-
1
-
-
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. PNAS 1993; 90: 1004-8.
-
(1993)
PNAS
, vol.90
, pp. 1004-1008
-
-
Dahlbäck, B.1
Carlsson, M.2
Svensson, P.J.3
-
2
-
-
0027428481
-
Anticoagulant protein C pathway defective in majority of thrombophilic patients
-
Griffin JH, Evatt B, Wideman C, Fernández JA. 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
Fernández, J.A.4
-
3
-
-
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
-
4
-
-
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 1994; 342: 1503-6
-
(1994)
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
-
5
-
-
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
-
6
-
-
0028352460
-
Activated protein C resistance causes by Arg 506 Gln mutation in factor Va
-
Greengard JS, Sun X, Xu X, Fernandez JA, Griffin JH, Evatt B. Activated protein C resistance causes by Arg 506 Gln mutation in factor Va. Lancet 1994; 343: 1361-2.
-
(1994)
Lancet
, vol.343
, pp. 1361-1362
-
-
Greengard, J.S.1
Sun, X.2
Xu, X.3
Fernandez, J.A.4
Griffin, J.H.5
Evatt, B.6
-
7
-
-
0028243401
-
506 of factor V
-
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
-
8
-
-
0028910906
-
Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis 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 thrombosis 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
-
9
-
-
0028988219
-
Arg506Gln Factor V mutation (Factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction
-
Kontula K, Ylikorkala A, Miettinen H, Vuorio A, Kauppinen-Mäkelin R, Hämäläinen L, Palomäki H, Kaste M. Arg506Gln Factor V mutation (Factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction. Thromb Haemost 1995; 73: 558-60.
-
(1995)
Thromb Haemost
, vol.73
, pp. 558-560
-
-
Kontula, K.1
Ylikorkala, A.2
Miettinen, H.3
Vuorio, A.4
Kauppinen-Mäkelin, R.5
Hämäläinen, L.6
Palomäki, H.7
Kaste, M.8
-
10
-
-
0027447258
-
Inherited predisposition to Thrombosis
-
Miletich JP, Prescott SM, White R, Majerus PW, Bovill EG. Inherited predisposition to Thrombosis. Cell 1993;72:477-80.
-
(1993)
Cell
, vol.72
, pp. 477-480
-
-
Miletich, J.P.1
Prescott, S.M.2
White, R.3
Majerus, P.W.4
Bovill, E.G.5
-
11
-
-
0028931717
-
High risk of thrombosis in patients homozygous for factor V Leiden (Activated Protein C-resistance)
-
Rosendaal FR, Koster T, Vandenbroucke 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
Vandenbroucke, J.P.3
Reitsma, P.H.4
-
12
-
-
0028000665
-
Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
-
Koeleman BPC, Reitsma PH, Allaart 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
Allaart, C.F.3
Bertina, R.M.4
-
13
-
-
0027995518
-
Massive thrombosis of venous cerebral sinuses in a 2-year-old boy with a combined inherited deficiency of antithrombin III and protein C
-
Gouault-Heilmann M, Quetin P, Dreyfus M, Gandrille S, Emmerich J, Leroy-Matheron C, Guesnu M. Massive thrombosis of venous cerebral sinuses in a 2-year-old boy with a combined inherited deficiency of antithrombin III and protein C. Thromb Haemost 1994; 72: 782-6.
-
(1994)
Thromb Haemost
, vol.72
, pp. 782-786
-
-
Gouault-Heilmann, M.1
Quetin, P.2
Dreyfus, M.3
Gandrille, S.4
Emmerich, J.5
Leroy-Matheron, C.6
Guesnu, M.7
-
14
-
-
0028132903
-
Deficiency of both protein C and protein S in a family with ischaemic strokes in young adults
-
Köller H, Stoll G, Sitzer M, Burk M, Schöttler B, Freund H-J. Deficiency of both protein C and protein S in a family with ischaemic strokes in young adults. Neurology 1994; 44: 1238-40.
-
(1994)
Neurology
, vol.44
, pp. 1238-1240
-
-
Köller, H.1
Stoll, G.2
Sitzer, M.3
Burk, M.4
Schöttler, B.5
Freund, H.-J.6
-
15
-
-
0025898867
-
Two cases of inherited triple deficiency in a large kindred with thrombotic diathesis and deficiencies of antithrombin III, heparin cofactor II, protein C and protein S
-
Jobin F, Lessard M. Two cases of inherited triple deficiency in a large kindred with thrombotic diathesis and deficiencies of antithrombin III, heparin cofactor II, protein C and protein S. Thromb Haemost 1991; 66: 295-9.
-
(1991)
Thromb Haemost
, vol.66
, pp. 295-299
-
-
Jobin, F.1
Lessard, M.2
-
16
-
-
0021914307
-
Assignment of the human antithrombin III structural gene to chromosome 1q23-25
-
Bock SC, Harris JF, Balazs I, Trent JM. Assignment of the human antithrombin III structural gene to chromosome 1q23-25. Cytogenet Cell Genet 1985; 39: 67-9.
-
(1985)
Cytogenet Cell Genet
, vol.39
, pp. 67-69
-
-
Bock, S.C.1
Harris, J.F.2
Balazs, I.3
Trent, J.M.4
-
17
-
-
0026774858
-
A Comprehensive genetic linkage map of the human genome
-
NIH/CEPH Collaborative Mapping Group. A Comprehensive genetic linkage map of the human genome. Science 1992; 258: 67-86.
-
(1992)
Science
, vol.258
, pp. 67-86
-
-
-
18
-
-
0024015532
-
Localization of the gene encoding human factor V to chromosome 1q21-25
-
Wang H, Riddell DC, Guinto ER, MacGillivray RT, Hamerton JL. Localization of the gene encoding human factor V to chromosome 1q21-25. Genomics 1988; 2: 324-8.
-
(1988)
Genomics
, vol.2
, pp. 324-328
-
-
Wang, H.1
Riddell, D.C.2
Guinto, E.R.3
MacGillivray, R.T.4
Hamerton, J.L.5
-
19
-
-
0027081969
-
Pleiotropic effects of antithrombin strand 1 C substitution mutations
-
Lane DA, Olds RJ, Conard J, Boisclair M, Bock SC, Hultin M, Abildgaard U, Ireland H, Thompson E, Sas G, Horellou MH, Tamponi G, Thein SL. Pleiotropic effects of antithrombin strand 1 C substitution mutations. J Clin Invest 1992; 90: 2422-5.
-
(1992)
J Clin Invest
, vol.90
, pp. 2422-2425
-
-
Lane, D.A.1
Olds, R.J.2
Conard, J.3
Boisclair, M.4
Bock, S.C.5
Hultin, M.6
Abildgaard, U.7
Ireland, H.8
Thompson, E.9
Sas, G.10
Horellou, M.H.11
Tamponi, G.12
Thein, S.L.13
-
20
-
-
0010736777
-
Different prevalence of thromboembolism in the subtypes of congenital antithrombin II1I deficiency: Review of 404 cases
-
Finazzi G, Caccia R, Barbui T. Different prevalence of thromboembolism in the subtypes of congenital antithrombin II1I deficiency: review of 404 cases. Thromb Haemost 1987; 58: 1094.
-
(1987)
Thromb Haemost
, vol.58
, pp. 1094
-
-
Finazzi, G.1
Caccia, R.2
Barbui, T.3
-
21
-
-
0027076617
-
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
-
22
-
-
0027291270
-
Antithrombin III mutation database: First update
-
Lane DA, Olds RJ, Boisclair M, Chowdhury V, Thein SL, Cooper DN, Blajchman MA, Perry DJ, Emmerich J, Aiach M. Antithrombin III mutation database: First update. Thromb Haemost 1993; 70: 361-9.
-
(1993)
Thromb Haemost
, vol.70
, pp. 361-369
-
-
Lane, D.A.1
Olds, R.J.2
Boisclair, M.3
Chowdhury, V.4
Thein, S.L.5
Cooper, D.N.6
Blajchman, M.A.7
Perry, D.J.8
Emmerich, J.9
Aiach, M.10
-
23
-
-
0027983874
-
Hereditary antithrombin deficiency: Heterogeneity of the molecular basis and mortality in Dutch families
-
van Boven HH, Olds RJ, Thein SL, Reitsma PH, Lane DA, Briët E, Vandenbroucke JP, Rosendaal FR. Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch families. Blood 1994; 84: 4209-13.
-
(1994)
Blood
, vol.84
, pp. 4209-4213
-
-
Van Boven, H.H.1
Olds, R.J.2
Thein, S.L.3
Reitsma, P.H.4
Lane, D.A.5
Briët, E.6
Vandenbroucke, J.P.7
Rosendaal, F.R.8
-
24
-
-
0027274861
-
Identification of nine novel mutations in type I antithrombin deficiency by heteroduplex screening
-
Chowdhury V, Olds RJ, Lane DA, Conard J, Pabinger I, Ryan K, Bauer KA, Bhavnani M, Abildgaard U, Finazzi G, Castaman G, Mannucci PM, Thein SL. Identification of nine novel mutations in type I antithrombin deficiency by heteroduplex screening. Br J Haematol 1993; 84: 656-61.
-
(1993)
Br J Haematol
, vol.84
, pp. 656-661
-
-
Chowdhury, V.1
Olds, R.J.2
Lane, D.A.3
Conard, J.4
Pabinger, I.5
Ryan, K.6
Bauer, K.A.7
Bhavnani, M.8
Abildgaard, U.9
Finazzi, G.10
Castaman, G.11
Mannucci, P.M.12
Thein, S.L.13
-
25
-
-
0028083284
-
Homozygous antithrombin deficiency: Report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis
-
Chowdhury V, Lane DA, Mille B, Auberger K, Gaudenberger-Bachem S, Pabinger I, Olds RJ, Thein SL. Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis. Thromb Haemost 1994; 72: 198-202.
-
(1994)
Thromb Haemost
, vol.72
, pp. 198-202
-
-
Chowdhury, V.1
Lane, D.A.2
Mille, B.3
Auberger, K.4
Gaudenberger-Bachem, S.5
Pabinger, I.6
Olds, R.J.7
Thein, S.L.8
-
26
-
-
0024296277
-
The relationship between defective heparin cofactor activities and thrombotic phenomena in at III abnormalities
-
Girolami A, Lazzaro AR, Simioni P. The relationship between defective heparin cofactor activities and thrombotic phenomena in AT III abnormalities. Thromb Haemost 1988; 59: 121.
-
(1988)
Thromb Haemost
, vol.59
, pp. 121
-
-
Girolami, A.1
Lazzaro, A.R.2
Simioni, P.3
-
27
-
-
0028037137
-
Identification of the same factor V gene mutation in 47 of 50 thrombosis-prone families with inherited resistance to activated protein C
-
Zöller B, Svensson PJ, He X, Dahlbäck B. Identification of the same factor V gene mutation in 47 of 50 thrombosis-prone families with inherited resistance to activated protein C J Clin Invest 1994; 94: 2521.
-
(1994)
J Clin Invest
, vol.94
, pp. 2521
-
-
Zöller, B.1
Svensson, P.J.2
He, X.3
Dahlbäck, B.4
-
28
-
-
0006071953
-
Antithrombin Frankfurt 1. Arginine to cysteine substitution at the reactive site and formation of a variant antithrombin-albumin covalent complex
-
Ireland H, Lane DA, Thompson E, Olds R, Thein SL, Hach Wunderle V, Scharrer I. Antithrombin Frankfurt 1. arginine to cysteine substitution at the reactive site and formation of a variant antithrombin-albumin covalent complex. Thromb Haemost 1991; 65: 913.
-
(1991)
Thromb Haemost
, vol.65
, pp. 913
-
-
Ireland, H.1
Lane, D.A.2
Thompson, E.3
Olds, R.4
Thein, S.L.5
Hach Wunderle, V.6
Scharrer, I.7
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