-
1
-
-
0041701487
-
Inherited platelet disorders
-
Hayward CPM. Inherited platelet disorders. Curr Opin Hematol 2003; 10: 362-8.
-
(2003)
Curr. Opin. Hematol.
, vol.10
, pp. 362-368
-
-
Hayward, C.P.M.1
-
2
-
-
0002764492
-
Congenital disorders of platelet secretion
-
Gresele P, Page C, Fuster V, Vermylen J, eds. Cambridge UK: The Press Syndicate of the University of Cambridge
-
Cattaneo M. Congenital disorders of platelet secretion. In: Gresele P, Page C, Fuster V, Vermylen J, eds. Platelets in thrombotic and non-thrombotic disorders. Pathophysiology, pharmacology and therapeutics. Cambridge UK: The Press Syndicate of the University of Cambridge; 2002; 655-73.
-
(2002)
Platelets in Thrombotic and Non-thrombotic Disorders. Pathophysiology, Pharmacology and Therapeutics
, pp. 655-673
-
-
Cattaneo, M.1
-
3
-
-
0142010841
-
Inherited Disorders of Platelet Function
-
Michelson AD (editor). San Diego, CA: Academic Press
-
Nurden AT, Nurden P. Inherited Disorders of Platelet Function. In: Michelson AD (editor). Platelets. San Diego, CA: Academic Press; 2002; 681-700.
-
(2002)
Platelets
, pp. 681-700
-
-
Nurden, A.T.1
Nurden, P.2
-
4
-
-
0002136770
-
Inherited abnormalities of the platelet membrane: Glanzmann thrombasthenia, Bernard-Soulier syndrome, and other disorders
-
Colman WR, Hirsh J, Marder VJ, Clowes AW, George JN (editors). 4th Ed. Philadelphia PA: Lippincott Williams and Wilkins
-
Nurden AT, George JN. Inherited abnormalities of the platelet membrane: Glanzmann thrombasthenia, Bernard-Soulier syndrome, and other disorders. In: Colman WR, Hirsh J, Marder VJ, Clowes AW, George JN (editors). Hemostasis and Thrombosis: Basic Principles and Clinical Practise. 4th Ed. Philadelphia PA: Lippincott Williams and Wilkins; 2001; 921-43.
-
(2001)
Hemostasis and Thrombosis: Basic Principles and Clinical Practise
, pp. 921-943
-
-
Nurden, A.T.1
George, J.N.2
-
5
-
-
0024259795
-
Guidelines on platelet function testing
-
The British Society for Haematology, BCSH Haemostasis and Thrombosis Task Force
-
The British Society for Haematology, BCSH Haemostasis and Thrombosis Task Force. Guidelines on platelet function testing. J Clin Pathol 1988; 41: 1322-30.
-
(1988)
J. Clin. Pathol.
, vol.41
, pp. 1322-1330
-
-
-
6
-
-
0042859862
-
Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects
-
Fontana P, Dupont A, Gandrille S, et al. Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects. Circulation 2003; 108: 989-95.
-
(2003)
Circulation
, vol.108
, pp. 989-995
-
-
Fontana, P.1
Dupont, A.2
Gandrille, S.3
-
7
-
-
0030061416
-
Prevalence of impaired responsiveness to epinephrine in platelets among Japanese
-
Kambayashi J, Shinoki N, Nakamura T, et al. Prevalence of impaired responsiveness to epinephrine in platelets among Japanese. Thromb Res 1996; 81: 85-90.
-
(1996)
Thromb. Res.
, vol.81
, pp. 85-90
-
-
Kambayashi, J.1
Shinoki, N.2
Nakamura, T.3
-
8
-
-
0034323126
-
Platelets from a patient heterozygous for the defect of P2cyc receptors for ADP have a secretion defect despite normal thromboxane A2 production and normal granule stores: Further evidence that some cases of platelet 'primary secretion defect' are heterozygous for a defect of P2cyc receptors
-
Cattaneo M, Lecchi A, Lombardi P, et al. Platelets from a patient heterozygous for the defect of P2cyc receptors for ADP have a secretion defect despite normal thromboxane A2 production and normal granule stores: further evidence that some cases of platelet 'primary secretion defect' are heterozygous for a defect of P2cyc receptors. Arterioscler Thromb Vasc Biol 2000; 20: e101-6.
-
(2000)
Arterioscler. Thromb. Vasc. Biol.
, vol.20
-
-
Cattaneo, M.1
Lecchi, A.2
Lombardi, P.3
-
9
-
-
0028942659
-
An inherited bleeding disorder linked to a defective interaction between ADP and its receptor on platelets
-
Nurden P, Savi P, Heilmann E, et al. An inherited bleeding disorder linked to a defective interaction between ADP and its receptor on platelets. J Clin Invest 1995; 95: 1612-22.
-
(1995)
J. Clin. Invest.
, vol.95
, pp. 1612-1622
-
-
Nurden, P.1
Savi, P.2
Heilmann, E.3
-
10
-
-
0023907023
-
Heterogeneous defects of platelet secretion and responses to weak agonists in patients with bleeding disorders
-
Lages B, Weiss HJ. Heterogeneous defects of platelet secretion and responses to weak agonists in patients with bleeding disorders. Br J Haematol 1988; 68: 53-62.
-
(1988)
Br. J. Haematol.
, vol.68
, pp. 53-62
-
-
Lages, B.1
Weiss, H.J.2
-
11
-
-
0034889515
-
The effect of human platelet alloantigen polymorphisms on the in vitro responsiveness to adrenaline and collagen
-
Theodoropoulos I, Christopoulos C, Metcalfe P, et al. The effect of human platelet alloantigen polymorphisms on the in vitro responsiveness to adrenaline and collagen. Br J Haematol 2001; 114: 387-93.
-
(2001)
Br. J. Haematol.
, vol.114
, pp. 387-393
-
-
Theodoropoulos, I.1
Christopoulos, C.2
Metcalfe, P.3
-
12
-
-
0022485174
-
Laboratory investigation of platelet function: A review of methodology
-
Yardumian DA, Mackie IJ, Machin SJ. Laboratory investigation of platelet function: a review of methodology. J Clin Pathol 1986; 39: 701-12.
-
(1986)
J. Clin. Pathol.
, vol.39
, pp. 701-712
-
-
Yardumian, D.A.1
Mackie, I.J.2
Machin, S.J.3
-
13
-
-
0035990305
-
The laboratory evaluation of platelet dysfunction
-
Peerschke EIB. The laboratory evaluation of platelet dysfunction. Clin Lab Med 2002; 22: 405-20.
-
(2002)
Clin. Lab. Med.
, vol.22
, pp. 405-420
-
-
Peerschke, E.I.B.1
-
14
-
-
0030299974
-
Pathogenic analysis of five cases with a platelet disorder characterized by the absence of thromboxane A2 (TXA2)-induced platelet aggregation in spite of normal TXA2 binding activity
-
Fuse I, Hattori A, Mito M, et al. Pathogenic analysis of five cases with a platelet disorder characterized by the absence of thromboxane A2 (TXA2)-induced platelet aggregation in spite of normal TXA2 binding activity. Thromb Haemost 1996; 76: 1080-5.
-
(1996)
Thromb. Haemost.
, vol.76
, pp. 1080-1085
-
-
Fuse, I.1
Hattori, A.2
Mito, M.3
-
15
-
-
0018750661
-
Inherited defective platelet aggregation with arachidonate as the main expression of a defective metabolism of arachidonic acid
-
Nyman D, Eriksson AW, Lehmann W, et al. Inherited defective platelet aggregation with arachidonate as the main expression of a defective metabolism of arachidonic acid. Thromb Res 1979; 14: 739-46.
-
(1979)
Thromb. Res.
, vol.14
, pp. 739-746
-
-
Nyman, D.1
Eriksson, A.W.2
Lehmann, W.3
-
16
-
-
0019781070
-
Epinephrine potentiation of arachidonate-induced aggregation of cyclooxygenase-deficient platelets
-
Rao GHR, White JG. Epinephrine potentiation of arachidonate-induced aggregation of cyclooxygenase-deficient platelets. Am J Hematol 1981; 11: 355-66.
-
(1981)
Am. J. Hematol.
, vol.11
, pp. 355-366
-
-
Rao, G.H.R.1
White, J.G.2
-
17
-
-
0023858616
-
Differential requirements for platelet aggregation and inhibition of adenylate cyclase by epinephrine. Studies of a familial platelet alpha2-adrenergic receptor defect
-
Rao AK, Willis J, Kowalska MA, et al. Differential requirements for platelet aggregation and inhibition of adenylate cyclase by epinephrine. Studies of a familial platelet alpha2-adrenergic receptor defect. Blood 1988; 71: 494-501.
-
(1988)
Blood
, vol.71
, pp. 494-501
-
-
Rao, A.K.1
Willis, J.2
Kowalska, M.A.3
-
18
-
-
0029952371
-
An autosomal dominant, qualitative platelet disorder associated with multimerin deficiency, abnormalities in platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen and an epinephrine aggregation defect
-
Hayward CPM, Rivard GE, Kane WH, et al. An autosomal dominant, qualitative platelet disorder associated with multimerin deficiency, abnormalities in platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen and an epinephrine aggregation defect. Blood 1996; 87: 4967-78.
-
(1996)
Blood
, vol.87
, pp. 4967-4978
-
-
Hayward, C.P.M.1
Rivard, G.E.2
Kane, W.H.3
-
19
-
-
0014664167
-
A familial defect in platelet function associated with impaired release of adenosine diphosphate
-
Weiss HJ, Chervenick PA, Zalusky R, et al. A familial defect in platelet function associated with impaired release of adenosine diphosphate. N Engl J Med 1969; 281: 1264-70.
-
(1969)
N. Engl. J. Med.
, vol.281
, pp. 1264-1270
-
-
Weiss, H.J.1
Chervenick, P.A.2
Zalusky, R.3
-
20
-
-
0018673733
-
Heterogeneity in storage pool deficiency: Studies on granule-bound substances in 18 patients including variants deficient in α-granules, platelet factor 4, β-thromboglobulin, and platelet-derived growth factor
-
Weiss HJ, Witte LD, Kaplan KL, et al. Heterogeneity in storage pool deficiency: studies on granule-bound substances in 18 patients including variants deficient in α-granules, platelet factor 4, β-thromboglobulin, and platelet-derived growth factor. Blood 1979; 54: 1296-319.
-
(1979)
Blood
, vol.54
, pp. 1296-1319
-
-
Weiss, H.J.1
Witte, L.D.2
Kaplan, K.L.3
-
21
-
-
0027411863
-
Heterogeneous abnormalities of platelet dense granule ultrastructure in 20 patients with congenital storage pool deficiency
-
Weiss HJ, Lages B, Vicic W, et al. Heterogeneous abnormalities of platelet dense granule ultrastructure in 20 patients with congenital storage pool deficiency. Br J Haematol 1993; 83: 282-95.
-
(1993)
Br. J. Haematol.
, vol.83
, pp. 282-295
-
-
Weiss, H.J.1
Lages, B.2
Vicic, W.3
-
22
-
-
0028201807
-
A revised classification of von Willebrand Disease
-
Sadler JE. A revised classification of von Willebrand Disease. Thromb Haemost 1994; 71: 520-5.
-
(1994)
Thromb. Haemost.
, vol.71
, pp. 520-525
-
-
Sadler, J.E.1
-
23
-
-
2342656365
-
The diagnosis of von Willebrand disease: A guideline from the UK haemophilia centre doctors' organization
-
Laffan M, Brown SA, Collins PW, et al. The diagnosis of von Willebrand disease: a guideline from the UK haemophilia centre doctors' organization. Haemophilia 2004; 10: 199-217.
-
(2004)
Haemophilia
, vol.10
, pp. 199-217
-
-
Laffan, M.1
Brown, S.A.2
Collins, P.W.3
-
24
-
-
0141609789
-
Inherited platelet-based bleeding disorders
-
Cattaneo M. Inherited platelet-based bleeding disorders. J Thromb Haemost 2003; 1: 1628-36.
-
(2003)
J. Thromb. Haemost.
, vol.1
, pp. 1628-1636
-
-
Cattaneo, M.1
|