-
1
-
-
0033843087
-
Genetics and ischaemic stroke
-
Hassan A, Markus HS. Genetics and ischaemic stroke. Brain 2000;123:1784-812.
-
(2000)
Brain
, vol.123
, pp. 1784-1812
-
-
Hassan, A.1
Markus, H.S.2
-
2
-
-
0033017646
-
Genetic susceptibility and ischemic stroke
-
Elbaz A, Amarenco P. Genetic susceptibility and ischemic stroke. Curr Opin Neurol 1999;12:47-55.
-
(1999)
Curr Opin Neurol
, vol.12
, pp. 47-55
-
-
Elbaz, A.1
Amarenco, P.2
-
3
-
-
0034878881
-
Evaluation of the roles of the Leiden V mutation and ACE I/D polymorphism in subtypes of ischaemic stroke
-
Szolnoki Z, Somogyvári F, Kondacs A, et al. Evaluation of the roles of the Leiden V mutation and ACE I/D polymorphism in subtypes of ischaemic stroke. J Neurol 2001;248:756-61.
-
(2001)
J Neurol
, vol.248
, pp. 756-761
-
-
Szolnoki, Z.1
Somogyvári, F.2
Kondacs, A.3
-
4
-
-
0033913898
-
A clustering of unfavourable common genetic mutations in stroke cases
-
Szolnoki Z, Somogyvári F, Szabó M, et al. A clustering of unfavourable common genetic mutations in stroke cases. Acta Neurol Scand 2000;102:124-8.
-
(2000)
Acta Neurol Scand
, vol.102
, pp. 124-128
-
-
Szolnoki, Z.1
Somogyvári, F.2
Szabó, M.3
-
5
-
-
0035106835
-
Common genetic mutations as possible aetiological factors in stroke
-
Szolnoki Z, Somogyvári F, Szólics M, et al. Common genetic mutations as possible aetiological factors in stroke. Eur Neurol 2001;45:119-20.
-
(2001)
Eur Neurol
, vol.45
, pp. 119-120
-
-
Szolnoki, Z.1
Somogyvári, F.2
Szólics, M.3
-
6
-
-
0034775236
-
Evaluation of the roles of common genetic mutations in leukoaraiosis
-
Szolnoki Z, Somogyvári F, Kondacs A, et al. Evaluation of the roles of common genetic mutations in leukoaraiosis. Acta Neurol Scand 2001;104:281-7.
-
(2001)
Acta Neurol Scand
, vol.104
, pp. 281-287
-
-
Szolnoki, Z.1
Somogyvári, F.2
Kondacs, A.3
-
7
-
-
0035128999
-
Interaction of heritable and estrogen-induced thrombophilia: Possible etiologies for ischaemic optic neuropathy and ischaemic stroke
-
Glueck CJ, Fontaine RN, Wang P. Interaction of heritable and estrogen-induced thrombophilia: possible etiologies for ischaemic optic neuropathy and ischaemic stroke. Thromb Haemosr 2001;85:256-9.
-
(2001)
Thromb Haemosr
, vol.85
, pp. 256-259
-
-
Glueck, C.J.1
Fontaine, R.N.2
Wang, P.3
-
9
-
-
0030833974
-
The inherited basis of venous thrombosis
-
Appleby RD, Olds RJ. The inherited basis of venous thrombosis. Pathology 1997;29:341-7.
-
(1997)
Pathology
, vol.29
, pp. 341-347
-
-
Appleby, R.D.1
Olds, R.J.2
-
10
-
-
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
-
11
-
-
0000730663
-
Factor V mutation and cryptogenic stroke in the young
-
Chimowitz M, Mansbach H, Schmaier A. Factor V mutation and cryptogenic stroke in the young. Stroke 1996;27:188.
-
(1996)
Stroke
, vol.27
, pp. 188
-
-
Chimowitz, M.1
Mansbach, H.2
Schmaier, A.3
-
12
-
-
0032786428
-
Association of elevated level of prothrombin fragment 1+2 and Arg506 to Gin mutation in patients with a history of ischemic stroke
-
De Lucia D, Papa ML, Ammendola F, et al. Association of elevated level of prothrombin fragment 1+2 and Arg506 to Gin mutation in patients with a history of ischemic stroke. J Neurosurg Sci 1999;43:45-50.
-
(1999)
J Neurosurg Sci
, vol.43
, pp. 45-50
-
-
De Lucia, D.1
Papa, M.L.2
Ammendola, F.3
-
13
-
-
0032142886
-
Arterial thromboembolic events in patients with the factor V Leiden mutation
-
Eskandari MK, Bontempo FA, Hassett AC, et al. Arterial thromboembolic events in patients with the factor V Leiden mutation. Am J Surg 1998;176:122-5.
-
(1998)
Am J Surg
, vol.176
, pp. 122-125
-
-
Eskandari, M.K.1
Bontempo, F.A.2
Hassett, A.C.3
-
14
-
-
0032783974
-
Thrombophilic predisposition in stroke and venous thromboembolism in Danish patients
-
Gaustadnes M, Rudiger N, Moller J, et al. Thrombophilic predisposition in stroke and venous thromboembolism in Danish patients. Blood Coagul Fibrinolysis 1999;10:251-9.
-
(1999)
Blood Coagul Fibrinolysis
, vol.10
, pp. 251-259
-
-
Gaustadnes, M.1
Rudiger, N.2
Moller, J.3
-
15
-
-
0034093930
-
Screening for thrombophilic risk factors among 25 german patients with cerebral venous thrombosis
-
Stolz E, Kemkes-Matthes B, Potzsch B, et al. Screening for thrombophilic risk factors among 25 german patients with cerebral venous thrombosis. Acta Neurol Scand 2000;102:31-6.
-
(2000)
Acta Neurol Scand
, vol.102
, pp. 31-36
-
-
Stolz, E.1
Kemkes-Matthes, B.2
Potzsch, B.3
-
16
-
-
0033556517
-
C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: A case-control study
-
Lalouschek W, Aull S, Serles W, et al. C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: a case-control study. Thromb Res 1999;93:61-9.
-
(1999)
Thromb Res
, vol.93
, pp. 61-69
-
-
Lalouschek, W.1
Aull, S.2
Serles, W.3
-
17
-
-
0344765521
-
Risk of stroke in young women and two prothrombic mutations: Factor V Leiden and prothrombin gene variant (G20210A)
-
Longstreth Jr WT, Rosendaal FR, Siscovick DS, et al. Risk of stroke in young women and two prothrombic 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
-
18
-
-
0345367477
-
Factor V Leiden mutation is a risk factor for cerebral venous thrombosis: A case control study of 55 patients
-
Ludemann P, Nabavi DG, Junker R, et al. Factor V Leiden mutation is a risk factor for cerebral venous thrombosis: a case control study of 55 patients. Stroke 1998;29:2507-10.
-
(1998)
Stroke
, vol.29
, pp. 2507-2510
-
-
Ludemann, P.1
Nabavi, D.G.2
Junker, R.3
-
19
-
-
0032961831
-
Factor V Leiden, prothrombin 20210G A and the MTHFRC677T mutations in childhood stroke
-
McColl MD, Chalmers EA, Thomas A, et al. Factor V Leiden, prothrombin 20210G A and the MTHFRC677T mutations in childhood stroke. Thromb Haemost 1999;81:690-4.
-
(1999)
Thromb Haemost
, vol.81
, pp. 690-694
-
-
McColl, M.D.1
Chalmers, E.A.2
Thomas, A.3
-
20
-
-
0031867746
-
Is hormone replacement a risk factor for ischemic stroke in women with factor V Leiden mutation?
-
Meschia JF, Biller J, Witt T, et al. Is hormone replacement a risk factor for ischemic stroke in women with factor V Leiden mutation? Arch Neurol 1998;55:1137-9.
-
(1998)
Arch Neurol
, vol.55
, pp. 1137-1139
-
-
Meschia, J.F.1
Biller, J.2
Witt, T.3
-
21
-
-
7344237914
-
Prevalence of factor V Leiden mutation in young adults with cerebral ischemia. A case-control study on 225 patients
-
Nabavi DG, Junker R, Wolff E, et al. Prevalence of factor V Leiden mutation in young adults with cerebral ischemia. A case-control study on 225 patients. J Neurol 1998;245:653-8.
-
(1998)
J Neurol
, vol.245
, pp. 653-658
-
-
Nabavi, D.G.1
Junker, R.2
Wolff, E.3
-
22
-
-
0032829537
-
Evaluation of genetic risk factors for silent brain infarction
-
Notsu Y, Nabika T, Park HY, et al. Evaluation of genetic risk factors for silent brain infarction. Stroke 1999;30:1881-6.
-
(1999)
Stroke
, vol.30
, pp. 1881-1886
-
-
Notsu, Y.1
Nabika, T.2
Park, H.Y.3
-
23
-
-
0031964217
-
Factor V Leiden mutation in a case with ischemic stroke: Which relationship?
-
Orlandi G, Pellegrinetti A, Fioretti C, et al. Factor V Leiden mutation in a case with ischemic stroke: which relationship? Angiology 1998;49:79-82.
-
(1998)
Angiology
, vol.49
, pp. 79-82
-
-
Orlandi, G.1
Pellegrinetti, A.2
Fioretti, C.3
-
24
-
-
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
-
25
-
-
0030978253
-
Age-specific incidence rates of venous thromboembolism among heterozygous carriers of factor V Leiden mutation
-
Ridker PM, Glynn RJ, Miletich JP, et al. Age-specific incidence rates of venous thromboembolism among heterozygous carriers of factor V Leiden mutation. Ann Intern Med 1997;126:528-31.
-
(1997)
Ann Intern Med
, vol.126
, pp. 528-531
-
-
Ridker, P.M.1
Glynn, R.J.2
Miletich, J.P.3
-
26
-
-
0031743737
-
Factor V Leiden and prothrombin gene G20210A variant in children with ischemic stroke
-
Zenz W, Bodo Z, Plotho J, et al. Factor V Leiden and prothrombin gene G20210A variant in children with ischemic stroke. Thromb Haemost 1998;80:763-6.
-
(1998)
Thromb Haemost
, vol.80
, pp. 763-766
-
-
Zenz, W.1
Bodo, Z.2
Plotho, J.3
-
27
-
-
0033044029
-
Protein S deficiency, activated protein C resistance and sticky platelet syndrome in a young woman with bilateral strokes
-
Chaturvedi S, Dzieczkowski JS. Protein S deficiency, activated protein C resistance and sticky platelet syndrome in a young woman with bilateral strokes. Cerebrovasc Dis 1999;9:127-30.
-
(1999)
Cerebrovasc Dis
, vol.9
, pp. 127-130
-
-
Chaturvedi, S.1
Dzieczkowski, J.S.2
-
28
-
-
0033954234
-
Hereditary thrombophilia in cerebral venous thrombosis
-
Weih M, Vetter B, Castell S, et al. Hereditary thrombophilia in cerebral venous thrombosis. Cerebrovasc Dis 2000;10:161-2.
-
(2000)
Cerebrovasc Dis
, vol.10
, pp. 161-162
-
-
Weih, M.1
Vetter, B.2
Castell, S.3
-
29
-
-
0028988219
-
Arg506Gln factor V mutation (factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction
-
Kontula K, Ylikorkala A, Miettinen H, et al. Arg506Gln factor V mutation (factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction. Thromb Haemost 1995;73:558-60.
-
(1995)
Thromb Haemost
, vol.73
, pp. 558-560
-
-
Kontula, K.1
Ylikorkala, A.2
Miettinen, H.3
-
30
-
-
0030803017
-
ACE gene polymorphism as a risk factor for ischemic cerebrovascular disease
-
Agerholm-Larsen B, Tybjaerg-Hansen A, Frikke-Schmidt R, et al. ACE gene polymorphism as a risk factor for ischemic cerebrovascular disease. Ann Intern Med 1997;127:346-55.
-
(1997)
Ann Intern Med
, vol.127
, pp. 346-355
-
-
Agerholm-Larsen, B.1
Tybjaerg-Hansen, A.2
Frikke-Schmidt, R.3
-
31
-
-
0030758043
-
Polymorphism of the angiotensin-converting enzyme (ACE) gene in patients with thrombotic brain infarction
-
Doi Y, Yoshinari M, Yoshizumi H, et al. Polymorphism of the angiotensin-converting enzyme (ACE) gene in patients with thrombotic brain infarction. Atherosclerosis 1997;132:145-50.
-
(1997)
Atherosclerosis
, vol.132
, pp. 145-150
-
-
Doi, Y.1
Yoshinari, M.2
Yoshizumi, H.3
-
32
-
-
0033044704
-
An angiotensin-converting enzyme gene polymorphism suggests a genetic distinction between ischaemic stroke and carotid stenosis
-
Kostulas K, Huang WX, Crisby M, et al. An angiotensin-converting enzyme gene polymorphism suggests a genetic distinction between ischaemic stroke and carotid stenosis. Eur J Clin Invest 1999;29:478-83.
-
(1999)
Eur J Clin Invest
, vol.29
, pp. 478-483
-
-
Kostulas, K.1
Huang, W.X.2
Crisby, M.3
-
33
-
-
0029094165
-
Angiotensin-converting enzyme gene deletion polymorphism. A new risk factor for lacunar stroke but not carotid atheroma
-
Markus HS, Barley J, Lunt R, et al. Angiotensin-converting enzyme gene deletion polymorphism. A new risk factor for lacunar stroke but not carotid atheroma. Stroke 1995;26:1329-33.
-
(1995)
Stroke
, vol.26
, pp. 1329-1333
-
-
Markus, H.S.1
Barley, J.2
Lunt, R.3
-
34
-
-
17344393902
-
Gene polymorphism of the renin-angiotensin system associated with risk for lacunar infarction. The Ohasama study
-
Takami S, Imai Y, Katsuya T, et al. Gene polymorphism of the renin-angiotensin system associated with risk for lacunar infarction. The Ohasama study. Am J Hypertens 2000;13:121-7.
-
(2000)
Am J Hypertens
, vol.13
, pp. 121-127
-
-
Takami, S.1
Imai, Y.2
Katsuya, T.3
-
35
-
-
0029557498
-
Lack of association between angiotensin converting enzyme gene insertion/deletion polymorphism and stroke
-
Ueda S, Weir CJ, Inglis GC, et al. Lack of association between angiotensin converting enzyme gene insertion/deletion polymorphism and stroke. J Hypertens 1995;13:1597-601.
-
(1995)
J Hypertens
, vol.13
, pp. 1597-1601
-
-
Ueda, S.1
Weir, C.J.2
Inglis, G.C.3
-
36
-
-
0032891439
-
Prospective evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of stroke
-
Zee RY, Ridker PM, Stampfer MJ, et al. Prospective evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of stroke. Circulation 1999;99:340-3.
-
(1999)
Circulation
, vol.99
, pp. 340-343
-
-
Zee, R.Y.1
Ridker, P.M.2
Stampfer, M.J.3
-
37
-
-
0033005234
-
Genetic analysis of the thermolabile variant of 5, 10- methylenetetrafolate reductase as a risk factor for ischaemic stroke
-
Harmon DL, Doyle RM, Meleady R, et al. Genetic analysis of the thermolabile variant of 5, 10-methylenetetrafolate reductase as a risk factor for ischaemic stroke. Arterioscler Thromb Vasc Biol 1999;19:208-11.
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 208-211
-
-
Harmon, D.L.1
Doyle, R.M.2
Meleady, R.3
-
38
-
-
0033031633
-
Role of a common mutation in the homocysteine regulatory enzyme methylenetetrahydrofolate reductase in ischaemic stroke
-
Press RD, Beamer N, Evans A, et al. Role of a common mutation in the homocysteine regulatory enzyme methylenetetrahydrofolate reductase in ischaemic stroke. Diagn Mol Pathol 1999;8:54-8.
-
(1999)
Diagn Mol Pathol
, vol.8
, pp. 54-58
-
-
Press, R.D.1
Beamer, N.2
Evans, A.3
-
39
-
-
0031847010
-
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;11:1019-23.
-
(1998)
Am J Hypertens
, vol.11
, pp. 1019-1023
-
-
Nakata, Y.1
Katsuya, T.2
Takami, S.3
-
40
-
-
0032438430
-
Methylenetetrahydrofolate reductase C677T genotype and stroke
-
Salooja N, Catto A, Carter A, et al. Methylenetetrahydrofolate reductase C677T genotype and stroke. Clin Lab Haematol 1998;20:357-61.
-
(1998)
Clin Lab Haematol
, vol.20
, pp. 357-361
-
-
Salooja, N.1
Catto, A.2
Carter, A.3
-
41
-
-
0032525101
-
Prothrombin G20210a mutant genotype is a risk factor for cerebrovascular ischaemic disease in young patients
-
De Stefano V, Chiusolo P, Paciaroni K, et al. Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischaemic disease in young patients. Blood 1998;91:3562-5.
-
(1998)
Blood
, vol.91
, pp. 3562-3565
-
-
De Stefano, V.1
Chiusolo, P.2
Paciaroni, K.3
-
42
-
-
0033515068
-
G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, venous thrombosis in large cohort of US men
-
Ridker PM, Hennekens CH, Miletich JP. G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, venous thrombosis in large cohort of US men. Circulation 1999;88:999-1004.
-
(1999)
Circulation
, vol.88
, pp. 999-1004
-
-
Ridker, P.M.1
Hennekens, C.H.2
Miletich, J.P.3
-
43
-
-
0028013309
-
Apolipaprotein E polymorphism and ischaemic cerebrovascular disease
-
Perdro-Botet J, Senti M, Rubies-Prat J. Apolipaprotein E polymorphism and ischaemic cerebrovascular disease. Stroke 1994;25:521.
-
(1994)
Stroke
, vol.25
, pp. 521
-
-
Perdro-Botet, J.1
Senti, M.2
Rubies-Prat, J.3
-
44
-
-
0028167816
-
Apolipoprotein E espilon 4 allele in Alzheimer's disease and vascular dementia
-
Frisoni GB, Calabresi L, Geroldi C, et al. Apolipoprotein E espilon 4 allele in Alzheimer's disease and vascular dementia. Dementia 1994;5:240-2.
-
(1994)
Dementia
, vol.5
, pp. 240-242
-
-
Frisoni, G.B.1
Calabresi, L.2
Geroldi, C.3
-
45
-
-
0035033632
-
Polymorphism of apoprotein E (APOE), methylenetetrahydrofolate reductase (MTHFR) and paraoxonase (PON1) genes in patients with cerebrovascular disease
-
Topic E, Timundic AM, Ttefanovic M, et al. Polymorphism of apoprotein E (APOE), methylenetetrahydrofolate reductase (MTHFR) and paraoxonase (PON1) genes in patients with cerebrovascular disease. Clin Chem Lab Med 2001;39:346-50.
-
(2001)
Clin Chem Lab Med
, vol.39
, pp. 346-350
-
-
Topic, E.1
Timundic, A.M.2
Ttefanovic, M.3
-
46
-
-
33847308837
-
Apolipoprotein E genetic polymorphism and stroke subtypes in a Bangladeshi hospital-based study
-
Chowdhury AH, Yokoyama T, Kokubo Y, et al. Apolipoprotein E genetic polymorphism and stroke subtypes in a Bangladeshi hospital-based study. J Epidemiol 2001;11:131-8.
-
(2001)
J Epidemiol
, vol.11
, pp. 131-138
-
-
Chowdhury, A.H.1
Yokoyama, T.2
Kokubo, Y.3
-
47
-
-
0034934732
-
Lack of association between apolipoprotein E genotype and ischaemic stroke in a Scottish population
-
Report of WHO study group
-
MacLeod MJ, De Lange RP, Breen G, et al. Lack of association between apolipoprotein E genotype and ischaemic stroke in a Scottish population. Eur J Clin Invest 2001;31:570-3. Report of WHO study group.
-
(2001)
Eur J Clin Invest
, vol.31
, pp. 570-573
-
-
MacLeod, M.J.1
De Lange, R.P.2
Breen, G.3
-
48
-
-
0003512785
-
Diabetes mellitus. Report of WHO study group
-
Group WS. Diabetes mellitus. Report of WHO study group. WHO Tech Rep Ser 1985;6:13-7.
-
(1985)
WHO Tech Rep Ser
, vol.6
, pp. 13-17
-
-
Group, W.S.1
-
49
-
-
0028820610
-
Alternative PCR method for diagnosis of mutation causing activated protein C resistant Gln506-factor V
-
Greengard JS, Xu X, Gandrile S, et al. Alternative PCR method for diagnosis of mutation causing activated protein C resistant Gln506-factor V. Thromb Res 1995;80:441-3.
-
(1995)
Thromb Res
, vol.80
, pp. 441-443
-
-
Greengard, J.S.1
Xu, X.2
Gandrile, S.3
-
50
-
-
0031757073
-
Genotyping method for methylenetetrahydrofalate reductase (C677T thermolabile variant) using heteroduplex technology
-
Clark ZE, Bowen DJ, Whatley SD, et al. Genotyping method for methylenetetrahydrofalate reductase (C677T thermolabile variant) using heteroduplex technology. Clin Chem 1998;44:2360-2.
-
(1998)
Clin Chem
, vol.44
, pp. 2360-2362
-
-
Clark, Z.E.1
Bowen, D.J.2
Whatley, S.D.3
-
51
-
-
0031934504
-
A reliable genotyping of the g-20210-a mutation of coagulation factor II (prothrombin)
-
Danneberg J, Abbes AP, Bruggeman BJM, et al. A reliable genotyping of the g-20210-a mutation of coagulation factor II (prothrombin). Clin Chem 1998;44:349-50.
-
(1998)
Clin Chem
, vol.44
, pp. 349-350
-
-
Danneberg, J.1
Abbes, A.P.2
Bruggeman, B.J.M.3
-
53
-
-
0034872435
-
Real-time PCR assay with fluorescent hybridization probes for exact and rapid genotyping of the angiotensin-converting enzyme gene insertion/deletion polymorphism
-
Somogyvári F, Szolnoki Z, Márki-Zay J, et al. Real-time PCR assay with fluorescent hybridization probes for exact and rapid genotyping of the angiotensin-converting enzyme gene insertion/deletion polymorphism. Clin Chem 2001;47:1728-9.
-
(2001)
Clin Chem
, vol.47
, pp. 1728-1729
-
-
Somogyvári, F.1
Szolnoki, Z.2
Márki-Zay, J.3
|