메뉴 건너뛰기




Volumn 45, Issue 11, 2007, Pages 661-664

The prevalence of clotting disorders in a series of cases of thrombosis of the cerebral venous sinuses;Prevalencia de los trastornos de la coagulación en una serie de trombosis de senos venosos cerebrales

Author keywords

Aetiology; Cerebral venous thrombosis; Coagulation; Prothrombotic; Thrombophilia; Thrombosis

Indexed keywords

BLOOD CLOTTING FACTOR; PROTHROMBIN;

EID: 37349121827     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.4511.2007096     Document Type: Article
Times cited : (12)

References (32)
  • 1
    • 34347242834 scopus 로고    scopus 로고
    • Cerebral venous thrombosis and plasma concentrations of factor VIII and von Willebrand factor: A case-control study
    • Bugnicourt JM, Roussel B, Tramier B, Lamy C, Godefroy O. Cerebral venous thrombosis and plasma concentrations of factor VIII and von Willebrand factor: a case-control study. J Neurol Neurosurg Psychiatry 2007; 78: 699-701.
    • (2007) J Neurol Neurosurg Psychiatry , vol.78 , pp. 699-701
    • Bugnicourt, J.M.1    Roussel, B.2    Tramier, B.3    Lamy, C.4    Godefroy, O.5
  • 2
    • 3142767412 scopus 로고    scopus 로고
    • Hyperhomocysteinemia and other thrombophilic risk factors in 26 patients with cerebral venous thrombosis
    • Boncoraglio G, Carriero MR, Chiapparini L, Ciceri E, Ciusani E, Erbetta A, et al. Hyperhomocysteinemia and other thrombophilic risk factors in 26 patients with cerebral venous thrombosis. Eur J Neurol 2004; 11: 405-9.
    • (2004) Eur J Neurol , vol.11 , pp. 405-409
    • Boncoraglio, G.1    Carriero, M.R.2    Chiapparini, L.3    Ciceri, E.4    Ciusani, E.5    Erbetta, A.6
  • 3
    • 1942531427 scopus 로고    scopus 로고
    • Hyperhomocysteinemia and other newly recognized inherited coagulation disorders (factor V Leiden and prothrombin gene mutation) in patients with idiopathic cerebral vein thrombosis
    • Ventura P, Cobelli M, Marietta M, Panini R, Rosa MC, Salvioli G. Hyperhomocysteinemia and other newly recognized inherited coagulation disorders (factor V Leiden and prothrombin gene mutation) in patients with idiopathic cerebral vein thrombosis. Cerebrovasc Dis 2004; 17: 153-9.
    • (2004) Cerebrovasc Dis , vol.17 , pp. 153-159
    • Ventura, P.1    Cobelli, M.2    Marietta, M.3    Panini, R.4    Rosa, M.C.5    Salvioli, G.6
  • 5
    • 0345367477 scopus 로고    scopus 로고
    • Factor V Leiden mutation is a risk factor for cerebral venous thrombosis
    • Lüdeman P, Nabavi DG, Junker R, Wolf E, Papke K, Buchner H, et al. Factor V Leiden mutation is a risk factor for cerebral venous thrombosis. Stroke 1998; 29: 2507-10.
    • (1998) Stroke , vol.29 , pp. 2507-2510
    • Lüdeman, P.1    Nabavi, D.G.2    Junker, R.3    Wolf, E.4    Papke, K.5    Buchner, H.6
  • 6
    • 0029768068 scopus 로고    scopus 로고
    • 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
  • 7
    • 0031756655 scopus 로고    scopus 로고
    • 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
  • 8
  • 10
    • 0035044598 scopus 로고    scopus 로고
    • Cerebral Venous Thrombosis Portuguese Collaborative Study Group (Venoport). Cerebral vein and dural sinus thrombosis in Portugal: 1980-1998
    • Ferro JM, Correia M, Pontes C, Baptista MV, Pita F, Cerebral Venous Thrombosis Portuguese Collaborative Study Group (Venoport). Cerebral vein and dural sinus thrombosis in Portugal: 1980-1998. Cerebrovasc Dis 2001; 11: 177-82.
    • (2001) Cerebrovasc Dis , vol.11 , pp. 177-182
    • Ferro, J.M.1    Correia, M.2    Pontes, C.3    Baptista, M.V.4    Pita, F.5
  • 11
    • 0034193350 scopus 로고    scopus 로고
    • 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
  • 12
    • 0029850530 scopus 로고    scopus 로고
    • 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
  • 13
    • 0031836809 scopus 로고    scopus 로고
    • Frequency of the 20210 G→A mutation in the 3′-untranslated region of the prothrombin gene in 35 cases of cerebral venous thrombosis
    • Biousse V, Conard J, Brouzes C, Horellou MH, Ameri A, Bousser MG. Frequency of the 20210 G→A mutation in the 3′-untranslated region of the prothrombin gene in 35 cases of cerebral venous thrombosis. Stroke 1998; 29: 1398-400.
    • (1998) Stroke , vol.29 , pp. 1398-1400
    • Biousse, V.1    Conard, J.2    Brouzes, C.3    Horellou, M.H.4    Ameri, A.5    Bousser, M.G.6
  • 14
    • 0031595694 scopus 로고    scopus 로고
    • Prothrombin gene 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 gene 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
  • 15
    • 0032543748 scopus 로고    scopus 로고
    • 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
  • 18
    • 0034091391 scopus 로고    scopus 로고
    • The A20210 allele in the prothrombin gene enhances the risk of venous thrombosis in carriers of inherited protein S deficiency
    • Castaman G, Tosetto A, Cappellari A, Ruggeri M, Rodeghiero F. The A20210 allele in the prothrombin gene enhances the risk of venous thrombosis in carriers of inherited protein S deficiency. Blood Coagul Fibrinolysis 2000; 11: 321-6.
    • (2000) Blood Coagul Fibrinolysis , vol.11 , pp. 321-326
    • Castaman, G.1    Tosetto, A.2    Cappellari, A.3    Ruggeri, M.4    Rodeghiero, F.5
  • 19
    • 0033017739 scopus 로고    scopus 로고
    • Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: Prevalence and risk assessment
    • Salomon O, Steinberg DM, Zivelin A, Gitel S, Dardik R, Rosenberg N, et al. Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment. Arterioscler Thromb Vasc Biol 1999; 19: 511-8.
    • (1999) Arterioscler Thromb Vasc Biol , vol.19 , pp. 511-518
    • Salomon, O.1    Steinberg, D.M.2    Zivelin, A.3    Gitel, S.4    Dardik, R.5    Rosenberg, N.6
  • 20
    • 4444301709 scopus 로고    scopus 로고
    • Lupus anticoagulant, factor V Leiden, and methylenetetrahydrofolate reductase gene mutation in a lupus patient with cerebral venous thrombosis
    • Uthman I, Khalil I, Sawaya R, Taher A. Lupus anticoagulant, factor V Leiden, and methylenetetrahydrofolate reductase gene mutation in a lupus patient with cerebral venous thrombosis. Clin Rheumatol 2004; 23: 362-3.
    • (2004) Clin Rheumatol , vol.23 , pp. 362-363
    • Uthman, I.1    Khalil, I.2    Sawaya, R.3    Taher, A.4
  • 21
    • 0036371958 scopus 로고    scopus 로고
    • Cerebral venous thrombosis associated to homozygous factor V Leiden mutation in a female of Syrian origin
    • Mira Y, Alfaro A, Estelles A, Vaya A, Ferrando F, Villa P. Cerebral venous thrombosis associated to homozygous factor V Leiden mutation in a female of Syrian origin. Haematologica 2002; 87: ELT02.
    • (2002) Haematologica , vol.87
    • Mira, Y.1    Alfaro, A.2    Estelles, A.3    Vaya, A.4    Ferrando, F.5    Villa, P.6
  • 22
    • 0032554293 scopus 로고    scopus 로고
    • Case-control study of risk of cerebral sinus thrombosis in oral contraceptive users and in (correction of who are) carriers of hereditary prothrombotic conditions. The Cerebral Venous Sinus Thrombosis Study Group
    • De Bruijn SF, Stam J, Koopman MM, Vandenbroucke JP. Case-control study of risk of cerebral sinus thrombosis in oral contraceptive users and in (correction of who are) carriers of hereditary prothrombotic conditions. The Cerebral Venous Sinus Thrombosis Study Group. BMJ 1998; 316: 589-92.
    • (1998) BMJ , vol.316 , pp. 589-592
    • De Bruijn, S.F.1    Stam, J.2    Koopman, M.M.3    Vandenbroucke, J.P.4
  • 23
    • 0029768069 scopus 로고    scopus 로고
    • Cerebral venous thrombosis and activated protein C resistance
    • Dulli DA, Luzzio CC, Williams EC, Schutta HS. Cerebral venous thrombosis and activated protein C resistance. Stroke 1996; 27: 1731-3.
    • (1996) Stroke , vol.27 , pp. 1731-1733
    • Dulli, D.A.1    Luzzio, C.C.2    Williams, E.C.3    Schutta, H.S.4
  • 24
  • 25
    • 0031726178 scopus 로고    scopus 로고
    • Activation of the protein C pathway in hereditary thrombophilia
    • Faioni EM, Franchi F, Asti D, Mannucci PM. Activation of the protein C pathway in hereditary thrombophilia. Thromb Haemost 1998; 80: 557-60.
    • (1998) Thromb Haemost , vol.80 , pp. 557-560
    • Faioni, E.M.1    Franchi, F.2    Asti, D.3    Mannucci, P.M.4
  • 26
    • 0031230720 scopus 로고    scopus 로고
    • APC resistance and factor V Leiden (FV:Q506) mutation in patients with ischemic cerebral events. Vienna Thrombophilia in Stroke Study Group (VITISS)
    • Halbmayer WM, Haushofer A, Angerer V, Finsterer J, Fischer M. APC resistance and factor V Leiden (FV:Q506) mutation in patients with ischemic cerebral events. Vienna Thrombophilia in Stroke Study Group (VITISS). Blood Coagul Fibrinolysis 1997; 8: 361-4.
    • (1997) Blood Coagul Fibrinolysis , vol.8 , pp. 361-364
    • Halbmayer, W.M.1    Haushofer, A.2    Angerer, V.3    Finsterer, J.4    Fischer, M.5
  • 28
    • 0034538371 scopus 로고    scopus 로고
    • Superior sagittal sinus and cerebral cortical venous thrombosis caused by congenital protein C deficiency: A case report
    • Kuwahara S, Abe T, Uga S, Mori K. Superior sagittal sinus and cerebral cortical venous thrombosis caused by congenital protein C deficiency: a case report. Neurol Med Chir (Tokyo) 2000; 40: 645-9.
    • (2000) Neurol Med Chir (Tokyo) , vol.40 , pp. 645-649
    • Kuwahara, S.1    Abe, T.2    Uga, S.3    Mori, K.4
  • 29
    • 0032018309 scopus 로고    scopus 로고
    • Cerebral venous thrombosis in pregnancy: The role of protein S deficiency
    • Gokcil Z, Odabasi Z, Vural O, Yardim M. Cerebral venous thrombosis in pregnancy: the role of protein S deficiency. Acta Neurol Belg 1998; 98: 36-8.
    • (1998) Acta Neurol Belg , vol.98 , pp. 36-38
    • Gokcil, Z.1    Odabasi, Z.2    Vural, O.3    Yardim, M.4
  • 30
    • 0034653996 scopus 로고    scopus 로고
    • Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S
    • Makris M, Leach M, Beauchamp NJ, Daly ME, Cooper PC, Hampton KK, et al. Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S. Blood 2000; 95: 1935-41.
    • (2000) Blood , vol.95 , pp. 1935-1941
    • Makris, M.1    Leach, M.2    Beauchamp, N.J.3    Daly, M.E.4    Cooper, P.C.5    Hampton, K.K.6
  • 31
    • 0038299175 scopus 로고    scopus 로고
    • Effect of hemostatic risk factors on the individual probability of thrombosis during pregnancy and the puerperium
    • Gerhardt A, Scharf RE, Zotz RB. Effect of hemostatic risk factors on the individual probability of thrombosis during pregnancy and the puerperium. Thromb Haemost 2003; 90: 77-85.
    • (2003) Thromb Haemost , vol.90 , pp. 77-85
    • Gerhardt, A.1    Scharf, R.E.2    Zotz, R.B.3
  • 32
    • 0031734147 scopus 로고    scopus 로고
    • Postpartum cerebral venous thrombosis, congenital protein C deficiency, and activated protein C resistance due to heterozygous factor V Leiden mutation
    • Derex L, Philippeau F, Nighoghossian N, Trouillas P, Berruyer M. Postpartum cerebral venous thrombosis, congenital protein C deficiency, and activated protein C resistance due to heterozygous factor V Leiden mutation. J Neurol Neurosurg Psychiatry 1998; 65: 801-2.
    • (1998) J Neurol Neurosurg Psychiatry , vol.65 , pp. 801-802
    • Derex, L.1    Philippeau, F.2    Nighoghossian, N.3    Trouillas, P.4    Berruyer, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.