-
1
-
-
0034922928
-
Factor V R506Q mutation-Leiden: An independent risk factor for venous thrombosis but not coronary artery disease
-
Irani-Hakime N, Tamim H, Elias G, Choueiry S, Kreidy R, Daccache JL, Almawi WY. Factor V R506Q mutation-Leiden: an independent risk factor for venous thrombosis but not coronary artery disease. J Thromb Thrombolysis 2001; 11: 111-6.
-
(2001)
J Thromb Thrombolysis
, vol.11
, pp. 111-116
-
-
Irani-Hakime, N.1
Tamim, H.2
Elias, G.3
Choueiry, S.4
Kreidy, R.5
Daccache, J.L.6
Almawi, W.Y.7
-
2
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, van der Velden PA, Reitsma PH. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369: 64-7.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
De Ronde, H.6
Van Der Velden, P.A.7
Reitsma, P.H.8
-
3
-
-
0033843870
-
The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese
-
Irani-Hakime N, Tamim H, Kreidy R, Almawi WY. The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese. Am J Hematol 2000; 65: 45-9.
-
(2000)
Am J Hematol
, vol.65
, pp. 45-49
-
-
Irani-Hakime, N.1
Tamim, H.2
Kreidy, R.3
Almawi, W.Y.4
-
4
-
-
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 SR, Rosendaal FR, Reitsma PH, Bertina RM. 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 1996; 88: 3698-703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
5
-
-
0033899336
-
Prevalence of factor V Leiden and prothrombin G20210A mutations in unselected patients with venous thromboembolism
-
De Moerloose P, Reber G, Perrier A, Perneger T, Bounameaux H. Prevalence of factor V Leiden and prothrombin G20210A mutations in unselected patients with venous thromboembolism. Br J Haematol 2000; 110: 125-9.
-
(2000)
Br J Haematol
, vol.110
, pp. 125-129
-
-
De Moerloose, P.1
Reber, G.2
Perrier, A.3
Perneger, T.4
Bounameaux, H.5
-
6
-
-
0031981017
-
Geographic distribution of the 20210 G to A prothrombin variant
-
Rosendaal FR, Doggen CJ, Zivelin A, Arruda VR, Aiach M, Siscovick DS, Hillarp A, Watzke HH, Bernardi F, Cumming AM, Preston FE, Reitsma PH. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 1998; 79: 706-8.
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.2
Zivelin, A.3
Arruda, V.R.4
Aiach, M.5
Siscovick, D.S.6
Hillarp, A.7
Watzke, H.H.8
Bernardi, F.9
Cumming, A.M.10
Preston, F.E.11
Reitsma, P.H.12
-
7
-
-
0036403373
-
Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease
-
Burzotta F, Paciaroni K, De Stefano V, Chiusolo P, Manzoli A, Casorelli I, Leone AM, Rossi E, Leone G, Maseri A, Andreotti F. Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease. Eur Heart J 2002; 23: 26-30.
-
(2002)
Eur Heart J
, vol.23
, pp. 26-30
-
-
Burzotta, F.1
Paciaroni, K.2
De Stefano, V.3
Chiusolo, P.4
Manzoli, A.5
Casorelli, I.6
Leone, A.M.7
Rossi, E.8
Leone, G.9
Maseri, A.10
Andreotti, F.11
-
8
-
-
0034111630
-
Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population
-
Angelopoulou K, Nicolaides A, Constantinou Deltas C. Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population. Clin Appl Thromb Hemost 2000; 6: 104-7.
-
(2000)
Clin Appl Thromb Hemost
, vol.6
, pp. 104-107
-
-
Angelopoulou, K.1
Nicolaides, A.2
Constantinou Deltas, C.3
-
9
-
-
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
-
10
-
-
0034487766
-
The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both
-
Martinelli I, Bucciarelli P, Margaglione M, De Stefano V, Castaman G, Mannucci PM. The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both. Br J Haematol 2000; 111: 1223-9.
-
(2000)
Br J Haematol
, vol.111
, pp. 1223-1229
-
-
Martinelli, I.1
Bucciarelli, P.2
Margaglione, M.3
De Stefano, V.4
Castaman, G.5
Mannucci, P.M.6
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