-
1
-
-
0028296057
-
The epidemiology of diagnosed pulmonary embolism and deep venous thrombosis in the elderly
-
Kniffin WD, Baron JA, Barret J, Birkmeyer JD, Anderson FA Jr. The epidemiology of diagnosed pulmonary embolism and deep venous thrombosis in the elderly. Arch Intern Med 1994; 154: 861-6.
-
(1994)
Arch Intern Med
, vol.154
, pp. 861-866
-
-
Kniffin, W.D.1
Baron, J.A.2
Barret, J.3
Birkmeyer, J.D.4
Anderson F.A., Jr.5
-
2
-
-
0030317948
-
The long-term clinical course of acute deep venous thrombosis
-
Prandoni P, Lensing AWA, Cogo A, Cuppini S, Villalta S, Carta M, Cattelan AM, Polistena P, Bernardi E, Prins MH. The long-term clinical course of acute deep 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
Cuppini, S.4
Villalta, S.5
Carta, M.6
Cattelan, A.M.7
Polistena, P.8
Bernardi, E.9
Prins, M.H.10
-
3
-
-
0029068453
-
The optimal duration of anticoagulation therapy for venous thromboembolism
-
Hirsh J. The optimal duration of anticoagulation therapy for venous thromboembolism. N Engl J Med 1995; 332: 1710-1.
-
(1995)
N Engl J Med
, vol.332
, pp. 1710-1711
-
-
Hirsh, J.1
-
4
-
-
0029876985
-
Inherited thrombophilia. Pathogenesis, clinical syndromes and management
-
De Stefano V, Finazzi G, Mannucci PM. Inherited thrombophilia. Pathogenesis, clinical syndromes and management. Blood 1996; 87: 3531-44.
-
(1996)
Blood
, vol.87
, pp. 3531-3544
-
-
De Stefano, V.1
Finazzi, G.2
Mannucci, P.M.3
-
5
-
-
10544253846
-
Inherited thrombophilia. Part 1
-
Lane DA, Mannucci PM, Bauer KA, Bertina RM, Bochkov NP, Boulyjenkov V, Chandy M, Dahlbäck B, Ginter EK, Miletich JP, Rosendaal FR, Seligsohn U. Inherited thrombophilia. Part 1. Thromb Haemost 1996; 76: 651-62.
-
(1996)
Thromb Haemost
, vol.76
, pp. 651-662
-
-
Lane, D.A.1
Mannucci, P.M.2
Bauer, K.A.3
Bertina, R.M.4
Bochkov, N.P.5
Boulyjenkov, V.6
Chandy, M.7
Dahlbäck, B.8
Ginter, E.K.9
Miletich, J.P.10
Rosendaal, F.R.11
Seligsohn, U.12
-
6
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BPC, Koester T, Rosendaal FR, Dirven RJ, de Ronde H, van der Velden PA, Reitsma PH. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369: 64-7.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koester, T.3
Rosendaal, F.R.4
Dirven, R.J.5
De Ronde, H.6
Van Der Velden, P.A.7
Reitsma, P.H.8
-
7
-
-
0027965649
-
Physiological anticoagulation. Resistance to activated protein C and venous thromboembolism
-
Dahlbäck B. Physiological anticoagulation. Resistance to activated protein C and venous thromboembolism. J Clin Invest 1994; 94: 923-7.
-
(1994)
J Clin Invest
, vol.94
, pp. 923-927
-
-
Dahlbäck, B.1
-
8
-
-
0029850530
-
A common genetic variation in the 3'untraslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort SR, Rosendaal FP, Reitsma PH, Bertina RM. A common genetic variation in the 3'untraslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.P.2
Reitsma, P.H.3
Bertina, R.M.4
-
9
-
-
0030792668
-
The prothrombin gene G20210A variant: Prevalence in an U.K. anticoagulant clinic population
-
Cumming AM, Keeney S, Salden A, Bhavnani M, Shwe KH, Hay CRM. The prothrombin gene G20210A variant: prevalence in an U.K. anticoagulant clinic population. Br J Haematol 1997; 98: 353-5.
-
(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
-
10
-
-
0031847816
-
20210 gene variant
-
20210 gene variant. Ann Intern Med 1998; 129: 89-93.
-
(1998)
Ann Intern Med
, vol.129
, pp. 89-93
-
-
Margaglione, M.1
Brancaccio, V.2
Giuliani, N.3
D'Andrea, G.4
Cappucci, G.5
Iannaccone, L.6
Vecchione, G.7
Grandone, E.8
Di Minno, G.9
-
11
-
-
0027971225
-
Clinical manifestations and management of inherited thrombophilia: Retrospective analysis and followup after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein S
-
De Stefano S, Leone G, Mastrangelo S, Tripodi A, Rodeghiero F, Castaman G, Barbui T, Finazzi G, Bizzi B, Mannucci PM.Clinical manifestations and management of inherited thrombophilia: retrospective analysis and followup after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein S. Thromb Haemost 1994; 72: 352-8.
-
(1994)
Thromb Haemost
, vol.72
, pp. 352-358
-
-
De Stefano, S.1
Leone, G.2
Mastrangelo, S.3
Tripodi, A.4
Rodeghiero, F.5
Castaman, G.6
Barbui, T.7
Finazzi, G.8
Bizzi, B.9
Mannucci, P.M.10
-
12
-
-
0028784353
-
Factor V Leiden and risk of recurrent idiopathic venous thromboembolism
-
Ridker PM, Miletich JP, Stampfer MJ, Goldhaber SZ, Lindpaintner K, Hennekens CH. Factor V Leiden and risk of recurrent idiopathic venous thromboembolism. Circulation 1995; 92: 2800-2.
-
(1995)
Circulation
, vol.92
, pp. 2800-2802
-
-
Ridker, P.M.1
Miletich, J.P.2
Stampfer, M.J.3
Goldhaber, S.Z.4
Lindpaintner, K.5
Hennekens, C.H.6
-
13
-
-
0031056991
-
506 → Gln mutation in the gene for factor V (factor V Leiden)
-
506 → Gln mutation in the gene for factor V (Factor V Leiden). N Engl J Med 1997; 336: 399-403.
-
(1997)
N Engl J Med
, vol.336
, pp. 399-403
-
-
Simioni, P.1
Prandoni, P.2
Lensing, A.W.A.3
Scudeller, A.4
Sardella, C.5
Prins, M.H.6
Villalta, S.7
Dazzi, F.8
Girolami, A.9
-
14
-
-
0028822703
-
Antiphospholipid antibodies and venous thromboembolism
-
Ginsberg JS, Wells PS, Brill-Edwards P, Donovan D, Moffatt K, Johnston M, Stevens P, Hirsh J. Antiphospholipid antibodies and venous thromboembolism. Blood 1995; 86: 3685-91.
-
(1995)
Blood
, vol.86
, pp. 3685-3691
-
-
Ginsberg, J.S.1
Wells, P.S.2
Brill-Edwards, P.3
Donovan, D.4
Moffatt, K.5
Johnston, M.6
Stevens, P.7
Hirsh, J.8
-
15
-
-
0029953246
-
Natural history and risk factors for thrombosis in 360 patients with antiphospholipid antibodies: A four years prospective study from the Italian registry
-
Finazzi G, Brancaccio V, Moia M, Ciavarella N, Mazzucconi MG, Schinco PC, Ruggeri M, Pogliani EM, Gamba G, Rossi E, Baudo F, Manotti C, D'Angelo A, Palareti G, De Stefano V, Berrettini M, Barbui T. Natural history and risk factors for thrombosis in 360 patients with antiphospholipid antibodies: a four years prospective study from the Italian registry. Am J Med 1996; 100: 530-6.
-
(1996)
Am J Med
, vol.100
, pp. 530-536
-
-
Finazzi, G.1
Brancaccio, V.2
Moia, M.3
Ciavarella, N.4
Mazzucconi, M.G.5
Schinco, P.C.6
Ruggeri, M.7
Pogliani, E.M.8
Gamba, G.9
Rossi, E.10
Baudo, F.11
Manotti, C.12
D'Angelo, A.13
Palareti, G.14
De Stefano, V.15
Berrettini, M.16
Barbui, T.17
-
16
-
-
0030924102
-
A retrospective review of 61 patients with antiphospholipid syndrome. Analysis of factors influencing recurrent thrombosis
-
Krnic-Barrie S, O'Connor CR, Looney SW, Pierangeli SS, Harris NE. A retrospective review of 61 patients with antiphospholipid syndrome. Analysis of factors influencing recurrent thrombosis. Arch Intern Med 1997; 157: 2101-8.
-
(1997)
Arch Intern Med
, vol.157
, pp. 2101-2108
-
-
Krnic-Barrie, S.1
O'Connor, C.R.2
Looney, S.W.3
Pierangeli, S.S.4
Harris, N.E.5
-
17
-
-
0029002411
-
Antiphospholipid antibodies, haemostatic variables and thrombosis. A survey of 144 patients
-
Ames PRJ, Pyke S, Iannaccone L, Brancaccio V. Antiphospholipid antibodies, haemostatic variables and thrombosis. A survey of 144 patients. Thromb Haemost 1995; 73: 768-73.
-
(1995)
Thromb Haemost
, vol.73
, pp. 768-773
-
-
Ames, P.R.J.1
Pyke, S.2
Iannaccone, L.3
Brancaccio, V.4
-
18
-
-
0029794426
-
Coagulation activation and fibrinolytic imbalance in subjects with idiopathic antiphospholipid antibodies. A crucial role for acquired free protein S deficiency
-
Ames PRJ, Catello T, Iannaccone L, Brillante M, Cimino R, Brancaccio V. Coagulation activation and fibrinolytic imbalance in subjects with idiopathic antiphospholipid antibodies. A crucial role for acquired free protein S deficiency. Thromb Haemost 1996; 76: 190-4.
-
(1996)
Thromb Haemost
, vol.76
, pp. 190-194
-
-
Ames, P.R.J.1
Catello, T.2
Iannaccone, L.3
Brillante, M.4
Cimino, R.5
Brancaccio, V.6
-
19
-
-
0028961140
-
Raised plasma fibrinogen concentrations in subjects attending a metabolic ward. Relation to family history and vascular risk factors
-
Margaglione M, Di Minno G, Grandone E, Vecchione G, Celentano E, Cappucci G, Giordano M, Grilli M, Simone P, Fusilli S, Panico S, Mancini M. Raised plasma fibrinogen concentrations in subjects attending a metabolic ward. Relation to family history and vascular risk factors. Thromb Haemost 1995; 73: 579-83.
-
(1995)
Thromb Haemost
, vol.73
, pp. 579-583
-
-
Margaglione, M.1
Di Minno, G.2
Grandone, E.3
Vecchione, G.4
Celentano, E.5
Cappucci, G.6
Giordano, M.7
Grilli, M.8
Simone, P.9
Fusilli, S.10
Panico, S.11
Mancini, M.12
-
20
-
-
0028000665
-
Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
-
Koeleman BPC, Reitsma PH, Allart CF, Bertina RM. Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families. Blood 1994; 84: 1031-5.
-
(1994)
Blood
, vol.84
, pp. 1031-1035
-
-
Koeleman, B.P.C.1
Reitsma, P.H.2
Allart, C.F.3
Bertina, R.M.4
-
21
-
-
0029966191
-
Detection of factor V Leiden mutation using SSCP
-
Margaglione M, D'Andrea G, Cappucci G, Grandone E, Giuliani N, Colaizzo D, Vecchione G, Di Minno G. Detection of factor V Leiden mutation using SSCP. Thromb Haemost 1996; 76: 814-5.
-
(1996)
Thromb Haemost
, vol.76
, pp. 814-815
-
-
Margaglione, M.1
D'Andrea, G.2
Cappucci, G.3
Grandone, E.4
Giuliani, N.5
Colaizzo, D.6
Vecchione, G.7
Di Minno, G.8
-
22
-
-
0029021115
-
A comparison of six weeks with six months of oral anticoagulant therapy after a first episode of venous thromboembolism
-
Schulman S, Rhedin AS, Lindmarker P, Carlsson A, Lärfars G, Nicol P, Loogna E, Svensson E, Ljungberg B, Walter H, Viering S, Nordlander S, Leijd B, Jönsson KA, Hjorth M, Linder O, Boberg J, and the Duration of Anticoagulation Trial Study Group. A comparison of six weeks with six months of oral anticoagulant therapy after a first episode of venous thromboembolism. N Engl J Med 1995; 332: 1661-5.
-
(1995)
N Engl J Med
, vol.332
, pp. 1661-1665
-
-
Schulman, S.1
Rhedin, A.S.2
Lindmarker, P.3
Carlsson, A.4
Lärfars, G.5
Nicol, P.6
Loogna, E.7
Svensson, E.8
Ljungberg, B.9
Walter, H.10
Viering, S.11
Nordlander, S.12
Leijd, B.13
Jönsson, K.A.14
Hjorth, M.15
Linder, O.16
Boberg, J.17
-
23
-
-
0033602514
-
A comparison of three month of anticoagulation with extended anticoagulation for a first episode of idiopathic venous thromboembolism
-
Kearon C, Gent M, Hirsh J, Weitz J, Kovacs MJ, Anderson DR, Turpie AG, Green D, Ginsberg JS, Wells P, MacKinnon B, Julian JA. A comparison of three month of anticoagulation with extended anticoagulation for a first episode of idiopathic venous thromboembolism. N Engl J Med 1999; 340: 901-7.
-
(1999)
N Engl J Med
, vol.340
, pp. 901-907
-
-
Kearon, C.1
Gent, M.2
Hirsh, J.3
Weitz, J.4
Kovacs, M.J.5
Anderson, D.R.6
Turpie, A.G.7
Green, D.8
Ginsberg, J.S.9
Wells, P.10
MacKinnon, B.11
Julian, J.A.12
-
24
-
-
0027520285
-
Venous thrombosis due to poor anticoagulation response to activated protein C: Leiden Thrombophilia study
-
Koster T, Rosendaal FR, de Ronde H, Briet E, Vandenbroucke JP, Bertina RM. Venous thrombosis due to poor anticoagulation response to activated protein C: Leiden Thrombophilia Study. Lancet 1993; 342: 1503-6.
-
(1993)
Lancet
, vol.342
, pp. 1503-1506
-
-
Koster, T.1
Rosendaal, F.R.2
De Ronde, H.3
Briet, E.4
Vandenbroucke, J.P.5
Bertina, R.M.6
-
25
-
-
0028098210
-
Resistance to activated protein C as a basis for venous thrombosis
-
Svensson JP, Dahlbäck B. Resistance to activated protein C as a basis for venous thrombosis. N Engl J Med 1994; 330: 517-22.
-
(1994)
N Engl J Med
, vol.330
, pp. 517-522
-
-
Svensson, J.P.1
Dahlbäck, B.2
-
26
-
-
0029050714
-
506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients
-
506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients. Blood 1995; 86: 219-24.
-
(1995)
Blood
, vol.86
, pp. 219-224
-
-
Gandrille, S.1
Greengard, J.S.2
Alhenc-Gelas, M.3
Juhan-Vague, I.4
Abgrall, J.F.5
Jude, B.6
Griffin, J.H.7
Aiach, M.8
-
27
-
-
0029022118
-
Factor V leiden. An additional risk factor for thrombosis in protein S deficient families?
-
Koeleman BPC, van Rumpt D, Halmulyàk K, Reitsma PH, Bertina RM. Factor V leiden. An additional risk factor for thrombosis in protein S deficient families? Thromb Haemost 1995; 74: 580-3.
-
(1995)
Thromb Haemost
, vol.74
, pp. 580-583
-
-
Koeleman, B.P.C.1
Van Rumpt, D.2
Halmulyàk, K.3
Reitsma, P.H.4
Bertina, R.M.5
-
28
-
-
0029873817
-
Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency
-
van Boven HH, Reitsma PH, Rosendaal FR, Bayston TA, Chowdhury V, Bauer KA, Scharre I. Conard J, Lane DA. Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency. Thromb Haemost 1996; 75: 417-21.
-
(1996)
Thromb Haemost
, vol.75
, pp. 417-421
-
-
Van Boven, H.H.1
Reitsma, P.H.2
Rosendaal, F.R.3
Bayston, T.A.4
Chowdhury, V.5
Bauer, K.A.6
Scharre, I.7
Conard, J.8
Lane, D.A.9
-
29
-
-
0030608645
-
Co-inheritance of the 2021OA allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia
-
Makris M, Preston FE, Beauchamp NJ, Cooper PC, Daly ME, Hampton KK, Bayliss P, Peake IR, Miller GJ. Co-inheritance of the 2021OA allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia. Thromh Haemost 1997; 78: 1426-9.
-
(1997)
Thromh Haemost
, vol.78
, pp. 1426-1429
-
-
Makris, M.1
Preston, F.E.2
Beauchamp, N.J.3
Cooper, P.C.4
Daly, M.E.5
Hampton, K.K.6
Bayliss, P.7
Peake, I.R.8
Miller, G.J.9
-
30
-
-
0031442537
-
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease
-
Ferraresi P, Marchetti G, Legnani C, Cavallari E, Castoldi E, Mascoli F, Ardissino D, Palareti G, Bernardi F. The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease. Arterioscler Thromb Vasc Biol 1997; 17: 2418-22.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 2418-2422
-
-
Ferraresi, P.1
Marchetti, G.2
Legnani, C.3
Cavallari, E.4
Castoldi, E.5
Mascoli, F.6
Ardissino, D.7
Palareti, G.8
Bernardi, F.9
-
31
-
-
0029930121
-
Probability of recurrence of thrombosis in patients with and without factor V Leiden
-
Rintelen C, Pabinger I, Knöbl P, Lechner K, Mannhalter Ch. Probability of recurrence of thrombosis in patients with and without factor V Leiden. Thromb Haemost 1996; 75: 229-32.
-
(1996)
Thromb Haemost
, vol.75
, pp. 229-232
-
-
Rintelen, C.1
Pabinger, I.2
Knöbl, P.3
Lechner, K.4
Mannhalter, Ch.5
-
32
-
-
20244369707
-
The risk of recurrent venous thromboembolism in patients with and without factor V Leiden
-
Eichinger S, Pabinger I, Stümpflen A, Hirschl M, Bialonczyk C, Schneider B, Mannhalter C, Minar E, Lechner K, Kyrle PA. The risk of recurrent venous thromboembolism in patients with and without factor V Leiden. Thromb Haemost 1997; 77: 624-8.
-
(1997)
Thromb Haemost
, vol.77
, pp. 624-628
-
-
Eichinger, S.1
Pabinger, I.2
Stümpflen, A.3
Hirschl, M.4
Bialonczyk, C.5
Schneider, B.6
Mannhalter, C.7
Minar, E.8
Lechner, K.9
Kyrle, P.A.10
-
33
-
-
0032954926
-
The risk of recurrent venous thromboembolism in carriers and non-carriers of the G1691A allele in coagulation factor V gene and the G20210A allele in the prothrombin gene
-
Lindmarker P, Schulman S, Sten-Linder M, Wiman B, Egberg N, Johnsson H and the DURAC Trial Study Group. The risk of recurrent venous thromboembolism in carriers and non-carriers of the G1691A allele in coagulation factor V gene and the G20210A allele in the prothrombin gene. Thromb Haemost 1999; 81: 684-9.
-
(1999)
Thromb Haemost
, vol.81
, pp. 684-689
-
-
Lindmarker, P.1
Schulman, S.2
Sten-Linder, M.3
Wiman, B.4
Egberg, N.5
Johnsson, H.6
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