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Volumn 87, Issue 3, 1996, Pages 887-892

Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in β-thalassemia/hemoglobin E disease

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; BETA GLOBIN; GAMMA GLOBIN; HEMOGLOBIN E; HEMOGLOBIN F; HYDROXYUREA;

EID: 13344259315     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v87.3.887.bloodjournal873887     Document Type: Article
Times cited : (127)

References (31)
  • 2
    • 0023112573 scopus 로고
    • Hemoglobinopathies in Southeast Asia
    • Fucharoen S, Winichagoon P: Hemoglobinopathies in Southeast Asia. Hemoglobin 11:65, 1989
    • (1989) Hemoglobin , vol.11 , pp. 65
    • Fucharoen, S.1    Winichagoon, P.2
  • 3
    • 0021137630 scopus 로고
    • Determination for different severity of anemia in thalassemia: Concordance and discordance among sib pairs
    • Fucharoen S, Winichagoon P, Pootrakul P, Wasi P: Determination for different severity of anemia in thalassemia: Concordance and discordance among sib pairs. Am J Med Genet 19:39, 1984
    • (1984) Am J Med Genet , vol.19 , pp. 39
    • Fucharoen, S.1    Winichagoon, P.2    Pootrakul, P.3    Wasi, P.4
  • 9
    • 0017880649 scopus 로고
    • Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects
    • Perrine RP, Pembrey ME, John P, Perrine S, Shoup F: Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects. Ann Intern Med 88:1, 1978
    • (1978) Ann Intern Med , vol.88 , pp. 1
    • Perrine, R.P.1    Pembrey, M.E.2    John, P.3    Perrine, S.4    Shoup, F.5
  • 10
    • 0025865223 scopus 로고
    • The pharmacology of hemoglobin switching of mice and men
    • Ley TJ: The pharmacology of hemoglobin switching of mice and men. Blood 77:1146, 1991
    • (1991) Blood , vol.77 , pp. 1146
    • Ley, T.J.1
  • 11
    • 0026749629 scopus 로고
    • Therapeutic approaches to hemoglobin switching in treatment of hemoglobinopathies
    • Stamatoyannopoulos JA, Neinhuis AW: Therapeutic approaches to hemoglobin switching in treatment of hemoglobinopathies. Annu Rev Med 43:497, 1992
    • (1992) Annu Rev Med , vol.43 , pp. 497
    • Stamatoyannopoulos, J.A.1    Neinhuis, A.W.2
  • 12
    • 0001941949 scopus 로고
    • Pharmacological modulation of fetal hemoglobin
    • Embury SH, Hebbel RP, Mohandas N, Steinberg MH (eds): New York, NY, Raven
    • Rodgers GP: Pharmacological modulation of fetal hemoglobin, in Embury SH, Hebbel RP, Mohandas N, Steinberg MH (eds): Sickle Cell Disease: Basic Principles and Clinical Practice. New York, NY, Raven, 1994, p 829
    • (1994) Sickle Cell Disease: Basic Principles and Clinical Practice , pp. 829
    • Rodgers, G.P.1
  • 15
    • 0028956292 scopus 로고
    • Clinical and laboratory effects of long-term administration of hydroxyurea to patients with sickle cell/β-thalassemia
    • Voskandou E, Kalotychou V, Loukopoulos D: Clinical and laboratory effects of long-term administration of hydroxyurea to patients with sickle cell/β-thalassemia. Br J Haematol 89:479, 1995
    • (1995) Br J Haematol , vol.89 , pp. 479
    • Voskandou, E.1    Kalotychou, V.2    Loukopoulos, D.3
  • 16
    • 0013813244 scopus 로고
    • Rapid electrophoresis and quantitation of hemoglobins on cellulose acetate
    • Marengo-Row AJ: Rapid electrophoresis and quantitation of hemoglobins on cellulose acetate. J Clin Pathol 18:790, 1965
    • (1965) J Clin Pathol , vol.18 , pp. 790
    • Marengo-Row, A.J.1
  • 18
    • 13344284163 scopus 로고
    • Structure, function, genetics and biosynthesis of hemoglobin
    • Weatherall DJ, Clegg JB (eds): Oxford, UK, Blackwell Scientific
    • Weatherall DJ, Clegg JB: Structure, function, genetics and biosynthesis of hemoglobin, in Weatherall DJ, Clegg JB (eds): The Thalassemia Syndromes. Oxford, UK, Blackwell Scientific, 1981, p 19
    • (1981) The Thalassemia Syndromes , pp. 19
    • Weatherall, D.J.1    Clegg, J.B.2
  • 21
    • 2442574561 scopus 로고
    • Resistance of hemoglobin Bart's to acid elution
    • Sanguantsermsri T: Resistance of hemoglobin Bart's to acid elution. J Med Assoc Thai 61:62, 1978
    • (1978) J Med Assoc Thai , vol.61 , pp. 62
    • Sanguantsermsri, T.1
  • 22
    • 0023484992 scopus 로고
    • Deaths in β-thalassemia/Hb E patients secondary to infections
    • Fucharoen S, Piankijagum A, Wasi P: Deaths in β-thalassemia/Hb E patients secondary to infections. Birth Defects 23:495, 1988
    • (1988) Birth Defects , vol.23 , pp. 495
    • Fucharoen, S.1    Piankijagum, A.2    Wasi, P.3
  • 23
    • 0028120456 scopus 로고
    • Pharmacologic treatment of thalassemia intermedia with hydroxyurea
    • Hajjar FM, Pearson HA: Pharmacologic treatment of thalassemia intermedia with hydroxyurea. J Pediatr 125:490, 1994
    • (1994) J Pediatr , vol.125 , pp. 490
    • Hajjar, F.M.1    Pearson, H.A.2
  • 24
    • 0028313169 scopus 로고
    • Potential alternatives to erythrocyte transfusion in hemoglobinopathies: Hydroxyurea, erythropoietin, butyrate derivatives, blood substitutes
    • Bachir D, Galacteros F: Potential alternatives to erythrocyte transfusion in hemoglobinopathies: Hydroxyurea, erythropoietin, butyrate derivatives, blood substitutes. Transfus Clin Biol 1:35, 1994
    • (1994) Transfus Clin Biol , vol.1 , pp. 35
    • Bachir, D.1    Galacteros, F.2
  • 25
    • 0029037422 scopus 로고
    • Hydroxyurea therapy in beta-thalassemia intermedia: Improvement in hematological parameters due to enhanced beta-globin synthesis
    • Huang SZ, Zeng YT, Lu ZH, Ren ZR, Schechter AN, Rodgers GP: Hydroxyurea therapy in beta-thalassemia intermedia: Improvement in hematological parameters due to enhanced beta-globin synthesis. Br J Haematol 90:557, 1995
    • (1995) Br J Haematol , vol.90 , pp. 557
    • Huang, S.Z.1    Zeng, Y.T.2    Lu, Zh.3    Ren, Z.R.4    Schechter, A.N.5    Rodgers, G.P.6
  • 26
    • 0018227087 scopus 로고
    • Individual variation in the production and survival of F-cells in sickle cell disease
    • Dover GJ, Boyer SH, Charache S, Heintzelman K: Individual variation in the production and survival of F-cells in sickle cell disease. N Engl J Med 299:1428, 1978
    • (1978) N Engl J Med , vol.299 , pp. 1428
    • Dover, G.J.1    Boyer, S.H.2    Charache, S.3    Heintzelman, K.4
  • 27
    • 0023218149 scopus 로고
    • Parvovirus associated aplastic crisis in homozygous sickle cell disease
    • Goldstein AR, Anderson MJ, Serjeant GR: Parvovirus associated aplastic crisis in homozygous sickle cell disease. Arch Dis Child 62:585, 1987
    • (1987) Arch Dis Child , vol.62 , pp. 585
    • Goldstein, A.R.1    Anderson, M.J.2    Serjeant, G.R.3
  • 28
    • 0027078611 scopus 로고
    • A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders
    • Perrine SP, Ginder GD, Faller DV, et al: A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders. N Engl J Med 328:81, 1993
    • (1993) N Engl J Med , vol.328 , pp. 81
    • Perrine, S.P.1    Ginder, G.D.2    Faller, D.V.3
  • 30
    • 0027496417 scopus 로고
    • Enhanced fetal hemoglobin production by phenylacetate and 4-phenylbutyrate in erythroid precursors derived from normal donors and patients with sickle cell anemia and beta-thalassemia
    • Fibach E, Prasanna P, Rodgers GP, Samid D: Enhanced fetal hemoglobin production by phenylacetate and 4-phenylbutyrate in erythroid precursors derived from normal donors and patients with sickle cell anemia and beta-thalassemia. Blood 82:2203, 1993
    • (1993) Blood , vol.82 , pp. 2203
    • Fibach, E.1    Prasanna, P.2    Rodgers, G.P.3    Samid, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.