-
1
-
-
19044397120
-
The hereditary factors that cause Thrombosis
-
Ozyurek HE, Gurgey A. The hereditary factors that cause Thrombosis. Katkι Pediatr 2001; 22: 170-177.
-
(2001)
Katkι Pediatr.
, vol.22
, pp. 170-177
-
-
Ozyurek, H.E.1
Gurgey, A.2
-
2
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BP, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369; 64-67.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.2
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
de Ronde, H.6
-
3
-
-
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: 3698-3703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
4
-
-
0028810738
-
World distribution of faktor V Leiden
-
Rees DC, Cox Clegg JB. World distribution of faktor V Leiden. Lancet 1995; 346: 1133-1134.
-
(1995)
Lancet
, vol.346
, pp. 1133-1134
-
-
Rees, D.C.1
Cox Clegg, J.B.2
-
5
-
-
0031181982
-
The prevalence of factor V Leiden (1691 G-A) mutation in Turkey
-
Gurgey A, Mesci L. The prevalence of factor V Leiden (1691 G-A) mutation in Turkey. Turk J Pediatr 1997; 39: 313-315.
-
(1997)
Turk. J. Pediatr.
, vol.39
, pp. 313-315
-
-
Gurgey, A.1
Mesci, L.2
-
6
-
-
0031007628
-
Frequency of factor V Leiden (Arg506Gln) in Turkey
-
Ozbek U, Tangun Y. Frequency of factor V Leiden (Arg506Gln) in Turkey. Br J Hematol 1997; 97: 504-505.
-
(1997)
Br. J. Hematol.
, vol.97
, pp. 504-505
-
-
Ozbek, U.1
Tangun, Y.2
-
7
-
-
0030747763
-
Prevalence of factor V Leiden mutation in various populations
-
Herrmann FH, Koesling M, Schroder W, Altman R, Jimenez Bonilla R, Lopaciuk S, et al. Prevalence of factor V Leiden mutation in various populations. Genet Epidemiology 1997; 14: 403-411.
-
(1997)
Genet. Epidemiology
, vol.14
, pp. 403-411
-
-
Herrmann, F.H.1
Koesling, M.2
Schroder, W.3
Altman, R.4
Jimenez Bonilla, R.5
Lopaciuk, S.6
-
8
-
-
0031468431
-
Use of first nucleotide change technology to determine the frequency of factor V Leiden in a population of Australian blood donors
-
Pecheniuk NM, March NA, Walsh NA, Dale JL. Use of first nucleotide change technology to determine the frequency of factor V Leiden in a population of Australian blood donors. Blood Coagulation Fibrinolysis 1997: 8: 491-495.
-
(1997)
Blood Coagulation Fibrinolysis
, vol.8
, pp. 491-495
-
-
Pecheniuk, N.M.1
March, N.A.2
Walsh, N.A.3
Dale, J.L.4
-
9
-
-
1842404736
-
Faktor V Leiden (R506Q) and risk of venous thromboembolism: A case-control study based or the Spanish population
-
Garcia-Gala JM, Alvarez V, Pinto CR, Soto I, Urgelles MF, Menender MJ, et al. Faktor V Leiden (R506Q) and risk of venous thromboembolism: a case-control study based or the Spanish population. Clin Genet 1997; 52: 206-210.
-
(1997)
Clin. Genet.
, vol.52
, pp. 206-210
-
-
Garcia-Gala, J.M.1
Alvarez, V.2
Pinto, C.R.3
Soto, I.4
Urgelles, M.F.5
Menender, M.J.6
-
10
-
-
0030955080
-
Ethnic distribution of factor V Leiden in 4047 men and women
-
Ridker PM, Miletich JP, Hennekens CH, Buring JE. Ethnic distribution of factor V Leiden in 4047 men and women. JAMA 1997; 277: 1305-1307.
-
(1997)
JAMA
, vol.277
, pp. 1305-1307
-
-
Ridker, P.M.1
Miletich, J.P.2
Hennekens, C.H.3
Buring, J.E.4
-
11
-
-
0029090538
-
APC-resistance and Mnl genotype (Gln 506) of coagulation factor V are rare in Japanese population
-
Takamiya O, Ishada F, Kodaira H, Kitano K. APC-resistance and Mnl genotype (Gln 506) of coagulation factor V are rare in Japanese population. Thromb Haemost 1995; 74: 996-1002.
-
(1995)
Thromb. Haemost.
, vol.74
, pp. 996-1002
-
-
Takamiya, O.1
Ishada, F.2
Kodaira, H.3
Kitano, K.4
-
13
-
-
0028861951
-
Coagulation faktor V Leiden mutation may have a racial background
-
Fujimura H, Kambayashi J, Monden M, Kato H, Miyata T. Coagulation faktor V Leiden mutation may have a racial background. Thromb Haemost 1996; 74: 1381-1382.
-
(1996)
Thromb. Haemost.
, vol.74
, pp. 1381-1382
-
-
Fujimura, H.1
Kambayashi, J.2
Monden, M.3
Kato, H.4
Miyata, T.5
-
14
-
-
1842290346
-
Resistance to activated protein C caused by factor V R506Q mutation is a common risk factor for venous thrombosis
-
Dahlback B. Resistance to activated protein C caused by factor V R506Q mutation is a common risk factor for venous thrombosis. Thromb Haemost 1997; 78: 483-488.
-
(1997)
Thromb. Haemost.
, vol.78
, pp. 483-488
-
-
Dahlback, B.1
-
15
-
-
0032186393
-
PG20210A mutation in Turkish Patients with Thrombosis
-
Gurgey A. Hiçsönmez G, Parlak H, Balta G, Celiker A. PG20210A mutation in Turkish Patients with Thrombosis. Am J Hematology 1998; 59: 179-180
-
(1998)
Am. J. Hematology
, vol.59
, pp. 179-180
-
-
Gurgey, A.1
Hiçsönmez, G.2
Parlak, H.3
Balta, G.4
Celiker, A.5
-
16
-
-
17744410104
-
Prothrombin gene 20210 G-A mutation in the Turkish population
-
Akar N, Misirlioglu M, Akar E, Avcu F, Yalcin A, Sozuoz A. Prothrombin gene 20210 G-A mutation in the Turkish population. Am J Hematol 1998; 58: 249.
-
(1998)
Am. J. Hematol.
, vol.58
, pp. 249
-
-
Akar, N.1
Misirlioglu, M.2
Akar, E.3
Avcu, F.4
Yalcin, A.5
Sozuoz, A.6
-
17
-
-
0031451539
-
Real-time fluorescence genotyping of factor V Leiden during rapid-cycle PCR
-
Lay MJ, Wittwer CT. Real-time fluorescence genotyping of factor V Leiden during rapid-cycle PCR. Clinical Chemistry 1997; 43: 2262-2267.
-
(1997)
Clinical Chemistry
, vol.43
, pp. 2262-2267
-
-
Lay, M.J.1
Wittwer, C.T.2
-
18
-
-
0343517715
-
Evaluation of the Roche Diagnostics Light Cycler-FVL Mutation Detection Kit and the Light Cycler-Prothrombin Mutation Detection Kit
-
Nauch M, Marz W, Wieland H. Evaluation of the Roche Diagnostics Light Cycler-FVL Mutation Detection Kit and the Light Cycler-Prothrombin Mutation Detection Kit. Clinical Biochemistry 2000; 33: 213-216.
-
(2000)
Clinical Biochemistry
, vol.33
, pp. 213-216
-
-
Nauch, M.1
Marz, W.2
Wieland, H.3
-
19
-
-
0034840147
-
Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism - Pooled analysis of 8 case-control studies including 2310 cases and 3204 controls
-
Study Group for Pooled-Analysis in Venous Thromboembolism
-
Emmerich J, Rosendaal FR, Cattaneo M, Margaglione M, De Stefano V, Cumming T, et al. Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism - pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism. Thromb Haemost 2001; 86: 809-816.
-
(2001)
Thromb. Haemost.
, vol.86
, pp. 809-816
-
-
Emmerich, J.1
Rosendaal, F.R.2
Cattaneo, M.3
Margaglione, M.4
De Stefano, V.5
Cumming, T.6
-
20
-
-
0036178694
-
Lower birth-weight in neonates of mothers carrying factor V G1691A and factor IIA(20210) mutations
-
Grandone E, Margaglione M, Colaizzo D, Pavone G, Paladini D, Martinelli P, et al. Lower birth-weight in neonates of mothers carrying factor V G1691A and factor IIA(20210) mutations. Haematologica 2002; 87: 177-181.
-
(2002)
Haematologica
, vol.87
, pp. 177-181
-
-
Grandone, E.1
Margaglione, M.2
Colaizzo, D.3
Pavone, G.4
Paladini, D.5
Martinelli, P.6
-
21
-
-
0030005015
-
Neonatal purpura fulminans in association with factor V R506Q mutation
-
Pipe SW, Schmaier AH, Nichols WC, Ginsburg D, Bozynski ME, Castle VP. Neonatal purpura fulminans in association with factor V R506Q mutation. J Pediatr 1996; 128: 706-709.
-
(1996)
J. Pediatr.
, vol.128
, pp. 706-709
-
-
Pipe, S.W.1
Schmaier, A.H.2
Nichols, W.C.3
Ginsburg, D.4
Bozynski, M.E.5
Castle, V.P.6
-
22
-
-
0030608860
-
Arg506 to Gln mutation in the factor V gene causes poor fibrinolytic response in children after venous occlusion
-
Nowak-Gottl U, Binder M, Dubbers A, Kehrel B, Koch HG, Veltmann H, et al. Arg506 to Gln mutation in the factor V gene causes poor fibrinolytic response in children after venous occlusion. Thromb Haemost 1997; 78: 1115-1118.
-
(1997)
Thromb. Haemost.
, vol.78
, pp. 1115-1118
-
-
Nowak-Gottl, U.1
Binder, M.2
Dubbers, A.3
Kehrel, B.4
Koch, H.G.5
Veltmann, H.6
-
23
-
-
0029875717
-
Factor V gene mutation is a risk factor for cerebral venous thrombosis
-
Martinelli I, Landi G, Merati G, Cella R, Tosetto A, Mannucci PM. Factor V gene mutation is a risk factor for cerebral venous thrombosis. Thromb Haemost 1996; 75: 393-394.
-
(1996)
Thromb. Haemost.
, vol.75
, pp. 393-394
-
-
Martinelli, I.1
Landi, G.2
Merati, G.3
Cella, R.4
Tosetto, A.5
Mannucci, P.M.6
-
24
-
-
0029762332
-
Factor V Leiden mutation in cerebral venous thrombosis
-
Zuber M, Toulon P, Marnet L, Mas JL. Factor V Leiden mutation in cerebral venous thrombosis. Stroke 1996; 27: 1721-1723.
-
(1996)
Stroke
, vol.27
, pp. 1721-1723
-
-
Zuber, M.1
Toulon, P.2
Marnet, L.3
Mas, J.L.4
-
25
-
-
0029877791
-
Activated protein C and retinal vein occlusion
-
Hunt BJ. Activated protein C and retinal vein occlusion. Br J Ophthalmol 1996; 80: 194.
-
(1996)
Br. J. Ophthalmol.
, vol.80
, pp. 194
-
-
Hunt, B.J.1
-
26
-
-
0029927375
-
Activated protein C resistance in young adults with central retinal vein occlusion
-
Larsson J, Olafsdottir E, Bauer B. Activated protein C resistance in young adults with central retinal vein occlusion. Br J Ophthalmol 1996; 80: 200-202.
-
(1996)
Br. J. Ophthalmol.
, vol.80
, pp. 200-202
-
-
Larsson, J.1
Olafsdottir, E.2
Bauer, B.3
-
27
-
-
0034657644
-
Sudden infant death syndrome, childhood thrombosis, and presence of genetic risk factors for thrombosis
-
Larsen TB, Norgaard-Pedersen B, Lundemose JB, Rudiger N, Gaustadnes M, Brandslund I. Sudden infant death syndrome, childhood thrombosis, and presence of genetic risk factors for thrombosis. Thromb Res 2000; 98: 233-239.
-
(2000)
Thromb. Res.
, vol.98
, pp. 233-239
-
-
Larsen, T.B.1
Norgaard-Pedersen, B.2
Lundemose, J.B.3
Rudiger, N.4
Gaustadnes, M.5
Brandslund, I.6
-
28
-
-
0034995461
-
Prothrombic disorders and abnormal neurodevelopmental outcome in infants with neonatal cerebral infarction
-
Mercuri E, Cowan F, Gupte G, Manning R, Laffan M, Rutherford M. Prothrombic disorders and abnormal neurodevelopmental outcome in infants with neonatal cerebral infarction. Pediatrics 2001; 107: 1400-1404.
-
(2001)
Pediatrics
, vol.107
, pp. 1400-1404
-
-
Mercuri, E.1
Cowan, F.2
Gupte, G.3
Manning, R.4
Laffan, M.5
Rutherford, M.6
-
29
-
-
0032863259
-
Factor V Leiden mutation is associated with ocular involvement in Behcet disease
-
Verity DH, Vaughan RW, Madanat W, Kondeatis E, Zureikat H, Fayyad F, et al. Factor V Leiden mutation is associated with ocular involvement in Behcet disease. Am J Ophthalmol 1999; 128: 352-356.
-
(1999)
Am. J. Ophthalmol.
, vol.128
, pp. 352-356
-
-
Verity, D.H.1
Vaughan, R.W.2
Madanat, W.3
Kondeatis, E.4
Zureikat, H.5
Fayyad, F.6
-
30
-
-
0031302336
-
Frequency of Factor V (1691 G-A) Mutation in Turkish Population
-
Akar N, Akar E, Dalgin G, Sözüöz A, Ömürlü K, Cin S. Frequency of Factor V (1691 G-A) Mutation in Turkish Population. Thromb Haemost 1997; 78: 1527-1528.
-
(1997)
Thromb. Haemost.
, vol.78
, pp. 1527-1528
-
-
Akar, N.1
Akar, E.2
Dalgin, G.3
Sözüöz, A.4
Ömürlü, K.5
Cin, S.6
-
31
-
-
0029858481
-
Coagulation Factor V Gene Mutation increases the risk of venous thrombosis in Behçet's Disease
-
Gul A, Ozbek U, Oztürk C, Inanç M, Koniçe M, Ozçelik T. Coagulation Factor V Gene Mutation increases the risk of venous thrombosis in Behçet's Disease. Br J Rheumatology 1996: 35: 1178-1180.
-
(1996)
Br. J. Rheumatology
, vol.35
, pp. 1178-1180
-
-
Gul, A.1
Ozbek, U.2
Oztürk, C.3
Inanç, M.4
Koniçe, M.5
Ozçelik, T.6
-
32
-
-
0033843870
-
The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese
-
Irani-Hakime N, Tamim H, Kreidy R, Almawi YW. The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese. Am J Hematology 2000; 65: 45-49.
-
(2000)
Am. J. Hematology
, vol.65
, pp. 45-49
-
-
Irani-Hakime, N.1
Tamim, H.2
Kreidy, R.3
Almawi, Y.W.4
-
33
-
-
0029782276
-
Large-scale screening for factor V Leiden mutation in north-eastern German population
-
Schroder W, Koesling M, Wulff K, Wehnert M, Herrmann FH. Large-scale screening for factor V Leiden mutation in north-eastern German population. Haemostasis 1996; 26: 233-236.
-
(1996)
Haemostasis
, vol.26
, pp. 233-236
-
-
Schroder, W.1
Koesling, M.2
Wulff, K.3
Wehnert, M.4
Herrmann, F.H.5
-
34
-
-
0032922667
-
High prevalence of factor V Leiden in healthy Jordanian Arabs
-
Awidi A, Shannak M, Bseiso A, Kailani MA, Anshasi B, Omar N, et al. High prevalence of factor V Leiden in healthy Jordanian Arabs. Thromb Haemost 1999; 81: 582-584.
-
(1999)
Thromb. Haemost.
, vol.81
, pp. 582-584
-
-
Awidi, A.1
Shannak, M.2
Bseiso, A.3
Kailani, M.A.4
Anshasi, B.5
Omar, N.6
-
35
-
-
0030587024
-
High Prevalence of the FVR506Q mutation causing APC resistance in a region of southern Sweden with a high incidence of venous thrombosis
-
Zoller B, Norlund L, Leksell H, Nilsson JE, von Schenck H, Rosen U, et al. High Prevalence of the FVR506Q mutation causing APC resistance in a region of southern Sweden with a high incidence of venous thrombosis. Thromb Res 1996; 83: 475-477.
-
(1996)
Thromb. Res.
, vol.83
, pp. 475-477
-
-
Zoller, B.1
Norlund, L.2
Leksell, H.3
Nilsson, J.E.4
von Schenck, H.5
Rosen, U.6
-
36
-
-
0033832644
-
Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population
-
Angchaisuksiri P, Pingsuthiwong S, Aryuchai K, Busabaratana M, Sura T, Atichartakarn V, et al. Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population. Am J Hematol 2000; 65: 119-122.
-
(2000)
Am. J. Hematol.
, vol.65
, pp. 119-122
-
-
Angchaisuksiri, P.1
Pingsuthiwong, S.2
Aryuchai, K.3
Busabaratana, M.4
Sura, T.5
Atichartakarn, V.6
-
37
-
-
0033862236
-
The factor V Leiden and prothrombin G20210A mutations in Kirghiz population
-
Gurgey A, Kudayarov DK, Tuncer M, Parlak H, Altay C. The factor V Leiden and prothrombin G20210A mutations in Kirghiz population. Thromb Haemost 2000; 84: 356.
-
(2000)
Thromb. Haemost.
, vol.84
, pp. 356
-
-
Gurgey, A.1
Kudayarov, D.K.2
Tuncer, M.3
Parlak, H.4
Altay, C.5
-
38
-
-
0034108641
-
Prevalence of the prothrombin gene G20210A mutation in Azerbaijan
-
Togrul J, Rustamov R, Gurgey A, Altay S, Altay C. Prevalence of the prothrombin gene G20210A mutation in Azerbaijan. Br J Haematol 2000; 108: 887-888.
-
(2000)
Br. J. Haematol.
, vol.108
, pp. 887-888
-
-
Togrul, J.1
Rustamov, R.2
Gurgey, A.3
Altay, S.4
Altay, C.5
-
39
-
-
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, Economou-Petersen E, Petersen MB. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors. Am J Hematol 1999; 61: 265-267.
-
(1999)
Am. J. Hematol.
, vol.61
, pp. 265-267
-
-
Antoniadi, T.1
Hatzis, T.2
Kroupis, C.3
Economou-Petersen, E.4
Petersen, M.B.5
-
40
-
-
0033058695
-
Factor V Leiden mutation in the Argentinean population
-
Hepner M, Roldan A, Pieroni G, Frontroth JP, Serviddio RM, Torres AF, et al. Factor V Leiden mutation in the Argentinean population. Thromb Haemost 1999; 81: 989.
-
(1999)
Thromb. Haemost.
, vol.81
, pp. 989
-
-
Hepner, M.1
Roldan, A.2
Pieroni, G.3
Frontroth, J.P.4
Serviddio, R.M.5
Torres, A.F.6
-
41
-
-
0032923430
-
High prevalence of factor V Leiden mutation and 20210A prothrombin variant in Hungary
-
Balogh I, Poka R, Pfliegler G, Dekany M, Boda Z, Muszbek L. High prevalence of factor V Leiden mutation and 20210A prothrombin variant in Hungary. Thromb Haemost 1999; 81: 660-661.
-
(1999)
Thromb. Haemost.
, vol.81
, pp. 660-661
-
-
Balogh, I.1
Poka, R.2
Pfliegler, G.3
Dekany, M.4
Boda, Z.5
Muszbek, L.6
-
42
-
-
0034020835
-
Factor V Leiden and prothrombin G20210A variant are risk factors for venous thromboembolism in the Argentinean population
-
Adamczuk Y, Iglesias Varela ML, Forastiero R, Martinuzzo M, Cerrato G, Pombo G, et al. Factor V Leiden and prothrombin G20210A variant are risk factors for venous thromboembolism in the Argentinean population. Thromb Haemost 2000; 83: 509-510.
-
(2000)
Thromb. Haemost.
, vol.83
, pp. 509-510
-
-
Adamczuk, Y.1
Iglesias Varela, M.L.2
Forastiero, R.3
Martinuzzo, M.4
Cerrato, G.5
Pombo, G.6
-
43
-
-
0031981017
-
Geographic distribution of the 20210 G to A prothrombin variant
-
Rosendaal FR, Doggen CJ, Zivelin A, Arruda VR, Aiach M, Siscovick DS, et al. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 1998; 79: 706-708.
-
(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
-
44
-
-
4344685226
-
Prothrombin G20210A gene mutation with light cycler polymerase chain reaction in venous thrombosis and healthy population in the southeast of Turkey
-
(in press)
-
Ayyildiz O, Kalkanli S, Batun S, Aybak M, Isikdogan A, Tiftik N et al. Prothrombin G20210A gene mutation with light cycler polymerase chain reaction in venous thrombosis and healthy population in the southeast of Turkey. Heart Vessels 2004 (in press).
-
(2004)
Heart Vessels
-
-
Ayyildiz, O.1
Kalkanli, S.2
Batun, S.3
Aybak, M.4
Isikdogan, A.5
Tiftik, N.6
|