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Volumn 9, Issue 8, 1998, Pages 757-760

Ischemic stroke in a young patient with protein C deficiency and prothrombin gene mutation G20210A

Author keywords

Protein C deficiency; Prothrombin gene mutation 20210A; Stroke

Indexed keywords

PROTEIN C; PROTHROMBIN;

EID: 0032464898     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001721-199811000-00006     Document Type: Article
Times cited : (7)

References (24)
  • 1
    • 0025358732 scopus 로고
    • Ischemic stroke due to protein C deficiency
    • Kohler J, Kasper J, Witt I, Von Reuthern G. Ischemic stroke due to protein C deficiency. Stroke 1990; 21: 1077-1080.
    • (1990) Stroke , vol.21 , pp. 1077-1080
    • Kohler, J.1    Kasper, J.2    Witt, I.3    Von Reuthern, G.4
  • 2
    • 0025183930 scopus 로고
    • Stroke in protein C deficiency
    • Grewal R, Goldberg M. Stroke in protein C deficiency. Am J Med 1990; 89: 5380-5389.
    • (1990) Am J Med , vol.89 , pp. 5380-5389
    • Grewal, R.1    Goldberg, M.2
  • 3
    • 0031445353 scopus 로고    scopus 로고
    • Protein C and S deficiency in children with ischemic cerebrovascular accident
    • Koh S, Chen L. Protein C and S deficiency in children with ischemic cerebrovascular accident. Pediat Neurol 1997; 17: 319-321.
    • (1997) Pediat Neurol , vol.17 , pp. 319-321
    • Koh, S.1    Chen, L.2
  • 4
    • 0030010119 scopus 로고    scopus 로고
    • Neonatal cerebral arterial thrombosis: Protein C deficiency
    • Gould RJ, Black K, Pavlakis SG. Neonatal cerebral arterial thrombosis: protein C deficiency. J Child Neurol 1996; 11: 250-251.
    • (1996) J Child Neurol , vol.11 , pp. 250-251
    • Gould, R.J.1    Black, K.2    Pavlakis, S.G.3
  • 6
    • 0028831847 scopus 로고
    • Cerebral infarction in a young adult associated with protein C deficiency
    • Kato H, Shirahama M, Ohmori K, Sunaga T. Cerebral infarction in a young adult associated with protein C deficiency. Angiology 1995; 46: 169-173.
    • (1995) Angiology , vol.46 , pp. 169-173
    • Kato, H.1    Shirahama, M.2    Ohmori, K.3    Sunaga, T.4
  • 9
    • 0027818498 scopus 로고
    • A case of protein C deficiency associated with cerebral infarction and obstruction of the deep leg and inferior mesenteric veins
    • Tsuda M, Miyazaki M, Takada T, Uda Y, Kuzuhara S. A case of protein C deficiency associated with cerebral infarction and obstruction of the deep leg and inferior mesenteric veins. Jpn J Psych Neurol 1993; 47: 887-892.
    • (1993) Jpn J Psych Neurol , vol.47 , pp. 887-892
    • Tsuda, M.1    Miyazaki, M.2    Takada, T.3    Uda, Y.4    Kuzuhara, S.5
  • 11
    • 0023689806 scopus 로고
    • Transient ischemic attack in a patient with congential protein C deficiency during treatment with stanzolol
    • DeStefano V, Leone G, Teofili L, Ferrelli R, Pollari G, Antonini V, Bizzi B. Transient ischemic attack in a patient with congential protein C deficiency during treatment with stanzolol. Am J Haematol 1988; 29: 120-121.
    • (1988) Am J Haematol , vol.29 , pp. 120-121
    • DeStefano, V.1    Leone, G.2    Teofili, L.3    Ferrelli, R.4    Pollari, G.5    Antonini, V.6    Bizzi, B.7
  • 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: 3698-3703.
    • (1996) Blood , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 13
    • 0030845360 scopus 로고    scopus 로고
    • The 20210A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep vein thrombosis
    • Hillarp A, Zoller B, Svenssen PJ, Dahlback B. The 20210A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep vein thrombosis. Thromb Haemost 1997; 78: 990-992.
    • (1997) Thromb Haemost , vol.78 , pp. 990-992
    • Hillarp, A.1    Zoller, B.2    Svenssen, P.J.3    Dahlback, B.4
  • 14
    • 0030792668 scopus 로고    scopus 로고
    • The prothrombin gene G20210A variant: Prevalence in a UK anticoagulant clinic population
    • Cumming AM, Keeney S, Salden A, Bhavnani M, Shwe KH, Hay CRM. The prothrombin gene G20210A variant: prevalence in a UK anticoagulant clinic population. Br J Haematol 1997; 98: 353-355.
    • (1997) Br J Haematol , vol.98 , pp. 353-355
    • Cumming, A.M.1    Keeney, S.2    Salden, A.3    Bhavnani, M.4    Shwe, K.H.5    Hay, C.R.M.6
  • 17
    • 0032525101 scopus 로고    scopus 로고
    • Prothrombin G20210A mutant genotype is a risk factor for cerebraovascular ischemic disease in young patients
    • DeStefano V, Chiusolo P, Paciaroni K, Casorelli I, Rossi E, Molinari M, et al. Prothrombin G20210A mutant genotype is a risk factor for cerebraovascular ischemic disease in young patients. Blood 1998; 91: 3562-3565.
    • (1998) Blood , vol.91 , pp. 3562-3565
    • DeStefano, V.1    Chiusolo, P.2    Paciaroni, K.3    Casorelli, I.4    Rossi, E.5    Molinari, M.6
  • 18
    • 25044476938 scopus 로고
    • Factor V assay as a functional test for the factor V Leiden/resistance to activated protein C syndrome
    • Arkel YS, Ku DH, Kamiyama M, Pajaro R, Alder H, Marchand A. Factor V assay as a functional test for the factor V Leiden/resistance to activated protein C syndrome [abstract]. Blood 1995; 86 (suppl): 202a.
    • (1995) Blood , vol.86 , Issue.SUPPL.
    • Arkel, Y.S.1    Ku, D.H.2    Kamiyama, M.3    Pajaro, R.4    Alder, H.5    Marchand, A.6
  • 19
    • 3543142333 scopus 로고    scopus 로고
    • A highly specific functional test for factor V Leiden; a modified tissue factor assay for activated protein C resistance
    • Arkel YS, Ku DH, Kamiyama M, Pajaro R, Alder H, Marchand A. A highly specific functional test for factor V Leiden; a modified tissue factor assay for activated protein C resistance. Haemostasis 1997; 27: 290-304.
    • (1997) Haemostasis , vol.27 , pp. 290-304
    • Arkel, Y.S.1    Ku, D.H.2    Kamiyama, M.3    Pajaro, R.4    Alder, H.5    Marchand, A.6
  • 20
    • 0029153954 scopus 로고
    • The polymerase chain reaction with sequence specific primers for the detection of the factor V mutation associated with activated protein C resistance
    • Kirschbaum NE, Foster PA. The polymerase chain reaction with sequence specific primers for the detection of the factor V mutation associated with activated protein C resistance. Thromb Haemost 1995; 74: 874-878.
    • (1995) Thromb Haemost , vol.74 , pp. 874-878
    • Kirschbaum, N.E.1    Foster, P.A.2
  • 21
    • 0025021850 scopus 로고
    • Protein C deficiency and anticardiolipin antibodies in a family with premature stroke
    • Haire W, Newland J. Protein C deficiency and anticardiolipin antibodies in a family with premature stroke. Am J Hematol 1990; 33: 61-63.
    • (1990) Am J Hematol , vol.33 , pp. 61-63
    • Haire, W.1    Newland, J.2
  • 22
    • 0027513602 scopus 로고
    • Childhood stroke associated with protein C or S deficiency and primary antiphospholipid syndrome
    • Devilat M, Toso M, Morales M. Childhood stroke associated with protein C or S deficiency and primary antiphospholipid syndrome. Ped Neurology 1993; 9: 67-70.
    • (1993) Ped Neurology , vol.9 , pp. 67-70
    • Devilat, M.1    Toso, M.2    Morales, M.3
  • 23
    • 0032499024 scopus 로고    scopus 로고
    • Homocysteine and atherothrombosis. Mechanisms of disease
    • Welch GN, Loscalzo J. Homocysteine and atherothrombosis. Mechanisms of disease. N Engl J Med 1998; 338: 1042-1050.
    • (1998) N Engl J Med , vol.338 , pp. 1042-1050
    • Welch, G.N.1    Loscalzo, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.