-
1
-
-
0020665028
-
Cerebral infarction in young adults: a practical approach
-
Hart R.G., and Miller V.T. Cerebral infarction in young adults: a practical approach. Stroke 14 (1983) 110-114
-
(1983)
Stroke
, vol.14
, pp. 110-114
-
-
Hart, R.G.1
Miller, V.T.2
-
3
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina R.M., Koeleman B.P.C., Koster T., et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 369 (1994) 64-67
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
-
4
-
-
33646821758
-
Factor V Leiden and increased risk for arterial thrombotic disease in young Brazilian patients
-
Adriano de P.S., Ribeiro D.D., das Gracas Carvaho M., Cardoso J., Sant'Ana Dusse L.M., and Fernandes A.P. Factor V Leiden and increased risk for arterial thrombotic disease in young Brazilian patients. Blood Coagul Fibrinolysis 17 (2006) 271-275
-
(2006)
Blood Coagul Fibrinolysis
, vol.17
, pp. 271-275
-
-
Adriano de, P.S.1
Ribeiro, D.D.2
das Gracas Carvaho, M.3
Cardoso, J.4
Sant'Ana Dusse, L.M.5
Fernandes, A.P.6
-
5
-
-
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 P.M., Hennekens C.H., Lindpainter K., Stampfer M.J., Eisenberg P.R., and Miletich J.P. 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 332 (1995) 912-917
-
(1995)
N Engl J Med
, vol.332
, pp. 912-917
-
-
Ridker, P.M.1
Hennekens, C.H.2
Lindpainter, K.3
Stampfer, M.J.4
Eisenberg, P.R.5
Miletich, J.P.6
-
6
-
-
0344765521
-
Risk of stroke in young women and two prothrombotic mutations: factor V Leiden and prothrombin gene variant (G20210A)
-
Longstreth Jr. W.T., Rosendaal F.R., Siscovick D.S., et al. Risk of stroke in young women and two prothrombotic mutations: factor V Leiden and prothrombin gene variant (G20210A). Stroke 29 (1998) 577-580
-
(1998)
Stroke
, vol.29
, pp. 577-580
-
-
Longstreth Jr., W.T.1
Rosendaal, F.R.2
Siscovick, D.S.3
-
7
-
-
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 19 (1999) 1751-1756
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 1751-1756
-
-
Margaglione, M.1
D'Andrea, G.2
Giuliani, N.3
-
8
-
-
0033960892
-
Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults
-
Voetsch B., Damasceno B.P., Camargo E.C.S., et al. Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults. Thromb Haemost 83 (2000) 229-233
-
(2000)
Thromb Haemost
, vol.83
, pp. 229-233
-
-
Voetsch, B.1
Damasceno, B.P.2
Camargo, E.C.S.3
-
9
-
-
0025278455
-
Elevated plasma homocysteine concentration as a possible independent risk factor for stroke
-
Coull B.M., Malinow M.R., Beamer N., Sexton G., Nordt F., and deGarmo P. Elevated plasma homocysteine concentration as a possible independent risk factor for stroke. Stroke 21 (1990) 572-576
-
(1990)
Stroke
, vol.21
, pp. 572-576
-
-
Coull, B.M.1
Malinow, M.R.2
Beamer, N.3
Sexton, G.4
Nordt, F.5
deGarmo, P.6
-
10
-
-
0025756673
-
Hyperhomocysteinemia: an independent risk factor for vascular disease
-
Clarke R., Daly L., Robinson K., et al. Hyperhomocysteinemia: an independent risk factor for vascular disease. N Engl J Med 324 (1991) 1149-1155
-
(1991)
N Engl J Med
, vol.324
, pp. 1149-1155
-
-
Clarke, R.1
Daly, L.2
Robinson, K.3
-
11
-
-
0028132586
-
A prospective study of plasma homocysteine and risk of ischemic stroke
-
Verhoef P., Hennekens C.H., Malinow M.R., Kok F.J., Willett W.C., and Stampfer M.J. A prospective study of plasma homocysteine and risk of ischemic stroke. Stroke 25 (1994) 1924-1930
-
(1994)
Stroke
, vol.25
, pp. 1924-1930
-
-
Verhoef, P.1
Hennekens, C.H.2
Malinow, M.R.3
Kok, F.J.4
Willett, W.C.5
Stampfer, M.J.6
-
12
-
-
0028845307
-
Prospective study of serum total homocysteine concentration and risk of stroke in middle-aged British men
-
Perry I.J., Refsum H., Morris R.W., Ebrahim S.B., Ueland P.M., and Shaper A.G. Prospective study of serum total homocysteine concentration and risk of stroke in middle-aged British men. Lancet 346 (1995) 1395-1398
-
(1995)
Lancet
, vol.346
, pp. 1395-1398
-
-
Perry, I.J.1
Refsum, H.2
Morris, R.W.3
Ebrahim, S.B.4
Ueland, P.M.5
Shaper, A.G.6
-
13
-
-
0029066299
-
A quantitative assessment of plasma homocysteine as a risk factor for vascular disease: probable benefits of increasing folic acid intakes
-
Boushey C.J., Beresford S.A.A., Omenn G.S., and Motulsky A.G. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease: probable benefits of increasing folic acid intakes. JAMA 274 (1995) 1049-1057
-
(1995)
JAMA
, vol.274
, pp. 1049-1057
-
-
Boushey, C.J.1
Beresford, S.A.A.2
Omenn, G.S.3
Motulsky, A.G.4
-
14
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
-
Frosst P., Blom H.J., Milos R., et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10 (1995) 111-113
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
-
15
-
-
0030880665
-
A common polymorphism in the methylenetetrahydrofolate reductase gene, homocysteine, and ischemic cerebrovascular disease
-
Markus H.S., Nadira A., Swaminathan R., Sankaralingam A., Molloy J., and Powell J. A common polymorphism in the methylenetetrahydrofolate reductase gene, homocysteine, and ischemic cerebrovascular disease. Stroke 28 (1997) 1739-1743
-
(1997)
Stroke
, vol.28
, pp. 1739-1743
-
-
Markus, H.S.1
Nadira, A.2
Swaminathan, R.3
Sankaralingam, A.4
Molloy, J.5
Powell, J.6
-
16
-
-
0031990486
-
The mutation C677T in the methylenetetrahydrofolate reductase gene and stroke
-
Reuner K.H., Ruf A., Kaps M., Druschky K.F., and Patscheke H. The mutation C677T in the methylenetetrahydrofolate reductase gene and stroke. Thromb Haemost 79 (1998) 450-451
-
(1998)
Thromb Haemost
, vol.79
, pp. 450-451
-
-
Reuner, K.H.1
Ruf, A.2
Kaps, M.3
Druschky, K.F.4
Patscheke, H.5
-
17
-
-
0033005234
-
Genetic analysis of the thermolabile variant of 5,10-methylenetetrahydrofolate reductase as a risk factor for ischemic stroke
-
Harmon D.L., Doyle R.M., Meleady R., et al. Genetic analysis of the thermolabile variant of 5,10-methylenetetrahydrofolate reductase as a risk factor for ischemic stroke. Arterioscler Thromb Vasc Biol 99 (1999) 208-211
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.99
, pp. 208-211
-
-
Harmon, D.L.1
Doyle, R.M.2
Meleady, R.3
-
18
-
-
17344372005
-
Methylene tetrahydrofolate reductase gene polymorphism and ischemic stroke in Japanese
-
Morita H., Kurihara H., Tsubaki S., et al. Methylene tetrahydrofolate reductase gene polymorphism and ischemic stroke in Japanese. Arterioscler Thromb Vasc Biol 18 (1998) 1465-1469
-
(1998)
Arterioscler Thromb Vasc Biol
, vol.18
, pp. 1465-1469
-
-
Morita, H.1
Kurihara, H.2
Tsubaki, S.3
-
19
-
-
0031711925
-
Endothelial nitric oxide synthase exon 7 polymorphism, ischemic cerebrovascular disease, and carotid atheroma
-
Markus H.S., Ruigrok Y., Ali N., and Powell J.F. Endothelial nitric oxide synthase exon 7 polymorphism, ischemic cerebrovascular disease, and carotid atheroma. Stroke 29 (1998) 1908-1911
-
(1998)
Stroke
, vol.29
, pp. 1908-1911
-
-
Markus, H.S.1
Ruigrok, Y.2
Ali, N.3
Powell, J.F.4
-
20
-
-
0036330557
-
Etiologic study of young ischemic stroke in Taiwan
-
Lee T.H., Hsu W.C., Chen C.J., and Chen S.T. Etiologic study of young ischemic stroke in Taiwan. Stroke 33 (2002) 1950-1955
-
(2002)
Stroke
, vol.33
, pp. 1950-1955
-
-
Lee, T.H.1
Hsu, W.C.2
Chen, C.J.3
Chen, S.T.4
-
21
-
-
0028942933
-
Ischemic stroke in young adults: experience in 329 patients enrolled in the Iowa Registry of Stroke in Young Adults
-
Adams Jr. H.P., Kappelle L.J., Biller J., et al. Ischemic stroke in young adults: experience in 329 patients enrolled in the Iowa Registry of Stroke in Young Adults. Arch Neurol 52 (1995) 491-495
-
(1995)
Arch Neurol
, vol.52
, pp. 491-495
-
-
Adams Jr., H.P.1
Kappelle, L.J.2
Biller, J.3
-
22
-
-
0028886559
-
Stroke in young black patients: risk factors, subtypes, and prognosis
-
Qureshi A.I., Safdar K., Patel M., Janssen R.S., and Frankel M.R. Stroke in young black patients: risk factors, subtypes, and prognosis. Stroke 26 (1995) 1995-1998
-
(1995)
Stroke
, vol.26
, pp. 1995-1998
-
-
Qureshi, A.I.1
Safdar, K.2
Patel, M.3
Janssen, R.S.4
Frankel, M.R.5
-
23
-
-
1442348272
-
Endothelial nitric oxide gene haplotypes and risk of cerebral small-vessel disease
-
Hassan A., Gormley K., O'Sullivan M., et al. Endothelial nitric oxide gene haplotypes and risk of cerebral small-vessel disease. Stroke 35 (2004) 654-659
-
(2004)
Stroke
, vol.35
, pp. 654-659
-
-
Hassan, A.1
Gormley, K.2
O'Sullivan, M.3
-
24
-
-
24644511646
-
Promoter polymorphisms in the nitric oxide synthase 3 gene are associated with ischemic stroke susceptibility in young black women
-
Timothy D., Wayne H., Jianfeng X., et al. Promoter polymorphisms in the nitric oxide synthase 3 gene are associated with ischemic stroke susceptibility in young black women. Stroke 36 (2005) 1848-1853
-
(2005)
Stroke
, vol.36
, pp. 1848-1853
-
-
Timothy, D.1
Wayne, H.2
Jianfeng, X.3
-
25
-
-
0035957122
-
Association of a 27-bp repeat polymorphism in ecNOS gene with ischemic stroke in Chinese patients
-
Hou L., Osei-Hyiaman D., Yu H., et al. Association of a 27-bp repeat polymorphism in ecNOS gene with ischemic stroke in Chinese patients. Neurol 56 (2001) 490-496
-
(2001)
Neurol
, vol.56
, pp. 490-496
-
-
Hou, L.1
Osei-Hyiaman, D.2
Yu, H.3
-
26
-
-
0030048029
-
A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene
-
Wang X.L., Sim A.S., Badenhop R.F., McCredie R.M., and Wicken D.E. A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene. Nat Med 2 (1996) 41-45
-
(1996)
Nat Med
, vol.2
, pp. 41-45
-
-
Wang, X.L.1
Sim, A.S.2
Badenhop, R.F.3
McCredie, R.M.4
Wicken, D.E.5
-
27
-
-
0031984045
-
Association of a polymorphism of the endothelial constitutive nitric oxide synthase gene with myocardial infarction in the Japanese population
-
Ichihara S., Yamada Y., Fujimura T., Nakashima N., and Yokota M. Association of a polymorphism of the endothelial constitutive nitric oxide synthase gene with myocardial infarction in the Japanese population. Am J Cardiol 81 (1998) 83-86
-
(1998)
Am J Cardiol
, vol.81
, pp. 83-86
-
-
Ichihara, S.1
Yamada, Y.2
Fujimura, T.3
Nakashima, N.4
Yokota, M.5
-
28
-
-
0032717816
-
The relationship between polymorphisms in the endothelial cell nitric oxide synthase gene and the platelet GPIIIa gene with myocardial infarction and venous thromboembolism in African Americans
-
Hooper W.C., Lally C., Austin H., et al. The relationship between polymorphisms in the endothelial cell nitric oxide synthase gene and the platelet GPIIIa gene with myocardial infarction and venous thromboembolism in African Americans. Chest 116 (1999) 880-886
-
(1999)
Chest
, vol.116
, pp. 880-886
-
-
Hooper, W.C.1
Lally, C.2
Austin, H.3
-
29
-
-
33745046171
-
Mutations and polymorphisms in genes affecting hemostasis proteins and homocysteine metabolism in children with arterial ischemic stroke
-
Komitopoulou A., Platokouki H., Kapsimali Z., Pergantou H., Adamtziki E., and Aronis S. Mutations and polymorphisms in genes affecting hemostasis proteins and homocysteine metabolism in children with arterial ischemic stroke. Cerebrovasc Dis 22 (2006) 13-20
-
(2006)
Cerebrovasc Dis
, vol.22
, pp. 13-20
-
-
Komitopoulou, A.1
Platokouki, H.2
Kapsimali, Z.3
Pergantou, H.4
Adamtziki, E.5
Aronis, S.6
-
30
-
-
0032499024
-
Homocysteine and atherothrombosis
-
Welch G.N., and Lascalzo J. Homocysteine and atherothrombosis. N Eng J Med 338 (1998) 1042-1050
-
(1998)
N Eng J Med
, vol.338
, pp. 1042-1050
-
-
Welch, G.N.1
Lascalzo, J.2
|