-
2
-
-
84866794231
-
Splenektomi sonrasi mezenter damar trombozu gelişen bir talessemia intermedia vakasi
-
Kale N, Hiçsönmez G, Gürgey A, Kale G, Altay Ç. Splenektomi sonrasi mezenter damar trombozu gelişen bir talessemia intermedia vakasi. Çocuk Saǧliǧi ve Hastaliklari Dergisi 1986; 29: 67-70.
-
(1986)
Çocuk Saǧliǧi Ve Hastaliklari Dergisi
, vol.29
, pp. 67-70
-
-
Kale, N.1
Hiçsönmez, G.2
Gürgey, A.3
Kale, G.4
Altay, Ç.5
-
3
-
-
0024366707
-
Plasma protein C levels in children with sickle cell disease
-
Karayalçin G, Lanzkowsky P. Plasma protein C levels in children with sickle cell disease. Am J Pediatr Hematol Oncol 1989; 11: 320-323.
-
(1989)
Am J Pediatr Hematol Oncol
, vol.11
, pp. 320-323
-
-
Karayalçin, G.1
Lanzkowsky, P.2
-
4
-
-
0028903653
-
Changes in coagulation and fibrinolysis in patients with sickle cell disease compared with healthy black controls
-
Hagger D, Wolff S, Owen J, Samson D. Changes in coagulation and fibrinolysis in patients with sickle cell disease compared with healthy black controls. Blood Coagul Fibrin 1995; 6: 93-99.
-
(1995)
Blood Coagul Fibrin
, vol.6
, pp. 93-99
-
-
Hagger, D.1
Wolff, S.2
Owen, J.3
Samson, D.4
-
5
-
-
0022966475
-
Is sickle cell crisis a thrombotic event?
-
Green D, Scott JP. Is sickle cell crisis a thrombotic event? Am J Hematol 1986; 23: 317-321.
-
(1986)
Am J Hematol
, vol.23
, pp. 317-321
-
-
Green, D.1
Scott, J.P.2
-
6
-
-
0030694226
-
Sickle cell disease: Relation between procoagulant activity of red blood cells from different phenotypes and in-vivo blood coagulation activation
-
Helley D, Girot R, Guillin MC, Bezeaurd A. Sickle cell disease: relation between procoagulant activity of red blood cells from different phenotypes and in-vivo blood coagulation activation. Br J Haematol 1997; 99: 268-272.
-
(1997)
Br J Haematol
, vol.99
, pp. 268-272
-
-
Helley, D.1
Girot, R.2
Guillin, M.C.3
Bezeaurd, A.4
-
8
-
-
0028350995
-
Hypercoagulability and thrombosis
-
Bick RL (ed). Common Bleeding and Clotting Disorders for the Internist
-
Bick LB. Hypercoagulability and thrombosis. In: Bick RL (ed). Common Bleeding and Clotting Disorders for the Internist. Med Clin North Am 1994; 78: 635-665.
-
(1994)
Med Clin North Am
, vol.78
, pp. 635-665
-
-
Bick, L.B.1
-
9
-
-
0027957535
-
Enhanced thrombin generation in children with sickle cell disease
-
Peters BE, ten Cate H, Wolters HJ, Weening RS, Brandjes DP. Enhanced thrombin generation in children with sickle cell disease. Thromb Haemost 1994; 71: 169-172.
-
(1994)
Thromb Haemost
, vol.71
, pp. 169-172
-
-
Peters, B.E.1
Ten Cate, H.2
Wolters, H.J.3
Weening, R.S.4
Brandjes, D.P.5
-
10
-
-
0026178580
-
Heparin cofactor II: An acute phase reactant in patients with deep vein thrombosis
-
Toulon P, Vitoux JF, Fiessenger JN, et al. Heparin cofactor II: an acute phase reactant in patients with deep vein thrombosis. Blood Coagul Fibrinolysis 1991; 3: 435-439.
-
(1991)
Blood Coagul Fibrinolysis
, vol.3
, pp. 435-439
-
-
Toulon, P.1
Vitoux, J.F.2
Fiessenger, J.N.3
-
11
-
-
0029075446
-
Low plasma heparin cofactor II levels in thalassemia syndromes are corrected by chronic blood transfusion
-
Driscol A, Mackie IJ, Porter B, Machin SJ. Low plasma heparin cofactor II levels in thalassemia syndromes are corrected by chronic blood transfusion. Br J Haematol 1995; 90: 65-70.
-
(1995)
Br J Haematol
, vol.90
, pp. 65-70
-
-
Driscol, A.1
Mackie, I.J.2
Porter, B.3
Machin, S.J.4
-
12
-
-
0031042922
-
Acquired von Willebrand disease: A concise reiew
-
Rinder MR, Richard RE, Rinder HM. Acquired von Willebrand disease: a concise reiew. Am J Hematol 1997; 54: 139-145.
-
(1997)
Am J Hematol
, vol.54
, pp. 139-145
-
-
Rinder, M.R.1
Richard, R.E.2
Rinder, H.M.3
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