-
1
-
-
0033168347
-
Contribution of distinct adhesive interactions to platelet aggregation in flowing blood
-
Ruggeri ZM, Dent JA, Saldivar E: Contribution of distinct adhesive interactions to platelet aggregation in flowing blood. Blood 1999;94:172-178.
-
(1999)
Blood
, vol.94
, pp. 172-178
-
-
Ruggeri, Z.M.1
Dent, J.A.2
Saldivar, E.3
-
2
-
-
0002136770
-
Inherited abnormalities of the platelet membrane: Glanzmann thrombasthenia, Bernard-Soulier syndrome, and other disorders
-
Colman RW, Hirsh J, Clowes AW, George JN (eds). Philadelphia, Lippincott Williams & Wilkins
-
Nurden AT, George JN: Inherited abnormalities of the platelet membrane: Glanzmann thrombasthenia, Bernard-Soulier syndrome, and other disorders; in Colman RW, Hirsh J, Clowes AW, George JN (eds): Hemostasis and Thrombosis: Basic Principles and Clinical Practice, ed 4. Philadelphia, Lippincott Williams & Wilkins, 2001, pp 921-943.
-
(2001)
Hemostasis and Thrombosis: Basic Principles and Clinical Practice, Ed 4
, pp. 921-943
-
-
Nurden, A.T.1
George, J.N.2
-
3
-
-
0033873109
-
Platelet glycoprotein polymorphisms as risk factors for thrombosis
-
Bray PF: Platelet glycoprotein polymorphisms as risk factors for thrombosis. Curr Opin Hematol 2000;7:284-289.
-
(2000)
Curr Opin Hematol
, vol.7
, pp. 284-289
-
-
Bray, P.F.1
-
4
-
-
0032952730
-
The number of platelet glycoprotein Ia molecules is associated with the genetically linked 807 C/T and HPA-5 polymorphisms
-
Corral J, Rivera J, Gonzalez-Conejero R, Vicente V: The number of platelet glycoprotein Ia molecules is associated with the genetically linked 807 C/T and HPA-5 polymorphisms. Transfusion 1999;39:372-378.
-
(1999)
Transfusion
, vol.39
, pp. 372-378
-
-
Corral, J.1
Rivera, J.2
Gonzalez-Conejero, R.3
Vicente, V.4
-
5
-
-
0026655919
-
Polymorphism of human glycoprotein Ibα results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macro-glycopeptide region
-
López JA, Ludwig EH, McCarthy BJ: Polymorphism of human glycoprotein Ibα results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macro-glycopeptide region. J Biol Chem 1992;267:10055-10061.
-
(1992)
J Biol Chem
, vol.267
, pp. 10055-10061
-
-
López, J.A.1
Ludwig, E.H.2
McCarthy, B.J.3
-
6
-
-
0029087909
-
Polymorphism of human membrane glycoproteins: Structure and clinical significance
-
Nurden AT: Polymorphism of human membrane glycoproteins: Structure and clinical significance. Thromb Haemost 1995;74:345-351.
-
(1995)
Thromb Haemost
, vol.74
, pp. 345-351
-
-
Nurden, A.T.1
-
7
-
-
0032189318
-
Reduced microvascular thrombosis and improved outcome in acute murine stroke by inhibition GP IIb/IIIa receptor-mediated platelet aggregation
-
Choudhri TF, Hoh BL, Zerwes HG, Prestigiacomo CJ, Kim SC, Connolly ES Jr, Kottirsch G, Pinsky DJ: Reduced microvascular thrombosis and improved outcome in acute murine stroke by inhibition GP IIb/IIIa receptor-mediated platelet aggregation. J Clin Invest 1998;102:1301-1310.
-
(1998)
J Clin Invest
, vol.102
, pp. 1301-1310
-
-
Choudhri, T.F.1
Hoh, B.L.2
Zerwes, H.G.3
Prestigiacomo, C.J.4
Kim, S.C.5
Connolly E.S., Jr.6
Kottirsch, G.7
Pinsky, D.J.8
-
8
-
-
0034085158
-
Integrin alpha (IIb) beta (3) inhibitor preserves microvascular patency in experimental acute focal cerebral ischemia
-
Abumiya T, Fitridge R, Mazur C, Copeland BR, Koziol JA, Tschopp JF, Pierschbacher MD, del Zoppo GJ: Integrin alpha (IIb) beta (3) inhibitor preserves microvascular patency in experimental acute focal cerebral ischemia. Stroke 2000;31:1402-1409.
-
(2000)
Stroke
, vol.31
, pp. 1402-1409
-
-
Abumiya, T.1
Fitridge, R.2
Mazur, C.3
Copeland, B.R.4
Koziol, J.A.5
Tschopp, J.F.6
Pierschbacher, M.D.7
Del Zoppo, G.J.8
-
9
-
-
0033137301
-
Low platelet alpha2beta1 levels in type I von Willebrand disease correlate with impaired platelet function in a high shear stress system
-
Di Paola J, Federici AB, Mannucci PM, Canciani MT, Kritzik M, Kunicki TJ, Nugent D: Low platelet alpha2beta1 levels in type I von Willebrand disease correlate with impaired platelet function in a high shear stress system. Blood 1999;93:3578-3582.
-
(1999)
Blood
, vol.93
, pp. 3578-3582
-
-
Di Paola, J.1
Federici, A.B.2
Mannucci, P.M.3
Canciani, M.T.4
Kritzik, M.5
Kunicki, T.J.6
Nugent, D.7
-
10
-
-
0035760865
-
Genetic variation in glycoprotein IIb/IIIa (GP IIb/IIIa) as a determinant of the responses to an oral GP IIb/IIIa antagonist in patients with unstable coronary syndromes
-
O'Connor FF, Shields DC, Fitzgerald A, Cannon CP, Braunwald E, Fitzgerald DJ: Genetic variation in glycoprotein IIb/IIIa (GP IIb/IIIa) as a determinant of the responses to an oral GP IIb/IIIa antagonist in patients with unstable coronary syndromes. Blood 2001;98:3256-3260.
-
(2001)
Blood
, vol.98
, pp. 3256-3260
-
-
O'Connor, F.F.1
Shields, D.C.2
Fitzgerald, A.3
Cannon, C.P.4
Braunwald, E.5
Fitzgerald, D.J.6
-
11
-
-
0001894742
-
Cerebrovascular diseases
-
Adams RD, Victor M, Ropper AH (eds). New York, McGraw-Hill
-
Adams RD, Victor M, Ropper AH: Cerebrovascular diseases; in Adams RD, Victor M, Ropper AH (eds): Principles of Neurology. New York, McGraw-Hill, 1997, pp 777-873.
-
(1997)
Principles of Neurology
, pp. 777-873
-
-
Adams, R.D.1
Victor, M.2
Ropper, A.H.3
-
13
-
-
0025253068
-
Glanzmann's thrombasthenia: The spectrum of clinical disease
-
George JN, Caen JP, Nurden AT: Glanzmann's thrombasthenia: The spectrum of clinical disease. Blood 1990;75:1383-1395.
-
(1990)
Blood
, vol.75
, pp. 1383-1395
-
-
George, J.N.1
Caen, J.P.2
Nurden, A.T.3
-
14
-
-
0034663250
-
Incidence of intracranial hemorrhage complicating treatment with glycoprotein IIb/IIIa receptor inhibitors: A pooled analysis of major clinical trials
-
Memon MA, Blankenship JC, Wood GC, Frey CM, Menapace FJ: Incidence of intracranial hemorrhage complicating treatment with glycoprotein IIb/IIIa receptor inhibitors: A pooled analysis of major clinical trials. Am J Med 2000;109:213-217.
-
(2000)
Am J Med
, vol.109
, pp. 213-217
-
-
Memon, M.A.1
Blankenship, J.C.2
Wood, G.C.3
Frey, C.M.4
Menapace, F.J.5
-
15
-
-
0029875770
-
A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis
-
Weiss EJ, Bray PF, Tayback M, Schulman SP, Kickler TS, Becker LC, Weiss JL, Gerstenblith G, Goldschmidt-Clermont PJ: A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis. N Engl J Med 1996;334:1090-1094.
-
(1996)
N Engl J Med
, vol.334
, pp. 1090-1094
-
-
Weiss, E.J.1
Bray, P.F.2
Tayback, M.3
Schulman, S.P.4
Kickler, T.S.5
Becker, L.C.6
Weiss, J.L.7
Gerstenblith, G.8
Goldschmidt-Clermont, P.J.9
-
16
-
-
0032532036
-
Polymorphisms of platelet membrane glycoprotein Ib associated with arterial thrombotic disease
-
González-Conejero R, Lozano ML, Rivera J, Corral J, Iniesta JA, Moraleda JM, Vicente V: Polymorphisms of platelet membrane glycoprotein Ib associated with arterial thrombotic disease. Blood 1998;92:2771-2776.
-
(1998)
Blood
, vol.92
, pp. 2771-2776
-
-
González-Conejero, R.1
Lozano, M.L.2
Rivera, J.3
Corral, J.4
Iniesta, J.A.5
Moraleda, J.M.6
Vicente, V.7
-
17
-
-
0034332876
-
Meta-analysis of the association of platelet glycoprotein IIIa PlA1/A2 polymorphism with myocardial infarction
-
Zhu MM, Weedon J, Clark LT: Meta-analysis of the association of platelet glycoprotein IIIa PlA1/A2 polymorphism with myocardial infarction. Am J Cardiol 2000;86:1000-1005.
-
(2000)
Am J Cardiol
, vol.86
, pp. 1000-1005
-
-
Zhu, M.M.1
Weedon, J.2
Clark, L.T.3
-
18
-
-
0028274014
-
The platelet glycoprotein Ib-IX complex
-
López JA: The platelet glycoprotein Ib-IX complex. Blood Coagul Fibrinolysis 1994;5:97-119.
-
(1994)
Blood Coagul Fibrinolysis
, vol.5
, pp. 97-119
-
-
López, J.A.1
-
19
-
-
0035874495
-
Polymorphisms of clotting factors modify the risk of primary intracranial hemorrhage
-
Corral J, Iniesta JA, González-Conejero R, Villalón M, Vicente V: Polymorphisms of clotting factors modify the risk of primary intracranial hemorrhage. Blood 2001;97:2979-2982.
-
(2001)
Blood
, vol.97
, pp. 2979-2982
-
-
Corral, J.1
Iniesta, J.A.2
González-Conejero, R.3
Villalón, M.4
Vicente, V.5
-
20
-
-
0029820281
-
Moderation of hemophilia A phenotype by the factor V R506Q mutation
-
Nichols WC, Amano K, Cacheris PM, Figueiredo MS, Michaelides K, Schwaab R, Hoyer L, Kaufman RJ, Ginsburg D: Moderation of hemophilia A phenotype by the factor V R506Q mutation. Blood 1996;88:1183-1187.
-
(1996)
Blood
, vol.88
, pp. 1183-1187
-
-
Nichols, W.C.1
Amano, K.2
Cacheris, P.M.3
Figueiredo, M.S.4
Michaelides, K.5
Schwaab, R.6
Hoyer, L.7
Kaufman, R.J.8
Ginsburg, D.9
-
21
-
-
0031594157
-
Factor V Q506 mutation (activated protein C resistance) associated with reduced intrapartum blood loss - A possible evolutionary selection mechanism
-
Lindqvist PG, Svensson PJ, Dahlbäck B, Marsál K: Factor V Q506 mutation (activated protein C resistance) associated with reduced intrapartum blood loss - a possible evolutionary selection mechanism. Thomb Haemost 1998;79:69-73.
-
(1998)
Thomb Haemost
, vol.79
, pp. 69-73
-
-
Lindqvist, P.G.1
Svensson, P.J.2
Dahlbäck, B.3
Marsál, K.4
-
22
-
-
0027935390
-
Platelet activation and arterial thrombosis. Report of a meeting of Physicians and Scientists, University of Texas Health Science Center at Houston and Texas Heart Institute, Houston
-
Platelet activation and arterial thrombosis. Report of a meeting of Physicians and Scientists, University of Texas Health Science Center at Houston and Texas Heart Institute, Houston. Lancet 1994;344:991-995.
-
(1994)
Lancet
, vol.344
, pp. 991-995
-
-
-
23
-
-
0033937685
-
Genetic variants of platelet glycoprotein receptors and risk of stroke in young women
-
Reiner AP, Kumar PN, Schwartz SM, Longstreth WT Jr, Pearce RM, Rosendaal FR, Psaty BM, Siscovick DS: Genetic variants of platelet glycoprotein receptors and risk of stroke in young women. Stroke 2000;31:1628-1633.
-
(2000)
Stroke
, vol.31
, pp. 1628-1633
-
-
Reiner, A.P.1
Kumar, P.N.2
Schwartz, S.M.3
Longstreth W.T., Jr.4
Pearce, R.M.5
Rosendaal, F.R.6
Psaty, B.M.7
Siscovick, D.S.8
-
24
-
-
0034016852
-
Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A
-
Lee DH, Walker IR, Teitel J, et al: Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A. Thromb Haemost 2000;83:387-391.
-
(2000)
Thromb Haemost
, vol.83
, pp. 387-391
-
-
Lee, D.H.1
Walker, I.R.2
Teitel, J.3
-
25
-
-
0035487920
-
Improved hemoglobin status and reduced menstrual blood loss among female carriers of factor V Leiden - An evolutionary advantage?
-
Lindqvist PG, Zoller B, Dahlback B: Improved hemoglobin status and reduced menstrual blood loss among female carriers of factor V Leiden - an evolutionary advantage? Thromb Haemost 2001;86:1122-1123.
-
(2001)
Thromb Haemost
, vol.86
, pp. 1122-1123
-
-
Lindqvist, P.G.1
Zoller, B.2
Dahlback, B.3
-
26
-
-
0035129399
-
Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors
-
Escuriola Ettingshausen C, Halimeh S, Kurnik K, et al: Symptomatic onset of severe hemo-philia A in childhood is dependent on the presence of prothrombotic risk factors. Thromb Haemost 2001;85:218-220.
-
(2001)
Thromb Haemost
, vol.85
, pp. 218-220
-
-
Escuriola Ettingshausen, C.1
Halimeh, S.2
Kurnik, K.3
-
27
-
-
0036195046
-
The prothrombin 20210 A allele influences clinical manifestation of hemophilia A in patients with intron 22 inversion and without inhibitors
-
Tizzano EF, Soria JM, Coll I, Guzmán B, Cornet M, Altisent C, Martorell M, Domenech M, del Rio E, Fontcuberta J, Baiget M: The prothrombin 20210 A allele influences clinical manifestation of hemophilia A in patients with intron 22 inversion and without inhibitors. Haematologica 2002;87:279-285.
-
(2002)
Haematologica
, vol.87
, pp. 279-285
-
-
Tizzano, E.F.1
Soria, J.M.2
Coll, I.3
Guzmán, B.4
Cornet, M.5
Altisent, C.6
Martorell, M.7
Domenech, M.8
Del Rio, E.9
Fontcuberta, J.10
Baiget, M.11
-
28
-
-
0034789084
-
Low prevalence of large intraventricular haemorrhage in very low birthweight infants carrying the factor V Leiden or prothrombin G20210A mutation
-
Gopel W, Gortner L, Kohlman T, Schultz C, Moller J: Low prevalence of large intraventricular haemorrhage in very low birthweight infants carrying the factor V Leiden or prothrombin G20210A mutation. Acta Paediatr 2001;90:1021-1024.
-
(2001)
Acta Paediatr
, vol.90
, pp. 1021-1024
-
-
Gopel, W.1
Gortner, L.2
Kohlman, T.3
Schultz, C.4
Moller, J.5
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