-
1
-
-
0345367477
-
Factor V Leiden mutation ia a risk factor for cerebral venous thrombosis
-
Lüdemann P, Nabavi DG, Junker R, Wolff E, Papke K, Buchner H, et al. Factor V Leiden mutation ia a risk factor for cerebral venous thrombosis. Stroke 1998;29:2507-10.
-
(1998)
Stroke
, vol.29
, pp. 2507-2510
-
-
Lüdemann, P.1
Nabavi, D.G.2
Junker, R.3
Wolff, E.4
Papke, K.5
Buchner, H.6
-
2
-
-
0029768068
-
Coagulation studies, factor V Leiden and anticardiolipin antibodies in 40 cases of cerebral venous thrombosis
-
Deschiens MA, Conrad J, Horellou MH, Ameri A, Preter M, Chendru F, et al. Coagulation studies, factor V Leiden and anticardiolipin antibodies in 40 cases of cerebral venous thrombosis. Stroke 1996;27:1724-30.
-
(1996)
Stroke
, vol.27
, pp. 1724-1730
-
-
Deschiens, M.A.1
Conrad, J.2
Horellou, M.H.3
Ameri, A.4
Preter, M.5
Chendru, F.6
-
3
-
-
0031756655
-
Inherited prothrombotic risk factors and cerebral venous thrombosis
-
Hillier CE, Collins PW, Bowen DJ, Bowley S, Wiles CM. Inherited prothrombotic risk factors and cerebral venous thrombosis. QJM 1998;91:677-80.
-
(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
-
4
-
-
0031836809
-
Frequency of the 20210 G→ A mutation in the 3′-untranslated region of the prothrombin gene in 35 cases of cereral venous thrombosis
-
Biousse V, Conard J, Brouzes C, Horellou NH, Ameri A, Bousser MG. Frequency of the 20210 G→ A mutation in the 3′-untranslated region of the prothrombin gene in 35 cases of cereral venous thrombosis. Stroke 1998;29:1398-400.
-
(1998)
Stroke
, vol.29
, pp. 1398-1400
-
-
Biousse, V.1
Conard, J.2
Brouzes, C.3
Horellou, N.H.4
Ameri, A.5
Bousser, M.G.6
-
5
-
-
0031595694
-
Prothrombin G20210→A transition is a risk factor for cerebral venous thrombosis
-
Reuner KH, Ruf A, Grau A, Rickmann H, Stolz E, Juttler E, et al. Prothrombin G20210→A transition is a risk factor for cerebral venous thrombosis. Stroke 1998;29:1765-9.
-
(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
-
6
-
-
0031442037
-
Cerebral venous thrombosis and anticardiolipin antibodies
-
Carhuapoma JR, Mitsias P, Levine SR. Cerebral venous thrombosis and anticardiolipin antibodies. Stroke 1997;28:2363-9.
-
(1997)
Stroke
, vol.28
, pp. 2363-2369
-
-
Carhuapoma, J.R.1
Mitsias, P.2
Levine, S.R.3
-
7
-
-
0034093930
-
Screening for thrombophilic factors among 25 german patients with cerebral venous thrombosis
-
Stolz E, Kemkes-Matthes B, Potzsch B, Hahn M, Kraus J, Wirbartz M. Screening for thrombophilic 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
Hahn, M.4
Kraus, J.5
Wirbartz, M.6
-
8
-
-
0034193350
-
Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis
-
Soria JM, Almasy L, Souto JC, Tirado I, Borell M, Mateo J, 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
Tirado, I.4
Borell, M.5
Mateo, J.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 SR, Rosendaal FR, Reitsma PH, Bertina RM. 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 1996;88:3698-703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
10
-
-
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, Mannucci PM. High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives. N Engl J Med 1998;338:1793-7.
-
(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
-
12
-
-
0011474264
-
Trombosis venosa cerebral asociada a la variante G20210A del gen de la protrombina
-
Sánchez-Marín B, Marta-Moreno E, Alarcía-Alejos R, López-Pérez A, Serrano-Ponz M, Latorre-Jimenez A. Trombosis venosa cerebral asociada a la variante G20210A del gen de la protrombina. Neurología 2000;15:473-584.
-
(2000)
Neurología
, vol.15
, pp. 473-584
-
-
Sánchez-Marín, B.1
Marta-Moreno, E.2
Alarcía-Alejos, R.3
López-Pérez, A.4
Serrano-Ponz, M.5
Latorre-Jimenez, A.6
-
13
-
-
0035899156
-
Trombosis venosa cerebral y mutación G20210A del gen de la protrombina familiar
-
Verdelho A, Ferro JM, Palmeiro A, Antunes C. Trombosis venosa cerebral y mutación G20210A del gen de la protrombina familiar. Rev Neurol 2001;33:335-8.
-
(2001)
Rev Neurol
, vol.33
, pp. 335-338
-
-
Verdelho, A.1
Ferro, J.M.2
Palmeiro, A.3
Antunes, C.4
-
14
-
-
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, del Rio E, Oliver A, Mateo J, 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
Del Rio, E.4
Oliver, A.5
Mateo, J.6
-
15
-
-
0028098210
-
Resistance to activated protein C as a basis for venous thrombosis
-
Svensson PJ, Dahlback B. Resistance to activated protein C as a basis for venous thrombosis. N Engl J Med 1994;330:517-22.
-
(1994)
N Engl J Med
, vol.330
, pp. 517-522
-
-
Svensson, P.J.1
Dahlback, B.2
-
16
-
-
0034446477
-
Trombosis cerebral neonatal y déficit de factor V Leiden
-
Moliner-Calderón E, López-Bernal E, Ginovart-Galiana G, Nadal-Amat J, Cubells-Riero J. Trombosis cerebral neonatal y déficit de factor V Leiden. An Pediatr 2000;52:52-5.
-
(2000)
An Pediatr
, vol.52
, pp. 52-55
-
-
Moliner-Calderón, E.1
López-Bernal, E.2
Ginovart-Galiana, G.3
Nadal-Amat, J.4
Cubells-Riero, J.5
-
17
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BPMC, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994;369:67-7.
-
(1994)
Nature
, vol.369
, pp. 67
-
-
Bertina, R.M.1
Koeleman, B.P.M.C.2
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
De Ronde, H.6
-
18
-
-
0027520285
-
Venous trombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia study
-
Koster T, Rosendaal FR, de Ronde F, Briët E, Vandenbroucke JP, Bertina RM. Venous trombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia study. Lancet 1993;342:1503-6.
-
(1993)
Lancet
, vol.342
, pp. 1503-1506
-
-
Koster, T.1
Rosendaal, F.R.2
De Ronde, F.3
Briët, E.4
Vandenbroucke, J.P.5
Bertina, R.M.6
-
19
-
-
0034628535
-
Prothrombin and factor V mutations in women with history of thrombosis during pregnancy and the puerperium
-
Gerhardt A, Scharf RE, Beckmann MW, Struve S, Bender HG, Pillny M, et al. Prothrombin and factor V mutations in women with history of thrombosis during pregnancy and the puerperium. N Engl J Med 2000;342:374-80.
-
(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.G.5
Pillny, M.6
-
20
-
-
0031904536
-
Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis
-
Weih M, Mehraein S, Valdueza JM, Einhäupl KM. Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis. Stroke 1998;29:1739-40.
-
(1998)
Stroke
, vol.29
, pp. 1739-1740
-
-
Weih, M.1
Mehraein, S.2
Valdueza, J.M.3
Einhäupl, K.M.4
-
21
-
-
0034131190
-
Combined heterozyosity of factor V Leiden and the G20210A prothrombin gene mutation in a patient with cerebral cortical thrombosis
-
Liu XY, Gabig TG, Bang NU. Combined heterozyosity of factor V Leiden and the G20210A prothrombin gene mutation in a patient with cerebral cortical thrombosis. Am J Hematol 2000;64:226-8.
-
(2000)
Am J Hematol
, vol.64
, pp. 226-228
-
-
Liu, X.Y.1
Gabig, T.G.2
Bang, N.U.3
-
22
-
-
0028845307
-
Prospective study of serum total homocysteine concentration and risk of stroke in middle-aged British men
-
Perry IJ, Refsum H, Morris RW, Ebrahim SB, Ueland PM, Shaper AG. Prospective study of serum total homocysteine concentration and risk of stroke in middle-aged British men. Lancet 1995;346:1395-8.
-
(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
-
23
-
-
0023696435
-
Intermediate homocysteinemia: A thermolabile variant of methylenetetrahydrofolate reductase
-
Kang SS, Zhou J, Wong PW, Kowalisyn J, Stroksch G. Intermediate homocysteinemia: A thermolabile variant of methylenetetrahydrofolate reductase. Am J Hum Genet 1988;43:414-21.
-
(1988)
Am J Hum Genet
, vol.43
, pp. 414-421
-
-
Kang, S.S.1
Zhou, J.2
Wong, P.W.3
Kowalisyn, J.4
Stroksch, G.5
-
24
-
-
0034606262
-
The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine
-
Kowa H, Yasui K, Takeshima T, Urakami K, Sakai F, Nakashima K. The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine. Am J Med Genet 2000;96:762-4.
-
(2000)
Am J Med Genet
, vol.96
, pp. 762-764
-
-
Kowa, H.1
Yasui, K.2
Takeshima, T.3
Urakami, K.4
Sakai, F.5
Nakashima, K.6
-
25
-
-
0025041014
-
Cerebral venous thrombosis in systemic lupus erythematosus
-
Vidailhet M, Piette JC, Wechsler B, Bousser MG, Brunet P. Cerebral venous thrombosis in systemic lupus erythematosus. Stroke 1990;21:1226-31.
-
(1990)
Stroke
, vol.21
, pp. 1226-1231
-
-
Vidailhet, M.1
Piette, J.C.2
Wechsler, B.3
Bousser, M.G.4
Brunet, P.5
-
27
-
-
0027965126
-
Antiphospholipid antibodies in patients without systemic lupus erythematosus: Neuroradiologic findings
-
Provenzale JM, Heinz ER, Ortel TL, Macik BG, Charles LA, Alberts MJ. Antiphospholipid antibodies in patients without systemic lupus erythematosus: Neuroradiologic findings. Radiology 1994;192:531-7.
-
(1994)
Radiology
, vol.192
, pp. 531-537
-
-
Provenzale, J.M.1
Heinz, E.R.2
Ortel, T.L.3
Macik, B.G.4
Charles, L.A.5
Alberts, M.J.6
-
28
-
-
0033512274
-
International consensus statement on preliminary classification criteria for definite antiphospholipid syndrome
-
Wilson WA, Gharavi AE, Koike T, Lockshin MD, Branch DW, Piette JC, et al. International consensus statement on preliminary classification criteria for definite antiphospholipid syndrome. Arthritis Rheumatism 1999;42:1309-11.
-
(1999)
Arthritis Rheumatism
, vol.42
, pp. 1309-1311
-
-
Wilson, W.A.1
Gharavi, A.E.2
Koike, T.3
Lockshin, M.D.4
Branch, D.W.5
Piette, J.C.6
-
29
-
-
0004750551
-
-
Haemostasis and Thrombosis Task Force of the British Committee for Standards in Haematology. Br J Haematol 2000;109:704-15.
-
(2000)
Br J Haematol
, vol.109
, pp. 704-715
-
-
-
30
-
-
0033710040
-
Extended anticogulation for prevention of recurrent venous thromboembolism in carriers of factor V Leiden
-
Marchetti M, Pistorio A, Barosi G. Extended anticogulation for prevention of recurrent venous thromboembolism in carriers of factor V Leiden. Thromb Haemost 2000;84:752-7.
-
(2000)
Thromb Haemost
, vol.84
, pp. 752-757
-
-
Marchetti, M.1
Pistorio, A.2
Barosi, G.3
|