메뉴 건너뛰기




Volumn 157, Issue 19, 1997, Pages 2227-2232

Recurrence of venous thromboembolism in patients with familial thrombophilia

Author keywords

[No Author keywords available]

Indexed keywords

ANTICOAGULANT AGENT; ANTITHROMBIN; PROTEIN C; PROTEIN S; WARFARIN;

EID: 0030868686     PISSN: 00039926     EISSN: None     Source Type: Journal    
DOI: 10.1001/archinte.157.19.2227     Document Type: Article
Times cited : (145)

References (69)
  • 1
    • 0001627642 scopus 로고
    • Inherited antithrombin deficiency causing thrombophilia
    • Egeberg O. Inherited antithrombin deficiency causing thrombophilia. Thromb Haemost. 1965;13:516-523.
    • (1965) Thromb Haemost , vol.13 , pp. 516-523
    • Egeberg, O.1
  • 2
    • 0001877945 scopus 로고
    • An approach to the thrombophilic patient
    • Colman RW, Hirsh J, Marder VL, Salzman EW, eds. Philadelphia, Pa: JB Lippincott
    • Hirsh J, Prins MH, Samama M. An approach to the thrombophilic patient. In: Colman RW, Hirsh J, Marder VL, Salzman EW, eds. Thrombosis and Haemostasis: Basic Principles and Practice. 3rd ed. Philadelphia, Pa: JB Lippincott; 1994:1543-1561.
    • (1994) Thrombosis and Haemostasis: Basic Principles and Practice. 3rd Ed. , pp. 1543-1561
    • Hirsh, J.1    Prins, M.H.2    Samama, M.3
  • 4
    • 1842267508 scopus 로고
    • The incidence of venous thromboembolism and superficial vein thrombosis in ATIII-, protein S- And protein C-deficient subjects
    • Friederich PW, Scudeller A, Sanson B-J, et al. The incidence of venous thromboembolism and superficial vein thrombosis in ATIII-, protein S- and protein C-deficient subjects. Thromb Haemost. 1995;73:1262.
    • (1995) Thromb Haemost , vol.73 , pp. 1262
    • Friederich, P.W.1    Scudeller, A.2    Sanson, B.-J.3
  • 5
    • 0027465837 scopus 로고
    • Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect
    • Allaart CF, Poort SR, Rosendaal FR, Reitsma PH, Bertina RM, Briet E. Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect. Lancet. 1993;341:134-138.
    • (1993) Lancet , vol.341 , pp. 134-138
    • Allaart, C.F.1    Poort, S.R.2    Rosendaal, F.R.3    Reitsma, P.H.4    Bertina, R.M.5    Briet, E.6
  • 6
    • 0028840258 scopus 로고
    • Hemorrhagic complications of anticoagulant treatment
    • Levine MM, Raskob G, Landefeld S, Hirsh J. Hemorrhagic complications of anticoagulant treatment. Chest 1995;108(suppl 4):276S-290S.
    • (1995) Chest , vol.108 , Issue.SUPPL. 4
    • Levine, M.M.1    Raskob, G.2    Landefeld, S.3    Hirsh, J.4
  • 7
    • 0029125979 scopus 로고
    • A review of mutations causing deficiencies of antithrombin, protein C and protein S
    • Aiach M, Gandrille S, Emmerich J. A review of mutations causing deficiencies of antithrombin, protein C and protein S. Thromb Haemost. 1995;74:81-89.
    • (1995) Thromb Haemost , vol.74 , pp. 81-89
    • Aiach, M.1    Gandrille, S.2    Emmerich, J.3
  • 9
    • 0019518691 scopus 로고
    • Hereditary antithrombin III deficiency in an English family
    • Scully MF, De Hass H, Chan P, Kakkar W. Hereditary antithrombin III deficiency in an English family. Br J Haematol. 1981;47:235-241.
    • (1981) Br J Haematol , vol.47 , pp. 235-241
    • Scully, M.F.1    De Hass, H.2    Chan, P.3    Kakkar, W.4
  • 10
    • 0017639859 scopus 로고
    • Deficit congenital en antithrombine m étude d'une famille Quebecosie
    • Thuot C, Marion D, Boucher H. Deficit congenital en antithrombine m étude d'une famille Quebecosie. Union Med Can. 1977;106:673-677.
    • (1977) Union Med Can , vol.106 , pp. 673-677
    • Thuot, C.1    Marion, D.2    Boucher, H.3
  • 11
    • 0018852768 scopus 로고
    • Heterogeneity of the 'classical' antithrombin III deficiency
    • Sas G, Peto I, Banhegyi D, Blasko G, Domjan G. Heterogeneity of the 'classical' antithrombin III deficiency. Thromb Haemost. 1980;43:133-137.
    • (1980) Thromb Haemost , vol.43 , pp. 133-137
    • Sas, G.1    Peto, I.2    Banhegyi, D.3    Blasko, G.4    Domjan, G.5
  • 12
    • 0019334957 scopus 로고
    • Inferior vena cava thrombosis in a child with familial antithrombin III deficiency
    • Leone G, Valori VM, Storti S, Myers TJ. Inferior vena cava thrombosis in a child with familial antithrombin III deficiency. Thromb Haemost. 1980;43:74-79.
    • (1980) Thromb Haemost , vol.43 , pp. 74-79
    • Leone, G.1    Valori, V.M.2    Storti, S.3    Myers, T.J.4
  • 13
    • 0018819101 scopus 로고
    • Inherited antithrombin III deficiency and cerebral thrombosis in a child
    • Ambruso DR, Jacobson LJ, Hathaway WE. Inherited antithrombin III deficiency and cerebral thrombosis in a child. Pediatrics. 1980;65:125-132.
    • (1980) Pediatrics , vol.65 , pp. 125-132
    • Ambruso, D.R.1    Jacobson, L.J.2    Hathaway, W.E.3
  • 14
    • 0015962737 scopus 로고
    • Familial thrombosis due to antithrombin deficiency
    • Marciniak E, Farley GH, DeSimone PA. Familial thrombosis due to antithrombin deficiency. Blood. 1974;43:219-225.
    • (1974) Blood , vol.43 , pp. 219-225
    • Marciniak, E.1    Farley, G.H.2    Desimone, P.A.3
  • 15
    • 0018576015 scopus 로고
    • Embolie pulmonaire severe et thrombophlebite recidivante en rapport avec un deficit hereditaire en antithrombine III
    • Rey JL, Delobel J, Claisse JF, Quiret JC, Bor P, Bernasconi P. Embolie pulmonaire severe et thrombophlebite recidivante en rapport avec un deficit hereditaire en antithrombine III. Arch Mal Coeur Vaiss. 1979;72:919-925.
    • (1979) Arch Mal Coeur Vaiss , vol.72 , pp. 919-925
    • Rey, J.L.1    Delobel, J.2    Claisse, J.F.3    Quiret, J.C.4    Bor, P.5    Bernasconi, P.6
  • 16
    • 0018763897 scopus 로고
    • Thrombose des veines portes et mesenterique superieure au cours d'un deficit congenital et familial en antithrombine III
    • Juillet Y, Vayssairat M, Fiessinger JN, Aiach M, Housset E. Thrombose des veines portes et mesenterique superieure au cours d'un deficit congenital et familial en antithrombine III. Ann Intern Med. 1979;130:53-58.
    • (1979) Ann Intern Med , vol.130 , pp. 53-58
    • Juillet, Y.1    Vayssairat, M.2    Fiessinger, J.N.3    Aiach, M.4    Housset, E.5
  • 17
    • 0020697148 scopus 로고
    • Heparin cofactor activities in a family with hereditary antithrombin III deficiency: Evidence for a second heparin cofactor in human plasma
    • Griffith MJ, Carraway T, White GC, Dombrose FA. Heparin cofactor activities in a family with hereditary antithrombin III deficiency: evidence for a second heparin cofactor in human plasma. Blood. 1983;61:111-116.
    • (1983) Blood , vol.61 , pp. 111-116
    • Griffith, M.J.1    Carraway, T.2    White, G.C.3    Dombrose, F.A.4
  • 18
    • 0023904864 scopus 로고
    • Cerebral thrombosis in a newborn with a congenital deficiency of antithrombin III
    • Brenner B, Fishman A, Goldsher D, Schreibman D, Tavory S. Cerebral thrombosis in a newborn with a congenital deficiency of antithrombin III. Am J Hematol. 1988;27:209-212.
    • (1988) Am J Hematol , vol.27 , pp. 209-212
    • Brenner, B.1    Fishman, A.2    Goldsher, D.3    Schreibman, D.4    Tavory, S.5
  • 20
    • 0024597624 scopus 로고
    • Antithrombin Sheffield: Amino acid substitution at the reactive site (Arg393 to His) causing thrombosis
    • Lane DA, Erdjument H, Flynn A, et al. Antithrombin Sheffield: amino acid substitution at the reactive site (Arg393 to His) causing thrombosis. Br J Haematol. 1989;71:91-96.
    • (1989) Br J Haematol , vol.71 , pp. 91-96
    • Lane, D.A.1    Erdjument, H.2    Flynn, A.3
  • 22
    • 0023795012 scopus 로고
    • Antithrombin III Avranches, a new variant with defective serine-protease inhibition: Comparison with antithrombin III Charleville
    • Aiach M, Roncato M, Chaduef G, Dezellus P, Capron L, Fiessinger JN. Antithrombin III Avranches, a new variant with defective serine-protease inhibition: comparison with antithrombin III Charleville. Thromb Haemost 1988;60:94-98.
    • (1988) Thromb Haemost , vol.60 , pp. 94-98
    • Aiach, M.1    Roncato, M.2    Chaduef, G.3    Dezellus, P.4    Capron, L.5    Fiessinger, J.N.6
  • 23
    • 0021149123 scopus 로고
    • Antithrombin III Trento: A new congential at III abnormality with a peculiar crossed immunoelectrophoretic pattern in absence of heparin
    • Girolami A, Marafioti F, Rubertelli M, Vicarioto MA, Cappellato G, Mazzuccato M. Antithrombin III Trento: a new congential AT III abnormality with a peculiar crossed immunoelectrophoretic pattern in absence of heparin. Acta Haematol. 1984;72:73-78.
    • (1984) Acta Haematol , vol.72 , pp. 73-78
    • Girolami, A.1    Marafioti, F.2    Rubertelli, M.3    Vicarioto, M.A.4    Cappellato, G.5    Mazzuccato, M.6
  • 24
    • 0018090254 scopus 로고
    • Deficit hereditaire en anti-thrombine III responsable d'accidents thrombo-emboliques recidivants
    • Bessot J-C, Ouoix E, Charbonneau J, et al. Deficit hereditaire en anti-thrombine III responsable d'accidents thrombo-emboliques recidivants. Nouv Presse Med. 1978;7:999-1003.
    • (1978) Nouv Presse Med , vol.7 , pp. 999-1003
    • Bessot, J.-C.1    Ouoix, E.2    Charbonneau, J.3
  • 26
    • 0021893717 scopus 로고
    • A functional abnormal antithrombin III (at III) deficiency: At III Charleville
    • Aiach M, Nora M, Fiessinger J-N, et al. A functional abnormal antithrombin III (AT III) deficiency: AT III Charleville. Thromb Res. 1985;39:559-561.
    • (1985) Thromb Res , vol.39 , pp. 559-561
    • Aiach, M.1    Nora, M.2    Fiessinger, J.-N.3
  • 27
    • 85047693725 scopus 로고
    • Immunoelectrophoretic evidence of a thrombin-induced abnormality in a new variant of hereditary dysfunctional antithrombin III (AT III 'Vicenza')
    • Barbui T, Finazzi G, Rodeghiero F, Dini E. Immunoelectrophoretic evidence of a thrombin-induced abnormality in a new variant of hereditary dysfunctional antithrombin III (AT III 'Vicenza'). Br J Haematol. 1983;54:561-564.
    • (1983) Br J Haematol , vol.54 , pp. 561-564
    • Barbui, T.1    Finazzi, G.2    Rodeghiero, F.3    Dini, E.4
  • 28
    • 0018698408 scopus 로고
    • Familial antithrombin III deficiency in a Japanese family
    • Matsuo T, Ohki Y, Kondo S, Matsuo O. Familial antithrombin III deficiency in a Japanese family. Thromb Res. 1979;16:815-822.
    • (1979) Thromb Res , vol.16 , pp. 815-822
    • Matsuo, T.1    Ohki, Y.2    Kondo, S.3    Matsuo, O.4
  • 29
    • 0018950972 scopus 로고
    • A South African family with antithrombin III deficiency
    • Beukes CA, Heyns ADP. A South African family with antithrombin III deficiency. S Afr Med J. 1980;58:528-533.
    • (1980) S Afr Med J , vol.58 , pp. 528-533
    • Beukes, C.A.1    Heyns, A.D.P.2
  • 30
    • 0017122255 scopus 로고
    • Hereditary antithrombin III deficiency: Effect of antithrombin III deficiency on platelet function
    • Carivalho A, Ellman L. Hereditary antithrombin III deficiency: effect of antithrombin III deficiency on platelet function. Am J Med. 1976;61:179-182.
    • (1976) Am J Med , vol.61 , pp. 179-182
    • Carivalho, A.1    Ellman, L.2
  • 31
    • 0017886633 scopus 로고
    • Antithrombin III deficiency, hypertriglyceridaemia, and venous thromboses
    • Gyde OHB, Middleton MD, Vaughan GR, Fletcher DJ. Antithrombin III deficiency, hypertriglyceridaemia, and venous thromboses. BMJ. 1978;1:621-623.
    • (1978) BMJ , vol.1 , pp. 621-623
    • Gyde, O.H.B.1    Middleton, M.D.2    Vaughan, G.R.3    Fletcher, D.J.4
  • 32
    • 0017104374 scopus 로고
    • Prophylactic and therapeutic use of anticoagulants in inherited antithrombin III deficiency
    • Zucker ML, Gomperts ED, Marcus RG. Prophylactic and therapeutic use of anticoagulants in inherited antithrombin III deficiency. S Afr Med J. 1976;50:1743-1745.
    • (1976) S Afr Med J , vol.50 , pp. 1743-1745
    • Zucker, M.L.1    Gomperts, E.D.2    Marcus, R.G.3
  • 34
    • 0020383416 scopus 로고
    • Familial antithrombin III deficiency
    • Winter JH, Fench A, Ridley W, et al. Familial antithrombin III deficiency. Q J Med. 1982;51:373-376.
    • (1982) Q J Med , vol.51 , pp. 373-376
    • Winter, J.H.1    Fench, A.2    Ridley, W.3
  • 35
    • 0020619944 scopus 로고
    • Familial antithrombin III deficiency: Its natural history, genetics, diagnosis and treatment
    • Cosgriff TM, Bishop DT, Hershgold EJ, et al. Familial antithrombin III deficiency: its natural history, genetics, diagnosis and treatment. Medicine. 1983;62:209-213.
    • (1983) Medicine , vol.62 , pp. 209-213
    • Cosgriff, T.M.1    Bishop, D.T.2    Hershgold, E.J.3
  • 36
    • 0017364618 scopus 로고
    • Antifactor Xa activity in thrombophilia: Studies in a family with AT-III deficiency
    • Odegard OR, Abildgaard U. Antifactor Xa activity in thrombophilia: studies in a family with AT-III deficiency. Scand J Haematol. 1977;18:86-90.
    • (1977) Scand J Haematol , vol.18 , pp. 86-90
    • Odegard, O.R.1    Abildgaard, U.2
  • 39
    • 0018253904 scopus 로고
    • Familial antithrombin III deficiency as pathogenesis of deep venous thrombosis
    • Johansson L, Hedner U, Nilsson IM. Familial antithrombin III deficiency as pathogenesis of deep venous thrombosis. Acta Med Scand. 1978;204:491-493.
    • (1978) Acta Med Scand , vol.204 , pp. 491-493
    • Johansson, L.1    Hedner, U.2    Nilsson, I.M.3
  • 40
    • 0021800065 scopus 로고
    • Antithrombin III 'Northwick Park': A variant antithrombin with normal affinity for heparin but reduced heparin cofactor activity
    • Howarth DJ, Samson D, Stirling Y, Seghatchian MJ. Antithrombin III 'Northwick Park': a variant antithrombin with normal affinity for heparin but reduced heparin cofactor activity. Thromb Haemost. 1985;53:314-317.
    • (1985) Thromb Haemost , vol.53 , pp. 314-317
    • Howarth, D.J.1    Samson, D.2    Stirling, Y.3    Seghatchian, M.J.4
  • 41
    • 0023114736 scopus 로고
    • Antithrombin III Pescara: A defective at III variant with no alterations of plasma crossed immunoelectrophoresis, but with an abnormal crossed immunoelectrofocusing pattern
    • Leone G, De Stefano V, Di Donfrancesco A, Ferrelli R, Traisci G, Bizzi B. Antithrombin III Pescara: a defective AT III variant with no alterations of plasma crossed immunoelectrophoresis, but with an abnormal crossed immunoelectrofocusing pattern. Br J Haematol. 1987;65:187-191.
    • (1987) Br J Haematol , vol.65 , pp. 187-191
    • Leone, G.1    De Stefano, V.2    Di Donfrancesco, A.3    Ferrelli, R.4    Traisci, G.5    Bizzi, B.6
  • 42
    • 0023272740 scopus 로고
    • Antithrombin III Glasgow: A variant with increased heparin affinity and reduced ability to inactivate thrombin, associated with familial thrombosis
    • Lane DA, Lowe GDO, Flynn A, Thompson E, Ireland H, Erdjument H. Antithrombin III Glasgow: a variant with increased heparin affinity and reduced ability to inactivate thrombin, associated with familial thrombosis. Br J Haematol. 1987;66:523-525.
    • (1987) Br J Haematol , vol.66 , pp. 523-525
    • Lane, D.A.1    Lowe, G.D.O.2    Flynn, A.3    Thompson, E.4    Ireland, H.5    Erdjument, H.6
  • 44
    • 0025695818 scopus 로고
    • Cerebral infarction and familial protein S deficiency
    • Davous P, Horellou MH, Conard J, Samama M. Cerebral infarction and familial protein S deficiency. Stroke. 1990;21:1760-1764.
    • (1990) Stroke , vol.21 , pp. 1760-1764
    • Davous, P.1    Horellou, M.H.2    Conard, J.3    Samama, M.4
  • 45
    • 18544395863 scopus 로고
    • Protein S deficiency associated with 'juvenile' arterial and venous thromboses
    • Mannucci PM, Tripodi A, Bertina RM. Protein S deficiency associated with 'juvenile' arterial and venous thromboses. Thromb Haemost. 1986;55:440-445.
    • (1986) Thromb Haemost , vol.55 , pp. 440-445
    • Mannucci, P.M.1    Tripodi, A.2    Bertina, R.M.3
  • 46
    • 0025169536 scopus 로고
    • Hereditary protein S deficiency in young adults with arterial occlusive disease
    • Allaart CF, Aronson DC, Ruys TH, et al. Hereditary protein S deficiency in young adults with arterial occlusive disease. Thromb Haemost. 1990;64:206-209.
    • (1990) Thromb Haemost , vol.64 , pp. 206-209
    • Allaart, C.F.1    Aronson, D.C.2    Ruys, T.H.3
  • 47
    • 1842341519 scopus 로고
    • Familial type 1 protein S deficiency associated with severe venous thrombosis: A study of five cases
    • Boyer-Neumann C, Wolf M, Amiral J, Guyader A-M, Meyer D, Larrieu JJ. Familial type 1 protein S deficiency associated with severe venous thrombosis: a study of five cases. Thromb Haemost. 1986;60:1298-1302.
    • (1986) Thromb Haemost , vol.60 , pp. 1298-1302
    • Boyer-Neumann, C.1    Wolf, M.2    Amiral, J.3    Guyader, A.-M.4    Meyer, D.5    Larrieu, J.J.6
  • 48
    • 0023204839 scopus 로고
    • Deficiency of plasma protein S, protein C or antithrombin III and arterial thrombosis
    • Coller BS, Owen J, Jesty J, et al. Deficiency of plasma protein S, protein C or antithrombin III and arterial thrombosis. Arteriosclerosis. 1987;7:456-461.
    • (1987) Arteriosclerosis , vol.7 , pp. 456-461
    • Coller, B.S.1    Owen, J.2    Jesty, J.3
  • 49
    • 0024605404 scopus 로고
    • Severe arterial cerebral thrombosis in patients with protein S deficiency (moderately reduced total and markedly reduced free protein S): A family study
    • Girolami A, Simioni P, Lazzaro AR, Cordiano I. Severe arterial cerebral thrombosis in patients with protein S deficiency (moderately reduced total and markedly reduced free protein S): a family study. Thromb Haemost. 1989;61:144-145.
    • (1989) Thromb Haemost , vol.61 , pp. 144-145
    • Girolami, A.1    Simioni, P.2    Lazzaro, A.R.3    Cordiano, I.4
  • 50
    • 0022632368 scopus 로고
    • Inherited deficiency of protein S in a Japanese family with recurrent venous thrombosis: A study of three generations
    • Kamiya T, Sugihara T, Ogata K, et al. Inherited deficiency of protein S in a Japanese family with recurrent venous thrombosis: a study of three generations. Blood. 1986;67:406-408.
    • (1986) Blood , vol.67 , pp. 406-408
    • Kamiya, T.1    Sugihara, T.2    Ogata, K.3
  • 53
    • 0021720421 scopus 로고
    • Recurrent venous thromboembolism in patients with a partial deficiency of protein S
    • Comp PC, Esmon C. Recurrent venous thromboembolism in patients with a partial deficiency of protein S. N Engl J Med. 1984;311:1525-1528.
    • (1984) N Engl J Med , vol.311 , pp. 1525-1528
    • Comp, P.C.1    Esmon, C.2
  • 56
    • 0023423944 scopus 로고
    • Thrombophilie infolge eines protein-C-defektes vom typ II
    • Vogel VG, Machulik M, Lauten G. Thrombophilie infolge eines protein-C-defektes vom typ II. Z Gesamte Inn Med. 1987;42:550-557.
    • (1987) Z Gesamte Inn Med , vol.42 , pp. 550-557
    • Vogel, V.G.1    Machulik, M.2    Lauten, G.3
  • 57
    • 0024595128 scopus 로고
    • Heterozygous protein C deficiency type I
    • Kemkes-Matthes B. Heterozygous protein C deficiency type I. Blut. 1989;58:201-204.
    • (1989) Blut , vol.58 , pp. 201-204
    • Kemkes-Matthes, B.1
  • 59
    • 0024507770 scopus 로고
    • The clinical spectrum of heterozygous protein C deficiency in a large New England kindred
    • Bovill EG, Bauer KA, Dickerman JD, Callas P, West B. The clinical spectrum of heterozygous protein C deficiency in a large New England kindred. Blood. 1989;73:712-715.
    • (1989) Blood , vol.73 , pp. 712-715
    • Bovill, E.G.1    Bauer, K.A.2    Dickerman, J.D.3    Callas, P.4    West, B.5
  • 62
    • 0024370505 scopus 로고
    • Congenital severe protein C deficiency in adults
    • Melissari E, Kakkar W. Congenital severe protein C deficiency in adults. Br J Haematol. 1989;72:222-226.
    • (1989) Br J Haematol , vol.72 , pp. 222-226
    • Melissari, E.1    Kakkar, W.2
  • 63
    • 0021101168 scopus 로고
    • Congenital protein C deficiency and venous thromboembolism: A study in three Dutch families
    • Broekmans AW, Velkamp JJ, Bertina RM. Congenital protein C deficiency and venous thromboembolism: a study in three Dutch families. N Engl J Med. 1983;309:340-344.
    • (1983) N Engl J Med , vol.309 , pp. 340-344
    • Broekmans, A.W.1    Velkamp, J.J.2    Bertina, R.M.3
  • 64
    • 0024097607 scopus 로고
    • Protein deficiency in three generations of one family
    • Zauber NP, Kudryk AB. Protein deficiency in three generations of one family. N J Med. 1988;85:805-809.
    • (1988) N J Med , vol.85 , pp. 805-809
    • Zauber, N.P.1    Kudryk, A.B.2
  • 65
    • 0002505687 scopus 로고
    • A venographic study of thromboembolism problems
    • Bauer GA. A venographic study of thromboembolism problems. Acta Chir Scand. 1940;84(suppl 61):1-75.
    • (1940) Acta Chir Scand , vol.84 , Issue.SUPPL. 61 , pp. 1-75
    • Bauer, G.A.1
  • 66
    • 0014497278 scopus 로고
    • Problems of acute deep venous thrombosis, I: The interpretation of signs and symptoms
    • Haeger K. Problems of acute deep venous thrombosis, I: the interpretation of signs and symptoms. Angiology. 1969;20:219-223.
    • (1969) Angiology , vol.20 , pp. 219-223
    • Haeger, K.1
  • 67
    • 0018600123 scopus 로고
    • Warfarin sodium versus low-dose heparin in the long-term treatment of venous thrombosis
    • Hull R, Delmore T, Genton E, et al. Warfarin sodium versus low-dose heparin in the long-term treatment of venous thrombosis. N Engl J Med. 1979;301:855-858.
    • (1979) N Engl J Med , vol.301 , pp. 855-858
    • Hull, R.1    Delmore, T.2    Genton, E.3
  • 68
    • 0026460878 scopus 로고
    • Acenocoumarol and heparin compared with acenocoumarol alone in the initial treatment of proximal-vein thrombosis
    • Brandjes DPM, Herjboer H, Büller HR, et al. Acenocoumarol and heparin compared with acenocoumarol alone in the initial treatment of proximal-vein thrombosis. N Engl J Med. 1992;327:1485-1489.
    • (1992) N Engl J Med , vol.327 , pp. 1485-1489
    • Brandjes, D.P.M.1    Herjboer, H.2    Büller, H.R.3
  • 69
    • 0030317948 scopus 로고    scopus 로고
    • The long-term clinical course of acute venous thrombosis
    • Prandoni P, Lensing AWA, Cogo A, et al. The long-term clinical course of acute venous thrombosis. Ann Intern Med. 1996;125:1-7.
    • (1996) Ann Intern Med , vol.125 , pp. 1-7
    • Prandoni, P.1    Lensing, A.W.A.2    Cogo, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.