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Volumn 107, Issue 6, 2006, Pages 2279-2285

Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease

Author keywords

[No Author keywords available]

Indexed keywords

ARGINASE; ASPARTATE AMINOTRANSFERASE; BILIRUBIN; BIOLOGICAL MARKER; CELL ADHESION MOLECULE; HAPTOGLOBIN; HEMOGLOBIN; LACTATE DEHYDROGENASE; LACTATE DEHYDROGENASE ISOENZYME; LACTATE DEHYDROGENASE ISOENZYME 1; LACTATE DEHYDROGENASE ISOENZYME 2; NITRIC OXIDE; UNCLASSIFIED DRUG;

EID: 33644775612     PISSN: 00064971     EISSN: 00064971     Source Type: Journal    
DOI: 10.1182/blood-2005-06-2373     Document Type: Article
Times cited : (527)

References (69)
  • 1
    • 10744233940 scopus 로고    scopus 로고
    • Pulmonary hypertension as a risk factor for death in patients with sickle cell disease
    • Gladwin MT, Sachdev V, Jison ML, et al. Pulmonary hypertension as a risk factor for death in patients with sickle cell disease. N Engl J Med. 2004;350:886-895.
    • (2004) N Engl J Med , vol.350 , pp. 886-895
    • Gladwin, M.T.1    Sachdev, V.2    Jison, M.L.3
  • 2
    • 27244435213 scopus 로고    scopus 로고
    • Levels of soluble endothelium-derived adhesion molecules in patients with sickle cell disease are associated with pulmonary hypertension, organ dysfunction, and mortality
    • Kato GJ, Martyr S, Blackwelder WC, et al. Levels of soluble endothelium-derived adhesion molecules in patients with sickle cell disease are associated with pulmonary hypertension, organ dysfunction, and mortality. Br J Haematol. 2005;130:943-953.
    • (2005) Br J Haematol , vol.130 , pp. 943-953
    • Kato, G.J.1    Martyr, S.2    Blackwelder, W.C.3
  • 3
    • 0035117938 scopus 로고    scopus 로고
    • Activation of vascular endothelial cell adhesion molecule expression by sickle blood cells
    • Brown MD, Wick TM, Eckman JR. Activation of vascular endothelial cell adhesion molecule expression by sickle blood cells. Pediatr Pathol Mol Med 2001;20:47-72.
    • (2001) Pediatr Pathol Mol Med , vol.20 , pp. 47-72
    • Brown, M.D.1    Wick, T.M.2    Eckman, J.R.3
  • 4
    • 0005991370 scopus 로고    scopus 로고
    • Enhanced levels of soluble VCAM-1 in sickle cell patients and their specific increment during vasoocclusive crisis
    • Duits AJ, Pieters RC, Saleh AW, et al. Enhanced levels of soluble VCAM-1 in sickle cell patients and their specific increment during vasoocclusive crisis. Clin Immunol Immunopathol. 1996;81:96-98.
    • (1996) Clin Immunol Immunopathol , vol.81 , pp. 96-98
    • Duits, A.J.1    Pieters, R.C.2    Saleh, A.W.3
  • 5
    • 0038690566 scopus 로고    scopus 로고
    • Erythropoiesis and serum sVCAM-1 levels in adults with sickle cell disease
    • Duits AJ, Rojer RA, van Endt T, et al. Erythropoiesis and serum sVCAM-1 levels in adults with sickle cell disease. Ann Hematol. 2003;82:171-174.
    • (2003) Ann Hematol , vol.82 , pp. 171-174
    • Duits, A.J.1    Rojer, R.A.2    Van Endt, T.3
  • 6
    • 0031877983 scopus 로고    scopus 로고
    • Cytokines and soluble adhesion molecules in sickle cell anemia patients during hydroxyurea therapy
    • Saleh AW, Duits AJ, Gerbers A, de Vries C, Hillen HF. Cytokines and soluble adhesion molecules in sickle cell anemia patients during hydroxyurea therapy. Acta Haematol. 1998;100:26-31.
    • (1998) Acta Haematol , vol.100 , pp. 26-31
    • Saleh, A.W.1    Duits, A.J.2    Gerbers, A.3    De Vries, C.4    Hillen, H.F.5
  • 7
    • 0032873984 scopus 로고    scopus 로고
    • Levels of endothelial, neutrophil and platelet-specific factors in sickle cell anemia patients during hydroxyurea therapy
    • Saleh AW, Hillen HF, Duits AJ. Levels of endothelial, neutrophil and platelet-specific factors in sickle cell anemia patients during hydroxyurea therapy. Acta Haematol. 1999;102:31-37.
    • (1999) Acta Haematol , vol.102 , pp. 31-37
    • Saleh, A.W.1    Hillen, H.F.2    Duits, A.J.3
  • 8
    • 0038014064 scopus 로고    scopus 로고
    • Steady-state sVCAM-1 serum levels in adults with sickle cell disease
    • Schnog JB, Rojer RA, Mac Gillavry MR, et al. Steady-state sVCAM-1 serum levels in adults with sickle cell disease. Ann Hematol. 2003;82:109-113.
    • (2003) Ann Hematol , vol.82 , pp. 109-113
    • Schnog, J.B.1    Rojer, R.A.2    Mac Gillavry, M.R.3
  • 9
    • 0034658663 scopus 로고    scopus 로고
    • Perfusion with sickle erythrocytes up-regulates ICAM-1 and VCAM-1 gene expression in cultured human endothelial cells
    • Shiu YT, Udden MM, McIntire LV. Perfusion with sickle erythrocytes up-regulates ICAM-1 and VCAM-1 gene expression in cultured human endothelial cells. Blood. 2000;95:3232-3241.
    • (2000) Blood , vol.95 , pp. 3232-3241
    • Shiu, Y.T.1    Udden, M.M.2    McIntire, L.V.3
  • 10
    • 0035312965 scopus 로고    scopus 로고
    • Modulation of endothelial cell activation in sickle cell disease: A pilot study
    • Solovey AA, Solovey AN, Harkness J, Hebbel RP. Modulation of endothelial cell activation in sickle cell disease: a pilot study. Blood. 2001;97:1937-1941.
    • (2001) Blood , vol.97 , pp. 1937-1941
    • Solovey, A.A.1    Solovey, A.N.2    Harkness, J.3    Hebbel, R.P.4
  • 11
    • 0026647352 scopus 로고
    • Hemolytic anemias. Diagnosis and management
    • Tabbara IA. Hemolytic anemias. Diagnosis and management. Med Clin North Am. 1992;76:649-668.
    • (1992) Med Clin North Am , vol.76 , pp. 649-668
    • Tabbara, I.A.1
  • 14
    • 0014558319 scopus 로고
    • Lactic acid dehydrogenase activity and plasma hemoglobin elevations in sickle cell disease
    • Neely CL, Wajima T, Kraus AP, Diggs LW, Barreras L. Lactic acid dehydrogenase activity and plasma hemoglobin elevations in sickle cell disease. Am J Clin Pathol. 1969;52:167-169.
    • (1969) Am J Clin Pathol , vol.52 , pp. 167-169
    • Neely, C.L.1    Wajima, T.2    Kraus, A.P.3    Diggs, L.W.4    Barreras, L.5
  • 15
    • 33644764856 scopus 로고    scopus 로고
    • Hyperhemolysis during the evolution of uncomplicated acute painful episodes in patients with sickle cell anemia
    • Ballas SK, Marcolina MJ. Hyperhemolysis during the evolution of uncomplicated acute painful episodes in patients with sickle cell anemia. Transfusion. 2006;46:105-110.
    • (2006) Transfusion , vol.46 , pp. 105-110
    • Ballas, S.K.1    Marcolina, M.J.2
  • 16
    • 0036908599 scopus 로고    scopus 로고
    • Cell-free hemoglobin limits nitric oxide bioavailability in sickle-cell disease
    • Reiter CD, Wang X, Tanus-Santos JE, et al. Cell-free hemoglobin limits nitric oxide bioavailability in sickle-cell disease. Nat Med. 2002;8:1383-1389.
    • (2002) Nat Med , vol.8 , pp. 1383-1389
    • Reiter, C.D.1    Wang, X.2    Tanus-Santos, J.E.3
  • 17
    • 0037458069 scopus 로고    scopus 로고
    • Divergent nitric oxide bioavailability in men and women with sickle cell disease
    • Gladwin MT, Schechter AN, Ognibene FP, et al. Divergent nitric oxide bioavailability in men and women with sickle cell disease. Circulation. 2003;107:271-278.
    • (2003) Circulation , vol.107 , pp. 271-278
    • Gladwin, M.T.1    Schechter, A.N.2    Ognibene, F.P.3
  • 18
    • 0043204998 scopus 로고    scopus 로고
    • Arginine therapy: A new treatment for pulmonary hypertension in sickle cell disease?
    • Morris CR, Morris SM, Jr., Hagar W, et al. Arginine therapy: a new treatment for pulmonary hypertension in sickle cell disease? Am J Crit Care Respir Med. 2003;168:63-69.
    • (2003) Am J Crit Care Respir Med , vol.168 , pp. 63-69
    • Morris, C.R.1    Morris Jr., S.M.2    Hagar, W.3
  • 19
    • 2542490292 scopus 로고    scopus 로고
    • Evidence for a metabolic shift of arginine metabolism in sickle cell disease
    • Schnog JJ, Jager EH, van der Dijs FP, et al. Evidence for a metabolic shift of arginine metabolism in sickle cell disease. Ann Hematol. 2004;83:371-375.
    • (2004) Ann Hematol , vol.83 , pp. 371-375
    • Schnog, J.J.1    Jager, E.H.2    Van Der Dijs, F.P.3
  • 20
    • 21444441271 scopus 로고    scopus 로고
    • Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension and mortality in sickle cell disease
    • Morris CR, Kato GJ, Poljakovic M, et al. Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension and mortality in sickle cell disease. JAMA. 2005;294:81-90.
    • (2005) JAMA , vol.294 , pp. 81-90
    • Morris, C.R.1    Kato, G.J.2    Poljakovic, M.3
  • 21
    • 0035909930 scopus 로고    scopus 로고
    • Oxygen radical inhibition of nitric oxide-dependent vascular function in sickle cell disease
    • U S A
    • Aslan M, Ryan TM, Adler B, et al. Oxygen radical inhibition of nitric oxide-dependent vascular function in sickle cell disease. Proc Natl Acad Sci U S A. 2001;98:15215-15220.
    • (2001) Proc Natl Acad Sci , vol.98 , pp. 15215-15220
    • Aslan, M.1    Ryan, T.M.2    Adler, B.3
  • 22
    • 20444468127 scopus 로고    scopus 로고
    • Endothelial cell NADPH oxidase mediates the cerebral microvascular dysfunction in sickle cell transgenic mice
    • Wood KC, Hebbel RP, Granger DN. Endothelial cell NADPH oxidase mediates the cerebral microvascular dysfunction in sickle cell transgenic mice. FASEB J 2005;19:989-991.
    • (2005) FASEB J , vol.19 , pp. 989-991
    • Wood, K.C.1    Hebbel, R.P.2    Granger, D.N.3
  • 23
    • 5144229735 scopus 로고    scopus 로고
    • Oxidant-mediated impairment of nitric oxide signaling in sickle cell disease - Mechanisms and consequences
    • Noisy-le-grand
    • Aslan M, Freeman BA. Oxidant-mediated impairment of nitric oxide signaling in sickle cell disease - mechanisms and consequences. Cell Mol Biol (Noisy-le-grand) 2004;50:95-105.
    • (2004) Cell Mol Biol , vol.50 , pp. 95-105
    • Aslan, M.1    Freeman, B.A.2
  • 24
    • 0037423394 scopus 로고    scopus 로고
    • Nitric oxide-dependent generation of reactive species in sickle cell disease. Actin tyrosine induces defective cytoskeletal polymerization
    • Aslan M, Ryan TM, Townes TM, et al. Nitric oxide-dependent generation of reactive species in sickle cell disease. Actin tyrosine induces defective cytoskeletal polymerization. J Biol Chem. 2003;278:4194-4204.
    • (2003) J Biol Chem , vol.278 , pp. 4194-4204
    • Aslan, M.1    Ryan, T.M.2    Townes, T.M.3
  • 26
    • 0035869387 scopus 로고    scopus 로고
    • Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilation
    • Belhassen L, Pelle G, Sediame S, et al. Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilation. Blood. 2001;97:1584-1589.
    • (2001) Blood , vol.97 , pp. 1584-1589
    • Belhassen, L.1    Pelle, G.2    Sediame, S.3
  • 27
    • 0141730299 scopus 로고    scopus 로고
    • Sickle cell anemia is associated with reduced nitric oxide bioactivity in peripheral conduit and resistance vessels
    • Eberhardt RT, McMahon L, Duffy SJ, et al. Sickle cell anemia is associated with reduced nitric oxide bioactivity in peripheral conduit and resistance vessels. Am J Hematol. 2003;74:104-111.
    • (2003) Am J Hematol , vol.74 , pp. 104-111
    • Eberhardt, R.T.1    McMahon, L.2    Duffy, S.J.3
  • 28
    • 0033637285 scopus 로고    scopus 로고
    • Mechanisms of vascular instability in a transgenic mouse model of sickle cell disease
    • Nath KA, Shah V, Haggard JJ, et al. Mechanisms of vascular instability in a transgenic mouse model of sickle cell disease. Am J Physiol Regul Integr Comp Physiol. 2000;279:R1949-R1955.
    • (2000) Am J Physiol Regul Integr Comp Physiol , vol.279
    • Nath, K.A.1    Shah, V.2    Haggard, J.J.3
  • 29
    • 9644260566 scopus 로고    scopus 로고
    • Effect of fetal hemoglobin on microvascular regulation in sickle transgenic-knockout mice
    • Kaul DK, Liu XD, Chang HY, Nagel RL, Fabry ME. Effect of fetal hemoglobin on microvascular regulation in sickle transgenic-knockout mice. J Clin Invest 2004;114:1136-1145.
    • (2004) J Clin Invest , vol.114 , pp. 1136-1145
    • Kaul, D.K.1    Liu, X.D.2    Chang, H.Y.3    Nagel, R.L.4    Fabry, M.E.5
  • 30
    • 31044445795 scopus 로고    scopus 로고
    • A novel mechanism of disease: Hemolysis-associated endothelial dysfunction mediated by accelerated NO inactivation by decompartmentalized oxyhemoglobin
    • Minneci PC, Deans KJ, Zhi H, et al. A novel mechanism of disease: hemolysis-associated endothelial dysfunction mediated by accelerated NO inactivation by decompartmentalized oxyhemoglobin. J Clin Invest. 2005;115:3409-3417.
    • (2005) J Clin Invest , vol.115 , pp. 3409-3417
    • Minneci, P.C.1    Deans, K.J.2    Zhi, H.3
  • 31
    • 0030594816 scopus 로고    scopus 로고
    • Methods for the separation of lactate dehydrogenases and clinical significance of the enzyme
    • Kopperschlager G, Kirchberger J. Methods for the separation of lactate dehydrogenases and clinical significance of the enzyme. J Chromatogr B Biomed Appl. 1996;684:25-49.
    • (1996) J Chromatogr B Biomed Appl , vol.684 , pp. 25-49
    • Kopperschlager, G.1    Kirchberger, J.2
  • 32
    • 0022893060 scopus 로고
    • Vasoocclusive crisis episodes in sickle cell disease
    • Adhikary PK, Hara S, Dwivedi C, et al. Vasoocclusive crisis episodes in sickle cell disease. J Med. 1986;17:227-240.
    • (1986) J Med , vol.17 , pp. 227-240
    • Adhikary, P.K.1    Hara, S.2    Dwivedi, C.3
  • 33
    • 84941841395 scopus 로고
    • Haemolysis as an interference factor in clinical chemistry
    • Sonntag O. Haemolysis as an interference factor in clinical chemistry. J Clin Chem Clin Biochem. 1986;24:127-139.
    • (1986) J Clin Chem Clin Biochem , vol.24 , pp. 127-139
    • Sonntag, O.1
  • 34
    • 15944398355 scopus 로고    scopus 로고
    • The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: A novel mechanism of human disease
    • Rother RP, Bell L, Hillmen P, Gladwin MT. The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: a novel mechanism of human disease. JAMA. 2005;293:1653-1662.
    • (2005) JAMA , vol.293 , pp. 1653-1662
    • Rother, R.P.1    Bell, L.2    Hillmen, P.3    Gladwin, M.T.4
  • 35
    • 14044254869 scopus 로고    scopus 로고
    • Impaired vasodilation by red blood cells in sickle cell disease
    • U S A
    • Pawloski JR, Hess DT, Stamler JS. Impaired vasodilation by red blood cells in sickle cell disease. Proc Natl Acad Sci U S A. 2005;102:2531-2536.
    • (2005) Proc Natl Acad Sci , vol.102 , pp. 2531-2536
    • Pawloski, J.R.1    Hess, D.T.2    Stamler, J.S.3
  • 36
    • 3042553343 scopus 로고    scopus 로고
    • Vasoactive factors in sickle cell disease: In vitro evidence for endothelin-1-mediated vasoconstriction
    • Ergul S, Brunson CY, Hutchinson J, et al. Vasoactive factors in sickle cell disease: in vitro evidence for endothelin-1-mediated vasoconstriction. Am J Hematol. 2004;76:245-251.
    • (2004) Am J Hematol , vol.76 , pp. 245-251
    • Ergul, S.1    Brunson, C.Y.2    Hutchinson, J.3
  • 37
    • 0242468086 scopus 로고    scopus 로고
    • Differential gene expression in the kidney of sickle cell transgenic mice: Upregulated genes
    • Rybicki AC, Fabry ME, Does MD, Kaul DK, Nagel RL. Differential gene expression in the kidney of sickle cell transgenic mice: upregulated genes. Blood Cells Mol Dis. 2003;31:370-380.
    • (2003) Blood Cells Mol Dis , vol.31 , pp. 370-380
    • Rybicki, A.C.1    Fabry, M.E.2    Does, M.D.3    Kaul, D.K.4    Nagel, R.L.5
  • 38
    • 0036225924 scopus 로고    scopus 로고
    • Exogenous nitric oxide inhibits VCAM-1 expression in human peritoneal mesothelial cells. Role of cyclic GMP and NF-kappaB
    • Lee SK, Kim JH, Yang WS, et al. Exogenous nitric oxide inhibits VCAM-1 expression in human peritoneal mesothelial cells. Role of cyclic GMP and NF-kappaB. Nephron. 2002;90:447-454.
    • (2002) Nephron , vol.90 , pp. 447-454
    • Lee, S.K.1    Kim, J.H.2    Yang, W.S.3
  • 39
    • 0029786764 scopus 로고    scopus 로고
    • Nitric oxide regulates vascular cell adhesion molecule 1 gene expression and redox-sensitive transcriptional events in human vascular endothelial cells
    • U S A
    • Khan BV, Harrison DG, Olbrych MT, Alexander RW, Medford RM. Nitric oxide regulates vascular cell adhesion molecule 1 gene expression and redox-sensitive transcriptional events in human vascular endothelial cells. Proc Natl Acad Sci U S A. 1996;93:9114-9119.
    • (1996) Proc Natl Acad Sci , vol.93 , pp. 9114-9119
    • Khan, B.V.1    Harrison, D.G.2    Olbrych, M.T.3    Alexander, R.W.4    Medford, R.M.5
  • 40
    • 0031572303 scopus 로고    scopus 로고
    • Endothelial cell adhesion molecule expression and lymphocyte adhesion to endothelial cells: Effect of nitric oxide
    • Cartwright JE, Whitley GS, Johnstone AP. Endothelial cell adhesion molecule expression and lymphocyte adhesion to endothelial cells: effect of nitric oxide. Exp Cell Res. 1997;235:431-434.
    • (1997) Exp Cell Res , vol.235 , pp. 431-434
    • Cartwright, J.E.1    Whitley, G.S.2    Johnstone, A.P.3
  • 41
    • 0034102968 scopus 로고    scopus 로고
    • Nitric oxide attenuates normal and sickle red blood cell adherence to pulmonary endothelium
    • Space SL, Lane PA, Pickett CK, Weil JV. Nitric oxide attenuates normal and sickle red blood cell adherence to pulmonary endothelium. Am J Hematol. 2000;63:200-204.
    • (2000) Am J Hematol , vol.63 , pp. 200-204
    • Space, S.L.1    Lane, P.A.2    Pickett, C.K.3    Weil, J.V.4
  • 42
    • 0029159779 scopus 로고
    • Nitric oxide decreases cytokine-induced endothelial activation. Nitric oxide selectively reduces endothelial expression of adhesion molecules and proinflammatory cytokines
    • De Caterina R, Libby P, Peng HB, et al. Nitric oxide decreases cytokine-induced endothelial activation. Nitric oxide selectively reduces endothelial expression of adhesion molecules and proinflammatory cytokines. J Clin Invest. 1995;96:60-68.
    • (1995) J Clin Invest , vol.96 , pp. 60-68
    • De Caterina, R.1    Libby, P.2    Peng, H.B.3
  • 43
    • 11844300366 scopus 로고    scopus 로고
    • Clinical relevance of vascular endothelial growth factor levels in sickle cell disease
    • Gurkan E, Tanriverdi K, Baslamisli F. Clinical relevance of vascular endothelial growth factor levels in sickle cell disease. Ann Hematol. 2005;84:71-75.
    • (2005) Ann Hematol , vol.84 , pp. 71-75
    • Gurkan, E.1    Tanriverdi, K.2    Baslamisli, F.3
  • 44
    • 0242266583 scopus 로고    scopus 로고
    • Hypoxaemia in sickle cell disease: Biomarker modulation and relevance to pathophysiology
    • Setty BN, Stuart MJ, Dampier C, Brodecki D, Allen JL. Hypoxaemia in sickle cell disease: biomarker modulation and relevance to pathophysiology. Lancet. 2003;362:1450-1455.
    • (2003) Lancet , vol.362 , pp. 1450-1455
    • Setty, B.N.1    Stuart, M.J.2    Dampier, C.3    Brodecki, D.4    Allen, J.L.5
  • 45
    • 0025969263 scopus 로고
    • Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells
    • Ballas SK. Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells. Am J Hematol. 1991;36:122-130.
    • (1991) Am J Hematol , vol.36 , pp. 122-130
    • Ballas, S.K.1
  • 46
    • 4143132048 scopus 로고    scopus 로고
    • Are there clinical phenotypes of homozygous sickle cell disease?
    • Alexander N, Higgs D, Dover G, Serjeant GR. Are there clinical phenotypes of homozygous sickle cell disease? Br J Haematol. 2004;126:606-611.
    • (2004) Br J Haematol , vol.126 , pp. 606-611
    • Alexander, N.1    Higgs, D.2    Dover, G.3    Serjeant, G.R.4
  • 49
    • 0020039135 scopus 로고
    • Juvenile leg ulceration in beta-thalassemia major and intermedia
    • Gimmon Z, Wexler MR, Rachmilewitz EA. Juvenile leg ulceration in beta-thalassemia major and intermedia. Plast Reconstr Surg. 1982;69:320-325.
    • (1982) Plast Reconstr Surg , vol.69 , pp. 320-325
    • Gimmon, Z.1    Wexler, M.R.2    Rachmilewitz, E.A.3
  • 50
    • 0025162619 scopus 로고
    • Thalassemia intermedia and recurrent priapism following splenectomy
    • Macchia P, Massei F, Nardi M, et al. Thalassemia intermedia and recurrent priapism following splenectomy. Haematologica. 1990;75:486-487.
    • (1990) Haematologica , vol.75 , pp. 486-487
    • Macchia, P.1    Massei, F.2    Nardi, M.3
  • 51
    • 0023018581 scopus 로고
    • Priapism and thalassaemia intermedia
    • Rao KR, Patel AR. Priapism and thalassaemia intermedia [letter]. Br J Surg. 1986;73:1048.
    • (1986) Br J Surg , vol.73 , pp. 1048
    • Rao, K.R.1    Patel, A.R.2
  • 52
    • 0022500608 scopus 로고
    • Recurrent priapism following splenectomy for thalassaemia intermedia
    • Jackson N, Franklin IM, Hughes MA. Recurrent priapism following splenectomy for thalassaemia intermedia. Br J Surg. 1986;73:678.
    • (1986) Br J Surg , vol.73 , pp. 678
    • Jackson, N.1    Franklin, I.M.2    Hughes, M.A.3
  • 53
    • 0042890574 scopus 로고    scopus 로고
    • Pulmonary arterial hypertension in previously splenectomized patients with beta-thalassemic disorders
    • Atichartakarn V, Likittanasombat K, Chuncharunee S, et al. Pulmonary arterial hypertension in previously splenectomized patients with beta-thalassemic disorders. Int J Hematol. 2003;78:139-145.
    • (2003) Int J Hematol , vol.78 , pp. 139-145
    • Atichartakarn, V.1    Likittanasombat, K.2    Chuncharunee, S.3
  • 54
    • 0032814056 scopus 로고    scopus 로고
    • Pulmonary hypertension in patients with thalassemia major
    • Derchi G, Fonti A, Forni GL, et al. Pulmonary hypertension in patients with thalassemia major [letter]. Am Heart J. 1999;138:384.
    • (1999) Am Heart J , vol.138 , pp. 384
    • Derchi, G.1    Fonti, A.2    Forni, G.L.3
  • 55
    • 0025897375 scopus 로고
    • Spherocytosis and pulmonary hypertension coincidental occurrence or causal relationship?
    • Verresen D, De Backer W, Van Meerbeeck J, et al. Spherocytosis and pulmonary hypertension coincidental occurrence or causal relationship? Eur Respir J 1991;4:629-631.
    • (1991) Eur Respir J , vol.4 , pp. 629-631
    • Verresen, D.1    De Backer, W.2    Van Meerbeeck, J.3
  • 56
    • 0031974567 scopus 로고    scopus 로고
    • Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: A case report and review of the literature
    • Hayag-Barin JE, Smith RE, Tucker FC Jr. Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: a case report and review of the literature. Am J Hematol. 1998;57:82-84.
    • (1998) Am J Hematol , vol.57 , pp. 82-84
    • Hayag-Barin, J.E.1    Smith, R.E.2    Tucker Jr., F.C.3
  • 57
    • 2442486442 scopus 로고    scopus 로고
    • Delayed pulmonary hypertension following splenectomy for congenital spherocytosis
    • Jardine DL, Laing AD. Delayed pulmonary hypertension following splenectomy for congenital spherocytosis. Intern Med J. 2004;34:214-216.
    • (2004) Intern Med J , vol.34 , pp. 214-216
    • Jardine, D.L.1    Laing, A.D.2
  • 60
    • 0017040486 scopus 로고
    • Priapism caused by glucose phosphate isomerase deficiency
    • Goulding FJ. Priapism caused by glucose phosphate isomerase deficiency. J Urol. 1976;116:819-820.
    • (1976) J Urol , vol.116 , pp. 819-820
    • Goulding, F.J.1
  • 61
    • 0030025396 scopus 로고    scopus 로고
    • Priapism following splenectomy in an unstable hemoglobin: Hemoglobin Olmsted beta 141 (H19) Leu→Arg
    • Thuret I, Bardakdjian J, Badens C, et al. Priapism following splenectomy in an unstable hemoglobin: hemoglobin Olmsted beta 141 (H19) Leu→Arg. Am J Hematol. 1996;51:133-136.
    • (1996) Am J Hematol , vol.51 , pp. 133-136
    • Thuret, I.1    Bardakdjian, J.2    Badens, C.3
  • 62
    • 0036136068 scopus 로고    scopus 로고
    • Priapism in a 15-year-old boy with congenital dyserythropoietic anemia type II (hereditary erythroblastic multinuclearity with positive acidified serum lysis test)
    • Edney MT, Schned AR, Cendron M, Chaffee S, Ellsworth PI. Priapism in a 15-year-old boy with congenital dyserythropoietic anemia type II (hereditary erythroblastic multinuclearity with positive acidified serum lysis test). J Urol. 2002;167:309-310.
    • (2002) J Urol , vol.167 , pp. 309-310
    • Edney, M.T.1    Schned, A.R.2    Cendron, M.3    Chaffee, S.4    Ellsworth, P.I.5
  • 63
    • 0025366445 scopus 로고
    • Comparison of homozygous sickle cell disease in northern Greece and Jamaica
    • Christakis J, Vavatsi N, Hassapopoulou H, et al. Comparison of homozygous sickle cell disease in northern Greece and Jamaica. Lancet. 1990;335:637-640.
    • (1990) Lancet , vol.335 , pp. 637-640
    • Christakis, J.1    Vavatsi, N.2    Hassapopoulou, H.3
  • 64
    • 0022977959 scopus 로고
    • Sickle cell disease in Orissa State, India
    • Kar BC, Satapathy RK, Kulozik AE, et al. Sickle cell disease in Orissa State, India. Lancet. 1986;2:1198-1201.
    • (1986) Lancet , vol.2 , pp. 1198-1201
    • Kar, B.C.1    Satapathy, R.K.2    Kulozik, A.E.3
  • 65
    • 0034139483 scopus 로고    scopus 로고
    • Priapism is rare in sickle cell disease in India
    • Dash BP, Kar BC. Priapism is rare in sickle cell disease in India. J Assoc Physicians India. 2000;48:255.
    • (2000) J Assoc Physicians India , vol.48 , pp. 255
    • Dash, B.P.1    Kar, B.C.2
  • 66
  • 68
    • 0027272159 scopus 로고
    • Pulse oximetry and factors associated with hemoglobin oxygen desaturation in children with sickle cell disease
    • Rackoff WR, Kunkel N, Silber JH, Asakura T, Ohene-Frempong K. Pulse oximetry and factors associated with hemoglobin oxygen desaturation in children with sickle cell disease. Blood. 1993;81:3422-3427.
    • (1993) Blood , vol.81 , pp. 3422-3427
    • Rackoff, W.R.1    Kunkel, N.2    Silber, J.H.3    Asakura, T.4    Ohene-Frempong, K.5
  • 69
    • 27744562780 scopus 로고    scopus 로고
    • Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease
    • Quinn CT, Ahmad N. Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease. Br J Haematol. 2005;131:129-134.
    • (2005) Br J Haematol , vol.131 , pp. 129-134
    • Quinn, C.T.1    Ahmad, N.2


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