-
1
-
-
55949104988
-
Inherited antithrombin deficiency: A review
-
Patnaik MM, Moll S. Inherited antithrombin deficiency: a review. Haemophilia 2008; 14: 1229-1239.
-
(2008)
Haemophilia
, vol.14
, pp. 1229-1239
-
-
Patnaik, M.M.1
Moll, S.2
-
2
-
-
78649854595
-
Cerebral Venous Thrombosis During Pregnancy in the Setting of Type I Antithrombin Deficiency: Case Report and Literature Review
-
Sharpe CJ, Crowther MA, Webert KE, et al. Cerebral Venous Thrombosis During Pregnancy in the Setting of Type I Antithrombin Deficiency: Case Report and Literature Review. Transfus Med Rev 2011; 25: 61-65.
-
(2011)
Transfus Med Rev
, vol.25
, pp. 61-65
-
-
Sharpe, C.J.1
Crowther, M.A.2
Webert, K.E.3
-
3
-
-
0031042986
-
Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
-
Lane DA, Bayston T, Olds RJ, et al. Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 1997; 77: 197-211.
-
(1997)
Thromb Haemost
, vol.77
, pp. 197-211
-
-
Lane, D.A.1
Bayston, T.2
Olds, R.J.3
-
4
-
-
77449093217
-
Detection and characterization of large SERPINC1 deletions in type I inherited antithrombin deficiency
-
Picard V, Chen JM, Tardy B, et al. Detection and characterization of large SERPINC1 deletions in type I inherited antithrombin deficiency. Hum Genet 2010; 127: 45-53.
-
(2010)
Hum Genet
, vol.127
, pp. 45-53
-
-
Picard, V.1
Chen, J.M.2
Tardy, B.3
-
5
-
-
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. Thromb Haemost 1987; 18: 1094.
-
(1987)
Thromb Haemost
, vol.18
, pp. 1094
-
-
Finazzi, G.1
Caccia, R.2
Barbui, T.3
-
6
-
-
33745289474
-
Molecular bases of antithrombin deficiency: Twenty- two novel mutations in the antithrombin gene
-
Picard V, Nowak-Göttl U, Biron-Andreani C, et al. Molecular bases of antithrombin deficiency: twenty- two novel mutations in the antithrombin gene. Hum Mutat 2006; 27: 600.
-
(2006)
Hum Mutat
, vol.27
, pp. 600
-
-
Picard, V.1
Nowak-Göttl, U.2
Biron-Andreani, C.3
-
7
-
-
77949263452
-
Altered fibrin clot structure/function in patients with idiopathic venous thromboembolism and in their relatives
-
Undas A, Zawilska K, Ciesla-Dul M, et al. Altered fibrin clot structure/function in patients with idiopathic venous thromboembolism and in their relatives. Blood 2009; 114: 4272-4278.
-
(2009)
Blood
, vol.114
, pp. 4272-4278
-
-
Undas, A.1
Zawilska, K.2
Ciesla-Dul, M.3
-
8
-
-
12844278573
-
Reduced plasma fibrinolytic potential is a risk factor for venous thrombosis
-
Lisman T, de Groot PG, Meijers JCM, et al. Reduced plasma fibrinolytic potential is a risk factor for venous thrombosis. Blood 2005; 15: 1102-1105.
-
(2005)
Blood
, vol.15
, pp. 1102-1105
-
-
Lisman, T.1
de Groot, P.G.2
Meijers, J.C.M.3
-
9
-
-
0021916917
-
Antithrombin Milano: A new variant with monomeric and dimeric inactive antithrombin III
-
Wolf M, Boyer C, Tripodi A, et al. Antithrombin Milano: A new variant with monomeric and dimeric inactive antithrombin III. Blood 1985; 65: 496-500.
-
(1985)
Blood
, vol.65
, pp. 496-500
-
-
Wolf, M.1
Boyer, C.2
Tripodi, A.3
-
10
-
-
4444376338
-
Genetic and environmental determinants of fibrin structure and function: Relevance to clinical disease
-
Scott EM, Ariëns RA, Grant PJ. Genetic and environmental determinants of fibrin structure and function: relevance to clinical disease. Arterioscler Thromb Vasc Biol 2004; 24: 1558-1566.
-
(2004)
Arterioscler Thromb Vasc Biol
, vol.24
, pp. 1558-1566
-
-
Scott, E.M.1
Ariëns, R.A.2
Grant, P.J.3
-
11
-
-
34047229067
-
Thrombin generation and fibrin clot structure
-
Wolberg AS. Thrombin generation and fibrin clot structure. Blood Rev 2007; 21: 131-142.
-
(2007)
Blood Rev
, vol.21
, pp. 131-142
-
-
Wolberg, A.S.1
-
12
-
-
57549089843
-
Cellular procoagulant activity dictates clot structure and stability as a function of distance from the cell surface
-
Campbell RA, Overmyer KA, Bagnell R, et al. Cellular procoagulant activity dictates clot structure and stability as a function of distance from the cell surface. Arterioscler Thromb Vasc Biol 2008; 28: 2247-2254.
-
(2008)
Arterioscler Thromb Vasc Biol
, vol.28
, pp. 2247-2254
-
-
Campbell, R.A.1
Overmyer, K.A.2
Bagnell, R.3
-
13
-
-
0029842962
-
Proneness to formation of tight and rigid fibrin gel structures in men with myocardial infarction at a young age
-
Fatah K, Silveira A, Tornvall P, et al. Proneness to formation of tight and rigid fibrin gel structures in men with myocardial infarction at a young age. Thromb Haemost 1996; 76: 535-540.
-
(1996)
Thromb Haemost
, vol.76
, pp. 535-540
-
-
Fatah, K.1
Silveira, A.2
Tornvall, P.3
-
14
-
-
0028047592
-
Antithrombin- Gly 424 Arg: A novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosis
-
Jochmans K, Lissens W, Vervoort R, et al. Antithrombin- Gly 424 Arg: a novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosis. Blood 1994; 83: 146-151.
-
(1994)
Blood
, vol.83
, pp. 146-151
-
-
Jochmans, K.1
Lissens, W.2
Vervoort, R.3
-
15
-
-
0034757282
-
Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism
-
Kuhle S, Lane DA, Johamanns A, et al. Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism. Thromb Haemost 2001; 86: 1007-1011.
-
(2001)
Thromb Haemost
, vol.86
, pp. 1007-1011
-
-
Kuhle, S.1
Lane, D.A.2
Johamanns, A.3
-
16
-
-
62549106201
-
Antithrombin Cambridge II (A384S) supports a role for antithrombin deficiency in arterial thrombosis
-
Roldán V, Ordoñez A, Marín F, et al. Antithrombin Cambridge II (A384S) supports a role for antithrombin deficiency in arterial thrombosis. Thromb Haemost 2009; 101: 483-486.
-
(2009)
Thromb Haemost
, vol.101
, pp. 483-486
-
-
Roldán, V.1
Ordoñez, A.2
Marín, F.3
|