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Volumn 80, Issue 1, 1998, Pages 167-170

Is plasminogen deficiency a thrombotic risk factor? - A study on 23 thrombophilic patients and their family members

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATED PROTEIN C; PLASMINOGEN;

EID: 0031878998     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1615157     Document Type: Article
Times cited : (44)

References (26)
  • 2
    • 0024334483 scopus 로고
    • Clinical disorders of fibrinolysis: A critical review
    • Francis RB Jr. Clinical disorders of fibrinolysis: a critical review. Blut 1989; 9: 1-14.
    • (1989) Blut , vol.9 , pp. 1-14
    • Francis Jr., R.B.1
  • 3
    • 0021889294 scopus 로고
    • Two different mechanisms in patients with venous thrombosis and defective fibrinolysis: Low concentration of plasminogen activator or increased concentration of plasminogen activator inhibitor
    • Nilsson IM, Ljungner H, Tengborn L. Two different mechanisms in patients with venous thrombosis and defective fibrinolysis: Low concentration of plasminogen activator or increased concentration of plasminogen activator inhibitor. Br Med J 1985; 290: 1453-5.
    • (1985) Br Med J , vol.290 , pp. 1453-1455
    • Nilsson, I.M.1    Ljungner, H.2    Tengborn, L.3
  • 4
    • 1842389053 scopus 로고
    • Plasminogen levels and putative prevalence of deficiency in 400 blood donors
    • Abstr
    • Tait RC, Walker ID, Islam SIA, Mitchell R, Davidson JF. Plasminogen levels and putative prevalence of deficiency in 400 blood donors. Br J Haematol 1991; 77 (S 1): 10 (Abstr).
    • (1991) Br J Haematol , vol.77 , Issue.S 1 , pp. 10
    • Tait, R.C.1    Walker, I.D.2    Islam, S.I.A.3    Mitchell, R.4    Davidson, J.F.5
  • 5
    • 2642596671 scopus 로고
    • Incidence of protein C deficiency in 132 juvenile thrombosis patients in comparison with other inherited fibrinolysis disorders
    • Abstr
    • Beck KH, Walter-Fincke R, Hach V, Scharrer I. Incidence of protein C deficiency in 132 juvenile thrombosis patients in comparison with other inherited fibrinolysis disorders. Thromb Haemost 1985; 54: 142 (Abstr).
    • (1985) Thromb Haemost , vol.54 , pp. 142
    • Beck, K.H.1    Walter-Fincke, R.2    Hach, V.3    Scharrer, I.4
  • 6
    • 0025241268 scopus 로고
    • Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep vein thrombosis
    • Heijboer H, Brandjes DPM. Büller HR, Sturk A, ten Cate JW. Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep vein thrombosis. N Engl J Med 1990; 323: 1512-6.
    • (1990) N Engl J Med , vol.323 , pp. 1512-1516
    • Heijboer, H.1    Brandjes, D.P.M.2    Büller, H.R.3    Sturk, A.4    Ten Cate, J.W.5
  • 7
    • 0009568096 scopus 로고
    • Thrombotic disease in three families with inherited plasminogen deficiency
    • Abstr
    • Hasegawa DK, Tyler BJ, Edson JR. Thrombotic disease in three families with inherited plasminogen deficiency. Blood (S 1) 1982; 60: 213a (Abstr).
    • (1982) Blood , vol.60 , Issue.S 1
    • Hasegawa, D.K.1    Tyler, B.J.2    Edson, J.R.3
  • 10
    • 0022472282 scopus 로고
    • Congenital heterozygous plasminogen deficiency associated with a severe thrombotic tendency
    • Girolami A, Marafioti F, Rubertelli M, Cappellato MG. Congenital heterozygous plasminogen deficiency associated with a severe thrombotic tendency. Acta haemat 1986; 75: 54-7.
    • (1986) Acta Haemat , vol.75 , pp. 54-57
    • Girolami, A.1    Marafioti, F.2    Rubertelli, M.3    Cappellato, M.G.4
  • 11
    • 0028556774 scopus 로고
    • Heterozygous type I plasminogen deficiency is associated with an increased risk for thrombosis: A statistical analysis in 20 kindreds
    • Sartori MT, Patrassi GM, Theodoridis P, Perin A, Pietrogrande F, Girolami A. Heterozygous type I plasminogen deficiency is associated with an increased risk for thrombosis: a statistical analysis in 20 kindreds. Blood Coag Fibrinol 1994; 5: 889-93.
    • (1994) Blood Coag Fibrinol , vol.5 , pp. 889-893
    • Sartori, M.T.1    Patrassi, G.M.2    Theodoridis, P.3    Perin, A.4    Pietrogrande, F.5    Girolami, A.6
  • 12
  • 13
    • 0024246493 scopus 로고
    • Thrombovascular disease and familial plasminogen deficiency: A report of three kindreds
    • Dolan G, Greaves M, Cooper P, Preston FE. Thrombovascular disease and familial plasminogen deficiency: a report of three kindreds. Br J Haematol 1988; 70: 417-421.
    • (1988) Br J Haematol , vol.70 , pp. 417-421
    • Dolan, G.1    Greaves, M.2    Cooper, P.3    Preston, F.E.4
  • 14
    • 0023880716 scopus 로고
    • Congenital deficiency of plasminogen and its relationship to venous thrombosis
    • Hach-Wunderle V, Scharrer I, Lottenberg R. Congenital deficiency of plasminogen and its relationship to venous thrombosis. Thromb Haemost 1988; 59: 277-80.
    • (1988) Thromb Haemost , vol.59 , pp. 277-280
    • Hach-Wunderle, V.1    Scharrer, I.2    Lottenberg, R.3
  • 16
    • 0030456454 scopus 로고    scopus 로고
    • Isolated familial plasminogen deficiency may not be a risk factor for thrombosis
    • Tait RC, Walker ID, Conkie JA, Islam IAM, McCall F. Isolated familial plasminogen deficiency may not be a risk factor for thrombosis. Thromb Haemost 1996; 76: 1004-8.
    • (1996) Thromb Haemost , vol.76 , pp. 1004-1008
    • Tait, R.C.1    Walker, I.D.2    Conkie, J.A.3    Islam, I.A.M.4    McCall, F.5
  • 17
    • 0030739571 scopus 로고    scopus 로고
    • Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis
    • Schuster V, Mingers A-M, Seidenspinner S, Nüssgens Z, Pukrop T, Kreth HW. Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis. Blood 1997; 90: 958-66.
    • (1997) Blood , vol.90 , pp. 958-966
    • Schuster, V.1    Mingers, A.-M.2    Seidenspinner, S.3    Nüssgens, Z.4    Pukrop, T.5    Kreth, H.W.6
  • 20
    • 0029837881 scopus 로고    scopus 로고
    • The VITA Project: Population based distributions of protein C, antithrombin III, heparin-cofactor II and plasminogen - Relationship with physiological variables and establishment of reference ranges
    • Rodeghiero F, Tosetto A. The VITA Project: Population based distributions of protein C, antithrombin III, heparin-cofactor II and plasminogen - relationship with physiological variables and establishment of reference ranges. Thromb Haemost 1996; 76: 226-33.
    • (1996) Thromb Haemost , vol.76 , pp. 226-233
    • Rodeghiero, F.1    Tosetto, A.2
  • 21
    • 0027081621 scopus 로고
    • Thrombophilieabklärung: Indikation und Durchführung
    • Demarmels Biasiutti F, Lämmle B. Thrombophilieabklärung: Indikation und Durchführung. Ther Umschau 1992; 49: 850-8.
    • (1992) Ther Umschau , vol.49 , pp. 850-858
    • Demarmels Biasiutti, F.1    Lämmle, B.2
  • 22
    • 0023932304 scopus 로고
    • Familial plasminogen deficiency and thromboembolism
    • Dolan G, Preston FE. Familial plasminogen deficiency and thromboembolism. Fibrinolysis 1988; 2 (S2): 26-34.
    • (1988) Fibrinolysis , vol.2 , Issue.S2 , pp. 26-34
    • Dolan, G.1    Preston, F.E.2
  • 24
    • 0028037137 scopus 로고
    • Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C
    • Zöller B, Svensson PJ, He X, Dahlbäck B. Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C. J Clin Invest 1994; 94: 2521-4.
    • (1994) J Clin Invest , vol.94 , pp. 2521-2524
    • Zöller, B.1    Svensson, P.J.2    He, X.3    Dahlbäck, B.4
  • 25
    • 0029864822 scopus 로고    scopus 로고
    • Resistance to activated protein C, the FV: Q506 allele, and venous thrombosis
    • Dahlbäck B, Hillarp A, Rosen S, Zöller B. Resistance to activated protein C, the FV: Q506 allele, and venous thrombosis. Ann Hematol 1996; 72: 166-76.
    • (1996) Ann Hematol , vol.72 , pp. 166-176
    • Dahlbäck, B.1    Hillarp, A.2    Rosen, S.3    Zöller, B.4
  • 26
    • 0029845099 scopus 로고    scopus 로고
    • Plasminogen deficiency: An additional risk factor for thrombosis in a family with factor VR506Q mutation?
    • Züger M, Demarmels Biasiutti F, Furlan M, Mannhalter Ch, Lämmle B. Plasminogen deficiency: An additional risk factor for thrombosis in a family with factor VR506Q mutation? Thromb Haemost 1996; 76: 475-6.
    • (1996) Thromb Haemost , vol.76 , pp. 475-476
    • Züger, M.1    Demarmels Biasiutti, F.2    Furlan, M.3    Mannhalter, Ch.4    Lämmle, B.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.