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1041 related items for PubMed ID: 20299254

  • 1. Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters.
    Charoenkwan P, Taweephol R, Sirichotiyakul S, Tantiprabha W, Sae-Tung R, Suanta S, Sakdasirisathaporn P, Sanguansermsri T.
    Blood Cells Mol Dis; 2010 Jun 15; 45(1):53-7. PubMed ID: 20299254
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  • 3. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.
    Tan J, Tay JS, Wong YC, Kham SK, Bte Abd Aziz N, Teo SH, Wong HB.
    Southeast Asian J Trop Med Public Health; 1995 Jun 15; 26 Suppl 1():252-6. PubMed ID: 8629117
    [Abstract] [Full Text] [Related]

  • 4. Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots.
    Jindatanmanusan P, Riolueang S, Glomglao W, Sukontharangsri Y, Chamnanvanakij S, Torcharus K, Viprakasit V.
    Ann Clin Biochem; 2014 Mar 15; 51(Pt 2):237-47. PubMed ID: 23901141
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  • 5. Hb Bart's in cord blood: an accurate indicator of alpha-thalassemia.
    Rugless MJ, Fisher CA, Stephens AD, Amos RJ, Mohammed T, Old JM.
    Hemoglobin; 2006 Mar 15; 30(1):57-62. PubMed ID: 16540417
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  • 7. Molecular and hematologic features of hemoglobin E heterozygotes with different forms of alpha-thalassemia in Thailand.
    Sanchaisuriya K, Fucharoen G, Sae-ung N, Jetsrisuparb A, Fucharoen S.
    Ann Hematol; 2003 Oct 15; 82(10):612-6. PubMed ID: 12955472
    [Abstract] [Full Text] [Related]

  • 8. Prevalence of hemoglobin E, alpha-thalassemia and glucose-6-phosphate dehydrogenase deficiency in 1,000 cord bloods studied in Bangkok.
    Tanphaichitr VS, Mahasandana C, Suvatte V, Yodthong S, Pung-amritt P, Seeloem J.
    Southeast Asian J Trop Med Public Health; 1995 Oct 15; 26 Suppl 1():271-4. PubMed ID: 8629122
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Red cell parameters in alpha-thalassemia with and without beta-thalassemia trait or hemoglobin E trait.
    Jindadamrongwech S, Wisedpanichkij R, Bunyaratvej A, Hathirat P.
    Southeast Asian J Trop Med Public Health; 1997 Jul 15; 28 Suppl 3():97-9. PubMed ID: 9640607
    [Abstract] [Full Text] [Related]

  • 12. Hemoglobin Lepore EF Bart's disease: a molecular, hematological, and diagnostic aspects.
    Chaibunruang A, Fucharoen G, Jetsrisuparb A, Fucharoen S.
    Ann Hematol; 2011 Nov 15; 90(11):1337-40. PubMed ID: 21302111
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  • 13. [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
    [Abstract] [Full Text] [Related]

  • 14. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.
    Fucharoen S, Fucharoen G.
    Hemoglobin; 2012 Oct 15; 36(1):18-24. PubMed ID: 22145566
    [Abstract] [Full Text] [Related]

  • 15. Biophysical changes of red cells with thalassemia-like abnormal hemoglobin.
    Bunyaratvej A, Fucharoen S, Tatsumi N.
    Southeast Asian J Trop Med Public Health; 1992 Oct 15; 23 Suppl 2():86-90. PubMed ID: 1299000
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 85(7):450-4. PubMed ID: 16565831
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  • 17. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients.
    Changtrakun Y, Fucharoen S, Ayukarn K, Siriratmanawong N, Fucharoen G, Sanchaisuriya K.
    Ann Hematol; 2002 Jul 15; 81(7):389-93. PubMed ID: 12185510
    [Abstract] [Full Text] [Related]

  • 18. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct 15; 64(4):1024-32. PubMed ID: 479366
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  • 19. Clinical phenotypes and molecular characterization of Hb H-Paksé disease.
    Viprakasit V, Tanphaichitr VS, Pung-Amritt P, Petrarat S, Suwantol L, Fisher C, Higgs DR.
    Haematologica; 2002 Feb 15; 87(2):117-25. PubMed ID: 11836160
    [Abstract] [Full Text] [Related]

  • 20. Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease.
    Sura T, Busabaratana M, Youngcharoen S, Wisedpanichkij R, Viprakasit V, Trachoo O.
    Eur J Haematol; 2007 Sep 15; 79(3):251-4. PubMed ID: 17655700
    [Abstract] [Full Text] [Related]

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