-
1
-
-
0022480477
-
Effort related axillosubclavian vein thrombosis
-
Aziz S, Straehley CJ, Whelan TJ: Effort related axillosubclavian vein thrombosis. Am J Surg 152:57-61, 1986.
-
(1986)
Am J Surg
, vol.152
, pp. 57-61
-
-
Aziz, S.1
Straehley, C.J.2
Whelan, T.J.3
-
2
-
-
0015155913
-
Effort thrombosis of the axillary and subclavian veins
-
Adams JT, Deweese JA: Effort thrombosis of the axillary and subclavian veins. J Trauma 11:923-930, 1971.
-
(1971)
J Trauma
, vol.11
, pp. 923-930
-
-
Adams, J.T.1
Deweese, J.A.2
-
3
-
-
0027446268
-
Familial thrombophilia due to previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C
-
Dahlbäck B, Carlsson M, Svensson PJ: Familial thrombophilia due to previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C. Proc Natl Acad Sci USA 90:1004-1008, 1993.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 1004-1008
-
-
Dahlbäck, B.1
Carlsson, M.2
Svensson, P.J.3
-
4
-
-
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 369:64-67, 1994.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
-
5
-
-
0028243401
-
Association of idiopathic venous thromboembolism with a single point mutation at Arg506 of factor V
-
Voorberg J, Roelse J, Koopman R, et al: Association of idiopathic venous thromboembolism with a single point mutation at Arg506 of factor V. Lancet 343:1535-1536, 1994.
-
(1994)
Lancet
, vol.343
, pp. 1535-1536
-
-
Voorberg, J.1
Roelse, J.2
Koopman, R.3
-
6
-
-
0028098210
-
Resistance to activated protein C as a basis of venous thromboembolism
-
Svensson PJ, Dahlbäck B: Resistance to activated protein C as a basis of venous thromboembolism. N Engl J Med 330:517-522, 1994.
-
(1994)
N Engl J Med
, vol.330
, pp. 517-522
-
-
Svensson, P.J.1
Dahlbäck, B.2
-
7
-
-
0029850530
-
A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated prothrombin levels and an increase in venous thrombosis
-
Port SR, Rosendaal FR, Reitsma PH, et al: A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated prothrombin levels and an increase in venous thrombosis. Blood 88:3698-3703, 1996.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Port, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
-
8
-
-
0018827254
-
Subclavian and axillary vein compression of musculoskeletal origin
-
Daskalakis E, Bouhoutsos J: Subclavian and axillary vein compression of musculoskeletal origin. Br J Surg 67:573-576, 1980.
-
(1980)
Br J Surg
, vol.67
, pp. 573-576
-
-
Daskalakis, E.1
Bouhoutsos, J.2
-
9
-
-
0024158892
-
Deep vein thrombosis of the axillary-subclavian veins: Epidemiologic data, effects of different types of treatment and late sequelae
-
Lindblad B, Tengborn L, Bergqvist D: Deep vein thrombosis of the axillary-subclavian veins: Epidemiologic data, effects of different types of treatment and late sequelae. Eur J Vasc Surg 2:161-165, 1988.
-
(1988)
Eur J Vasc Surg
, vol.2
, pp. 161-165
-
-
Lindblad, B.1
Tengborn, L.2
Bergqvist, D.3
-
10
-
-
84965185923
-
Thromboembolism: Analysis of cases at Charity Hospital in New Orleans over a 12-year period
-
Ochsner A, DeBakey M, DeCamp PT, et al: Thromboembolism: Analysis of cases at Charity Hospital in New Orleans over a 12-year period. Arch Surg 134:405, 1951.
-
(1951)
Arch Surg
, vol.134
, pp. 405
-
-
Ochsner, A.1
DeBakey, M.2
DeCamp, P.T.3
-
11
-
-
0001052516
-
The prevalence of factor V Leiden mutation in Turkish population
-
Gürgey A, Mesci L: The prevalence of factor V Leiden mutation in Turkish population. Turk J Pediatr 39:310-315, 1997.
-
(1997)
Turk J Pediatr
, vol.39
, pp. 310-315
-
-
Gürgey, A.1
Mesci, L.2
-
12
-
-
0029841485
-
Factor V Leiden mutation in children with thrombosis
-
Gürgey A, Mesci L, Renda Y, et al: Factor V Leiden mutation in children with thrombosis. Am J Hematol 53:37-39, 1996.
-
(1996)
Am J Hematol
, vol.53
, pp. 37-39
-
-
Gürgey, A.1
Mesci, L.2
Renda, Y.3
-
13
-
-
0028931717
-
High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance)
-
Rosendaal FR, Koster T, Vandenbrouke JP, et al: High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance). Blood 85:1504-1508, 1995.
-
(1995)
Blood
, vol.85
, pp. 1504-1508
-
-
Rosendaal, F.R.1
Koster, T.2
Vandenbrouke, J.P.3
-
14
-
-
0028910906
-
Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke and venous thromboembolism 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 thromboembolism in apparently healthy men. N Engl J Med 332:912-917, 1995.
-
(1995)
N Engl J Med
, vol.332
, pp. 912-917
-
-
Ridker, P.M.1
Hennekens, C.H.2
Lindpaintner, K.3
-
15
-
-
0029162113
-
Resistance to activated protein C as a basis for venous thromboembolism associated with pregnancy and oral contraceptives
-
Hellgren M, Svensson PJ, Dahlbäck B: Resistance to activated protein C as a basis for venous thromboembolism associated with pregnancy and oral contraceptives. Am J Obstet Gynecol 173:210-213, 1995.
-
(1995)
Am J Obstet Gynecol
, vol.173
, pp. 210-213
-
-
Hellgren, M.1
Svensson, P.J.2
Dahlbäck, B.3
-
16
-
-
0030792668
-
The prothrombin gene G20210a variant: Prevalence in a U.K. anticoagulant clinic population
-
Cumming AM, Keeney S, Salden A, et al: The prothrombin gene G20210A variant: Prevalence in a U.K. anticoagulant clinic population. Br J Haematol 98:353-355, 1997.
-
(1997)
Br J Haematol
, vol.98
, pp. 353-355
-
-
Cumming, A.M.1
Keeney, S.2
Salden, A.3
-
17
-
-
0032521209
-
The prothrombin 20210 A allele is frequently coinherited in young carriers of the factor V Arg 506 to Gln mutation with venous thrombophilia
-
Ehrenforth S, Ludwing G, Klinke S, et al: The prothrombin 20210 A allele is frequently coinherited in young carriers of the factor V Arg 506 to Gln mutation with venous thrombophilia. Blood 91:2209-2210, 1998.
-
(1998)
Blood
, vol.91
, pp. 2209-2210
-
-
Ehrenforth, S.1
Ludwing, G.2
Klinke, S.3
-
18
-
-
0032520927
-
The 20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families
-
Zöller B, Svensson PJ, Dahlbäck B, et al. The 20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families. Blood 91:2210-2211, 1998.
-
(1998)
Blood
, vol.91
, pp. 2210-2211
-
-
Zöller, B.1
Svensson, P.J.2
Dahlbäck, B.3
-
19
-
-
0030608645
-
Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia
-
Makris M, Preston FE, Beauchamp NJ, et al: Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia. Thromb Haemost 78:1426-1429, 1997.
-
(1997)
Thromb Haemost
, vol.78
, pp. 1426-1429
-
-
Makris, M.1
Preston, F.E.2
Beauchamp, N.J.3
|