-
1
-
-
0012829027
-
Gesammalte Abhandlungen zur wissenschaftlichen Medtzin
-
Virchow R. Gesammalte Abhandlungen zur wissenschaftlichen Medtzin. Medinger Sohn. 1856:219-732.
-
(1856)
Medinger Sohn
, pp. 219-732
-
-
Virchow, R.1
-
2
-
-
0034922804
-
An update on hypercoagulable disorders
-
Federman DG, Kirsner RS. An update on hypercoagulable disorders. Arch Intern Med. 2001;161:1051-1056.
-
(2001)
Arch Intern Med
, vol.161
, pp. 1051-1056
-
-
Federman, D.G.1
Kirsner, R.S.2
-
3
-
-
0035912152
-
Genetic susceptibility to venous thrombosis
-
Seligsohn U, Lubetsky A. Genetic susceptibility to venous thrombosis. N Engl J Med. 2001;344:1222-1231.
-
(2001)
N Engl J Med
, vol.344
, pp. 1222-1231
-
-
Seligsohn, U.1
Lubetsky, A.2
-
4
-
-
0028008663
-
Venous thromboembolic complications (VTE) in children: First analyses of the Canadian Registry of VTE
-
Andrew M, David M, Adams M, et al. Venous thromboembolic complications (VTE) in children: First analyses of the Canadian Registry of VTE. Blood. 1994;83:1251-1257.
-
(1994)
Blood
, vol.83
, pp. 1251-1257
-
-
Andrew, M.1
David, M.2
Adams, M.3
-
5
-
-
0029876985
-
Inherited thrombophilia: Pathogenesis, clinical syndromes, and management
-
De Stefano V, Finazzi G, Mannucci PM. Inherited thrombophilia: Pathogenesis, clinical syndromes, and management. Blood. 1996;87:3531-3544. Genetic susceptibility to venous thrombosis. N Engl J Med. 2001;344:1222-1231.
-
(1996)
Blood
, vol.87
, pp. 3531-3544
-
-
De Stefano, V.1
Finazzi, G.2
Mannucci, P.M.3
-
6
-
-
0035912152
-
Genetic susceptibility to venous thrombosis
-
De Stefano V, Finazzi G, Mannucci PM. Inherited thrombophilia: Pathogenesis, clinical syndromes, and management. Blood. 1996;87:3531-3544. Genetic susceptibility to venous thrombosis. N Engl J Med. 2001;344:1222-1231.
-
(2001)
N Engl J Med
, vol.344
, pp. 1222-1231
-
-
-
9
-
-
0028805001
-
Neonatal thrombosis: Report of a prospective Canadian and international registry
-
Schmidt B, Andrew M. Neonatal thrombosis: Report of a prospective Canadian and international registry. Pediatrics. 1995;96(5 Pt 1):939-943.
-
(1995)
Pediatrics
, vol.96
, Issue.5 PART 1
, pp. 939-943
-
-
Schmidt, B.1
Andrew, M.2
-
10
-
-
0035196351
-
Venous thromboembolism in childhood: A prospective two-year registry in the Netherlands
-
van Ommen CH, Heijboer H, Buller HR, et al. Venous thromboembolism in childhood: A prospective two-year registry in The Netherlands. J Pediatr. 2001;139:676-681.
-
(2001)
J Pediatr
, vol.139
, pp. 676-681
-
-
Van Ommen, C.H.1
Heijboer, H.2
Buller, H.R.3
-
11
-
-
0025266246
-
Development of the hemostatic system in the neonate and young infant
-
Andrew M, Paes B, Johnston M. Development of the hemostatic system in the neonate and young infant. Am J Pediatr Hematol Oncol. 1990;12:95-104.
-
(1990)
Am J Pediatr Hematol Oncol
, vol.12
, pp. 95-104
-
-
Andrew, M.1
Paes, B.2
Johnston, M.3
-
13
-
-
0037458240
-
Congenital thrombophilic states associated with venous thrombosis: A qualitative overview and proposed classification system
-
Crowther MA, Kelton JG. Congenital thrombophilic states associated with venous thrombosis: A qualitative overview and proposed classification system. Ann Intern Med. 2003;138:128-134.
-
(2003)
Ann Intern Med
, vol.138
, pp. 128-134
-
-
Crowther, M.A.1
Kelton, J.G.2
-
14
-
-
0030951829
-
Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism - Results of the Spanish Multicentric Study on Thrombophilia (EMET-Study)
-
Mateo J, Oliver A, Borrell M, et al. Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism - results of the Spanish Multicentric Study on Thrombophilia (EMET-Study). Thromb Haemost. 1997;77:444-451.
-
(1997)
Thromb Haemost
, vol.77
, pp. 444-451
-
-
Mateo, J.1
Oliver, A.2
Borrell, M.3
-
15
-
-
0033515068
-
G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men
-
Ridker PM, Hennekens CH, Miletich JP. G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men. Circulation. 1999;99:999-1004.
-
(1999)
Circulation
, vol.99
, pp. 999-1004
-
-
Ridker, P.M.1
Hennekens, C.H.2
Miletich, J.P.3
-
16
-
-
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. Thromb Haemost. 1989;61:50-54.
-
(1989)
Thromb Haemost
, vol.61
, pp. 50-54
-
-
Ben-Tal, O.1
Zivelin, A.2
Seligsohn, U.3
-
17
-
-
0028217433
-
Prevalence of antithrombin deficiency in healthy blood donors: A cross-sectional study
-
Wells PS, Blajchman MA, Henderson P, et al. Prevalence of antithrombin deficiency in healthy blood donors: A cross-sectional study. Am J Hematol. 1994;45:321-324.
-
(1994)
Am J Hematol
, vol.45
, pp. 321-324
-
-
Wells, P.S.1
Blajchman, M.A.2
Henderson, P.3
-
18
-
-
0028234593
-
Prevalence of antithrombin deficiency in the healthy population
-
Tait RC, Walker ID, Perry DJ, et al. Prevalence of antithrombin deficiency in the healthy population. Br J Haematol. 1994;87:106-112.
-
(1994)
Br J Haematol
, vol.87
, pp. 106-112
-
-
Tait, R.C.1
Walker, I.D.2
Perry, D.J.3
-
19
-
-
0028851046
-
Prevalence of protein C deficiency in the healthy population
-
Tait RC, Walker ID, Reitsma PH, et al. Prevalence of protein C deficiency in the healthy population. Thromb Haemost. 1995;73:87-93.
-
(1995)
Thromb Haemost
, vol.73
, pp. 87-93
-
-
Tait, R.C.1
Walker, I.D.2
Reitsma, P.H.3
-
20
-
-
0034006558
-
Studies on congenital protein C deficiency in Japanese: Prevalence, genetic analysis, and relevance to the onset of arterial occlusive diseases
-
Sakata T, Kario K, Katayama Y, et al. Studies on congenital protein C deficiency in Japanese: prevalence, genetic analysis, and relevance to the onset of arterial occlusive diseases. Semin Thromb Hemost. 2000;26:11-16.
-
(2000)
Semin Thromb Hemost
, vol.26
, pp. 11-16
-
-
Sakata, T.1
Kario, K.2
Katayama, Y.3
-
21
-
-
0026465569
-
Hereditary deficiency of antithrombin III, protein C and protein S: Prevalence in patients with a history of venous thrombosis and criteria for rational patient screening
-
Pabinger I, Brucker S, Kyrle PA, et al. Hereditary deficiency of antithrombin III, protein C and protein S: Prevalence in patients with a history of venous thrombosis and criteria for rational patient screening. Blood Coagul Fibrinolysis. 1992;3:547-553.
-
(1992)
Blood Coagul Fibrinolysis
, vol.3
, pp. 547-553
-
-
Pabinger, I.1
Brucker, S.2
Kyrle, P.A.3
-
22
-
-
0001627642
-
Inherited antithrombin deficiency causing thrombophilia
-
Egeberg O. Inherited antithrombin deficiency causing thrombophilia. Thromb Diath Haemorrh. 1965;13:516-530.
-
(1965)
Thromb Diath Haemorrh
, vol.13
, pp. 516-530
-
-
Egeberg, O.1
-
23
-
-
0028098218
-
Inherited resistance to activated protein C is corrected by anticoagulant cofactor activity found to be a property of factor V
-
21a. Dahlback B, Hildebrand B. Inherited resistance to activated protein C is corrected by anticoagulant cofactor activity found to be a property of factor V. Proc Natl Acad Sci USA. 1994;91:1396-1400.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 1396-1400
-
-
Dahlback, B.1
Hildebrand, B.2
-
24
-
-
0033586755
-
Activated protein C resistance and factor V Leiden mutation are independent risk factors for venous thromboembolism
-
Rodeghiero F, Tosetto A. Activated protein C resistance and factor V Leiden mutation are independent risk factors for venous thromboembolism. Ann Intern Med. 1999;130:643-650.
-
(1999)
Ann Intern Med
, vol.130
, pp. 643-650
-
-
Rodeghiero, F.1
Tosetto, A.2
-
25
-
-
0033028586
-
Hyperhomocysteinemia, atherosclerosis and thrombosis
-
Cattaneo M. Hyperhomocysteinemia, atherosclerosis and thrombosis. Thromb Haemost. 1999;81:165-176.
-
(1999)
Thromb Haemost
, vol.81
, pp. 165-176
-
-
Cattaneo, M.1
-
26
-
-
0032569645
-
Meta-analysis of hyperhomo cysteinemia as a risk factor for venous thromboembolic disease
-
Ray JG. Meta-analysis of hyperhomo cysteinemia as a risk factor for venous thromboembolic disease. Arch Intern Med. 1998;158:2101-2106.
-
(1998)
Arch Intern Med
, vol.158
, pp. 2101-2106
-
-
Ray, J.G.1
-
27
-
-
0029655724
-
Molecular genetic analysis in mild hyperhomocysteine-mia: A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease
-
Kluijtmans LA, van den Heuvel LP, Boers GH, et al. Molecular genetic analysis in mild hyperhomocysteine-mia: A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease. Am J Hum Genet. 1996;58:35-41.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 35-41
-
-
Kluijtmans, L.A.1
Van Den Heuvel, L.P.2
Boers, G.H.3
-
28
-
-
0030027668
-
Relation between folate status, a common mutation in methylenete- trahydrofolate reductase, and plasma homocysteine concentrations
-
Jacques PF, Bostom AG, Williams RR, et al. Relation between folate status, a common mutation in methylenete-trahydrofolate reductase, and plasma homocysteine concentrations. Circulation. 1996;93:7-9.
-
(1996)
Circulation
, vol.93
, pp. 7-9
-
-
Jacques, P.F.1
Bostom, A.G.2
Williams, R.R.3
-
29
-
-
0033817681
-
Hyperhomocysteinemia, vascular pathology, and endothelial dysfunction
-
van Guldener C, Stehouwer CD. Hyperhomocysteinemia, vascular pathology, and endothelial dysfunction. Semin Thromb Hemost. 2000;26:281-289.
-
(2000)
Semin Thromb Hemost
, vol.26
, pp. 281-289
-
-
Van Guldener, C.1
Stehouwer, C.D.2
-
30
-
-
0035014266
-
Homocysteine-induced endoplasmic reticulum stress causes dysregulation of the cholesterol and triglyceride biosynthetic pathways
-
Werstuck GH, Lentz SR, Dayal S, et al. Homocysteine-induced endoplasmic reticulum stress causes dysregulation of the cholesterol and triglyceride biosynthetic pathways. J Clin Invest. 2001;107:1263-1273.
-
(2001)
J Clin Invest
, vol.107
, pp. 1263-1273
-
-
Werstuck, G.H.1
Lentz, S.R.2
Dayal, S.3
-
31
-
-
0036786363
-
The incidence of venous thromboembolism in thrombophilic children: A prospective cohort study
-
Tormene D, Simioni P, Prandoni P, et al. The incidence of venous thromboembolism in thrombophilic children: A prospective cohort study. Blood. 2002;100:2403-2405.
-
(2002)
Blood
, vol.100
, pp. 2403-2405
-
-
Tormene, D.1
Simioni, P.2
Prandoni, P.3
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