigation of risk factors in children with arterial ischemic stroke
    • Ganesan V., Prengler M., McShane M. et al. Investigation of risk factors in children with arterial ischemic stroke. Ann Neurol 2003; 53: 167-173.
    • (2003) Ann Neurol , vol.53 , pp. 167-173
    • Ganesan, V.1    Prengler, M.2    McShane, M.3
  • 48
    • 34248211683 scopus 로고    scopus 로고
    • Influence of combined methionine synthase (MTR 2756A>G) andmethylenetetrahydrofolate reductase (MTHFR 677C>T) polymorphisms to plasma homocysteine levels in Korean patients with ischemic stroke
    • Kim O.J., Hong S.P., Ahn J.Y. et al. Influence of combined methionine synthase (MTR 2756A>G) andmethylenetetrahydrofolate reductase (MTHFR 677C>T) polymorphisms to plasma homocysteine levels in Korean patients with ischemic stroke. YonseiMed J 2007; 48: 2: 201-209.
    • (2007) YonseiMed J , vol.48 , Issue.2 , pp. 201-209
    • Kim, O.J.1    Hong, S.P.2    Ahn, J.Y.3


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