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Journal Abstract Search

1103 related items for PubMed ID: 16627247

  • 1. 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]

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

  • 3. Prevention of beta-thalassemia major and Hb Bart's hydrops fetalis syndrome.
    Beris P, Darbellay R, Extermann P.
    Semin Hematol; 1995 Oct; 32(4):244-61. PubMed ID: 8560282
    [No 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 Oct; 22(4):264-8. PubMed ID: 17369692
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  • 6. 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
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  • 7. Prenatal eradication of Hb Bart's hydrops fetalis.
    Tongsong T, Wanapirak C, Sirivatanapa P, Sa-nguansermsri T, Sirichotiyakul S, Piyamongkol W, Chanprapaph P, Steger HF, Sekararithi R, Tuggapichitti A.
    J Reprod Med; 2001 Jan; 46(1):18-22. PubMed ID: 11209626
    [Abstract] [Full Text] [Related]

  • 8. Co-inheritance of alpha-and beta-thalassemia in Khuzestan Province, Iran.
    Rahim F, Kaikhaei B, Zandian K, Hoseini A.
    Hematology; 2008 Feb; 13(1):59-64. PubMed ID: 18534068
    [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; 83(1):57-65. PubMed ID: 19226360
    [Abstract] [Full Text] [Related]

  • 10. Alpha-thalassaemia prenatal diagnosis by two PCR-based methods.
    Kleanthous M, Kyriacou K, Kyrri A, Kalogerou E, Vassiliades P, Drousiotou A, Kallikas I, Ioannou P, Angastiniotis M.
    Prenat Diagn; 2001 May; 21(5):413-7. PubMed ID: 11360286
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  • 12. [A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province].
    Zhou YQ, Mo QH, Lu JH, Li LY, Liang X, Jia SQ, Xiao GF, Zhou WJ, Xiao QZ, Xu XM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Jun; 25(3):256-61. PubMed ID: 18543211
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  • 14. 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]

  • 15. Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis.
    Chui DH.
    Ann N Y Acad Sci; 2005 Jun; 1054():25-32. PubMed ID: 16339648
    [Abstract] [Full Text] [Related]

  • 16. Beta-thalassemia in association with a new delta-chain hemoglobin variant [delta116(g18)Arg-->Leu]: implications for carrier screening and prenatal diagnosis.
    Waye JS, Patterson M, Walker L, Eng B, Nakamura LM, Lafferty JD, Yong SL, Wu JK, Chui DH.
    Am J Hematol; 2003 Nov; 74(3):179-81. PubMed ID: 14587045
    [Abstract] [Full Text] [Related]

  • 17. [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
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  • 18. 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]

  • 19. Screening for (--SEA) alpha-globin gene deletion in beta-thalassemia carriers and prevention of hydrops fetalis.
    Kwan Ma ES, Yin Chan AY, Yin Ha S, Fung Chan GC, Lung Lau Y, Chan LC.
    Haematologica; 2000 Sep; 85(9):991-3. PubMed ID: 10980643
    [No Abstract] [Full Text] [Related]

  • 20. A multicenter trial of the effectiveness of zeta-globin enzyme-linked immunosorbent assay and hemoglobin H inclusion body screening for the detection of alpha0-thalassemia trait.
    Lafferty JD, Barth DS, Sheridan BL, McFarlane AG, Halchuk LM, Raby A, Crowther MA.
    Am J Clin Pathol; 2008 Feb; 129(2):309-15. PubMed ID: 18208812
    [Abstract] [Full Text] [Related]

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