-
1
-
-
0033519051
-
Venous thrombosis: A multicausal disease
-
Rosendaal FR. Venous thrombosis: a multicausal disease. Lancet, 1999, 353:1167-73.
-
(1999)
Lancet
, vol.353
, pp. 1167-1173
-
-
Rosendaal, F.R.1
-
2
-
-
0028939318
-
Characterization of the molecular defect in factor V R506Q
-
Kalafatis M et al. Characterization of the molecular defect in factor V R506Q. Journal of biological chemistry, 1995, 270:4053-7.
-
(1995)
Journal of biological chemistry
, vol.270
, pp. 4053-4057
-
-
Kalafatis, M.1
-
3
-
-
25444438704
-
Completed three-dimensional model of human coagulation factor Va. Molecular dynamics simulations and structural analysis
-
Orban T, Kalafatis M, Gogonea V. Completed three-dimensional model of human coagulation factor Va. Molecular dynamics simulations and structural analysis. Biochemistry, 2005, 44:13082-90.
-
(2005)
Biochemistry
, vol.44
, pp. 13082-13090
-
-
Orban, T.1
Kalafatis, M.2
Gogonea, V.3
-
4
-
-
33750807530
-
Sequence variations within the genes related to hemostatic imbalance and their impact on coronary artery disease in Turkish population
-
Taymaz H et al. Sequence variations within the genes related to hemostatic imbalance and their impact on coronary artery disease in Turkish population. Thrombosis research, 2007, 119:55-62.
-
(2007)
Thrombosis research
, vol.119
, pp. 55-62
-
-
Taymaz, H.1
-
5
-
-
0034922928
-
Factor V R506Q mutation-Leiden: An independent risk factor for venous thrombosis but not coronary artery disease
-
Irani-Hakime N et al. Factor V R506Q mutation-Leiden: an independent risk factor for venous thrombosis but not coronary artery disease. Journal of thrombosis and thrombolysis, 2001, 11:111-6.
-
(2001)
Journal of thrombosis and thrombolysis
, vol.11
, pp. 111-116
-
-
Irani-Hakime, N.1
-
6
-
-
21644464818
-
Comparison of the prevalence of APC-resistance in vascular patients and in a normal population cohort in Western Germany
-
Aleksic M et al. Comparison of the prevalence of APC-resistance in vascular patients and in a normal population cohort in Western Germany. European journal of vascular and endovascular surgery, 2005, 30:160-3.
-
(2005)
European journal of vascular and endovascular surgery
, vol.30
, pp. 160-163
-
-
Aleksic, M.1
-
7
-
-
0036854180
-
Acquired and inherited thrombophilia in women with unexplained fetal losses
-
Alonso A et al. Acquired and inherited thrombophilia in women with unexplained fetal losses. American journal of obstetrics and gynaecology, 2002, 187:1337-42.
-
(2002)
American journal of obstetrics and gynaecology
, vol.187
, pp. 1337-1342
-
-
Alonso, A.1
-
8
-
-
33646446730
-
High frequency of thrombophilic disorders in women with recurrent fetal miscarriage
-
Onderoglu L et al. High frequency of thrombophilic disorders in women with recurrent fetal miscarriage. Clinical and experimental obstetrics & gynecology, 2006, 33:50-4.
-
(2006)
Clinical and experimental obstetrics & gynecology
, vol.33
, pp. 50-54
-
-
Onderoglu, L.1
-
10
-
-
26244460048
-
Factor V Leiden, prothrombin 20210, methylenetetrahydrofolate reductase 677T, and population genetics
-
Bauduer F, Lacombe D. Factor V Leiden, prothrombin 20210, methylenetetrahydrofolate reductase 677T, and population genetics. Molecular genetics and metabolism, 2005, 86:91-9.
-
(2005)
Molecular genetics and metabolism
, vol.86
, pp. 91-99
-
-
Bauduer, F.1
Lacombe, D.2
-
11
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic acids research, 1988, 16:1215.
-
(1988)
Nucleic acids research
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
12
-
-
0342437523
-
Factor V Leiden: Detection in whole blood by ASA PCR using an additional mismatch in antepenultimate position
-
Hezard N et al. Factor V Leiden: detection in whole blood by ASA PCR using an additional mismatch in antepenultimate position. Thrombosis research, 1997, 88:59-66.
-
(1997)
Thrombosis research
, vol.88
, pp. 59-66
-
-
Hezard, N.1
-
13
-
-
0023784942
-
The putative factor IX gene promoter in hemophilia B Leyden
-
Reitsma PH et al. The putative factor IX gene promoter in hemophilia B Leyden. Blood, 1988, 72:1074-6.
-
(1988)
Blood
, vol.72
, pp. 1074-1076
-
-
Reitsma, P.H.1
-
14
-
-
3042585338
-
Deep vein thrombosis and pulmonary embolism in two cohorts: The longitudinal investigation of thromboembolism etiology
-
Cushman M et al. Deep vein thrombosis and pulmonary embolism in two cohorts: the longitudinal investigation of thromboembolism etiology. American journal of medicine, 2004, 117:516-22.
-
(2004)
American journal of medicine
, vol.117
, pp. 516-522
-
-
Cushman, M.1
-
15
-
-
34250743644
-
Gain-of-function gene mutations and venous thromboembolism: Distinct roles in different clinical settings
-
Colaizzo D et al. Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings. Journal of medical genetics, 2007, 44:412-6.
-
(2007)
Journal of medical genetics
, vol.44
, pp. 412-416
-
-
Colaizzo, D.1
-
16
-
-
1442357145
-
Factor V Leiden and the risk for venous thromboembolism in the adult Danish population
-
Juul K et al. Factor V Leiden and the risk for venous thromboembolism in the adult Danish population. Annals of internal medicine, 2004, 140:330-7.
-
(2004)
Annals of internal medicine
, vol.140
, pp. 330-337
-
-
Juul, K.1
-
17
-
-
32144432660
-
Hereditary thrombophilia in ethnic Omani patients
-
Pathare A et al. Hereditary thrombophilia in ethnic Omani patients. American journal of haematology, 2006, 81:101-6.
-
(2006)
American journal of haematology
, vol.81
, pp. 101-106
-
-
Pathare, A.1
-
18
-
-
0033832644
-
Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population
-
Angchaisuksiri P et al. Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population. American journal of haematology, 2000, 65:119-22.
-
(2000)
American journal of haematology
, vol.65
, pp. 119-122
-
-
Angchaisuksiri, P.1
-
19
-
-
1842637226
-
Allelic frequency of the factor V Leiden mutation and of the prothrombin gene 20210A mutation in healthy Tunisian population
-
Bouaziz L et al. Allelic frequency of the factor V Leiden mutation and of the prothrombin gene 20210A mutation in healthy Tunisian population. Thrombosis and haemostasis, 2004, 91:824-5.
-
(2004)
Thrombosis and haemostasis
, vol.91
, pp. 824-825
-
-
Bouaziz, L.1
-
20
-
-
27944450847
-
Varied prevalence of factor V G1691A (Leiden) and prothrombin G20210A single nucleotide polymorphisms among Arabs
-
Almawi WY et al. Varied prevalence of factor V G1691A (Leiden) and prothrombin G20210A single nucleotide polymorphisms among Arabs. Journal of thrombosis and thrombolysis, 2005, 20:163-8.
-
(2005)
Journal of thrombosis and thrombolysis
, vol.20
, pp. 163-168
-
-
Almawi, W.Y.1
-
21
-
-
1842584394
-
Laboratory markers in the diagnosis of venous thromboembolism
-
Caprini JA et al. Laboratory markers in the diagnosis of venous thromboembolism. Circulation, 2004, 109:14-8.
-
(2004)
Circulation
, vol.109
, pp. 14-18
-
-
Caprini, J.A.1
-
23
-
-
33645555323
-
Multi-locus candidate gene polymorphisms and risk of myocardial infarction: A population-based, prospective genetic analysis
-
Zee RY et al. Multi-locus candidate gene polymorphisms and risk of myocardial infarction: a population-based, prospective genetic analysis. Journal of thrombosis and haemostasis, 2006, 4:341-8.
-
(2006)
Journal of thrombosis and haemostasis
, vol.4
, pp. 341-348
-
-
Zee, R.Y.1
-
24
-
-
27644456837
-
Arterial thrombosis associated with heterozygous factor V Leiden disorder, hyperhomocysteinemia, and peripheral arterial disease: Importance of synergistic factors
-
Page C et al. Arterial thrombosis associated with heterozygous factor V Leiden disorder, hyperhomocysteinemia, and peripheral arterial disease: importance of synergistic factors. Journal of vascular surgery, 2005, 42:1014-8.
-
(2005)
Journal of vascular surgery
, vol.42
, pp. 1014-1018
-
-
Page, C.1
|