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Journal Abstract Search

146 related items for PubMed ID: 15001953

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  • 3. Molecular and hematological profiles of hemoglobin EE disease with different forms of alpha-thalassemia.
    Fucharoen G, Trithipsombat J, Sirithawee S, Yamsri S, Changtrakul Y, Sanchaisuriya K, Fucharoen S.
    Ann Hematol; 2006 Jul; 85(7):450-4. PubMed ID: 16565831
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  • 5. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand.
    Yamsri S, Sanchaisuriya K, Fucharoen G, Sae-Ung N, Fucharoen S.
    Blood Cells Mol Dis; 2011 Aug 15; 47(2):120-4. PubMed ID: 21664157
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  • 6. Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.
    Luo HY, Heeney M, Wang WC, Eung SH, Ware RE, Steinberg MH, Chui DH.
    Am J Hematol; 2006 May 15; 81(5):361-5. PubMed ID: 16628724
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  • 7. Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia.
    Ma ES, Chan AY, Au WY, Yeung YM, Chan LC.
    Haematologica; 2001 Apr 15; 86(4):432-3. PubMed ID: 11325652
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  • 8. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Eur J Haematol; 2009 Jul 15; 83(1):57-65. PubMed ID: 19226360
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  • 13. Molecular and clinical features of Hb H disease in northern Thailand.
    Charoenkwan P, Taweephon R, Sae-Tung R, Thanarattanakorn P, Sanguansermsri T.
    Hemoglobin; 2005 Jul 15; 29(2):133-40. PubMed ID: 15921165
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  • 15. [Alpha 2 codon 30 deletion (deltaGAG) causing non-deletional hemoglobin H disease in Guangxi province].
    Chen P, Li SQ, Wu H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct 15; 21(5):435-9. PubMed ID: 15476164
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  • 16. High frequency of deletional alpha-thalassemia in beta-thalassemia trait: implications for genetic counseling.
    Panigrahi I, Rafeeq PH, Choudhry VP, Saxena R.
    Am J Hematol; 2004 Jul 15; 76(3):297-9. PubMed ID: 15224373
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  • 17. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis.
    Fucharoen S, Fucharoen G, Sae-ung N, Sanchaisuriya K.
    Blood Cells Mol Dis; 2007 Jul 15; 39(2):195-8. PubMed ID: 17587614
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  • 18. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
    Li D, Liao C, Li J, Xie X, Huang Y, Zhong H.
    Haematologica; 2006 May 15; 91(5):649-51. PubMed ID: 16627247
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  • 20. The prevalence and molecular basis of hemoglobinopathies in Cambodia.
    Carnley BP, Prior JF, Gilbert A, Lim E, Devenish R, Sing H, Sarin E, Guhadasan R, Sullivan SG, Wise CA, Bittles AH, Chan K, Wong MS, Chan V, Erber WN.
    Hemoglobin; 2006 May 15; 30(4):463-70. PubMed ID: 16987801
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