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Volumn 11, Issue 2, 2004, Pages 195-208

Pathophysiology of stroke in sickle cell disease

Author keywords

Hypercoagulable state; Nitric oxide; Oxidative endothelial injury; Red cell adhesion; Sickle cell disease; Stroke

Indexed keywords

ACENOCOUMAROL; ACETYLSALICYLIC ACID; ACETYLSALICYLIC ACID PLUS DIPYRIDAMOLE; ANTICOAGULANT AGENT; ANTIINFLAMMATORY AGENT; ANTIOXIDANT; ANTITHROMBOCYTIC AGENT; BLOOD CLOTTING FACTOR 8; DEFEROXAMINE; ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE 1; FIBRINOGEN; HEPARIN; HYDROXYUREA; PADGEM PROTEIN; TICLOPIDINE; VASCULAR CELL ADHESION MOLECULE 1; VITRONECTIN RECEPTOR; VON WILLEBRAND FACTOR; WARFARIN;

EID: 3242753073     PISSN: 10739688     EISSN: None     Source Type: Journal    
DOI: 10.1080/10739680490278600     Document Type: Review
Times cited : (74)

References (116)
  • 5
    • 10244259849 scopus 로고
    • Cerebral vascular lesions accompanying sickle-cell anemia
    • Arena JM. (1939). Cerebral vascular lesions accompanying sickle-cell anemia. J Pediatr 14:745-751.
    • (1939) J. Pediatr. , vol.14 , pp. 745-751
    • Arena, J.M.1
  • 6
    • 15844366370 scopus 로고    scopus 로고
    • Cognitive functioning and brain magnetic resonance imaging in children with sickle Cell disease
    • Neuropsychology Commitee of the Cooperative Study of Sickle Cell Disease
    • Armstrong FD, Thompson RJ, Jr., Wang W, Zimmerman R, Pegelow CH, Miller S, Moser F, Bello J, Hurtig A, Vass K. (1996). Cognitive functioning and brain magnetic resonance imaging in children with sickle Cell disease. Neuropsychology Commitee of the Cooperative Study of Sickle Cell Disease. Pediatrics 97:864-870.
    • (1996) Pediatrics , vol.97 , pp. 864-870
    • Armstrong, F.D.1    Thompson Jr., R.J.2    Wang, W.3    Zimmerman, R.4    Pegelow, C.H.5    Miller, S.6    Moser, F.7    Bello, J.8    Hurtig, A.9    Vass, K.10
  • 8
    • 0033512569 scopus 로고    scopus 로고
    • Correlation of the C677T MTHFR genotype with homocysteine levels in children with sickle cell disease
    • Balasa VV, Gruppo RA, Gartside PS, Kalinyak KA. (1999). Correlation of the C677T MTHFR genotype with homocysteine levels in children with sickle cell disease. J Pediatr Hematol Oncol 21:397-400.
    • (1999) J. Pediatr. Hematol. Oncol. , vol.21 , pp. 397-400
    • Balasa, V.V.1    Gruppo, R.A.2    Gartside, P.S.3    Kalinyak, K.A.4
  • 10
    • 0024328119 scopus 로고
    • Platelet activation during pain crisis in sickle cell anemia patients
    • Beurling-Harbury C Schade SG. (1989). Platelet activation during pain crisis in sickle cell anemia patients. Am J Hematol 31:237-241.
    • (1989) Am. J. Hematol. , vol.31 , pp. 237-241
    • Beurling-Harbury, C.1    Schade, S.G.2
  • 11
    • 0001246993 scopus 로고
    • Cerebral vascular disease accompanying sickle cell anemia
    • Bridgers WH. (1939). Cerebral vascular disease accompanying sickle cell anemia. Am J Pathol 15:353-361.
    • (1939) Am. J. Pathol. , vol.15 , pp. 353-361
    • Bridgers, W.H.1
  • 12
    • 0029979392 scopus 로고    scopus 로고
    • Disturbance of plasma and platelet thrombospondin levels in sickle cell disease
    • Browne PV, Mosher DF, Steinberg MH, Hebbel RP. (1996). Disturbance of plasma and platelet thrombospondin levels in sickle cell disease. Am J Hematol 51:296-301.
    • (1996) Am. J. Hematol. , vol.51 , pp. 296-301
    • Browne, P.V.1    Mosher, D.F.2    Steinberg, M.H.3    Hebbel, R.P.4
  • 13
    • 85047691411 scopus 로고
    • Evidence against enhanced platelet activity in sickle cell anaemia
    • Buchanan GR, Holtkamp CA. (1983). Evidence against enhanced platelet activity in sickle cell anaemia. Br J Haematol 54:595-603.
    • (1983) Br. J. Haematol. , vol.54 , pp. 595-603
    • Buchanan, G.R.1    Holtkamp, C.A.2
  • 14
    • 0036828422 scopus 로고    scopus 로고
    • Arterial strokes in children
    • Carvalho KS, Garg BP. (2002). Arterial strokes in children. Neurol Clin 20:1079-1100.
    • (2002) Neurol. Clin. , vol.20 , pp. 1079-1100
    • Carvalho, K.S.1    Garg, B.P.2
  • 17
    • 0027515584 scopus 로고
    • Neuropsychologic effects of stroke in children with sickle cell anemia
    • Craft S, Schatz J, Glauser TA, Lee B, DeBaun MR. (1993). Neuropsychologic effects of stroke in children with sickle cell anemia J Pediatr 123:712-717.
    • (1993) J. Pediatr. , vol.123 , pp. 712-717
    • Craft, S.1    Schatz, J.2    Glauser, T.A.3    Lee, B.4    DeBaun, M.R.5
  • 18
    • 0032752359 scopus 로고    scopus 로고
    • The methylenete-trahydrofolate reductase gene C677T polymorphisim in patients with homozygous sickle cell disease and stroke
    • Cumming AM, Olujohungbe A, Keeney S, Singh H, Hay CR, Serjeant GR. (1999). The methylenete-trahydrofolate reductase gene C677T polymorphisim in patients with homozygous sickle cell disease and stroke. Br J Haematol 107:569-571.
    • (1999) Br. J. Haematol. , vol.107 , pp. 569-571
    • Cumming, A.M.1    Olujohungbe, A.2    Keeney, S.3    Singh, H.4    Hay, C.R.5    Serjeant, G.R.6
  • 19
    • 0033979993 scopus 로고    scopus 로고
    • Inflammation and stroke: Putative role for cytokines. adhesion molecules and iNOS in brain response to ischemia
    • del Zoppo G, Ginis I, Hallenbeck JM, Iadecola C, Wang X, Feuerstein GZ. (2000). Inflammation and stroke: putative role for cytokines. adhesion molecules and iNOS in brain response to ischemia. Brain Pathol 10:95-112.
    • (2000) Brain Pathol. , vol.10 , pp. 95-112
    • del Zoppo, G.1    Ginis, I.2    Hallenbeck, J.M.3    Iadecola, C.4    Wang, X.5    Feuerstein, G.Z.6
  • 20
    • 0036216168 scopus 로고    scopus 로고
    • Stroke and the child's brain: An overview of epidemiology, syndromes and risk factors
    • DeVeber G. (2002). Stroke and the child's brain: an overview of epidemiology, syndromes and risk factors. Curr Opin Neurol 15:133-138.
    • (2002) Curr. Opin. Neurol. , vol.15 , pp. 133-138
    • DeVeber, G.1
  • 21
    • 0036566530 scopus 로고    scopus 로고
    • Moyamoya syndrome in childhood sickle cell disease: A predictive factor for recurrent, cerebrovascular events
    • Dobson SR, Holden KR, Nietert PJ, Cure JK, Laver JH, Disco D, Abboud MR. (2002). Moyamoya syndrome in childhood sickle cell disease: a predictive factor for recurrent, cerebrovascular events. Blood 99:3144-3150.
    • (2002) Blood , vol.99 , pp. 3144-3150
    • Dobson, S.R.1    Holden, K.R.2    Nietert, P.J.3    Cure, J.K.4    Laver, J.H.5    Disco, D.6    Abboud, M.R.7
  • 23
    • 85112371006 scopus 로고    scopus 로고
    • Increased fibrin deposition at sites of vasoocclusion in transgenic sickle mice
    • (Abstr)
    • Du LM, Holzman SL, Mohandas N, Scott JP, Trost BA, Hillery CA. (2000). Increased fibrin deposition at sites of vasoocclusion in transgenic sickle mice. Blood 96:16 (Abstr).
    • (2000) Blood , vol.96 , pp. 16
    • Du, L.M.1    Holzman, S.L.2    Mohandas, N.3    Scott, J.P.4    Trost, B.A.5    Hillery, C.A.6
  • 26
    • 0028118673 scopus 로고
    • Nitric oxide and the cerebral circulation
    • Faraci FM, Brian JE Jr. (1994). Nitric oxide and the cerebral circulation. Stroke 25:692-703.
    • (1994) Stroke , vol.25 , pp. 692-703
    • Faraci, F.M.1    Brian Jr., J.E.2
  • 28
    • 0023941202 scopus 로고
    • Protein S deficiency in sickle cell anemia
    • Francis RB Jr. (1988). Protein S deficiency in sickle cell anemia. J Lab Clin Med 111:571-576.
    • (1988) J. Lab. Clin. Med. , vol.111 , pp. 571-576
    • Francis Jr., R.B.1
  • 29
    • 0024596417 scopus 로고
    • Elevated fibrin D-dimer fragment in sickle cell anemia: Evidence for activation of coagulation during the steady state as well as in painful crisis
    • Francis RB Jr. (1989). Elevated fibrin D-dimer fragment in sickle cell anemia: evidence for activation of coagulation during the steady state as well as in painful crisis. Haemostasis 19:105-111.
    • (1989) Haemostasis , vol.19 , pp. 105-111
    • Francis Jr., R.B.1
  • 30
    • 0026145807 scopus 로고
    • Platelets, coagulation, and fibrinolysis in sickle cell disease: Their possible role in vascular occlusion
    • Francis RB Jr. (1991). Platelets, coagulation, and fibrinolysis in sickle cell disease: their possible role in vascular occlusion. Blood Coagul Fibrinolysis 2:341-353.
    • (1991) Blood Coagul. Fibrinolysis , vol.2 , pp. 341-353
    • Francis Jr., R.B.1
  • 31
    • 0026145807 scopus 로고
    • Platelets, coagulation, and fibrinolysis in sickle cell disease: Their possible role in vascular occlusion
    • Francis RB Jr. (1991). Platelets, coagulation, and fibrinolysis in sickle cell disease: their possible role in vascular occlusion. Blood Coagul Fibrinolysis 2:341-353.
    • (1991) Blood Coagul. Fibrinolysis , vol.2 , pp. 341-353
    • Francis Jr., R.B.1
  • 33
    • 0030912619 scopus 로고    scopus 로고
    • Mechanisms of stroke in sickle cell disease: Sickle erythrocytes decrease cerebral blood flow in rats after nitric oxide synthase inhibition
    • French JA, II, Kenny D, Scott JP, Hoffmann RG, Wood JD, Hudetz AG, Hillery CA. (1997). Mechanisms of stroke in sickle cell disease: sickle erythrocytes decrease cerebral blood flow in rats after nitric oxide synthase inhibition. Blood 89:4591-4599.
    • (1997) Blood , vol.89 , pp. 4591-4599
    • French II, J.A.1    Kenny, D.2    Scott, J.P.3    Hoffmann, R.G.4    Wood, J.D.5    Hudetz, A.G.6    Hillery, C.A.7
  • 35
    • 0028894111 scopus 로고
    • Sickle reticulocytes adhere to VCAM-1
    • Gee BE, Platt OS. (1995). Sickle reticulocytes adhere to VCAM-1 Blood 85:268-274.
    • (1995) Blood , vol.85 , pp. 268-274
    • Gee, B.E.1    Platt, O.S.2
  • 36
    • 0018819967 scopus 로고
    • Cerebral infarction secondary to sickle cell disease: Arteriographic findings
    • Gerald B, Sebes JI, Langston JW. (1980). Cerebral infarction secondary to sickle cell disease: arteriographic findings. AJR Am J Roentgenol 134:1209-1212.
    • (1980) AJR Am. J. Roentgenol. , vol.134 , pp. 1209-1212
    • Gerald, B.1    Sebes, J.I.2    Langston, J.W.3
  • 37
    • 0028957256 scopus 로고
    • Accuracy of neurologic examination and history in detecting evidence of MRI-diagnosed cerebral infarctions in children with sickle cell hemoglobinopathy
    • Glauser TA, Siegel MJ, Lee BC, DeBaun MR. (1995). Accuracy of neurologic examination and history in detecting evidence of MRI-diagnosed cerebral infarctions in children with sickle cell hemoglobinopathy. J Child Neurol 10:88-92.
    • (1995) J. Child Neurol. , vol.10 , pp. 88-92
    • Glauser, T.A.1    Siegel, M.J.2    Lee, B.C.3    DeBaun, M.R.4
  • 38
    • 10244240031 scopus 로고    scopus 로고
    • Congenital and aquired prothrombotic risk factors in stroke
    • Grabowski EF. (2002). Congenital and aquired prothrombotic risk factors in stroke. Curr Opin Neurol 15:139-144.
    • (2002) Curr. Opin. Neurol. , vol.15 , pp. 139-144
    • Grabowski, E.F.1
  • 40
    • 0022966475 scopus 로고
    • Is sickle cell crisis a thrombotic event?
    • Green D, Scott JP. (1986). Is sickle cell crisis a thrombotic event? Am J Hematol 23:317-321.
    • (1986) Am. J. Hematol. , vol.23 , pp. 317-321
    • Green, D.1    Scott, J.P.2
  • 42
    • 0029897658 scopus 로고    scopus 로고
    • Increased adhesion of erythrocytes to components of the extracellular matrix: Isolation and characterization of a red blood cell lipid that binds thrombospondin and laminin
    • Hillery CA, Du MC, Montgomery RR, Scott JP. (1996). Increased adhesion of erythrocytes to components of the extracellular matrix: isolation and characterization of a red blood cell lipid that binds thrombospondin and laminin. Blood 87:4879-4886.
    • (1996) Blood , vol.87 , pp. 4879-4886
    • Hillery, C.A.1    Du, M.C.2    Montgomery, R.R.3    Scott, J.P.4
  • 43
    • 0038107362 scopus 로고    scopus 로고
    • Distinct HLA associations by stroke subtype in children with sickle cell anemia
    • Hoppe C, Klitz W, Noble J, Vigil L, Vichinsky E, Styles L. (2003). Distinct HLA associations by stroke subtype in children with sickle cell anemia. Blood 101:2865-2869.
    • (2003) Blood , vol.101 , pp. 2865-2869
    • Hoppe, C.1    Klitz, W.2    Noble, J.3    Vigil, L.4    Vichinsky, E.5    Styles, L.6
  • 47
    • 12144289379 scopus 로고    scopus 로고
    • Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and beta-thalassemia
    • Iannone R, Casella JF, Fuch EJ, et al. (2003). Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and beta-thalassemia. Biol Blood Marrow Transplant 9:519-528.
    • (2003) Biol. Blood Marrow Transplant. , vol.9 , pp. 519-528
    • Iannone, R.1    Casella, J.F.2    Fuch, E.J.3
  • 48
    • 0030670561 scopus 로고    scopus 로고
    • Analysis of class II genes of human leukocyte antigen in patients with moyamoya disease
    • Inoue TK, Ikezaki K, Sasazuki T, Matsushima T, Fukui M. (1997). Analysis of class II genes of human leukocyte antigen in patients with moyamoya disease. Clin Neurol Neurosurg 99(Suppl 2 ):S234-S237.
    • (1997) Clin. Neurol. Neurosurg. , vol.99 , Issue.SUPPL. 2
    • Inoue, T.K.1    Ikezaki, K.2    Sasazuki, T.3    Matsushima, T.4    Fukui, M.5
  • 49
    • 0031012245 scopus 로고    scopus 로고
    • Factor V Leiden is not responsible for stroke in patients with sickling disorders and is uncommon in African Americans with sickle cell disease
    • Kahn MJ, Scher C, Rozans M, Michaels RK, Leissinger C, Krause J. (1997). Factor V Leiden is not responsible for stroke in patients with sickling disorders and is uncommon in African Americans with sickle cell disease. Am J Hematol 54:12-15.
    • (1997) Am. J. Hematol. , vol.54 , pp. 12-15
    • Kahn, M.J.1    Scher, C.2    Rozans, M.3    Michaels, R.K.4    Leissinger, C.5    Krause, J.6
  • 50
    • 0033624253 scopus 로고    scopus 로고
    • Hypoxia/reoxygenation causes inflammatory response in transgenic sickle mice but not in normal mice
    • Kaul DK, Hebbel RP. (2000). Hypoxia/ reoxygenation causes inflammatory response in transgenic sickle mice but not in normal mice. J Clin Invest 106:411-420.
    • (2000) J. Clin. Invest. , vol.106 , pp. 411-420
    • Kaul, D.K.1    Hebbel, R.P.2
  • 53
    • 0025528264 scopus 로고
    • Vascular lesions in the central nervous system in sickle cell disease
    • Koshy M, Thomas C, Goodwin J. (1990). Vascular lesions in the central nervous system in sickle cell disease. J Assoc Acad Minor Phys 1:71-78.
    • (1990) J. Assoc. Acad. Minor Phys. , vol.1 , pp. 71-78
    • Koshy, M.1    Thomas, C.2    Goodwin, J.3
  • 54
    • 0028322292 scopus 로고
    • Elevated urinary levels of thromboxane and prostacyclin metabolities in sickle cell disease reflects activated platelets in the circulation
    • Kurantsin-Mills J, Ibe BO, Natta CL, Raj JU, Siegel RS, Lessin LS. (1994). Elevated urinary levels of thromboxane and prostacyclin metabolities in sickle cell disease reflects activated platelets in the circulation. Br J Haematol 87:580-585.
    • (1994) Br. J. Haematol. , vol.87 , pp. 580-585
    • Kurantsin-Mills, J.1    Ibe, B.O.2    Natta, C.L.3    Raj, J.U.4    Siegel, R.S.5    Lessin, L.S.6
  • 55
    • 0026743902 scopus 로고
    • Plasma factor VII and thrombin-antithrombin III levels indicate increased tissue factor activity in sickle cell patients
    • Kurantsin-Mills J, Ofosu FA, Safa TK, Siegel RS, Lessin LS. (1992). Plasma factor VII and thrombin-antithrombin III levels indicate increased tissue factor activity in sickle cell patients. Br J Haematol 81:539-544.
    • (1992) Br. J. Haematol. , vol.81 , pp. 539-544
    • Kurantsin-Mills, J.1    Ofosu, F.A.2    Safa, T.K.3    Siegel, R.S.4    Lessin, L.S.5
  • 56
    • 0030020463 scopus 로고    scopus 로고
    • Detection of altered membrane phospholopid assymmetry in subpopulations of human red blood cells using flourescently labeled Annexin V
    • Kuypers FA, Lewis RA, Hua M, Schott MA, Discher D, Ernest JD, Lubin BH. (1996). Detection of altered membrane phospholopid assymmetry in subpopulations of human red blood cells using flourescently labeled Annexin V. Blood 87:1179-1187.
    • (1996) Blood , vol.87 , pp. 1179-1187
    • Kuypers, F.A.1    Lewis, R.A.2    Hua, M.3    Schott, M.A.4    Discher, D.5    Ernest, J.D.6    Lubin, B.H.7
  • 57
  • 58
  • 62
    • 0035134405 scopus 로고    scopus 로고
    • The panoply of animal models for sickle cell anaemia
    • Nagel RL, Fabry ME. (2001). The panoply of animal models for sickle cell anaemia. Br J Haematol 112:19-25.
    • (2001) Br. J. Haematol. , vol.112 , pp. 19-25
    • Nagel, R.L.1    Fabry, M.E.2
  • 63
    • 0029973833 scopus 로고    scopus 로고
    • Adhesion of sickle red blood cells and damage to interleukin-1 beta stimulated endothelial cells under flow in vitro
    • Natarajan M, Udden MM, McIntire LV. (1996). Adhesion of sickle red blood cells and damage to interleukin-1 beta stimulated endothelial cells under flow in vitro. Blood 87:4845-4852.
    • (1996) Blood , vol.87 , pp. 4845-4852
    • Natarajan, M.1    Udden, M.M.2    McIntire, L.V.3
  • 75
    • 0025797296 scopus 로고
    • Sickle cell anemia: Beta s-gene-cluster haplotypes as prognostic indicators of vital organ failure
    • Powars DR. (1991). Sickle cell anemia: beta s-gene-cluster haplotypes as prognostic indicators of vital organ failure. Semin Hematol 28:202-208.
    • (1991) Semin. Hematol. , vol.28 , pp. 202-208
    • Powars, D.R.1
  • 78
    • 10244227423 scopus 로고    scopus 로고
    • Chondroitin sulfate-A limits cerebral ischemia induced by nitric oxide inhibition in sickle erthrocyte-infused rats
    • (Abstr)
    • Punzalan RC, Trost BA, Scott JP, Huderz AG, Hillery CA. (1998). Chondroitin sulfate-A limits cerebral ischemia induced by nitric oxide inhibition in sickle erthrocyte-infused rats. Blood 92:329a (Abstr).
    • (1998) Blood , vol.92
    • Punzalan, R.C.1    Trost, B.A.2    Scott, J.P.3    Huderz, A.G.4    Hillery, C.A.5
  • 79
    • 0023002273 scopus 로고
    • Sickle cell anemia and central nervous system infarction: A neuropathological study
    • Rothman SM, Fulling KH, Nelson JS. (1986). Sickle cell anemia and central nervous system infarction: a neuropathological study. Ann Neurol 20:684-690.
    • (1986) Ann. Neurol. , vol.20 , pp. 684-690
    • Rothman, S.M.1    Fulling, K.H.2    Nelson, J.S.3
  • 80
    • 0021335218 scopus 로고
    • Effect of transfusion therapy on arteriographic abnormalities and on recurrence of stroke in sickle cell disease
    • Russell MO, Goldberg HI, Hodson A, Kim HC, Halus J, Reivich M, Schwartz E. (1984). Effect of transfusion therapy on arteriographic abnormalities and on recurrence of stroke in sickle cell disease. Blood 63:162-169.
    • (1984) Blood , vol.63 , pp. 162-169
    • Russell, M.O.1    Goldberg, H.I.2    Hodson, A.3    Kim, H.C.4    Halus, J.5    Reivich, M.6    Schwartz, E.7
  • 81
    • 0030725279 scopus 로고    scopus 로고
    • Knockout-transgenic mouse model of sickle cell disease
    • Ryan TM, Ciavatta DJ, Townes TM. (1997). Knockout-transgenic mouse model of sickle cell disease. Science 278:873-876.
    • (1997) Science , vol.278 , pp. 873-876
    • Ryan, T.M.1    Ciavatta, D.J.2    Townes, T.M.3
  • 83
    • 0034969365 scopus 로고    scopus 로고
    • Molecular characteristics of pediatric patients with sickle cell anemia and stroke
    • Sarnaik SA, Ballas SK. (2001). Molecular characteristics of pediatric patients with sickle cell anemia and stroke. Am J Hematol 67:179-182.
    • (2001) Am. J. Hematol. , vol.67 , pp. 179-182
    • Sarnaik, S.A.1    Ballas, S.K.2
  • 84
    • 0035942334 scopus 로고    scopus 로고
    • Poor school and cognitive functioning with silent cerebral infarcts and sickle cell disease
    • Schatz J, Brown RT, Pascual JM, Hsu L, DeBaun MR. (2001). Poor school and cognitive functioning with silent cerebral infarcts and sickle cell disease. Neurology 56:1109-1111.
    • (2001) Neurology , vol.56 , pp. 1109-1111
    • Schatz, J.1    Brown, R.T.2    Pascual, J.M.3    Hsu, L.4    DeBaun, M.R.5
  • 89
    • 0029040383 scopus 로고
    • Sickle cell vasoocclusive crisis is associated with abnormalities in the ratio of vasoconstrictor to vasodilator prostanoids
    • Setty BN, Chen D, Stuart MJ. (1995). Sickle cell vasoocclusive crisis is associated with abnormalities in the ratio of vasoconstrictor to vasodilator prostanoids. Pediatr Res 38:95-102.
    • (1995) Pediatr. Res. , vol.38 , pp. 95-102
    • Setty, B.N.1    Chen, D.2    Stuart, M.J.3
  • 90
    • 0034254238 scopus 로고    scopus 로고
    • Fetal hemoglobin in sickle cell disease: Relationship to erythrocyte phosphatidylserine exposure and coagulation activation
    • Setty BN, Kulkarni S, Rao AK, Stuart MJ. (2000). Fetal hemoglobin in sickle cell disease: relationship to erythrocyte phosphatidylserine exposure and coagulation activation. Blood 96:1119-1124.
    • (2000) Blood , vol.96 , pp. 1119-1124
    • Setty, B.N.1    Kulkarni, S.2    Rao, A.K.3    Stuart, M.J.4
  • 91
    • 0032080802 scopus 로고    scopus 로고
    • Tissue factor expression by endothelial cells in sickle cell anemia
    • Solovey A, Gui L, Key NS, Hebbel RP. (1998), Tissue factor expression by endothelial cells in sickle cell anemia. J Clin Invest 101: 1899-1904.
    • (1998) J. Clin. Invest. , vol.101 , pp. 1899-1904
    • Solovey, A.1    Gui, L.2    Key, N.S.3    Hebbel, R.P.4
  • 93
    • 0035132563 scopus 로고    scopus 로고
    • Improved cerebrovascular patency following therapy in patients with sickle cell disease: Initial results in 4 patients who received HLA-identical hematopoietic stem cell allografts
    • Steen RG, Helton KJ, Horwitz EM, Benaim E, Thompson S, Bowman LC, Krance R, Wang WC, Cunningham JM. (2001). Improved cerebrovascular patency following therapy in patients with sickle cell disease: initial results in 4 patients who received HLA-identical hematopoietic stem cell allografts. Ann Neurol 49:222-229.
    • (2001) Ann. Neurol. , vol.49 , pp. 222-229
    • Steen, R.G.1    Helton, K.J.2    Horwitz, E.M.3    Benaim, E.4    Thompson, S.5    Bowman, L.C.6    Krance, R.7    Wang, W.C.8    Cunningham, J.M.9
  • 96
    • 0033198521 scopus 로고    scopus 로고
    • Sickle cell acute chest syndrome: Pathogenesis and rationale for treatment
    • Stuart MJ, Setty BN. (1999). Sickle cell acute chest syndrome: pathogenesis and rationale for treatment. Blood 94:1555-1560.
    • (1999) Blood , vol.94 , pp. 1555-1560
    • Stuart, M.J.1    Setty, B.N.2
  • 97
    • 0016277663 scopus 로고
    • Abnormalities of platelet aggregation in the vasoocclusive crisis of sickle-cell anemia
    • Stuart MJ, Stockman JA, Oski FA. (1974). Abnormalities of platelet aggregation in the vasoocclusive crisis of sickle-cell anemia. J Pediatr 85:629-632.
    • (1974) J. Pediatr. , vol.85 , pp. 629-632
    • Stuart, M.J.1    Stockman, J.A.2    Oski, F.A.3
  • 98
    • 0036829459 scopus 로고    scopus 로고
    • Hydroxyurea (HU) for prevention of recurrent stroke in sickle cell anemia (SCA)
    • Sumoza A, de Bisotti R, Sumoza D, Fairbanks V. (2002). Hydroxyurea (HU) for prevention of recurrent stroke in sickle cell anemia (SCA). Am J Hematol 71:161-165.
    • (2002) Am. J. Hematol. , vol.71 , pp. 161-165
    • Sumoza, A.1    de Bisotti, R.2    Sumoza, D.3    Fairbanks, V.4
  • 99
    • 0027184968 scopus 로고
    • 1-integrin expression on sickle reticulocytes: Vascular cell adhesion molecule-l-dependent binding to endothelium
    • 1-integrin expression on sickle reticulocytes: vascular cell adhesion molecule-l-dependent binding to endothelium. Blood 82:1891-1899.
    • (1993) Blood , vol.82 , pp. 1891-1899
    • Swerlick, R.A.1    Eckman, J.R.2    Kumar, A.3    Jeitler, M.4    Wick, T.M.5
  • 100
    • 0001499987 scopus 로고
    • Sickle cell anemia: Report of two cases in children, with necropsy in one case
    • Sydenstricker VP, Mulherin WA, Houseal RW. (1923). Sickle cell anemia: report of two cases in children, with necropsy in one case. Am J Dis Child 26:132-154.
    • (1923) Am. J. Dis. Child , vol.26 , pp. 132-154
    • Sydenstricker, V.P.1    Mulherin, W.A.2    Houseal, R.W.3
  • 101
    • 0028921559 scopus 로고
    • Detailed examination of vascular lesions triggered by an inhibitor of endothelium-derived relaxing factor
    • Tagami M, Ikeda K, Nara Y, Fujino H, Kubota A, Numano F, Yamori Y. (1995). Detailed examination of vascular lesions triggered by an inhibitor of endothelium-derived relaxing factor. Lab Invest 72:174-182.
    • (1995) Lab. Invest. , vol.72 , pp. 174-182
    • Tagami, M.1    Ikeda, K.2    Nara, Y.3    Fujino, H.4    Kubota, A.5    Numano, F.6    Yamori, Y.7
  • 102
    • 1842338762 scopus 로고    scopus 로고
    • Protein C and protein S activity in sickle cell disease and stroke
    • Tam DA. (1997). Protein C and protein S activity in sickle cell disease and stroke. J Child Neurol 12:19-21.
    • (1997) J. Child Neurol. , vol.12 , pp. 19-21
    • Tam, D.A.1
  • 103
    • 0034776219 scopus 로고    scopus 로고
    • Polymorphisms within the angiotensinogen gene (GT-repeat) and the risk of stroke in pediatric patients with sickle cell disease: A case-control study
    • Tang DC, Prauner R, Liu WL, Kim KH, Hirsch RP, Driscoll MC, Rodgers GP. (2001). Polymorphisms within the angiotensinogen gene (GT-repeat) and the risk of stroke in pediatric patients with sickle cell disease: a case-control study. Am J Hematol 68:164-169.
    • (2001) Am. J. Hematol. , vol.68 , pp. 164-169
    • Tang, D.C.1    Prauner, R.2    Liu, W.L.3    Kim, K.H.4    Hirsch, R.P.5    Driscoll, M.C.6    Rodgers, G.P.7
  • 105
    • 0345451539 scopus 로고    scopus 로고
    • Internal carotid artery occlusion in a child with sickle cell disease: Case report and immunohistochemical study
    • Tuohy AM, McKie V, Manci EA, Adams RJ. (1997). Internal carotid artery occlusion in a child with sickle cell disease: case report and immunohistochemical study. J Pediatr Hematol Oncol 19:455-458.
    • (1997) J. Pediatr. Hematol. Oncol. , vol.19 , pp. 455-458
    • Tuohy, A.M.1    McKie, V.2    Manci, E.A.3    Adams, R.J.4
  • 106
    • 0028053133 scopus 로고
    • A cautionary note regarding hydroxyurea in sickle cell disease
    • Vichinsky EP, Lubin BH. (1994). A cautionary note regarding hydroxyurea in sickle cell disease. Blood 83:1124-1128.
    • (1994) Blood , vol.83 , pp. 1124-1128
    • Vichinsky, E.P.1    Lubin, B.H.2
  • 108
    • 0034828316 scopus 로고    scopus 로고
    • Neuropsychologic performance in school-aged children with sickle cell disease: A report from the Cooperative Study of Sickle Cell Disease
    • Wang W, Enos L, Gallagher D, Thompson R, Guarini L, Vichinsky E, Wright E, Zimmerman R, Armstrong FD. (2001). Neuropsychologic performance in school-aged children with sickle cell disease: a report from the Cooperative Study of Sickle Cell Disease. J Pediatr 139:391-397.
    • (2001) J. Pediatr. , vol.139 , pp. 391-397
    • Wang, W.1    Enos, L.2    Gallagher, D.3    Thompson, R.4    Guarini, L.5    Vichinsky, E.6    Wright, E.7    Zimmerman, R.8    Armstrong, F.D.9
  • 109
    • 0026034335 scopus 로고
    • High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease
    • Wang WC, Kovnar EH, Tonkin IL, Mulhern RK, Langston JW, Day SW, Schell MJ, Wilimas JA. (1991). High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease. J Pediatr 118:377-382.
    • (1991) J. Pediatr. , vol.118 , pp. 377-382
    • Wang, W.C.1    Kovnar, E.H.2    Tonkin, I.L.3    Mulhern, R.K.4    Langston, J.W.5    Day, S.W.6    Schell, M.J.7    Wilimas, J.A.8
  • 110
    • 0033229703 scopus 로고    scopus 로고
    • Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease
    • Ware RE, Zimmerman SA, Schultz WH. (1999). Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease. Blood 94:3022-3026.
    • (1999) Blood , vol.94 , pp. 3022-3026
    • Ware, R.E.1    Zimmerman, S.A.2    Schultz, W.H.3
  • 113
    • 0031147997 scopus 로고    scopus 로고
    • Platelet activation and platelet-erythrocyte aggregates in patients with sickle cell anemia
    • Wun T, Paglieroni T, Tablin F, Welborn J, Nelson K, Cheung A. (1997). Platelet activation and platelet-erythrocyte aggregates in patients with sickle cell anemia. J Lab Clin Med 129:507-516.
    • (1997) J. Lab. Clin. Med. , vol.129 , pp. 507-516
    • Wun, T.1    Paglieroni, T.2    Tablin, F.3    Welborn, J.4    Nelson, K.5    Cheung, A.6
  • 116
    • 0031724415 scopus 로고    scopus 로고
    • Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease
    • Zimmerman SA, Ware RE. (1998). Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease. Am J Hematol 59:267-272.
    • (1998) Am. J. Hematol. , vol.59 , pp. 267-272
    • Zimmerman, S.A.1    Ware, R.E.2


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