-
1
-
-
0019579602
-
Antithrombin III deficiency and thromboembolism
-
Thaler E, Lechner K. Antithrombin III deficiency and thromboembolism. Clin Haematol 1981; 10: 369-90.
-
(1981)
Clin Haematol
, vol.10
, pp. 369-390
-
-
Thaler, E.1
Lechner, K.2
-
2
-
-
0026025457
-
Role of antithrombin III as a regulator of in vivo coagulation
-
Bauer KA, Rosenberg RD. Role of antithrombin III as a regulator of in vivo coagulation. Semin Haematol 1991; 28: 10-8.
-
(1991)
Semin Haematol
, vol.28
, pp. 10-18
-
-
Bauer, K.A.1
Rosenberg, R.D.2
-
3
-
-
0021101168
-
Congenital protein C deficiency and venous thromboembolism: A study in three Dutch families
-
Broekmans AW, Veltkamp JJ, Bertina RM. Congenital protein C deficiency and venous thromboembolism: a study in three Dutch families. N Engl J Med 1983; 309: 340-4.
-
(1983)
N Engl J Med
, vol.309
, pp. 340-344
-
-
Broekmans, A.W.1
Veltkamp, J.J.2
Bertina, R.M.3
-
4
-
-
0023227876
-
Hereditary protein S deficiency: Clinical manifestations
-
Engesser L, Broekmans AW, Briët E, Brommer EJP, Bertina RM. Hereditary protein S deficiency: clinical manifestations. Ann Intern Med 1987; 106: 677-82.
-
(1987)
Ann Intern Med
, vol.106
, pp. 677-682
-
-
Engesser, L.1
Broekmans, A.W.2
Briët, E.3
Brommer, E.J.P.4
Bertina, R.M.5
-
5
-
-
0026591793
-
The protein C anticoagulant pathway
-
Esmon CT. The protein C anticoagulant pathway. Arterioscler Thromb 1992; 12: 135-45.
-
(1992)
Arterioscler Thromb
, vol.12
, pp. 135-145
-
-
Esmon, C.T.1
-
6
-
-
0028272987
-
The risk of thromboembolism in patients with protein S or protein C deficiency: Prospective cohort study
-
Pabinger I, Kyrle PA, Heistinger M, Eichinger S, Lechner K. The risk of thromboembolism in patients with protein S or protein C deficiency: 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
Eichinger, S.4
Lechner, K.5
-
7
-
-
0027446268
-
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
-
8
-
-
0028098210
-
Resistance to activated protein C as a basis for venous thrombosis
-
Svensson PJ, 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, P.J.1
Dahlbäck, B.2
-
9
-
-
0027428481
-
Anticoagulant protein C pathway defective in majority of thrombophilic patients
-
Griffin JH, Evatt B, Wideman C, Fernandez J. Anticoagulant protein C pathway defective in majority of thrombophilic patients. Blood 1993; 82: 1989-93.
-
(1993)
Blood
, vol.82
, pp. 1989-1993
-
-
Griffin, J.H.1
Evatt, B.2
Wideman, C.3
Fernandez, J.4
-
10
-
-
0027520285
-
Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study
-
Koster T, Rosendaal FR, de Ronde H, Briët E, Vandenbroucke JP, Bertina RM. Venous thrombosis due to poor anticoagulant 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
Briët, E.4
Vandenbroucke, J.P.5
Bertina, R.M.6
-
11
-
-
0027742936
-
Resistance to activated protein C in nine thrombophilic families: Interference in a protein S functional assay
-
Faioni EM, Franchi F, Asti D, Sacchi E, Bernardi F, Mannucci PM. Resistance to activated protein C in nine thrombophilic families: interference in a protein S functional assay. Thromb Haemost 1993; 70: 1067-71.
-
(1993)
Thromb Haemost
, vol.70
, pp. 1067-1071
-
-
Faioni, E.M.1
Franchi, F.2
Asti, D.3
Sacchi, E.4
Bernardi, F.5
Mannucci, P.M.6
-
12
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BPC, Koster 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
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
De Ronde, H.6
Van Der Velden, P.A.7
Reitsma, P.H.8
-
13
-
-
0028352460
-
Activated protein C resistance caused by Arg 506 Gln mutation in FVa
-
Greengard JS, Sun X, Xu X, Fernandez JY. Griffin JH, Evatt B. Activated protein C resistance caused by Arg 506 Gln mutation in FVa. Lancet 1994; 343: 1361-2.
-
(1994)
Lancet
, vol.343
, pp. 1361-1362
-
-
Greengard, J.S.1
Sun, X.2
Xu, X.3
Fernandez, J.Y.4
Griffin, J.H.5
Evatt, B.6
-
14
-
-
0028243401
-
Association of idiopathic venous thromboembolism with single point mutation at Arg 506 of factor V
-
Voorberg J, Roelse J, Koopman R, Büller H, Berends F, ten Cate JW, Mertens K, van Mourik JA. Association of idiopathic venous thromboembolism with single point mutation at Arg 506 of factor V. Lancet 1994; 343: 1535-6.
-
(1994)
Lancet
, vol.343
, pp. 1535-1536
-
-
Voorberg, J.1
Roelse, J.2
Koopman, R.3
Büller, H.4
Berends, F.5
Ten Cate, J.W.6
Mertens, K.7
Van Mourik, J.A.8
-
15
-
-
0028931717
-
High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance)
-
Rosendaal FR, Koster T, Vandenbrouke JP, Reitsma PH. High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance). Blood 1995; 85: 1504-8.
-
(1995)
Blood
, vol.85
, pp. 1504-1508
-
-
Rosendaal, F.R.1
Koster, T.2
Vandenbrouke, J.P.3
Reitsma, P.H.4
-
16
-
-
0028910906
-
Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thromboembolism in apparently healthy men
-
Ridker PM, Hennekens CH, Lindpaintner K, Stampfer MJ, Eisenberg PR, Miletich JP. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thromboembolism in apparently healthy men. N Engl J Med 1995; 332: 912-7.
-
(1995)
N Engl J Med
, vol.332
, pp. 912-917
-
-
Ridker, P.M.1
Hennekens, C.H.2
Lindpaintner, K.3
Stampfer, M.J.4
Eisenberg, P.R.5
Miletich, J.P.6
-
17
-
-
0028219638
-
Duration of oral anticoagulant therapy after proximal deep vein thrombosis: A decision analysis
-
Sarasiti F, Bounameaux H. Duration of oral anticoagulant therapy after proximal deep vein thrombosis: a decision analysis. Thromb Haemost 1994; 71 (3): 286-91.
-
(1994)
Thromb Haemost
, vol.71
, Issue.3
, pp. 286-291
-
-
Sarasiti, F.1
Bounameaux, H.2
-
18
-
-
0027971225
-
Clinical manifestations of inherited thrombophilia: A 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, Tripodi A, Rodeghiero F, Castaman G, Barbui T, Finazzi G, Bizzi B, Mannucci PM. Clinical manifestations of inherited thrombophilia: a 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
Tripodi, A.4
Rodeghiero, F.5
Castaman, G.6
Barbui, T.7
Finazzi, G.8
Bizzi, B.9
Mannucci, P.M.10
-
19
-
-
9044240641
-
Molekularbiologie in der medizinischen Diagnostik
-
Springer Verlag; Berlin, Heidelberg, New York
-
Mannhalter C, Huber H, Löffler H, Faber V. Molekularbiologie in der medizinischen Diagnostik. In "Methoden der diagnostischen Hämatologie". Springer Verlag; Berlin, Heidelberg, New York 1994; 215-261.
-
(1994)
Methoden der Diagnostischen Hämatologie
, pp. 215-261
-
-
Mannhalter, C.1
Huber, H.2
Löffler, H.3
Faber, V.4
-
20
-
-
0028037137
-
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 P, 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.2
He, X.3
Dahlbäck, B.4
-
21
-
-
0024507770
-
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: 712-7.
-
(1989)
Blood
, vol.73
, pp. 712-717
-
-
Bovill, E.G.1
Bauer, K.A.2
Dickerman, J.D.3
Callas, P.4
West, B.5
-
22
-
-
0028908094
-
The management of thrombosis in the anti-phospholipid-antibody syndrome
-
Khamashta MA, Cuadrano MJ, Mujic F, Taub NA, Hunt BJ, Hughes GR. The management of thrombosis in the anti-phospholipid-antibody syndrome. N Engl J Med 1995; 332 (15): 993-7.
-
(1995)
N Engl J Med
, vol.332
, Issue.15
, pp. 993-997
-
-
Khamashta, M.A.1
Cuadrano, M.J.2
Mujic, F.3
Taub, N.A.4
Hunt, B.J.5
Hughes, G.R.6
-
23
-
-
0021166727
-
Impaired fibrinolytic capacity predisposes for recurrence of venous thrombosis
-
Korninger C, Lechner K, Niessner H, Gössinger H, Kundi M. Impaired fibrinolytic capacity predisposes for recurrence of venous thrombosis. Thromb Haemost 1984; 52 (2): 127-30.
-
(1984)
Thromb Haemost
, vol.52
, Issue.2
, pp. 127-130
-
-
Korninger, C.1
Lechner, K.2
Niessner, H.3
Gössinger, H.4
Kundi, M.5
-
24
-
-
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, Läfars G, Nicol P, Loogna E, Svensson E, Ljungeberg B, Walter H, Viering S, Nordlander S, Leijd B, Jönsson KA, Hlorth M, Linder O, Borberg J and the duration of anticoagulant 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
Läfars, G.5
Nicol, P.6
Loogna, E.7
Svensson, E.8
Ljungeberg, B.9
Walter, H.10
Viering, S.11
Nordlander, S.12
Leijd, B.13
Jönsson, K.A.14
Hlorth, M.15
Linder, O.16
Borberg, J.17
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