-
1
-
-
0035164329
-
Risk factors, outcome, and treatment in subtypes of ischemic stroke: The German stroke data bank
-
GRAU AJ, WEIMAR CH, BUGGLE F et al. on behalf of the German Stroke Data Bank Collaborators. Risk factors, outcome, and treatment in subtypes of ischemic stroke: the German stroke data bank. Stroke 2001;32:2559-66.
-
(2001)
Stroke
, vol.32
, pp. 2559-2566
-
-
Grau, A.J.1
Weimar, C.H.2
Buggle, F.3
-
2
-
-
0031727435
-
The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population
-
SOUTO JC, COLL I, LLOBET D et al. The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population. Thromb Haemost 1998;80:366-9.
-
(1998)
Thromb Haemost
, vol.80
, pp. 366-369
-
-
Souto, J.C.1
Coll, I.2
Llobet, D.3
-
3
-
-
0031981017
-
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;79:706-8.
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.2
Zivelin, A.3
-
4
-
-
0033515068
-
G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men
-
RIDKER PM, HENNEKENS CH, MILETICH JP. G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men. Circulation 1999;99:999-1004.
-
(1999)
Circulation
, vol.99
, pp. 999-1004
-
-
Ridker, P.M.1
Hennekens, C.H.2
Miletich, J.P.3
-
5
-
-
0032954926
-
The risk of recurrent venous thromboembolism in carriers and non-carriers of the G1691A allele in the coagulation factor V gene and the G20210A allele in the prothrombin gene. DURAC Trial Study Group. Duration of Anticoagulation
-
LINDMARKER P, SCHULMAN S, STEN-LINDER M, WIMAN B, EGBERG N, JOHNSSON H. The risk of recurrent venous thromboembolism in carriers and non-carriers of the G1691A allele in the coagulation factor V gene and the G20210A allele in the prothrombin gene. DURAC Trial Study Group. Duration of Anticoagulation. Thromb Haemost 1999;81:684-9.
-
(1999)
Thromb Haemost
, vol.81
, pp. 684-689
-
-
Lindmarker, P.1
Schulman, S.2
Sten-Linder, M.3
Wiman, B.4
Egberg, N.5
Johnsson, H.6
-
6
-
-
0034082445
-
Prothrombin G20210A polymorphism and thrombophilia
-
NGUYEN A. Prothrombin G20210A polymorphism and thrombophilia. Mayo Clin Proc 2000;75:595-604.
-
(2000)
Mayo Clin Proc
, vol.75
, pp. 595-604
-
-
Nguyen, A.1
-
7
-
-
0028910906
-
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, LINDPAINTNER K, STAMPFER MJ, EISENBERG 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;332:912-7.
-
(1995)
N Engl J Med
, vol.332
, pp. 912-917
-
-
Ridker, P.M.1
Hennekens, C.H.2
Lindpaintner, K.3
Stampfer, M.J.4
Eisenberg, P.R.5
Miletich, J.P.6
-
8
-
-
0033653710
-
Genetic susceptibility to thrombosis and its relationship to physiological risk factors: The GAIT study. Genetic analysis of idiopathic thrombophilia
-
SOUTO JC, ALMASY L, BORRELL M et al. Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic analysis of idiopathic thrombophilia. Am J Hum Genet 2000;67:1452-9.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1452-1459
-
-
Souto, J.C.1
Almasy, L.2
Borrell, M.3
-
9
-
-
0028810738
-
World distribution of factor V Leiden
-
REES DC, COX M, CLEGG JB. World distribution of factor V Leiden. Lancet 1995;346:1133-4.
-
(1995)
Lancet
, vol.346
, pp. 1133-1134
-
-
Rees, D.C.1
Cox, M.2
Clegg, J.B.3
-
10
-
-
0033667435
-
Diagnostic testing for coagulopathies in patients with ischemic stroke
-
BUSHNELL CD, GOLDSTEIN LB. Diagnostic testing for coagulopathies in patients with ischemic stroke. Stroke 2000;31:3067-78.
-
(2000)
Stroke
, vol.31
, pp. 3067-3078
-
-
Bushnell, C.D.1
Goldstein, L.B.2
-
11
-
-
0034883626
-
Inherited thrombophilia in ischemic stroke and its pathogenic subtypes
-
HANKEY GJ, EIKELBOOM JW, VAN BOCKXMEER FM, LOFTHOUSE E, STAPLES N, BAKER RI. Inherited thrombophilia in ischemic stroke and its pathogenic subtypes. Stroke 2001;32:1793-9.
-
(2001)
Stroke
, vol.32
, pp. 1793-1799
-
-
Hankey, G.J.1
Eikelboom, J.W.2
Van Bockxmeer, F.M.3
Lofthouse, E.4
Staples, N.5
Baker, R.I.6
-
12
-
-
0042905777
-
Ethnic differences in markers of thrombophilia: Implications for the investigation of ischemic stroke in multiethnic populations: The South London Ethnicity and Stroke Study
-
JERRARD-DUNNE P, EVANS A, MCGOVERN R et al. Ethnic differences in markers of thrombophilia: implications for the investigation of ischemic stroke in multiethnic populations: the South London Ethnicity and Stroke Study. Stroke 2003;34:1821-6.
-
(2003)
Stroke
, vol.34
, pp. 1821-1826
-
-
Jerrard-Dunne, P.1
Evans, A.2
Mcgovern, R.3
-
13
-
-
0036903587
-
Cryptogenic stroke in relation to genetic variation in clotting factors and other genetic polymorphisms among young men and women
-
Genetics and Stroke in the Young Study Group
-
AUSTIN H, CHIMOWITZ MI, HILL HA et al. Genetics and Stroke in the Young Study Group. Cryptogenic stroke in relation to genetic variation in clotting factors and other genetic polymorphisms among young men and women. Stroke 2002;33:2762-8.
-
(2002)
Stroke
, vol.33
, pp. 2762-2768
-
-
Austin, H.1
Chimowitz, M.I.2
Hill, H.A.3
-
14
-
-
17644434948
-
Risk of ischemic stroke associated with functional thrombin-activable fibrinolysis inhibitor plasma levels
-
SANTAMARÍA A, OLIVER A, BORRELL M et al. Risk of ischemic stroke associated with functional thrombin-activable fibrinolysis inhibitor plasma levels. Stroke 2003;34:2387-91.
-
(2003)
Stroke
, vol.34
, pp. 2387-2391
-
-
Santamaría, A.1
Oliver, A.2
Borrell, M.3
-
15
-
-
0027514354
-
Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial
-
ADAMS HP JR, BENDIXEN BH, KAPPELLE LJ et al. Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. Stroke 1993;24:35-41.
-
(1993)
Stroke
, vol.24
, pp. 35-41
-
-
Adams Jr., H.P.1
Bendixen, B.H.2
Kappelle, L.J.3
-
17
-
-
0018135382
-
A sensitive test demonstrating lupus anticoagulant and its behavioural patterns
-
EXNER T, RICHARD A, KRONENBERG H. A sensitive test demonstrating lupus anticoagulant and its behavioural patterns. B J Haematol 1978;40:143-51.
-
(1978)
B J Haematol
, vol.40
, pp. 143-151
-
-
Exner, T.1
Richard, A.2
Kronenberg, H.3
-
18
-
-
0034193350
-
Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis
-
SORIA JM, ALMASY L, SOUTO JC et al. Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis. Blood 2000;95:2780-5.
-
(2000)
Blood
, vol.95
, pp. 2780-2785
-
-
Soria, J.M.1
Almasy, L.2
Souto, J.C.3
-
19
-
-
0004360975
-
Infrequency of stroke caused by specific coagulation disorders
-
HABERL RL, BINIASCH O, OTT M, PEINEMANN A, WICK M, KEMPTER B. Infrequency of stroke caused by specific coagulation disorders. Cerebrovasc Dis 1995;5:391-6.
-
(1995)
Cerebrovasc Dis
, vol.5
, pp. 391-396
-
-
Haberl, R.L.1
Biniasch, O.2
Ott, M.3
Peinemann, A.4
Wick, M.5
Kempter, B.6
-
20
-
-
0035852984
-
Use of specialized coagulation testing in the evaluation of patients with acute ischemic stroke
-
BUSHNELL C, SIDDIQI Z, MORGENLANDER JC, GOLDSTEIN LB. Use of specialized coagulation testing in the evaluation of patients with acute ischemic stroke. Neurology 2001;56:624-7.
-
(2001)
Neurology
, vol.56
, pp. 624-627
-
-
Bushnell, C.1
Siddiqi, Z.2
Morgenlander, J.C.3
Goldstein, L.B.4
-
21
-
-
0028998202
-
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;15:783-5.
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 783-785
-
-
Catto, A.1
Carter, A.2
Ireland, H.3
-
22
-
-
0030060241
-
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;27:44-8.
-
(1996)
Stroke
, vol.27
, pp. 44-48
-
-
Press, R.D.1
Liu, X.Y.2
Beamer, N.3
Coull, B.M.4
-
23
-
-
0030664938
-
The venous thrombosis risk factor 20210 a allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease
-
CORRAL J, GONZALEZ-CONEJERO R, LOZANO ML, RIVERA J, HERAS I, VICENTE V. The venous thrombosis risk factor 20210 A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease. Br J Haematol 1997;99:304-7.
-
(1997)
Br J Haematol
, vol.99
, pp. 304-307
-
-
Corral, J.1
Gonzalez-Conejero, R.2
Lozano, M.L.3
Rivera, J.4
Heras, I.5
Vicente, V.6
-
24
-
-
0031442537
-
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease
-
FERRARESI P, MARCHETTI G, LEGNANI C et al. The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease. Arterioscler Thromb Vasc Biol 1997;17:2418-22.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 2418-2422
-
-
Ferraresi, P.1
Marchetti, G.2
Legnani, C.3
-
25
-
-
0344765521
-
Risk of stroke in young women and two prothrombotic mutations: Factor V Leiden and prothrombin gene variant (G20210A)
-
LONGSTRETH WT JR, ROSENDAAL FR, SISCOVICK DS et al. Risk of stroke in young women and two prothrombotic mutations: factor V Leiden and prothrombin gene variant (G20210A). Stroke 1998;29:577-80.
-
(1998)
Stroke
, vol.29
, pp. 577-580
-
-
Longstreth Jr., W.T.1
Rosendaal, F.R.2
Siscovick, D.S.3
-
26
-
-
0033002257
-
Inherited prothrombotic conditions and premature ischemic stroke: Sex difference in the association with factor V Leiden
-
MARGAGLIONE M, D'ANDREA G, GIULIANI N et al. Inherited prothrombotic conditions and premature ischemic stroke: sex difference in the association with factor V Leiden. Arterioscler Thromb Vasc Biol 1999;19:1751-6.
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 1751-1756
-
-
Margaglione, M.1
D'Andrea, G.2
Giuliani, N.3
-
27
-
-
0033960892
-
Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults
-
VOETSCH B, DAMASCENO BP, CAMARGO EC et al. Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults. Thromb Haemost 2000;83:229-33.
-
(2000)
Thromb Haemost
, vol.83
, pp. 229-233
-
-
Voetsch, B.1
Damasceno, B.P.2
Camargo, E.C.3
-
28
-
-
0036403874
-
Evaluation of the interactions of common genetic mutations in stroke subtypes
-
SZOLNOKI Z, SOMOGYVARI F, KONDACS A, SZABO M, FODOR L. Evaluation of the interactions of common genetic mutations in stroke subtypes. J Neurol 2002;249:1391-7.
-
(2002)
J Neurol
, vol.249
, pp. 1391-1397
-
-
Szolnoki, Z.1
Somogyvari, F.2
Kondacs, A.3
Szabo, M.4
Fodor, L.5
-
29
-
-
0036144087
-
Hyperhomocysteinemia and other inherited prothrombotic conditions in young adults with a history of ischemic stroke
-
MADONNA P, DE STEFANO V, COPPOLA A et al. Hyperhomocysteinemia and other inherited prothrombotic conditions in young adults with a history of ischemic stroke. Stroke 2002;33:51-6.
-
(2002)
Stroke
, vol.33
, pp. 51-56
-
-
Madonna, P.1
De Stefano, V.2
Coppola, A.3
-
30
-
-
0028888446
-
Myocardial infarction, Arg 506 to Gln factor V mutation, and activated protein C resistance
-
EMMERICH J, POIRIER O, EVANS A et al. Myocardial infarction, Arg 506 to Gln factor V mutation, and activated protein C resistance. Lancet 1995;345:321.
-
(1995)
Lancet
, vol.345
, pp. 321
-
-
Emmerich, J.1
Poirier, O.2
Evans, A.3
-
31
-
-
0030921663
-
A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women
-
ROSENDAAL FR, SISCOVICK DS, SCHWARTZ SM, PSATY BM, RAGHUNATHAN TE, VOS HL. A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women. Blood 1997;90:1747-50.
-
(1997)
Blood
, vol.90
, pp. 1747-1750
-
-
Rosendaal, F.R.1
Siscovick, D.S.2
Schwartz, S.M.3
Psaty, B.M.4
Raghunathan, T.E.5
Vos, H.L.6
-
32
-
-
0032562254
-
Interaction of coagulation defects and cardiovascular risk factors: Increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A
-
DOGGEN CJ, CATS VM, BERTINA RM, ROSENDAAL FR. Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A. Circulation 1998;97:1037-41.
-
(1998)
Circulation
, vol.97
, pp. 1037-1041
-
-
Doggen, C.J.1
Cats, V.M.2
Bertina, R.M.3
Rosendaal, F.R.4
-
33
-
-
3142596443
-
Screening for hypercoagulable syndromes following stroke
-
BUSHNELL C, GOLDSTEIN LB. Screening for hypercoagulable syndromes following stroke. Curr Atheroscler Rep 2003;5:291-8.
-
(2003)
Curr Atheroscler Rep
, vol.5
, pp. 291-298
-
-
Bushnell, C.1
Goldstein, L.B.2
-
34
-
-
3242748377
-
Homozigosity of the T allele of the 46C-> T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population
-
SANTAMARÍA A, MATEO J, TIRADO I et al. Homozigosity of the T allele of the 46C-> T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population. Stroke 2004;35:1795-9.
-
(2004)
Stroke
, vol.35
, pp. 1795-1799
-
-
Santamaría, A.1
Mateo, J.2
Tirado, I.3
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