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418 related items for PubMed ID: 24330258

  • 1. Detection of alpha(0)-thalassemia South-East Asian-type deletion by droplet digital PCR.
    Pornprasert S, Prasing W.
    Eur J Haematol; 2014 Mar; 92(3):244-8. PubMed ID: 24330258
    [Abstract] [Full Text] [Related]

  • 2. Semi-nested Taqman real-time quantitative PCR for noninvasive prenatal diagnosis of Bart's hydrops fetalis.
    Pornprasert S, Sukunthamala K, Kunyanone N, Sittiprasert S, Thungkham K, Junorse S, Pongsawatkul K, Pattanaporn W, Jitwong C.
    J Med Assoc Thai; 2012 Jan; 95(1):6-9. PubMed ID: 22379734
    [Abstract] [Full Text] [Related]

  • 3. Analysis of real-time PCR cycle threshold of alpha-thalassemia-1 Southeast Asian type deletion using fetal cell-free DNA in maternal plasma for noninvasive prenatal diagnosis of Bart's hydrops fetalis.
    Pornprasert S, Sukunthamala K, Kunyanone N, Sittiprasert S, Thungkham K, Junorse S, Pongsawatkul K, Pattanaporn W, Jitwong C, Sanguansermsri T.
    J Med Assoc Thai; 2010 Nov; 93(11):1243-8. PubMed ID: 21114201
    [Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N, Pinmuang-Ngam C, Fucharoen G, Fucharoen S.
    Fetal Diagn Ther; 2007 Nov; 22(4):264-8. PubMed ID: 17369692
    [Abstract] [Full Text] [Related]

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  • 6. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R, Fucharoen G, Fucharoen S, Sae-ung N, Sanchaisuriya K, Ratanasiri T.
    Acta Haematol; 2009 Nov; 121(4):227-33. PubMed ID: 19546525
    [Abstract] [Full Text] [Related]

  • 7. Detection of alpha-thalassemia-1 Southeast Asian type using real-time gap-PCR with SYBR Green1 and high resolution melting analysis.
    Pornprasert S, Phusua A, Suanta S, Saetung R, Sanguansermsri T.
    Eur J Haematol; 2008 Jun; 80(6):510-4. PubMed ID: 18284625
    [Abstract] [Full Text] [Related]

  • 8. Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (- -SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart's Hydrops Fetalis Syndrome in Thailand.
    Jomoui W, Tepakhan W, Karnpean R.
    Hemoglobin; 2019 Jun; 43(4-5):236-240. PubMed ID: 31635494
    [Abstract] [Full Text] [Related]

  • 9. Characterization of Hb Bart's Hydrops Fetalis Caused by - -SEA and a Large Novel α0-Thalassemia Deletion.
    He S, Li J, Huang P, Zhang S, Lin L, Zuo Y, Tian X, Zheng C, Qiu X, Chen B.
    Hemoglobin; 2018 Jan; 42(1):61-64. PubMed ID: 29493331
    [Abstract] [Full Text] [Related]

  • 10. Analysis of real-time SYBR-polymerase chain reaction cycle threshold for diagnosis of the alpha-thalassemia-1 Southeast Asian type deletion: application to carrier screening and prenatal diagnosis of Hb Bart's hydrops fetalis.
    Pornprasert S, Sukunthamala K, Sacome J, Phusua A, Saetung R, Sanguansermsri T, Leechanachai P.
    Hemoglobin; 2008 Jan; 32(4):393-402. PubMed ID: 18654890
    [Abstract] [Full Text] [Related]

  • 11. [Molecular screening and prenatal diagnosis of the deletional alpha-thalassemia by polymerase chain reaction amplification].
    Xu XM, Cai XH, Li J.
    Zhonghua Yi Xue Za Zhi; 1994 Aug; 74(8):495-7, 520. PubMed ID: 7994662
    [Abstract] [Full Text] [Related]

  • 12. Genetic origin of α0-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart's hydrops fetalis syndrome.
    Jomoui W, Fucharoen G, Sanchaisuriya K, Charoenwijitkul P, Maneesarn J, Xu X, Fucharoen S.
    J Hum Genet; 2017 Aug; 62(8):747-754. PubMed ID: 28381876
    [Abstract] [Full Text] [Related]

  • 13. Diagnosis of alpha-thalassemia-1 Southeast Asian type deletion and fetal gender by single-tube multiplex real-time PCR.
    Srithep S, Kongthai K, Pornprasert S.
    Clin Lab; 2013 Aug; 59(1-2):193-7. PubMed ID: 23505926
    [Abstract] [Full Text] [Related]

  • 14. 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; 91(5):649-51. PubMed ID: 16627247
    [Abstract] [Full Text] [Related]

  • 15. Invasive prenatal diagnosis of α-thalassemia to control Hb Bart's hydrops fetalis syndrome: 15 years of experience.
    Lai K, Li S, Lin W, Yang D, Chen W, Li M, Pang L, Chen P.
    Arch Gynecol Obstet; 2018 Aug; 298(2):307-311. PubMed ID: 29948167
    [Abstract] [Full Text] [Related]

  • 16. Detection of α-thalassemia South-East Asian deletion based on a fully integrated digital polymerase chain reaction system DropXpert S6.
    Li Y, Ye J, Liang L, Tan X, Zheng L, Qin T, Yu L.
    Hematology; 2024 Dec; 29(1):2365596. PubMed ID: 38864494
    [Abstract] [Full Text] [Related]

  • 17. Rapid prenatal diagnosis of Hb Bart's hydrops fetalis in southeast Asia area by polymerase chain reaction.
    Chang JG, Chen CP, Ho HJ, Lin CP, Lee LS, Chen PH.
    Int J Hematol; 1992 Oct; 56(2):155-9. PubMed ID: 1421177
    [Abstract] [Full Text] [Related]

  • 18. Development and application of a real-time quantitative PCR for prenatal detection of fetal alpha(0)-thalassemia from maternal plasma.
    Tungwiwat W, Fucharoen S, Fucharoen G, Ratanasiri T, Sanchaisuriya K.
    Ann N Y Acad Sci; 2006 Sep; 1075():103-7. PubMed ID: 17108198
    [Abstract] [Full Text] [Related]

  • 19. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
    [Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis of homozygous alpha-thalassemia-1 by cell-free fetal DNA in maternal plasma.
    Sirichotiyakul S, Charoenkwan P, Sanguansermsri T.
    Prenat Diagn; 2012 Jan; 32(1):45-9. PubMed ID: 22031039
    [Abstract] [Full Text] [Related]

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