-
2
-
-
10544253846
-
Inherited thrombophilia: Part 1
-
Lane, D.A. et al. (1996) Inherited thrombophilia: part 1, Thromb. Haemost. 76, 651-662
-
(1996)
Thromb. Haemost.
, vol.76
, pp. 651-662
-
-
Lane, D.A.1
-
3
-
-
0347516652
-
Inherited thrombophilia: Part 2
-
Lane, D.A. et al. (1996) Inherited thrombophilia: part 2, Thromb. Haemost. 76, 824-834
-
(1996)
Thromb. Haemost.
, vol.76
, pp. 824-834
-
-
Lane, D.A.1
-
4
-
-
0028246930
-
Clinical syndromes associated with lupus anticoagulants
-
Kampe, C.E. (1994) Clinical syndromes associated with lupus anticoagulants, Semin. Thromb. Hemost. 20, 16-26
-
(1994)
Semin. Thromb. Hemost.
, vol.20
, pp. 16-26
-
-
Kampe, C.E.1
-
5
-
-
0026760990
-
Deep-vein thrombosis and the incidence of subsequent symptomatic cancer
-
Prandoni, P. et al. (1992) Deep-vein thrombosis and the incidence of subsequent symptomatic cancer, New Engl. J. Med. 327, 1128-1133
-
(1992)
New Engl. J. Med.
, vol.327
, pp. 1128-1133
-
-
Prandoni, P.1
-
6
-
-
0028109413
-
Antithrombin: The principal inhibitor of thrombin
-
Olds, R.J. et al. (1994) Antithrombin: the principal inhibitor of thrombin, Semin. Thromb. Hemost. 20, 353-372
-
(1994)
Semin. Thromb. Hemost.
, vol.20
, pp. 353-372
-
-
Olds, R.J.1
-
7
-
-
0021914307
-
Assignment of the human antithrombin III structural gene to chromosome 1q23-25
-
Bock, S.C., Harris, J.F., Balazs, I. and Trent, J.M. (1985) Assignment of the human antithrombin III structural gene to chromosome 1q23-25, Cytogenet. Cell. Genet. 39, 67-69
-
(1985)
Cytogenet. Cell. Genet.
, vol.39
, pp. 67-69
-
-
Bock, S.C.1
Harris, J.F.2
Balazs, I.3
Trent, J.M.4
-
8
-
-
0025970806
-
Mortality in hereditary antithrombin-III deficiency - 1830 to 1989
-
Rosendaal, F.R. et al. (1991) Mortality in hereditary antithrombin-III deficiency - 1830 to 1989, Lancet 337, 260-262
-
(1991)
Lancet
, vol.337
, pp. 260-262
-
-
Rosendaal, F.R.1
-
9
-
-
0010736777
-
Different prevalence of thromboembolism in the subtypes of congenital antithrombin III deficiency: Review of 404 cases
-
Finazzi, G., Caccia, R. and Barbui, T. (1987) Different prevalence of thromboembolism in the subtypes of congenital antithrombin III deficiency: review of 404 cases, Thromb. Haemost. 58, 1094
-
(1987)
Thromb. Haemost.
, vol.58
, pp. 1094
-
-
Finazzi, G.1
Caccia, R.2
Barbui, T.3
-
10
-
-
0028083284
-
Homozygous antithrombin deficiency: Report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis
-
Chowdhury, V. et al. (1994) Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis, Thromb. Haemost. 72, 198-202
-
(1994)
Thromb. Haemost.
, vol.72
, pp. 198-202
-
-
Chowdhury, V.1
-
11
-
-
0002624539
-
Antithrombin and heparin
-
Carrell, R., Skinner, R., Wardell, M. and Whisstock, J. (1995) Antithrombin and heparin, Mol. Med. Today 1, 226-231
-
(1995)
Mol. Med. Today
, vol.1
, pp. 226-231
-
-
Carrell, R.1
Skinner, R.2
Wardell, M.3
Whisstock, J.4
-
12
-
-
0027081969
-
Pleiotropic effects of antithrombin strand 1C substitution mutations
-
Lane, D.A. et al. (1992) Pleiotropic effects of antithrombin strand 1C substitution mutations, J. Clin. Invest. 90, 2422-2433
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 2422-2433
-
-
Lane, D.A.1
-
13
-
-
0027291270
-
Antithrombin III mutation database: First update. for the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
-
Lane, D.A. et al. (1993) Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis, Thromb. Haemost. 70, 361-369
-
(1993)
Thromb. Haemost.
, vol.70
, pp. 361-369
-
-
Lane, D.A.1
-
14
-
-
0024532084
-
Sublocalization of the human protein C gene on chromosome 2q13-q14
-
Patracchini, P. et al. (1989) Sublocalization of the human protein C gene on chromosome 2q13-q14, Hum. Genet. 81, 191-192
-
(1989)
Hum. Genet.
, vol.81
, pp. 191-192
-
-
Patracchini, P.1
-
15
-
-
0029043736
-
Protein C deficiency: A database of mutations, 1995 update. on behalf of the Subcommittee on plasma coagulation inhibitors of the Scientific and Standardization Committee of the ISTH
-
Reitsma, P.H. et al. (1995) Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on plasma coagulation inhibitors of the Scientific and Standardization Committee of the ISTH, Thromb. Haemost. 73, 876-889
-
(1995)
Thromb. Haemost.
, vol.73
, pp. 876-889
-
-
Reitsma, P.H.1
-
16
-
-
0026722694
-
The effect of phospholipids, calcium ions and protein S on rate constants of human factor Va inactivation by activated human protein C
-
Bakker, H.M. et al. (1992) The effect of phospholipids, calcium ions and protein S on rate constants of human factor Va inactivation by activated human protein C, Eur. J. Biochem. 208, 171-178
-
(1992)
Eur. J. Biochem.
, vol.208
, pp. 171-178
-
-
Bakker, H.M.1
-
17
-
-
0029017118
-
Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease
-
Zoller, B., Garcia de Frutos, P. and Dahlback, B. (1995) Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease, Blood 85, 3524-3531
-
(1995)
Blood
, vol.85
, pp. 3524-3531
-
-
Zoller, B.1
Garcia De Frutos, P.2
Dahlback, B.3
-
18
-
-
85088086007
-
Genetic and phenotypic analysis of a large (122 member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes
-
in press
-
Simmonds, R.E. et al. Genetic and phenotypic analysis of a large (122 member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes, Blood (in press)
-
Blood
-
-
Simmonds, R.E.1
-
19
-
-
0027742936
-
Resistance to activated protein C in nine thrombophilic families: Interference in a protein S functional assay
-
Faioni, E.M. et al. (1993) Resistance to activated protein C in nine thrombophilic families: interference in a protein S functional assay, Thromb. Haemost. 70, 1067-1071
-
(1993)
Thromb. Haemost.
, vol.70
, pp. 1067-1071
-
-
Faioni, E.M.1
-
20
-
-
0028871033
-
Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene
-
Gandrille, S. et al. (1995) Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene. Blood 85, 130-138
-
(1995)
Blood
, vol.85
, pp. 130-138
-
-
Gandrille, S.1
-
21
-
-
0029060076
-
Identification of eight point mutations in protein S deficiency type I - Analysis of 15 pedigrees
-
Gomez, E., Poort, S.R., Bertina, R.M. and Reitsma, P.H. (1995) Identification of eight point mutations in protein S deficiency type I - analysis of 15 pedigrees, Thromb. Haemost. 73, 750-755
-
(1995)
Thromb. Haemost.
, vol.73
, pp. 750-755
-
-
Gomez, E.1
Poort, S.R.2
Bertina, R.M.3
Reitsma, P.H.4
-
22
-
-
23444453692
-
Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I
-
Reitsma, P.H., Ploos van Amstel, H. and Bertina, R.M. (1994) Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I, J. Clin. Invest. 93, 486-492
-
(1994)
J. Clin. Invest.
, vol.93
, pp. 486-492
-
-
Reitsma, P.H.1
Ploos Van Amstel, H.2
Bertina, R.M.3
-
23
-
-
0027465837
-
Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect
-
Allaart, C.F. et al. (1993) Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect, Lancet 341, 134-138
-
(1993)
Lancet
, vol.341
, pp. 134-138
-
-
Allaart, C.F.1
-
24
-
-
0024507770
-
The clinical spectrum of heterozygous protein C deficiency in a large New England kindred
-
Bovill, E.G. et al. (1989) The clinical spectrum of heterozygous protein C deficiency in a large New England kindred. Blood 73, 712-717
-
(1989)
Blood
, vol.73
, pp. 712-717
-
-
Bovill, E.G.1
-
25
-
-
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
-
Dahlback, B., Carlsson, M. and Svensson, P.J. (1993) 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. U. S. A. 90, 1004-1008
-
(1993)
Proc. Natl. Acad. Sci. U. S. A.
, vol.90
, pp. 1004-1008
-
-
Dahlback, B.1
Carlsson, M.2
Svensson, P.J.3
-
26
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina, R.M. et al. (1994) Mutation in blood coagulation factor V associated with resistance to activated protein C, Nature 369, 64-67
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
-
27
-
-
0029090538
-
APC-resistance and Mnl I genotype (Gln506) of coagulation factor V are rare in Japanese population
-
Takamiya, O., Ishida, F., Kodaira, H. and Kitano, K. (1995) APC-resistance and Mnl I genotype (Gln506) of coagulation factor V are rare in Japanese population, Thromb. Haemost. 74, 996
-
(1995)
Thromb. Haemost.
, vol.74
, pp. 996
-
-
Takamiya, O.1
Ishida, F.2
Kodaira, H.3
Kitano, K.4
-
28
-
-
0028810738
-
World distribution of factor V Leiden
-
Rees, D.C., Cox, M. and Clegg, J.B. (1995) World distribution of factor V Leiden, Lancet 346, 1133-1134
-
(1995)
Lancet
, vol.346
, pp. 1133-1134
-
-
Rees, D.C.1
Cox, M.2
Clegg, J.B.3
-
29
-
-
0027520285
-
Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study
-
Koster, T. et al. (1993) Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study, Lancet 342, 1503-1506
-
(1993)
Lancet
, vol.342
, pp. 1503-1506
-
-
Koster, T.1
-
30
-
-
0028931717
-
High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance)
-
Rosendaal, F.R., Koster, T., Vandenbroucke, J.P. and Reitsma, P.H. (1995) High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance). Blood 85, 1504-1508
-
(1995)
Blood
, vol.85
, pp. 1504-1508
-
-
Rosendaal, F.R.1
Koster, T.2
Vandenbroucke, J.P.3
Reitsma, P.H.4
-
31
-
-
0028814316
-
Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep vein thrombosis
-
Koster, T. et al. (1995) Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep vein thrombosis, Lancet 345, 152-155
-
(1995)
Lancet
, vol.345
, pp. 152-155
-
-
Koster, T.1
-
32
-
-
0025241268
-
Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep-vein thrombosis
-
Heijboer, H. et al. (1990) Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep-vein thrombosis. New Engl. J. Med. 323, 1512-1516
-
(1990)
New Engl. J. Med.
, vol.323
, pp. 1512-1516
-
-
Heijboer, H.1
-
33
-
-
0028029477
-
Increased risk of venous thrombosis in oral-contraceptive users who are carriers of factor V Leiden mutation
-
Vandenbroucke, J.P. et al. (1994) Increased risk of venous thrombosis in oral-contraceptive users who are carriers of factor V Leiden mutation, Lancet 344, 1453-1457
-
(1994)
Lancet
, vol.344
, pp. 1453-1457
-
-
Vandenbroucke, J.P.1
-
34
-
-
0023634855
-
Deficient t-PA release and elevated PA inhibitor levels in patients with spontaneous or recurrent deep venous thrombosis
-
Juhan, V.I. et al. (1987) Deficient t-PA release and elevated PA inhibitor levels in patients with spontaneous or recurrent deep venous thrombosis, Thromb. Haemost. 57, 67-72
-
(1987)
Thromb. Haemost.
, vol.57
, pp. 67-72
-
-
Juhan, V.I.1
-
35
-
-
0027311245
-
The two allele sequences of a common polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene respond differently to interleukin-1 in HepG2 cells
-
Dawson, S.J. et al. (1993) The two allele sequences of a common polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene respond differently to interleukin-1 in HepG2 cells, J. Biol. Chem. 268, 10739-10745
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 10739-10745
-
-
Dawson, S.J.1
-
36
-
-
0024246493
-
Thrombovascular disease and familial plasminogen deficiency: A report of three kindreds
-
Dolan, G., Greaves, M., Cooper, P. and Preston, F.E. (1988) Thrombovascular disease and familial plasminogen deficiency: a report of three kindreds, Br J. Haematol. 70, 417-421
-
(1988)
Br J. Haematol.
, vol.70
, pp. 417-421
-
-
Dolan, G.1
Greaves, M.2
Cooper, P.3
Preston, F.E.4
-
37
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst, P. et al. (1995) A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase, Nat. Genet. 10, 111-113
-
(1995)
Nat. Genet.
, vol.10
, pp. 111-113
-
-
Frosst, P.1
-
38
-
-
0028949953
-
Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?
-
den Heijer, M. et al. (1995) Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis? Lancet 345, 882-885
-
(1995)
Lancet
, vol.345
, pp. 882-885
-
-
Den Heijer, M.1
-
39
-
-
0029850530
-
A common genetic variation in the 3′ untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort, S., Rosendaal, F., Reitsma, P. and Bertina, R. (1996) A common genetic variation in the 3′ untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis, Blood 88, 3698-3703
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.1
Rosendaal, F.2
Reitsma, P.3
Bertina, R.4
-
40
-
-
0028000665
-
Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
-
Koeleman, B.P., Reitsma, P.H., Allaart, C.F. and Bertina, R.M. (1994) Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families. Blood 84, 1031-1035
-
(1994)
Blood
, vol.84
, pp. 1031-1035
-
-
Koeleman, B.P.1
Reitsma, P.H.2
Allaart, C.F.3
Bertina, R.M.4
-
41
-
-
0029016883
-
Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S
-
Zoller, B., Berntsdotter, A., Garcia de Frutos, P. and Dahlback, B. (1995) Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S, Blood 85, 3518-3523
-
(1995)
Blood
, vol.85
, pp. 3518-3523
-
-
Zoller, B.1
Berntsdotter, A.2
Garcia De Frutos, P.3
Dahlback, B.4
-
42
-
-
0029873817
-
Factor V Leiden (FVR506Q) in families with inherited antithrombin deficiency
-
van Boven, H.A. et al. (1996) Factor V Leiden (FVR506Q) in families with inherited antithrombin deficiency, Thromb. Haemost. 75, 417-421
-
(1996)
Thromb. Haemost.
, vol.75
, pp. 417-421
-
-
Van Boven, H.A.1
-
43
-
-
0029933176
-
Coexistence of hereditary homocystinuria and factor V Leiden - Effect on thrombosis
-
Mandel, H. et al. (1996) Coexistence of hereditary homocystinuria and factor V Leiden - effect on thrombosis. New Engl. J. Med. 334, 763-768
-
(1996)
New Engl. J. Med.
, vol.334
, pp. 763-768
-
-
Mandel, H.1
|