-
1
-
-
0025253068
-
Glanzmann's thrombasthenia: the spectrum of clinical disease
-
George J.N., Caen J.P., and Nurden A.T. Glanzmann's thrombasthenia: the spectrum of clinical disease. Blood 75 (1990) 1383-1395
-
(1990)
Blood
, vol.75
, pp. 1383-1395
-
-
George, J.N.1
Caen, J.P.2
Nurden, A.T.3
-
2
-
-
0031929048
-
The molecular genetics of Glanzmann's thrombasthenia
-
French D.L. The molecular genetics of Glanzmann's thrombasthenia. Platelets 9 (1998) 5-20
-
(1998)
Platelets
, vol.9
, pp. 5-20
-
-
French, D.L.1
-
3
-
-
0034103571
-
Platelet glycoprotein IIb/IIIa receptors and Glanzmann's thrombasthenia
-
French D.L., and Seligsohn U. Platelet glycoprotein IIb/IIIa receptors and Glanzmann's thrombasthenia. Arterioscler Thromb Vasc Biol 20 (2000) 607-610
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
, pp. 607-610
-
-
French, D.L.1
Seligsohn, U.2
-
4
-
-
0036436932
-
Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease
-
Ghosh K., Kulkarni B., Nair S., Shetty S., and Mohanty D. Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease. Br J Haematol 119 (2002) 348-353
-
(2002)
Br J Haematol
, vol.119
, pp. 348-353
-
-
Ghosh, K.1
Kulkarni, B.2
Nair, S.3
Shetty, S.4
Mohanty, D.5
-
5
-
-
3042701610
-
Milder bleeding tendency in Glanzmann's thrombasthenia patients inheriting HPA-1b in the homozygous state
-
Ghosh K., Nair S., Kulkarni B., Shetty S., and Mohanty D. Milder bleeding tendency in Glanzmann's thrombasthenia patients inheriting HPA-1b in the homozygous state. J Thromb Haemost 1 (2003) 2255-2256
-
(2003)
J Thromb Haemost
, vol.1
, pp. 2255-2256
-
-
Ghosh, K.1
Nair, S.2
Kulkarni, B.3
Shetty, S.4
Mohanty, D.5
-
6
-
-
0346102708
-
Glansmann's Thrombasthemia Italian Team (GLATIT). Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism
-
D'Andrea G., and Margaglione M. Glansmann's Thrombasthemia Italian Team (GLATIT). Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. Haematologica 88 (2003) 1378-1382
-
(2003)
Haematologica
, vol.88
, pp. 1378-1382
-
-
D'Andrea, G.1
Margaglione, M.2
-
7
-
-
0031833274
-
Screening for factor V Leiden and a prothrombin gene polymorphism in patients with Glanzmann's thrombasthenia
-
Duperat V.G., Vergnes C., Nurden P., and Nurden A.T. Screening for factor V Leiden and a prothrombin gene polymorphism in patients with Glanzmann's thrombasthenia. Br J Haematol 101 (1998) 593-594
-
(1998)
Br J Haematol
, vol.101
, pp. 593-594
-
-
Duperat, V.G.1
Vergnes, C.2
Nurden, P.3
Nurden, A.T.4
-
8
-
-
0141561924
-
The role of platelets in venous thrombosis: a patient with Glanzmann's thrombasthenia and a factor V Leiden mutation suffering from deep venous thrombosis
-
Ten Cate H., Brandjes D.P., Smits P.H., and van Mourik J.A. The role of platelets in venous thrombosis: a patient with Glanzmann's thrombasthenia and a factor V Leiden mutation suffering from deep venous thrombosis. J Thromb Haemost 1 (2003) 394-395
-
(2003)
J Thromb Haemost
, vol.1
, pp. 394-395
-
-
Ten Cate, H.1
Brandjes, D.P.2
Smits, P.H.3
van Mourik, J.A.4
-
9
-
-
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 S.R., Rosendaal F.R., Reitsma P.H., and Bertina R.M. 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 88 (1996) 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
-
10
-
-
0034193350
-
Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis
-
Soria J.M., Almasy L., Souto J.C., et al. Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis. Blood 95 (2000) 2780-2785
-
(2000)
Blood
, vol.95
, pp. 2780-2785
-
-
Soria, J.M.1
Almasy, L.2
Souto, J.C.3
-
11
-
-
0028335097
-
High prevalence of hyperhomocyst(e)inemia in patients with juvenile venous thrombosis
-
Falcon C.R., Cattaneo M., Panzeri D., Martinelli I., and Mannucci P.M. High prevalence of hyperhomocyst(e)inemia in patients with juvenile venous thrombosis. Arterioscler Thromb 14 (1994) 1080-1083
-
(1994)
Arterioscler Thromb
, vol.14
, pp. 1080-1083
-
-
Falcon, C.R.1
Cattaneo, M.2
Panzeri, D.3
Martinelli, I.4
Mannucci, P.M.5
-
12
-
-
0028853921
-
Prevalence of moderate hyperhomocysteinemia in patients with early-onset venous and arterial occlusive disease
-
Fermo I., Vigano' D'Angelo S., Paroni R., et al. Prevalence of moderate hyperhomocysteinemia in patients with early-onset venous and arterial occlusive disease. Ann Intern Med 123 (1995) 747-753
-
(1995)
Ann Intern Med
, vol.123
, pp. 747-753
-
-
Fermo, I.1
Vigano' D'Angelo, S.2
Paroni, R.3
-
13
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
-
Frosst P., Blom H.J., Milos R., et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10 (1995) 111-113
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
-
14
-
-
2642701740
-
Analysis of the 677 C->T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups
-
Franco R.F., Araujo A.G., Guerreiro J.F., Elion J., and Zago M.A. Analysis of the 677 C->T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups. Thromb Haemost 79 (1998) 119-121
-
(1998)
Thromb Haemost
, vol.79
, pp. 119-121
-
-
Franco, R.F.1
Araujo, A.G.2
Guerreiro, J.F.3
Elion, J.4
Zago, M.A.5
-
15
-
-
0028890671
-
Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia
-
Engbersen A.M., Franken D.G., Boers G.H., et al. Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia. Am J Hum Genet 56 (1995) 142-150
-
(1995)
Am J Hum Genet
, vol.56
, pp. 142-150
-
-
Engbersen, A.M.1
Franken, D.G.2
Boers, G.H.3
-
16
-
-
0012749942
-
Factor V Leiden-the commonest molecular defect in arterial and venous thrombophilia in India
-
Ahmed R., Gupta P.K., Kannan M., Choudhry V.P., and Saxena R. Factor V Leiden-the commonest molecular defect in arterial and venous thrombophilia in India. Thromb Res 110 (2003) 9-21
-
(2003)
Thromb Res
, vol.110
, pp. 9-21
-
-
Ahmed, R.1
Gupta, P.K.2
Kannan, M.3
Choudhry, V.P.4
Saxena, R.5
-
17
-
-
0037241181
-
Does the MTHFR 677T allele alter the clinical phenotype in severe haemophilia A?
-
Ahmed R., Kannan M., Choudhry V.P., and Saxena R. Does the MTHFR 677T allele alter the clinical phenotype in severe haemophilia A?. Thromb Res 109 (2003) 71-72
-
(2003)
Thromb Res
, vol.109
, pp. 71-72
-
-
Ahmed, R.1
Kannan, M.2
Choudhry, V.P.3
Saxena, R.4
|