-
1
-
-
0022656226
-
Vascular complications of inflammatory bowel disease
-
Talbot RW, Heppell J, Dozois RR, et al. Vascular complications of inflammatory bowel disease. Mayo Clin Proc 1986; 61(2): 140-5.
-
(1986)
Mayo Clin Proc
, vol.61
, Issue.2
, pp. 140-145
-
-
Talbot, R.W.1
Heppell, J.2
Dozois, R.R.3
-
2
-
-
0035085024
-
The incidence of deep venous thrombosis and pulmonary embolism among patients with inflammatory bowel disease: A population-based cohort study
-
Bernstein CN, Blanchard JF, Houston DS et al. The incidence of deep venous thrombosis and pulmonary embolism among patients with inflammatory bowel disease: a population-based cohort study. Thromb Haemost 2001; 85(3): 430-4.
-
(2001)
Thromb Haemost
, vol.85
, Issue.3
, pp. 430-434
-
-
Bernstein, C.N.1
Blanchard, J.F.2
Houston, D.S.3
-
3
-
-
0033938933
-
Inflammatory bowel disease promotes venous thrombosis earlier in life
-
Grip O, Svensson PJ, Lindgren S. Inflammatory bowel disease promotes venous thrombosis earlier in life. Scand J Gastroenterol 2000; 35(6): 619-23.
-
(2000)
Scand J Gastroenterol
, vol.35
, Issue.6
, pp. 619-623
-
-
Grip, O.1
Svensson, P.J.2
Lindgren, S.3
-
4
-
-
0037149297
-
Relative risk of cardiovascular events in patients with rheumatoid arthritis
-
DeMaria AN. Relative risk of cardiovascular events in patients with rheumatoid arthritis. Am J Cardiol 2002; 89(6A): 33D-38D.
-
(2002)
Am J Cardiol
, vol.89
, Issue.6 A
-
-
DeMaria, A.N.1
-
5
-
-
12244269685
-
Latent coeliac disease, hyperhomocysteinemia and pulmonary thromboembolism: A close link?
-
Gabrielli M, Santoliquido A, Gasbarrini G, et al. Latent coeliac disease, hyperhomocysteinemia and pulmonary thromboembolism: a close link? Thromb Haemost 2003; 89(1): 203-4.
-
(2003)
Thromb Haemost
, vol.89
, Issue.1
, pp. 203-204
-
-
Gabrielli, M.1
Santoliquido, A.2
Gasbarrini, G.3
-
6
-
-
0031680257
-
The factor V Leiden mutation increases the risk of venous thrombosis in patients with inflammatory bowel disease
-
Liebman HA, Kashani N, Sutherland D, et al. The factor V Leiden mutation increases the risk of venous thrombosis in patients with inflammatory bowel disease. Gastroenterology 1998; 115(4): 830-4.
-
(1998)
Gastroenterology
, vol.115
, Issue.4
, pp. 830-834
-
-
Liebman, H.A.1
Kashani, N.2
Sutherland, D.3
-
7
-
-
2142659242
-
Spontaneous venous thrombosis in inflammatory bowel disease: Relevance of factor V Leiden and the prothrombin gene mutation
-
Wong T, Nightingale J, Winter M, et al. Spontaneous venous thrombosis in inflammatory bowel disease: relevance of factor V Leiden and the prothrombin gene mutation. J Thromb Haemost 2003; 1(6): 1326-8.
-
(2003)
J Thromb Haemost
, vol.1
, Issue.6
, pp. 1326-1328
-
-
Wong, T.1
Nightingale, J.2
Winter, M.3
-
8
-
-
0036860856
-
Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease
-
Kader HA, Berman WF, Al-Seraihy AS, et al. Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease. J Pediatr Gastroenterol Nutr 2002; 35(5): 629-35.
-
(2002)
J Pediatr Gastroenterol Nutr
, vol.35
, Issue.5
, pp. 629-635
-
-
Kader, H.A.1
Berman, W.F.2
Al-Seraihy, A.S.3
-
9
-
-
0033869354
-
Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis
-
Vecchi M, Sacchi E, Saibeni S, et al. Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis. Dig Dis Sci 2000; 45(7): 1465-9.
-
(2000)
Dig Dis Sci
, vol.45
, Issue.7
, pp. 1465-1469
-
-
Vecchi, M.1
Sacchi, E.2
Saibeni, S.3
-
10
-
-
0034771941
-
Factor V Leiden and prothrombin gene mutation in inflammatory bowel disease in a Mediterranean area
-
Turri D, Roselli M, Simioni P, et al. Factor V Leiden and prothrombin gene mutation in inflammatory bowel disease in a Mediterranean area. Dig Liver Dis 2001; 33(7): 559-62.
-
(2001)
Dig Liver Dis
, vol.33
, Issue.7
, pp. 559-562
-
-
Turri, D.1
Roselli, M.2
Simioni, P.3
-
11
-
-
0030610090
-
The mutation Ala677→Val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis
-
Arruda VR, von Zuben PM, Chiparini LC, et al. The mutation Ala677→Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis. Thromb Haemost 1997; 77(5): 818-21.
-
(1997)
Thromb Haemost
, vol.77
, Issue.5
, pp. 818-821
-
-
Arruda, V.R.1
Von Zuben, P.M.2
Chiparini, L.C.3
-
12
-
-
0343238134
-
Prevalence of prothrombin 20210A allele and methylenetetrahydrofolate reductase C677T genetic mutations in the Chinese population
-
Ho CH. Prevalence of prothrombin 20210A allele and methylenetetrahydrofolate reductase C677T genetic mutations in the Chinese population. Ann Hematol 2000; 79(5): 239-42.
-
(2000)
Ann Hematol
, vol.79
, Issue.5
, pp. 239-242
-
-
Ho, C.H.1
-
13
-
-
0032840589
-
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors
-
Antoniadi T, Hatzis T, Kroupis C, et al. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors. Am J Hematol 1999; 61(4): 265-7.
-
(1999)
Am J Hematol
, vol.61
, Issue.4
, pp. 265-267
-
-
Antoniadi, T.1
Hatzis, T.2
Kroupis, C.3
-
14
-
-
0141888580
-
Methylenetetrahydrofolate reductase gene C677T mutation and plasma homocysteine level in Behcet's disease
-
Canataroglu A, Tanriverdi K, Inal T, et al. Methylenetetrahydrofolate reductase gene C677T mutation and plasma homocysteine level in Behcet's disease. Rheumatol Int 2003; 23(5): 236-40.
-
(2003)
Rheumatol Int
, vol.23
, Issue.5
, pp. 236-240
-
-
Canataroglu, A.1
Tanriverdi, K.2
Inal, T.3
-
15
-
-
17744410104
-
Prothrombin gene 20210 G-A mutation in the Turkish population
-
Akar N, Misirlioglu M, Akar E, et al. Prothrombin gene 20210 G-A mutation in the Turkish population. Am J Hematol 1998; 58(3): 249.
-
(1998)
Am J Hematol
, vol.58
, Issue.3
, pp. 249
-
-
Akar, N.1
Misirlioglu, M.2
Akar, E.3
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