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Volumn 88, Issue 2, 2009, Pages 179-180

Erythropoietin for hemoglobin H disease

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; HEMOGLOBIN A; HEMOGLOBIN A2; NOVEL ERYTHROPOIESIS STIMULATING PROTEIN; RECOMBINANT ERYTHROPOIETIN;

EID: 58149092124     PISSN: 09395555     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00277-008-0556-y     Document Type: Letter
Times cited : (2)

References (11)
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    • Dozy AM, Kan YW, Embury SH, Mentzer WC, Wang WC (1979) a-Globin gene organization in blacks precludes the severe form of a-thalassemia. Nature 280(5723):605-607 doi: 10.1038/280605a0
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  • 2
    • 0018902027 scopus 로고
    • Unequal crossing-over: A common basis of single a-globin genes in Asians and American Blacks with Hemoglobin H disease
    • Phillips JA III, Vik TA, Scott AF, Young KE, Kazazian HH Jr, Smith KD et al (1980) Unequal crossing-over: A common basis of single a-globin genes in Asians and American Blacks with Hemoglobin H disease. Blood 55(6):1066-1069
    • (1980) Blood , vol.55 , Issue.6 , pp. 1066-1069
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  • 3
    • 0037305250 scopus 로고    scopus 로고
    • Hemoglobin H disease: Not necessarily a benign disorder
    • doi: 10.1182/blood-2002-07-1975
    • Chui DH, Fucharoen S, Chan V (2003) Hemoglobin H disease: Not necessarily a benign disorder. Blood 101(3):791-800 doi: 10.1182/ blood-2002-07-1975
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    • Chui, D.H.1    Fucharoen, S.2    Chan, V.3
  • 5
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    • Common a-thalassemia deletions in transfusion-dependent thalassemia patients in the Southeast Asia region of Myanmar
    • doi: 10.1532/LH96.06017
    • Ne-Win, Harano K, Harano T, Thein-Thein-Myint, Rai-Mra, Aye-Aye-Myint, Shimono K, Okada S (2006) Common a-thalassemia deletions in transfusion-dependent thalassemia patients in the Southeast Asia region of Myanmar. Lab Hematol 12(3):139-142 doi: 10.1532/LH96.06017
    • (2006) Lab Hematol , vol.12 , Issue.3 , pp. 139-142
    • Ne-Win1    Harano, K.2    Harano, T.3    Thein-Thein-Myint4    Rai-Mra5    Aye-Aye-Myint6    Shimono, K.7    Okada, S.8
  • 6
    • 33845878540 scopus 로고    scopus 로고
    • Clinical and molecular analysis of hemoglobin H disease in Sardinia: Hematological, obstetric and cardiac aspects in patients with different genotypes
    • doi: 10.1111/j.1365-2141.2006.06423.x
    • Origa R, Sollaino MC, Giagu N, Barella S, Campus S, Mandas C et al (2007) Clinical and molecular analysis of hemoglobin H disease in Sardinia: Hematological, obstetric and cardiac aspects in patients with different genotypes. Br J Haematol 136(2):326-332 doi: 10.1111/ j.1365-2141.2006.06423.x
    • (2007) Br J Haematol , vol.136 , Issue.2 , pp. 326-332
    • Origa, R.1    Sollaino, M.C.2    Giagu, N.3    Barella, S.4    Campus, S.5    Mandas, C.6
  • 8
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    • Erythropoietin dose requirement in a patient with HbH disease and renal failure
    • Winearls CG, Hughes RT, Pippard MJ, Cotes PM (1992) Erythropoietin dose requirement in a patient with HbH disease and renal failure. Nephrol Dial Transplant 7(10):1052-1054
    • (1992) Nephrol Dial Transplant , vol.7 , Issue.10 , pp. 1052-1054
    • Winearls, C.G.1    Hughes, R.T.2    Pippard, M.J.3    Cotes, P.M.4
  • 9
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    • Treatment of b-thalassemia patients with recombinant human erythropoietin: Effect on transfusion requirements and soluble adhesion molecules
    • doi: 10.1159/000077551
    • Chaidos A, Makis A, Hatzimichael E, Tsiara S, Gouva M, Tzouvara E et al (2004) Treatment of b-thalassemia patients with recombinant human erythropoietin: Effect on transfusion requirements and soluble adhesion molecules. Acta Haematol 111(4):189-195 doi: 10.1159/000077551
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  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.