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Volumn 90, Issue 1, 2003, Pages 17-26

Risk of venous thromboembolism in relatives of symptomatic probands with thrombophilia: A systematic review

Author keywords

Genetics; Risk factors; Systematic review; Thrombophilia; Thrombosis

Indexed keywords

ANTICOAGULANT AGENT; BLOOD CLOTTING FACTOR 5 LEIDEN;

EID: 0037623698     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1613594     Document Type: Review
Times cited : (57)

References (62)
  • 2
    • 0035806950 scopus 로고    scopus 로고
    • The thrombophilias: Well-defined risk factors with uncertain therapeutic implications
    • Bauer KA. The thrombophilias: Well-defined risk factors with uncertain therapeutic implications. Ann Intern Med 2001; 135(5): 367-73.
    • (2001) Ann Intern Med , vol.135 , Issue.5 , pp. 367-373
    • Bauer, K.A.1
  • 3
    • 0031765181 scopus 로고    scopus 로고
    • Inherited thrombophilia and pregnancy: The obstetric perspective
    • Bonnar J, Green R, Norris L. Inherited thrombophilia and pregnancy: The obstetric perspective. Semin Thromb Hemost 1998; 24(suppl 1): 49-53.
    • (1998) Semin Thromb Hemost , vol.24 , Issue.SUPPL. 1 , pp. 49-53
    • Bonnar, J.1    Green, R.2    Norris, L.3
  • 4
    • 0032767244 scopus 로고    scopus 로고
    • Thrombophilic polymorphisms are common in women with fetal loss without apparent cause
    • Brenner B, Sarig G, Weiner Z, et al. Thrombophilic polymorphisms are common in women with fetal loss without apparent cause. Thromb Haemost 1999; 82: 6-9.
    • (1999) Thromb Haemost , vol.82 , pp. 6-9
    • Brenner, B.1    Sarig, G.2    Weiner, Z.3
  • 5
    • 0005517354 scopus 로고    scopus 로고
    • Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecendent
    • Gris J-C, Quere I, Monpeyroux F, et al. Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecendent. Thromb Haemost 1999; 81: 891-9.
    • (1999) Thromb Haemost , vol.81 , pp. 891-899
    • Gris, J.-C.1    Quere, I.2    Monpeyroux, F.3
  • 7
    • 0035912152 scopus 로고    scopus 로고
    • Genetic susceptibility to venous thrombosis
    • Seligsohn U, Lubetsky A. Genetic susceptibility to venous thrombosis. N Engl J Med 2001; 344(16): 1222-31.
    • (2001) N Engl J Med , vol.344 , Issue.16 , pp. 1222-1231
    • Seligsohn, U.1    Lubetsky, A.2
  • 8
    • 0035412353 scopus 로고    scopus 로고
    • Genetic hypercoagulability: Screening should be an informed choice
    • Green D. Genetic hypercoagulability: Screening should be an informed choice. Blood 2001; 98(1): 20.
    • (2001) Blood , vol.98 , Issue.1 , pp. 20
    • Green, D.1
  • 9
    • 0035412379 scopus 로고    scopus 로고
    • Genetic hypercoagulability: Prevention suggests testing family members
    • Mannucci PM. Genetic hypercoagulability: Prevention suggests testing family members. Blood 2001; 98(1): 21-2.
    • (2001) Blood , vol.98 , Issue.1 , pp. 21-22
    • Mannucci, P.M.1
  • 11
    • 0034791001 scopus 로고    scopus 로고
    • Investigation and management of heritable thrombophilia
    • Walker ID, Greaves M, Preston FE. Investigation and management of heritable thrombophilia. Br J Haematol 2001; 114: 512-28.
    • (2001) Br J Haematol , vol.114 , pp. 512-528
    • Walker, I.D.1    Greaves, M.2    Preston, F.E.3
  • 12
    • 0034100330 scopus 로고    scopus 로고
    • Management of patients with hereditary hypercoagulable disorders
    • Kearon C, Crowther M, Hirsh J. Management of patients with hereditary hypercoagulable disorders. Annu Rev Med 2000; 51: 169-85.
    • (2000) Annu Rev Med , vol.51 , pp. 169-185
    • Kearon, C.1    Crowther, M.2    Hirsh, J.3
  • 13
    • 0030053275 scopus 로고
    • Guidelines for the management of thrombophilia
    • Cavenagh JD, Colvin BT. Guidelines for the management of thrombophilia. Postgrad Med J 1995; 72(844): 87-94.
    • (1995) Postgrad Med J , vol.72 , Issue.844 , pp. 87-94
    • Cavenagh, J.D.1    Colvin, B.T.2
  • 14
    • 0030929276 scopus 로고    scopus 로고
    • Familial thrombophilia: Genetic risk factors and management
    • Makris M, Rosenthal FR, Preston FE. Familial thrombophilia: Genetic risk factors and management. J Intern Med 1997; 242(Suppl 740): 9-15.
    • (1997) J Intern Med , vol.242 , Issue.SUPPL. 740 , pp. 9-15
    • Makris, M.1    Rosenthal, F.R.2    Preston, F.E.3
  • 15
    • 0029876985 scopus 로고    scopus 로고
    • Inherited thrombophilia: Pathogenesis, clinical syndromes, and management
    • De Stefano V, Finazzi G, Mannucci PM. Inherited thrombophilia: Pathogenesis, clinical syndromes, and management. Blood 1996; 87(9): 3531-44.
    • (1996) Blood , vol.87 , Issue.9 , pp. 3531-3544
    • De Stefano, V.1    Finazzi, G.2    Mannucci, P.M.3
  • 16
    • 0034461758 scopus 로고    scopus 로고
    • Aspects of the clinical management of hereditary thrombophilia: A personal perspective
    • Mannucci PM. Aspects of the clinical management of hereditary thrombophilia: A personal perspective. Haemostasis 2000; 30(Suppl 2): 11-15.
    • (2000) Haemostasis , vol.30 , Issue.SUPPL. 2 , pp. 11-15
    • Mannucci, P.M.1
  • 18
    • 0034665430 scopus 로고    scopus 로고
    • Evaluation of the hypercoagulable state. Whom to screen, how to test and treat
    • Barger AP, Hurley R. Evaluation of the hypercoagulable state. Whom to screen, how to test and treat. Postgrad Med 2000; 108(4): 59-66.
    • (2000) Postgrad Med , vol.108 , Issue.4 , pp. 59-66
    • Barger, A.P.1    Hurley, R.2
  • 19
    • 0344678336 scopus 로고    scopus 로고
    • Thrombophilia as a multigenic disease
    • Zoller B, Garcia DF, Hillarp A, et al. Thrombophilia as a multigenic disease. Haematologica 1999; 84(1): 59-70.
    • (1999) Haematologica , vol.84 , Issue.1 , pp. 59-70
    • Zoller, B.1    Garcia, D.F.2    Hillarp, A.3
  • 20
    • 0032910075 scopus 로고    scopus 로고
    • The investigation and management of inherited thrombophilia
    • Cumming AM, Shiach CR. The investigation and management of inherited thrombophilia. Clin Lab Haematol 1999; 21(2): 77-92.
    • (1999) Clin Lab Haematol , vol.21 , Issue.2 , pp. 77-92
    • Cumming, A.M.1    Shiach, C.R.2
  • 21
    • 0031764835 scopus 로고    scopus 로고
    • Inherited thrombophilic states
    • Rao AK, Kaplan R, Sheth S. Inherited thrombophilic states. Semin Thromb Hemost 1998; 24(Suppl 1): 3-12.
    • (1998) Semin Thromb Hemost , vol.24 , Issue.SUPPL. 1 , pp. 3-12
    • Rao, A.K.1    Kaplan, R.2    Sheth, S.3
  • 23
    • 0034685429 scopus 로고    scopus 로고
    • Meta-analysis of observational studies in epidemiology: A proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group
    • Stroup DF, Berlin JA, Morton SC, et al. Meta-analysis of observational studies in epidemiology: A proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group. JAMA 2000; 283(15): 2008-12.
    • (2000) JAMA , vol.283 , Issue.15 , pp. 2008-2012
    • Stroup, D.F.1    Berlin, J.A.2    Morton, S.C.3
  • 24
    • 0028861454 scopus 로고
    • Best evidence synthesis: An intelligent alternative to meta-analysis
    • Slavin RE. Best evidence synthesis: An intelligent alternative to meta-analysis. J Clin Epidemiol 1995; 48(1): 9-18.
    • (1995) J Clin Epidemiol , vol.48 , Issue.1 , pp. 9-18
    • Slavin, R.E.1
  • 25
    • 0035806996 scopus 로고    scopus 로고
    • A prospective study of asymptomatic carriers of the factor V leiden mutation to determine the incidence of venous thromboembolism
    • Middeldorp S, Meinardi JR, Koopman MMW, et al. A prospective study of asymptomatic carriers of the factor V leiden mutation to determine the incidence of venous thromboembolism. Ann Intern Med 2001; 135(5): 322-7.
    • (2001) Ann Intern Med , vol.135 , Issue.5 , pp. 322-327
    • Middeldorp, S.1    Meinardi, J.R.2    Koopman, M.M.W.3
  • 26
    • 0037085791 scopus 로고    scopus 로고
    • Incidence of venous thromboembolism in asymptomatic family members who are carriers of factor V Leiden: A prospective cohort study
    • Simioni P, Tormene D, Prandoni P, et al. Incidence of venous thromboembolism in asymptomatic family members who are carriers of factor V Leiden: A prospective cohort study. Blood 2002; 99(6): 1938-42.
    • (2002) Blood , vol.99 , Issue.6 , pp. 1938-1942
    • Simioni, P.1    Tormene, D.2    Prandoni, P.3
  • 27
    • 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, et al. The risk of thromboembolism in asymptomatic patients with Protein C and Protein S deficiency: A prospective cohort study. Thromb Haemost 1994; 71(4): 441-5.
    • (1994) Thromb Haemost , vol.71 , Issue.4 , pp. 441-445
    • Pabinger, I.1    Kyrle, P.A.2    Heistinger, M.3
  • 28
    • 0033485887 scopus 로고    scopus 로고
    • The incidence of venous thromboembolism in asymptomatic carriers of a deficiency of antithrombin, Protein C or Protein S: A prospective cohort study
    • Sanson BJ, Simioni P, Tormene D, et al. The incidence of venous thromboembolism in asymptomatic carriers of a deficiency of antithrombin, Protein C or Protein S: A prospective cohort study. Blood 1999; 94(11): 3702-6.
    • (1999) Blood , vol.94 , Issue.11 , pp. 3702-3706
    • Sanson, B.J.1    Simioni, P.2    Tormene, D.3
  • 29
    • 0000662461 scopus 로고    scopus 로고
    • Incidence of venous thromboembolism in families with inherited thrombophilia
    • Simioni P, Sanson BJ, Prandoni P, et al. Incidence of venous thromboembolism in families with inherited thrombophilia. Thromb Haemost 1999; 81(2): 198-202.
    • (1999) Thromb Haemost , vol.81 , Issue.2 , pp. 198-202
    • Simioni, P.1    Sanson, B.J.2    Prandoni, P.3
  • 30
    • 0032892955 scopus 로고    scopus 로고
    • Risk of venous thromboembolism and clinical manifestations in carriers of antithrombin, protein C, protein S deficiency, or activated protein C resistance: A multicenter collaborative family study
    • Bucciarelli P, Rosendaal FR, Tripodi A, et al. Risk of venous thromboembolism and clinical manifestations in carriers of antithrombin, protein C, protein S deficiency, or activated protein C resistance: A multicenter collaborative family study. Arterioscler Thromb Vasc Biol 1999; 19(4): 1026-33.
    • (1999) Arterioscler Thromb Vasc Biol , vol.19 , Issue.4 , pp. 1026-1033
    • Bucciarelli, P.1    Rosendaal, F.R.2    Tripodi, A.3
  • 31
    • 0033230321 scopus 로고    scopus 로고
    • Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden)
    • Faioni EM, Franchi F, Bucciarelli P, et al. Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden). Blood 1999; 94(9): 3062-6.
    • (1999) Blood , vol.94 , Issue.9 , pp. 3062-3066
    • Faioni, E.M.1    Franchi, F.2    Bucciarelli, P.3
  • 32
    • 0034887216 scopus 로고    scopus 로고
    • High factor VIII levels contribute to the thrombotic risk in families with factor V Leiden
    • Lensen R, Bertina RM, Vandenbroucke JP, et al. High factor VIII levels contribute to the thrombotic risk in families with Factor V Leiden. Br J Haematol 2001; 114(2): 380-6.
    • (2001) Br J Haematol , vol.114 , Issue.2 , pp. 380-386
    • Lensen, R.1    Bertina, R.M.2    Vandenbroucke, J.P.3
  • 33
    • 0031985328 scopus 로고    scopus 로고
    • The incidence of venous thromboembolism in family members of patients with Factor V Leiden mutation and venous thrombosis
    • Middeldorp S, Koopman MMW, Van Pampus ECM, et al. The incidence of venous thromboembolism in family members of patients with Factor V Leiden mutation and venous thrombosis. Ann Intern Med 1998; 128(1): 15-20.
    • (1998) Ann Intern Med , vol.128 , Issue.1 , pp. 15-20
    • Middeldorp, S.1    Koopman, M.M.W.2    Van Pampus, E.C.M.3
  • 34
    • 0032816611 scopus 로고    scopus 로고
    • Pseudohomozygosity for activated protein C resistance is a risk factor for venous thrombosis
    • Castaman G, Tosetto A, Ruggeri M, et al. Pseudohomozygosity for activated protein C resistance is a risk factor for venous thrombosis. Br J Haematol 1999; 106(1): 232-6.
    • (1999) Br J Haematol , vol.106 , Issue.1 , pp. 232-236
    • Castaman, G.1    Tosetto, A.2    Ruggeri, M.3
  • 35
    • 0028000665 scopus 로고
    • Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
    • Koeleman BP, Reitsma PH, Allaart CF, et al. Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families. Blood 1994; 84(4): 1031-5.
    • (1994) Blood , vol.84 , Issue.4 , pp. 1031-1035
    • Koeleman, B.P.1    Reitsma, P.H.2    Allaart, C.F.3
  • 36
    • 0029022118 scopus 로고
    • Factor V Leiden: An additional risk factor for thrombosis in protein S deficient families?
    • Koeleman BP, Van Rumpt D, Hamulyak K, et al. Factor V Leiden: An additional risk factor for thrombosis in protein S deficient families? Thromb Haemost 1995; 74(2): 580-3.
    • (1995) Thromb Haemost , vol.74 , Issue.2 , pp. 580-583
    • Koeleman, B.P.1    Van Rumpt, D.2    Hamulyak, K.3
  • 37
    • 0033760132 scopus 로고    scopus 로고
    • Factor V Leiden: The venous thrombotic risk in thrombophilic families
    • Lensen R, Rosendaal F, Vandenbroucke J, et al. Factor V Leiden: The venous thrombotic risk in thrombophilic families. Br J Haematol 2000; 110(4): 939-45.
    • (2000) Br J Haematol , vol.110 , Issue.4 , pp. 939-945
    • Lensen, R.1    Rosendaal, F.2    Vandenbroucke, J.3
  • 38
    • 0035196953 scopus 로고    scopus 로고
    • Impact of the factor II: G20210A variant on the risk of venous thromboembolism in relatives from families with the factor V: R506Q mutation
    • Rintelen C, Pabinger I, Bettelheim P, et al. Impact of the factor II: G20210A variant on the risk of venous thromboembolism in relatives from families with the factor V: R506Q mutation. Eur J Haematol 2001; 67(3): 165-9.
    • (2001) Eur J Haematol , vol.67 , Issue.3 , pp. 165-169
    • Rintelen, C.1    Pabinger, I.2    Bettelheim, P.3
  • 39
    • 0035142673 scopus 로고    scopus 로고
    • Familial clustering of high factor VIII levels in patients with venous thromboembolism
    • Schambeck CM, Hinney K, Haubitz I, et al. Familial clustering of high factor VIII levels in patients with venous thromboembolism. Arterioscler Thromb Vasc Biol 2001; 21(2): 289-92.
    • (2001) Arterioscler Thromb Vasc Biol , vol.21 , Issue.2 , pp. 289-292
    • Schambeck, C.M.1    Hinney, K.2    Haubitz, I.3
  • 40
    • 0032829036 scopus 로고    scopus 로고
    • Gene-gene and gene-environment interactions determine risk of thrombosis in families with inherited antithrombin deficiency
    • Van Boven HH, Vandenbroucke JP, Briet E, et al. Gene-gene and gene-environment interactions determine risk of thrombosis in families with inherited antithrombin deficiency. Blood 1999; 94(8): 2590-4.
    • (1999) Blood , vol.94 , Issue.8 , pp. 2590-2594
    • Van Boven, H.H.1    Vandenbroucke, J.P.2    Briet, E.3
  • 41
    • 0034839785 scopus 로고    scopus 로고
    • Phenotypic APC resistance in carriers of the A20210 prothrombin mutation is associated with an increased risk of venous thrombosis
    • Castaman G, Tosetto A, Simioni M, et al. Phenotypic APC resistance in carriers of the A20210 prothrombin mutation is associated with an increased risk of venous thrombosis. Thromb Haemost 2001; 86(3): 804-8.
    • (2001) Thromb Haemost , vol.86 , Issue.3 , pp. 804-808
    • Castaman, G.1    Tosetto, A.2    Simioni, M.3
  • 43
    • 0032190251 scopus 로고    scopus 로고
    • Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: A study of 150 families
    • Martinelli I, Mannucci PM, De Stefano V, et al. Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: A study of 150 families. Blood 1998; 92(7): 2353-8.
    • (1998) Blood , vol.92 , Issue.7 , pp. 2353-2358
    • Martinelli, I.1    Mannucci, P.M.2    De Stefano, V.3
  • 45
    • 0034487766 scopus 로고    scopus 로고
    • The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both
    • Martinelli I, Bucciarelli P, Margaglione M, et al. The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both. Br J Haematol 2000; 114(4): 1223-9.
    • (2000) Br J Haematol , vol.111 , Issue.4 , pp. 1223-1229
    • Martinelli, I.1    Bucciarelli, P.2    Margaglione, M.3
  • 46
    • 0027465837 scopus 로고
    • Increaed risk of venous thrombosis in carriers of hereditary protein C deficiency defect
    • Allaart CF, Poort SR, Rosendaal FR, et al. Increaed risk of venous thrombosis in carriers of hereditary protein C deficiency defect. Lancet 1993; 341(8838): 134-8.
    • (1993) Lancet , vol.341 , Issue.8838 , pp. 134-138
    • Allaart, C.F.1    Poort, S.R.2    Rosendaal, F.R.3
  • 47
    • 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, et al. Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis, in families with inherited deficiencies of protein S. Blood 2000; 95(6): 1935-41.
    • (2000) Blood , vol.95 , Issue.6 , pp. 1935-1941
    • Makris, M.1    Leach, M.2    Beauchamp, N.J.3
  • 48
    • 0029975366 scopus 로고    scopus 로고
    • Thrombotic risk in hereditary antithrombin III, protein C, or protein S deficiency. A cooperative, retrospective study. Gesellschaft fur Thrombose- und Hamostaseforschung (GTH) Study Group on Natural Inhibitors
    • Pabinger I, Schneider B. Thrombotic risk in hereditary antithrombin III, protein C, or protein S deficiency. A cooperative, retrospective study. Gesellschaft fur Thrombose- und Hamostaseforschung (GTH) Study Group on Natural Inhibitors. Arterioscler Thromb Vasc Biol 1996; 16(6): 742-8.
    • (1996) Arterioscler Thromb Vasc Biol , vol.16 , Issue.6 , pp. 742-748
    • Pabinger, I.1    Schneider, B.2
  • 49
    • 0031916587 scopus 로고    scopus 로고
    • Increased risk of venous thrombosis in carriers of natural anticoagulant deficiencies. Results of the family studies of the Spanish Multicenter Study on Thrombophilia (EMET study)
    • Mateo J, Oliver A, Borrell M, et al. Increased risk of venous thrombosis in carriers of natural anticoagulant deficiencies. Results of the family studies of the Spanish Multicenter Study on Thrombophilia (EMET study). Blood Coagul Fibrinolysis 1998; 9(1): 71-8.
    • (1998) Blood Coagul Fibrinolysis , vol.9 , Issue.1 , pp. 71-78
    • Mateo, J.1    Oliver, A.2    Borrell, M.3
  • 50
    • 0029873817 scopus 로고    scopus 로고
    • Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency
    • Van Boven HH, Reitsma PH, Rosendaal FR, et al. Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency. Thromb Haemost 1996; 75(3): 417-21.
    • (1996) Thromb Haemost , vol.75 , Issue.3 , pp. 417-421
    • Van Boven, H.H.1    Reitsma, P.H.2    Rosendaal, F.R.3
  • 51
    • 0027971225 scopus 로고
    • Clinical manifestations and management of inherited thrombophilia: Retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein S
    • De Stefano V, Leone G, Mastrangelo S, et al. Clinical manifestations and management of inherited thrombophilia: Retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein S. Thromb Haemost 1994; 72(3): 352-8.
    • (1994) Thromb Haemost , vol.72 , Issue.3 , pp. 352-358
    • De Stefano, V.1    Leone, G.2    Mastrangelo, S.3
  • 52
    • 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
    • Zoller P, Svensson PJ, He X, et al. 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
    • Zoller, P.1    Svensson, P.J.2    He, X.3
  • 53
    • 0035162185 scopus 로고    scopus 로고
    • Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies
    • Tirado I, Mateo J, Soria JM, et al. Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies. Haematologica 2001; 86(11): 1200-8.
    • (2001) Haematologica , vol.86 , Issue.11 , pp. 1200-1208
    • Tirado, I.1    Mateo, J.2    Soria, J.M.3
  • 54
    • 0034786549 scopus 로고    scopus 로고
    • Risk of thrombosis associated with oral contraceptives of women from 97 families with inherited thrombophilia: High risk of thrombosis in carriers of the G20210A mutation of the prothrombin gene
    • Santamaria A, Mateo J, Oliver A, et al. Risk of thrombosis associated with oral contraceptives of women from 97 families with inherited thrombophilia: High risk of thrombosis in carriers of the G20210A mutation of the prothrombin gene. Haematologica 2001; 86(9): 965-71.
    • (2001) Haematologica , vol.86 , Issue.9 , pp. 965-971
    • Santamaria, A.1    Mateo, J.2    Oliver, A.3
  • 55
    • 0034666737 scopus 로고    scopus 로고
    • Prothrombotic risk factors in children with spontaneous venous thrombosis and their asymptomatic parents: A family study
    • Kosch A, Junker R, Kurnik K, et al. Prothrombotic risk factors in children with spontaneous venous thrombosis and their asymptomatic parents: A family study. Thromb Res 2000; 99(6): 531-7.
    • (2000) Thromb Res , vol.99 , Issue.6 , pp. 531-537
    • Kosch, A.1    Junker, R.2    Kurnik, K.3
  • 56
    • 0028324624 scopus 로고
    • Thrombotic risk of women with hereditary antithrombin III-, protein C- and protein S-deficiency taking oral contraceptive medication. The GTH Study Group on Natural Inhibitors
    • Pabinger I, Schneider B. Thrombotic risk of women with hereditary antithrombin III-, protein C- and protein S-deficiency taking oral contraceptive medication. The GTH Study Group on Natural Inhibitors. Thromb Haemost 1994; 71(5): 548-52.
    • (1994) Thromb Haemost , vol.71 , Issue.5 , pp. 548-552
    • Pabinger, I.1    Schneider, B.2
  • 57
    • 0033574197 scopus 로고    scopus 로고
    • Low rate of venous thromboembolism in asymptomatic relatives of probands with factor V Leiden mutation
    • Simioni P, Prandoni P, Girolami A. Low rate of venous thromboembolism in asymptomatic relatives of probands with factor V Leiden mutation. Ann Intern Med 1999; 130(6): 538.
    • (1999) Ann Intern Med , vol.130 , Issue.6 , pp. 538
    • Simioni, P.1    Prandoni, P.2    Girolami, A.3
  • 58
    • 0033768444 scopus 로고    scopus 로고
    • Factor XIII Val34Leu and the risk of venous thromboembolism in factor V Leiden carriers
    • Franco RF, Middeldorp S, Meinardi JR, et al. Factor XIII Val34Leu and the risk of venous thromboembolism in factor V Leiden carriers. Br J Haematol 2000; 111(1): 118-21.
    • (2000) Br J Haematol , vol.111 , Issue.1 , pp. 118-121
    • Franco, R.F.1    Middeldorp, S.2    Meinardi, J.R.3
  • 59
    • 0002510810 scopus 로고
    • Evaluating coding decisions
    • Cooper H, Hedges LV, editors. New York: Russell Sage Foundation
    • Orwin RG. Evaluating coding decisions. In: The Handbook of Research Synthesis. Cooper H, Hedges LV, editors. New York: Russell Sage Foundation, 1994; 140-60.
    • (1994) The Handbook of Research Synthesis , pp. 140-160
    • Orwin, R.G.1
  • 60
    • 0036786363 scopus 로고    scopus 로고
    • The incidence of venous thromboembolism in thrombophilic children: A prospective cohort study
    • Tormene D, Simioni P, Prandoni P, et al. The incidence of venous thromboembolism in thrombophilic children: A prospective cohort study. Blood 2002; 100(7): 2403-5.
    • (2002) Blood , vol.100 , Issue.7 , pp. 2403-2405
    • Tormene, D.1    Simioni, P.2    Prandoni, P.3
  • 61
    • 0033519051 scopus 로고    scopus 로고
    • Venous thrombosis: A multicausal disease
    • Rosendaal FR. Venous thrombosis: A multicausal disease. Lancet 1999; 353: 1167-73.
    • (1999) Lancet , vol.353 , pp. 1167-1173
    • Rosendaal, F.R.1
  • 62
    • 0002487281 scopus 로고
    • Publication bias
    • In: Cooper H, Hedges LV, editors.; New York: Russell Sage Foundation
    • Begg CB. Publication bias. In: Cooper H, Hedges LV, editors. The Handbook of Research Synthesis. New York: Russell Sage Foundation, 1994: 399-409.
    • (1994) The Handbook of Research Synthesis , pp. 399-409
    • Begg, C.B.1


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