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276 related items for PubMed ID: 29678852
21. Noninvasive prenatal detection of hemoglobin Bart hydrops fetalis via maternal plasma dispensed with parental haplotyping using the semiconductor sequencing platform. Yang J, Peng CF, Qi Y, Rao XQ, Guo F, Hou Y, He W, Wu J, Chen YY, Zhao X, Wang YN, Peng H, Wang D, Du L, Luo MY, Huang QF, Liu HL, Yin A. Am J Obstet Gynecol; 2020 Feb; 222(2):185.e1-185.e17. PubMed ID: 31394068 [Abstract] [Full Text] [Related]
22. 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]
23. Ten years' experience in prenatal diagnosis of α-thalassemia in a municipal hospital and retrospective analysis of ultrasonic abnormalities. Li H, Wang J, Wang D, Gan Y, Xiong Y. Int J Hematol; 2023 Sep; 118(3):355-363. PubMed ID: 37477864 [Abstract] [Full Text] [Related]
24. 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 Sep; 43(4-5):245-248. PubMed ID: 31687860 [Abstract] [Full Text] [Related]
25. [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; 47(2):85-9. PubMed ID: 22455737 [Abstract] [Full Text] [Related]
26. 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 [Abstract] [Full Text] [Related]
27. 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]
28. Misdiagnosis of Hb Bart's disease: prenatal screening and diagnosis of thalassemia in special population. Gan G, Li Y, Bai J, Jiang M, Zheng L, Li Y. Clin Chem Lab Med; 2023 Sep 26; 61(10):e210-e213. PubMed ID: 37114924 [No Abstract] [Full Text] [Related]
29. Impact of the detection of ζ-globin chains and hemoglobin Bart's using immunochromatographic strip tests for α0-thalassemia (--SEA) differential diagnosis. Pata S, Laopajon W, Pongpaiboon M, Thongkum W, Polpong N, Munkongdee T, Paiboonsukwong K, Fucharoen S, Tayapiwatana C, Kasinrerk W. PLoS One; 2019 Sep 26; 14(10):e0223996. PubMed ID: 31661492 [Abstract] [Full Text] [Related]
30. Prenatal diagnosis of homozygous alpha-thalassemia-1 by cell-free fetal DNA in maternal plasma. Sirichotiyakul S, Charoenkwan P, Sanguansermsri T. Prenat Diagn; 2012 Jan 26; 32(1):45-9. PubMed ID: 22031039 [Abstract] [Full Text] [Related]
31. Detection of alpha-thalassemia-1 Southeast Asian type using real-time gap-PCR with SYBR Green1 and high resolution melting analysis. Pornprasert S, Phusua A, Suanta S, Saetung R, Sanguansermsri T. Eur J Haematol; 2008 Jun 26; 80(6):510-4. PubMed ID: 18284625 [Abstract] [Full Text] [Related]
32. Development and application of a real-time quantitative PCR for prenatal detection of fetal alpha(0)-thalassemia from maternal plasma. Tungwiwat W, Fucharoen S, Fucharoen G, Ratanasiri T, Sanchaisuriya K. Ann N Y Acad Sci; 2006 Sep 26; 1075():103-7. PubMed ID: 17108198 [Abstract] [Full Text] [Related]
33. [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]
34. 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 Jun 28; 80(2):129-132. PubMed ID: 31841045 [Abstract] [Full Text] [Related]
35. [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 28; 74(8):495-7, 520. PubMed ID: 7994662 [Abstract] [Full Text] [Related]
36. Co-inheritance of α0 -thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications. Singha K, Srivorakun H, Fucharoen G, Fucharoen S. Int J Lab Hematol; 2017 Oct 28; 39(5):508-512. PubMed ID: 28497611 [Abstract] [Full Text] [Related]
37. PCR-based analysis of alpha-thalassemia in Southern Taiwan. Chen TP, Liu TC, Chang CS, Chang JG, Tsai HJ, Lin SF. Int J Hematol; 2002 Apr 28; 75(3):277-80. PubMed ID: 11999355 [Abstract] [Full Text] [Related]
38. Amniotic fluid metabolomic and lipidomic alterations associated with hemoglobin Bart's diseases. Chen X, Chen H, Nie H, Li G, Su J, Cao X, Cao Y, Wei F. Metabolomics; 2021 Sep 06; 17(9):82. PubMed ID: 34490587 [Abstract] [Full Text] [Related]
39. 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 Sep 06; 14(2):122-4. PubMed ID: 10085512 [Abstract] [Full Text] [Related]