These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

308 related items for PubMed ID: 25116001

  • 1. Treatment of alpha(0)-thalassemia (--(SEA)/--(SEA)) via serial fetal and post-natal transfusions: Can early fetal intervention improve outcomes?
    Chmait RH, Baskin JL, Carson S, Randolph LM, Hamilton A.
    Hematology; 2015 May; 20(4):217-22. PubMed ID: 25116001
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Alpha thalassemia major--new mutations, intrauterine management, and outcomes.
    Vichinsky EP.
    Hematology Am Soc Hematol Educ Program; 2009 Jan; ():35-41. PubMed ID: 20008180
    [Abstract] [Full Text] [Related]

  • 4. Early onset of fetal hydrops associated with the α-thalassemia - -(THAI) deletion.
    Yang Y, Li DZ.
    Hemoglobin; 2014 Jan; 38(6):431-4. PubMed ID: 25370866
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Homozygous alpha-thalassemia treated with intrauterine transfusions and unrelated donor hematopoietic cell transplantation.
    Yi JS, Moertel CL, Baker KS.
    J Pediatr; 2009 May; 154(5):766-8. PubMed ID: 19364562
    [Abstract] [Full Text] [Related]

  • 7. 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]

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

  • 9. [Prenatal diagnosis of Thailand deletion of alpha-thalassemia 1].
    Chen P, Li SQ, Li MQ, Pang LH, Lin WX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):247-50. PubMed ID: 17557230
    [Abstract] [Full Text] [Related]

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

  • 11. 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]

  • 12. 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]

  • 13. 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]

  • 14. Prevention of Hb Bart's (γ4) Disease Associated with the - -(THAI) α(0)-Thalassemia Deletion in Mainland China.
    Li DZ, Li Y, Li J, Li SC, Li R.
    Hemoglobin; 2015 Feb 10; 39(6):412-4. PubMed ID: 26212676
    [Abstract] [Full Text] [Related]

  • 15. 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 10; 83(1):57-65. PubMed ID: 19226360
    [Abstract] [Full Text] [Related]

  • 16. [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 10; 47(2):85-9. PubMed ID: 22455737
    [Abstract] [Full Text] [Related]

  • 17. An increase of the cardiothoracic ratio leads to a diagnosis of Bart's hydrops.
    Phupong V.
    J Med Assoc Thai; 2006 Apr 10; 89(4):509-12. PubMed ID: 16696397
    [Abstract] [Full Text] [Related]

  • 18. Carrier screening and prenatal diagnosis for alpha-thalassemia with biphasic polymerase chain reaction.
    Kuo PL, Lin TM, Huang KF, Yeh NG, Wu DB, Wu RC, Tzeng CC, Wu HL, Huang KE.
    J Formos Med Assoc; 1994 Sep 10; 93(9):765-9. PubMed ID: 7735005
    [Abstract] [Full Text] [Related]

  • 19. 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 10; 32(1):180-5. PubMed ID: 11485083
    [Abstract] [Full Text] [Related]

  • 20. Antenatal diagnosis of Bart's hydrops fetalis [correction of homozygous alpha thalassemia]. A case report.
    Doridot V, Sibony O, Luton D, Reyal F, Feraud O, Multon O, Oury JF, Blot P.
    Fetal Diagn Ther; 1999 Mar 10; 14(2):122-4. PubMed ID: 10085512
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.