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Volumn 37, Issue 3, 2015, Pages 150-152

The compound state: Hb S/beta-thalassemia

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN A2;

EID: 84930090789     PISSN: 15168484     EISSN: 18060870     Source Type: Journal    
DOI: 10.1016/j.bjhh.2015.02.008     Document Type: Note
Times cited : (20)

References (16)
  • 1
    • 84856279998 scopus 로고    scopus 로고
    • Biomarkers in sickle cell disease
    • Rees D.C., Gibson J.S. Biomarkers in sickle cell disease. Br J Haematol 2012, 156(4):433-445.
    • (2012) Br J Haematol , vol.156 , Issue.4 , pp. 433-445
    • Rees, D.C.1    Gibson, J.S.2
  • 2
    • 5044239523 scopus 로고    scopus 로고
    • Sickle-cell disease
    • Stuart M.J., Nagel R.L. Sickle-cell disease. Lancet 2004, 364(9442):1343-1360.
    • (2004) Lancet , vol.364 , Issue.9442 , pp. 1343-1360
    • Stuart, M.J.1    Nagel, R.L.2
  • 4
    • 81055147553 scopus 로고    scopus 로고
    • Genetic modifiers of sickle cell disease
    • Thein S.L. Genetic modifiers of sickle cell disease. Hemoglobin 2011, 35(5-6):589-606.
    • (2011) Hemoglobin , vol.35 , Issue.5-6 , pp. 589-606
    • Thein, S.L.1
  • 5
    • 0001719775 scopus 로고    scopus 로고
    • Compound heterozygous and other sickle hemoglobinopathies
    • Cambridge University Press, Cambridge, UK, M.H. Steinberg, B.G. Forget, D.R. Higgs, R.L. Nagel (Eds.)
    • Steinberg M.H. Compound heterozygous and other sickle hemoglobinopathies. Disorders of hemoglobin: genetics, pathophysiology, and clinical management 2001, 786-810. Cambridge University Press, Cambridge, UK. 1st ed. M.H. Steinberg, B.G. Forget, D.R. Higgs, R.L. Nagel (Eds.).
    • (2001) Disorders of hemoglobin: genetics, pathophysiology, and clinical management , pp. 786-810
    • Steinberg, M.H.1
  • 6
    • 84878982472 scopus 로고    scopus 로고
    • Classification of the disorders of hemoglobin
    • Forget B.G., Bunn H.F. Classification of the disorders of hemoglobin. Cold Spring Harb Perspect Med 2013, 3(2):a011684.
    • (2013) Cold Spring Harb Perspect Med , vol.3 , Issue.2 , pp. a011684
    • Forget, B.G.1    Bunn, H.F.2
  • 7
    • 0035096303 scopus 로고    scopus 로고
    • Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemia
    • Rigano P., Rodgers G.P., Renda D., Renda M.C., Aquino A., Maggio A. Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemia. Hemoglobin 2001, 25(1):9-17.
    • (2001) Hemoglobin , vol.25 , Issue.1 , pp. 9-17
    • Rigano, P.1    Rodgers, G.P.2    Renda, D.3    Renda, M.C.4    Aquino, A.5    Maggio, A.6
  • 8
    • 45849104274 scopus 로고    scopus 로고
    • The Hb S/beta+-thalassemia phenotype demonstrates that the IVS-I (-2) (A>C) mutation is a mild beta-thalassemia allele
    • Schmugge M., Waye J.S., Basran R.K., Zurbriggen K., Frischknecht H. The Hb S/beta+-thalassemia phenotype demonstrates that the IVS-I (-2) (A>C) mutation is a mild beta-thalassemia allele. Hemoglobin 2008, 32(3):303-307.
    • (2008) Hemoglobin , vol.32 , Issue.3 , pp. 303-307
    • Schmugge, M.1    Waye, J.S.2    Basran, R.K.3    Zurbriggen, K.4    Frischknecht, H.5
  • 9
    • 0345327621 scopus 로고    scopus 로고
    • Mild Hb S-beta(+)-thalassemia with a deletion of five nucleotides at the polyadenylation site of the beta-globin gene
    • Lacan P., Ponceau B., Aubry M., Francina A. Mild Hb S-beta(+)-thalassemia with a deletion of five nucleotides at the polyadenylation site of the beta-globin gene. Hemoglobin 2003, 27(4):257-259.
    • (2003) Hemoglobin , vol.27 , Issue.4 , pp. 257-259
    • Lacan, P.1    Ponceau, B.2    Aubry, M.3    Francina, A.4
  • 10
    • 0028098232 scopus 로고
    • Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations
    • Boletini E., Svobodova M., Divoky V., Baysal E., Curuk M.A., Dimovski A.J., et al. Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations. Hum Genet 1994, 93(2):182-187.
    • (1994) Hum Genet , vol.93 , Issue.2 , pp. 182-187
    • Boletini, E.1    Svobodova, M.2    Divoky, V.3    Baysal, E.4    Curuk, M.A.5    Dimovski, A.J.6
  • 12
    • 0027474960 scopus 로고
    • A mild type of Hb S-beta(+)-thalassemia [-92(C→T)] in a Sicilian family
    • Divoky V., Baysal E., Schiliro G., Dibenedetto S.P., Huisman T.H. A mild type of Hb S-beta(+)-thalassemia [-92(C→T)] in a Sicilian family. Am J Hematol 1993, 42(2):225-226.
    • (1993) Am J Hematol , vol.42 , Issue.2 , pp. 225-226
    • Divoky, V.1    Baysal, E.2    Schiliro, G.3    Dibenedetto, S.P.4    Huisman, T.H.5
  • 13
    • 0000650711 scopus 로고
    • Compound heterozygous states
    • Raven Press Ltd., New York, S.H. Embury, R.P. Hebbel, N. Mohandas, M.H. Steinberg (Eds.)
    • Kinney T.R., Ware R.E. Compound heterozygous states. Sickle cell disease: basic principles and clinical practice 1994, 437-451. Raven Press Ltd., New York. 1st ed. S.H. Embury, R.P. Hebbel, N. Mohandas, M.H. Steinberg (Eds.).
    • (1994) Sickle cell disease: basic principles and clinical practice , pp. 437-451
    • Kinney, T.R.1    Ware, R.E.2
  • 15
    • 84878959132 scopus 로고    scopus 로고
    • The natural history of sickle cell disease
    • Serjeant G.R. The natural history of sickle cell disease. Cold Spring Harb Perspect Med 2013, 3(10):a011783.
    • (2013) Cold Spring Harb Perspect Med , vol.3 , Issue.10 , pp. a011783
    • Serjeant, G.R.1
  • 16
    • 84930085319 scopus 로고    scopus 로고
    • Very mild forms of Hb S/beta+-thalassemia in Brazilian children
    • Belisario A.R., Sales R.R., Viana M.B. Very mild forms of Hb S/beta+-thalassemia in Brazilian children. Rev Bras Hematol Hemoter 2015, 37(3):198-201.
    • (2015) Rev Bras Hematol Hemoter , vol.37 , Issue.3 , pp. 198-201
    • Belisario, A.R.1    Sales, R.R.2    Viana, M.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.