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Journal Abstract Search

242 related items for PubMed ID: 21114201

  • 1. 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]

  • 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. 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 Jan; 121(4):227-33. PubMed ID: 19546525
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  • 5. 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
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  • 7. 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 Mar; 32(4):393-402. PubMed ID: 18654890
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  • 9. 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 Mar; 43(4-5):236-240. PubMed ID: 31635494
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  • 11. Noninvasive prenatal detection of hemoglobin Bart hydrops fetalis via maternal plasma dispensed with parental haplotyping using the semiconductor sequencing platform.
    Yang J, Peng CF, Qi Y, Rao XQ, Guo F, Hou Y, He W, Wu J, Chen YY, Zhao X, Wang YN, Peng H, Wang D, Du L, Luo MY, Huang QF, Liu HL, Yin A.
    Am J Obstet Gynecol; 2020 Feb; 222(2):185.e1-185.e17. PubMed ID: 31394068
    [Abstract] [Full Text] [Related]

  • 12. Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy.
    Singha K, Yamsri S, Chaibunruang A, Srivorakun H, Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Orphanet J Rare Dis; 2022 Feb 10; 17(1):45. PubMed ID: 35144630
    [Abstract] [Full Text] [Related]

  • 13. 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 10; 62(8):747-754. PubMed ID: 28381876
    [Abstract] [Full Text] [Related]

  • 14. [Prenatal diagnosis of Thailand deletion of α-thalassemia 1 families].
    Lin N, Lin Y, Huang HL, Lin XL, He DQ, He SQ, Guo DH, Li Y, Xu LP.
    Zhonghua Yi Xue Za Zhi; 2016 Jun 28; 96(24):1919-22. PubMed ID: 27373361
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of Hb Bart's hydrops fetalis by PCR technique: Pramongkutklao experience.
    Torcharus K, Sriphaisal T, Krutvecho T, Ketupanya A, Vuthiwong C, Suwanasophon C, Noonai A.
    Southeast Asian J Trop Med Public Health; 1995 Jun 28; 26 Suppl 1():287-90. PubMed ID: 8629126
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  • 16. An increase of the cardiothoracic ratio leads to a diagnosis of Bart's hydrops.
    Phupong V.
    J Med Assoc Thai; 2006 Apr 28; 89(4):509-12. PubMed ID: 16696397
    [Abstract] [Full Text] [Related]

  • 17. Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -SEA/) Deletion.
    Yang X, Yan JM, Li J, Xie XM, Zhou JY, Li Y, Li DZ.
    Hemoglobin; 2016 Sep 28; 40(5):353-355. PubMed ID: 27686733
    [Abstract] [Full Text] [Related]

  • 18. Characterization and identification of Hb Bart's hydrops fetalis caused by a compound heterozygous mutation --SEA /--CR , a novel α0 -thalassemia deletion.
    Ruengdit C, Panyasai S, Kunyanone N, Phornsiricharoenphant W, Ngamphiw C, Tongsima S, Sripichai O, Pissard S, Pornprasert S.
    Int J Lab Hematol; 2020 Jun 28; 42(3):e116-e120. PubMed ID: 31943793
    [No Abstract] [Full Text] [Related]

  • 19. 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 28; 56(2):155-9. PubMed ID: 1421177
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  • 20. Noninvasive prenatal diagnosis for hemoglobin Bart's hydrops fetalis.
    Winichagoon P, Sithongdee S, Kanokpongsakdi S, Tantisirin P, Bernini LF, Fucharoen S.
    Int J Hematol; 2005 Jun 28; 81(5):396-9. PubMed ID: 16158819
    [Abstract] [Full Text] [Related]

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