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231 related items for PubMed ID: 24051347

  • 1. Two unusual cases of haemoglobin Bart's hydrops fetalis due to uniparental disomy or non-paternity.
    Kou KO, Lee H, Lau B, Wong WS, Kan A, Tang M, Lau ET, Poon CF, Leung KY.
    Fetal Diagn Ther; 2014; 35(4):306-8. PubMed ID: 24051347
    [Abstract] [Full Text] [Related]

  • 2. A Rare Case of Hemoglobin Bart's Hydrops Fetalis due to Uniparental Disomy of Chromosome 16.
    Tan YR, Tan HK.
    J Med Cases; 2021 Jul; 12(7):275-279. PubMed ID: 34434471
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 4. An increase of the cardiothoracic ratio leads to a diagnosis of Bart's hydrops.
    Phupong V.
    J Med Assoc Thai; 2006 Apr; 89(4):509-12. PubMed ID: 16696397
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  • 6. Electrophoresis features and genotypes of Hb bart's hydrops fetalis.
    Li Y, Liang L, Tian M, Qing T, Wu X.
    Scand J Clin Lab Invest; 2020 Apr; 80(2):129-132. PubMed ID: 31841045
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  • 7. A Fetus with Hb Bart's Disease Due to Maternal Uniparental Disomy for Chromosome 16.
    Au PK, Kan AS, Tang MH, Leung KY, Chan KY, Tang TW, Lau ET.
    Hemoglobin; 2016 Apr; 40(1):66-9. PubMed ID: 26574185
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  • 8. 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 Apr; 22(4):264-8. PubMed ID: 17369692
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  • 9. Prenatal control of Hb Bart's hydrops fetalis: a two-year experience at a mainland Chinese hospital.
    Liao C, Pan M, Han J, Yang X, Zhen L, Li J, Li R, Li DZ.
    J Matern Fetal Neonatal Med; 2015 Mar; 28(4):413-5. PubMed ID: 24766075
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  • 10. Re-emergence of late presentations of fetal haemoglobin Bart's disease in Hong Kong.
    Kwan WY, So CH, Chan WP, Leung WC, Chow KM.
    Hong Kong Med J; 2011 Dec; 17(6):434-40. PubMed ID: 22147311
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  • 11. Maternal uniparental disomy of chromosome 16 resulting in hemoglobin Bart's hydrops fetalis.
    Wattanasirichaigoon D, Promsonthi P, Chuansumrit A, Leopairut J, Yanatatsaneejit P, Rattanatanyong P, Munkongdee T, Fucharoen S, Mutirangura A.
    Clin Genet; 2008 Sep; 74(3):284-7. PubMed ID: 18564363
    [No Abstract] [Full Text] [Related]

  • 12. 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
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  • 13. 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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  • 14. Comparison of red blood cell hematology among normal, alpha-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy.
    Srisupundit K, Piyamongkol W, Tongsong T.
    Am J Hematol; 2008 Dec; 83(12):908-10. PubMed ID: 18932192
    [Abstract] [Full Text] [Related]

  • 15. Characterisation of two unusual cases of haemoglobin Bart's hydrops foetalis caused by -SEA and large novel α-globin gene cluster deletions.
    Wang Y, Xiong Y, Liu C, Lu J, Wang J, Qin D, Liu L, Wu J, Zhao X, Fang L, Du L, Yin A.
    J Int Med Res; 2021 Feb; 49(2):300060521993642. PubMed ID: 33596700
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  • 17. 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]

  • 18. Fetal splenic artery peak velocity (SPA-PSV) at mid-pregnancy as a predictor of Hb Bart's disease.
    Tongsong T, Piyamongkol W, Tongprasert F, Srisupundit K, Luewan S.
    Ultraschall Med; 2011 Jan 10; 32 Suppl 1():S41-5. PubMed ID: 21225551
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