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158 related items for PubMed ID: 18654890

  • 1. 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; 32(4):393-402. PubMed ID: 18654890
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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 Nov; 43(4-5):236-240. PubMed ID: 31635494
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR.
    Wang W, Yap CH, Loh SF, Tan AS, Lim MN, Prasath EB, Chan ML, Tan WC, Jiang B, Yeo GH, Mathew J, Ho A, Ho SS, Wong PC, Choolani MA, Chong SS.
    Reprod Biomed Online; 2010 Nov; 21(5):642-8. PubMed ID: 20864413
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 Mar; 22(4):264-8. PubMed ID: 17369692
    [Abstract] [Full Text] [Related]

  • 8. 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 Mar; 121(4):227-33. PubMed ID: 19546525
    [Abstract] [Full Text] [Related]

  • 9. Analysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart's on Capillary Electrophoresis.
    Khongthai K, Ruengdit C, Panyasai S, Pornprasert S.
    Hemoglobin; 2019 Mar; 43(4-5):245-248. PubMed ID: 31687860
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Rapid diagnosis of the alpha-thalassemia-1 Southeast Asian type deletion using a single tube real-time SYBR-polymerase chain reaction combined with dissociation curve analysis.
    Liu JZ, Xiao B, Wang QT, Wang LR.
    Hemoglobin; 2009 Aug; 33(6):546-9. PubMed ID: 19958205
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. 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]

  • 14. 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]

  • 15. Prenatal diagnosis of hemoglobin Bart's hydrops fetalis by HPLC analysis of hemoglobin in fetal blood samples.
    Sanguansermsri T, Thanaratanakorn P, Steger HF, Tongsong T, Sirivatanapa P, Wanapirak C, Sirichotiyakul S, Chanprapas P, Flatz G.
    Southeast Asian J Trop Med Public Health; 2001 Mar; 32(1):180-5. PubMed ID: 11485083
    [Abstract] [Full Text] [Related]

  • 16. 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; 40(5):353-355. PubMed ID: 27686733
    [Abstract] [Full Text] [Related]

  • 17. Whole Blood PCR for Rapid Screening of α0-Thalassemia.
    Wichian P, Yamsri S, Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Ann Clin Lab Sci; 2018 Mar; 48(2):231-235. PubMed ID: 29678852
    [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; 42(3):e116-e120. PubMed ID: 31943793
    [No Abstract] [Full Text] [Related]

  • 19. 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; 26 Suppl 1():287-90. PubMed ID: 8629126
    [Abstract] [Full Text] [Related]

  • 20. Hb Bart's Hydrops Fetalis Syndrome and Hb H Disease Caused by Deletional Chiang Rai (- -CR) α0-Thalassemia in Two Unrelated Thai Families.
    Ruengdit C, Khamphikham P, Jinorose N, Pornprasert S.
    Hemoglobin; 2021 Mar; 45(2):75-79. PubMed ID: 33821735
    [Abstract] [Full Text] [Related]

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