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

231 related items for PubMed ID: 24051347

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. 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; 26 Suppl 1():287-90. PubMed ID: 8629126
    [Abstract] [Full Text] [Related]

  • 23. Inferior vena cava Doppler indices in fetuses with hemoglobin Bart's hydrops fetalis.
    Luewan S, Tongprasert F, Srisupundit K, Tongsong T.
    Prenat Diagn; 2014 Jun; 34(6):577-80. PubMed ID: 24609794
    [Abstract] [Full Text] [Related]

  • 24. [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]

  • 25. An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations.
    Lee HH, Mak AS, Kou KO, Poon CF, Wong WS, Chiu KH, Au PK, Chan KY, Kan AS, Tang MH, Leung KY.
    Hemoglobin; 2016 Nov 28; 40(6):431-434. PubMed ID: 28361594
    [Abstract] [Full Text] [Related]

  • 26. Early onset of fetal hydrops associated with the α-thalassemia - -(THAI) deletion.
    Yang Y, Li DZ.
    Hemoglobin; 2014 Nov 28; 38(6):431-4. PubMed ID: 25370866
    [Abstract] [Full Text] [Related]

  • 27. Ventricular Diastolic Function in Normal Fetuses and Fetuses with Hb Bart's Disease Assessed by Color M-Mode Propagation Velocity using Cardio-STIC-M (Spatio-Temporal Image Correlation M-Mode).
    Tongsong T, Tongprasert F, Srisupundit K, Luewan S, Traisrisilp K.
    Ultraschall Med; 2016 Oct 28; 37(5):492-496. PubMed ID: 26529356
    [Abstract] [Full Text] [Related]

  • 28. Fetal myocardial performance (Tei) index in fetal hemoglobin Bart's disease.
    Luewan S, Tongprasert F, Srisupundit K, Tongsong T.
    Ultraschall Med; 2013 Aug 28; 34(4):355-8. PubMed ID: 23386484
    [Abstract] [Full Text] [Related]

  • 29. Hydrops fetalis caused by severe alpha-thalassemia.
    Hsieh FJ, Ko TM, Chen HY.
    Early Hum Dev; 1992 Aug 28; 29(1-3):233-6. PubMed ID: 1396245
    [Abstract] [Full Text] [Related]

  • 30. Prenatal diagnosis of hemoglobin Bart's disease caused by co-inheritance of two different alpha 0-thalassemia defects in China.
    Li DZ, Li J, Liao C.
    Prenat Diagn; 2009 Jun 28; 29(6):632-3. PubMed ID: 19294754
    [No Abstract] [Full Text] [Related]

  • 31. 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 28; 91(5):649-51. PubMed ID: 16627247
    [Abstract] [Full Text] [Related]

  • 32. 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 May 28; 43(4-5):236-240. PubMed ID: 31635494
    [Abstract] [Full Text] [Related]

  • 33. Detection of alpha(0)-thalassemia South-East Asian-type deletion by droplet digital PCR.
    Pornprasert S, Prasing W.
    Eur J Haematol; 2014 Mar 28; 92(3):244-8. PubMed ID: 24330258
    [Abstract] [Full Text] [Related]

  • 34. 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]

  • 35. Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome.
    Chen M, Chan JK, Nadarajah S, Tan AS, Chan ML, Mathew J, Saw EE, Lim C, Wong W, Cheah FS, Law HY, Wong PC, Chong SS.
    Prenat Diagn; 2015 Jun 28; 35(6):534-43. PubMed ID: 25641621
    [Abstract] [Full Text] [Related]

  • 36. Prenatal diagnosis of haemoglobin Bart's disease by cordocentesis at 12-14 weeks' gestation.
    Lam YH, Tang MH.
    Prenat Diagn; 1997 Jun 28; 17(6):501-4. PubMed ID: 9203207
    [Abstract] [Full Text] [Related]

  • 37. 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 28; 32(1):180-5. PubMed ID: 11485083
    [Abstract] [Full Text] [Related]

  • 38. α-Thalassemia with Haemoglobin Adana mutation: prenatal diagnosis.
    Zainal NZ, Alauddin H, Ahmad S, Hussin NH.
    Malays J Pathol; 2014 Dec 28; 36(3):207-11. PubMed ID: 25500521
    [Abstract] [Full Text] [Related]

  • 39. 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 28; 95(1):6-9. PubMed ID: 22379734
    [Abstract] [Full Text] [Related]

  • 40. 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]

    Page: [Previous] [Next] [New Search]
    of 12.