-
1
-
-
0034628404
-
The challenge of thrombophilia in maternal-fetal medicine
-
Greer I.A. The challenge of thrombophilia in maternal-fetal medicine. N Engl J Med 342 (2000) 424-425
-
(2000)
N Engl J Med
, vol.342
, pp. 424-425
-
-
Greer, I.A.1
-
2
-
-
0021079081
-
Cerebral venous and arterial thrombosis in pregnancy and puerperium. A study of 135 patients
-
Srinivasan K. Cerebral venous and arterial thrombosis in pregnancy and puerperium. A study of 135 patients. Angiology 34 (1983) 731-746
-
(1983)
Angiology
, vol.34
, pp. 731-746
-
-
Srinivasan, K.1
-
3
-
-
0345062283
-
The prothrombin gene variant 20210A in venous and arterial thromboembolism
-
Vicente V., Gonzalez-Conejero R., Rivera J., et al. The prothrombin gene variant 20210A in venous and arterial thromboembolism. Haematologica 84 (1999) 356-362
-
(1999)
Haematologica
, vol.84
, pp. 356-362
-
-
Vicente, V.1
Gonzalez-Conejero, R.2
Rivera, J.3
-
4
-
-
0031981017
-
Geographic distribution of the 20210 G to A prothrombin variant
-
Rosendaal F.R., Doggen C.J., and Zivelin A. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 79 (1998) 706-708
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.2
Zivelin, A.3
-
5
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller S.A., Dykes D.D., and Polesky H.F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucl Acids Res 16 (1988) 1215
-
(1988)
Nucl Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
6
-
-
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.R., Rosendaal F.R., Reitsma P.H., et al. 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 (1996) 3698-3703
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
-
7
-
-
0036339190
-
Treatment of cerebral sinus/venous thrombosis
-
Nagaraja D., and Sarma G.R. Treatment of cerebral sinus/venous thrombosis. Neurol India 50 (2002) 114-116
-
(2002)
Neurol India
, vol.50
, pp. 114-116
-
-
Nagaraja, D.1
Sarma, G.R.2
-
8
-
-
0023230641
-
Nucleotide sequence of the gene for human prothrombin
-
Degan S.J.F., and Davie E.W. Nucleotide sequence of the gene for human prothrombin. Biochemistry 26 (1987) 6165
-
(1987)
Biochemistry
, vol.26
, pp. 6165
-
-
Degan, S.J.F.1
Davie, E.W.2
-
9
-
-
0034939628
-
Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing to hereditary thrombophilia
-
Gehring N.H., Frede U., Neu-Yilik G., et al. Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing to hereditary thrombophilia. Nat Genet 28 (2001) 389-392
-
(2001)
Nat Genet
, vol.28
, pp. 389-392
-
-
Gehring, N.H.1
Frede, U.2
Neu-Yilik, G.3
-
10
-
-
0034310731
-
Hyperprothrombinemia may result in acquired activated protein C resistance
-
Tripodi A., Chantarangkul V., Mannucci P.M., et al. Hyperprothrombinemia may result in acquired activated protein C resistance. Blood 96 (2000) 3295-3296
-
(2000)
Blood
, vol.96
, pp. 3295-3296
-
-
Tripodi, A.1
Chantarangkul, V.2
Mannucci, P.M.3
-
11
-
-
0030792668
-
The prothrombin gene G20210A variant: prevalence in a UK anticoagulant clinic population
-
Cumming A.M., Keeney S., Salden A., et al. The prothrombin gene G20210A variant: prevalence in a UK anticoagulant clinic population. Br J Haematol 98 (1997) 353-355
-
(1997)
Br J Haematol
, vol.98
, pp. 353-355
-
-
Cumming, A.M.1
Keeney, S.2
Salden, A.3
-
12
-
-
0032387846
-
Prevalence of the prothrombin 20210 G-to-A variant in blacks: infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects
-
Dilley A., Austin H., Hooper W.C., et al. Prevalence of the prothrombin 20210 G-to-A variant in blacks: infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects. J Lab Clin Med 132 (1998) 452-455
-
(1998)
J Lab Clin Med
, vol.132
, pp. 452-455
-
-
Dilley, A.1
Austin, H.2
Hooper, W.C.3
-
13
-
-
0031618374
-
Frequencies of prothrombin 20210 G → A mutation may be different among races-studies on Japanese populations with various forms of thrombotic disorders and healthy subjects
-
Isshiki I., Murata M., Watanabe R., et al. Frequencies of prothrombin 20210 G → A mutation may be different among races-studies on Japanese populations with various forms of thrombotic disorders and healthy subjects. Blood Coagul Fibrinolysis 9 (1998) 105-106
-
(1998)
Blood Coagul Fibrinolysis
, vol.9
, pp. 105-106
-
-
Isshiki, I.1
Murata, M.2
Watanabe, R.3
-
14
-
-
0030845360
-
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
-
Hillarp A., Zoller B., Svensson P.J., et al. The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis. Thromb Haemost 78 (1997) 990-992
-
(1997)
Thromb Haemost
, vol.78
, pp. 990-992
-
-
Hillarp, A.1
Zoller, B.2
Svensson, P.J.3
-
15
-
-
20044382874
-
Clinical manifestations of the prothrombin G20210A mutation in children: a pediatric coagulation consortium study
-
Young G., Manco-Johnson M., Gill J.C., et al. Clinical manifestations of the prothrombin G20210A mutation in children: a pediatric coagulation consortium study. J Thromb Haemost 1 (2003) 958-962
-
(2003)
J Thromb Haemost
, vol.1
, pp. 958-962
-
-
Young, G.1
Manco-Johnson, M.2
Gill, J.C.3
-
16
-
-
0031756655
-
Inherited prothrombotic risk factors and cerebral venous thrombosis
-
Hillier C.E., Collins P.W., Bowen D.J., et al. Inherited prothrombotic risk factors and cerebral venous thrombosis. QJM 91 (1998) 677-680
-
(1998)
QJM
, vol.91
, pp. 677-680
-
-
Hillier, C.E.1
Collins, P.W.2
Bowen, D.J.3
-
17
-
-
0033920794
-
G20210A PRTH gene mutation and other thrombophilic polymorphisms in cerebral venous thrombosis
-
Madonna P., de Stefano A., Coppola A., et al. G20210A PRTH gene mutation and other thrombophilic polymorphisms in cerebral venous thrombosis. Stroke 31 (2000) 1787-1788
-
(2000)
Stroke
, vol.31
, pp. 1787-1788
-
-
Madonna, P.1
de Stefano, A.2
Coppola, A.3
-
18
-
-
0032543748
-
High risk of cerebral-vein thrombosis in carriers of a prothrombin gene mutation and in users of oral contraceptives
-
Martinelli I., Sacchi E., Landi G., et al. High risk of cerebral-vein thrombosis in carriers of a prothrombin gene mutation and in users of oral contraceptives. N Engl J Med 338 (1998) 1793-1797
-
(1998)
N Engl J Med
, vol.338
, pp. 1793-1797
-
-
Martinelli, I.1
Sacchi, E.2
Landi, G.3
-
19
-
-
0031595694
-
Prothrombin gene G20210-A transition is a risk factor for cerebral venous thrombosis
-
Reuner K.H., Ruf A., Grau A., et al. Prothrombin gene G20210-A transition is a risk factor for cerebral venous thrombosis. Stroke 29 (1998) 1765-1769
-
(1998)
Stroke
, vol.29
, pp. 1765-1769
-
-
Reuner, K.H.1
Ruf, A.2
Grau, A.3
-
20
-
-
11444268843
-
Prothrombin G20210A mutation, and not factor V Leiden mutation, is a risk factor for cerebral venous thrombosis in Brazilian patients
-
Rodrigues C.A., Rocha L.K., Morelli V.M., et al. Prothrombin G20210A mutation, and not factor V Leiden mutation, is a risk factor for cerebral venous thrombosis in Brazilian patients. J Thromb Haemost 2 (2004) 1211-1212
-
(2004)
J Thromb Haemost
, vol.2
, pp. 1211-1212
-
-
Rodrigues, C.A.1
Rocha, L.K.2
Morelli, V.M.3
-
21
-
-
11444253333
-
Prothrombin 20210A and oral contraceptive use as risk factors for cerebral venous thrombosis
-
Gadelha T., Andre C., Juca A.A., et al. Prothrombin 20210A and oral contraceptive use as risk factors for cerebral venous thrombosis. Cerebrovasc Dis 19 (2005) 49-52
-
(2005)
Cerebrovasc Dis
, vol.19
, pp. 49-52
-
-
Gadelha, T.1
Andre, C.2
Juca, A.A.3
-
22
-
-
33644933673
-
Risk of cerebral venous thrombosis and novel gene polymorphisms of the coagulation and fibrinolytic systems
-
Lichy C., Dong-Si T., Reuner K., et al. Risk of cerebral venous thrombosis and novel gene polymorphisms of the coagulation and fibrinolytic systems. J Neurol 253 (2006) 16-20
-
(2006)
J Neurol
, vol.253
, pp. 16-20
-
-
Lichy, C.1
Dong-Si, T.2
Reuner, K.3
-
23
-
-
33645510408
-
Thrombophilic abnormalities, oral contraceptives and risk of cerebral vein thrombosis: a meta-analysis
-
Dentali F., Crowther M., and Dentali W.A. Thrombophilic abnormalities, oral contraceptives and risk of cerebral vein thrombosis: a meta-analysis. Blood 107 (2006) 2766-2773
-
(2006)
Blood
, vol.107
, pp. 2766-2773
-
-
Dentali, F.1
Crowther, M.2
Dentali, W.A.3
-
24
-
-
0031904536
-
Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis
-
Weih M., Mehraein S., Valdueza J.M., et al. Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis. Stroke 29 (1998) 1739-1740
-
(1998)
Stroke
, vol.29
, pp. 1739-1740
-
-
Weih, M.1
Mehraein, S.2
Valdueza, J.M.3
-
25
-
-
2442637355
-
Prothrombin 20210A is not prevalent in North India
-
Garewal G., Das R., Ahluwalia J., et al. Prothrombin 20210A is not prevalent in North India. J Thromb Haemost 1 (2003) 2253-2254
-
(2003)
J Thromb Haemost
, vol.1
, pp. 2253-2254
-
-
Garewal, G.1
Das, R.2
Ahluwalia, J.3
-
26
-
-
0035088186
-
Venous thromboembolism in young patients from western India: a study
-
Ghosh K., Shetty S., Madkaikar M., et al. Venous thromboembolism in young patients from western India: a study. Clin Appl Thromb Hemost 7 (2001) 158-165
-
(2001)
Clin Appl Thromb Hemost
, vol.7
, pp. 158-165
-
-
Ghosh, K.1
Shetty, S.2
Madkaikar, M.3
-
27
-
-
30644460368
-
Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis
-
Koshy A., and Jeyakumari M. Prothrombin G20210A gene variant is not associated with idiopathic portal vein thrombosis in an area endemic for portal vein thrombosis. Ann Hematol 85 (2006) 126-128
-
(2006)
Ann Hematol
, vol.85
, pp. 126-128
-
-
Koshy, A.1
Jeyakumari, M.2
-
28
-
-
22144472522
-
Prevalence of the Factor V G1691A and the Factor II/prothrombin G20210A gene polymorphisms among Tamilians
-
Angeline T., Bentley H.A., Hawk A.B., et al. Prevalence of the Factor V G1691A and the Factor II/prothrombin G20210A gene polymorphisms among Tamilians. Exp Mol Pathol 79 (2005) 9-13
-
(2005)
Exp Mol Pathol
, vol.79
, pp. 9-13
-
-
Angeline, T.1
Bentley, H.A.2
Hawk, A.B.3
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