-
1
-
-
0002350130
-
Familial venous thrombophilia
-
Bloom AL et al., eds. Edinburgh, Churchill Livingstone
-
Allaart CF, Briet E. Familial venous thrombophilia. In: Bloom AL et al., eds. Haemostasis and thrombosis. Edinburgh, Churchill Livingstone, 1994: 1349-1360.
-
(1994)
Haemostasis and Thrombosis
, pp. 1349-1360
-
-
Allaart, C.F.1
Briet, E.2
-
2
-
-
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, 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. Proceedings of the National Academy of Sciences of the United States of America, 1993, 90: 1004-1008.
-
(1993)
Proceedings of the National Academy of Sciences of the United States of America
, vol.90
, pp. 1004-1008
-
-
Dahlback, B.1
Carlsson, M.2
Svensson, P.J.3
-
3
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature, 1994, 369: 64-67.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
-
4
-
-
0028931717
-
High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance)
-
Rosendaal FR et al. High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance). Blood, 1995, 85: 1504-1508.
-
(1995)
Blood
, vol.85
, pp. 1504-1508
-
-
Rosendaal, F.R.1
-
5
-
-
0028243401
-
Association of idiopathic venous thromboembolism with single point-mutation at Arg506 of factor V
-
Voorberg J et al. Association of idiopathic venous thromboembolism with single point-mutation at Arg506 of factor V. Lancet, 1994, 343: 1535-1536.
-
(1994)
Lancet
, vol.343
, pp. 1535-1536
-
-
Voorberg, J.1
-
6
-
-
0027081969
-
Pleiotropic effects of antithrombin strand 1C substitution mutations
-
Lane DA et al. Pleiotropic effects of antithrombin strand 1C substitution mutations. Journal of clinical investigation, 1992, 90: 2422-2433.
-
(1992)
Journal of Clinical Investigation
, vol.90
, pp. 2422-2433
-
-
Lane, D.A.1
-
7
-
-
0027291270
-
Antithrombin III mutation database: First update
-
Lane DA et al. Antithrombin III mutation database: first update. Thrombosis and haemostasis, 1993, 70: 361-369.
-
(1993)
Thrombosis and Haemostasis
, vol.70
, pp. 361-369
-
-
Lane, D.A.1
-
8
-
-
0010736777
-
Different prevalence of thromboembolism in the subtypes of congenital antithrombin III deficiency: Review of 404 cases
-
Finazzi G, Caccia R, Barbui T. Different prevalence of thromboembolism in the subtypes of congenital antithrombin III deficiency: review of 404 cases. Thrombosis and haemostasis, 1987, 58: 1094.
-
(1987)
Thrombosis and Haemostasis
, vol.58
, pp. 1094
-
-
Finazzi, G.1
Caccia, R.2
Barbui, T.3
-
9
-
-
0028228952
-
(ATT) trinucleotide repeats in the antithrombin gene and their use in determining the origin of repeated mutations
-
Olds RJ et al. (ATT) trinucleotide repeats in the antithrombin gene and their use in determining the origin of repeated mutations. Human mutation, 1994, 4: 31-41.
-
(1994)
Human Mutation
, vol.4
, pp. 31-41
-
-
Olds, R.J.1
-
10
-
-
0029043736
-
Protein C deficiency: A database of mutations, 1995 update
-
Reitsma PH et al. Protein C deficiency: a database of mutations, 1995 update. Thrombosis and haemostasis, 1995, 73: 876-889.
-
(1995)
Thrombosis and Haemostasis
, vol.73
, pp. 876-889
-
-
Reitsma, P.H.1
-
11
-
-
0029125979
-
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. Thrombosis and haemostasis, 1995, 74: 81-89.
-
(1995)
Thrombosis and Haemostasis
, vol.74
, pp. 81-89
-
-
Aiach, M.1
Gandrille, S.2
Emmerich, J.3
-
12
-
-
1842349339
-
Molecular defects responsible for type I and IIa protein S (PS) deficiencies in a panel of 120 French families
-
Borgel D et al. Molecular defects responsible for type I and IIa protein S (PS) deficiencies in a panel of 120 French families. Thrombosis and haemostasis, 1995, 73: 1256.
-
(1995)
Thrombosis and Haemostasis
, vol.73
, pp. 1256
-
-
Borgel, D.1
-
14
-
-
0029060076
-
Identification of eight point mutations in protein S deficiency type I - Analysis of 15 pedigrees
-
Gomez E et al. Identification of eight point mutations in protein S deficiency type I - analysis of 15 pedigrees. Thrombosis and haemostasis, 1995, 73: 750-755.
-
(1995)
Thrombosis and Haemostasis
, vol.73
, pp. 750-755
-
-
Gomez, E.1
-
15
-
-
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. 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, 1995, 85: 130-138.
-
(1995)
Blood
, vol.85
, pp. 130-138
-
-
Gandrille, S.1
-
16
-
-
0027953010
-
Protein S Tokushima: Abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S
-
Hayashi T et al. Protein S Tokushima: abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S. Blood, 1994, 83: 683-690.
-
(1994)
Blood
, vol.83
, pp. 683-690
-
-
Hayashi, T.1
-
17
-
-
0028290275
-
Factor V and protein S as synergistic cofactors to activated protein C in degradation of factor Villa
-
Shen L, Dahlback B. Factor V and protein S as synergistic cofactors to activated protein C in degradation of factor Villa. Journal of biological chemistry, 1994, 269: 18735-18738.
-
(1994)
Journal of Biological Chemistry
, vol.269
, pp. 18735-18738
-
-
Shen, L.1
Dahlback, B.2
-
18
-
-
0001978360
-
The physiology and biochemistry of factor V
-
Bloom AL et al., eds. Edinburgh, Churchill Livingstone
-
Jenny RJ, Tracy PB, Mann KG. The physiology and biochemistry of factor V. In: Bloom AL et al., eds. Haemostasis and thrombosis. Edinburgh, Churchill Livingstone, 1994: 465-476.
-
(1994)
Haemostasis and Thrombosis
, pp. 465-476
-
-
Jenny, R.J.1
Tracy, P.B.2
Mann, K.G.3
-
19
-
-
0028352460
-
Activated protein C resistance caused by Arg506Gln mutation in factor Va
-
Greengard JS et al. Activated protein C resistance caused by Arg506Gln mutation in factor Va. Lancet, 1994, 343: 1361-1362.
-
(1994)
Lancet
, vol.343
, pp. 1361-1362
-
-
Greengard, J.S.1
-
20
-
-
0028810738
-
World distribution of factor V Leiden
-
Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet, 1995, 346: 1133-1334.
-
(1995)
Lancet
, vol.346
, pp. 1133-1334
-
-
Rees, D.C.1
Cox, M.2
Clegg, J.B.3
-
21
-
-
0028954459
-
The first mutation identified in the thrombomodulin gene in a 45-year-old man presenting with thromboembolic disease
-
Ohlin AK, Marlar RA. The first mutation identified in the thrombomodulin gene in a 45-year-old man presenting with thromboembolic disease. Blood, 1995, 85: 330-336.
-
(1995)
Blood
, vol.85
, pp. 330-336
-
-
Ohlin, A.K.1
Marlar, R.A.2
-
22
-
-
0028877613
-
Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen
-
Haverkate F, Samama M. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen. Thrombosis and haemostasis, 1995, 73: 151-161.
-
(1995)
Thrombosis and Haemostasis
, vol.73
, pp. 151-161
-
-
Haverkate, F.1
Samama, M.2
-
23
-
-
0028335097
-
High prevalence of hyperhomocysteinemia in patients with juvenile venous thrombosis
-
Falcon CR et al. High prevalence of hyperhomocysteinemia in patients with juvenile venous thrombosis. Arteriosclerosis and thrombosis, 1994, 14: 1080-1083.
-
(1994)
Arteriosclerosis and Thrombosis
, vol.14
, pp. 1080-1083
-
-
Falcon, C.R.1
-
24
-
-
0000638414
-
A natural anticoagulant pathway: Protein C, S, C4b-binding protein and thrombomodulin
-
Bloom AL et al., eds. Edinburgh, Churchill Livingstone
-
Dahlback B, Stenflo J. A natural anticoagulant pathway: protein C, S, C4b-binding protein and thrombomodulin. In: Bloom AL et al., eds. Haemostasis and thrombosis. Edinburgh, Churchill Livingstone, 1994: 671-698.
-
(1994)
Haemostasis and Thrombosis
, pp. 671-698
-
-
Dahlback, B.1
Stenflo, J.2
-
25
-
-
0023932304
-
Familial plasminogen deficiency and thromboembolism
-
Dolan G, Preston FE. Familial plasminogen deficiency and thromboembolism. Fibrinolysis, 1988, 2 (suppl. 2): 26-34.
-
(1988)
Fibrinolysis
, vol.2
, Issue.2 SUPPL.
, pp. 26-34
-
-
Dolan, G.1
Preston, F.E.2
-
26
-
-
0023818347
-
The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous throm-bosis
-
Gladson CL et al. The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous throm-bosis. Thrombosis and haemostasis, 1988, 59: 18-22.
-
(1988)
Thrombosis and Haemostasis
, vol.59
, pp. 18-22
-
-
Gladson, C.L.1
-
27
-
-
1842389053
-
Plasminogen levels and putative prevalence of deficiency in 4500 blood donors
-
Tait RC et al. Plasminogen levels and putative prevalence of deficiency in 4500 blood donors. British journal of haematology, 1991, 77 (suppl. 1): 10.
-
(1991)
British Journal of Haematology
, vol.77
, Issue.1 SUPPL.
, pp. 10
-
-
Tait, R.C.1
-
28
-
-
0019174107
-
Isolation and characterization of a human plasma protein with affinity for the lysine binding sites in plasminogen. Role in the regulation of fibrinolysis and identification as histidine rich glycoprotein
-
Lijnen HR, Hoylaerts M, Collen D. Isolation and characterization of a human plasma protein with affinity for the lysine binding sites in plasminogen. Role in the regulation of fibrinolysis and identification as histidine rich glycoprotein. Journal of biological chemistry, 1980, 255: 10214-10222.
-
(1980)
Journal of Biological Chemistry
, vol.255
, pp. 10214-10222
-
-
Lijnen, H.R.1
Hoylaerts, M.2
Collen, D.3
-
29
-
-
0023612120
-
Familial elevation of plasma histidine-rich glycoprotein in a family with thrombophilia
-
Engesser L et al. Familial elevation of plasma histidine-rich glycoprotein in a family with thrombophilia. British journal of haematology, 1987, 67: 355-358.
-
(1987)
British Journal of Haematology
, vol.67
, pp. 355-358
-
-
Engesser, L.1
-
30
-
-
0027535155
-
High levels of histidine-rich glycoprotein and thrombotic diathesis. Report of two unrelated families
-
Castaman G et al. High levels of histidine-rich glycoprotein and thrombotic diathesis. Report of two unrelated families. Thrombosis research, 1993, 69: 279-305.
-
(1993)
Thrombosis Research
, vol.69
, pp. 279-305
-
-
Castaman, G.1
-
31
-
-
0028814316
-
Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep vein thrombosis
-
Koster T et al. Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep vein thrombosis. Lancet, 1995, 345: 152-155.
-
(1995)
Lancet
, vol.345
, pp. 152-155
-
-
Koster, T.1
-
32
-
-
0027428481
-
Anticoagulant protein C pathway defective in majority of thrombophilic patients
-
Griffin JH et al. Anticoagulant protein C pathway defective in majority of thrombophilic patients. Blood, 1993, 82: 1989-1993.
-
(1993)
Blood
, vol.82
, pp. 1989-1993
-
-
Griffin, J.H.1
-
33
-
-
0000352678
-
Prevalence of antithrombin III deficiency subtypes in 4000 healthy blood donors
-
Tait RC et al. Prevalence of antithrombin III deficiency subtypes in 4000 healthy blood donors. Thrombosis and haemostasis, 1991, 65: 839.
-
(1991)
Thrombosis and Haemostasis
, vol.65
, pp. 839
-
-
Tait, R.C.1
-
34
-
-
0028851046
-
Prevalence of protein C deficiency in the healthy population
-
Tait RC et al. Prevalence of protein C deficiency in the healthy population. Thrombosis and haemostasis, 1995, 73: 87-93.
-
(1995)
Thrombosis and Haemostasis
, vol.73
, pp. 87-93
-
-
Tait, R.C.1
-
35
-
-
0023233223
-
Absence of thrombosis in subjects with heterozygous protein C deficiency
-
Miletich J, Sherman L, Broze G, Jr. Absence of thrombosis in subjects with heterozygous protein C deficiency. New England journal of medicine, 1987, 317: 991-996.
-
(1987)
New England Journal of Medicine
, vol.317
, pp. 991-996
-
-
Miletich, J.1
Sherman, L.2
Broze Jr., G.3
-
36
-
-
0028098210
-
Resistance to activated protein C as a basis for venous thrombosis
-
Svensson PJ, Dahlback B. Resistance to activated protein C as a basis for venous thrombosis. New England journal of medicine, 1994, 330: 517-522.
-
(1994)
New England Journal of Medicine
, vol.330
, pp. 517-522
-
-
Svensson, P.J.1
Dahlback, B.2
-
37
-
-
0028910906
-
Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction
-
Ridker PM et al. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction. New England journal of medicine, 1995, 332: 912-917.
-
(1995)
New England Journal of Medicine
, vol.332
, pp. 912-917
-
-
Ridker, P.M.1
-
38
-
-
0027520285
-
Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study
-
Koster T et al. Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study. Lancet, 1993, 342: 1503-1506.
-
(1993)
Lancet
, vol.342
, pp. 1503-1506
-
-
Koster, T.1
-
39
-
-
0028008773
-
Different incidence of venous thrombosis in patients with inherited deficiencies of antithrombin III, protein C and protein S
-
Finazzi G, Barbui T. Different incidence of venous thrombosis in patients with inherited deficiencies of antithrombin III, protein C and protein S. Thrombosis and haemostasis, 1994, 71: 15-18.
-
(1994)
Thrombosis and Haemostasis
, vol.71
, pp. 15-18
-
-
Finazzi, G.1
Barbui, T.2
-
40
-
-
0027971225
-
Clinical manifestations and management of inherited thrombophilia: Retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein S
-
De Stefano V et al. Clinical manifestations and management of inherited thrombophilia: retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein S. Thrombosis and haemostasis, 1994, 72: 352-358.
-
(1994)
Thrombosis and Haemostasis
, vol.72
, pp. 352-358
-
-
De Stefano, V.1
-
41
-
-
0002096711
-
Hereditary protein S deficiency
-
Bertina RM, ed. Edinburgh, Churchill Livingstone
-
Briet E, Broekmans AW. Hereditary protein S deficiency. In: Bertina RM, ed. Protein C and related proteins. Edinburgh, Churchill Livingstone, 1988: 203-212.
-
(1988)
Protein C and Related Proteins
, pp. 203-212
-
-
Briet, E.1
Broekmans, A.W.2
-
42
-
-
0000581205
-
Hereditary protein C deficiency
-
Bertina RM, ed. Edinburgh, Churchill Livingstone
-
Broekmans AW, Conard J. Hereditary protein C deficiency. In: Bertina RM, ed. Protein C and related proteins. Edinburgh, Churchill Livingstone, 1988: 160-202.
-
(1988)
Protein C and Related Proteins
, pp. 160-202
-
-
Broekmans, A.W.1
Conard, J.2
-
43
-
-
0027076617
-
Thrombosis in antithrombin-III-deficient persons. Report of a large kindred and literature review
-
Demers C et al. Thrombosis in antithrombin-III-deficient persons. Report of a large kindred and literature review. Annals of internal medicine, 1992, 116: 754-761.
-
(1992)
Annals of Internal Medicine
, vol.116
, pp. 754-761
-
-
Demers, C.1
-
44
-
-
0028037137
-
Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C
-
Zoller B et al. Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C. Journal of clinical investigation, 1994, 94: 2521-2524.
-
(1994)
Journal of Clinical Investigation
, vol.94
, pp. 2521-2524
-
-
Zoller, B.1
-
45
-
-
0028364515
-
Thrombosis during pregnancy and surgery in patients with congenital deficiency of antithrombin III, protein C, protein S
-
De Stefano V et al. Thrombosis during pregnancy and surgery in patients with congenital deficiency of antithrombin III, protein C, protein S. Thrombosis and haemostasis, 1994, 71: 799-800.
-
(1994)
Thrombosis and Haemostasis
, vol.71
, pp. 799-800
-
-
De Stefano, V.1
-
46
-
-
0029057110
-
Thrombotic risk during pregnancy and puerperium in women with APC-resistance. Effective subcutaneous heparin in prophylaxis in a pregnant patient
-
De Stefano V et al. Thrombotic risk during pregnancy and puerperium in women with APC-resistance. Effective subcutaneous heparin in prophylaxis in a pregnant patient. Thrombosis and haemostasis, 1995, 74: 793-794.
-
(1995)
Thrombosis and Haemostasis
, vol.74
, pp. 793-794
-
-
De Stefano, V.1
-
47
-
-
0028083284
-
Homozygous antithrombin deficiency: Report of two new cases (99Leuto Phe) associated with arterial and venous thrombosis
-
Chowdhury V et al. Homozygous antithrombin deficiency: report of two new cases (99Leuto Phe) associated with arterial and venous thrombosis. Thrombosis and haemostasis, 1994, 72: 198-202.
-
(1994)
Thrombosis and Haemostasis
, vol.72
, pp. 198-202
-
-
Chowdhury, V.1
-
48
-
-
0001924054
-
Two cases of homozygous antithrombin III deficiency in a family with congenital deficiency of ATIII
-
Senzinger H, Vinazzer H, eds. Schmitt & Meyer GmbH, Würzburg
-
Hakten et al. Two cases of homozygous antithrombin III deficiency in a family with congenital deficiency of ATIII. In: Senzinger H, Vinazzer H, eds. Thrombosis and haemorrhagic disorders. Schmitt & Meyer GmbH, Würzburg, 1989: 177-181.
-
(1989)
Thrombosis and Haemorrhagic Disorders
, pp. 177-181
-
-
Hakten1
-
49
-
-
0025269656
-
Asymptomatic homozygous protein C deficiency
-
Tripodi A et al. Asymptomatic homozygous protein C deficiency. Acta haematologica, 1990, 83: 152-155.
-
(1990)
Acta Haematologica
, vol.83
, pp. 152-155
-
-
Tripodi, A.1
-
50
-
-
0025064295
-
Neonatal purpura fulminans associated with homozygous protein S deficiency
-
Mahasandana C et al. Neonatal purpura fulminans associated with homozygous protein S deficiency. Lancet, 1990, 335: 61-62.
-
(1990)
Lancet
, vol.335
, pp. 61-62
-
-
Mahasandana, C.1
-
51
-
-
0026022024
-
A standard heparin monogram for the management of heparin therapy
-
Cruickshank MK et al. A standard heparin monogram for the management of heparin therapy. Archives of internal medicine, 1991, 151: 333-337.
-
(1991)
Archives of Internal Medicine
, vol.151
, pp. 333-337
-
-
Cruickshank, M.K.1
-
52
-
-
0027517894
-
The weight-based heparin dosing nomogram compared with a standard care nomogram
-
Raschke RA et al. The weight-based heparin dosing nomogram compared with a standard care nomogram. Annals of internal medicine, 1993, 199: 874-881.
-
(1993)
Annals of Internal Medicine
, vol.199
, pp. 874-881
-
-
Raschke, R.A.1
-
53
-
-
0024418642
-
Clinical experiences with antithrombin III concentrate in treatment of congenital and acquired deficiency of antithrombin
-
Schwartz RS et al. Clinical experiences with antithrombin III concentrate in treatment of congenital and acquired deficiency of antithrombin. American journal of medicine, 1989, 87: 53S-60S.
-
(1989)
American Journal of Medicine
, vol.87
-
-
Schwartz, R.S.1
-
54
-
-
0029021115
-
A comparison of six weeks with six months of oral anticoagulation after a first episode of venous thromboembolism
-
Schulman S et al. A comparison of six weeks with six months of oral anticoagulation after a first episode of venous thromboembolism. New England journal of medicine, 1995, 332: 1661-1665.
-
(1995)
New England Journal of Medicine
, vol.332
, pp. 1661-1665
-
-
Schulman, S.1
-
55
-
-
0029059797
-
Optimal duration of oral anticoagulant therapy: A randomised trial comparing four weeks with three months of warfarin in patients with proximal deep venous thrombosis
-
Levine MN, Hirsh J, Gent M. Optimal duration of oral anticoagulant therapy: a randomised trial comparing four weeks with three months of warfarin in patients with proximal deep venous thrombosis. Thrombosis and haemostasis, 1995, 74: 606-611.
-
(1995)
Thrombosis and Haemostasis
, vol.74
, pp. 606-611
-
-
Levine, M.N.1
Hirsh, J.2
Gent, M.3
-
56
-
-
0026573466
-
Estrogen replacement therapy and the risk of venous thrombosis
-
Devor M et al. Estrogen replacement therapy and the risk of venous thrombosis. American journal of medicine, 1992, 92: 275-285.
-
(1992)
American Journal of Medicine
, vol.92
, pp. 275-285
-
-
Devor, M.1
-
57
-
-
0025216068
-
Thrombosis and pregnancy in congenital deficiencies in at III, protein C or protein S: Study of 78 women
-
Conard J et al. Thrombosis and pregnancy in congenital deficiencies in AT III, protein C or protein S: study of 78 women. Thrombosis and haemostasis, 1990, 63: 319-320.
-
(1990)
Thrombosis and Haemostasis
, vol.63
, pp. 319-320
-
-
Conard, J.1
-
59
-
-
1842352327
-
Protein C (PC) and coumarin-induced skin necrosis
-
Broekmans AW et al. Protein C (PC) and coumarin-induced skin necrosis. Thrombosis research, 1986, 6: 137.
-
(1986)
Thrombosis Research
, vol.6
, pp. 137
-
-
Broekmans, A.W.1
-
60
-
-
0000771986
-
Warfarin-induced skin necrosis in a patient with protein S deficiency
-
Friedman KD et al. Warfarin-induced skin necrosis in a patient with protein S deficiency. Blood, 1986, 68 (suppl): 333a.
-
(1986)
Blood
, vol.68
, Issue.SUPPL.
-
-
Friedman, K.D.1
-
61
-
-
0027164283
-
Treatment of coumarin-induced skin necrosis with a monoclonal antibody purified protein C concentrate
-
Schramm W et al. Treatment of coumarin-induced skin necrosis with a monoclonal antibody purified protein C concentrate. Archives of dermatology, 1993, 129: 753-756.
-
(1993)
Archives of Dermatology
, vol.129
, pp. 753-756
-
-
Schramm, W.1
-
62
-
-
0022656222
-
Purpura fulminans in a Chinese boy with congenital protein C deficiency
-
Yuen P et al. Purpura fulminans in a Chinese boy with congenital protein C deficiency. Pediatrics, 1986, 77: 670-677.
-
(1986)
Pediatrics
, vol.77
, pp. 670-677
-
-
Yuen, P.1
-
63
-
-
85047692272
-
Decrease in protein C antigen and formation of an abnormal protein soon after starting oral anticoagulant therapy
-
Vigano et al. Decrease in protein C antigen and formation of an abnormal protein soon after starting oral anticoagulant therapy. British journal of haematology, 1984, 57: 213-220.
-
(1984)
British Journal of Haematology
, vol.57
, pp. 213-220
-
-
Vigano1
-
64
-
-
0025241268
-
Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep-vein thrombosis
-
Heijboer H et al. Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep-vein thrombosis. New England journal of medicine, 1990, 323: 1512-1516.
-
(1990)
New England Journal of Medicine
, vol.323
, pp. 1512-1516
-
-
Heijboer, H.1
-
65
-
-
0029033740
-
Protein C deficiency in a controlled series of unselected outpatients: An infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study)
-
Koster T et al. Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study). Blood, 1995, 85: 2756-2761.
-
(1995)
Blood
, vol.85
, pp. 2756-2761
-
-
Koster, T.1
-
66
-
-
0002521955
-
Thrombophilia: Its causes and a rough estimate of its prevalence
-
Briët E et al. Thrombophilia: its causes and a rough estimate of its prevalence. Thrombosis and haemostasis, 1987, 58: 39.
-
(1987)
Thrombosis and Haemostasis
, vol.58
, pp. 39
-
-
Briët, E.1
-
67
-
-
0003111160
-
Incidence of defective tPA release in 158 unrelated young patients with venous thrombosis in comparison to PC-, PS-, ATIII-, fibrinogen-, and plasminogen-deficiency
-
Scharrer I et al. Incidence of defective tPA release in 158 unrelated young patients with venous thrombosis in comparison to PC-, PS-, ATIII-, fibrinogen-, and plasminogen-deficiency. Thrombosis and haemostasis, 1987, 58: 72.
-
(1987)
Thrombosis and Haemostasis
, vol.58
, pp. 72
-
-
Scharrer, I.1
-
68
-
-
0024563172
-
The relative frequency of hereditary thrombotic disorders among 107 patients with thrombophilia in Israel
-
Ben Tal O, Zivelin A, Seligsohn U. The relative frequency of hereditary thrombotic disorders among 107 patients with thrombophilia in Israel. Thrombosis and haemostasis, 1989, 61: 50-54.
-
(1989)
Thrombosis and Haemostasis
, vol.61
, pp. 50-54
-
-
Ben Tal, O.1
Zivelin, A.2
Seligsohn, U.3
-
69
-
-
0025855781
-
Incidence and clinical characteristics of hereditary disorders associated with venous thrombosis
-
Tabernero MD et al. Incidence and clinical characteristics of hereditary disorders associated with venous thrombosis. American journal of hematology, 1991, 36: 249-254.
-
(1991)
American Journal of Hematology
, vol.36
, pp. 249-254
-
-
Tabernero, M.D.1
|