-
1
-
-
33750502781
-
Brain veins and their diseases
-
Toole J.F. (Ed), Lippincott Williams and Wilkins, New York
-
Nagaraja D. Brain veins and their diseases. In: Toole J.F. (Ed). Cerebrovascular disorders (2004), Lippincott Williams and Wilkins, New York 481-506
-
(2004)
Cerebrovascular disorders
, pp. 481-506
-
-
Nagaraja, D.1
-
2
-
-
0021079081
-
Cerebral venous and arterial thrombosis in pregnancy and puerperium. A study of 135 patients
-
Srinivasan K. Cerebral venous and arterial thrombosis in pregnancy and puerperium. A study of 135 patients. Angiology 34 (1983) 731-746
-
(1983)
Angiology
, vol.34
, pp. 731-746
-
-
Srinivasan, K.1
-
3
-
-
0019304283
-
Stroke during pregnancy and puerperium in young females below the age of 40 years as a result of cerebral venous/venous sinus thrombosis
-
Bansal B.C., Gupta R.R., and Prakash C. Stroke during pregnancy and puerperium in young females below the age of 40 years as a result of cerebral venous/venous sinus thrombosis. Jpn Heart J 21 (1980) 171-183
-
(1980)
Jpn Heart J
, vol.21
, pp. 171-183
-
-
Bansal, B.C.1
Gupta, R.R.2
Prakash, C.3
-
4
-
-
0025735996
-
Cerebrovascular accidents complicating pregnancy and the puerperium
-
Simolke G.A., Cox S.M., and Cunningham F.G. Cerebrovascular accidents complicating pregnancy and the puerperium. Obstet Gynecol 78 (1991) 37-42
-
(1991)
Obstet Gynecol
, vol.78
, pp. 37-42
-
-
Simolke, G.A.1
Cox, S.M.2
Cunningham, F.G.3
-
5
-
-
0031805031
-
Stroke in pregnancy and the puerperium
-
Mas J.L., and Lamy C. Stroke in pregnancy and the puerperium. J Neurol 245 (1998) 305-313
-
(1998)
J Neurol
, vol.245
, pp. 305-313
-
-
Mas, J.L.1
Lamy, C.2
-
6
-
-
13844315228
-
Genetic testing for thrombophilia mutations
-
Hertzberg M.S. Genetic testing for thrombophilia mutations. Semin Thromb Hemost 31 (2005) 33-38
-
(2005)
Semin Thromb Hemost
, vol.31
, pp. 33-38
-
-
Hertzberg, M.S.1
-
7
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller S.A., Dykes D.D., and Polesky H.F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16 (1988) 1215
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
8
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina R.M., Koeleman B.P., Koster T., Rosendaal F.R., Dirven R.J., de Ronde H., 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.2
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
de Ronde, H.6
-
9
-
-
0029850530
-
A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort S.R., Rosendaal F.R., Reitsma P.H., and Bertina R.M. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 88 (1996) 3698-3703
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
10
-
-
0032529506
-
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene
-
Zivelin A., Rosenberg N., Faier S., Kornbrot N., Peretz H., Mannhalter C., et al. A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene. Blood 92 (1998) 1119-1124
-
(1998)
Blood
, vol.92
, pp. 1119-1124
-
-
Zivelin, A.1
Rosenberg, N.2
Faier, S.3
Kornbrot, N.4
Peretz, H.5
Mannhalter, C.6
-
11
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: a common mutation in methylene tetrahydrofolate reductase gene
-
Frosst P., Blom H.J., Milos R., Goyette P., Sheppard C.A., Matthews R.G., et al. A candidate genetic risk factor for vascular disease: a common mutation in methylene tetrahydrofolate reductase gene. Nat Genet 10 (1995) 111-113
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
-
12
-
-
0035912152
-
Genetic susceptibility to venous thrombosis
-
Seligsohn U., and Lubetsky A. Genetic susceptibility to venous thrombosis. N Engl J Med 344 (2001) 1222-1231
-
(2001)
N Engl J Med
, vol.344
, pp. 1222-1231
-
-
Seligsohn, U.1
Lubetsky, A.2
-
13
-
-
0031023757
-
A single genetic origin for a common Caucasian risk factor for venous thrombosis
-
Zivelin A., Griffin J.H., Xu X., Pabinger I., Samama M., Conard J., et al. A single genetic origin for a common Caucasian risk factor for venous thrombosis. Blood 89 (1997) 397-402
-
(1997)
Blood
, vol.89
, pp. 397-402
-
-
Zivelin, A.1
Griffin, J.H.2
Xu, X.3
Pabinger, I.4
Samama, M.5
Conard, J.6
-
14
-
-
7244231457
-
Absence of factor V Leiden (G1691A) mutation, FII G20210A allele in coronary artery disease in north India
-
Gupta N., Khan F., Tripathi M., Singh V.P., Tewari S., Ramesh V., et al. Absence of factor V Leiden (G1691A) mutation, FII G20210A allele in coronary artery disease in north India. Indian J Med Sci 57 (2003) 535-542
-
(2003)
Indian J Med Sci
, vol.57
, pp. 535-542
-
-
Gupta, N.1
Khan, F.2
Tripathi, M.3
Singh, V.P.4
Tewari, S.5
Ramesh, V.6
-
16
-
-
0034628535
-
Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium
-
Gerhardt A., Scharf R.E., Beckmann M.W., Struve S., Bender H.F., Pillny M., et al. Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium. N Engl J Med 342 (2000) 374-380
-
(2000)
N Engl J Med
, vol.342
, pp. 374-380
-
-
Gerhardt, A.1
Scharf, R.E.2
Beckmann, M.W.3
Struve, S.4
Bender, H.F.5
Pillny, M.6
-
17
-
-
0035659849
-
Factor V Leiden mutation and the risk of venous thromboembolism in pregnant women
-
Tormene D., Simioni P., Prandoni P., Luni S., Zerbinati P., Sartor D., et al. Factor V Leiden mutation and the risk of venous thromboembolism in pregnant women. Haematologica 86 (2001) 1305-1309
-
(2001)
Haematologica
, vol.86
, pp. 1305-1309
-
-
Tormene, D.1
Simioni, P.2
Prandoni, P.3
Luni, S.4
Zerbinati, P.5
Sartor, D.6
-
18
-
-
0029762332
-
Factor V Leiden mutation in cerebral venous thrombosis
-
Zuber M., Toulon P., Mamet L., and Mas J.L. Factor V Leiden mutation in cerebral venous thrombosis. Stroke 27 (1996) 1721-1723
-
(1996)
Stroke
, vol.27
, pp. 1721-1723
-
-
Zuber, M.1
Toulon, P.2
Mamet, L.3
Mas, J.L.4
-
19
-
-
0345367477
-
Factor V Leiden mutation is a risk factor for cerebral vein thrombosis: a case-control study of 55 patients
-
Ludemann P., Nabavi D.G., Junker R., Wolff E., Papke K., Buchner H., et al. Factor V Leiden mutation is a risk factor for cerebral vein thrombosis: a case-control study of 55 patients. Stroke 29 (1998) 2507-2510
-
(1998)
Stroke
, vol.29
, pp. 2507-2510
-
-
Ludemann, P.1
Nabavi, D.G.2
Junker, R.3
Wolff, E.4
Papke, K.5
Buchner, H.6
-
20
-
-
0031891060
-
Increased rate of factor V Leiden mutation in patients with cerebral venous thrombosis
-
Weih M., Vetter B., Ziemer S., Mehraein S., Valdueza J.M., Koscielny J., et al. Increased rate of factor V Leiden mutation in patients with cerebral venous thrombosis. J Neurol 245 (1998) 149-152
-
(1998)
J Neurol
, vol.245
, pp. 149-152
-
-
Weih, M.1
Vetter, B.2
Ziemer, S.3
Mehraein, S.4
Valdueza, J.M.5
Koscielny, J.6
-
21
-
-
0029875717
-
Factor V gene mutation is a risk factor for cerebral venous thrombosis
-
Martinelli I., Landi G., Merati G., Cella R., Tosetto A., and Mannucci P.M. Factor V gene mutation is a risk factor for cerebral venous thrombosis. Thromb Haemost 75 (1996) 393-394
-
(1996)
Thromb Haemost
, vol.75
, pp. 393-394
-
-
Martinelli, I.1
Landi, G.2
Merati, G.3
Cella, R.4
Tosetto, A.5
Mannucci, P.M.6
-
22
-
-
0037342033
-
No association between thrombosis and factor V gene polymorphisms in Chinese Han population
-
Yanqing H., Fangping C., Qinzhi X., Zaifu J., Guangping W., Xiaoxia Z., et al. No association between thrombosis and factor V gene polymorphisms in Chinese Han population. Thromb Haemost 89 (2003) 446-451
-
(2003)
Thromb Haemost
, vol.89
, pp. 446-451
-
-
Yanqing, H.1
Fangping, C.2
Qinzhi, X.3
Zaifu, J.4
Guangping, W.5
Xiaoxia, Z.6
-
23
-
-
33644800098
-
Low frequency of factor V Leiden and prothrombin G20210A mutations in patients with hepatic venous outflow tract obstruction in northern India: a case-control study
-
Kumar S.I., Kumar A., Srivastava S., Saraswat V.A., and Aggarwal R. Low frequency of factor V Leiden and prothrombin G20210A mutations in patients with hepatic venous outflow tract obstruction in northern India: a case-control study. Indian J Gastroenterol 24 (2005) 211-215
-
(2005)
Indian J Gastroenterol
, vol.24
, pp. 211-215
-
-
Kumar, S.I.1
Kumar, A.2
Srivastava, S.3
Saraswat, V.A.4
Aggarwal, R.5
-
24
-
-
0035088186
-
Venous thromboembolism in young patients from western India: a study
-
Ghosh K., Shetty S., Madkaikar M., Pawar A., Nair S., Khare A., et al. Venous thromboembolism in young patients from western India: a study. Clin Appl Thromb Hemost 7 (2001) 158-165
-
(2001)
Clin Appl Thromb Hemost
, vol.7
, pp. 158-165
-
-
Ghosh, K.1
Shetty, S.2
Madkaikar, M.3
Pawar, A.4
Nair, S.5
Khare, A.6
-
25
-
-
11444268843
-
Prothrombin G20210A mutation, and not factor V Leiden mutation, is a risk factor for cerebral venous thrombosis in Brazilian patients
-
Rodrigues C.A., Rocha L.K., Morelli V.M., Franco R.F., and Lourenco D.M. Prothrombin G20210A mutation, and not factor V Leiden mutation, is a risk factor for cerebral venous thrombosis in Brazilian patients. J Thromb Haemost 2 (2004) 1211-1212
-
(2004)
J Thromb Haemost
, vol.2
, pp. 1211-1212
-
-
Rodrigues, C.A.1
Rocha, L.K.2
Morelli, V.M.3
Franco, R.F.4
Lourenco, D.M.5
-
26
-
-
2142717279
-
Heterogeneous distribution of factor V Leiden in patients from north India with venous thromboembolism
-
Garewal G., Das R., Varma S., Chawla Y., and Prabhakar S. Heterogeneous distribution of factor V Leiden in patients from north India with venous thromboembolism. J Thromb Haemost 1 (2003) 1329-1330
-
(2003)
J Thromb Haemost
, vol.1
, pp. 1329-1330
-
-
Garewal, G.1
Das, R.2
Varma, S.3
Chawla, Y.4
Prabhakar, S.5
-
27
-
-
0031981017
-
Geographic distribution of the 20210 G to A prothrombin variant
-
Rosendaal F.R., Doggen C.J., and Zivelin A. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 79 (1998) 706-708
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.2
Zivelin, A.3
-
28
-
-
0032729187
-
Coexistence of factor V Leiden and factor II A20210 mutation and recurrent venous thromboembolism
-
Margaglione M., D'Andrea G., Colaizzo D., Cappucci G., del Popolo A., Brancaccio V., et al. Coexistence of factor V Leiden and factor II A20210 mutation and recurrent venous thromboembolism. Thromb Haemost 82 (1999) 1583-1587
-
(1999)
Thromb Haemost
, vol.82
, pp. 1583-1587
-
-
Margaglione, M.1
D'Andrea, G.2
Colaizzo, D.3
Cappucci, G.4
del Popolo, A.5
Brancaccio, V.6
-
29
-
-
0031756655
-
Inherited prothrombotic risk factors and cerebral venous thrombosis
-
Hillier C.E., Collins P.W., Bowen D.J., Bowley S., and Wiles C.M. Inherited prothrombotic risk factors and cerebral venous thrombosis. QJM 91 (1998) 677-680
-
(1998)
QJM
, vol.91
, pp. 677-680
-
-
Hillier, C.E.1
Collins, P.W.2
Bowen, D.J.3
Bowley, S.4
Wiles, C.M.5
-
30
-
-
0033920794
-
G20210A PRTH gene mutation and other thrombophilic polymorphisms in cerebral venous thrombosis
-
Madonna P., de Stefano A., Coppola A., Albisinni R., and Cerbone A.M. G20210A PRTH gene mutation and other thrombophilic polymorphisms in cerebral venous thrombosis. Stroke 31 (2000) 1787-1788
-
(2000)
Stroke
, vol.31
, pp. 1787-1788
-
-
Madonna, P.1
de Stefano, A.2
Coppola, A.3
Albisinni, R.4
Cerbone, A.M.5
-
31
-
-
0032543748
-
High risk of cerebral-vein thrombosis in carriers of a prothrombin gene mutation and in users of oral contraceptives
-
Martinelli I., Sacchi E., Landi G., Taioli E., Duca F., and Mannucci P.M. High risk of cerebral-vein thrombosis in carriers of a prothrombin gene mutation and in users of oral contraceptives. N Engl J Med 338 (1998) 1793-1797
-
(1998)
N Engl J Med
, vol.338
, pp. 1793-1797
-
-
Martinelli, I.1
Sacchi, E.2
Landi, G.3
Taioli, E.4
Duca, F.5
Mannucci, P.M.6
-
32
-
-
11444253333
-
Prothrombin 20210A and oral contraceptive use as risk factors for cerebral venous thrombosis
-
Gadelha T., Andre C., Juca A.A., and Nucci M. Prothrombin 20210A and oral contraceptive use as risk factors for cerebral venous thrombosis. Cerebrovasc Dis 19 (2005) 49-52
-
(2005)
Cerebrovasc Dis
, vol.19
, pp. 49-52
-
-
Gadelha, T.1
Andre, C.2
Juca, A.A.3
Nucci, M.4
-
33
-
-
0031595694
-
Prothrombin gene G20210-A transition is a risk factor for cerebral venous thrombosis
-
Reuner K.H., Ruf A., Grau A., Rickmann H., Stolz E., Juttler E., et al. Prothrombin gene G20210-A transition is a risk factor for cerebral venous thrombosis. Stroke 29 (1998) 1765-1769
-
(1998)
Stroke
, vol.29
, pp. 1765-1769
-
-
Reuner, K.H.1
Ruf, A.2
Grau, A.3
Rickmann, H.4
Stolz, E.5
Juttler, E.6
-
34
-
-
0034093930
-
Screening for thrombophilic risk factors among 25 German patients with cerebral venous thrombosis
-
Solz E., Kemkes-Matthes B., Potzsch B., Hahn M., Kraus J., Wirbartz A., et al. Screening for thrombophilic risk factors among 25 German patients with cerebral venous thrombosis. Acta Neurol Scand 102 (2000) 31-36
-
(2000)
Acta Neurol Scand
, vol.102
, pp. 31-36
-
-
Solz, E.1
Kemkes-Matthes, B.2
Potzsch, B.3
Hahn, M.4
Kraus, J.5
Wirbartz, A.6
-
35
-
-
33644933673
-
Risk of cerebral venous thrombosis and novel gene polymorphisms of the coagulation and fibrinolytic systems
-
Lichy C., Dong-Si T., Reuner K., Genius J., Rickmann H., Hampe T., et al. Risk of cerebral venous thrombosis and novel gene polymorphisms of the coagulation and fibrinolytic systems. J Neurol 253 (2006) 316-320
-
(2006)
J Neurol
, vol.253
, pp. 316-320
-
-
Lichy, C.1
Dong-Si, T.2
Reuner, K.3
Genius, J.4
Rickmann, H.5
Hampe, T.6
-
36
-
-
0033665792
-
Hereditary thrombophilia with ischemic stroke and sinus thrombosis. Diagnosis, therapy and meta-analysis
-
Weih M., Junge-Hulsing J., Mehraein S., Ziemer S., and Einhaupl K.M. Hereditary thrombophilia with ischemic stroke and sinus thrombosis. Diagnosis, therapy and meta-analysis. Nervenarzt 71 (2000) 936-945
-
(2000)
Nervenarzt
, vol.71
, pp. 936-945
-
-
Weih, M.1
Junge-Hulsing, J.2
Mehraein, S.3
Ziemer, S.4
Einhaupl, K.M.5
-
37
-
-
33645510408
-
Thrombophilic abnormalities, oral contraceptives and risk of cerebral vein thrombosis: a meta-analysis
-
Dentali F., Crowther M., and Dentali W.A. Thrombophilic abnormalities, oral contraceptives and risk of cerebral vein thrombosis: a meta-analysis. Blood 107 (2006) 2766-2773
-
(2006)
Blood
, vol.107
, pp. 2766-2773
-
-
Dentali, F.1
Crowther, M.2
Dentali, W.A.3
-
38
-
-
30644460368
-
Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis
-
Koshy A., and Jeyakumari M. Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis. Ann Hematol 85 (2006) 126-128
-
(2006)
Ann Hematol
, vol.85
, pp. 126-128
-
-
Koshy, A.1
Jeyakumari, M.2
-
39
-
-
2442637355
-
Prothrombin 20210A is not prevalent in north India
-
Garewal G., Das R., Ahluwalia J., Mittal N., and Varma S. Prothrombin 20210A is not prevalent in north India. J Thromb Haemost 1 (2003) 2253-2254
-
(2003)
J Thromb Haemost
, vol.1
, pp. 2253-2254
-
-
Garewal, G.1
Das, R.2
Ahluwalia, J.3
Mittal, N.4
Varma, S.5
-
40
-
-
0032921209
-
Born to clot: the European burden
-
Rees D.C., Chapman N.H., Webster M.T., Guerreiro J.F., Rochette J., and Clegg J.B. Born to clot: the European burden. Br J Haematol 105 (1999) 564-566
-
(1999)
Br J Haematol
, vol.105
, pp. 564-566
-
-
Rees, D.C.1
Chapman, N.H.2
Webster, M.T.3
Guerreiro, J.F.4
Rochette, J.5
Clegg, J.B.6
-
41
-
-
0029806746
-
Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians
-
Ma J., Stampfer M.J., Hennekens C.H., Frosst P., Selhub J., Horsford J., et al. Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians. Circulation 94 (1996) 2410-2416
-
(1996)
Circulation
, vol.94
, pp. 2410-2416
-
-
Ma, J.1
Stampfer, M.J.2
Hennekens, C.H.3
Frosst, P.4
Selhub, J.5
Horsford, J.6
-
42
-
-
0030612756
-
The 677C→T mutation in the methylenetetra hydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease
-
Verhoef P., Kok F.J., Kluijtmans L.A., Blom H.J., Refsum H., Ueland P.M., et al. The 677C→T mutation in the methylenetetra hydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease. Atherosclerosis 132 (1997) 105-113
-
(1997)
Atherosclerosis
, vol.132
, pp. 105-113
-
-
Verhoef, P.1
Kok, F.J.2
Kluijtmans, L.A.3
Blom, H.J.4
Refsum, H.5
Ueland, P.M.6
-
43
-
-
20444445722
-
Homocysteine, MTHFR and risk of venous thrombosis: a meta-analysis of published epidemiological studies
-
Den Heijer M., Lewington S., and Clarke R. Homocysteine, MTHFR and risk of venous thrombosis: a meta-analysis of published epidemiological studies. J Thromb Haemost 3 (2005) 292-299
-
(2005)
J Thromb Haemost
, vol.3
, pp. 292-299
-
-
Den Heijer, M.1
Lewington, S.2
Clarke, R.3
-
44
-
-
0033768636
-
Methylenetetrahydrofolate reductase 677 C→T mutation and coronary heart disease risk in UK Indian Asians
-
Chambers J.C., Ireland H., Thompson E., Reilly P., Obeid O.A., Refsum H., et al. Methylenetetrahydrofolate reductase 677 C→T mutation and coronary heart disease risk in UK Indian Asians. Arterioscler Thromb Vasc Biol 20 (2000) 2448-2452
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
, pp. 2448-2452
-
-
Chambers, J.C.1
Ireland, H.2
Thompson, E.3
Reilly, P.4
Obeid, O.A.5
Refsum, H.6
-
45
-
-
22144472522
-
Prevalence of the factor V G1691A and the factor II/prothrombin G20210A gene polymorphisms among Tamilians
-
Angeline T., Bentley H.A., Hawk A.B., Manners R.J., Mokashi H.A., Jeyaraj N., et al. Prevalence of the factor V G1691A and the factor II/prothrombin G20210A gene polymorphisms among Tamilians. Exp Mol Pathol 79 (2005) 9-13
-
(2005)
Exp Mol Pathol
, vol.79
, pp. 9-13
-
-
Angeline, T.1
Bentley, H.A.2
Hawk, A.B.3
Manners, R.J.4
Mokashi, H.A.5
Jeyaraj, N.6
-
46
-
-
0043240188
-
Hyperhomocysteinemia in cerebral vein thrombosis
-
Martinelli I., Battaglioli T., Pedotti P., Cattaneo M., and Mannucci P.M. Hyperhomocysteinemia in cerebral vein thrombosis. Blood 102 (2003) 1363-1366
-
(2003)
Blood
, vol.102
, pp. 1363-1366
-
-
Martinelli, I.1
Battaglioli, T.2
Pedotti, P.3
Cattaneo, M.4
Mannucci, P.M.5
-
47
-
-
3242750748
-
Hyperhomocysteinemia, low folate and vitamin B12 concentrations, and methylene tetrahydrofolate reductase mutation in cerebral venous thrombosis
-
Cantu C., Alonso E., Jara A., Martinez L., Rios C., Fernandez Mde L., et al. Hyperhomocysteinemia, low folate and vitamin B12 concentrations, and methylene tetrahydrofolate reductase mutation in cerebral venous thrombosis. Stroke 35 (2004) 1790-1794
-
(2004)
Stroke
, vol.35
, pp. 1790-1794
-
-
Cantu, C.1
Alonso, E.2
Jara, A.3
Martinez, L.4
Rios, C.5
Fernandez Mde, L.6
|