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Volumn 77, Issue 3, 1997, Pages 444-451

Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism - Results of the Spanish multicentric study on thrombophilia (EMET-Study)

Author keywords

[No Author keywords available]

Indexed keywords

ANTITHROMBIN; HEPARIN COFACTOR II; LUPUS ANTICOAGULANT; PHOSPHOLIPID ANTIBODY; PLASMINOGEN; PROTEIN C; PROTEIN S;

EID: 0030951829     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0038-1655986     Document Type: Article
Times cited : (247)

References (48)
  • 1
    • 0018966649 scopus 로고
    • Incidence of acute deep vein thrombosis in two districts: A phlebographic study
    • Kierkegaard A. Incidence of acute deep vein thrombosis in two districts: a phlebographic study. Acta Chir Scand 1980; 146: 267-9.
    • (1980) Acta Chir Scand , vol.146 , pp. 267-269
    • Kierkegaard, A.1
  • 3
    • 0027076617 scopus 로고
    • Thrombosis in antithrombin-III-deficient persons. Report of a large kindred and literature review
    • Demers C, Ginsberg JS, Hirsh J, Henderson P, Blajchman MA. Thrombosis in antithrombin-III-deficient persons. Report of a large kindred and literature review. Ann Intern Med 1992;116:754-61.
    • (1992) Ann Intern Med , vol.116 , pp. 754-761
    • Demers, C.1    Ginsberg, J.S.2    Hirsh, J.3    Henderson, P.4    Blajchman, M.A.5
  • 4
    • 0028272987 scopus 로고
    • The risk of thromboembolism in asymptomatic patients with protein C and protein S deficiency: A prospective cohort study
    • Pabinger I, Kyrle PA, Heistinger M, Eichinger S, Wittmann E, Lechner K. The risk of thromboembolism in asymptomatic patients with protein C and protein S deficiency: A prospective cohort study. Thromb Haemost 1994; 71: 441-5.
    • (1994) Thromb Haemost , vol.71 , pp. 441-445
    • Pabinger, I.1    Kyrle, P.A.2    Heistinger, M.3    Eichinger, S.4    Wittmann, E.5    Lechner, K.6
  • 6
    • 0027465837 scopus 로고
    • Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect
    • Allart CF, Poort SR, Rosendaal FR, Reitsma PH, Bertina RM, Briët E. Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect. Lancet 1993; 341: 134-8.
    • (1993) Lancet , vol.341 , pp. 134-138
    • Allart, C.F.1    Poort, S.R.2    Rosendaal, F.R.3    Reitsma, P.H.4    Bertina, R.M.5    Briët, E.6
  • 9
    • 0021741550 scopus 로고
    • Familial protein S deficiency is associated with recurrent thrombosis
    • Comp PC, Nixon RR, Cooper MR, Esmon CT. Familial protein S deficiency is associated with recurrent thrombosis. J Clin Invest 1984; 74: 2082-8.
    • (1984) J Clin Invest , vol.74 , pp. 2082-2088
    • Comp, P.C.1    Nixon, R.R.2    Cooper, M.R.3    Esmon, C.T.4
  • 11
    • 0029016883 scopus 로고
    • Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S
    • Zöller B, Berntsdotter A, García de Frutos P, Dahlbäck B. Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S. Blood 1995; 85: 3518-23.
    • (1995) Blood , vol.85 , pp. 3518-3523
    • Zöller, B.1    Berntsdotter, A.2    De García Frutos, P.3    Dahlbäck, B.4
  • 12
    • 0025833619 scopus 로고
    • Protein S and C4b-binding protein: Proteins involved in the regulation of the protein C anticoagulant system
    • Dahlbäck B. Protein S and C4b-binding protein: proteins involved in the regulation of the protein C anticoagulant system. Thromb Haemost 1991; 66:49-61.
    • (1991) Thromb Haemost , vol.66 , pp. 49-61
    • Dahlbäck, B.1
  • 13
    • 0029017118 scopus 로고
    • Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease
    • Zöller B, García de Frutos P, Dahlbäck B. Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease. Blood 1995; 85: 3524-31.
    • (1995) Blood , vol.85 , pp. 3524-3531
    • Zöller, B.1    De García Frutos, P.2    Dahlbäck, B.3
  • 14
    • 0027446268 scopus 로고
    • Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C
    • Dahlbäck B, Carlsson M, Svensson PJ. Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C. Proc Natl Acad Sci USA 1993; 90: 1004-8.
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 1004-1008
    • Dahlbäck, B.1    Carlsson, M.2    Svensson, P.J.3
  • 16
    • 0028959158 scopus 로고
    • Inherited thrombophilia: Resistance to activated protein C as a pathogenic factor of venous thrombosis
    • Dahlbäck B. Inherited thrombophilia: Resistance to activated protein C as a pathogenic factor of venous thrombosis. Blood 1995; 85: 607-14.
    • (1995) Blood , vol.85 , pp. 607-614
    • Dahlbäck, B.1
  • 17
    • 0021995981 scopus 로고
    • Association of hereditary heparin cofactor-II deficiency with thrombosis
    • Tran TH, Marbet GH, Duckert F. Association of hereditary heparin cofactor-II deficiency with thrombosis. Lancet 1985; 2:413-4.
    • (1985) Lancet , vol.2 , pp. 413-414
    • Tran, T.H.1    Marbet, G.H.2    Duckert, F.3
  • 18
    • 0021995982 scopus 로고
    • Constitutional heparin cofactor-II deficiency associated with recurrent thrombosis
    • Sié P, Dupouy D, Pichon J, Boneu B. Constitutional heparin cofactor-II deficiency associated with recurrent thrombosis. Lancet 1985; 2: 414-6.
    • (1985) Lancet , vol.2 , pp. 414-416
    • Sié, P.1    Dupouy, D.2    Pichon, J.3    Boneu, B.4
  • 19
    • 0017807269 scopus 로고
    • Abnormal plasminogen, a hereditary molecular abnormality found in a patient with recurrent thrombosis
    • Aoki N, Moroi M, Sakata Y, Yoshida N. Abnormal plasminogen, a hereditary molecular abnormality found in a patient with recurrent thrombosis. J Clin Invest 1978; 61: 1186-95.
    • (1978) J Clin Invest , vol.61 , pp. 1186-1195
    • Aoki, N.1    Moroi, M.2    Sakata, Y.3    Yoshida, N.4
  • 20
    • 0022538164 scopus 로고
    • Investigation of a congenital abnormal plasminogen, Frankfurt I, and its relationship with thrombosis
    • Scharrer IM, Wohl RC, Hach V, Sinio L, Boreisha I, Robbins KC. Investigation of a congenital abnormal plasminogen, Frankfurt I, and its relationship with thrombosis. Thromb Haemost 1986; 55: 396-401.
    • (1986) Thromb Haemost , vol.55 , pp. 396-401
    • Scharrer, I.M.1    Wohl, R.C.2    Hach, V.3    Sinio, L.4    Boreisha, I.5    Robbins, K.C.6
  • 21
    • 0022396322 scopus 로고
    • Hereditary dysfibrinogenemia
    • Bithell TC. Hereditary dysfibrinogenemia.Clin Chem 1985;31:509-16.
    • (1985) Clin Chem , vol.31 , pp. 509-516
    • Bithell, T.C.1
  • 23
    • 0029146539 scopus 로고
    • Protean clinical presentation of antiphospholipid-protein antibodies
    • Triplett DA. Protean clinical presentation of antiphospholipid-protein antibodies. Thromb Haemost 1995; 74: 329-37.
    • (1995) Thromb Haemost , vol.74 , pp. 329-337
    • Triplett, D.A.1
  • 25
    • 0023818347 scopus 로고
    • The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis
    • Gladson CL, Scharrer I, Hach V, Beck KH, Griffin JH. The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis. Thromb Haemost 1988; 59: 18-22.
    • (1988) Thromb Haemost , vol.59 , pp. 18-22
    • Gladson, C.L.1    Scharrer, I.2    Hach, V.3    Beck, K.H.4    Griffin, J.H.5
  • 26
    • 0024563172 scopus 로고
    • The relative frequency of hereditary thrombotic disorders among 107 patients with thrombophilia in Israel
    • Ben-Tal O, Zivelin A, Seligsohn U. The relative frequency of hereditary thrombotic disorders among 107 patients with thrombophilia in Israel. Thromb Haemost 1990; 61: 50-4.
    • (1990) Thromb Haemost , vol.61 , pp. 50-54
    • Ben-Tal, O.1    Zivelin, A.2    Seligsohn, U.3
  • 27
    • 0024441258 scopus 로고
    • Elevated plasminogen activator inhibitor (PAI), a cause of thrombophilia?. a study in 203 patients with familial or sporadic thrombophilia
    • Engesser L, Brommer EJP, Kluft C, Briët E. Elevated plasminogen activator inhibitor (PAI), a cause of thrombophilia?. A study in 203 patients with familial or sporadic thrombophilia. Thromb Haemost 1989; 62: 673-80.
    • (1989) Thromb Haemost , vol.62 , pp. 673-680
    • Engesser, L.1    Brommer, E.J.P.2    Kluft, C.3    Briët, E.4
  • 28
    • 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 LW. 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, L.W.5
  • 30
    • 0026749276 scopus 로고
    • Deep vein thrombosis: Prevalence of etiologic factors and results of management in 100 consecutive patients
    • Bick RL, Jakway J, Baker WF. Deep vein thrombosis: prevalence of etiologic factors and results of management in 100 consecutive patients. Sem Thromb Hemost 1992; 18: 267-74.
    • (1992) Sem Thromb Hemost , vol.18 , pp. 267-274
    • Bick, R.L.1    Jakway, J.2    Baker, W.F.3
  • 32
    • 0026695880 scopus 로고
    • Thromboembolic disease. Critical evaluation of laboratory investigation
    • Malm J, Laurell M, Nilsson IM, Dahlbäck B. Thromboembolic disease. Critical evaluation of laboratory investigation. Thromb Haemost 1992; 68: 2-13.
    • (1992) Thromb Haemost , vol.68 , pp. 2-13
    • Malm, J.1    Laurell, M.2    Nilsson, I.M.3    Dahlbäck, B.4
  • 33
    • 0026465569 scopus 로고
    • Hereditary deficiency of antithrombin III, protein C and protein S: Prevalence in patients with a history of venous thrombosis and criteria for rational patient screening
    • Pabinger I, Brücker S, Kyrie PA, Schneider B, Korninger HC, Niessner H, Lechner K. Hereditary deficiency of antithrombin III, protein C and protein S: prevalence in patients with a history of venous thrombosis and criteria for rational patient screening. Blood Coagul Fibrinol 1992;3:547-53.
    • (1992) Blood Coagul Fibrinol , vol.3 , pp. 547-553
    • Pabinger, I.1    Brücker, S.2    Kyrie, P.A.3    Schneider, B.4    Korninger, H.C.5    Niessner, H.6    Lechner, K.7
  • 34
    • 0022636454 scopus 로고
    • An abnormal plasma distribution of protein S occurs in functional protein S deficiency
    • Comp PC, Doray D, Patton D, Esmon CT. An abnormal plasma distribution of protein S occurs in functional protein S deficiency. Blood 1986; 67: 504-8.
    • (1986) Blood , vol.67 , pp. 504-508
    • Comp, P.C.1    Doray, D.2    Patton, D.3    Esmon, C.T.4
  • 35
    • 0028098080 scopus 로고
    • The influence of low protein S plasma levels in young women, on the definition of normal range
    • Garí M, Falkon L, UrrutiaT, Vallvé C, Borrell M, Fontcuberta J. The influence of low protein S plasma levels in young women, on the definition of normal range. Thromb Res 1994; 73: 149-52.
    • (1994) Thromb Res , vol.73 , pp. 149-152
    • Garí, M.1    Falkon, L.2    Urrutia, T.3    Vallvé, C.4    Borrell, M.5    Fontcuberta, J.6
  • 36
    • 33745551242 scopus 로고
    • Gerinnungsphysiologische Schenellmethode zur Bestimmung des Fibrinogens
    • Clauss A. Gerinnungsphysiologische Schenellmethode zur Bestimmung des Fibrinogens. Acta Haematol 1957; 17: 237-46.
    • (1957) Acta Haematol , vol.17 , pp. 237-246
    • Clauss, A.1
  • 37
    • 0018135382 scopus 로고
    • A sensitive test demonstrating lupus anticoagulant and its behavioural patterns
    • Exner T, Rickard KA, Kronenberg H. A sensitive test demonstrating lupus anticoagulant and its behavioural patterns. Br J Haematol 1978; 40: 143-51.
    • (1978) Br J Haematol , vol.40 , pp. 143-151
    • Exner, T.1    Rickard, K.A.2    Kronenberg, H.3
  • 38
    • 0023121840 scopus 로고
    • Anticardiolipin antibodies: Isotype distribution and phospholipid specificity
    • Gharavi AE, Harris EN, Asherson RA, Hughes GRV. Anticardiolipin antibodies: isotype distribution and phospholipid specificity. Ann Rheum Dis 1987; 46: 1-6.
    • (1987) Ann Rheum Dis , vol.46 , pp. 1-6
    • Gharavi, A.E.1    Harris, E.N.2    Asherson, R.A.3    Hughes, G.R.V.4
  • 40
    • 0023233223 scopus 로고
    • Absence of thrombosis in subjects with heterozygous protein C deficiency
    • Miletich J, Sherman L, Broze G. Absence of thrombosis in subjects with heterozygous protein C deficiency. N Engl J Med 1987; 317: 991-6.
    • (1987) N Engl J Med , vol.317 , pp. 991-996
    • Miletich, J.1    Sherman, L.2    Broze, G.3
  • 41
    • 0023644095 scopus 로고
    • Fibrinogen and risk of cardiovascular disease; the Framingham Study
    • Kannel WB, Wolf PA, Castelli WP, D'Agostino RB. Fibrinogen and risk of cardiovascular disease; the Framingham Study. JAMA 1987; 258: 1183-6.
    • (1987) JAMA , vol.258 , pp. 1183-1186
    • Kannel, W.B.1    Wolf, P.A.2    Castelli, W.P.3    D'Agostino, R.B.4
  • 42
    • 0028342850 scopus 로고
    • Factor VII and fibrinogen levels as risk factors for venous thrombosis. a case-control study of plasma levels and DNA polymorphisms. the Leiden Thrombophilia Study
    • Koster T, Rosendaal FR, Reitsma PH, van der Velden PA, Briët E, Vandenbroucke JP. Factor VII and fibrinogen levels as risk factors for venous thrombosis. A case-control study of plasma levels and DNA polymorphisms. The Leiden Thrombophilia Study. Thromb Haemost 1994; 71: 719-22.
    • (1994) Thromb Haemost , vol.71 , pp. 719-722
    • Koster, T.1    Rosendaal, F.R.2    Reitsma, P.H.3    Van Der Velden, P.A.4    Briët, E.5    Vandenbroucke, J.P.6
  • 43
    • 0027930963 scopus 로고
    • Prevalence, follow-up and clinical significance of the anticardiolipin antibodies in normal subjects
    • Vila P, Hernández MC, López-Fernández MF, Batlle J. Prevalence, follow-up and clinical significance of the anticardiolipin antibodies in normal subjects. Thromb Haemost 1994;72:209-13.
    • (1994) Thromb Haemost , vol.72 , pp. 209-213
    • Vila, P.1    Hernández, M.C.2    López-Fernández, M.F.3    Batlle, J.4
  • 44
    • 0028120405 scopus 로고
    • Differences in protein S and C4b-binding protein levels in different groups of patients with antiphospholipid antibodies
    • Forastiero RR, Kordich L, Basilotta, Carreras LO. Differences in protein S and C4b-binding protein levels in different groups of patients with antiphospholipid antibodies. Blood Coagul Fibrinol 1994; 5: 609-16.
    • (1994) Blood Coagul Fibrinol , vol.5 , pp. 609-616
    • Forastiero, R.R.1    Kordich, L.2    Basilotta3    Carreras, L.O.4
  • 45
    • 84920292673 scopus 로고
    • The prevalence of antiphospholipid antibodies in women with recurrent spontaneous abortion, women with successful pregnancies, and women who have never been pregnant
    • Parke AL, Wilson D, Maier D. The prevalence of antiphospholipid antibodies in women with recurrent spontaneous abortion, women with successful pregnancies, and women who have never been pregnant. Arthritis Rheum 1987;30:601-6.
    • (1987) Arthritis Rheum , vol.30 , pp. 601-606
    • Parke, A.L.1    Wilson, D.2    Maier, D.3
  • 48
    • 0028765167 scopus 로고
    • Bad blood by mutation
    • Majerus PW. Bad blood by mutation. Nature 1994; 369: 14-5.
    • (1994) Nature , vol.369 , pp. 14-15
    • Majerus, P.W.1


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