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Volumn 2, Issue 8, 2012, Pages

The hemoglobin E thalassemias

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLSALICYLIC ACID; ERYTHROPOIETIN; FERRITIN; HEMOGLOBIN A; HEMOGLOBIN ALPHA CHAIN; HEMOGLOBIN E; HEMOGLOBIN F; HEMOGLOBIN H; HYDROXYUREA; MESSENGER RNA; PHENOBARBITAL; PROTEIN MYB; PYRIMIDINE 5' NUCLEOTIDE NUCLEOSIDASE; 5' NUCLEOTIDASE;

EID: 84886690091     PISSN: None     EISSN: 21571422     Source Type: Journal    
DOI: 10.1101/cshperspect.a011734     Document Type: Article
Times cited : (160)

References (68)
  • 2
    • 0023513146 scopus 로고
    • A study of infective episodes in patients with β-thalassemia/Hb E disease in Thailand
    • Aswapokee N, Aswapokee P, Fucharoen S, Wasi P. 1988a. A study of infective episodes in patients with β-thalassemia/Hb E disease in Thailand. Birth Defects 23: 513-520.
    • (1988) Birth Defects , vol.23 , pp. 513-520
    • Aswapokee, N.1    Aswapokee, P.2    Fucharoen, S.3    Wasi, P.4
  • 5
    • 0036105903 scopus 로고    scopus 로고
    • Increased circulating activated endothelial cells, vascular endothelial growth factor, and tumor necrosis factor in thalassemia
    • Butthep P, Rummavas S, Wisedpanichkij R, Jindadamrongwech S, Fucharoen S, Bunyaratvej A. 2002. Increased circulating activated endothelial cells, vascular endothelial growth factor, and tumor necrosis factor in thalassemia. Am J Hematol 70: 100-106.
    • (2002) Am J Hematol , vol.70 , pp. 100-106
    • Butthep, P.1    Rummavas, S.2    Wisedpanichkij, R.3    Jindadamrongwech, S.4    Fucharoen, S.5    Bunyaratvej, A.6
  • 8
    • 2542545445 scopus 로고
    • Studies on hemoglobin E: I. The clinical, hematologic, and genetic characteristics of the hemoglobin E syndromes
    • Chernoff AI, Minnich V, Na-Nakorn S, Tuchinda S, Kashamsant C, Chernoff RR. 1956. Studies on hemoglobin E: I. The clinical, hematologic, and genetic characteristics of the hemoglobin E syndromes. J Lab Clin Med 47: 490-498.
    • (1956) J Lab Clin Med , vol.47 , pp. 490-498
    • Chernoff, A.I.1    Minnich, V.2    Na-Nakorn, S.3    Tuchinda, S.4    Kashamsant, C.5    Chernoff, R.R.6
  • 10
    • 0016736939 scopus 로고
    • Hemoglobin E, an oxidatively unstable mutation
    • Frischer H, Bowman J. 1975. Hemoglobin E, an oxidatively unstable mutation. J Lab Clin Med 85: 531-539.
    • (1975) J Lab Clin Med , vol.85 , pp. 531-539
    • Frischer, H.1    Bowman, J.2
  • 11
    • 84932638322 scopus 로고    scopus 로고
    • Hemoglobin E disorders
    • In, (ed. Steinberg MH, Forget BG, Higgs DR, Weatherall DJ), Cambridge University Press, Cambridge
    • Fucharoen S, Weatherall DJ. 2009. Hemoglobin E disorders. In Disorders of hemoglobin (ed. Steinberg MH, Forget BG, Higgs DR, Weatherall DJ), pp. 417-433. Cambridge University Press, Cambridge.
    • (2009) Disorders of hemoglobin , pp. 417-433
    • Fucharoen, S.1    Weatherall, D.J.2
  • 12
    • 61849144756 scopus 로고    scopus 로고
    • Prevention and control of thalassemia in Asia
    • Fucharoen S, Winichagoon P. 2007. Prevention and control of thalassemia in Asia. Asian Biomed 1: 1-6.
    • (2007) Asian Biomed , vol.1 , pp. 1-6
    • Fucharoen, S.1    Winichagoon, P.2
  • 14
    • 0023806678 scopus 로고
    • Beta-thalassemia associated with α-thalassemia in Thailand
    • Fucharoen S, Winichagoon P, Thonglairuam V. 1988a. Beta-thalassemia associated with α-thalassemia in Thailand. Hemoglobin 12: 581-592.
    • (1988) Hemoglobin , vol.12 , pp. 581-592
    • Fucharoen, S.1    Winichagoon, P.2    Thonglairuam, V.3
  • 15
    • 0023904470 scopus 로고
    • EF Bart's disease: Interaction of the abnormal α-and β-globin genes
    • Fucharoen S, Winichagoon P, Thonglairuam V, Wasi P. 1988b. EF Bart's disease: Interaction of the abnormal α-and β-globin genes. Eur J Haematol 40: 75-78.
    • (1988) Eur J Haematol , vol.40 , pp. 75-78
    • Fucharoen, S.1    Winichagoon, P.2    Thonglairuam, V.3    Wasi, P.4
  • 18
    • 84866124484 scopus 로고    scopus 로고
    • The molecular basis of α thalassemia
    • doi: 10. 1101/cshperspect a011718
    • Higgs DR. 2012. The molecular basis of α thalassemia. Cold Spring Harb Perspect Med doi: 10. 1101/cshperspect a011718.
    • (2012) Cold Spring Harb Perspect Med
    • Higgs, D.R.1
  • 19
    • 0028339754 scopus 로고
    • Bone marrow transplantation in Thailand
    • Issaragrisil S. 1994. Bone marrow transplantation in Thailand. Bone Marrow Transplant 13: 721-723.
    • (1994) Bone Marrow Transplant , vol.13 , pp. 721-723
    • Issaragrisil, S.1
  • 20
    • 0019481026 scopus 로고
    • Spinal cord compression in thalassemia. Report of 12 cases and recommendations for treatment
    • Issaragrisil S, Piankigagum A, Wasi P. 1981. Spinal cord compression in thalassemia. Report of 12 cases and recommendations for treatment. Arch Intern Med 141: 1033-1036.
    • (1981) Arch Intern Med , vol.141 , pp. 1033-1036
    • Issaragrisil, S.1    Piankigagum, A.2    Wasi, P.3
  • 21
    • 0040982401 scopus 로고
    • Identification of a fourth abnormal human hemoglobin
    • Itano HA, Bergren WR, Sturgeon P. 1954. Identification of a fourth abnormal human hemoglobin. J Am Chem Soc 76: 2278.
    • (1954) J Am Chem Soc , vol.76 , pp. 2278
    • Itano, H.A.1    Bergren, W.R.2    Sturgeon, P.3
  • 22
    • 0025441923 scopus 로고
    • Cardiac involvement in β-thalassemia/hemoglobin E disease: Clinical and hemodynamic findings
    • Jootar P, Fucharoen S. 1990. Cardiac involvement in β-thalassemia/hemoglobin E disease: Clinical and hemodynamic findings. Southeast Asian J Trop Med Public Health 21: 269-273.
    • (1990) Southeast Asian J Trop Med Public Health , vol.21 , pp. 269-273
    • Jootar, P.1    Fucharoen, S.2
  • 23
    • 77955333676 scopus 로고    scopus 로고
    • A cost-utility and budget impact analysis of allogeneic hematopoietic stem cell transplantation for severe thalassemic patients in Thailand
    • Leelahavarong P, Chaikledkaew U, Hongeng S, Kasemsup V, Lubell Y, Teerawattananon Y. 2010. A cost-utility and budget impact analysis of allogeneic hematopoietic stem cell transplantation for severe thalassemic patients in Thailand. BMC Health Serv Res 10: 209.
    • (2010) BMC Health Serv Res , vol.10 , pp. 209
    • Leelahavarong, P.1    Chaikledkaew, U.2    Hongeng, S.3    Kasemsup, V.4    Lubell, Y.5    Teerawattananon, Y.6
  • 26
    • 84877309853 scopus 로고    scopus 로고
    • Pathophysiology and clinical manifestations of the β thalassemias
    • doi: 10. 1101/cshperspect. a011726
    • Nienhuis AW, Nathan DG. 2012. Pathophysiology and clinical manifestations of the β thalassemias. Cold Spring Harb Perspect Med doi: 10. 1101/cshperspect. a011726.
    • (2012) Cold Spring Harb Perspect Med
    • Nienhuis, A.W.1    Nathan, D.G.2
  • 34
    • 0019311766 scopus 로고
    • Increased transferrin iron saturation in splenectomized thalassaemia patients
    • Pootrakul P, Rugkiatsakul R, Wasi P. 1980. Increased transferrin iron saturation in splenectomized thalassaemia patients. Brit J Haematol 46: 143-145.
    • (1980) Brit J Haematol , vol.46 , pp. 143-145
    • Pootrakul, P.1    Rugkiatsakul, R.2    Wasi, P.3
  • 35
    • 0019814079 scopus 로고
    • Serum ferritin levels in thalassemias and the effect of splenectomy
    • Pootrakul P, Vougsmasa V, Laongpanich P, Wasi P. 1981. Serum ferritin levels in thalassemias and the effect of splenectomy. Acta Haematol 66: 244-250.
    • (1981) Acta Haematol , vol.66 , pp. 244-250
    • Pootrakul, P.1    Vougsmasa, V.2    Laongpanich, P.3    Wasi, P.4
  • 37
    • 0038351780 scopus 로고    scopus 로고
    • The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): Hematologic and evolutionary implications
    • Premawardhena A, Fisher CA, Liu YT, Verma IC, de Silva S, Arambepola M, Clegg JB, Weatherall DJ. 2003. The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): Hematologic and evolutionary implications. Blood Cells Mol Dis 31: 98-101.
    • (2003) Blood Cells Mol Dis , vol.31 , pp. 98-101
    • Premawardhena, A.1    Fisher, C.A.2    Liu, Y.T.3    Verma, I.C.4    de Silva, S.5    Arambepola, M.6    Clegg, J.B.7    Weatherall, D.J.8
  • 40
    • 0032530271 scopus 로고    scopus 로고
    • Is hemoglobin instability important in the interaction between hemoglobin E and β thalassemia?
    • Rees DC, Clegg JB, Weatherall DJ. 1998. Is hemoglobin instability important in the interaction between hemoglobin E and β thalassemia? Blood 92: 2141-2146.
    • (1998) Blood , vol.92 , pp. 2141-2146
    • Rees, D.C.1    Clegg, J.B.2    Weatherall, D.J.3
  • 42
    • 84878411727 scopus 로고    scopus 로고
    • The switch from fetal to adult hemoglobin
    • doi: 10. 1101/cshperspect. a011643
    • Sankaran VG, Orkin SH. 2012. The switch from fetal to adult hemoglobin. Cold Spring Harb Perspect Med doi: 10. 1101/cshperspect. a011643.
    • (2012) Cold Spring Harb Perspect Med
    • Sankaran, V.G.1    Orkin, S.H.2
  • 46
    • 0023780965 scopus 로고
    • Pathologic findings in 76 autopsy cases of thalassemia
    • Sonakul D, Pacharee P, Thakerngpol K. 1988. Pathologic findings in 76 autopsy cases of thalassemia. Birth Defects 23: 157-176.
    • (1988) Birth Defects , vol.23 , pp. 157-176
    • Sonakul, D.1    Pacharee, P.2    Thakerngpol, K.3
  • 49
    • 84878995335 scopus 로고    scopus 로고
    • Molecular basis of β thalassemia
    • doi: 10. 1101/cshperspect a011700
    • Thein SL. 2012. Molecular basis of β thalassemia. Cold Spring Harb Perspect Med doi: 10. 1101/cshperspect a011700.
    • (2012) Cold Spring Harb Perspect Med
    • Thein, S.L.1
  • 52
    • 0019316743 scopus 로고
    • Defective synthesis of Hb E is due to reduced levels of βE mRNA
    • Traeger J, Wood WG, Clegg JB, Weatherall DJ, Wasi P. 1980. Defective synthesis of Hb E is due to reduced levels of βE mRNA. Nature 288: 497-499.
    • (1980) Nature , vol.288 , pp. 497-499
    • Traeger, J.1    Wood, W.G.2    Clegg, J.B.3    Weatherall, D.J.4    Wasi, P.5
  • 53
    • 80051598243 scopus 로고    scopus 로고
    • Molecular analysis of globin gene expression in different thalassaemia disorders: Individual variation of β(E) pre-mRNA splicing determine disease severity
    • Tubsuwan A, Munkongdee T, Jearawiriyapaisarn N, Boonchoy C, WinichagoonP, Fucharoen S, Svasti S. 2011. Molecular analysis of globin gene expression in different thalassaemia disorders: Individual variation of β(E) pre-mRNA splicing determine disease severity. Brit J Haematol 154: 635-643.
    • (2011) Brit J Haematol , vol.154 , pp. 635-643
    • Tubsuwan, A.1    Munkongdee, T.2    Jearawiriyapaisarn, N.3    Boonchoy, C.4    Winichagoon, P.5    Fucharoen, S.6    Svasti, S.7
  • 56
    • 84877102409 scopus 로고    scopus 로고
    • Natural history and clinical manifestations of the α thalassemias
    • doi: 10. 1101/cshperspect. a011742
    • Vichinsky E. 2012. Natural history and clinical manifestations of the α thalassemias. Cold Spring Harb Perspect Med doi: 10. 1101/cshperspect. a011742.
    • (2012) Cold Spring Harb Perspect Med
    • Vichinsky, E.1
  • 60
    • 0018178479 scopus 로고
    • A syndrome of hypertension, convulsions, and cerebral haemorrhage in thalassaemic patients after multiple blood transfusions
    • Wasi P, Na-Nakorn S, Pootrakul P, Sonakul D, Piankijagum A, Pacharee P. 1978. A syndrome of hypertension, convulsions, and cerebral haemorrhage in thalassaemic patients after multiple blood transfusions. Lancet ii: 602-604.
    • (1978) Lancet , vol.2 , pp. 602-604
    • Wasi, P.1    Na-Nakorn, S.2    Pootrakul, P.3    Sonakul, D.4    Piankijagum, A.5    Pacharee, P.6
  • 63
    • 0030733896 scopus 로고    scopus 로고
    • Observations on the relationship between g-globin chain content and globin chain precipitation in thalassaemic erythroblasts and on the composition of erythroblastic inclusions in Hb E/β-thalassaemia
    • Wickramasinghe SN, Lee MJ. 1997. Observations on the relationship between g-globin chain content and globin chain precipitation in thalassaemic erythroblasts and on the composition of erythroblastic inclusions in Hb E/β-thalassaemia. Eur J Haematol 59: 305-309.
    • (1997) Eur J Haematol , vol.59 , pp. 305-309
    • Wickramasinghe, S.N.1    Lee, M.J.2
  • 64
    • 84879287709 scopus 로고    scopus 로고
    • World distribution, population genetics, and health burden of the hemoglobinopathies
    • doi: 10. 1101/cshperspecta011692
    • Williams TN, Weatherall DJ. 2012. World distribution, population genetics, and health burden of the hemoglobinopathies. Cold Spring Harb Perspect Med doi: 10. 1101/cshperspecta011692.
    • (2012) Cold Spring Harb Perspect Med
    • Williams, T.N.1    Weatherall, D.J.2
  • 66
    • 0023192479 scopus 로고
    • Different severity of homozygous β-thalassemia among siblings
    • Winichagoon P, Fucharoen S, Thonglairoam V, Wasi P. 1987. Different severity of homozygous β-thalassemia among siblings. Hum Genet 76: 296-297.
    • (1987) Hum Genet , vol.76 , pp. 296-297
    • Winichagoon, P.1    Fucharoen, S.2    Thonglairoam, V.3    Wasi, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.