-
1
-
-
0019985276
-
Budd-Chiari syndrome: Etiology, diagnosis and management
-
Mitchell MC, Boinott JK, Kaufman S, et al. Budd-Chiari syndrome: etiology, diagnosis and management. Medicine (Baltimore) 1982;61:199-218.
-
(1982)
Medicine (Baltimore)
, vol.61
, pp. 199-218
-
-
Mitchell, M.C.1
Boinott, J.K.2
Kaufman, S.3
-
2
-
-
0026516360
-
Adult "idiopathic" extrahepatic venous thrombosis. Importance of putative "latent" myeloproliferative disorders and comparison with cases with known etiology
-
Cardin F, Graffeo M, McCormick PA, et al. Adult "idiopathic" extrahepatic venous thrombosis. Importance of putative "latent" myeloproliferative disorders and comparison with cases with known etiology. Dig Dis Sci 1992;37:335-9.
-
(1992)
Dig Dis Sci
, vol.37
, pp. 335-339
-
-
Cardin, F.1
Graffeo, M.2
McCormick, P.A.3
-
3
-
-
0023945861
-
Etiology of portal vein thrombosis in adults. A prospective evaluation of primary myeloproliferative disorders
-
Valla D, Casadevall N, Huisse MG, et al. Etiology of portal vein thrombosis in adults. A prospective evaluation of primary myeloproliferative disorders. Gastroenterology 1988;94:1063-9.
-
(1988)
Gastroenterology
, vol.94
, pp. 1063-1069
-
-
Valla, D.1
Casadevall, N.2
Huisse, M.G.3
-
4
-
-
0024639346
-
Portal and mesenteric thrombosis revealing constitutional protein C deficiency
-
Prat F, Ouzan D, Trecziak N, et al. Portal and mesenteric thrombosis revealing constitutional protein C deficiency. Gut 1989;30:416.
-
(1989)
Gut
, vol.30
, pp. 416
-
-
Prat, F.1
Ouzan, D.2
Trecziak, N.3
-
5
-
-
17444435818
-
A protein S deficient family with portal vein thrombosis
-
Sas G. Blaskó G, Petr I, et al. A protein S deficient family with portal vein thrombosis. Thromb Haemost 1985;54:724.
-
(1985)
Thromb Haemost
, vol.54
, pp. 724
-
-
Sas, G.1
Blaskó, G.2
Petr, I.3
-
6
-
-
0023185643
-
Mesenteric venous thrombosis and antithrombin III deficiency
-
Wilson C, Walker ID, Davidson JF, et al. Mesenteric venous thrombosis and antithrombin III deficiency. J Clin Pathol 1987; 40:906-8.
-
(1987)
J Clin Pathol
, vol.40
, pp. 906-908
-
-
Wilson, C.1
Walker, I.D.2
Davidson, J.F.3
-
7
-
-
0026465569
-
Hereditary deficiency of antithrombin III, protein C and protein S: Prevalence in patients with a history of venous thrombosis and criteria for rational patient screening
-
Pabinger I, Brucker S, Kyrle PA, et al. Hereditary deficiency of antithrombin III, protein C and protein S: prevalence in patients with a history of venous thrombosis and criteria for rational patient screening. Blood Coag Fibrinol 1992;3:547-53.
-
(1992)
Blood Coag Fibrinol
, vol.3
, pp. 547-553
-
-
Pabinger, I.1
Brucker, S.2
Kyrle, P.A.3
-
8
-
-
0027428481
-
Anticoagulant protein C pathway defective in majority of thrombophilic patients
-
Griffin JH, Evatt B, Wideman C, et al. Anticoagulant protein C pathway defective in majority of thrombophilic patients. Blood 1993;82:1989-93.
-
(1993)
Blood
, vol.82
, pp. 1989-1993
-
-
Griffin, J.H.1
Evatt, B.2
Wideman, C.3
-
9
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BPC, Koster T, et al. 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
-
11
-
-
0028291210
-
Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis
-
Zoller B, Dahlback B. Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis. Lancet 1994;343:1536-8.
-
(1994)
Lancet
, vol.343
, pp. 1536-1538
-
-
Zoller, B.1
Dahlback, B.2
-
12
-
-
0031056991
-
The risk of recurrent venous thromboembolism in patients with an Arg506-Gln mutation in the gene for factor V (Factor Leiden)
-
Simioni P, Prandoni P, Lensing AWA, et al. The risk of recurrent venous thromboembolism in patients with an Arg506-Gln mutation in the gene for factor V (Factor Leiden). N Engl J Med 1997;336:399-403.
-
(1997)
N Engl J Med
, vol.336
, pp. 399-403
-
-
Simioni, P.1
Prandoni, P.2
Lensing, A.W.A.3
-
13
-
-
0029933176
-
Coexistence of hereditary homocystinuria and Factor V leiden. Effect on thrombosis
-
Mandel H, Brenner B, Berant M, et al. Coexistence of hereditary homocystinuria and Factor V leiden. Effect on thrombosis. N Engl J Med 1996;334:763-8.
-
(1996)
N Engl J Med
, vol.334
, pp. 763-768
-
-
Mandel, H.1
Brenner, B.2
Berant, M.3
-
14
-
-
0028029477
-
Increased risk of venous thrombosis in oral-contraceptive users who are carriers of factor V Leiden mutation
-
Vandenbroucke JP, Koster T, Briet E, et al. Increased risk of venous thrombosis in oral-contraceptive users who are carriers of factor V Leiden mutation. Lancet 1994;344:1453-7.
-
(1994)
Lancet
, vol.344
, pp. 1453-1457
-
-
Vandenbroucke, J.P.1
Koster, T.2
Briet, E.3
-
15
-
-
0028000665
-
Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
-
Koeleman BP, Reitsma PH, Allaart CF, et al. Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families. Blood 1994;84:1031-5.
-
(1994)
Blood
, vol.84
, pp. 1031-1035
-
-
Koeleman, B.P.1
Reitsma, P.H.2
Allaart, C.F.3
-
16
-
-
0029873817
-
Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency
-
Van Boven HH, Reitsma PH, Rosendaal FR, et al. Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency. Thromb Haemost 1996;75:417-21.
-
(1996)
Thromb Haemost
, vol.75
, pp. 417-421
-
-
Van Boven, H.H.1
Reitsma, P.H.2
Rosendaal, F.R.3
-
17
-
-
0028788691
-
Une nouvelle cause hereditaire de thrombose portale:La resistance anormale a la proteine C activée par mutation Arg506-Gln du gene du facteur V
-
Levoir D, Aubertine JM, Almenc-Gelas M, et al. Une nouvelle cause hereditaire de thrombose portale:la resistance anormale a la proteine C activée par mutation Arg506-Gln du gene du facteur V. Gastroenterol Clin Biol 1995;19:729-31.
-
(1995)
Gastroenterol Clin Biol
, vol.19
, pp. 729-731
-
-
Levoir, D.1
Aubertine, J.M.2
Almenc-Gelas, M.3
-
18
-
-
0029851052
-
Acute Budd-Chiari syndrome with fulminant hepatic failure in pregnant woman with factor V Leiden mutation
-
Fickert P, Ramschak H, Kenner L, et al. Acute Budd-Chiari syndrome with fulminant hepatic failure in pregnant woman with factor V Leiden mutation. Gastroenterology 1996;111:1670-3.
-
(1996)
Gastroenterology
, vol.111
, pp. 1670-1673
-
-
Fickert, P.1
Ramschak, H.2
Kenner, L.3
-
19
-
-
0028910906
-
Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men
-
Ridker PM, Hennekens CH, Lindpaintner K, et al. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men. N Engl J Med 1995;332:912-7.
-
(1995)
N Engl J Med
, vol.332
, pp. 912-917
-
-
Ridker, P.M.1
Hennekens, C.H.2
Lindpaintner, K.3
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