-
1
-
-
0028335097
-
High prevalence of hyperhomocyst(e)inemia in patients with juvenile venous thrombosis
-
1. Falcon CR, Marco C, Panzari D, Martinelli I, Mannucci PM. High prevalence of hyperhomocyst(e)inemia in patients with juvenile venous thrombosis. Arteriosder Thromb 1994; 14: 1080-1083.
-
(1994)
Arteriosder Thromb
, vol.14
, pp. 1080-1083
-
-
Falcon, C.R.1
Marco, C.2
Panzari, D.3
Martinelli, I.4
Mannucci, P.M.5
-
2
-
-
0028853921
-
Prevalence of moderate hyperhomocysteinemia in patients with early-onset venous and arterial occlusive disease
-
2. Fermo I, Vigano S, D'Angelo S, Paroni R, Mazzola G, Calori G, D'Angelo A. Prevalence of moderate hyperhomocysteinemia in patients with early-onset venous and arterial occlusive disease. Ann Intern Med 1995; 123: 747-753.
-
(1995)
Ann Intern Med
, vol.123
, pp. 747-753
-
-
Fermo, I.1
Vigano, S.2
D'Angelo, S.3
Paroni, R.4
Mazzola, G.5
Calori, G.6
D'Angelo, A.7
-
3
-
-
0028949953
-
Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?
-
3. Den Heijer M, Blom HJ, Gerrits WBJ, Rosendaal FR, Haak HL, Wijermans PW, et al. Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis? Lancet 1995; 345: 882-885.
-
(1995)
Lancet
, vol.345
, pp. 882-885
-
-
Den Heijer, M.1
Blom, H.J.2
Gerrits, W.B.J.3
Rosendaal, F.R.4
Haak, H.L.5
Wijermans, P.W.6
-
4
-
-
0029921114
-
Hyperhomocysteinaemia as a risk factor for deep vein thrombosis
-
4. Den Heijer M, Koster T, Blom H, Bos GMJ, Briët E, Reitsma PH, et al. Hyperhomocysteinaemia as a risk factor for deep vein thrombosis. N Engl J Med 1996; 334: 759-762.
-
(1996)
N Engl J Med
, vol.334
, pp. 759-762
-
-
Den Heijer, M.1
Koster, T.2
Blom, H.3
Bos, G.M.J.4
Briët, E.5
Reitsma, P.H.6
-
5
-
-
0030058721
-
Genetic and nongenetic factors for moderate hyperhomocysteinemia
-
5. Kang SS, Wong PWK. Genetic and nongenetic factors for moderate hyperhomocysteinemia. Atherosclerosis 1996; 119: 135.
-
(1996)
Atherosclerosis
, vol.119
, pp. 135
-
-
Kang, S.S.1
Wong, P.W.K.2
-
6
-
-
0029049553
-
A candidate genetic risk for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
6. Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, et al. A candidate genetic risk for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nature Genet 1995; 10: 111-113.
-
(1995)
Nature Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
-
7
-
-
0029655724
-
Molecular genetic analysis in mild hyperhomocysteinemia. A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease
-
7. Kluijtmans LAJ, von den Heuvel LPWJ, Boers GHJ, Frosst P, Stevens EMB, van Oost BA, et al. Molecular genetic analysis in mild hyperhomocysteinemia. 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.J.1
Von Den Heuvel, L.P.W.J.2
Boers, G.H.J.3
Frosst, P.4
Stevens, E.M.B.5
Van Oost, B.A.6
-
8
-
-
0000182299
-
Thermolabile methylene tetra hydrofolate reductase (MTHFR) does not modify the risk for venous thromboembolism in subjects with heterozygous factor V Leiden
-
8. Trillot N, Preudhomme C, Alhenc-Gelas M, Gaveriaux V, Bauters A, Gandrille S, et al. Thermolabile methylene tetra hydrofolate reductase (MTHFR) does not modify the risk for venous thromboembolism in subjects with heterozygous factor V Leiden. Blood 1996; 88 (suppl 1): 284a.
-
(1996)
Blood
, vol.88
, Issue.SUPPL. 1
-
-
Trillot, N.1
Preudhomme, C.2
Alhenc-Gelas, M.3
Gaveriaux, V.4
Bauters, A.5
Gandrille, S.6
-
9
-
-
0031886677
-
Thermolabile methylenetetrahydrofolate reductase and factor V Leiden in the risk of deep-vein thrombosis
-
9. Kluijtmans LAJ, den Heijer M, Reitsma PH, Heil SG, Blom HJ, Rosendaal FR. Thermolabile methylenetetrahydrofolate reductase and factor V Leiden in the risk of deep-vein thrombosis. Thromb Haemost 1998; 79: 254-258.
-
(1998)
Thromb Haemost
, vol.79
, pp. 254-258
-
-
Kluijtmans, L.A.J.1
Den Heijer, M.2
Reitsma, P.H.3
Heil, S.G.4
Blom, H.J.5
Rosendaal, F.R.6
-
10
-
-
0013564268
-
Hyperhomocyst(e)inaemia and a common methylene-tetrahydrofolate reductase mutation (Ala223 Val MTHFR) are not associated with a history of thrombosis with inherited thrombophilia
-
10. Legnani C, Palareti G, Sassi S, Grauso F, Bargossi A, Bernardi F, et al. Hyperhomocyst(e)inaemia and a common methylene-tetrahydrofolate reductase mutation (Ala223 Val MTHFR) are not associated with a history of thrombosis with inherited thrombophilia. Thromb Haemost 1997; (suppl): 568.
-
(1997)
Thromb Haemost
, Issue.SUPPL.
, pp. 568
-
-
Legnani, C.1
Palareti, G.2
Sassi, S.3
Grauso, F.4
Bargossi, A.5
Bernardi, F.6
-
13
-
-
0029930121
-
Probability of recurrence of thrombosis in patients with and without factor V Leiden
-
13. Rintelen C, Pabinger P, Knöbl P, Lechner K, Mannhalter C. Probability of recurrence of thrombosis in patients with and without factor V Leiden. Thromb Haemost 1996, 75: 229-232.
-
(1996)
Thromb Haemost
, vol.75
, pp. 229-232
-
-
Rintelen, C.1
Pabinger, P.2
Knöbl, P.3
Lechner, K.4
Mannhalter, C.5
-
14
-
-
0029850530
-
A common genetic variation in the 3′ untranslated region of the prothrombin gene is associated with elevated plasma thrombin levels and an increase in venous thrombosis
-
14. 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 thrombin levels and an increase in venous thrombosis. Blood 1994; 10: 3698-3703.
-
(1994)
Blood
, vol.10
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
15
-
-
0028000665
-
Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
-
15. Koeleman BPC, Reitsma PH, Allaart CF, Bertina RM. Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families. Blood 1994; 84: 1031-1035.
-
(1994)
Blood
, vol.84
, pp. 1031-1035
-
-
Koeleman, B.P.C.1
Reitsma, P.H.2
Allaart, C.F.3
Bertina, R.M.4
-
16
-
-
0029022118
-
Factor V Leiden: An additional risk factor for thrombosis in protein S deficient families?
-
16. Koeleman BPC, van Rumpf D, Hamulyak K, Reitsma PH, Bertina RM. Factor V Leiden: an additional risk factor for thrombosis in protein S deficient families? Thromb Haemost 1995; 74: 580-583.
-
(1995)
Thromb Haemost
, vol.74
, pp. 580-583
-
-
Koeleman, B.P.C.1
Van Rumpf, D.2
Hamulyak, K.3
Reitsma, P.H.4
Bertina, R.M.5
-
17
-
-
0029050714
-
Incidence of activated protein C resistance caused by ARG 506 GLN mutation in 113 unrelated symptomatic protein C deficient patients
-
17. Gandrille S, Greengard JS, Alhenc-Gelas M, Juhan-Vague I, Abgrall JF, Griffin JH, Aiach M, and the French Network on the behalf of INSERM. Incidence of activated protein C resistance caused by ARG 506 GLN mutation in 113 unrelated symptomatic protein C deficient patients. Blood 1995; 86: 219-224.
-
(1995)
Blood
, vol.86
, pp. 219-224
-
-
Gandrille, S.1
Greengard, J.S.2
Alhenc-Gelas, M.3
Juhan-Vague, I.4
Abgrall, J.F.5
Griffin, J.H.6
Aiach, M.7
-
18
-
-
0029016883
-
Resistance to activated protein C as an additional risk factor in hereditary deficiency of protein S
-
18. Zöller B, Berntsdotter A, Garcia de Frutos P, Dahlbäck B. Resistance to activated protein C as an additional risk factor in hereditary deficiency of protein S. Blood 1995; 85: 3518-3523.
-
(1995)
Blood
, vol.85
, pp. 3518-3523
-
-
Zöller, B.1
Berntsdotter, A.2
Garcia De Frutos, P.3
Dahlbäck, B.4
-
19
-
-
0031893697
-
Clinical feature in thrombophilia in families with gene defects in protein C or protein S combined with factor V Leiden
-
19. Mustafa S, Mannhalter C, Rintelen C, Kyrle PA, Knoebl P, Lechner K, et al. Clinical feature in thrombophilia in families with gene defects in protein C or protein S combined with factor V Leiden. Blood Coag Fibrinol 1998; 9: 85-89.
-
(1998)
Blood Coag Fibrinol
, vol.9
, pp. 85-89
-
-
Mustafa, S.1
Mannhalter, C.2
Rintelen, C.3
Kyrle, P.A.4
Knoebl, P.5
Lechner, K.6
-
20
-
-
0030855797
-
Hyperhomocysteinaemia and thrombosis: Acquired conditions
-
20. Selhub J, D'Angelo A. Hyperhomocysteinaemia and thrombosis: acquired conditions. Thromb Haemost 1997; 78: 527-531.
-
(1997)
Thromb Haemost
, vol.78
, pp. 527-531
-
-
Selhub, J.1
D'Angelo, A.2
-
21
-
-
0030850024
-
The prevalence of two genetic traits to venous thrombosis in whites and African-Americans
-
21. Austin H, Hooper CW, Dilley A, Drews C, Renshaw M, Ellinsen D, et al. The prevalence of two genetic traits to venous thrombosis in whites and African-Americans. Thromb Res 1997; 86: 409-415.
-
(1997)
Thromb Res
, vol.86
, pp. 409-415
-
-
Austin, H.1
Hooper, C.W.2
Dilley, A.3
Drews, C.4
Renshaw, M.5
Ellinsen, D.6
-
22
-
-
0029933176
-
Coexistence of hereditary homocystinuria and factor V Leiden-effect on thrombosis
-
22. Mandel H, Brenner B, Berant M, Rosenberg N, Lanir N, Jakobs C, et al. Coexistence of hereditary homocystinuria and factor V Leiden-effect on thrombosis. N Engl J Med 1996; 334: 763-768.
-
(1996)
N Engl J Med
, vol.334
, pp. 763-768
-
-
Mandel, H.1
Brenner, B.2
Berant, M.3
Rosenberg, N.4
Lanir, N.5
Jakobs, C.6
|